COMPOUNDS AND MEDICAMENTS USING SAME

Abstract

The present disclosure provides a compound that is useful for the treatment and prophylaxis of rabies. The present disclosure provides a compound represented by formula XXIF or formula XXIB:

Description

TECHNICAL FIELD

The present disclosure relates to a novel fused tricyclic compound that is useful as a medicament, an enantiomer thereof, or a pharmaceutically acceptable salt thereof, or a solvate thereof. More specifically, the present disclosure relates to a pharmaceutical composition comprising the fused tricyclic compound or an enantiomer thereof, or a pharmaceutically acceptable salt thereof, or a solvate thereof. The present disclosure also relates to a therapeutic agent comprising the fused tricyclic compound or an enantiomer thereof, or a pharmaceutically acceptable salt thereof, or a solvate thereof.

BACKGROUND ART

Rabies is an infection induced by a rabies virus. The mortality after the onset in humans is almost 100%. While over 15 million people worldwide are vaccinated postexposure for the prophylaxis of rabies every year, the worldwide number of fatalities due to rabies is about 55000 annually. An effective therapeutic method for rabies still has not been established. There is still a demand for the establishment thereof.

SUMMARY OF INVENTION

Solution to Problem

The present disclosure provides a compound and a method for the treatment of rabies and other diseases.

The present disclosure was completed by the inventors from finding that compounds represented by the following formula IF, IB, IIF, IIB, XXIF, XXIB, XXIIF, or XXIIB and the structural formulas related thereto, or a pharmaceutically acceptable salt thereof (hereinafter, also referred to as “the compound(s) of the present disclosure” or “the present compound(s)”) can achieve the objects as a result of diligent study.

The present disclosure provides the following items.

[Item 1]

A compound represented by formula XXIF:

or an enantiomer thereof, or a salt thereof, or a solvate thereof, wherein

R₁, R₃, and R₄ are each independently hydrogen, an optionally substituted hydrocarbon group, an optionally substituted heterocycle, optionally substituted carbonyl, or an optionally substituted functional group, and

R_2A and R_2B are each independently hydrogen, an optionally substituted hydrocarbon group, an optionally substituted heterocycle, optionally substituted carbonyl, or an optionally substituted functional group, or R_2A and R_2B, together with the nitrogen atom to which they are attached, form a heterocycle, wherein the heterocycles are each independently and optionally substituted.

[Item 1B]

The compound represented by formula XXIF:

or an enantiomer thereof, or a salt thereof, or a solvate thereof according to item 1, wherein

R₁, R₃, and R₄ are each independently hydrogen, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, or optionally substituted carbonyl,

R_2A and R_2B are each independently hydrogen, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, or optionally substituted carbonyl, or R_2A and R_2B, together with the nitrogen atom to which they are attached, form a non-aryl heterocycle or heteroaryl ring, wherein the non-aryl heterocycle and the heteroaryl ring are each independently and optionally substituted.

[Item 2]

A compound represented by formula XXIB:

or an enantiomer thereof, or a salt thereof, or a solvate thereof, wherein

R₁, R₃, and R₄ are each independently hydrogen, an optionally substituted hydrocarbon group, an optionally substituted heterocycle, optionally substituted carbonyl, or an optionally substituted functional group,

R_2A and R_2B are each independently hydrogen, an optionally substituted hydrocarbon group, an optionally substituted heterocycle, optionally substituted carbonyl, or an optionally substituted functional group, or R_2A and R_2B, together with the nitrogen atom to which they are attached, form a heterocycle, wherein the heterocycles are each independently and optionally substituted.

[Item 2B]

The compound represented by formula XXIB:

or an enantiomer thereof, or a salt thereof, or a solvate thereof according to item 2, wherein

R₁, R₃, and R₄ are each independently hydrogen, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, or optionally substituted carbonyl,

R_2A and R_2B are each independently hydrogen, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, or optionally substituted carbonyl, or R_2A and R_2B, together with the nitrogen atom to which they are attached, form a non-aryl heterocycle or heteroaryl ring, wherein the non-aryl heterocycle and the heteroaryl ring are each independently and optionally substituted.

[Item 3]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

the alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, and carbonyl of R₁, R₃, and R₄ are each independently and optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group I, and

the alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, carbonyl, and the non-aryl heterocycle and the heteroaryl ring of R_2A and R_2B are each independently and optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group I.

[Item 4]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁, R₃, and R₄ are each independently hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, or optionally substituted carbonyl, and

R_2A and R_2B are each independently hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, or optionally substituted carbonyl, or R_2A and R_2B, together with the nitrogen atom to which they are attached, form a non-aryl heterocycle or heteroaryl ring, wherein the non-aryl heterocycle and the heteroaryl ring are each independently and optionally substituted.

[Item 4B]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁, R₃, and R₄ are each independently hydrogen, optionally substituted C_1-12 alkyl, optionally substituted C_3-10 cycloalkyl, optionally substituted 5- to 10-membered heterocycloalkyl, optionally substituted C_6-10 aryl, optionally substituted 5- to 10-membered heteroaryl, or optionally substituted carbonyl, and

R_2A and R_2B are each independently hydrogen, optionally substituted C_1-12 alkyl, optionally substituted C_3-10 cycloalkyl, optionally substituted 5- to 10-membered heterocycloalkyl, optionally substituted C_6-10 aryl, optionally substituted 5- to 10-membered heteroaryl, or optionally substituted carbonyl, or R_2A and R_2B, together with the nitrogen atom to which they are attached, form a non-aryl heterocycle or heteroaryl ring, wherein the non-aryl heterocycle and the heteroaryl ring are each independently and optionally substituted.

[Item 5]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁, R₃, and R₄ are each independently hydrogen, optionally substituted alkyl, optionally substituted arylalkyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, formyl, optionally substituted alkylcarbonyl, optionally substituted alkoxycarbonyl, optionally substituted arylcarbonyl, optionally substituted aryloxycarbonyl, optionally substituted heteroarylcarbonyl, optionally substituted heteroaryloxycarbonyl, optionally substituted cycloalkylcarbonyl, optionally substituted cycloalkyloxycarbonyl, optionally substituted heterocycloalkylcarbonyl, optionally substituted heterocycloalkyloxycarbonyl, carbamoyl, optionally substituted alkylcarbamoyl, optionally substituted alkoxycarbamoyl, optionally substituted arylcarbamoyl, optionally substituted heteroarylcarbamoyl, optionally substituted cycloalkylcarbamoyl, or optionally substituted heterocycloalkylcarbamoyl, wherein the groups of R₁, R₃, and R₄ are optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group II, and

R_2A and R_2B are each independently hydrogen, optionally substituted alkyl, optionally substituted arylalkyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, formyl, optionally substituted alkylcarbonyl, optionally substituted alkoxycarbonyl, optionally substituted arylcarbonyl, optionally substituted aryloxycarbonyl, optionally substituted heteroarylcarbonyl, optionally substituted heteroaryloxycarbonyl, optionally substituted cycloalkylcarbonyl, optionally substituted cycloalkyloxycarbonyl, optionally substituted heterocycloalkylcarbonyl, optionally substituted heterocycloalkyloxycarbonyl, carbamoyl, optionally substituted alkylcarbamoyl, optionally substituted alkoxycarbamoyl, optionally substituted arylcarbamoyl, optionally substituted heteroarylcarbamoyl, optionally substituted cycloalkylcarbamoyl, or optionally substituted heterocycloalkylcarbamoyl, wherein the groups of R_2A and R_2B are optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group II, or R_2A and R_2B, together with the nitrogen atom to which they are attached, form a 5- to 6-membered non-aryl heterocycle or heteroaryl ring, wherein the non-aryl heterocycle and the heteroaryl ring are optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group II.

[Item 5B]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁, R₃, and R₄ are each independently hydrogen, optionally substituted C_1-12 alkyl, optionally substituted C_6-10 aryl C_1-12 alkyl, optionally substituted C_3-10cycloalkyl, optionally substituted 5- to 10-membered heterocycloalkyl, formyl, optionally substituted C_1-12 alkylcarbonyl, optionally substituted C_1-12 alkoxycarbonyl, optionally substituted C_6-10 arylcarbonyl, optionally substituted C_6-10 aryloxycarbonyl, optionally substituted 5- to 10-membered heteroarylcarbonyl, optionally substituted 5- to 10-membered heteroaryloxycarbonyl, optionally substituted C_3-10 cycloalkylcarbonyl, optionally substituted C_3-10 cycloalkyloxycarbonyl, optionally substituted 5- to 10-membered heterocycloalkylcarbonyl, optionally substituted 5- to 10-membered heterocycloalkyloxycarbonyl, carbamoyl, optionally substituted C_1-12 alkylcarbamoyl, optionally substituted C_1-12 alkoxycarbamoyl, optionally substituted C_6-10 arylcarbamoyl, optionally substituted 5- to 10-membered heteroarylcarbamoyl, optionally substituted C_3-10 cycloalkylcarbamoyl, or optionally substituted 5- to 10-membered heterocycloalkylcarbamoyl, wherein the groups of R₁, R₃, and R₄ are optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group III, and

R_2A and R_2B are each independently hydrogen, optionally substituted C_1-12 alkyl, optionally substituted C_6-10 aryl C_1-12 alkyl, optionally substituted C_3-10 cycloalkyl, optionally substituted 5- to 10-membered heterocycloalkyl, formyl, optionally substituted C_1-12 alkylcarbonyl, optionally substituted C_1-12 alkoxycarbonyl, optionally substituted C_6-10 arylcarbonyl, optionally substituted C_6-10 aryloxycarbonyl, optionally substituted 5- to 10-membered heteroarylcarbonyl, optionally substituted 5- to 10-membered heteroaryloxycarbonyl, optionally substituted C_3-10 cycloalkylcarbonyl, optionally substituted C_3-10 cycloalkyloxycarbonyl, optionally substituted 5- to 10-membered heterocycloalkylcarbonyl, optionally substituted 5- to 10-membered heterocycloalkyloxycarbonyl, carbamoyl, optionally substituted C_1-12 alkylcarbamoyl, optionally substituted C_1-12 alkoxycarbamoyl, optionally substituted C_6-10 arylcarbamoyl, optionally substituted 5- to 10-membered heteroarylcarbamoyl, optionally substituted C_3-10 cycloalkylcarbamoyl, or optionally substituted 5- to 10-membered heterocycloalkylcarbamoyl, wherein the groups of R_2A and R_2B are optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group III, or R_2A and R_2B, together with the nitrogen atom to which they are attached, form a 5- to 6-membered non-aryl heterocycle, wherein the non-aryl heterocycle is optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group V.

[Item 6]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁ and R₄ are each independently hydrogen, optionally substituted alkyl, optionally substituted arylalkyl, optionally substituted cycloalkyl, formyl, optionally substituted alkylcarbonyl, optionally substituted alkoxycarbonyl, optionally substituted arylcarbonyl, optionally substituted aryloxycarbonyl, optionally substituted cycloalkylcarbonyl, optionally substituted cycloalkyloxycarbonyl, optionally substituted heterocycloalkylcarbonyl, optionally substituted heterocycloalkyloxycarbonyl, carbamoyl, optionally substituted alkylcarbamoyl, optionally substituted alkoxycarbamoyl, optionally substituted arylcarbamoyl, optionally substituted heteroarylcarbamoyl, optionally substituted cycloalkylcarbamoyl, or optionally substituted heterocycloalkylcarbamoyl, wherein the groups of R₁ and R₄ are optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group III.

[Item 6B]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁ and R₄ are each independently hydrogen, optionally substituted C_1-12 alkyl, optionally substituted C_6-10 aryl C_1-12 alkyl, optionally substituted C_3-10 cycloalkyl, formyl, optionally substituted C_1-12 alkylcarbonyl, optionally substituted C_1-12 alkoxycarbonyl, optionally substituted C_6-10 arylcarbonyl, optionally substituted C_6-10 aryloxycarbonyl, optionally substituted C_3-10 cycloalkylcarbonyl, optionally substituted C_3-10 cycloalkyloxycarbonyl, optionally substituted 5- to 10-membered heterocycloalkylcarbonyl, optionally substituted 5- to 10-membered heterocycloalkyloxycarbonyl, carbamoyl, optionally substituted C_1-12 alkylcarbamoyl, optionally substituted C_1-12 alkoxycarbamoyl, optionally substituted C_6-10 arylcarbamoyl, optionally substituted 5- to 10-membered heteroarylcarbamoyl, optionally substituted C_3-10 cycloalkylcarbamoyl, or optionally substituted 5- to 10-membered heterocycloalkylcarbamoyl, wherein the groups of R₁ and R₄ are optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group III.

[Item 7]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁ and R₄ are each independently hydrogen, optionally substituted alkyl, optionally substituted arylalkyl, formyl, optionally substituted alkylcarbonyl, optionally substituted alkoxycarbonyl, optionally substituted arylcarbonyl, optionally substituted aryloxycarbonyl, carbamoyl, or optionally substituted alkylcarbamoyl, wherein the groups of R₁ and R₄ are optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group III.

[Item 7B]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁ and R₄ are each independently hydrogen, optionally substituted C_1-12 alkyl, optionally substituted C_6-10 aryl C_1-12 alkyl, formyl, optionally substituted C_1-12 alkylcarbonyl, optionally substituted C_1-12 alkoxycarbonyl, optionally substituted C_6-10 arylcarbonyl, optionally substituted C_6-10 aryloxycarbonyl, carbamoyl, or optionally substituted C_1-12 alkylcarbamoyl, wherein the groups of R₁ and R₄ are optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group III.

[Item 8]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁ and R₄ are each independently hydrogen; alkyl; alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amino, substituted amino, substituted oxy, substituted carbonyl, cycloalkyl, and substituted cycloalkyl; arylalkyl; arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, alkyl, substituted alkyl, hydroxy, substituted oxy, amino, substituted amino, and nitro; formyl; substituted carbonyl; or substituted oxycarbonyl, wherein the substituted amino, substituted oxy, substituted alkyl, substituted carbonyl, substituted cycloalkyl, substituted carbonyl, and substituted oxycarbonyl in R₁ and R₄ each independently have one to the maximum substitutable number of the same or different substituents selected from substituent group IV.

[Item 8B]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁ and R₄ are each independently hydrogen; C_1-12 alkyl; C_1-12 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amino, substituted amino, substituted oxy, substituted carbonyl, C_3-10 cycloalkyl, and substituted C_3-10 cycloalkyl; C_6-10 aryl C_1-6 alkyl; C_6-10 aryl C_1-6 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, C_1-6 alkyl, substituted alkyl, hydroxy, substituted oxy, amino, substituted amino, and nitro; formyl; substituted carbonyl; or substituted oxycarbonyl, wherein the substituted amino, substituted oxy, substituted alkyl, substituted carbonyl, substituted cycloalkyl, substituted carbonyl, and substituted oxycarbonyl in R₁ and R₄ each independently have one to the maximum substitutable number of the same or different substituents selected from substituent group IV.

[Item 9]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁ and R₄ are each independently hydrogen; alkyl; alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amidinoamino, alkoxy, alkoxycarbonyl, carbamoyl, carboxy, hydroxy, trialkylsilyloxy, and cycloalkyl; arylalkyl; arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, alkyl, haloalkyl, alkoxy, haloalkoxy, amino, substituted amino, nitro, and hydroxy; formyl; alkylcarbonyl; arylalkylcarbonyl; arylalkyloxycarbonyl; alkoxycarbonyl; arylcarbonyl; aryloxycarbonyl; carbamoyl; alkylcarbamoyl; or arylalkylcarbamoyl, wherein the substituted amino each independently have one to the maximum substitutable number of the same or different substituents selected from substituent group IV.

[Item 9B]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁ and R₄ are each independently hydrogen; C_1-12 alkyl; C_1-12 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amidinoamino, C_1-6 alkoxy, C_1-6 alkoxycarbonyl, carbamoyl, carboxy, hydroxy, tri-C_1-6 alkylsilyloxy, and C_3-10 cycloalkyl; C_6-10 aryl C_1-6 alkyl; C_6-10 aryl C_1-6 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, C_1-6 alkyl, C_1-6 haloalkyl, C_1-6 alkoxy, C_1-6 haloalkoxy, amino, substituted amino, nitro, and hydroxy; formyl; C_1-12 alkylcarbonyl; C_6-10 aryl C_1-6 alkylcarbonyl; C_6-10 aryl C_1-6 alkyloxycarbonyl; C_1-12 alkoxycarbonyl; C_6-10 arylcarbonyl; C_6-10 aryloxycarbonyl; carbamoyl; C_1-12 alkylcarbamoyl; or C_6-10 aryl C_1-6 alkylcarbamoyl, wherein the substituted amino have one to the maximum substitutable number of the same or different substituents selected from substituent group IV.

[Item 10]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₃ is hydrogen; alkyl; alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amino, substituted amino, carboxy, substituted oxycarbonyl, carbamoyl, substituted aminocarbonyl, hydroxy, substituted oxy, cycloalkyl, and substituted cycloalkyl; arylalkyl; or arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, alkyl, substituted alkyl, carboxy, substituted oxycarbonyl, hydroxy, and substituted oxy, wherein the substituted amino, substituted oxy, substituted oxycarbonyl, substituted aminocarbonyl, substituted alkyl, substituted cycloalkyl, substituted carbonyl, and substituted oxycarbonyl in R₃ each independently have one to the maximum substitutable number of the same or different substituents selected from substituent group IV.

[Item 11]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₃ is hydrogen; alkyl; alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amidinoamino, alkoxycarbonyl, carbamoyl, carboxy, hydroxy, trialkylsilyloxy, amino, alkoxycarbonylamino, and cycloalkyl; arylalkyl; or arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, alkyl, alkoxycarbonyl, and hydroxy.

[Item 11B]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₃ is hydrogen; C_1-12 alkyl; C_1-12 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amidinoamino, C_1-6 alkoxycarbonyl, carbamoyl, carboxy, hydroxy, tri-C_1-6 alkylsilyloxy, amino, C_1-6 alkoxycarbonylamino, and C_3-10 cycloalkyl; C_6-10 aryl C_1-6 alkyl; or C_6-10 aryl C_1-6 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, C_1-6 alkyl, C_1-6 alkoxycarbonyl, and hydroxy.

[Item 12]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R_2A and R_2B are each independently hydrogen; alkyl; alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of formyl, substituted carbonyl, hydroxy, substituted oxy, amino, substituted amino, cycloalkyl, substituted cycloalkyl, heterocycloalkyl, and substituted heterocycloalkyl; arylalkyl; arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, alkyl, substituted alkyl, hydroxy, and substituted oxy; heteroarylalkyl; substituted heteroarylalkyl; cycloalkyl; or substituted cycloalkyl, wherein the substituted carbonyl, substituted oxy, substituted amino, substituted cycloalkyl, substituted heterocycloalkyl, substituted heteroarylalkyl, and substituted alkyl in R_2A and R_2B each independently have one to the maximum substitutable number of the same or different substituents selected from substituent group IV, or R_2A and R_2B, together with the nitrogen atom to which they are attached, form a non-aryl heterocycle, wherein the non-aryl heterocycle is optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group VI.

[Item 13]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R_2A and R_2B are each independently hydrogen; alkyl; alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amidinoamino, alkoxy, alkoxycarbonyl, carbamoyl, carboxy, hydroxy, amino, alkoxycarbonylamino, cycloalkyl, and heterocycloalkyl; arylalkyl; arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, alkyl, haloalkyl, alkoxy, and hydroxy; heteroarylalkyl; alkoxycarbonyl-substituted heteroarylalkyl; or cycloalkyl, or R_2A and R_2B, together with the nitrogen atom to which they are attached, form a 5- to 6-membered non-aryl heterocycle, wherein the non-aryl heterocycle is optionally substituted with one or up to the maximum substitutable number of the same or different substituents selected from substituent group VI.

[Item 13B]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R_2A and R_2B are each independently hydrogen; C_1-12 alkyl; C_1-12 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amidinoamino, C_1-6 alkoxy, C_1-6 alkoxycarbonyl, carbamoyl, carboxy, hydroxy, amino, C_1-6 alkoxycarbonylamino, C_3-10 cycloalkyl, and 5- to 10-membered heterocycloalkyl; C_6-10 aryl C_1-6 alkyl; C_6-10 aryl C_1-6 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, C_1-6 alkyl, C_1-6 haloalkyl, C_1-6 alkoxy, and hydroxy; 5- to 10-membered heteroaryl C_1-6 alkyl; C_1-6 alkoxycarbonyl-substituted 5- to 10-membered heteroaryl C_1-6 alkyl; or C_3-10 cycloalkyl, or R_2A and R_2B, together with the nitrogen atom to which they are attached, form a 5- to 6-membered non-aryl heterocycle, wherein the non-aryl heterocycle is optionally substituted with one or up to the maximum substitutable number of the same or different substituents selected from substituent group VI.

[Item 14]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁ is alkyl; alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amidinoamino, carbamoyl, carboxy, hydroxy, and cycloalkyl; arylalkyl; or arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, alkyl, haloalkyl, alkoxy, substituted amino, and hydroxy, wherein the substituted amino has one to the maximum substitutable number of the same or different substituents selected from substituent group IV.

[Item 14B]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁ is C_1-12 alkyl; C_1-12 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amidinoamino, carbamoyl, carboxy, hydroxy, and C_3-10 cycloalkyl; C_6-10 aryl C_1-6 alkyl; or C_6-10 aryl C_1-6 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, C_1-6 alkyl, C_1-6 haloalkyl, C_1-6 alkoxy, substituted amino, and hydroxy, wherein the substituted amino has one to the maximum substitutable number of the same or different substituents selected from substituent group IV.

[Item 15]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R_2A is hydrogen, and R_2B is alkyl; alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amidinoamino, carbamoyl, carboxy, hydroxy, and cycloalkyl; arylalkyl; arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, alkyl, haloalkyl, alkoxy, and hydroxy; or cycloalkyl.

[Item 15B]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R_2A is hydrogen, and R_2B is C_1-12 alkyl; C_1-12 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amidinoamino, carbamoyl, carboxy, hydroxy, and C_3-10 cycloalkyl; C_6-10 aryl C_1-6 alkyl; C_6-10 aryl C_1-6 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, C_1-6 alkyl, C_1-6 haloalkyl, C_1-6 alkoxy, and hydroxy; or C_3-10 cycloalkyl.

[Item 16]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₃ is alkyl; alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amidinoamino, carbamoyl, carboxy, hydroxy, and cycloalkyl; arylalkyl; or arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of alkyl and hydroxy.

[Item 16B]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₃ is C_1-12 alkyl; C_1-12 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amidinoamino, carbamoyl, carboxy, hydroxy, and C_3-10 cycloalkyl; C_6-10 aryl C_1-6 alkyl; or C_6-10 aryl C_1-6 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of C_1-6 alkyl and hydroxy.

[Item 17]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₄ is hydrogen, alkyl, alkylcarbonyl, arylalkylcarbonyl, arylalkyloxycarbonyl, alkoxycarbonyl, carbamoyl, or arylalkylcarbamoyl.

[Item 17B]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₄ is hydrogen, C_1-12 alkyl, C_1-12 alkylcarbonyl, C_6-10 aryl C_1-6 alkylcarbonyl, C_6-10 aryl C_1-6 alkyloxycarbonyl, C_1-12 alkoxycarbonyl, carbamoyl, or C_6-10 aryl C_1-6 alkylcarbamoyl.

[Item 17C]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁ is hydrogen, methyl, ethyl, isobutyl, isopentyl, amidinoaminopropyl, tert-butoxyethyl, tert-butoxypropyl, (tert-butoxycarbonyl)ethyl, carbamoylmethyl, carboxyethyl, hydroxyethyl, hydroxypropyl, cyclopentylmethyl, cyclohexylmethyl, benzyl, phenylethyl, naphthalenylmethyl, fluorobenzyl, chlorobenzyl, dichlorobenzyl, methylbenzyl, tert-butylbenzyl, (trifluoromethyl)benzyl, methoxybenzyl, ethoxybenzyl, tert-butoxybenzyl, aminobenzyl, (cyclopentylcarbonylamino)benzyl, (cyclopentylmethylamino)benzyl, (dimethylamino)benzyl, (carbamoylethylcarbonylamino)benzyl, (carboxyethylcarbonylamino)benzyl, nitrobenzyl, hydroxybenzyl, 3-methylbutanoyl, isobutylcarbonyl, 2-phenylacetyl, isopropyloxycarbonyl, benzoyl, or phenyloxycarbonyl.

[Item 17D]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R_2A is hydrogen, R_2B is methyl, isopropyl, isobutyl, n-pentyl, isopentyl, n-hexyl, heptyl, amidinoaminopropyl, tert-butoxyethyl, tert-butoxycarbonylmethyl, carbamoylmethyl, carbamoylethyl, carboxyethyl, hydroxyethyl, aminobutyl, ((tert-butoxycarbonyl)amino)butyl, cyclohexylmethyl, (tetrahydro-2H-pyran-2-yl)methyl, benzyl, phenylethyl, naphthalenylmethyl, naphthalenylethyl, fluorobenzyl, chlorobenzyl, dichlorobenzyl, (fluorophenyl)ethyl, methylbenzyl, (trifluoromethyl)benzyl, methoxybenzyl, tert-butoxybenzyl, hydroxybenzyl, α-hydroxymethylphenethyl, β-hydroxyphenethyl, pyridinylmethyl, (1H-indol-3-yl)ethyl, (1-(tert-butoxycarbonyl)-1H-indol-3-yl)ethyl, cyclopentyl, or cyclohexyl, or R_2A and R_2B, together with the nitrogen atom to which they are attached, form a pyrrolidine ring or piperidine ring.

[Item 17E]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₃ is n-propyl, isobutyl, isopentyl, amidinoaminopropyl, (methoxycarbonyl)ethyl, (tert-butoxycarbonyl)ethyl, carbamoylmethyl, carboxyethyl, hydroxymethyl, hydroxyethyl, (tert-butyldimethylsilyloxy)ethyl, aminobutyl, ((tert-butoxycarbonyl)amino)butyl, cyclohexylmethyl, cyclohexylethyl, benzyl, phenylethyl, phenylpropyl, phenylbutyl, naphthalenylmethyl, naphthalenylethyl, chlorobenzyl, methylbenzyl, (methylphenyl)ethyl, (isopropylphenyl)ethyl, or hydroxybenzyl.

[Item 17F]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₄ is hydrogen, methyl, ethyl, isobutyl, formyl, acetyl, 3-methylbutanoyl, 2-phenylacetyl, methoxycarbonyl, ethoxycarbonyl, 2-methylpropyloxycarbonyl, tert-butoxycarbonyl, benzoyl, benzyl, benzyloxycarbonyl, aminocarbonyl, N-benzylaminocarbonyl, propylcarbamoyl, N-isobutylaminocarbonyl, or N-benzylaminocarbonyl.

[Item 17G]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

the compound is a compound selected from the group consisting of compound numbers IB-1 to IB-995 and IF-1 to IF-931.

[Item 18]

A compound represented by formula XXIIF:

or an enantiomer thereof, or a salt thereof, or a solvate thereof, wherein

R₁ and R₃ are each independently hydrogen, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, or optionally substituted carbonyl, and

R_2A and R_2B are each independently hydrogen, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, or optionally substituted carbonyl, or R_2A and R_2B, together with the nitrogen atom to which they are attached, form a non-aryl heterocycle or heteroaryl ring, wherein the non-aryl heterocycle and the heteroaryl ring are each independently and optionally substituted.

[Item 19]

A compound represented by formula XXIIB:

or an enantiomer thereof, or a salt thereof, or a solvate thereof, wherein

R₁ and R₃ are each independently hydrogen, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, or optionally substituted carbonyl, and

R_2A and R_2B are each independently hydrogen, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, or optionally substituted carbonyl, or R_2A and R_2B, together with the nitrogen atom to which they are attached, form a non-aryl heterocycle or heteroaryl ring, wherein the non-aryl heterocycle and the heteroaryl ring are each independently and optionally substituted.

[Item 20]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

the alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, and carbonyl of R₁ and R₃ are each independently and optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group I, and

the alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, carbonyl, and the non-aryl heterocycle and the heteroaryl ring of R_2A and R_2B are each independently and optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group I.

[Item 21]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁ and R₃ are each independently hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, or optionally substituted carbonyl, and

R_2A and R_2B are each independently hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, or optionally substituted carbonyl, or R_2A and R_2B, together with the nitrogen atom to which they are attached, form a non-aryl heterocycle or heteroaryl ring, wherein the non-aryl heterocycle and the heteroaryl ring are each independently and optionally substituted.

[Item 22]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁ and R₃ are each independently hydrogen, optionally substituted alkyl, optionally substituted arylalkyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, formyl, optionally substituted alkylcarbonyl, optionally substituted alkoxycarbonyl, optionally substituted arylcarbonyl, optionally substituted aryloxycarbonyl, optionally substituted heteroarylcarbonyl, optionally substituted heteroaryloxycarbonyl, optionally substituted cycloalkylcarbonyl, optionally substituted cycloalkyloxycarbonyl, optionally substituted heterocycloalkylcarbonyl, optionally substituted heterocycloalkyloxycarbonyl, carbamoyl, optionally substituted alkylcarbamoyl, optionally substituted alkoxycarbamoyl, optionally substituted arylcarbamoyl, optionally substituted heteroarylcarbamoyl, optionally substituted cycloalkylcarbamoyl, or optionally substituted heterocycloalkylcarbamoyl, wherein the groups of R₁ and R₃ are optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group II, and

R_2A and R_2B are each independently hydrogen, optionally substituted alkyl, optionally substituted arylalkyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, formyl, optionally substituted alkylcarbonyl, optionally substituted alkoxycarbonyl, optionally substituted arylcarbonyl, optionally substituted aryloxycarbonyl, optionally substituted heteroarylcarbonyl, optionally substituted heteroaryloxycarbonyl, optionally substituted cycloalkylcarbonyl, optionally substituted cycloalkyloxycarbonyl, optionally substituted heterocycloalkylcarbonyl, optionally substituted heterocycloalkyloxycarbonyl, carbamoyl, optionally substituted alkylcarbamoyl, optionally substituted alkoxycarbamoyl, optionally substituted arylcarbamoyl, optionally substituted heteroarylcarbamoyl, optionally substituted cycloalkylcarbamoyl, or optionally substituted heterocycloalkylcarbamoyl, wherein the groups of R_2A and R_2B are optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group II, or R_2A and R_2B, together with the nitrogen atom to which they are attached, form a 5- to 6-membered non-aryl heterocycle, wherein the non-aryl heterocycle is optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group II.

[Item 23]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁ and R₃ are each independently hydrogen, optionally substituted C_1-12 alkyl, optionally substituted C_6-10 aryl C_1-12 alkyl, optionally substituted C_3-10 cycloalkyl, optionally substituted 5- to 10-membered heterocycloalkyl, formyl, optionally substituted C_1-12 alkylcarbonyl, optionally substituted C_1-12 alkoxycarbonyl, optionally substituted C_6-10 arylcarbonyl, optionally substituted C_6-10 aryloxycarbonyl, optionally substituted 5- to 10-membered heteroarylcarbonyl, optionally substituted 5- to 10-membered heteroaryloxycarbonyl, optionally substituted C_3-10 cycloalkylcarbonyl, optionally substituted C_3-10 cycloalkyloxycarbonyl, optionally substituted 5- to 10-membered heterocycloalkylcarbonyl, optionally substituted 5- to 10-membered heterocycloalkyloxycarbonyl, carbamoyl, optionally substituted C_1-12 alkylcarbamoyl, optionally substituted C_1-12 alkoxycarbamoyl, optionally substituted C_6-10 arylcarbamoyl, optionally substituted 5- to 10-membered heteroarylcarbamoyl, optionally substituted C_3-10 cycloalkylcarbamoyl, or optionally substituted 5- to 10-membered heterocycloalkylcarbamoyl, wherein the groups of R₁ and R₃ are optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group III, and R_2A and R_2B are each independently hydrogen, optionally substituted C_1-12 alkyl, optionally substituted C_6-10 aryl C_1-12 alkyl, optionally substituted C_3-10 cycloalkyl, optionally substituted 5- to 10-membered heterocycloalkyl, formyl, optionally substituted C_1-12 alkylcarbonyl, optionally substituted C_1-12 alkoxycarbonyl, optionally substituted C_6-10 arylcarbonyl, optionally substituted C_6-10 aryloxycarbonyl, optionally substituted 5- to 10-membered heteroarylcarbonyl, optionally substituted 5- to 10-membered heteroaryloxycarbonyl, optionally substituted C_3-10 cycloalkylcarbonyl, optionally substituted C_3-10 cycloalkyloxycarbonyl, optionally substituted 5- to 10-membered heterocycloalkylcarbonyl, optionally substituted 5- to 10-membered heterocycloalkyloxycarbonyl, carbamoyl, optionally substituted C_1-12 alkylcarbamoyl, optionally substituted C_1-12 alkoxycarbamoyl, optionally substituted C_6-10 arylcarbamoyl, optionally substituted 5- to 10-membered heteroarylcarbamoyl, optionally substituted C_3-10 cycloalkylcarbamoyl, or optionally substituted 5- to 10-membered heterocycloalkylcarbamoyl, wherein the groups of R_2A and R_2B are optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group III, or R_2A and R_2B, together with the nitrogen atom to which they are attached, form a 5- to 6-membered non-aryl heterocycle, wherein the non-aryl heterocycle is optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group III.

[Item 24]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁ and R₃ are each independently hydrogen, optionally substituted alkyl, optionally substituted arylalkyl, optionally substituted cycloalkyl, formyl, optionally substituted alkylcarbonyl, optionally substituted alkoxycarbonyl, optionally substituted arylcarbonyl, optionally substituted aryloxycarbonyl, optionally substituted cycloalkylcarbonyl, optionally substituted cycloalkyloxycarbonyl, optionally substituted heterocycloalkylcarbonyl, optionally substituted heterocycloalkyloxycarbonyl, carbamoyl, optionally substituted alkylcarbamoyl, optionally substituted alkoxycarbamoyl, optionally substituted arylcarbamoyl, optionally substituted heteroarylcarbamoyl, optionally substituted cycloalkylcarbamoyl, or optionally substituted heterocycloalkylcarbamoyl, wherein the groups of R₁ and R₃ are optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group III.

[Item 25B]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁ and R₃ are each independently hydrogen, optionally substituted C_1-12 alkyl, optionally substituted C_6-10 aryl C_1-12 alkyl, optionally substituted C_3-10 cycloalkyl, formyl, optionally substituted C_1-12 alkylcarbonyl, optionally substituted C_1-12 alkoxycarbonyl, optionally substituted C_6-10 arylcarbonyl, optionally substituted C_6-10 aryloxycarbonyl, optionally substituted C_3-10 cycloalkylcarbonyl, optionally substituted C_3-10 cycloalkyloxycarbonyl, optionally substituted 5- to 10-membered heterocycloalkylcarbonyl, optionally substituted 5- to 10-membered heterocycloalkyloxycarbonyl, carbamoyl, optionally substituted C_1-12 alkylcarbamoyl, optionally substituted C_1-12 alkoxycarbamoyl, optionally substituted C_6-10 arylcarbamoyl, optionally substituted 5- to 10-membered heteroarylcarbamoyl, optionally substituted C_3-10 cycloalkylcarbamoyl, or optionally substituted 5- to 10-membered heterocycloalkylcarbamoyl, wherein the groups of R₁ and R₃ are optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group III.

[Item 25]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁ is hydrogen; alkyl; C_1-12 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amino, substituted amino, hydroxy, substituted oxy, formyl, substituted carbonyl, cycloalkyl, and substituted cycloalkyl; arylalkyl; arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, alkyl, substituted alkyl, hydroxy, substituted oxy, amino, substituted amino, and nitro; formyl; or substituted carbonyl, wherein the substituted amino, substituted oxy, substituted carbonyl, substituted cycloalkyl, and substituted alkyl in R₁ each independently have one to the maximum substitutable number of the same or different substituents selected from substituent group IV.

[Item 26]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁ is hydrogen; alkyl; C_1-12 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amidinoamino, alkoxycarbonyl-substituted amidinoamino, alkoxy, alkoxycarbonyl, carbamoyl, carboxy, hydroxy, trialkylsilyloxy, and cycloalkyl; arylalkyl; arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, alkyl, haloalkyl, alkoxy, haloalkoxy, amino, substituted amino, nitro, and hydroxy; formyl; alkylcarbonyl; arylalkylcarbonyl; alkoxycarbonyl; arylcarbonyl; aryloxycarbonyl; carbamoyl; alkylcarbamoyl; or arylalkylcarbamoyl, wherein the substituted amino has one to the maximum substitutable number of the same or different substituents selected from substituent group IV.

[Item 27B]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁ is hydrogen; C_1-12 alkyl; C_1-12 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amidinoamino, C_1-6 alkoxycarbonyl-substituted amidinoamino, C_1-6 alkoxy, C_1-6 alkoxycarbonyl, carbamoyl, carboxy, hydroxy, tri-C_1-6 alkylsilyloxy, and C_3-10 cycloalkyl; C_6-10 aryl C_1-6 alkyl; C_6-10 aryl C_1-6 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, C_1-6 alkyl, C_1-6 haloalkyl, C_1-6 alkoxy, C_1-6 haloalkoxy, amino, substituted amino, nitro, and hydroxy; formyl; C_1-12 alkylcarbonyl; C_6-10 aryl C_1-6 alkylcarbonyl; C_1-12 alkoxycarbonyl; C_6-10 arylcarbonyl; C_6-10 aryloxycarbonyl; carbamoyl; C_1-12 alkylcarbamoyl; or C_6-10 aryl C_1-6 alkylcarbamoyl, wherein the substituted amino has one to the maximum substitutable number of the same or different substituents selected from substituent group IV.

[Item 27C]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁ is C_1-12 alkyl; C_1-12 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amidinoamino, C_1-6 alkoxycarbonyl-substituted amidinoamino, C_1-6 alkoxy, C_1-6 alkoxycarbonyl, carbamoyl, carboxy, hydroxy, tri-C_1-6 alkylsilyloxy, and C_3-10 cycloalkyl; C_6-10 aryl C_1-6 alkyl; or C_6-10 aryl C_1-6 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, C_1-6 alkyl, C_1-6 haloalkyl, C_1-6 alkoxy, C_1-6 haloalkoxy, amino, substituted amino, nitro, and hydroxy, wherein the substituted amino has one to the maximum substitutable number of the same or different substituents selected from substituent group IV.

[Item 28]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₃ is hydrogen; alkyl; formyl; substituted carbonyl; alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of hydroxy, substituted oxy, substituted carbonyl, amino, substituted amino, cycloalkyl, substituted cycloalkyl, heterocycloalkyl, and substituted heterocycloalkyl; arylalkyl; arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, nitro, hydroxy, substituted oxy, amino, substituted amino, alkyl, and substituted alkyl; heteroarylalkyl; or substituted heteroarylalkyl, wherein the substituted carbonyl, substituted oxy, substituted amino, substituted cycloalkyl, substituted heterocycloalkyl, substituted alkyl, and substituted heteroarylalkyl in R₃ each independently have one to the maximum substitutable number of the same or different substituents selected from substituent group IV.

[Item 29B]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₃ is hydrogen; alkyl; formyl; alkylcarbonyl; arylalkylcarbonyl; alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of hydroxy, trialkylsilyloxy, alkoxy, alkoxycarbonyl, alkoxycarbonylamino, cycloalkyl, carboxy, amino, amidinoamino, alkoxycarbonyl-substituted amidinoamino, carbamoyl, and heterocycloalkyl; arylalkyl; arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, nitro, hydroxy, amino, monoalkylamino, dialkylamino, alkyl, haloalkyl, alkoxy, haloalkoxy, carboxyalkylcarbonylamino, carbamoylalkylcarbonylamino, cycloalkylcarbonylamino, and cycloalkylalkylamino; heteroarylalkyl; or alkoxycarbonyl-substituted heteroarylalkyl.

[Item 29C]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₃ is hydrogen; C_1-12 alkyl; formyl; C_1-6 alkylcarbonyl; C_6-10 aryl C_1-6 alkylcarbonyl; C_1-12 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of hydroxy, tri-C_1-6 alkylsilyloxy, C_1-6 alkoxy, C_1-6 alkoxycarbonyl, C_1-6 alkoxycarbonylamino, C_3-6 cycloalkyl, carboxy, amino, amidinoamino, C_1-6 alkoxycarbonyl-substituted amidinoamino, carbamoyl, and 5- to 6-membered heterocycloalkyl; C_6-10 aryl C_1-6 alkyl; C_6-10 aryl C_1-12 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, nitro, hydroxy, amino, mono-C_1-6 alkylamino, di-C_1-6 alkylamino, C_1-6 alkyl, C_1-6 haloalkyl, C_1-6 alkoxy, C_1-6 haloalkoxy, carboxy C_1-6 alkylcarbonylamino, carbamoyl C_1-6 alkylcarbonylamino, C_3-6 cycloalkylcarbonylamino, and C_3-6 cycloalkyl C_1-6 alkylamino; 5- to 10-membered heteroaryl C_1-6 alkyl; or C_1-6 alkoxycarbonyl-substituted 5- to 10-membered heteroaryl C_1-6 alkyl.

[Item 29D]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₃ is C_1-12 alkyl; C_1-12 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of hydroxy, tri-C_1-6 alkylsilyloxy, C_1-6 alkoxy, C_1-6 alkoxycarbonyl, C_1-6 alkoxycarbonylamino, C_3-6 cycloalkyl, carboxy, amino, amidinoamino, C_1-6 alkoxycarbonyl-substituted amidinoamino, carbamoyl, and 5- to 6-membered heterocycloalkyl; C_6-10 aryl C_1-6 alkyl; or C_6-10 aryl C_1-12 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, nitro, hydroxy, amino, mono-C_1-6 alkylamino, di-C_1-6 alkylamino, C_1-6 alkyl, C_1-6 haloalkyl, C_1-6 alkoxy, C_1-6 haloalkoxy, carboxy C_1-6 alkylcarbonylamino, carbamoyl C_1-6 alkylcarbonylamino, C_3-6 cycloalkylcarbonylamino, and C_3-6 cycloalkyl C_1-6 alkylamino.

[Item 29]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R_2A and R_2B are each independently hydrogen; alkyl; formyl; substituted carbonyl; alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of hydroxy, substituted oxy, substituted carbonyl, amino, substituted amino, cycloalkyl, substituted cycloalkyl, heterocycloalkyl, and substituted heterocycloalkyl; arylalkyl; arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, nitro, hydroxy, substituted oxy, amino, substituted amino, alkyl, and substituted alkyl; heteroarylalkyl; or substituted heteroarylalkyl, wherein the substituted carbonyl, substituted oxy, substituted amino, substituted cycloalkyl, substituted heterocycloalkyl, substituted alkyl, and substituted heteroarylalkyl in R_2A and R_2B each independently have one to the maximum substitutable number of the same or different substituents selected from substituent group IV, or R_2A and R_n, together with the nitrogen atom to which they are attached, form a non-aryl heterocycle, wherein the non-aryl heterocycle is optionally substituted with one or up to the maximum substitutable number of the same or different substituents selected from substituent group VI.

[Item 30B]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R_2A and R_2B are each independently hydrogen; alkyl; formyl; alkylcarbonyl; arylalkylcarbonyl; alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of hydroxy, trialkylsilyloxy, alkoxy, alkoxycarbonyl, alkoxycarbonylamino, cycloalkyl, carboxy, amino, amidinoamino, alkoxycarbonyl-substituted amidinoamino, carbamoyl, and heterocycloalkyl; arylalkyl; arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, nitro, hydroxy, amino, monoalkylamino, dialkylamino, alkyl, haloalkyl, alkoxy, carboxyalkylcarbonylamino, carbamoylalkylcarbonylamino, cycloalkylcarbonylamino, and cycloalkylalkylamino; heteroarylalkyl; or alkoxycarbonyl-substituted heteroarylalkyl, or R_2A and R_2B, together with the nitrogen atom to which they are attached, form a non-aryl heterocycle, wherein the non-aryl heterocycle is optionally substituted with one or up to the maximum substitutable number of the same or different substituents selected from substituent group VI.

[Item 30C]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R_2A and R_2B are each independently hydrogen; C_1-12 alkyl; formyl; C_1-6 alkylcarbonyl; C_6-10 aryl C_1-6 alkylcarbonyl; C_1-12 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of hydroxy, tri-C_1-6 alkylsilyloxy, C_1-6 alkoxy, C_1-6 alkoxycarbonyl, C_1-6 alkoxycarbonylamino, C_3-10 cycloalkyl, carboxy, amino, amidinoamino, C_1-6 alkoxycarbonyl-substituted amidinoamino, carbamoyl, and 5- to 6-membered heterocycloalkyl; C_6-10 aryl C_1-12 alkyl; C_6-10 aryl C_1-12 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, nitro, hydroxy, amino, mono-C_1-6 alkylamino, di-C_1-6 alkylamino, C_1-6 alkyl, C_1-6 haloalkyl, C_1-6 alkoxy, carboxy C_1-6 alkylcarbonylamino, carbamoyl C_1-6 alkylcarbonylamino, C_3-6 cycloalkylcarbonylamino, and C_3-6 cycloalkyl C_1-6 alkylamino; 5- to 10-membered heteroaryl C_1-12 alkyl; or C_1-6 alkoxycarbonyl-substituted 5- to 10-membered heteroaryl C_1-12 alkyl, or R_2A and R_2B, together with the nitrogen atom to which they are attached, form a 5- to 6-membered non-aryl heterocycle, wherein the non-aryl heterocycle is optionally substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, nitro, hydroxy, amino, C_1-6alkyl, C_1-6 haloalkyl, C_1-6 alkoxy, C_1-6 alkoxycarbonyl, C_3-6 cycloalkylcarbonylamino, and C_3-6 cycloalkyl C_1-6 alkylamino.

[Item 30D]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R_2A and R_2B are each independently hydrogen; C_1-12 alkyl; C_1-12 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of hydroxy, tri-C_1-6 alkylsilyloxy, C_1-6 alkoxy, C_1-6 alkoxycarbonyl, C_1-6 alkoxycarbonylamino, C_3-10 cycloalkyl, carboxy, amino, amidinoamino, C_1-6 alkoxycarbonyl-substituted amidinoamino, carbamoyl, and 5- to 6-membered heterocycloalkyl; C_6-10 aryl C_1-12 alkyl; C_6-10 aryl C_1-12 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, nitro, hydroxy, amino, mono-C_1-6 alkylamino, di-C_1-6 alkylamino, C_1-6 alkyl, C_1-6 haloalkyl, C_1-6 alkoxy, carboxy C_1-6 alkylcarbonylamino, carbamoyl C_1-6 alkylcarbonylamino, C_3-6 cycloalkylcarbonylamino, and C_3-6 cycloalkyl C_1-6 alkylamino; 5- to 10-membered heteroaryl C_1-12 alkyl; or C_1-6 alkoxycarbonyl-substituted 5- to 10-membered heteroaryl C_1-12 alkyl, or R_2A and R_2B, together with the nitrogen atom to which they are attached, form a 5- to 6-membered non-aryl heterocycle, wherein the non-aryl heterocycle is optionally substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, nitro, hydroxy, amino, C_1-6alkyl, C_1-6 haloalkyl, C_1-6 alkoxy, C_1-6 alkoxycarbonyl, C_3-6 cycloalkylcarbonylamino, and C_3-6 cycloalkyl C_1-6 alkylamino.

[Item 30]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁ is alkyl; alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amidinoamino, carbamoyl, carboxy, hydroxy, and cycloalkyl; arylalkyl; or arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, alkyl, haloalkyl, alkoxy, haloalkoxy, substituted amino, and hydroxy, wherein the substituted amino has one to the maximum substitutable number of the same or different substituents selected from substituent group IV.

[Item 31B]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁ is C_1-12 alkyl; C_1-12 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amidinoamino, carbamoyl, carboxy, hydroxy, and C_3-10 cycloalkyl; C_6-10 aryl C_1-6 alkyl; or C_6-10 aryl C_1-6 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, C_1-6 alkyl, C_1-6 haloalkyl, C_1-6 alkoxy, C_1-6 haloalkoxy, substituted amino, and hydroxy, wherein the substituted amino has one to the maximum substitutable number of the same or different substituents selected from substituent group IV.

[Item 31]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R_2A is hydrogen, and R_2B is alkyl; alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amidinoamino, carbamoyl, carboxy, hydroxy, and cycloalkyl; arylalkyl; or arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen and alkyl.

[Item 32B]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R_2A is hydrogen, and R_2B is C_1-12 alkyl; C_1-12 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amidinoamino, carbamoyl, carboxy, hydroxy, and C_3-10 cycloalkyl; C_6-10 aryl C_1-6 alkyl; or C_6-10 aryl C_1-6 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen and C_1-6 alkyl.

[Item 32]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₃ is alkyl; alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amidinoamino, carbamoyl, carboxy, hydroxy, and cycloalkyl; or arylalkyl.

[Item 32B]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₃ is C_1-12 alkyl; alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amidinoamino, carbamoyl, carboxy, hydroxy, and cycloalkyl; C_6-10 aryl C_1-6 alkyl; or arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of alkyl and hydroxy.

[Item 32C]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁ is methyl, n-propyl, isobutyl, isopentyl, amidinoaminopropyl, tert-butoxycarbonyl-substituted amidinoaminopropyl, tert-butoxyethyl, tert-butoxypropyl, (tert-butoxycarbonyl)ethyl, carboxyethyl, hydroxyethyl, hydroxypropyl, aminopropyl, 2-(tert-butyl-dimethylsilyloxy)ethyl, cyclopentylmethyl, cyclohexylmethyl, benzyl, phenylethyl, naphthalenylmethyl, fluorobenzyl, chlorobenzyl, dichlorobenzyl, methylbenzyl, (tert-butyl)benzyl, methoxybenzyl, ethoxybenzyl, (tert-butoxy)benzyl, (trifluoromethoxy)benzyl, (dimethylamino)benzyl, nitrobenzyl, or hydroxybenzyl.

[Item 32D]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R_2A and R_2B are each independently isopropyl, isobutyl, sec-butyl, pentyl, isopentyl, n-hexyl, heptyl, amidinoaminopropyl, tert-butoxycarbonyl-substituted amidinoaminopropyl, tert-butoxyethyl, tert-butoxycarbonylmethyl, (tert-butoxycarbonyl)ethyl, carbamoylethyl, carboxyethyl, hydroxyethyl, aminopropyl, aminobutyl, ((tert-butoxycarbonyl)amino)butyl, cyclopentylmethyl, cyclohexylmethyl, (1,2,3,4-tetrahydronaphthalenyl)methyl, (tetrahydro-2H-pyranyl)methyl, benzyl, phenylethyl, naphthalenylmethyl, (naphthalenyl)ethyl, β,-hydroxyphenethyl, α-(hydroxymethyl)phenethyl, fluorobenzyl, chlorobenzyl, dichlorobenzyl, (fluorophenyl)ethyl, methylbenzyl, (trifluoromethyl)benzyl, methoxybenzyl, (tert-butoxy)benzyl, hydroxybenzyl, pyridinylmethyl, quinolinylethyl, (1-(tert-butoxycarbonyl)-1H-indolyl)ethyl, cyclopentyl, or cyclohexyl, or R_2A and R_2B, together with the nitrogen atom to which they are attached, form a pyrrolidine ring or piperidine ring.

[Item 32E]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₃ is n-propyl, isobutyl, isopentyl, amidinoaminopropyl, tert-butoxycarbonyl-substituted amidinoaminopropyl, (methoxycarbonyl)ethyl, (tert-butoxycarbonyl)ethyl, carboxyethyl, hydroxyethyl, aminopropyl, (tert-butyldimethylsilyloxy)ethyl, ((tert-butoxycarbonyl)amino)butyl, cyclopentylmethyl, cyclohexylmethyl, cyclohexylethyl, benzyl, phenylethyl, phenylpropyl, phenylbutyl, naphthalenylmethyl, naphthalenylethyl, chlorobenzyl, methylbenzyl, (methylphenyl)ethyl, (isopropylphenyl)ethyl, (tert-butoxy)benzyl, or hydroxybenzyl.

[Item 32F]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

the compound is a compound selected from the group consisting of compound numbers IIB-1 to IIB-1129 and IIF-1 to IIF-1047.

[Item 33]

An antiviral agent for a virus in the Lyssavirus genus, comprising the compound according to any one of the preceding items or a pharmaceutically acceptable salt thereof.

[Item 34]

The antiviral agent according to any one of the preceding items, wherein the virus in the Lyssavirus genus comprises a rabies virus.

[Item 35]

A medicament comprising the compound according to any one of the preceding items or a pharmaceutically acceptable salt thereof.

[Item 36]

The medicament according to any one of the preceding items, which is a prophylactic agent or a therapeutic agent for rabies.

[Item 37]

A pharmaceutical composition comprising the compound according to any one of the preceding items or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier.

[Item 38]

A pharmaceutical composition for the prophylaxis or treatment of rabies, comprising the compound according to any one of the preceding items or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier.

[Item 39]

An anticancer agent comprising the compound according to any one of the preceding items or a pharmaceutically acceptable salt thereof.

[Item 40]

The medicament according to any one of the preceding items, which is a prophylactic agent or a therapeutic agent for cancer.

[Item 41]

A pharmaceutical composition for the prophylaxis or treatment of cancer, comprising the compound according to any one of the preceding items or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier.

[Item 42]

A method for the prophylaxis or treatment of rabies, characterized by administering a prophylactically or therapeutically effective amount of the compound according to any one of the preceding items or a pharmaceutically acceptable salt thereof, the antiviral agent according to any one of the preceding items, the medicament according to any one of the preceding items, or the pharmaceutical composition according to any one of the preceding items to a patient in need thereof.

[Item 43]

Use of the compound according to any one of the preceding items or a pharmaceutically acceptable salt thereof, or the antiviral agent according to any one of the preceding items, for the manufacture of a medicament for the prophylaxis or treatment of rabies.

[Item 44]

A method for the prophylaxis or treatment of cancer, characterized by administering a prophylactically or therapeutically effective amount of the compound according to any one of the preceding items or a pharmaceutically acceptable salt thereof, the anticancer agent according to any one of the preceding items, the medicament according to any one of the preceding items, or the pharmaceutical composition according to any one of the preceding items to a patient in need thereof.

[Item 45]

Use of the compound according to any one of the preceding items or a pharmaceutically acceptable salt thereof, or the anticancer agent according to any one of the preceding items, for the manufacture of a medicament for the prophylaxis or treatment of cancer.

[Item 46]

A method for the prophylaxis or treatment of rabies, comprising administering an effective amount of the compound according to any one of the preceding items or a pharmaceutically acceptable salt thereof to a subject in need thereof.

[Item 47]

A method for the prophylaxis or treatment of cancer, comprising administering an effective amount of the compound according to any one of the preceding items or a pharmaceutically acceptable salt thereof to a subject in need thereof.

The present disclosure also provides the following items.

[Item A1]

A compound represented by formula IF:

or an enantiomer thereof, or a salt thereof, or a solvate thereof, wherein

R₁, R₂ and R₃ are each independently optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted arylalkyl, optionally substituted heteroarylalkyl, optionally substituted cycloalkylalkyl, or optionally substituted heterocycloalkylalkyl, and

R₄ is hydrogen, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted arylalkyl, optionally substituted heteroarylalkyl, optionally substituted cycloalkylalkyl, optionally substituted heterocycloalkylalkyl, optionally substituted alkylcarbonyl, optionally substituted alkoxycarbonyl, optionally substituted arylcarbonyl, optionally substituted heteroarylcarbonyl, or optionally substituted carbamoyl.

[Item A2]

A compound represented by formula IB:

or an enantiomer thereof, or a salt thereof, or a solvate thereof, wherein

R₁, R₂ and R₃ are each independently optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted arylalkyl, optionally substituted heteroarylalkyl, optionally substituted cycloalkylalkyl, or optionally substituted heterocycloalkylalkyl, and

R₄ is hydrogen, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted arylalkyl, optionally substituted heteroarylalkyl, optionally substituted cycloalkylalkyl, optionally substituted heterocycloalkylalkyl, optionally substituted alkylcarbonyl, optionally substituted alkoxycarbonyl, optionally substituted arylcarbonyl, optionally substituted heteroarylcarbonyl, or optionally substituted carbamoyl.

[Item A3]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁, R₂ and R₃ are each independently optionally substituted alkyl, optionally substituted arylalkyl, optionally substituted heteroarylalkyl, or optionally substituted cycloalkylalkyl, and

R₄ is hydrogen, optionally substituted alkyl, optionally substituted alkylcarbonyl, optionally substituted arylcarbonyl, optionally substituted alkoxycarbonyl, or optionally substituted carbamoyl.

[Item A3a]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁, R₂ and R₃ are each independently optionally substituted alkyl, optionally substituted arylalkyl, optionally substituted heteroarylalkyl, or optionally substituted cycloalkylalkyl, and

R₄ is hydrogen, optionally substituted alkyl, optionally substituted alkylcarbonyl, optionally substituted arylcarbonyl, or optionally substituted alkoxycarbonyl.

[Item A4]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁, R₂ and R₃ are each independently optionally substituted C_1-6 alkyl, optionally substituted C_6-10 aryl C_1-6 alkyl, optionally substituted 5- to 10-membered heteroaryl C_1-6 alkyl, or optionally substituted C_3-6 cycloalkyl C_1-6 alkyl, and

R₄ is hydrogen, optionally substituted C_1-6 alkyl, optionally substituted C_1-6 alkylcarbonyl, optionally substituted C_6-10 arylcarbonyl, optionally substituted C_1-6 alkoxycarbonyl, or optionally substituted C_1-6 alkylcarbamoyl.

[Item A4b]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁, R₂ and R₃ are each independently optionally substituted C_1-6 alkyl, optionally substituted C_6-10 aryl C_1-6 alkyl, optionally substituted 5- to 10-membered heteroaryl C_1-6 alkyl, or optionally substituted C_3-6 cycloalkyl C_1-6 alkyl, and

R₄ is hydrogen, optionally substituted C_1-6 alkyl, optionally substituted C_1-6 alkylcarbonyl, optionally substituted C_6-10 arylcarbonyl, or optionally substituted C_1-6 alkoxycarbonyl.

[Item A5]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁, R₂ and R₃ are each independently C_1-6 alkyl, hydroxy-substituted C_1-6 alkyl, carbamoyl-substituted C_1-6 alkyl, amino-substituted C_1-6 alkyl, amidinoamino-substituted C_1-6 alkyl, carboxy-substituted C_1-6 alkyl, C_6-10 aryl C_1-6 alkyl, C_1-4 alkoxycarbonyl-substituted 5- to 10-membered heteroaryl C_1-6 alkyl, C_1-4 alkyl-substituted C_6-10 aryl C_1-6 alkyl, hydroxy-substituted C_6-10 aryl C_1-6 alkyl, halogen-substituted C_6-10 aryl C_1-6 alkyl, C_1-4 alkoxy-substituted C_6-10 aryl C_1-6 alkyl, (optionally substituted amino)-C_6-10 aryl C_1-6 alkyl, C_1-4 alkoxycarbonyl-substituted C_1-6 alkyl, C_1-4 alkoxycarbonylamino-substituted C_1-6 alkyl, 5- to 6-membered heterocycloalkyl-substituted C_1-6 alkyl, or C_3-6 cycloalkyl C_1-6 alkyl.

[Item A5a]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁, R₂ and R₃ are each independently C_1-6 alkyl, hydroxy-substituted C_1-6 alkyl, carbamoyl-substituted C_1-6 alkyl, amino-substituted C_1-6 alkyl, amidinoamino-substituted C_1-6 alkyl, carboxy-substituted C_1-6 alkyl, C_6-10 aryl C_1-6 alkyl, C_1-4 alkoxycarbonyl-substituted 5- to 10-membered heteroaryl C_1-6 alkyl, C_1-4 alkyl-substituted C_6-10 aryl C_1-6 alkyl, hydroxy-substituted C_6-10 aryl C_1-6 alkyl, halogen-substituted C_6-10 aryl C_1-6 alkyl, C_1-4 alkoxy-substituted C_6-10 aryl C_1-6 alkyl, C_1-4 alkoxycarbonyl-substituted C_1-6 alkyl, C_1-4 alkoxycarbonylamino-substituted C_1-6 alkyl, 5- to 6-membered heterocycloalkyl-substituted C_1-6 alkyl, or C_3-6 cycloalkyl C_1-6 alkyl.

[Item A5b]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₄ is hydrogen, optionally substituted C_1-6 alkyl, optionally substituted C_1-6 alkylcarbonyl, optionally substituted C_6-10 aryl C_1-6 alkylcarbonyl, optionally substituted C_6-10 arylcarbonyl, optionally substituted C_1-6 alkoxycarbonyl, optionally substituted C_6-10 aryl C_1-6 alkoxycarbonyl, carbamoyl, optionally substituted C_1-6 alkylcarbamoyl, or optionally substituted C_6-10 aryl C_1-6 alkylcarbamoyl.

[Item A5c]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁, R₂ and R₃ are each independently optionally substituted alkyl or optionally substituted arylalkyl.

[Item A5d]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁, R₂ and R₃ are each independently optionally substituted C_1-6 alkyl or optionally substituted C_6-10 aryl C_1-6 alkyl.

[Item A5e]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁, R₂ and R₃ are each independently C_1-6 alkyl, C_6-10 aryl C_1-6 alkyl, C_1-4 alkyl-substituted C_6-10 aryl C_1-6 alkyl, halogen-substituted C_6-10 aryl C_1-6 alkyl, C_1-4 alkoxy-substituted C_6-10 aryl C_1-6 alkyl, or (optionally substituted amino)-C_6-10 aryl C_1-6 alkyl.

[Item A5f]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₂ is naphthalen-1-ylmethyl or optionally substituted benzyl.

[Item A5g]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁ and R₃ are each independently alkyl or optionally substituted benzyl, and R₂ is optionally substituted benzyl.

[Item A5h]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁ and R₃ are each independently C_1-6 alkyl, benzyl, C_1-4 alkyl-substituted benzyl, chloro-substituted benzyl, C_1-4 alkoxy-substituted benzyl, or amino-substituted benzyl, and R₂ is benzyl or chloro-substituted benzyl.

[Item A5i]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁ and R₃ are each independently isobutyl, isopentyl, 4-(dimethylamino)benzyl, 4-methylbenzyl, 4-methoxybenzyl, 3-chlorobenzyl, 4-chlorobenzyl, or 3,4-dichlorobenzyl, and R₂ is benzyl, 3-chlorobenzyl, or 3,4-dichlorobenzyl.

[Item A6]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₄ is hydrogen, C_1-6 alkyl, C_1-6 alkylcarbonyl, C_6-lo arylcarbonyl, C_6-10 aryl C_1-6 alkylcarbonyl, C_1-6 alkoxycarbonyl, C_6-10 aryl C_1-6 alkoxycarbonyl, carbamoyl, C_1-6 alkylcarbamoyl, or C_6-10 aryl C_1-6 alkylcarbamoyl.

[Item A6b]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₄ is hydrogen, C_1-6 alkyl, C_1-6 alkylcarbonyl, C_6-10 arylcarbonyl, or C_1-6 alkoxycarbonyl.

[Item A7]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₄ is hydrogen, C_1-4 alkyl, C_1-4 alkylcarbonyl, C₆ arylcarbonyl, C₆ aryl C_1-4 alkylcarbonyl, C_1-4 alkoxycarbonyl, C₆ aryl C_1-4 alkoxycarbonyl, carbamoyl, C_1-4 alkylcarbamoyl, or C₆ aryl C_1-4 alkylcarbamoyl.

[Item A7b]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₄ is hydrogen, C_1-4 alkyl, C_1-4 alkylcarbonyl, C₆ arylcarbonyl, or C_1-4 alkoxycarbonyl.

[Item A8]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₄ is hydrogen, methyl, ethyl, acetyl, benzoyl, methoxycarbonyl, tert-butoxycarbonyl, or propylcarbamoyl.

[Item A8b]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₄ is hydrogen, methyl, ethyl, acetyl, benzoyl, methoxycarbonyl, or tert-butoxycarbonyl.

[Item A9]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₂ is C_1-4 alkyl, hydroxy-substituted C_1-4 alkyl, carbamoyl-substituted C_1-4 alkyl, amino-substituted C_1-4 alkyl, amidinoamino-substituted C_1-4 alkyl, carboxy-substituted C_1-4 alkyl, C_6-10 aryl C_1-4 alkyl, C_1-4 alkoxycarbonyl-substituted 5- to 10-membered heteroaryl C_1-4 alkyl, C_1-4 alkyl-substituted C_6-10 aryl C_1-4 alkyl, hydroxy-substituted C_6-10 aryl C_1-4 alkyl, halogen-substituted C_6-10 aryl C_1-4 alkyl, C_1-4 alkoxy-substituted C_6-10 aryl C_1-4 alkyl, C_1-4 alkoxycarbonyl-substituted C_1-4 alkyl, C_1-4 alkoxycarbonylamino-substituted C_1-4 alkyl, 5- to 6-membered heterocycloalkyl-substituted C_1-4 alkyl, or C_5-6 cycloalkyl C_1-4 alkyl.

[Item A9b]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₂ is isopropyl, 1-methylpropyl, isobutyl, isopentyl, n-hexyl, hydroxymethyl, 2-hydroxyethyl, carbamoylmethyl, 3-amino-3-oxopropyl, 4-aminobutyl, 3-(amidinoamino)propyl, 2-carboxyethyl, benzyl, phenethyl, naphthalen-1-ylmethyl, 2-(naphthalen-1-yl)ethyl, 2-(1-(tert-butoxycarbonyl)-1H-indol-3-yl)ethyl, 3-methylbenzyl, 4-methylbenzyl, 4-hydroxybenzyl, 4-fluorobenzyl, 3-chlorobenzyl, 4-chlorobenzyl, 3,4-dichlorobenzyl, 4-(tert-butoxy)benzyl, 2-(tert-butoxy)-2-oxoethyl, 4-((tert-butoxycarbonyl)amino)butyl, (tetrahydro-2H-pyran-2-yl)methyl, or cyclohexylmethyl.

[Item A10]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₂ is isobutyl, 2-hydroxyethyl, 3-amino-3-oxopropyl, 4-aminobutyl, 2-carboxyethyl, benzyl, phenethyl, naphthalen-1-ylmethyl, 2-(naphthalen-1-yl)ethyl, 2-(1-(tert-butoxycarbonyl)-1H-indol-3-yl)ethyl, 3-methylbenzyl, 4-methylbenzyl, 4-hydroxybenzyl, 3-chlorobenzyl, 4-chlorobenzyl, 3,4-dichlorobenzyl, 4-(tert-butoxy)benzyl, 2-(tert-butoxy)-2-oxoethyl, 4-((tert-butoxycarbonyl)amino)butyl, (tetrahydro-2H-pyran-2-yl)methyl, or cyclohexylmethyl.

[Item A10b]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₂ is 1-methylpropyl, isopropyl, isobutyl, isopentyl, n-hexyl, benzyl, 4-hydroxybenzyl, 4-fluorobenzyl, 2-carboxyethyl, carbamoylmethyl, carbamoylethyl, 3-(amidinoamino)propyl, hydroxymethyl, 2-hydroxyethyl, phenethyl, naphthalen-1-ylmethyl, or cyclohexylmethyl.

[Item A11]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₂ is isopropyl, isobutyl, isopentyl, benzyl, 4-hydroxybenzyl, 4-fluorobenzyl, 2-carboxyethyl, carbamoylmethyl, 3-(amidinoamino)propyl, 2-hydroxyethyl, phenethyl, naphthalen-1-ylmethyl, or n-hexyl.

[Item A11b]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₂ is 1-methylpropyl, isopropyl, isobutyl, benzyl, 4-hydroxybenzyl, 2-carboxyethyl, 3-(amidinoamino)propyl, or naphthalen-1-ylmethyl.

[Item A12]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁ is C_1-6 alkyl, hydroxy-substituted C_1-4 alkyl, carbamoyl-substituted C_1-4 alkyl, amino-substituted C_1-6 alkyl, amidinoamino-substituted C_1-4 alkyl, carboxy-substituted C_1-4 alkyl, C_1-4 alkoxycarbonyl-substituted C_1-4 alkyl, C_6-10 aryl C_1-4 alkyl, hydroxy-substituted C_6-10 aryl C₁-4 alkyl, C_1-4 alkoxy-substituted C_6-10 aryl C_1-4 alkyl, halo-substituted C_6-10 aryl C_1-4 alkyl, or C_5-6 cycloalkyl C_1-4 alkyl.

[Item A12b]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁ is methyl, isopropyl, isobutyl, isopentyl, n-hexyl, 3-amino-3-oxopropyl, 3-(tert-butoxy)-3-oxopropyl, benzyl, naphthalen-1-ylmethyl, 2-carboxyethyl, carbamoylmethyl, 3-(amidinoamino)propyl, 4-fluorobenzyl, 4-hydroxybenzyl, 4-(tert-butoxy)benzyl, 3,4-dichlorobenzyl, naphthalen-1-ylmethyl, phenethyl, hydroxymethyl, 2-hydroxyethyl, or cyclohexylmethyl.

[Item A13]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁ is methyl, isobutyl, isopentyl, 3-(tert-butoxy)-3-oxopropyl, benzyl, naphthalen-1-ylmethyl, 4-hydroxybenzyl, 4-(tert-butoxy)benzyl, 3,4-dichlorobenzyl, or cyclohexylmethyl.

[Item A14]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁ is isopropyl, isobutyl, isopentyl, n-hexyl, cyclohexylmethyl, benzyl, phenethyl, naphthalen-1-ylmethyl, 4-hydroxybenzyl, 4-fluorobenzyl, 2-carboxyethyl, carbamoylmethyl, carbamoylethyl, 3-(amidinoamino)propyl, hydroxymethyl, or hydroxyethyl.

[Item A14b]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁ is isobutyl, isopentyl, cyclohexylmethyl, benzyl, phenethyl, naphthalen-1-ylmethyl, 4-hydroxybenzyl, 4-fluorobenzyl, 2-carboxyethyl, carbamoylmethyl, 3-(amidinoamino) propyl, or hydroxyethyl.

[Item A14c]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁ is isobutyl, benzyl, 4-hydroxybenzyl, 2-carboxyethyl, 3-(amidinoamino)propyl, or naphthalen-1-ylmethyl.

[Item A15]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₃ is C_1-4 alkyl, hydroxy-substituted C_1-4 alkyl, carbamoyl-substituted C_1-4 alkyl, C_1-4 alkoxycarbonyl-substituted C_1-4 alkyl, amino-substituted C_1-4 alkyl, amidinoamino-substituted C_1-4 alkyl, carboxy-substituted C_1-4 alkyl, C_6-10 aryl C_1-4 alkyl, C_1-4 alkyl-substituted C_6-10 aryl C_1-4 alkyl, hydroxy-substituted C_6-10 aryl C_1-4 alkyl, or C_5-6 cycloalkyl C_1-4 alkyl.

[Item A15b]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, which is isopropyl, isobutyl, isopentyl, n-hexyl, hydroxymethyl, 2-hydroxyethyl, carbamoylmethyl, 3-amino-3-oxopropyl, 4-aminobutyl, 3-(amidinoamino)propyl, 2-carboxyethyl, benzyl, phenethyl, naphthalen-1-ylmethyl, 4-hydroxybenzyl, 4-fluorobenzyl, 3-methylbenzyl, 4-methylbenzyl, 3-methoxy-3-oxopropyl, 4-((tert-butoxycarbonyl)amino)butyl, or cyclohexylmethyl.

[Item A16]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₃ is isobutyl, isopentyl, 3-amino-3-oxopropyl, 3-methoxy-3-oxopropyl, 4-aminobutyl, 2-carboxyethyl, benzyl, phenethyl, 3-methylbenzyl, 4-methylbenzyl, 4-hydroxybenzyl, 4-((tert-butoxycarbonyl)amino)butyl, or cyclohexylmethyl. [Item A17] The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₃ is isopropyl, isobutyl, isopentyl, n-hexyl, cyclohexylmethyl, benzyl, phenethyl, naphthalen-1-ylmethyl, 4-hydroxybenzyl, 4-fluorobenzyl, 2-carboxyethyl, carbamoylmethyl, carbamoylethyl, 3-(amidinoamino)propyl, hydroxymethyl, or hydroxyethyl.

[Item A17b]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₃ is isobutyl, isopentyl, benzyl, phenethyl, 4-hydroxybenzyl, 2-carboxyethyl, carbamoylmethyl, 3-(amidinoamino) propyl, hydroxymethyl, or naphthalen-1-ylmethyl.

[Item A17c]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₃ is isobutyl, benzyl, 4-hydroxybenzyl, 2-carboxyethyl, 3-(amidinoamino)propyl, or naphthalen-1-ylmethyl.

[Item A18]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₄ is hydrogen or alkyl.

[Item A18a]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₄ is hydrogen or C_1-6 alkyl.

[Item A18b]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₄ is hydrogen or ethyl.

[Item A19]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₄ is hydrogen.

[Item A20]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein R₁ is C_1-6 alkyl or C_6-10 aryl C_1-6 alkyl, and R₂ and R₃ are each independently C_1-6 alkyl or optionally substituted C_6-10 aryl C_1-6 alkyl.

[Item A21]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁ is isobutyl, isopentyl, or benzyl, R₂ is isobutyl, benzyl, phenethyl, 3-methylbenzyl, 4-methylbenzyl, or 3,4-dichlorobenzyl, and R₃ is isobutyl, benzyl, phenethyl, 3-methylbenzyl, or 4-methylbenzyl.

[Item A22]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

the compound is a compound of formula IF, R₁ is isobutyl, R₂ is benzyl, and R₃ is benzyl.

[Item A23]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

the compound is compound of formula IF, R₁ is benzyl, R₂ is benzyl, and R₃ is isobutyl.

[Item A24]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

the compound is a compound of formula IF, R₁ is isobutyl, R₂ is benzyl, and R₃ is 3-methylbenzyl.

[Item A25]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

the compound is a compound of formula IF, R₁ is benzyl, R₂ is 3,4-dichlorobenzyl, and R₃ is isobutyl.

[Item A26]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein the compound of formula IF is a compound selected from the group consisting of IF-1, IF-2, IF-3, IF-4, IF-5, IF-6, IF-7, IF-8, IF-9, IF-10, IF-11, IF-12, IF-13, IF-14, IF-15, IF-16, IF-17, IF-18, IF-19, IF-20, IF-22, IF-23, IF-24, IF-25, IF-26, IF-27, IF-28, IF-29, IF-30, IF-31, IF-32, IF-33, IF-34, IF-35, IF-36, IF-38, IF-39, IF-40, IF-41, IF-42, IF-43, IF-44, IF-45, IF-46, IF-47, IF-49, IF-50, IF-54, IF-57, IF-58, IF-68, IF-69, IF-70, IF-71, IF-72, IF-73, IF-74, IF-76, IF-77, IF-80, and IF-81 to IF-884.

[Item A26b]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein the compound of formula IF is (3S*,3aS*,6S*,7R*,7aS*)—N,7-dibenzyl-1-isobutyloctahydro-6H-3,6-methanopyrrolo[3,2-c]pyridine-6-caboxamide, (3S*,3aS*,6S*,7R*,7aS*)-1,7-dibenzyl-N-isobutyloctahydro-6H-3,6-methanopyrrolo[3,2-c]pyridine-6-caboxamide, (3S*,3aS*,6S*,7R*,7aS*)—N,1-dibenzyl-7-isobutyloctahydro-6H-3,6-methanopyrrolo[3,2-c]pyridine-6-caboxamide, (3S*,3aS*,6S*,7R*,7aS*)—N,7-dibenzyl-1-isopentyloctahydro-6H-3,6-methanopyrrolo[3,2-c]pyridine-6-caboxamide, (3S*,3aS*,6S*,7R*,7aS*)—N-benzyl-1-isobutyl-7-phenethyloctahydro-6H-3,6-methanopyrrolo[3,2-c]pyridine-6-caboxamide, (3S*,3aS*,6S*,7R*,7aS*)—N-benzyl-1-isobutyl-7-(3-methylbenzyl)octahydro-6H-3,6-methanopyrrolo[3,2-c]pyridine-6-caboxamide, (3S*,3aS*,6S*,7R*,7aS*)—N-benzyl-1-isobutyl-7-(4-methylbenzyl)octahydro-6H-3,6-methanopyrrolo[3,2-c]pyridine-6-caboxamide, (3S*,3aS*,6S*,7R*,7aS*)-7-benzyl-1-isobutyl-N-(3-methylbenzyl)octahydro-6H-3,6-methanopyrrolo[3,2-c]pyridine-6-caboxamide, (3S*,3aS*,6S*,7R*,7aS*)-1-benzyl-N-(3,4-dichlorobenzyl)-7-isobutyloctahydro-6H-3,6-methanopyrrolo[3,2-c]pyridine-6-caboxamide, or (3S*,3aS*,6S*,7R*,7aS*)—N,7-dibenzyl-4-ethyl-1-isobutyloctahydro-6H-3,6-methanopyrrolo[3,2-c]pyridine-6-caboxamide.

[Item A27]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein the compound of formula IB is a compound selected from the group consisting of IB-1, IB-2, IB-3, IB-4, IB-5, IB-6, IB-7, IB-8, IB-9, IB-10, IB-11, IB-12, IB-13, IB-14, IB-15, IB-16, IB-17, IB-18, IB-19, IB-20, IB-21, IB-22, IB-23, IB-24, IB-25, IB-26, IB-27, IB-28, IB-29, IB-30, IB-31, IB-32, IB-33, IB-34, IB-35, IB-36, IB-37, IB-38, IB-39, IB-40, IB-41, IB-42, IB-43, IB-44, IB-45, IB-46, IB-47, IB-49, IB-50, IB-54, IB-57, IB-58, IB-64, IB-68, IB-69, IB-70, IB-71, IB-72, IB-73, IB-74, IB-75, IB-76, IB-77, IB-78, IB-79, IB-80, and IB-81 to IB-923.

[Item A27b]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein the compound of formula IB is (3S*,3aS*,6R*,7R*,7aS*)-7-benzyl-N,1-diisobutyloctahydro-3aH-3,6-methanopyrrolo[3,2-b]pyridine-3a-caboxamide, (3S*,3aS*,6R*,7R*,7aS*)-1-benzyl-N,7-diisobutyloctahydro-3aH-3,6-methanopyrrolo[3,2-b]pyridine-3a-caboxamide, (3S*,3aS*,6R*,7R*,7aS*)—N-benzyl-1,7-diisobutyloctahydro-3aH-3,6-methanopyrrolo[3,2-b]pyridine-3a-caboxamide, (3S*,3aS*,6R*,7R*,7aS*)—N,7-dibenzyl-1-isopentyloctahydro-3aH-3,6-methanopyrrolo[3,2-b]pyridine-3a-caboxamide, (3S*,3aS*,6R*,7R*,7aS*)-1-benzyl-7-isobutyl-N-phenethyloctahydro-3aH-3,6-methanopyrrolo[3,2-b]pyridine-3a-caboxamide, (3S*,3aS*,6R*,7R*,7aS*)—N-benzyl-1-isobutyl-7-(3-methylbenzyl)octahydro-3aH-3,6-methanopyrrolo[3,2-b]pyridine-3a-caboxamide, or (3S*,3aS*,6R*,7R*,7aS*)-7-benzyl-1-isobutyl-N-(3-methylbenzyl)octahydro-3aH-3,6-methanopyrrolo[3,2-b]pyridine-3a-caboxamide.

[Item A28]

A compound represented by formula IIF:

or an enantiomer thereof, or a salt thereof, or a solvate thereof, wherein

R₁, R₂ and R₃ are each independently optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted arylalkyl, optionally substituted heteroarylalkyl, optionally substituted cycloalkylalkyl, or optionally substituted heterocycloalkylalkyl.

[Item A29]

A compound represented by formula IIB:

or an enantiomer thereof, or a salt thereof, or a solvate thereof, wherein

R₁, R₂ and R₃ are each independently optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted arylalkyl, optionally substituted heteroarylalkyl, optionally substituted cycloalkylalkyl, or optionally substituted heterocycloalkylalkyl.

[Item A30]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁, R₂ and R₃ are each independently optionally substituted alkyl, optionally substituted arylalkyl, optionally substituted heteroarylalkyl, or optionally substituted cycloalkylalkyl.

[Item A31]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁, R₂ and R₃ are each independently optionally substituted C_1-6 alkyl, optionally substituted C_6-10 aryl C_1-6 alkyl, optionally substituted 5- to 10-membered heteroaryl C_1-6 alkyl, or optionally substituted C_3-6 cycloalkyl C_1-6 alkyl.

[Item A32]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁, R₂ and R₃ are each independently C_1-6 alkyl, hydroxy-substituted C_1-6 alkyl, carbamoyl-substituted C_1-6 alkyl, amino-substituted C_1-6 alkyl, amidinoamino-substituted C_1-6 alkyl, carboxy-substituted C_1-6 alkyl, C_6-10 aryl C_1-6 alkyl, C_1-4 alkoxycarbonyl-substituted 5- to 10-membered heteroaryl C_1-6 alkyl, C_1-4 alkyl-substituted C_6-10 aryl C_1-6 alkyl, hydroxy-substituted C_6-10 aryl C_1-6 alkyl, halogen-substituted C_6-10 aryl C_1-6 alkyl, C_1-4 alkoxy-substituted C_6-10 aryl C_1-6 alkyl, (optionally substituted amino)-C_6-10 aryl C_1-6 alkyl, C_1-4 alkoxycarbonyl-substituted C_1-6 alkyl, C_1-4 alkoxycarbonylamino-substituted C_1-6 alkyl, 5- to 6-membered heterocycloalkyl-substituted C_1-6 alkyl, or C_3-6 cycloalkyl C_1-6 alkyl.

[Item A32a]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁, R₂ and R₃ are each independently C_1-6 alkyl, hydroxy-substituted C_1-6 alkyl, carbamoyl-substituted C_1-6 alkyl, amino-substituted C_1-6 alkyl, amidinoamino-substituted C_1-6 alkyl, carboxy-substituted C_1-6 alkyl, C_6-10 aryl C_1-6 alkyl, C_1-4 alkoxycarbonyl-substituted 5- to 10-membered heteroaryl C_1-6 alkyl, C_1-4 alkyl-substituted C_6-10 aryl C_1-6 alkyl, hydroxy-substituted C_6-10 aryl C_1-6 alkyl, halogen-substituted C_6-20 aryl C_1-6 alkyl, C_1-4 alkoxy-substituted C_6-10 aryl C_1-6 alkyl, C_1-4 alkoxycarbonyl-substituted C_1-6 alkyl, C_1-4 alkoxycarbonylamino-substituted C_1-6 alkyl, 5- to 6-membered heterocycloalkyl-substituted C_1-6 alkyl, or C_3-6 cycloalkylC_1-6alkyl.

[Item A32b]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁, R₂ and R₃ are each independently optionally substituted alkyl or optionally substituted arylalkyl.

[Item A32c]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁, R₂ and R₃ are each independently optionally substituted C_1-6 alkyl or optionally substituted C_6-10 aryl C_1-6 alkyl.

[Item A33]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₂ is C_1-4 alkyl, hydroxy-substituted C_1-4 alkyl, carbamoyl-substituted C_1-4 alkyl, amino-substituted C_1-4 alkyl, amidinoamino-substituted C_1-4 alkyl, carboxy-substituted C_1-4 alkyl, C_6-10 aryl C_1-4 alkyl, C_1-4 alkoxycarbonyl-substituted 5- to 10-membered heteroaryl C_1-4 alkyl, C_1-4 alkyl-substituted C_6-10 aryl C_1-4 alkyl, hydroxy-substituted C_6-10 aryl C_1-4 alkyl, halogen-substituted C_6-10 aryl C_1-4 alkyl, C_1-4 alkoxy-substituted C_6-10 aryl C_1-4 alkyl, C_1-4 alkoxycarbonyl-substituted C_1-4 alkyl, C_1-4 alkoxycarbonylamino-substituted C_1-4 alkyl, 5- to 6-membered heterocycloalkyl-substituted C_1-4 alkyl, or C_5-6 cycloalkyl C_1-4 alkyl.

[Item A33b]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₂ is isopropyl, 1-methylpropyl, isobutyl, isopentyl, n-hexyl, hydroxymethyl, 2-hydroxyethyl, carbamoylmethyl, 3-amino-3-oxopropyl, 4-aminobutyl, 3-(amidinoamino)propyl, 2-carboxyethyl, benzyl, phenethyl, naphthalen-1-ylmethyl, 2-(naphthalen-1-yl)ethyl, 2-(1-(tert-butoxycarbonyl)-1H-indol-3-yl)ethyl, 3-methylbenzyl, 4-methylbenzyl, 4-hydroxybenzyl, 4-fluorobenzyl, 3-chlorobenzyl, 4-chlorobenzyl, 3,4-dichlorobenzyl, 4-(tert-butoxy)benzyl, 2-(tert-butoxy)-2-oxoethyl, 3-(tert-butoxy)-3-oxopropyl, 4-((tert-butoxycarbonyl)amino)butyl, (tetrahydro-2H-pyran-2-yl)methyl, cyclohexylmethyl, or

[Item A34]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₂ is isobutyl, 2-hydroxyethyl, 3-amino-3-oxopropyl, 4-aminobutyl, 2-carboxyethyl, benzyl, phenethyl, naphthalen-1-ylmethyl, 2-(naphthalen-1-yl)ethyl, 2-(1-(tert-butoxycarbonyl)-1H-indol-3-yl)ethyl, 3-methylbenzyl, 4-methylbenzyl, 4-hydroxybenzyl, 3-chlorobenzyl, 4-chlorobenzyl, 3,4-dichlorobenzyl, 4-(tert-butoxy)benzyl, 2-(tert-butoxy)-2-oxoethyl, 4-((tert-butoxycarbonyl)amino)butyl, (tetrahydro-2H-pyran-2-yl)methyl, or cyclohexylmethyl.

[Item A35]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₂ is isopropyl, isobutyl, isopentyl, benzyl, 4-hydroxybenzyl, 4-fluorobenzyl, 2-carboxyethyl, carbamoylmethyl, 3-(amidinoamino)propyl, hydroxyethyl, phenethyl, naphthalen-1-ylmethyl, or n-hexyl.

[Item A35b]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₂ is isopropyl, 1-methylpropyl, isobutyl, 3-(amidinoamino)propyl, 2-carboxyethyl, benzyl, naphthalen-1-ylmethyl, 4-hydroxybenzyl, 4-(tert-butoxy)benzyl, 3-(tert-butoxy)-3-oxopropyl, or

[Item A36]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁ is C_1-6 alkyl, hydroxy-substituted C_1-4 alkyl, carbamoyl-substituted C_1-4 alkyl, amino-substituted C_1-6 alkyl, amidinoamino-substituted C_1-4 alkyl, carboxy-substituted C_1-4 alkyl, C_1-4 alkoxycarbonyl-substituted C_1-4 alkyl, C_6-10 aryl C_1-4 alkyl, hydroxy-substituted C_6-10 aryl C_1-4 alkyl, C_1-4 alkoxy-substituted C_6-10 aryl C_1-4 alkyl, halo-substituted C_6-10 aryl C_1-4 alkyl, or C_5-6 cycloalkyl C_1-4 alkyl.

[Item A36b]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁ is methyl, isopropyl, isobutyl, isopentyl, n-hexyl, 2-hydroxyethyl, carbamoylmethyl, 3-amino-3-oxopropyl, 3-(amidinoamino)propyl, 2-carboxyethyl, benzyl, phenethyl, naphthalen-1-ylmethyl, 4-hydroxybenzyl, 4-fluorobenzyl, 3,4-dichlorobenzyl, 4-(tert-butoxy)benzyl, 3-(tert-butoxy)-3-oxopropyl, hydroxymethyl, cyclohexylmethyl, or

[Item A37]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁ is methyl, isobutyl, isopentyl, 3-(tert-butoxy)-3-oxopropyl, benzyl, naphthalen-1-ylmethyl, 4-hydroxybenzyl, 4-(tert-butoxy)benzyl, 3,4-dichlorobenzyl, or cyclohexylmethyl.

[Item A38]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁ is isobutyl, isopentyl, cyclohexylmethyl, benzyl, phenethyl, naphthalen-1-ylmethyl, 4-hydroxybenzyl, 4-fluorobenzyl, 2-carboxyethyl, carbamoylmethyl, 3-(amidinoamino) propyl, or hydroxyethyl.

[Item A38b]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁ is isobutyl, 3-(amidinoamino)propyl, 2-carboxyethyl, benzyl, naphthalen-1-ylmethyl, 4-hydroxybenzyl, 4-(tert-butoxy)benzyl, 3-(tert-butoxy)-3-oxopropyl, or

[Item A39]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₃ is C_1-4 alkyl, hydroxy-substituted C_1-4 alkyl, carbamoyl-substituted C_1-4 alkyl, C_1-4 alkoxycarbonyl-substituted C_1-4 alkyl, amino-substituted C_1-4 alkyl, amidinoamino-substituted C_1-4 alkyl, carboxy-substituted C_1-4 alkyl, C_6-10 aryl C_1-4 alkyl, C_1-4 alkyl-substituted C_6-10 aryl C_1-4 alkyl, hydroxy-substituted C_6-10 aryl C_1-4 alkyl, or C_5-6 cycloalkyl C_1-4 alkyl.

[Item A39b]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₃ is isopropyl, isobutyl, isopentyl, n-hexyl, hydroxymethyl, 2-hydroxyethyl, carbamoylmethyl, 3-amino-3-oxopropyl, 4-aminobutyl, 3-(amidinoamino)propyl, 2-carboxyethyl, benzyl, phenethyl, naphthalen-1-ylmethyl, 3-methylbenzyl, 4-methylbenzyl, 4-hydroxybenzyl, 4-fluorobenzyl, 4-(tert-butoxy)benzyl, 3-methoxy-3-oxopropyl, 3-(tert-butoxy)-3-oxopropyl, 4-((tert-butoxycarbonyl)amino)butyl, cyclohexylmethyl, or

[Item A40]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₃ is isobutyl, isopentyl, 3-amino-3-oxopropyl, 3-methoxy-3-oxopropyl, 4-aminobutyl, 2-carboxyethyl, benzyl, phenethyl, 3-methylbenzyl, 4-methylbenzyl, 4-hydroxybenzyl, 4-((tert-butoxycarbonyl)amino)butyl, or cyclohexylmethyl.

[Item A41]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₃ is isobutyl, isopentyl, benzyl, phenethyl, 4-hydroxybenzyl, 2-carboxyethyl, carbamoylmethyl, 3-(amidinoamino) propyl, hydroxymethyl, or naphthalen-1-ylmethyl.

[Item A41b]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₃ is isobutyl, 2-carboxyethyl, 3-(amidinoamino)propyl, benzyl, naphthalen-1-ylmethyl, 4-hydroxybenzyl, 4-(tert-butoxy)benzyl, 3-(tert-butoxy)-3-oxopropyl, or

[Item A42]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁ is C_1-6 alkyl or C_6-10 aryl C_1-6 alkyl, R₂ and R₃ are each independently C_1-6 alkyl or optionally substituted C_6-10 aryl C_1-6 alkyl.

[Item A42b]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁, R₂, and R₃ are each independently C_1-6 alkyl or optionally substituted C_6-10 aryl C_1-6 alkyl.

[Item A42c]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁, R₂, and R₃ are each independently C_1-6 alkyl, C_6-10 aryl C_1-6 alkyl, C_1-4 alkyl-substituted C_6-20 aryl C_1-6 alkyl, halogen-substituted C_6-10 aryl C_1-6 alkyl, C_1-4 alkoxy-substituted C_6-10 aryl C_1-6 alkyl, or (optionally substituted amino)-C_6-10 aryl C_1-6 alkyl.

[Item A42d]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁ is C_1-6 alkyl or C₆ aryl C_1-4 alkyl, R₂ is C_1-6 alkyl or C_1-4 alkyl-substituted benzyl, and R₃ is C_1-6 alkyl or C₆ aryl C_1-4 alkyl.

[Item A43]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁ is isobutyl, benzyl, 4-(dimethylamino)benzyl, 4-methylbenzyl, 4-tert-butylbenzyl, 4-methoxybenzyl, 3-chlorobenzyl, 4-chlorobenzyl, or 3,4-dichlorobenzyl, R₂ is isobutyl, benzyl, naphthalen-1-ylmethyl, 4-methylbenzyl, 4-chlorobenzyl, or 3,4-dichlorobenzyl, and R₃ is isobutyl, isopentyl, or benzyl.

[Item A43b]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein

R₁ is isobutyl, isopentyl, or benzyl, R₂ is isobutyl, benzyl, phenethyl, 3-methylbenzyl, 4-methylbenzyl, or 3,4-dichlorobenzyl, and R₃ is isobutyl, benzyl, phenethyl, 3-methylbenzyl, or 4-methylbenzyl.

[Item A44]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein the compound is a compound of formula IIF, R₁ is isobutyl, R₂ is 4-methylbenzyl, and R₃ is benzyl.

[Item A45]

The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to any one of the preceding items, wherein the compound is a compound of formula IIB, R₁ is benzyl, R₂ is isobutyl, and R₃ is isobutyl.

[Item A46]

An antiviral agent for a virus in the Lyssavirus genus, comprising the compound according to any one of the preceding items or a pharmaceutically acceptable salt thereof.

[Item A47]

The antiviral agent according to any one of the preceding items, wherein the virus in the Lyssavirus genus comprises a rabies virus.

[Item A48]

A medicament comprising the compound according to any one of the preceding items or a pharmaceutically acceptable salt thereof, or the antiviral agent according to any one of the preceding items.

[Item A49]

The medicament according to any one of the preceding items, which is a prophylactic agent or a therapeutic agent for rabies.

[Item A50]

A pharmaceutical composition comprising the compound according to any one of the preceding items or a pharmaceutically acceptable salt thereof, or the antiviral agent according to any one of the preceding items, and a pharmaceutically acceptable carrier.

[Item A51]

A pharmaceutical composition for the prophylaxis or treatment of rabies, comprising the compound according to any one of the preceding items or a pharmaceutically acceptable salt thereof, or the antiviral agent according to any one of the preceding items, and a pharmaceutically acceptable carrier.

[Item A52]

The compound according to any one of the preceding items or a pharmaceutically acceptable salt thereof for use as an antiviral agent for a virus in the Lyssavirus genus, preferably a rabies virus, or for the prophylaxis or treatment of rabies.

[Item A53]

A method for the prophylaxis or treatment of rabies, characterized by administering a prophylactically or therapeutically effective amount of the compound according to any one of the preceding items or a pharmaceutically acceptable salt thereof, the antiviral agent according to any one of the preceding items, the medicament according to any one of the preceding items, or the pharmaceutical composition according to any one of the preceding items to a patient in need thereof

[Item A54]

Use of the compound according to any one of the preceding items or a pharmaceutically acceptable salt thereof, or the antiviral agent according to any one of the preceding items, for the manufacture of a medicament for the prophylaxis or treatment of rabies.

The present disclosure is intended so that one or more of the features described above can be provided not only as the explicitly disclosed combinations, but also as other combinations thereof. Additional embodiments and advantages of the present disclosure are recognized by those skilled in the art by reading and understanding the following detailed description as needed.

Advantageous Effects of Invention

The compounds of the present disclosure exhibit an excellent antiviral action on viruses in the Lyssavirus genus including the rabies virus. Therefore, the compounds of the present disclosure are useful as a therapeutic agent and/or prophylactic agent for rabies.

BRIEF DESCRIPTION OF DRAWINGS

FIG. 1 shows an ORTEP diagram for the results of X-ray crystallography in Synthesis Example: IF-1.

FIG. 2 shows a chromatogram upon separation of the racemate in Synthesis Example: IF-1 using a chiral column, CHIRALPAK IG (5 μm, 4.6×150 mm), mobile phase: methanol:diethylamine (100:0.1).

FIG. 3 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 4 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 5 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 6 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 7 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 8 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 9 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 10 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 11 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 12 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 13 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 14 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 15 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 16 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 17 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 18 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 19 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 20 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 21 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 22 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 23 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 24 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 25 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 26 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 27 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 28 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 29 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 30 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 31 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 32 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 33 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 34 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 35 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 36 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 37 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 38 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 39 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 40 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 41 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 42 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 43 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 44 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 45 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 46 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 47 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 48 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 49 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 50 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 51 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 52 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 53 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 54 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 55 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 56 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 57 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 58 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 59 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 60 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 61 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 62 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 63 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 64 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 65 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 66 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 67 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 68 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 69 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 70 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 71 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 72 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 73 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 74 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 75 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 76 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 77 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 78 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 79 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 80 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

FIG. 81 shows the ¹H-NMR chart for an exemplary compound of the present disclosure (formula in the figure).

DESCRIPTION OF EMBODIMENTS

Hereinafter, the present disclosure is described in more detail.

Throughout the entire specification, a singular expression should be understood as encompassing the concept thereof in the plural form, unless specifically noted otherwise. Thus, singular articles (e.g., “a”, “an”, “the”, and the like in the case of English) should also be understood as encompassing the concept thereof in the plural form, unless specifically noted otherwise. The terms used herein should also be understood as being used in the meaning that is commonly used in the art, unless specifically noted otherwise. Thus, unless defined otherwise, all terminologies and scientific technical terms that are used herein have the same meaning as the general understanding of those skilled in the art to which the present disclosure pertains. In case of a contradiction, the present specification (including the definitions) takes precedence.

Definitions

The terms and the general technology used in the present disclosure are first described.

As used herein, the term “group” refers to a monovalent group, unless especially noted otherwise. Examples of a group that is not a monovalent group include alkylene group (divalent) and the like. The term “group” may also be abbreviated in the following description of substituents or the like.

As used herein, the number of substituents when a group is defined as “optionally substituted” or “substituted” is not particularly limited as long as it is substitutable and is one or more. The description for each group is also applicable when the substituent is a part of or a substituent on another substituent, unless specifically noted otherwise.

As used herein, “maximum substitutable number” is the maximum number of substituents that a group can have. The number can vary for each group. For example, the number is 3 for a methyl group, 5 for an ethyl group, 7 for a benzyl group, and 10 for a naphthalenyl ethyl group.

For a group that is modified by “optionally substituted” or “substituted” herein, any portion of the group can be substituted. For example, “optionally substituted arylalkyl” and “substituted arylalkyl” can have the aryl moiety substituted, the alkyl moiety substituted, or both the aryl moiety and the alkyl moiety substituted.

As used herein, the substituent used when “optionally substituted” can be one or more of the same or different substituents selected from any one of the following substituent groups I to VI. While the types of atoms within a substituent associated with attachment are not particularly limited by the type of substituent, if the atom to which a substituent attaches is an oxygen atom, a nitrogen atom, or a sulfur atom, the atom is limited to and selected from those with an attachment point in the following substituents that is a carbon atom.

Substituent group I consists of halogen, hydroxy, oxo, carboxy, amino, imino, hydroxyamino, hydroxyimino, formyl, formyloxy, carbamoyl, sulfamoyl, sulfanyl, sulfino, sulfo, thioformyl, thiocarboxy, dithiocarboxy, thiocarbamoyl, cyano, nitro, nitroso, azide, hydrazino, ureide, amidino, amidinoamino, unsubstituted or substituted alkyl, unsubstituted or substituted alkenyl, unsubstituted or substituted alkynyl, unsubstituted or substituted aryl, unsubstituted or substituted cycloalkyl, unsubstituted or substituted heteroaryl, unsubstituted or substituted heterocycloalkyl, unsubstituted or substituted alkyloxy, unsubstituted or substituted alkenyloxy, unsubstituted or substituted alkynyloxy, unsubstituted or substituted aryl-L_X-oxy, unsubstituted or substituted cycloalkyl-L_X-oxy, unsubstituted or substituted heteroaryl-L_X-oxy, unsubstituted or substituted heterocycloalkyl-L_X-oxy, unsubstituted or substituted alkyloxyalkyl, unsubstituted or substituted alkenyloxyalkyl, unsubstituted or substituted alkynyloxyalkyl, unsubstituted or substituted aryloxyalkyl, unsubstituted or substituted cycloalkyloxyalkyl, unsubstituted or substituted heteroaryloxyalkyl, unsubstituted or substituted heterocycloalkyloxyalkyl, unsubstituted or substituted alkyloxyalkyloxy, unsubstituted or substituted alkenyloxyalkyloxy, unsubstituted or substituted alkynyloxyalkyloxy, unsubstituted or substituted aryloxyalkyloxy, unsubstituted or substituted cycloalkyloxyalkyloxy, unsubstituted or substituted heteroaryloxyalkyloxy, unsubstituted or substituted heterocycloalkyloxyalkyloxy, unsubstituted or substituted alkylcarbonyl, unsubstituted or substituted alkenylcarbonyl, unsubstituted or substituted alkynylcarbonyl, unsubstituted or substituted aryl-L_X-carbonyl, unsubstituted or substituted cycloalkyl-L_X-carbonyl, unsubstituted or substituted heteroaryl-L_X-carbonyl, unsubstituted or substituted heterocycloalkyl-L_X-carbonyl, unsubstituted or substituted alkylcarbonyloxy, unsubstituted or substituted alkenylcarbonyloxy, unsubstituted or substituted alkynylcarbonyloxy, unsubstituted or substituted aryl-L_X-carbonyloxy, unsubstituted or substituted cycloalkyl-L_X-carbonyloxy, unsubstituted or substituted heteroaryl-L_X-carbonyloxy, unsubstituted or substituted heterocycloalkyl-L_X-carbonyloxy, unsubstituted or substituted alkylcarbonylamino, unsubstituted or substituted alkenylcarbonylamino, unsubstituted or substituted alkynylcarbonylamino, unsubstituted or substituted aryl-L_X-carbonylamino, unsubstituted or substituted cycloalkyl-L_X-carbonylamino, unsubstituted or substituted heteroaryl-L_X-carbonylamino, unsubstituted or substituted heterocycloalkyl-L_X-carbonylamino, unsubstituted or substituted alkylcarbonylthio, unsubstituted or substituted alkenylcarbonylthio, unsubstituted or substituted alkynylcarbonylthio, unsubstituted or substituted aryl-L_X-carbonylthio, unsubstituted or substituted cycloalkyl-L_X-carbonylthio, unsubstituted or substituted heteroaryl-L_X-carbonylthio, unsubstituted or substituted heterocycloalkyl-L_X-carbonylthio, unsubstituted or substituted alkylcarbonylimino, unsubstituted or substituted alkenylcarbonylimino, unsubstituted or substituted alkynylcarbonylimino, unsubstituted or substituted aryl-L_X-carbonylimino, unsubstituted or substituted cycloalkyl-L_X-carbonylimino, unsubstituted or substituted heteroaryl-L_X-carbonylimino, unsubstituted or substituted heterocycloalkyl-L_X-carbonylimino, unsubstituted or substituted alkylthio, unsubstituted or substituted alkenylthio, unsubstituted or substituted alkynylthio, unsubstituted or substituted aryl-L_X-thio, unsubstituted or substituted cycloalkyl-L_X-thio, unsubstituted or substituted heteroaryl-L_X-thio, unsubstituted or substituted heterocycloalkyl-L_X-thio, unsubstituted or substituted alkylamino, unsubstituted or substituted alkenylamino, unsubstituted or substituted alkynylamino, unsubstituted or substituted alkynylamino, unsubstituted or substituted aryl-L_X-amino, unsubstituted or substituted cycloalkyl-L_X-amino, unsubstituted or substituted heteroaryl-L_X-amino, unsubstituted or substituted heterocycloalkyl-L_X-amino, unsubstituted or substituted alkylsulfonyl, unsubstituted or substituted alkenylsulfonyl, unsubstituted or substituted alkynylsulfonyl, unsubstituted or substituted aryl-L_X-sulfonyl, unsubstituted or substituted cycloalkyl-L_X-sulfonyl, unsubstituted or substituted heteroaryl-L_X-sulfonyl, unsubstituted or substituted heterocycloalkyl-L_X-sulfonyl, unsubstituted or substituted alkylsulfonylamino, unsubstituted or substituted alkenylsulfonylamino, unsubstituted or substituted alkynylsulfonylamino, unsubstituted or substituted aryl-L_X-sulfonylamino, unsubstituted or substituted cycloalkyl-L_X-sulfonylamino, unsubstituted or substituted heteroaryl-L_X-sulfonylamino, unsubstituted or substituted heterocycloalkyl-L_X-sulfonylamino, unsubstituted or substituted alkylimino, unsubstituted or substituted alkenylimino, unsubstituted or substituted alkynylimino, unsubstituted or substituted aryl-L_X-imino, unsubstituted or substituted cycloalkyl-L_X-imino, unsubstituted or substituted heteroaryl-L_X-imino, unsubstituted or substituted heterocycloalkyl-L_X-imino, unsubstituted or substituted alkyloxyimino, unsubstituted or substituted alkenyloxyimino, unsubstituted or substituted alkynyloxyimino, unsubstituted or substituted aryl-L_X-oxyimino, unsubstituted or substituted cycloalkyl-L_X-oxyimino, unsubstituted or substituted heteroaryl-L_X-oxyimino, unsubstituted or substituted heterocycloalkyl-L_X-oxyimino, unsubstituted or substituted alkyloxycarbonyl, unsubstituted or substituted alkenyloxycarbonyl, unsubstituted or substituted alkynyloxycarbonyl, unsubstituted or substituted aryl-L_X-oxycarbonyl, unsubstituted or substituted cycloalkyl-L_X-oxycarbonyl, unsubstituted or substituted heteroaryl-L_X-oxycarbonyl, unsubstituted or substituted heterocycloalkyl-L_X-oxycarbonyl, unsubstituted or substituted alkyloxycarbonylamino, unsubstituted or substituted alkenyloxycarbonylamino, unsubstituted or substituted alkynyloxycarbonylamino, unsubstituted or substituted aryl-L_X-oxycarbonylamino, unsubstituted or substituted cycloalkyl-L_X-oxycarbonylamino, unsubstituted or substituted heteroaryl-L_X-oxycarbonylamino, unsubstituted or substituted heterocycloalkyl-L_X-oxycarbonylamino, unsubstituted or substituted alkylsulfanyl, unsubstituted or substituted alkenylsulfanyl, unsubstituted or substituted alkynylsulfanyl, unsubstituted or substituted aryl-L_X-sulfanyl, unsubstituted or substituted cycloalkyl-L_X-sulfanyl, unsubstituted or substituted heteroaryl-L_X-sulfanyl, unsubstituted or substituted heterocycloalkyl-L_X-sulfanyl, unsubstituted or substituted alkylsulfinyl, unsubstituted or substituted alkenylsulfinyl, unsubstituted or substituted alkynylsulfinyl, unsubstituted or substituted aryl-L_X-sulfinyl, unsubstituted or substituted cycloalkyl-L_X-sulfinyl, unsubstituted or substituted heteroaryl-L_X-sulfinyl, unsubstituted or substituted heterocycloalkyl-L_X-sulfinyl, unsubstituted or substituted alkylcarbamoyl, unsubstituted or substituted alkenylcarbamoyl, unsubstituted or substituted alkynylcarbamoyl, unsubstituted or substituted aryl-L_X-carbamoyl, unsubstituted or substituted cycloalkyl-L_X-carbamoyl, unsubstituted or substituted heteroaryl-L_X-carbamoyl, unsubstituted or substituted heterocycloalkyl-L_X-carbamoyl, unsubstituted or substituted alkylsulfamoyl, unsubstituted or substituted alkenylsulfamoyl, unsubstituted or substituted alkynylsulfamoyl, unsubstituted or substituted aryl-L_X-sulfamoyl, unsubstituted or substituted cycloalkyl-L_X-sulfamoyl, unsubstituted or substituted heteroaryl-L_X-sulfamoyl, and unsubstituted or substituted heterocycloalkyl-L_X-sulfamoyl, wherein L_X is a single bond or unsubstituted or substituted alkylene,

wherein the substituted alkyl, substituted alkenyl, substituted alkynyl, substituted aryl, substituted cycloalkyl, substituted heteroaryl, substituted heterocycloalkyl, and substituted alkylene moieties (fully or partially) in the substituent group each independently have one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, hydroxy, oxo, carboxy, amino, imino, hydroxyamino, hydroxyimino, formyl, formyloxy, carbamoyl, sulfamoyl, sulfanyl, sulfino, sulfa, thioformyl, thiocarboxy, dithiocarboxy, thiocarbamoyl, cyano, nitro, nitroso, azide, hydrazino, ureide, amidino, amidinoamino, alkyl, alkenyl, alkynyl, aryl, cycloalkyl, heteroaryl, heterocycloalkyl, alkyloxy, alkenyloxy, alkynyloxy, aryl-L_X-oxy, cycloalkyl-L_X-oxy, heteroaryl-L_X-oxy, heterocycloalkyl-L_X-oxy, alkyloxyalkyl, alkenyloxyalkyl, alkynyloxyalkyl, aryloxyalkyl, cycloalkyloxyalkyl, heteroaryloxyalkyl, heterocycloalkyloxyalkyl, alkyloxyalkyloxy, alkenyloxyalkyloxy, alkynyloxyalkyloxy, aryloxyalkyloxy, cycloalkyloxyalkyloxy, heteroaryloxyalkyloxy, heterocycloalkyloxyalkyloxy, alkylcarbonyl, alkenylcarbonyl, alkynylcarbonyl, aryl-L_X-carbonyl, cycloalkyl-L_X-carbonyl, heteroaryl-L_X-carbonyl, heterocycloalkyl-L_X-carbonyl, alkylcarbonyloxy, alkenylcarbonyloxy, alkynylcarbonyloxy, aryl-L_X-carbonyloxy, cycloalkyl-L_X-carbonyloxy, heteroaryl-L_X-carbonyloxy, heterocycloalkyl-L_X-carbonyloxy, alkylcarbonylamino, alkenylcarbonylamino, alkynylcarbonylamino, aryl-L_X-carbonylamino, cycloalkyl-L_X-carbonylamino, heteroaryl-L_X-carbonylamino, heterocycloalkyl-L_X-carbonylamino, alkylcarbonylthio, alkenylcarbonylthio, alkynylcarbonylthio, aryl-L_X-carbonylthio, cycloalkyl-L_X-carbonylthio, heteroaryl-L_X-carbonylthio, heterocycloalkyl-L_X-carbonylthio, alkylcarbonylimino, alkenylcarbonylimino, alkynylcarbonylimino, aryl-L_X-carbonylimino, cycloalkyl-L_X-carbonylimino, heteroaryl-L_X-carbonylimino, heterocycloalkyl-L_X-carbonylimino, alkylthio, alkenylthio, alkynylthio, aryl-L_X-thio, cycloalkyl-L_X-thio, heteroaryl-L_X-thio, heterocycloalkyl-L_X-thio, alkylamino, alkenylamino, alkynylamino, alkynylamino, aryl-L_X-amino, cycloalkyl-L_X-amino, heteroaryl-L_X-amino, heterocycloalkyl-L_X-amino, alkylsulfonyl, alkenylsulfonyl, alkynylsulfonyl, aryl-L_X-sulfonyl, cycloalkyl-L_X-sulfonyl, heteroaryl-L_X-sulfonyl, heterocycloalkyl-L_X-sulfonyl, alkylsulfonylamino, alkenylsulfonylamino, alkynylsulfonylamino, aryl-L_X-sulfonylamino, cycloalkyl-L_X-sulfonylamino, heteroaryl-L_X-sulfonylamino, heterocycloalkyl-L_X-sulfonylamino, alkylimino, alkenylimino, alkynylimino, aryl-L_X-imino, cycloalkyl-L_X-imino, heteroaryl-L_X-imino, heterocycloalkyl-L_X-imino, alkyloxyimino, alkenyloxyimino, alkynyloxyimino, aryl-L_X-oxyimino, cycloalkyl-L_X-oxyimino, heteroaryl-L_X-oxyimino, heterocycloalkyl-L_X-oxyimino, alkyloxycarbonyl, alkenyloxycarbonyl, alkynyloxycarbonyl, aryl-L_X-oxycarbonyl, cycloalkyl-L_X-oxycarbonyl, heteroaryl-L_X-oxycarbonyl, heterocycloalkyl-L_X-oxycarbonyl, alkyloxycarbonylamino, alkenyloxycarbonylamino, alkynyloxycarbonylamino, aryl-L_X-oxycarbonylamino, cycloalkyl-L_X-oxycarbonylamino, heteroaryl-L_X-oxycarbonylamino, heterocycloalkyl-L_X-oxycarbonylamino, alkylsulfanyl, alkenylsulfanyl, alkynylsulfanyl, aryl-L_X-sulfanyl, cycloalkyl-L_X-sulfanyl, heteroaryl-L_X-sulfanyl, heterocycloalkyl-L_X-sulfanyl, alkylsulfinyl, alkenylsulfinyl, alkynylsulfinyl, aryl-L_X-sulfinyl, cycloalkyl-L_X-sulfinyl, heteroaryl-L_X-sulfinyl, heterocycloalkyl-L_X-sulfinyl, alkylcarbamoyl, alkenylcarbamoyl, alkynylcarbamoyl, aryl-L_X-carbamoyl, cycloalkyl-L_X-carbamoyl, heteroaryl-L_X-carbamoyl, heterocycloalkyl-L_X-carbamoyl, alkylsulfamoyl, alkenylsulfamoyl, alkynylsulfamoyl, aryl-L_X-sulfamoyl, cycloalkyl-L_X-sulfamoyl, heteroaryl-L_X-sulfamoyl, and heterocycloalkyl-L_X-sulfamoyl.

Substituent group II consists of halogen, hydroxy, oxo, carboxy, amino, imino, hydroxyamino, hydroxyimino, formyl, formyloxy, carbamoyl, sulfamoyl, sulfanyl, sulfino, sulfo, thioformyl, thiocarboxy, dithiocarboxy, thiocarbamoyl, cyano, nitro, nitroso, azide, hydrazino, ureide, amidino, amidinoamino, unsubstituted or substituted C_1-12 alkyl, unsubstituted or substituted C_2-12 alkenyl, unsubstituted or substituted C_2-12 alkynyl, unsubstituted or substituted C_0-10 aryl, unsubstituted or substituted C_3-10 cycloalkyl, unsubstituted or substituted 5- to 10-membered heteroaryl, unsubstituted or substituted 5- to 10-membered heterocycloalkyl, unsubstituted or substituted C_1-12 alkyloxy, unsubstituted or substituted C_2-12 alkenyloxy, unsubstituted or substituted C_2-12 alkynyloxy, unsubstituted or substituted C_6-10 aryl-L_X-oxy, unsubstituted or substituted C_3-10 cycloalkyl-L_X-oxy, unsubstituted or substituted 5- to 10-membered heteroaryl-L_X-oxy, unsubstituted or substituted 5- to 10-membered heterocycloalkyl-L_X-oxy, unsubstituted or substituted C_1-12 alkyloxy C_1-12 alkyl, unsubstituted or substituted C_2-12 alkenyloxy C_1-12 alkyl, unsubstituted or substituted C_2-12 alkynyloxy C_1-12 alkyl, unsubstituted or substituted C_0-10 aryloxy C_1-12 alkyl, unsubstituted or substituted C_3-10 cycloalkyloxy C_1-12 alkyl, unsubstituted or substituted 5- to 10-membered heteroaryloxy C_1-12 alkyl, unsubstituted or substituted 5- to 10-membered heterocycloalkyloxy C_1-12 alkyl, unsubstituted or substituted C_1-12 alkyloxy C_1-12 alkyloxy, unsubstituted or substituted C_2-12 alkenyloxy C_1-12 alkyloxy, unsubstituted or substituted C_2-12 alkynyloxy C_1-12 alkyloxy, unsubstituted or substituted C_6-10 aryloxy C_1-12 alkyloxy, unsubstituted or substituted C_3-10 cycloalkyloxy C_1-12 alkyloxy, unsubstituted or substituted 5- to 10-membered heteroaryloxy C_1-12 alkyloxy, unsubstituted or substituted 5- to 10-membered heterocycloalkyloxy C_1-12 alkyloxy, unsubstituted or substituted C_1-12 alkylcarbonyl, unsubstituted or substituted C_2-12 alkenylcarbonyl, unsubstituted or substituted C_2-12 alkynylcarbonyl, unsubstituted or substituted C_6-10 aryl-L_X-carbonyl, unsubstituted or substituted C_3-10 cycloalkyl-L_X-carbonyl, unsubstituted or substituted 5- to 10-membered heteroaryl-L_X-carbonyl, unsubstituted or substituted 5- to 10-membered heterocycloalkyl-L_X-carbonyl, unsubstituted or substituted C_1-12 alkylcarbonyloxy, unsubstituted or substituted C_2-12 alkenylcarbonyloxy, unsubstituted or substituted C_2-12 alkynylcarbonyloxy, unsubstituted or substituted C_6-10 aryl-L_X-carbonyloxy, unsubstituted or substituted C_3-10 cycloalkyl-L_X-carbonyloxy, unsubstituted or substituted 5- to 10-membered heteroaryl-L_X-carbonyloxy, unsubstituted or substituted 5- to 10-membered heterocycloalkyl-L_X-carbonyloxy, unsubstituted or substituted C_1-12 alkylcarbonylamino, unsubstituted or substituted C_2-12 alkenylcarbonylamino, unsubstituted or substituted C_2-12 alkynylcarbonylamino, unsubstituted or substituted C_6-10 aryl-L_X-carbonylamino, unsubstituted or substituted C_3-10 cycloalkyl-L_X-carbonylamino, unsubstituted or substituted 5- to 10-membered heteroaryl-L_X-carbonylamino, unsubstituted or substituted 5- to 10-membered heterocycloalkyl-L_X-carbonylamino, unsubstituted or substituted C_1-12 alkylcarbonylthio, unsubstituted or substituted C_2-12 alkenylcarbonylthio, unsubstituted or substituted C_2-12 alkynylcarbonylthio, unsubstituted or substituted C_6-10 aryl-L_X-carbonylthio, unsubstituted or substituted C_3-10 cycloalkyl-L_X-carbonylthio, unsubstituted or substituted 5- to 10-membered heteroaryl-L_X-carbonylthio, unsubstituted or substituted 5- to 10-membered heterocycloalkyl-L_X-carbonylthio, unsubstituted or substituted C_1-12 alkylcarbonylimino, unsubstituted or substituted C_2-12 alkenylcarbonylimino, unsubstituted or substituted C_2-12 alkynylcarbonylimino, unsubstituted or substituted C_6-10 aryl-L_X-carbonylimino, unsubstituted or substituted C_3-10 cycloalkyl-L_X-carbonylimino, unsubstituted or substituted 5- to 10-membered heteroaryl-L_X-carbonylimino, unsubstituted or substituted 5- to 10-membered heterocycloalkyl-L_X-carbonylimino, unsubstituted or substituted C_1-12 alkylthio, unsubstituted or substituted C_2-12 alkenylthio, unsubstituted or substituted C_2-12 alkynylthio, unsubstituted or substituted C_6-10 aryl-L_X-thio, unsubstituted or substituted C_3-10 cycloalkyl-L_X-thio, unsubstituted or substituted 5- to 10-membered heteroaryl-L_X-thio, unsubstituted or substituted 5- to 10-membered heterocycloalkyl-L_X-thio, unsubstituted or substituted C_1-12 alkylamino, unsubstituted or substituted C_2-12 alkenylamino, unsubstituted or substituted C_2-12 alkynylamino, unsubstituted or substituted C_2-12 alkynylamino, unsubstituted or substituted C_6-10 aryl-L_X-amino, unsubstituted or substituted C_3-10 cycloalkyl-L_X-amino, unsubstituted or substituted 5- to 10-membered heteroaryl-L_X-amino, unsubstituted or substituted 5- to 10-membered heterocycloalkyl-L_X-amino, unsubstituted or substituted C_1-12 alkylsulfonyl, unsubstituted or substituted C_2-12 alkenylsulfonyl, unsubstituted or substituted C_2-12 alkynylsulfonyl, unsubstituted or substituted C_6-10 aryl-L_X-sulfonyl, unsubstituted or substituted C_3-10 cycloalkyl-L_X-sulfonyl, unsubstituted or substituted 5- to 10-membered heteroaryl-L_X-sulfonyl, unsubstituted or substituted 5- to 10-membered heterocycloalkyl-L_X-sulfonyl, unsubstituted or substituted C_1-12 alkylsulfonylamino, unsubstituted or substituted C_2-12 alkenylsulfonylamino, unsubstituted or substituted C_2-12 alkynylsulfonylamino, unsubstituted or substituted C_6-10 aryl-L_X-sulfonylamino, unsubstituted or substituted C_3-10 cycloalkyl-L_X-sulfonylamino, unsubstituted or substituted 5- to 10-membered heteroaryl-L_X-sulfonylamino, unsubstituted or substituted 5- to 10-membered heterocycloalkyl-L_X-sulfonylamino, unsubstituted or substituted C_1-12 alkylimino, unsubstituted or substituted C_2-12 alkenylimino, unsubstituted or substituted C_2-12 alkynylimino, unsubstituted or substituted C_6-10 aryl-L_X-imino, unsubstituted or substituted C_3-10 cycloalkyl-L_X-imino, unsubstituted or substituted 5- to 10-membered heteroaryl-L_X-imino, unsubstituted or substituted 5- to 10-membered heterocycloalkyl-L_X-imino, unsubstituted or substituted C_1-12 alkyloxyimino, unsubstituted or substituted C_2-12 alkenyloxyimino, unsubstituted or substituted C_2-12 alkynyloxyimino, unsubstituted or substituted C_6-10 aryl-L_X-oxyimino, unsubstituted or substituted C_3-10 cycloalkyl-L_X-oxyimino, unsubstituted or substituted 5- to 10-membered heteroaryl-L_X-oxyimino, unsubstituted or substituted 5- to 10-membered heterocycloalkyl-L_X-oxyimino, unsubstituted or substituted C_1-12 alkyloxycarbonyl, unsubstituted or substituted C_2-12 alkenyloxycarbonyl, unsubstituted or substituted C_2-12 alkynyloxycarbonyl, unsubstituted or substituted C_6-10 aryl-L_X-oxycarbonyl, unsubstituted or substituted C_3-10 cycloalkyl-L_X-oxycarbonyl, unsubstituted or substituted 5- to 10-membered heteroaryl-L_X-oxycarbonyl, unsubstituted or substituted 5- to 10-membered heterocycloalkyl-L_X-oxycarbonyl, unsubstituted or substituted C_1-12 alkyloxycarbonylamino, unsubstituted or substituted C_2-12 alkenyloxycarbonylamino, unsubstituted or substituted C_2-12 alkynyloxycarbonylamino, unsubstituted or substituted C_6-10 aryl-L_X-oxycarbonylamino, unsubstituted or substituted C_3-10 cycloalkyl-L_X-oxycarbonylamino, unsubstituted or substituted 5- to 10-membered heteroaryl-L_X-oxycarbonylamino, unsubstituted or substituted 5- to 10-membered heterocycloalkyl-L_X-oxycarbonylamino, unsubstituted or substituted C_1-12 alkylsulfanyl, unsubstituted or substituted C_2-12 alkenylsulfanyl, unsubstituted or substituted C_2-12 alkynylsulfanyl, unsubstituted or substituted C_6-10 aryl-L_X-sulfanyl, unsubstituted or substituted C_3-10 cycloalkyl-L_X-sulfanyl, unsubstituted or substituted 5- to 10-membered heteroaryl-L_X-sulfanyl, unsubstituted or substituted 5- to 10-membered heterocycloalkyl-L_X-sulfanyl, unsubstituted or substituted C_1-12 alkylsulfinyl, unsubstituted or substituted C_2-12 alkenylsulfinyl, unsubstituted or substituted C_2-12 alkynylsulfinyl, unsubstituted or substituted C_6-10 aryl-L_X-sulfinyl, unsubstituted or substituted C_3-10 cycloalkyl-L_X-sulfinyl, unsubstituted or substituted 5- to 10-membered heteroaryl-L_X-sulfinyl, unsubstituted or substituted 5- to 10-membered heterocycloalkyl-L_X-sulfinyl, unsubstituted or substituted C_1-12 alkylcarbamoyl, unsubstituted or substituted C_2-12 alkenylcarbamoyl, unsubstituted or substituted C_2-12 alkynylcarbamoyl, unsubstituted or substituted C_6-10 aryl-L_X-carbamoyl, unsubstituted or substituted C_3-10 cycloalkyl-L_X-carbamoyl, unsubstituted or substituted 5- to 10-membered heteroaryl-L_X-carbamoyl, unsubstituted or substituted 5- to 10-membered heterocycloalkyl-L_X-carbamoyl, unsubstituted or substituted C_1-12 alkylsulfamoyl, unsubstituted or substituted C_2-12 alkenylsulfamoyl, unsubstituted or substituted C_2-12 alkynylsulfamoyl, unsubstituted or substituted C_6-10 aryl-L_X-sulfamoyl, unsubstituted or substituted C_3-10 cycloalkyl-L_X-sulfamoyl, unsubstituted or substituted 5- to 10-membered heteroaryl-L_X-sulfamoyl, and unsubstituted or substituted 5- to 10-membered heterocycloalkyl-L_X-sulfamoyl, wherein L_X is a single bond or unsubstituted or substituted C_1-12 alkylene,

wherein the substituted C_1-12 alkyl, substituted C_2-12 alkenyl, substituted C_2-12 alkynyl, substituted C_6-10 aryl, substituted C_3-10 cycloalkyl, substituted 5- to 10-membered heteroaryl, substituted 5- to 10-membered heterocycloalkyl, and substituted alkylene moieties (fully or partially) in the substituent group each independently have one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, hydroxy, oxo, carboxy, amino, imino, hydroxyamino, hydroxyimino, formyl, formyloxy, carbamoyl, sulfamoyl, sulfanyl, sulfino, sulfa, thioformyl, thiocarboxy, dithiocarboxy, thiocarbamoyl, cyano, nitro, nitroso, azide, hydrazino, ureide, amidino, amidinoamino, C_1-12 alkyl, C_1-12 haloalkyl, C_2-12 alkenyl, C_2-12 alkynyl, C_6-10 aryl, C_3-10 cycloalkyl, 5- to 10-membered heteroaryl, 5- to 10-membered heterocycloalkyl, C_1-12 alkyloxy, C_1-12 haloalkyloxy, C_2-12 alkenyloxy, C_2-12 alkynyloxy, C_6-10 aryl-L_X-oxy, C_3-10 cycloalkyl-L_X-oxy, 5- to 10-membered heteroaryl-L_X-oxy, 5- to 10-membered heterocycloalkyl-L_X-oxy, C_1-12 alkyloxyalkyl, C_2-12 alkenyloxyalkyl, C_2-12 alkynyloxyalkyl, C_6-10 aryloxyalkyl, C_3-10 cycloalkyloxyalkyl, 5- to 10-membered heteroaryloxyalkyl, 5- to 10-membered heterocycloalkyloxyalkyl, C_1-12 alkyloxyalkyloxy, C_2-12 alkenyloxyalkyloxy, C_2-12 alkynyloxyalkyloxy, C_6-10 aryloxyalkyloxy, C_3-10 cycloalkyloxyalkyloxy, 5- to 10-membered heteroaryloxyalkyloxy, 5- to 10-membered heterocycloalkyloxyalkyloxy, C_1-12 alkylcarbonyl, C_2-12 alkenylcarbonyl, C_2-12 alkynylcarbonyl, C_6-10 aryl-L_X-carbonyl, C_3-10 cycloalkyl-L_X-carbonyl, 5- to 10-membered heteroaryl-L_X-carbonyl, 5- to 10-membered heterocycloalkyl-L_X-carbonyl, C_1-12 alkylcarbonyloxy, C_2-12 alkenylcarbonyloxy, C_2-12 alkynylcarbonyloxy, C_6-10 aryl-L_X-carbonyloxy, C_3-10 cycloalkyl-L_X-carbonyloxy, 5- to 10-membered heteroaryl-L_X-carbonyloxy, 5- to 10-membered heterocycloalkyl-L_X-carbonyloxy, C_1-12 alkylcarbonylamino, C_2-12 alkenylcarbonylamino, C_2-12 alkynylcarbonylamino, C_6-10 aryl-L_X-carbonylamino, C_3-10 cycloalkyl-L_X-carbonylamino, 5- to 10-membered heteroaryl-L_X-carbonylamino, 5- to 10-membered heterocycloalkyl-L_X-carbonylamino, C_1-12 alkylcarbonylthio, C_2-12 alkenylcarbonylthio, C_2-12 alkynylcarbonylthio, C_6-10 aryl-L_X-carbonylthio, C_3-10 cycloalkyl-L_X-carbonylthio, 5- to 10-membered heteroaryl-L_X-carbonylthio, 5- to 10-membered heterocycloalkyl-L_X-carbonylthio, C_1-12 alkylcarbonylimino, C_2-12 alkenylcarbonylimino, C_2-12 alkynylcarbonylimino, C_6-10 aryl-L_X-carbonylimino, C_3-10 cycloalkyl-L_X-carbonylimino, 5- to 10-membered heteroaryl-L_X-carbonylimino, 5- to 10-membered heterocycloalkyl-L_X-carbonylimino, C_1-12 alkylthio, C_2-12 alkenylthio, C_2-12 alkynylthio, C_6-10 aryl-L_X-thio, C_3-10 cycloalkyl-L_X-thio, 5- to 10-membered heteroaryl-L_X-thio, 5- to 10-membered heterocycloalkyl-L_X-thio, C_1-12 alkylamino, C_2-12 alkenylamino, C_2-12 alkynylamino, C_2-12 alkynylamino, C_6-10 aryl-L_X-amino, C_3-10 cycloalkyl-L_X-amino, 5- to 10-membered heteroaryl-L_X-amino, 5- to 10-membered heterocycloalkyl-L_X-amino, C_1-12 alkylsulfonyl, C_2-12 alkenylsulfonyl, C_2-12 alkynylsulfonyl, C_6-10 aryl-L_X-sulfonyl, C_3-10 cycloalkyl-L_X-sulfonyl, 5- to 10-membered heteroaryl-L_X-sulfonyl, 5- to 10-membered heterocycloalkyl-L_X-sulfonyl, C_1-12 alkylsulfonylamino, C_2-12 alkenylsulfonylamino, C_2-12 alkynylsulfonylamino, C_6-10 aryl-L_X-sulfonylamino, C_3-10 cycloalkyl-L_X-sulfonylamino, 5- to 10-membered heteroaryl-L_X-sulfonylamino, 5- to 10-membered heterocycloalkyl-L_X-sulfonylamino, C_1-12 alkylimino, C_2-12 alkenylimino, C_2-12 alkynylimino, C_6-10 aryl-L_X-imino, C_3-10 cycloalkyl-L_X-imino, 5- to 10-membered heteroaryl-L_X-imino, 5- to 10-membered heterocycloalkyl-L_X-imino, C_1-12 alkyloxyimino, C_2-12 alkenyloxyimino, C_2-12 alkynyloxyimino, C_6-10 aryl-L_X-oxyimino, C_3-10 cycloalkyl-L_X-oxyimino, 5- to 10-membered heteroaryl-L_X-oxyimino, 5- to 10-membered heterocycloalkyl-L_X-oxyimino, C_1-12 alkyloxycarbonyl, C_2-12 alkenyloxycarbonyl, C_2-12 alkynyloxycarbonyl, C_6-10 aryl-L_X-oxycarbonyl, C_3-10 cycloalkyl-L_X-oxycarbonyl, 5- to 10-membered heteroaryl-L_X-oxycarbonyl, 5- to 10-membered heterocycloalkyl-L_X-oxycarbonyl, C_1-12 alkyloxycarbonylamino, C_2-12 alkenyloxycarbonylamino, C_2-12 alkynyloxycarbonylamino, C_6-10 aryl-L_X-oxycarbonylamino, C_3-10 cycloalkyl-L_X-oxycarbonylamino, 5- to 10-membered heteroaryl-L_X-oxycarbonylamino, 5- to 10-membered heterocycloalkyl-L_X-oxycarbonylamino, C_1-12 alkylsulfanyl, C_2-12 alkenylsulfanyl, C_2-12 alkynylsulfanyl, C_6-10 aryl-L_X-sulfanyl, C_3-10 cycloalkyl-L_X-sulfanyl, 5- to 10-membered heteroaryl-L_X-sulfanyl, 5- to 10-membered heterocycloalkyl-L_X-sulfanyl, C_1-12 alkylsulfinyl, C_2-12 alkenylsulfinyl, C_2-12 alkynylsulfinyl, C_6-10 aryl-L_X-sulfinyl, C_3-10 cycloalkyl-L_X-sulfinyl, 5- to 10-membered heteroaryl-L_X-sulfinyl, 5- to 10-membered heterocycloalkyl-L_X-sulfinyl, C_1-12 alkylcarbamoyl, C_2-12 alkenylcarbamoyl, C_2-12 alkynylcarbamoyl, C_6-10 aryl-L_X-carbamoyl, C_3-10 cycloalkyl-L_X-carbamoyl, 5- to 10-membered heteroaryl-L_X-carbamoyl, 5- to 10-membered heterocycloalkyl-L_X-carbamoyl, C_1-12 alkylsulfamoyl, C_2-12 alkenylsulfamoyl, C_2-12 alkynylsulfamoyl, C_6-10 aryl-L_X-sulfamoyl, C_3-10 cycloalkyl-L_X-sulfamoyl, 5- to 10-membered heteroaryl-L_X-sulfamoyl, and 5- to 10-membered heterocycloalkyl-L_X-sulfamoyl.

Substituent group III consists of halogen, hydroxy, carboxy, amino, carbamoyl, nitro, amidinoamino, alkyl, aryl, cycloalkyl, heteroaryl, alkyloxy, alkylcarbonyl, cycloalkylcarbonyl, alkylcarbonylamino, cycloalkylcarbonylamino, alkylamino, cycloalkylalkylamino, alkyloxycarbonyl, and trialkylsilyloxy, and these groups of the substituent group are optionally substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, hydroxy, carboxy, amino, carbamoyl, nitro, alkyl, haloalkyl, alkyloxy, haloalkyloxy, and alkyloxycarbonyl.

Substituent group III is preferably substituent group III′, which consists of halogen, hydroxy, carboxy, amino, carbamoyl, nitro, amidinoamino, C_1-12 alkyl, C_6-10 aryl, C_3-10 cycloalkyl, 5- to 10-membered heteroaryl, C_1-12 alkyloxy, C₁-alkylcarbonyl, C_3-10 cycloalkylcarbonyl, C_1-12 alkylcarbonylamino, C_3-10 cycloalkylcarbonylamino, C_1-12 alkylamino, C_3-10 cycloalkyl C_1-6 alkylamino, C_1-12 alkyloxycarbonyl, and tri-C_1-6 alkylsilyloxy, wherein these groups of the substituent group are optionally substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, hydroxy, carboxy, amino, carbamoyl, nitro, C_1-12 alkyl, C_1-12 haloalkyl, C_1-12 alkyloxy, C_1-12 haloalkyloxy, and C_1-12 alkyloxycarbonyl.

Substituent group IV consists of halogen, hydroxy, carboxy, amino, carbamoyl, nitro, amidino, alkyl, aryl, cycloalkyl, heteroarylheterocycloalkyl, arylalkyl, cycloalkylalkyl, alkyloxy, aryloxy, alkylcarbonyl, cycloalkylcarbonyl, alkyloxycarbonyl, and trialkylsilyloxy, and these groups of the substituent group are optionally substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, hydroxy, carboxy, amino, carbamoyl, nitro, alkyl, haloalkyl, alkyloxy, haloalkyloxy, and alkyloxycarbonyl.

Substituent group IV is preferably substituent group IV′, which consists of halogen, hydroxy, carboxy, amino, carbamoyl, nitro, amidino, C_1-6 alkyl, C_6-10 aryl, C_3-10 cycloalkyl, 5- to 10-membered heteroaryl, 5- to 10-membered heterocycloalkyl, C_6-10 aryl C_1-6 alkyl, C_3-10 cycloalkyl C_1-6 alkyl, C_1-6 alkyloxy, C_6-10 aryloxy, C_1-6 alkylcarbonyl, C_3-10 cycloalkylcarbonyl, C_1-6 alkyloxycarbonyl, and tri-C_1-6 alkylsilyloxy, and these groups of the substituent group are each independently and optionally substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, hydroxy, carboxy, amino, carbamoyl, nitro, C_1-6 alkyl, C_1-6 haloalkyl, C_1-6 alkyloxy, C_1-6 haloalkyloxy, and C_1-6 alkyloxycarbonyl.

Substituent group V consists of halogen, hydroxy, carboxy, amino, formyl, carbamoyl, cyano, nitro, amidino, amidinoamino, alkyl, aryl, cycloalkyl, heteroaryl, heterocycloalkyl, alkyloxy, aryloxy, cycloalkyloxy, heteroaryloxy, heterocycloalkyloxy, alkyloxyoxy, alkylamino, arylamino, cycloalkylamino, heteroarylamino, heterocycloalkylamino, formyl, alkylcarbonyl, arylcarbonyl, cycloalkylcarbonyl, heteroarylcarbonyl, heterocycloalkylcarbonyl, alkyloxycarbonyl, aryloxycarbonyl, cycloalkyloxycarbonyl, heteroaryloxycarbonyl, heterocycloalkyloxycarbonyl, alkylcarbamoyl, arylcarbamoyl, cycloalkylcarbamoyl, heteroarylcarbamoyl, and heterocycloalkylcarbamoyl, wherein these groups of the substituent group are each independently and optionally substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, hydroxy, carboxy, amino, formyl, carbamoyl, cyano, nitro, amidino, amidinoamino, alkyl, alkyloxy, haloalkyl, haloalkyloxy, alkylamino, formyl, alkylcarbonyl, alkyloxycarbonyl, and alkylcarbamoyl.

Substituent group V is preferably substituent group V′, which consists of halogen, hydroxy, carboxy, amino, formyl, carbamoyl, cyano, nitro, amidino, amidinoamino, C_1-12 alkyl, C_6-10 aryl, C_3-10 cycloalkyl, 5- to 10-membered heteroaryl, 5- to 10-membered heterocycloalkyl, C_1-12 alkyloxy, C_6-10 aryloxy, C_3-10 cycloalkyloxy, 5- to 10-membered heteroaryloxy, 5- to 10-membered heterocycloalkyloxy, C_1-12 alkylamino, C_6-10 arylamino, C_3-10 cycloalkylamino, 5- to 10-membered heteroarylamino, 5- to 10-membered heterocycloalkylamino, formyl, C_1-12 alkylcarbonyl, C_6-10 arylcarbonyl, C_3-10 cycloalkylcarbonyl, 5- to 10-membered heteroarylcarbonyl, 5- to 10-membered heterocycloalkylcarbonyl, C_1-12 alkyloxycarbonyl, C_6-10 aryloxycarbonyl, C_3-10 cycloalkyloxycarbonyl, 5- to 10-membered heteroaryloxycarbonyl, 5- to 10-membered heterocycloalkyloxycarbonyl, C_1-12 alkylcarbamoyl, C_6-10 arylcarbamoyl, C_3-10 cycloalkylcarbamoyl, 5- to 10-membered heteroarylcarbamoyl, and 5- to 10-membered heterocycloalkylcarbamoyl, wherein these groups of the substituent group are each independently and optionally substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, hydroxy, carboxy, amino, formyl, carbamoyl, cyano, nitro, amidino, amidinoamino, C_1-6 alkyl, C_1-6 alkyloxy, C_1-6 haloalkyl, C_1-6 haloalkyloxy, C_1-6 alkylamino, formyl, C_1-6 alkylcarbonyl, C_1-6 alkyloxycarbonyl, and C_1-6 alkylcarbamoyl.

Substituent group VI consists of halogen, hydroxy, carboxy, amino, formyl, carbamoyl, cyano, nitro, amidino, amidinoamino, alkyl, alkyloxy, haloalkyl, haloalkyloxy, alkylamino, formyl, alkylcarbonyl, alkyloxycarbonyl, and alkylcarbamoyl.

Substituent group VI is preferably substituent group VI′, which consists of halogen, hydroxy, carboxy, amino, formyl, carbamoyl, cyano, nitro, amidino, amidinoamino, C_1-6 alkyl, C_1-6 alkyloxy, C_1-6 haloalkyl, C_1-6 haloalkyloxy, C_1-6 alkylamino, formyl, C_1-6 alkylcarbonyl, C_1-6 alkyloxycarbonyl, and C_1-6 alkylcarbamoyl.

As used herein, examples of substituents used when “optionally substituted” include substituent group α and substituent group β. Substituent group a can be substituent group α1, substituent group α2, or substituent group α3. Substituent group β can be substituent group β1, substituent group β2, or substituent group β3. Substituents used when “optionally substituted” can be selected from substituent group α1, and substitution can be performed with 1 to 5 of the same or different substituents. While the types of atoms within a substituent associated with attachment are not particularly limited by the type of substituent, if the atom to which a substituent attaches is an oxygen atom, a nitrogen atom, or a sulfur atom, the substituent is limited to those with an attaching atom that is a carbon atom from the following substituents.

Substituent group α1 includes

1) halogen atom2) hydroxyl group3) carboxyl group4) cyano group5) C_1-6 alkyl6) C_2-6 alkenyl7) C_2-6 alkynyl8) C_1-6 alkoxy9) C_1-6 alkylthio10) C_1-6 alkylcarbonyl11) C_1-6 alkylsulfonyl(however, each substituent from 5) to 11) is optionally substituted with 1 to 5 of the same or different substituents selected from substituent group (1)12) C_3-10 alicyclic group13) C_3-10 alicyclic oxy14) C_6-10 aryloxy15) 5- to 6-membered heteroaryloxy16) 4- to 10-membered non-aryl heterocyclyloxy17) C_3-10 alicyclic thio18) C_6-10 arylthio19) 5- to 6-membered heteroarylthio20) 4- to 10-membered non-aryl heterocyclylthio21) C_6-10 aryl22) 5- to 6-membered heteroaryl23) 4- to 10-membered non-aryl heterocycle24) C_3-10 alicyclic carbonyl25) C_6-10 arylcarbonyl26) 5- to 6-membered heteroarylcarbonyl27) 4- to 10-membered non-aryl heterocyclylcarbonyl28) C_3-10 alicyclic sulfonyl29) C_6-10 aryl sulfonyl30) 5- to 6-membered heteroarylsulfonyl31) 4- to 10-membered non-aryl heterocyclylsulfonyl(however, each substituent from 12) to 31) is optionally substituted with 1 to 5 substituents in substituent group β1 or 5) C_1-6 alkyl)32) —NR^10aR^11a 33) —SO₂—NR^10bR^11b 34) —NR^10c—C(═O) R^11c 35) —NR^10d—C(═O) OR^11d 36) —NR^12a—C(═P) NR^10eR^11e 37) —NR¹⁰ⁱ—SO₂—R¹¹ⁱ 38) —NR^12c—SO₂—NR^10jR^11j

39) —C(═O) OR^10k

40) —C(═O) NR^10lR^11k 41) —C(═O) NR^10mOR^11l 42) —C(═O)NR^12d—NR¹⁰ⁿR^11m 43) —C(═NR^13a)R^10s 44) —C(═NR^13c)NR^10tR^11q 45) —C(═NR^13d) NR^12f—NR^10uR^11r 46) —NR^17c—C(═NR^13k)R^17d 47) —NR^12g—C(═NR^13e)—NR^10vR^11s 48) —NR¹⁴—C(═NR^13f)—NR^12h—NR^10wR^11t

49) —OC(═O)R^10x

50) —OC(═O)OR^10y

51) —OC(═O)—NR^10z1R^11u 52) —NR¹²ⁱ—NR^10z2R^11v 53) —NR^10z3OR^11w, and54) protecting group, and

substituent group β1 is a group consisting of

1) halogen atom,2) hydroxyl group,3) carboxyl group,4) cyano group,5) C_3-10 alicyclic group,6) C_1-6 alkoxy,7) C_3-10 alicyclic oxy,8) C_1-6 alkylthio,9) 5- to 6-membered heteroarylthio,10) C_6-10 aryl,11) 5- to 6-membered heteroaryl,12) 4- to 10-membered non-aryl heterocycle,13) C_1-6 alkylcarbonyl,14) C_3-10 alicyclic carbonyl,15) C_6-10 arylcarbonyl,16) 5- to 6-membered heteroarylcarbonyl,17) 4- to 10-membered non-aryl heterocyclylcarbonyl,18) —NR^15aR^16a,19) —SO₂—NR^15bR^16b,20) —NR^15c—C(═O)R^16c 21) —NR^17a—C(═O)NR^15dR^16d 22) —C(═O)NR^15eR^15e,23) —C(═NR^13g)R^15f,24) —C(═NR^13h) NR^15gR^16f 25) —NR^16g—C(═NR¹³ⁱ)R^15h 26) —NR^17b—C(═NR^13j)—NR¹⁵ⁱR^16h, and27) protecting group(however, each substituent from 5) to 17) in substituent group β1 is optionally substituted with 1 to 5 substituents selected from the group consisting of a halogen atom, hydroxyl group, cyano group, carboxyl group, and —NR^18aR^18b), wherein

R^13a, R^13a2, R^13c, R^13c2, R^13d, R^13d2, R^13e, R^13f, R^13g, R^13g2, R^13h, R^13h2, R¹³ⁱ, R^13j, and R^13k are each independently the same or different hydrogen atom, hydroxyl group, C_1-6 alkyl, C_1-6 alkoxy, or C_1-6 alkoxycarbonyl,

R^10a, R^10b, R^10c, R^10d, R^10e, R¹⁰ⁱ, R^10j, R^10k, R^10l, R^10m, R¹⁰ⁿ, R^10s, R^10s2, R^10t, R^10t2, R^10u, R^10u2, R^10v, R^10w, R^10x, R^10y, R^10z1, R^10z2, R^10z3, R^11a, R^11b, R^11c, R^11d, R^11e, R¹¹ⁱ, R^11j, R^11k, R^11l, R^11m, R^11q, R^11q2, R^11r, R^11r2, R^11s, R^11t, R^11u, R^11v, R^11w, R^12a, R^12c, R^12d, R^12f, R^12f2, R^12g, R^12h, R¹²ⁱ, R¹⁴, R^15a, R^15b, R^15c, R^15d, R^15e, R^15f, R^15f2, R^15g, R^15g2, R^15h, R¹⁵ⁱ, R^16a, R^16b, R^16c, R^16d, R^16e, R^16f, R^16f2, R^16g, R^16h, R^17a, R^17b, R^17c, and R^17d are each independently the same or different hydrogen atom, C_1-6 alkyl (the C_1-6 alkyl is optionally substituted with 1 to 3 of the same or different substituents selected from a hydroxyl group, cyano group, C_1-6 alkoxy, and —NR^18aR^18b), or C_1-6 alkoxycarbonyl, and

R^18a and R^18b are each independently the same or different hydrogen atom or C_1-6 alkyl.

In an exemplary embodiment, hydrogen of any hydroxyl group in substituent groups α1 and β1 is optionally substituted with a protecting group.

Examples of preferred substituents as the substituent used when “optionally substituted” herein include the following.

Substituent group α2 preferably includes

1) halogen atom2) hydroxyl group3) carboxyl group4) cyano group5) C_1-6 alkyl6) C_1-6 alkoxy7) C_1-6 alkylthio8) C_1-6 alkylcarbonyl(however, each substituent from 5) to 8) is optionally substituted with 1 to 5 same or different substituents selected from substituent group (2)9) C_3-10 alicyclic group10) C_3-10 alicyclic oxy11) C_6-10 aryloxy12) 5- to 6-membered heteroaryloxy13) 4- to 10-membered non-aryl heterocyclyloxy14) C_3-10 alicyclic thio15) C_6-10 arylthio16) 5- to 6-membered heteroarylthio17) 4- to 10-membered non-aryl heterocyclylthio18) C_6-10 aryl19) 5- to 6-membered heteroaryl20) 4- to 10-membered non-aryl heterocycle21) C_3-10 alicyclic carbonyl22) C_6-10 arylcarbonyl23) 5- to 6-membered heteroarylcarbonyl24) 4- to 10-membered non-aryl heterocyclylcarbonyl(however, each substituent from 9) to 24) is optionally substituted with 1 to 5 substituents in substituent group β2 or 1) C_1-6 alkyl)25) —NR^10aR^11a 26) —SO₂—NR^10bR^11b 27) —NR^10c—C(═O)R^11c 28) —NR^12a—C(═O) NR^10dR^11d 29) —NR^10e_SO₂—R^11e 30) —NR^12b—SO₂—NR^10fR^11f 31) —C(═O)—NR^10gR^11g 32) —C(═NR^13a)R^10h 33) —C(═NR^13b)R¹⁰ⁱR^11h 34) —NR^11f2—C(═NR^13c)R^10g2, and35) —NR^12c—C(═NR^13d) and

substituent group (2 is preferably a group consisting of

1) halogen atom2) hydroxyl group3) cyano group4) C_3-10 alicyclic group5) C_1-6 alkoxy6) C_1-6 alkylthio7) 5- to 6-membered heteroarylthio8) 5- to 6-membered heteroaryl9) 4- to 10-membered non-aryl heterocycle10) C_1-6 alkylcarbonyl11) C_3-10 alicyclic carbonyl12) C_6-10 arylcarbonyl13) 5- to 6-membered heteroarylcarbonyl14) 4- to 10-membered non-aryl heterocyclylcarbonyl15) —NR^15aR^16a 16) —NR^15b—C(═O)R^16b 17) —NR^17a—C(═O)NR^15cR^16c 18) —C(═O)NR^15dR^16d 19) —C(═NR^13e)R^15e 20) —C(═NR^13f)NR^15fR^16e 21) —NR^16f—C(═NR^13g)R^15g 22) —NR^17b—C(═NR^13h)—NR^15hR^16g 23) —C(═N—OR^13e2)R^15e2, and24) —C(═N—OR^13f2)NR^15f2R^16e2 (however, each substituent from 4) to 14) in substituent group β2 is optionally substituted with 1 to 5 substituents selected from the group consisting of a halogen atom, hydroxyl group, cyano group, carboxyl group, and —NR^18aR^18b,

R^13a, R^13a2, R^13b, R^13b2, R^13c, R^13d, R^13e, R^13e2, R^13f, R^13f2, R^13g, and R^13h are each independently the same or different hydrogen atom, hydroxyl group, C_1-6 alkyl, C_1-6 alkoxy, or C_1-6 alkoxycarbonyl,

R^10a, R^10b, R^10c, R^10d, R^10e, R^10f, R^10g, R^10g2, R^10h, R^10h2, R¹⁰ⁱ, R¹⁰ⁱ², R^10j, R^11a, R^11b, R^11c, R^11d, R^11e, R^11f, R^11f2, R^11g, R^11h, R^11h2, R¹¹ⁱ, R^12a, R^12b, R^12c, R^15a, R^15b, R^15c, R^15d, R^15e, R^15e2, R^15f, R^15f2, R^15g, R^15h, R^16a, R^16b, R^16c, R^16d, R^16e, R^16e2, R^16f, R^16g, R^17a, and R^17b are each independently the same or different hydrogen atom, C_1-6 alkyl (the C_1-6 alkyl is optionally substituted with 1 to 3 same or different substituents selected from a hydroxyl group, cyano group, C_1-6 alkoxy, and —NR^18aR^18b), or C_1-6 alkoxycarbonyl, and

R^18a and R^18b are each independently the same or different hydrogen atom or C_1-6 alkyl.

In an exemplary embodiment, hydrogen of any hydroxy group in substituent groups α2 and β2 is optionally substituted with a protecting group.

Examples of more preferred substituents used when “optionally substituted” herein include the following substituents.

Substituent group α3 more preferably includes

1) halogen atom2) hydroxyl group3) cyano group4) C_1-6 alkyl5) C_1-6 alkoxy6) C_1-6 alkylthio7) C_1-6 alkylcarbonyl(however, each substituent from 4) to 7) is optionally substituted with 1 to 5 same or different substituents selected from substituent group β3)8) C_3-10 alicyclic group9) 5- to 6-membered heteroaryloxy10) 4- to 10-membered non-aryl heterocyclyloxy11) 5- to 6-membered heteroarylthio12) 4- to 10-membered non-aryl heterocyclylthio13) C_6-10 aryl14) 5- to 6-membered heteroaryl15) 4- to 10-membered non-aryl heterocycle(however, each substituent from 8) to 15) is optionally substituted with 1 to 5 substituents in substituent group β3 or 1) C_1-6 alkyl)16) —NR^10aR^11a 17) —NR^11b—C(═O)R^10b 18) —NR^12a—C(═O) NR^10cR^11c 19) —C(═O)—NR^10dR^11d 20) —C(═NR^13a)R^10e 21) —C(═NR^13b)NR^10fR^11e 22) —NR^11f—C(═NR^13c) R^10g, and23) —NR^12b—C(═NR^13d)—NR^10hR^11g, and substituent group β3 is more preferably1) halogen atom,2) hydroxyl group,3) cyano group,4) —NR^15aR^16a,5) —NR^15b—C(═O)R^16b,6) —NR^17a—C(═O) NR^15cR^16c,7) —C(═O) NR^15dR^16d,8) —C(═NR^13e)R^15e,9) —C(═NR^13f) NR^15fR^16e,10) —NR^16f—C(═NR^13g)R^15g, and11) —NR^17b—C(═NR^13h)—NR^15hR^16g, wherein

R^13a, R^13a2, R^13b, R^13b2, R^13c, R^13d, R^13e, R^13e2, R^13f, R^13f2, R^13g, and R^13h are each independently the same or different hydrogen atom, hydroxyl group, C_1-6 alkyl, C_1-6 alkoxy, or C_1-6 alkoxycarbonyl,

R^10a, R^10b, R^10c, R^10d, R^10e, R^10f, R^10e2, R^10f2, R^10g, R^10h, R^11a, R^11b, R^11c, R^11d, R^11e, R^11e2, R^11f, R^11g, R^12a, R^12b, R^15a, R^15b, R^15c, R^15d, R^15e, R^15e2, R^15f, R^15f2, R^15g, R^15h, R^16a, R^16b, R^16c, R^16d, R^16e, R^16e2, R^16f, R^16g, R^17a, and R^17b are each independently the same or different hydrogen atom, C_1-6 alkyl (the C_1-6 alkyl is optionally substituted with 1 to 3 same or different substituents selected from hydroxyl group, cyano group, C_1-6 alkoxy, and —NR^18aR^18b), or C_1-6 alkoxycarbonyl, and

R^18a, and R^18b are each independently the same or different hydrogen atom or C_1-6 alkyl.

In an exemplary embodiment, hydrogen of any hydroxyl group in substituent groups α3 and β3 is optionally substituted with a protecting group.

In an exemplary embodiment, a hydroxyl group in the aforementioned substituent group (e.g., α (α1 or the like) β (β1 or the like), or I to VI) is also optionally substituted with a protecting group. In an exemplary embodiment, an amino group in substituent groups I to VI is also optionally protected with a nitrogen protecting group.

As used herein, “C_1-6” means that the number of carbon atoms is 1 to 6. The same applies to other numbers. For example, “C_1-4” means that the number of carbon atoms is 1 to 4, and “C_1-3” means that the number of carbon atoms is 1 to 3. A description with a limitation in the number of carbons herein is only a preferred numerical range. It is intended so that groups with a substituent with a number of carbons other than the number of carbons specified in the present disclosure are also within the scope of the present disclosure.

As used herein, “hydrocarbon group” is also referred to as a hydrocarbyl group, referring to a group generated by removing at least one hydrogen from “hydrocarbon” comprising at least one carbon and at least one hydrogen.

As used herein, “functional group” refers to any group conferring some type of functionality, encompassing a carboxyl group, nitrile group, carbonyl group, hydroxyl group, amino group, imino group, nitro group, halogen group, as well as alkyl group, and more broadly acid anhydrides and groups formed by a bond such as an ester bond, amide bond, or ether bond.

As used herein, “heteroatom” refers to atoms other than carbon atoms and hydrogen atoms such as oxygen atoms, nitrogen atoms, and sulfur atoms. A group comprising a heteroatom is also known as a hetero . . . group (e.g., heteroaryl group (means that an aryl group comprises at least a heteroatom) or heterocyclic group (means that a cyclic group (carbon ring group) comprises at least one heteroatom)) or the like.

As used herein, “halogen atom” is an atom belonging to the halogen group, referring to a fluorine atom, chlorine atom, bromine atom, iodine atom, or the like, and is preferably a fluorine atom or chlorine atom, and still more preferably a fluorine atom. A “halogen atom” is also referred to as “halogen” or “halo”.

As used herein, “hydroxyl group” is a monovalent group of —OH. This group is also referred to as a “hydroxy group” or “hydroxy”.

As used herein, “carboxyl group” is a monovalent group of —COOH. This group is also referred to as a “carboxy group”, “carboxy”, or “carboxyl”.

As used herein, “cyano group” is a monovalent group of —CN.

As used herein, “amino” is a monovalent group of —NH₂.

This group is also referred to as an “amino group”.

As used herein, “alkyl” refers to a linear or branched saturated aliphatic hydrocarbon group. “C_1-12 alkyl” is an alkyl group with 1 to 12 carbon atoms. Examples thereof include, but are not limited to, C_1-6 alkyl, heptyl, isoheptyl, octyl, isooctyl, nonyl, isnonyl, decyl, isodecyl, undecyl, isoundecyl, dodecyl, isododecy, and the like. “C_1-6 alkyl” is an alkyl group with 1 to 6 carbon atoms, which is preferably “C_1-4 alkyl”, more preferably “C_1-3 alkyl”, and still more preferably “C_1-2 alkyl”. Specific examples of “C_1-4 alkyl” include methyl, ethyl, propyl, isopropyl, n-butyl, isobutyl, tert-butyl, sec-butyl, and the like. Specific examples of “C_1-6alkyl” include, but are not limited to, C_1-4 alkyl, n-pentyl, isopentyl, neopentyl, tert-pentyl, 1,2-dimethylpropyl, n-hexyl, and the like.

As used herein, “alkenyl” refers to a linear or branched unsaturated aliphatic hydrocarbon group comprising at least one carbon-carbon double bond. “C_2-12 alkenyl” is an alkenyl group with 2 to 12 carbon atoms. Examples thereof include, but are not limited to, heptenyl, isoheptenyl, octenyl, isooctenyl, nonenyl, isononenyl, decenyl, isodecenyl, undecenyl, isoundecenyl, dodecenyl, isododecenyl, and the like. “C_2-6 alkenyl” is an alkenyl group with 2 to 6 carbon atoms. Preferred examples thereof include “C_2-4 alkenyl”. Specific examples of “C_2-6 alkenyl” include, but are not limited to, vinyl, 1-propenyl, 2-propenyl, 1-butenyl, 2-butenyl, 3-butenyl, 2-methyl-1-propenyl, 2-methyl-2-propenyl, and the like.

As used herein, “alkynyl” refers to a linear or branched unsaturated aliphatic hydrocarbon group comprising at least one carbon-carbon triple bond. “C_2-12 alkynyl” is an alkynyl group with 2 to 12 carbon atoms. Examples thereof include, but are not limited to, heptynyl, isoheptynyl, octynyl, isooctynyl, nonynyl, isononynyl, decynyl, isodecynyl, undecynyl, isoundecynyl, dodecynyl, isododecynyl, and the like. “C_2-6 alkynyl” is an alkynyl group with 2 to 6 carbon atoms. Preferred examples thereof include “C_2-4 alkynyl”. Specific examples of “C_2-6 alkynyl” include, but are not limited to, ethynyl, 1-propynyl, 2-propynyl, 1-butynyl, 1-methyl-2-propynyl, 3-butynyl, 1-pentynyl, 1-hexynyl, and the like.

As used herein, “aryl” refers to a monovalent group of a monocyclic or bicyclic aromatic hydrocarbon ring. “C_6-10 aryl” refers to an aryl group with 6 to 10 carbon atoms. Examples of “aryl” include, but are not limited to, C₆ aryl, C₁₀ aryl, and the like. Specific examples of C₆ aryl include, but are not limited to, phenyl and the like. Specific examples of C₁₀ aryl include, but are not limited to, 1-naphthyl, 2-naphthyl, and the like.

An aryl group as a substituent or a portion thereof may be fused to an alicyclic group. For example, a phenyl group may be fused to a cyclohexane ring to form a 1,2,3,4-tetrahydronaphthalenyl group. In such a case, one of the possible carbon atoms on a benzene ring attaches to the backbone, or to a group near the backbone, or to its atom. An aryl group encompasses 5,6,7,8-tetrahydronaphthalen-1-yl and 5,6,7,8-tetrahydronaphthalen-2-yl.

As used herein, “arylalkyl” refers to alkyl substituted with at least one aryl. C₀“_6-1 aryl C_1-6 alkyl” refers to C_1-6 alkyl substituted with at least one C_6-10 aryl. Specific examples of C_6-10 aryl C_1-6 alkyl include, but are not limited to, benzyl(phenyl-CH₂—), phenethyl (phenyl-CH₂CH₂—), naphthalen-1-ylmethyl, naphthalen-2-ylmethyl, 2-(naphthalen-1-yl)ethyl, 2-(naphthalen-2-yl)ethyl, and the like.

As used herein, “(optionally substituted amino)-arylalkyl” refers to arylalkyl substituted with an optionally substituted amino group, wherein the alkyl group, the aryl group, or both is substituted with an amino group. An amino group of such an arylalkyl group may be unsubstituted, or substituted with 1, 2, or 3 substituents, such as optionally substituted alkyl (e.g., unsubstituted C_1-6 alkyl, C_3-6 cycloalkyl-C_1-6 alkyl, C_3-6 cycloalkylcarbonyl, or the like). Examples of (optionally substituted amino)-C_6-10 aryl C_1-6 alkyl include, but are not limited to, (di(alkyl)amino)benzyl, ((cycloalkylalkyl)amino)benzyl, ((cycloalkylcarbonyl)amino)benzyl, ((carbamoylalkyl) carbonylamino)benzyl, ((carboxyalkyl)carbonyl)aminobenzyl, (di(alkyl)amino)naphthalenylmethyl, ((cycloalkylalkyl)amino)naphthalenylmethyl, ((cycloalkylcarbonyl)amino)naphthalenylmethyl, ((carbamoylalkyl)carbonylamino)naphthalenylmethyl, ((carboxyalkyl)carbonyl)aminonaphthalenylmethyl, and the like.

As used herein, the aryl moiety of “arylthio” is defined the same as the aforementioned aryl. Preferred examples of “C_6-10 arylthio” include “C₆ or C₁₀ arylthio”. Specific examples of “C_6-10 aryloxy” include, but are not limited to, phenylthio, 1-naphthylthio, 2-naphthylthio, and the like.

As used herein, “aryl sulfonyl” refers to sulfonyl substituted with the aforementioned “aryl”. “C_6-10 aryl sulfonyl” is preferably “C₆ or C₁₀ aryl sulfonyl”. Specific examples of “C_6-10 aryl sulfonyl” include, but are not limited to, phenylsulfonyl, 1-naphthylsulfonyl, 2-naphthylsulfonyl, and the like.

As used herein, “heteroaryl” refers to a monovalent group of a monocyclic or bicyclic aromatic heterocycle comprising 1 to 4 same or different heteroatoms selected from the group consisting of an oxygen atom, nitrogen atom, and sulfur atom.

As used herein, “5- to 6-membered heteroaryl” refers to a monovalent group of a monocyclic aromatic heterocycle consisting 5 to 6 atoms, comprising 1 to 4 same or different heteroatoms selected from the group consisting of an oxygen atom, nitrogen atom, and sulfur atom. Specific examples of “5- to 6-membered heteroaryl” include, but are not limited to, pyrrolyl, furyl, thienyl, pyrazolyl, imidazolyl, oxazolyl, isooxazolyl, oxadiazolyl, thiazolyl, isothiazolyl, thiadiazolyl, tetrazolyl, pyridyl, furyl, pyridazinyl, pyrimidinyl, pyrazinyl, and the like.

As used herein, “5- to 10-membered heteroaryl” refers to a monovalent group of a monocyclic or bicyclic aromatic heterocycle consisting of 5 to 10 atoms, comprising 1 to 4 same or different heteroatoms selected from the group consisting of an oxygen atom, nitrogen atom, and sulfur atom. Specific examples of “5- to 10-membered heteroaryl” include, but are not limited to, 5- to 6-membered heteroaryl, quinolyl, isoquinolyl, naphthyridinyl, quinoxalinyl, cinnolinyl, quinazolinyl, phthalazinyl, imidazopyridyl, imidazothiazolyl, imidazooxazolyl, benzothiazolyl, benzooxazolyl, benzoimidazolyl, indolyl, isoindolyl, indazolyl, pyrrolopyridyl, thienopyridyl, furopyridyl, benzothiadiazolyl, benzooxadiazolyl, pyridopyrimidinyl, benzofuryl, benzothienyl, benzo[1,3]dioxole, thienofuryl, chromenyl, chromanyl, coumarinyl, quinolonyl, and the like.

As used herein, “heteroarylalkyl” refers to alkyl substituted with at least one heteroaryl. “5- to 10-membered heteroaryl C_1-6 alkyl” refers to C_1-6 alkyl substituted with at least one 5- to 10-membered heteroaryl. Specific examples of 5- to 10-membered heteroaryl C_1-6 alkyl include, but are not limited to, pyridin-2-ylmethyl, pyridin-4-ylmethyl, 2-(quinolin-8-yl)ethyl, 2-(quinolin-5-yl)ethyl, 2-(quinoxalin-5-yl)ethyl, 2-(1H-indol-3-yl)ethyl, and the like.

As used herein, “alicyclic group” refers to a monovalent group of a monocyclic, bicyclic, or tricyclic non-aromatic hydrocarbon ring, including those that have a partially unsaturated bond, those that have a partially crosslinked structure, those that are partially a spiro, and those having 1, 2, or more carbonyl structures. An “alicyclic group” encompasses cycloalkyl, cycloalkenyl, and cycloalkynyl. “C_3-20 alicyclic group” is preferably a “C_3-10 alicyclic group”, more preferably a “C_3-6 alicyclic group”. Specific examples of “C_3-20 alicyclic group” include, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, cyclohexadinyl, cycloheptadinyl, cyclooctadinyl, adamantyl, norbornyl, and the like.

An alicyclic group can be a fused ring between a non-aryl ring and an aryl and/or heteroaryl ring. For example, cycloalkyl fused with C_6-10 aryl or 5- to 6-membered heteroaryl is encompassed by an alicyclic group. Examples of fused alicyclic groups include a monovalent group with one hydrogen atom removed from 1,2,3,4-tetrahydronaphthalene, indane, 1,2,3,4-tetrahydroanthracene, and 5,6,7,8-tetrahydroquinoline. Specific examples thereof include 1,2,3,4-tetrahydronaphthalen-1-yl, 1,2,3,4-tetrahydronaphthalen-2-yl, indan-1-yl, indan-2-yl, 5,6,7,8-tetrahydroquinolin-5-yl, 5,6,7,8-tetrahydroquinolin-6-yl, and the like. A fused alicyclic group attaches from any one of the possible cyclic structure atoms on a non-aryl ring to the backbone.

As used herein, “C_3-10 alicyclic group” refers to a substituent with “C_3-10 alicyclic group” that is a monovalent group among the aforementioned C₀“_3-2 alicyclic group”.

As used herein, “alicyclic oxy” refers to an (alicyclic group)-O— group, and the alicyclic moiety is defined the same as an alicyclic group. “C_3-6 alicyclic oxy” refers to a (C_3-6 alicyclic group)-O— group, and the C_3-6 alicyclic moiety is defined the same as a C_3-6 alicyclic group. “C_3-6 alicyclic oxy” is preferably “C_3-5 alicyclic oxy”. Specific examples of “C_3-6 alicyclic oxy” include, but are not limited to, cyclopropyloxy, cyclobutyloxy, cyclopentyloxy, cyclohexyloxy, and the like.

As used herein, “alicyclic carbonyl” refers to carbonyl substituted with the “alicyclic group” described above. “C_3-10 alicyclic carbonyl” is preferably “C_3-6 alicyclic carbonyl”. Specific examples of “C_3-10 alicyclic carbonyl” include, but are not limited to, cyclopropylcarbonyl, cyclobutylcarbonyl, cyclopentylcarbonyl, cyclohexylcarbonyl, and the like.

As used herein, “alicyclic thio” refers to an (alicyclic group)-S— group, and the alicyclic moiety is defined the same as above. “C_3-10 alicyclic thio” is preferably “C_3-6 alicyclic thio”. Specific examples of “C_3-6 alicyclic thio” include, but are not limited to, cyclopropylthio, cyclobutylthio, cyclopentylthio, cyclohexylthio, and the like.

As used herein, “alicyclic sulfonyl” refers to a sulfonyl group substituted with the “alicyclic group” described above. “C_3-10 alicyclic sulfonyl” is preferably “C_3-6 alicyclic sulfonyl”. Specific examples of “C_3-10 alicyclic sulfonyl” include, but are not limited to, cyclopropylsulfonyl, cyclobutylsulfonyl, cyclopentylsulfonyl, cyclohexylsulfonyl, and the like.

As used herein, “cycloalkyl” refers to a non-aromatic saturated hydrocarbon ring group, including those that have a partially crosslinked structure, those that are partially spiro, those having 1, 2, or more carbonyl structures. “C_3-20 cycloalkyl” refers to monocyclic or bicyclic cycloalkyl with 3 to 20 carbon atoms. “C_3-6 cycloalkyl” refers to monocyclic cycloalkyl with 3 to 6 carbon atoms. Specific examples of C_3-6 cycloalkyl include, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl, and cyclohexyl.

A cycloalkyl group can be fused to aryl and/or heteroaryl ring as a substituent or a portion thereof. For example, a cyclohexyl group can be fused to a benzene ring to form a 1,2,3,4-tetrahydronaphthalenyl group. In such a case, one of the possible carbon atoms on the cyclohexane ring attaches to the backbone, to a group near the backbone, or to its atom. A cycloalkyl group encompasses 1,2,3,4-tetrahydronaphthalen-1-yl, 1,2,3,4-tetrahydronaphthalen-2-yl, indan-1-yl, indan-2-yl, 5,6,7,8-tetrahydroquinolin-5-yl, and 5,6,7,8-tetrahydroquinolin-6-yl.

As used herein, “cycloalkylalkyl” refers to alkyl substituted with at least one cycloalkyl. “C_3-6 cycloalkyl C_1-6 alkyl” refers to C_1-6 alkyl substituted with at least one C_3-6 cycloalkyl. Specific examples of C_3-6 cycloalkyl C_1-6 alkyl include, but are not limited to, cyclopropylmethyl, cyclobutylmethyl, cyclopentylmethyl, cyclohexylmethyl, 2-cyclopropylethyl, 2-cyclobutylethyl, 2-cyclopentylethyl, 2-cyclohexylethyl, 3-cyclopropylpropyl, 3-cyclobutylpropyl, 3-cyclopentylpropyl, 3-cyclohexylpropyl, and the like.

As used herein, “heterocycloalkyl” refers to a non-aromatic saturated or partially unsaturated heterocycle comprised of 3 or more atoms, copmrising 1, 2, or more same or different heteroatoms selected from the group consisting of an oxygen atom, nitrogen atom, and sulfur atom, including those that have a partially crosslinked structure and those that are partially spiro. “Heterocycloalkyl” encompasses “non-aryl heterocycle”. Heterocycloalkyl can have a structure where a non-aromatic heterocycle is fused to an aryl ring and/or heteroaryl ring.

As used herein, “non-aryl heterocycle” refers to a monocyclic or bicyclic non-aromatic heterocycle comprised of 3 or more atoms, comprising 1, 2, or more same or different heteroatoms selected from the group consisting of an oxygen atom, nitrogen atom, and sulfur atom, including saturated non-aryl heterocycles, those that have a partially unsaturated attachment, those that have a partially crosslinked structure, and those that are partially spiro. A non-aryl heterocycle can form a fused ring with aryl or heteroaryl. For example, a non-aryl heterocycle fused to C_6-10 aryl or 5- to 6-membered heteroaryl is also encompassed by a heterocycle. 1, 2, or more carbonyl, thiocarbonyl, sulfinyl, or sulfonyl can be comprised to constitute the non-aryl heterocycle. For example, lactam, thiolactam, lactone, thiolactone, cyclic imide, cyclic carbamate, cyclic thiocarbamate, and other cyclic groups are also encompassed by the non-aryl heterocycle. In this regard, an oxygen atom of carbonyl, sulfinyl, and sulfonyl and a sulfur atom of thiocarbonyl are not included in the number of members of the ring (ring size) or the number of heteroatoms constituting the ring.

As used herein, “4- to 10-membered non-aryl heterocycle” refers to a substituent with “4- to 10-membered non-aryl heterocycle” that is a monovalent group among the “non-aryl heterocycle” described above.

As used herein, the non-aryl heterocycle moiety of “non-aryl heterocyclyloxy” is defined the same as the “non-aryl heterocycle” described above. “4- to 10-membered non-aryl heterocyclyloxy” is preferably “4- to 6-membered non-aryl heterocyclyloxy”. Specific examples of “4- to 10-membered non-aryl heterocyclyloxy” include, but are not limited to, tetrahydrofuranyloxy, tetrahydropyranyloxy, azetidinyloxy, pyrrolidinyloxy, piperidinyloxy, and the like.

As used herein, the non-aryl heterocycle moiety of “non-aryl heterocyclylthio” is defined the same as the “non-aryl heterocycle” described above. “4- to 10-membered non-aryl heterocyclylthio” is preferably “4- to 6-membered non-aryl heterocyclylthio”. Specific examples of “4- to 10-membered non-aryl heterocyclylthio” include, but are not limited to, tetrahydropyranylthio, piperidinylthio, and the like.

As used herein, “non-aryl heterocyclylcarbonyl” refers to a carbonyl group substituted with the “non-aryl heterocycle” described above. “4- to 10-membered non-aryl heterocyclylcarbonyl” is preferably “4- to 6-membered non-aryl heterocyclylcarbonyl”. Specific examples of “4- to 10-membered non-aryl heterocyclylcarbonyl” include, but are not limited to, azetidinylcarbonyl, pyrrolidinylcarbonyl, piperidinylcarbonyl, morpholinylcarbonyl, and the like.

As used herein, “non-aryl heterocyclylsulfonyl” refers to a sulfonyl group substituted with the “non-aryl heterocycle” described above. “4- to 10-membered non-aryl heterocyclylsulfonyl” is preferably “4- to 6-membered non-aryl heterocyclylsulfonyl”. Specific examples of “4- to 10-membered non-aryl heterocyclylsulfonyl” include, but are not limited to, azetidinylsulfonyl, pyrrolidinylsulfonyl, piperidinylsulfonyl, morpholinylsulfonyl, and the like.

As used herein, “5- to 6-membered heterocycloalkyl” refers to heterocycloalkyl comprised of 5 to 6 cyclic atoms, comprising 1 or more same or different heteroatoms selected from the group consisting of an oxygen atom, nitrogen atom, and sulfur atom.

As used herein, “heterocycloalkylalkyl” refers to alkyl substituted with at least one heterocycloalkyl.

As used herein, “alkylcarbonyl” is a monovalent group of —C(═O)-alkyl. Preferred examples of alkylcarbonyl include C_1-6 alkylcarbonyl. Specific examples of C_1-6 alkylcarbonyl include, but are not limited to, acetyl (CH₃C(═O)—), n-propanoyl (CH₃CH₂C(═O)—), n-butanoyl (CH₃CH₂CH₂C(═O)—), n-pentanoyl (CH₃ (CH₂)₃C(═O)—), n-hexanoyl (CH₃ (CH₂)₄C(═O)—), n-heptanoyl (CH₃ (CH₂)₅C(═O)—), and the like.

As used herein, “alkoxy” is a monovalent group of —O-alkyl. Preferred examples of alkoxy include C_1-6 alkoxy (i.e., C_1-6 alkyl-O—), C_1-4 alkoxy (i.e., C_1-4 alkyl-O—), and the like. Specific examples of C_1-4 alkoxy include methoxy (CH₃O—), ethoxy (CH₃CH₂O—), n-propoxy (CH₃(CH₂)₂O—), isopropoxy ((CH₃)₂CHO—), n-butoxy (CH₃(CH₂)₃O—), isobutoxy ((CH₃)₂CHCH₂O—), tert-butoxy ((CH₃)₃CO—), sec-butoxy (CH₃CH₂CH(CH₃)O—), and the like. Specific examples of C_1-6 alkoxy include, but are not limited to, C_1-4 alkoxy, n-pentyloxy (CH₃(CH₂)₄O—), isopentyloxy ((CH₃)₂CHCH₂CH₂O—), neopentyloxy ((CH₃)₃CCH₂O—), tert-pentyloxy (CH₃CH₂C(CH₃)₂O—), 1,2-dimethylpropoxy (CH₃CH(CH₃)CH(CH₃)O—), and the like.

As used herein, “alkoxycarbonyl” is a monovalent group of —C(═O)—O-alkyl. Examples of alkoxycarbonyl include, but are not limited to, C_1-6 alkoxycarbonyl, preferably C_1-4 alkoxycarbony. Specific examples of C_1-4 alkoxycarbonyl include methoxycarbonyl, ethoxycarbonyl, n-propoxycarbonyl, isopropoxycarbonyl, n-butoxycarbonyl, sec-butoxycarbonyl, tert-butoxycarbonyl, isobutoxycarbonyl, and the like. Specific examples of C_1-6 alkoxycarbonyl include, but are not limited to, C_1-4 alkoxycarbonyl, n-pentyloxycarbonyl, isopentyloxycarbonyl, neopentyloxycarbonyl, tert-pentyloxycarbonyl, 1,2-dimethylpropyloxycarbonyl, n-hexyloxycarbonyl, and the like.

As used herein, “alkoxycarbonylamino” is a monovalent group of —NH—C(═O)—O-alkyl. Examples of alkoxycarbonylamino include, but are not limited to, C_1-6 alkoxycarbonylamino, preferably C_1-4 alkoxycarbonylamino. Specific examples of C_1-4 alkoxycarbonylamino include methoxycarbonylamino, ethoxycarbonylamino, n-propoxycarbonylamino, isopropoxycarbonylamino, n-butoxycarbonylamino, sec-butoxycarbonylamino, tert-butoxycarbonylamino, isobutoxycarbonylamino, and the like. Specific examples of C_1-6 alkoxycarbonylamino include, but are not limited to, C_1-4 alkoxycarbonylamino, n-pentyloxycarbonylamino, isopentyloxycarbonylamino, neopentyloxycarbonylamino, tert-pentyloxycarbonylamino, 1,2-dimethylpropyloxycarbonylamino, n-hexyloxycarbonylamino, and the like.

As used herein, “haloalkyl” is a monovalent group of halogenated alkyl, having one or more hydrogen on an alkyl group substituted with halogen. The term “perhaloalkyl” refers to haloalkyl with all hydrogen on the alkyl group substituted with halogen. For example, perfluoroethyl is —CF₂CF₃, and perchloro-n-propyl is —CCl₂CCl₂CCl₃. Examples of haloalkyl include C_1-6 haloalkyl, C_1-4 haloalkyl, C_1-3 haloalkyl, and the like. Specific examples of C_1-3 alkyl include, but are not limited to, fluoromethyl, chloromethyl, bromomethyl, difluoromethyl, dichloromethyl, dibromomethyl, trifluoromethyl, trichloromethyl, tribromomethyl, fluorochloromethyl, difluorochloromethyl, fluorodichloromethyl, fluoroethyl, chloroethyl, bromoethyl, trifluoroethyl, trichloroethyl, tribromoethyl, perfluoroethyl, perchloroethyl, perbromoethyl, perfluoropropyl, perchloropropyl, perbromopropyl, perfluoroisopropyl, perchloroisopropyl, perbromoisopropyl, and the like. Specific examples of C_1-4 alkyl include, but are not limited to, C_1-3 haloalkyl, perfluorobutyl, perchlorobutyl, perbromobutyl, perfluoroisobutyl, perfluoro-t-butyl, and the like. Specific examples of C_1-6 alkyl include, but are not limited to, C_1-4 haloalkyl, perfluoro-n-pentyl, perfluoroisopentyl, perfluoroneopentyl, perfluorotert-pentyl, perfluoro-1,2-dimethylpropyl, and the like.

As used herein, “haloalkoxy” as well as “haloalkyloxy” is a monovalent group of —O-haloalkyl with one or more hydrogen on the alkyl group substitututed with halogen. The term “perhaloalkoxy” refers to haloalkoxy with all hydrogen on the alkyl group substituted with halogen. For example, perfluoroethoxy is —OCF₂CF₃, and perchloro-n-propoxy is —OCCl₂CCl₂CCl₃. Preferred examples of haloalkoxy include C_1-6 haloalkoxy, C_1-4 haloalkoxy, C_1-3 haloalkoxy, and the like. Specific examples of C_1-3 alkoxy include, but are not limited to, fluoromethoxy, chloromethoxy, bromomethoxy, difluoromethoxy, dichloromethoxy, dibromomethoxy, tri fluoromethoxy, trichloromethoxy, tribromomethoxy, fluorochloromethoxy, difluorochloromethoxy, fluorodichloromethoxy, fluoroethoxy, chloroethoxy, bromoethoxy, trifluoroethoxy, trichloroethoxy, tribromoethoxy, perfluoroethoxy, perchloroethoxy, perbromoethoxy, perfluoropropoxy, perchloropropoxy, perbromopropoxy, perfluoroisopropoxy, perchloroisopropoxy, perbromoisopropoxy, and the like. Specific examples of C_1-4 alkoxy include, but are not limited to, C_1-3 haloalkoxy, perfluorobutoxy, perchlorobutoxy, perbromobutoxy, perfluoroisobutoxy, perfluoro-t-butoxy, and the like. Specific examples of C_1-6 alkoxy include, but are not limited to, C_1-4 haloalkoxy, perfluoro-n-pentyloxy, perfluoroisopentyloxy, perfluoroneopentyloxy, perfluorotert-pentyloxy, perfluoro-1,2-dimethylpropoxy, and the like.

As used herein, “alkylsulfonyl” refers to a sulfonyl group substituted with the “alkyl” described above. “C_1-6 alkylsulfonyl” is preferably “C_1-4 alkylsulfonyl”. Specific examples of “C_1-6 alkylsulfonyl” include, but are not limited to, methylsulfonyl, propionylsulfonyl, butyrylsulfonyl, and the like.

As used herein, the alkyl moiety of “alkylthio” is defined the same as the alkyl described above. Examples of “C_1-6 alkylthio” include “C_1-4 alkylthio”, and preferred examples thereof include “C_1-3 alkylthio”. Specific examples of “C_1-6 alkylthio” include, but are not limited to, methylthio, ethylthio, propylthio, butylthio, isopropylthio, isobutylthio, tert-butylthio, sec-butylthio, isopentylthio, neopentylthio, tert-pentylthio, 1,2-dimethylpropylthio, and the like.

As used herein, “arylcarbonyl” is a monovalent group of —C(═O)-aryl. Preferred examples of arylcarbonyl include C_6-10 arylcarbonyl. Specific examples of C_6-10 arylcarbonyl include, but are not limited to, benzoyl (i.e., phenyl-C(═O)—), 1-naphthylcarbonyl, 2-naphthylcarbonyl, and the like.

As used herein, the aryl moiety of “aryloxy” is defined the same as the aryl described above. Preferred examples of “C_6-10 aryloxy” include “C₆ or C₁₀ aryloxy”. Specific examples of “C_6-10 aryloxy group” include, but are not limited to, a phenoxy group, 1-naphthyloxy group, 2-naphthyloxy group, and the like.

As used herein, “heteroarylcarbonyl” is a monovalent group of —C(═O)-heteroaryl.

As used herein, “heteroarylcarbonyl group” refers to a carbonyl group substituted with the “heteroaryl” described above. Specific examples of “5- to 6-membered heteroarylcarbonyl group” include, but are not limited to, pyrazoylcarbonyl group, triazoylcarbonyl group, triazoylcarbonyl group, thiadiazoylcarbonyl group, pyridylcarbonyl group, pyridazoylcarbonyl group, and the like.

As used herein, the heteroaryl moiety of the “heteroaryloxy group” is defined the same as the “heteroaryl” described above. The 5- to 6-membered heteroaryl moiety of the “5- to 6-membered heteroaryloxy group” is defined the same as “5-membered heteroaryl” or “6-membered heteroaryl”, respectively. Specific examples of “5- to 6-membered heteroaryloxy group” include, but are not limited to, a pyrazoyloxy group, triazoyloxy group, triazoyloxy group, thiadiazoyloxy group, pyridyloxy group, pyridazoyloxy group, and the like.

As used herein, the heteroaryl moiety of a “heteroarylthio group” is defined the same as the “heteroaryl” described above. The 5- to 6-membered heteroaryl moiety of “5- to 6-membered heteroarylthio group” is defined the same as “5-membered heteroaryl” or “6-membered heteroaryl”, respectively. Specific examples of “5- to 6-membered heteroarylthio group” include, but are not limited to, pyrazoylthio group, triazoylthio group, thiazoylthio group, thiadiazoylthio group, pyridylthio group, pyridazoylthio group, and the like.

As used herein, the heteroaryl moiety of a “heteroarylsulfonyl group” is defined the same as the “heteroaryl” described above. A “5- to 6-membered heteroarylsulfonyl group” refers to a sulfonyl group substituted with a “5- to 6-membered heteroaryl”. Specific examples of “5- to 6-membered heteroarylsulfonyl group” include, but are not limited to, pyrazoylsulfonyl group, triazoylsulfonyl group, triazoylsulfonyl group, thiadiazoylsulfonyl group, pyridylsulfonyl group, pyridazoylsulfonyl group, and the like.

As used herein, “acyl” refers to a monovalent group of —C(═O)—R_acyl, wherein R_acyl is hydrogen, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted aryl, optionally substituted heteroaryl, or optionally substituted heterocycloalkyl. Specific examples of acyl include, but are not limited to, formyl, groups exemplified as alkylcarbonyl, arylcarbonyl, and heteroarylcarbonyl, and the like.

As used herein, “optionally substituted carbonyl” group refers to a monovalent group of —C(═O)— (hydrogen or any group selected from a substituent group described herein). Examples of “optionally substituted carbonyl” group include, but are not limited to, formyl, and optionally substituted carbamoyl, alkylcarbonyl, alkoxycarbonyl, alkenylcarbonyl, alkenyloxycarbonyl, alkynylcarbonyl, alkynyloxycarbonyl, arylcarbonyl, aryloxycarbonyl, cycloalkylcarbonyl, cycloalkyloxycarbonyl, heteroarylcarbonyl, heteroaryloxycarbonyl, heterocycloalkylcarbonyl, heterocycloalkyloxycarbonyl, and the like. A carbonyl group substituted with hydrogen is a formyl group. A carbonyl group substituted with amino is a carbamoyl group.

As used herein, “optionally substituted oxy” group refers to a monovalent group of —O— (hydrogen or any group selected from a substituent group described herein). Examples of “optionally substituted oxy” group include, but are not limited to, hydroxy, and optionally substituted alkyloxy, alkenyloxy, alkynyloxy, aryloxy, heteroaryloxy, heterocycloalkyloxy, alkylcarbonyloxy, alkenylcarbonyloxy, alkynylcarbonyloxy, arylcarbonyloxy, heteroarylcarbonyloxy, heterocycloalkylcarbonyloxy, and the like. An oxy group substituted with hydrogen is a hydroxy group.

As used herein, “carbamoyl” is a monovalent group of —C(═O)—NH₂.

As used herein, “amidinoamino” is a monovalent group of —NH—C(═NH)—NH₂.

As used herein, the phrase “a substituent-substituted group” means that the group is substituted with at least one substituent. For example, “hydroxy-substituted C_1-6 alkyl” refers to C_1-6 alkyl that has at least one hydroxy substitution.

As used herein, “carbamoyl-substituted C_1-6alkyl” is C_1-6 alkyl substituted with at least one —C(═O)—NH₂ group. Examples of “carbamoyl-substituted C_1-6 alkyl” include, but are not limited to, carbamoyl-substituted C_1-4 alkyl. Specific examples of “carbamoyl-substituted C_1-4 alkyl” include, but are not limited to, 2-amino-2-oxoethyl (i.e., H₂NC(═O)—CH₂— or carbamoylmethyl), 3-amino-3-oxopropyl (i.e., H₂NC(═O)—CH₂CH₂— or carbamoylethyl), 4-amino-4-oxobutyl (i.e., H₂NC(═O)—(CH₂)₃— or carbamoylpropyl), 5-amino-5-oxopentyl (i.e., H₂NC(═O)—(CH₂)₄— or carbamoylbutyl), and the like. Specific examples of “carbamoyl-substituted C_1-6 alkyl” include, but are not limited to, carbamoyl-substituted C_1-4 alkyl, 6-amino-6-oxohexyl (i.e., H₂NC(═O)—(CH₂)₅— or carbamoylpentyl), 7-amino-7-oxoheptyl (i.e., H₂NC(═O)—(CH₂)₆— or carbamoylhexyl), and the like.

As used herein, “amidinoamino-substituted alkyl” or “guanidino-substituted alkyl” is alkyl substituted with at least one —NH—C(═NH)—NH₂ group, wherein the nitrogen atom of the amidinoamino group can be protected with a nitrogen protecting group (e.g., tert-butoxycarbonyl group). Examples of “amidinoamino-substituted C_1-6 alkyl” include, but are not limited to, “amidinoamino-substituted C_1-4 alkyl” and the like. Specific examples of “amidinoamino-substituted C_1-4 alkyl” include, but are not limited to, (amidinoamino)methyl, 2-(amidinoamino)ethyl, 3-(amidinoamino)propyl, 4-(amidinoamino)butyl, and the like. Specific examples of “amidinoamino-substituted C_1-6 alkyl” include, but are not limited to, amidinoamino-substituted C_1-4 alkyl, 5-(amidinoamino)pentyl, 6-(amidinoamino)hexyl, and the like. Examples of amidinoamino groups protected with a nitrogen protecting group include

As used herein, “amidinoamino” is synonymous with “guanidino”.

As used herein, “carboxy-substituted alkyl” is alkyl substituted with at least one —COOH group. Examples of “carboxy-substituted C_1-6 alkyl” include, but are not limited to, “carboxy-substituted C_1-4 alkyl” and the like. Specific examples of “carboxy-substituted C_1-4 alkyl” include, but are not limited to, carboxymethyl, 2-carboxyethyl, 3-carboxypropyl, 4-carboxybutyl, and the like. Specific examples of “carboxy-substituted C_1-6 alkyl” include, but are not limited to, carboxy-substituted C_1-4 alkyl, 5-carboxypentyl, 6-carboxyhexyl, and the like.

A “protecting group” refers to a group of atoms that blocks, reduces, or prevents reactivity of a functional group when attached to a reactive functional group in a molecule. The compound of the present disclosure can have a substitution with a protecting group when appropriate or needed at any of R₁ to R₄ or any position of a substituent thereof or other substituents or the like. Compounds comprising such a protecting group are also within the scope of the present disclosure. Typically, a protecting group can be selectively removed during a synthesis process if desired. Examples of protecting groups are found in Greene and Wuts, Protective Groups in Organic Chemistry, 5th Edition, 2014, John Wiley & Sons, NY and Harrison et al., Compendium of Synthetic Organic Methods, Vol. 1 to 8, John Wiley & Sons, NY, or the like. As used herein, a “protecting group” can fall under the definitions for 1) to 53) of substituent a and 1) to 26) of substituent β. In such a case, “54) protecting group” can be described as “54) protecting group other than 1) to 53)” in substituent group α1, and “27) protecting group” can be described as “protecting group other than 1) to 26)” in substituent group β1. Representative examples of nitrogen protecting groups include, but are not limited to, formyl, acetyl, trifluoroacetyl, benzyl, benzyloxycarbonyl (“CBZ”), tert-butoxycarbonyl (“Boc”), trimethylsilyl (“TMS”), 2-trimethylsilylethanesulfonyl (“TES”), trityl and substituted trityl group, allyloxycarbonyl, 9-fluorenylmethyloxycarbonyl (“FMOC”), nitro-veratryloxycarbonyl (“NVOC”), groups represented by “Protect” herein, and the like. Representative examples of hydroxyl protecting groups include, but are not limited to, groups that acylate (esterify) or alkylate a hydroxyl group, such as benzyl and trityl ether, as well as alkyl ether, tetrahydropyranyl ether, trialkylsilyl ether (e.g., TMS, triethylsilyl, t-butyldimethylsilyl (TBDMS), and triisopropylsilyl (TIPS)), alkyldiarylsilyl ether (e.g., t-butyldiphenylsilyl (TBDPS)), triarylsilyl ether (e.g., triphenylsilyl), glycol ether (e.g., ethylene glycol ether, propylene glycol ether, and the like), and allyl ether.

An amino group of the compound of the present disclosure (e.g., amino group of the backbone, amino group as a substituent, amino group in a substituent of said compound, or the like) can be protected with a nitrogen protecting group or a group represented by “Protect”. An amino group in a substituent listed in a substituent group can be further protected with a nitrogen protecting group or a group represented by “Protect”. A protected substituent can also be used as a substituent.

A hydroxy group of the compound of the present disclosure (e.g., hydroxy group as a substituent, a hydroxy group in a substituent of said compound, a hydroxy group in a substituent group described above, or the like) can also be protected with a protecting group of a hydroxy group. A hydroxy group in a substituent listed in a substituent group can be further protected with a hydroxyl protecting group described herein. A protected substituent can also be used as a substituent.

Preferred Embodiments

The preferred embodiments of the present disclosure are described hereinafter. It is understood that the embodiments provided hereinafter are provided for the better understanding of the present disclosure, so that the scope of the present disclosure should not be limited by the following descriptions. Thus, it is apparent that those skilled in the art can refer to the descriptions herein to make appropriate modifications within the scope of the present disclosure. It is also understood that the following embodiments of the present disclosure can be used individually or as a combination.

(Compound and Composition of the Present Disclosure)

In one aspect, the compound of the present disclosure can be exemplified as a compound represented by formula XXIF:

or an enantiomer thereof, or a salt thereof, or a solvate thereof, wherein

R₁, R₃, and R₄ are each independently hydrogen, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, or optionally substituted carbonyl, and

R_2A and R_2B are each independently hydrogen, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, or optionally substituted carbonyl, or R_2A and R₂₃, together with the nitrogen atom to which they are attached, form a non-aryl heterocycle or heteroaryl ring, wherein the non-aryl heterocycle and the heteroaryl ring are each independently and optionally substituted.

If one of R_2A or R_2B is hydrogen herein, it is understood that the same definition as R₂ described herein can be used.

In another aspect, the compound of the present disclosure can be exemplified as a compound represented by formula XXIB:

or an enantiomer thereof, or a salt thereof, or a solvate thereof, wherein R₁, R_2a, R_2B, and R₃ are defined the same as those for formula XXIF described herein.

In still another aspect, the compound of the present disclosure can be exemplified as a compound represented by formula XXIIF:

or an enantiomer thereof, or a salt thereof, or a solvate thereof, wherein R₁, R_2A, R_2B, and R₃ are defined the same as those for formula XXIF described herein.

In still another aspect, the compound of the present disclosure can be exemplified as a compound represented by formula XXIIB:

or an enantiomer thereof, or a salt thereof, or a solvate thereof, wherein R₁, R₂, and R₃ are defined the same as those for formula XXIF described herein.

In one embodiment, the alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, and carbonyl of R₁, R₃, and if present R₄ are each independently and optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group I, and

the alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, carbonyl, and the non-aryl heterocycle and the heteroaryl ring of R_2A and R_2B are each independently and optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group I.

In one embodiment, R₁, R₃, and if present R₄ are each independently hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, or optionally substituted carbonyl, and

R_2A and R_2B are each independently hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, or optionally substituted carbonyl, or R_2A and R_n, together with the nitrogen atom to which they are attached, form a non-aryl heterocycle or heteroaryl ring, wherein the non-aryl heterocycle and the heteroaryl ring are each independently and optionally substituted.

In some cases for substituents in this embodiment, R_2A and R_2B are each independently hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, or optionally substituted heteroaryl and/or R_2A and R_2B, together with the nitrogen atom to which they are attached, form a non-aryl heterocycle, wherein the non-aryl heterocycles are each independently and optionally substituted.

Alternatively, in another embodiment for (an imine form), R₁ and R₃ are each independently hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, or optionally substituted carbonyl, and R_2A and R_2B are each independently hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, or optionally substituted carbonyl, or R_2A and R_n, together with the nitrogen atom to which they are attached, form a non-aryl heterocycle or heteroaryl ring, wherein the non-aryl heterocycle and the heteroaryl ring are each independently and optionally substituted.

In some cases, R₁ and R₃ are each independently hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, or optionally substituted heteroaryl, and R_2A and R_2B are each independently hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, or optionally substituted heteroaryl, and/or R_2A and R_2B, together with the nitrogen atom to which they are attached, form a non-aryl heterocycle, wherein the non-aryl heterocycles are each independently and optionally substituted.

In one embodiment, R₁, R₃, and if present R₄ are each independently hydrogen, optionally substituted C_1-12 alkyl, optionally substituted C_3-10 cycloalkyl, optionally substituted 5- to 10-membered heterocycloalkyl, optionally substituted C_6-10 aryl, optionally substituted 5- to 10-membered heteroaryl, or optionally substituted carbonyl, and

R_2A and R_2B are each independently hydrogen, optionally substituted C_1-12 alkyl, optionally substituted C_3-10 cycloalkyl, optionally substituted 5- to 10-membered heterocycloalkyl, optionally substituted C_6-10 aryl, optionally substituted 5- to 10-membered heteroaryl, or optionally substituted carbonyl, or R_2A and R_n, together with the nitrogen atom to which they are attached, form a non-aryl heterocycle or heteroaryl ring, wherein the non-aryl heterocycle and the heteroaryl ring are each independently and optionally substituted.

In some cases, R_2A and R_2B are each independently hydrogen, optionally substituted C_1-12 alkyl, optionally substituted C_3-10 cycloalkyl, optionally substituted 5- to 10-membered heterocycloalkyl, optionally substituted C_6-10 aryl, or optionally substituted 5- to 10-membered heteroaryl, and/or R_2A and R_n, together with the nitrogen atom to which they are attached, form a non-aryl heterocycle, wherein the non-aryl heterocycles are each independently and optionally substituted.

In one embodiment, R₁, R₃, and if present R₄ are each independently hydrogen, optionally substituted alkyl, optionally substituted arylalkyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, formyl, optionally substituted alkylcarbonyl, optionally substituted alkoxycarbonyl, optionally substituted arylcarbonyl, optionally substituted aryloxycarbonyl, optionally substituted heteroarylcarbonyl, optionally substituted heteroaryloxycarbonyl, optionally substituted cycloalkylcarbonyl, optionally substituted cycloalkyloxycarbonyl, optionally substituted heterocycloalkylcarbonyl, optionally substituted heterocycloalkyloxycarbonyl, carbamoyl, optionally substituted alkylcarbamoyl, optionally substituted alkoxycarbamoyl, optionally substituted arylcarbamoyl, optionally substituted heteroarylcarbamoyl, optionally substituted cycloalkylcarbamoyl, or optionally substituted heterocycloalkylcarbamoyl, wherein the groups of R₁, R₃, and R₄ are optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group II, and

R_2A and R_2B are each independently hydrogen, optionally substituted alkyl, optionally substituted arylalkyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, formyl, optionally substituted alkylcarbonyl, optionally substituted alkoxycarbonyl, optionally substituted arylcarbonyl, optionally substituted aryloxycarbonyl, optionally substituted heteroarylcarbonyl, optionally substituted heteroaryloxycarbonyl, optionally substituted cycloalkylcarbonyl, optionally substituted cycloalkyloxycarbonyl, optionally substituted heterocycloalkylcarbonyl, optionally substituted heterocycloalkyloxycarbonyl, carbamoyl, optionally substituted alkylcarbamoyl, optionally substituted alkoxycarbamoyl, optionally substituted arylcarbamoyl, optionally substituted heteroarylcarbamoyl, optionally substituted cycloalkylcarbamoyl, or optionally substituted heterocycloalkylcarbamoyl, wherein the groups of R_2A and R_2B are optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group II, or R_2A and R_n, together with the nitrogen atom to which they are attached, form a 5- to 6-membered non-aryl heterocycle or heteroaryl ring, wherein the non-aryl heterocycle and the heteroaryl ring are optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group II.

In one embodiment, R₁, R₃, and if present R₄ are each independently hydrogen, optionally substituted C_1-12 alkyl, optionally substituted C_6-10 aryl C_1-12 alkyl, optionally substituted C_3-10 cycloalkyl, optionally substituted 5- to 10-membered heterocycloalkyl, formyl, optionally substituted C_1-12 alkylcarbonyl, optionally substituted C_1-12 alkoxycarbonyl, optionally substituted C_6-10 arylcarbonyl, optionally substituted C_6-10 aryloxycarbonyl, optionally substituted 5- to 10-membered heteroarylcarbonyl, optionally substituted 5- to 10-membered heteroaryloxycarbonyl, optionally substituted C_3-10 cycloalkylcarbonyl, optionally substituted C_3-10 cycloalkyloxycarbonyl, optionally substituted 5- to 10-membered heterocycloalkylcarbonyl, optionally substituted 5- to 10-membered heterocycloalkyloxycarbonyl, carbamoyl, optionally substituted C_1-12 alkylcarbamoyl, optionally substituted C_1-12 alkoxycarbamoyl, optionally substituted C_6-10 arylcarbamoyl, optionally substituted 5- to 10-membered heteroarylcarbamoyl, optionally substituted C_3-10 cycloalkylcarbamoyl, or optionally substituted 5- to 10-membered heterocycloalkylcarbamoyl, wherein the groups of R₁, R₃, and R₄ are optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group III, and

R_2A and R_2B are each independently hydrogen, optionally substituted C_1-12 alkyl, optionally substituted C_6-10 aryl C_1-12 alkyl, optionally substituted C_3-10 cycloalkyl, optionally substituted 5- to 10-membered heterocycloalkyl, formyl, optionally substituted C_1-12 alkylcarbonyl, optionally substituted C_1-12 alkoxycarbonyl, optionally substituted C_6-10 arylcarbonyl, optionally substituted C_6-10 aryloxycarbonyl, optionally substituted 5- to 10-membered heteroarylcarbonyl, optionally substituted 5- to 10-membered heteroaryloxycarbonyl, optionally substituted C_3-10 cycloalkylcarbonyl, optionally substituted C_3-10 cycloalkyloxycarbonyl, optionally substituted 5- to 10-membered heterocycloalkylcarbonyl, optionally substituted 5- to 10-membered heterocycloalkyloxycarbonyl, carbamoyl, optionally substituted C_1-12 alkylcarbamoyl, optionally substituted C_1-12 alkoxycarbamoyl, optionally substituted C_6-10 arylcarbamoyl, optionally substituted 5- to 10-membered heteroarylcarbamoyl, optionally substituted C_3-10 cycloalkylcarbamoyl, or optionally substituted 5- to 10-membered heterocycloalkylcarbamoyl, wherein the groups of R_2A and R_2B are optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group III, or R_2A and R_2B, together with the nitrogen atom to which they are attached, form a 5- to 6-membered non-aryl heterocycle, wherein the non-aryl heterocycle is optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group V.

In some cases, R_2A and R_2B are each independently hydrogen, optionally substituted C_1-12 alkyl, optionally substituted C_6-10 aryl C_1-12 alkyl, optionally substituted C₃-cycloalkyl, optionally substituted 5- to 10-membered heterocycloalkyl, or formyl, wherein the groups of R_2A and R_2B are optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group III.

In one embodiment, R₁ and if present R₄ are each independently hydrogen, optionally substituted alkyl, optionally substituted arylalkyl, optionally substituted cycloalkyl, formyl, optionally substituted alkylcarbonyl, optionally substituted alkoxycarbonyl, optionally substituted arylcarbonyl, optionally substituted aryloxycarbonyl, optionally substituted cycloalkylcarbonyl, optionally substituted cycloalkyloxycarbonyl, optionally substituted heterocycloalkylcarbonyl, optionally substituted heterocycloalkyloxycarbonyl, carbamoyl, optionally substituted alkylcarbamoyl, optionally substituted alkoxycarbamoyl, optionally substituted arylcarbamoyl, optionally substituted heteroarylcarbamoyl, optionally substituted cycloalkylcarbamoyl, or optionally substituted heterocycloalkylcarbamoyl, wherein the groups of R₁ and R₄ are optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group III.

In some cases, R₁ and if present R₄ are each independently hydrogen, optionally substituted alkyl, optionally substituted arylalkyl, optionally substituted cycloalkyl, or formyl, wherein the groups of R₁ and R₄ are optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group III.

In one embodiment, R₁ and if present R₄ are each independently hydrogen, optionally substituted C_1-12 alkyl, optionally substituted C_6-10 aryl C_1-12 alkyl, optionally substituted C_3-10 cycloalkyl, formyl, optionally substituted C_1-12 alkylcarbonyl, optionally substituted C_1-12 alkoxycarbonyl, optionally substituted C_6-10 arylcarbonyl, optionally substituted C_6-10 aryloxycarbonyl, optionally substituted C_3-10 cycloalkylcarbonyl, optionally substituted C_3-10 cycloalkyloxycarbonyl, optionally substituted 5- to 10-membered heterocycloalkylcarbonyl, optionally substituted 5- to 10-membered heterocycloalkyloxycarbonyl, carbamoyl, optionally substituted C_1-12 alkylcarbamoyl, optionally substituted C_1-12 alkoxycarbamoyl, optionally substituted C_6-10 arylcarbamoyl, optionally substituted 5- to 10-membered heteroarylcarbamoyl, optionally substituted C_3-10 cycloalkylcarbamoyl, or optionally substituted 5- to 10-membered heterocycloalkylcarbamoyl, wherein the groups of R₁ and R₄ are optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group III.

In one embodiment, R₁ and if present R₄ are each independently hydrogen, optionally substituted alkyl, optionally substituted arylalkyl, formyl, optionally substituted alkylcarbonyl, optionally substituted alkoxycarbonyl, optionally substituted arylcarbonyl, optionally substituted aryloxycarbonyl, carbamoyl, or optionally substituted alkylcarbamoyl, wherein the groups of R₁ and R₄ are optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group III.

In one embodiment, R₁ and if present R₄ are each independently hydrogen, optionally substituted C_1-12 alkyl, optionally substituted C_6-10 aryl C_1-12 alkyl, formyl, optionally substituted C_1-12 alkylcarbonyl, optionally substituted C_1-12 alkoxycarbonyl, optionally substituted C_6-10 arylcarbonyl, optionally substituted C_6-10 aryloxycarbonyl, carbamoyl, or optionally substituted C_1-12 alkylcarbamoyl, wherein the groups of R₁ and R₄ are optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group III.

In one embodiment, R₁ and if present R₄ are each independently hydrogen, alkyl, alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amino, substituted amino, substituted oxy, substituted carbonyl, cycloalkyl, and substituted cycloalkyl, arylalkyl, arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, alkyl, substituted alkyl, hydroxy, substituted oxy, amino, substituted amino, and nitro, formyl, substituted carbonyl, or substituted oxycarbonyl, wherein the substituted amino, substituted oxy, substituted alkyl, substituted carbonyl, substituted cycloalkyl, substituted carbonyl, and substituted oxycarbonyl in R₁ and R₄ each independently have one to the maximum substitutable number of the same or different substituents selected from substituent group IV.

In one embodiment, R₁ and if present R₄ are each independently hydrogen, C_1-12 alkyl, C_1-12 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amino, substituted amino, substituted oxy, substituted carbonyl, C_3-10 cycloalkyl, and substituted C_3-10 cycloalkyl, C_6-10 aryl C_1-6 alkyl, C_6-10 aryl C_1-6 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, C_1-6 alkyl, substituted alkyl, hydroxy, substituted oxy, amino, substituted amino, and nitro, formyl, substituted carbonyl, or substituted oxycarbonyl, wherein the substituted amino, substituted oxy, substituted alkyl, substituted carbonyl, substituted cycloalkyl, substituted carbonyl, and substituted oxycarbonyl in R₁ and R₄ each independently have one to the maximum substitutable number of the same or different substituents selected from substituent group IV.

In one embodiment, R₁ and R₃ are each independently hydrogen, optionally substituted alkyl, optionally substituted arylalkyl, optionally substituted cycloalkyl, formyl, optionally substituted alkylcarbonyl, optionally substituted alkoxycarbonyl, optionally substituted arylcarbonyl, optionally substituted aryloxycarbonyl, optionally substituted cycloalkylcarbonyl, optionally substituted cycloalkyloxycarbonyl, optionally substituted heterocycloalkylcarbonyl, optionally substituted heterocycloalkyloxycarbonyl, carbamoyl, optionally substituted alkylcarbamoyl, optionally substituted alkoxycarbamoyl, optionally substituted arylcarbamoyl, optionally substituted heteroarylcarbamoyl, optionally substituted cycloalkylcarbamoyl, or optionally substituted heterocycloalkylcarbamoyl, wherein the groups of R₁ and R₃ are optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group III.

In one embodiment, and R₃ are each independently hydrogen, optionally substituted C_1-12 alkyl, optionally substituted C_6-10 aryl C_1-12 alkyl, optionally substituted C_3-10 cycloalkyl, formyl, optionally substituted C_1-12 alkylcarbonyl, optionally substituted C_1-12 alkoxycarbonyl, optionally substituted C_6-10 arylcarbonyl, optionally substituted C_6-10 aryloxycarbonyl, optionally substituted C_3-10 cycloalkylcarbonyl, optionally substituted C_3-10 cycloalkyloxycarbonyl, optionally substituted 5- to 10-membered heterocycloalkylcarbonyl, optionally substituted 5- to 10-membered heterocycloalkyloxycarbonyl, carbamoyl, optionally substituted C_1-12 alkylcarbamoyl, optionally substituted C_1-12 alkoxycarbamoyl, optionally substituted C_6-10 arylcarbamoyl, optionally substituted 5- to 10-membered heteroarylcarbamoyl, optionally substituted C_3-10 cycloalkylcarbamoyl, or optionally substituted 5- to 10-membered heterocycloalkylcarbamoyl, wherein the groups of R₁ and R₃ are optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group III.

In one embodiment, R₁ and if present R₄ are each independently hydrogen, alkyl, alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amidinoamino, alkoxy, alkoxycarbonyl, carbamoyl, carboxy, hydroxy, trialkylsilyloxy, and cycloalkyl, arylalkyl, arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, alkyl, haloalkyl, alkoxy, haloalkoxy, amino, substituted amino, nitro, and hydroxy, formyl, alkylcarbonyl, arylalkylcarbonyl, arylalkyloxycarbonyl, alkoxycarbonyl, arylcarbonyl, aryloxycarbonyl, carbamoyl, alkylcarbamoyl, or arylalkylcarbamoyl, wherein the substituted amino each independently has one to the maximum substitutable number of the same or different substituents selected from substituent group IV.

In one embodiment, R₁ and if present R₄ are each independently hydrogen, C_1-12 alkyl, C_1-12 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amidinoamino, C_1-6 alkoxy, C_1-6 alkoxycarbonyl, carbamoyl, carboxy, hydroxy, tri-C_1-6 alkylsilyloxy, and C_3-10 cycloalkyl, C_6-10 aryl C_1-6 alkyl, C_6-10 aryl C_1-6 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, C_1-6 alkyl, C_1-6 haloalkyl, C_1-6 alkoxy, C_1-6 haloalkoxy, amino, substituted amino, nitro, and hydroxy, formyl, C_1-12 alkylcarbonyl, C_6-10 aryl C_1-6 alkylcarbonyl, C_6-10 aryl C_1-6 alkyloxycarbonyl, C_1-12 alkoxycarbonyl, C_6-10 arylcarbonyl, C_6-10 aryloxycarbonyl, carbamoyl, C_1-12 alkylcarbamoyl, or C_6-10 aryl C_1-6 alkylcarbamoyl, wherein the substituted amino has one to the maximum substitutable number of the same or different substituents selected from substituent group IV.

In one embodiment, R₁ and if present R₄ are each independently, C_1-12 alkyl, C_1-12 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amidinoamino, C_1-6 alkoxycarbonyl-substituted amidinoamino, C_1-6 alkoxy, C_1-6 alkoxycarbonyl, carbamoyl, carboxy, hydroxy, tri-C_1-6 alkylsilyloxy, and C_3-10 cycloalkyl, C_6-10 aryl C_1-6 alkyl, or C_6-10 aryl C_1-6 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, C_1-6 alkyl, C_1-6 haloalkyl, C_1-6 alkoxy, C_1-6 haloalkoxy, amino, substituted amino, nitro, and hydroxy, wherein the substituted amino optionally has one to the maximum substitutable number of the same or different substituents selected from substituent group IV.

In one embodiment, R₃ is hydrogen, alkyl, alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of formyl, substituted carbonyl, hydroxy, substituted oxy, substituted carbonyl, amino, substituted amino, cycloalkyl, substituted cycloalkyl, heterocycloalkyl, and substituted heterocycloalkyl, arylalkyl, arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, nitro, hydroxy, substituted oxy, amino, substituted amino, alkyl, and substituted alkyl, heteroarylalkyl, or substituted heteroarylalkyl, wherein the substituted carbonyl, substituted oxy, substituted amino, substituted cycloalkyl, substituted heterocycloalkyl, substituted alkyl, and substituted heteroarylalkyl in R₃ each independently and optionally have one to the maximum substitutable number of the same or different substituents selected from substituent group IV.

In some cases, R₃ is hydrogen, alkyl, alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of hydroxy, substituted oxy, substituted carbonyl, amino, substituted amino, cycloalkyl, substituted cycloalkyl, heterocycloalkyl, and substituted heterocycloalkyl, arylalkyl, arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, nitro, hydroxy, substituted oxy, amino, substituted amino, alkyl, and substituted alkyl, heteroarylalkyl, or substituted heteroarylalkyl, wherein the substituted oxy, substituted amino, substituted cycloalkyl, substituted heterocycloalkyl, substituted alkyl, and substituted heteroarylalkyl in R₃ each independently and optionally have one to the maximum substitutable number of the same or different substituents selected from substituent group IV.

In one embodiment, R₃ can be hydrogen, alkyl, formyl, alkylcarbonyl, arylalkylcarbonyl, alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of hydroxy, trialkylsilyloxy, alkoxy, alkoxycarbonyl, alkoxycarbonylamino, cycloalkyl, carboxy, amino, amidinoamino, alkoxycarbonyl-substituted amidinoamino, carbamoyl, and heterocycloalkyl, arylalkyl, arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, nitro, hydroxy, amino, monoalkylamino, dialkylamino, alkyl, haloalkyl, alkoxy, haloalkoxy, carboxyalkylcarbonylamino, carbamoylalkylcarbonylamino, cycloalkylcarbonylamino, and cycloalkylalkylamino, heteroarylalkyl, or alkoxycarbonyl-substituted heteroarylalkyl.

In some cases, R₃ can be hydrogen, alkyl, alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of hydroxy, trialkylsilyloxy, alkoxy, alkoxycarbonyl, alkoxycarbonylamino, cycloalkyl, carboxy, amino, amidinoamino, alkoxycarbonyl-substituted amidinoamino, carbamoyl, and heterocycloalkyl, arylalkyl, arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, nitro, hydroxy, amino, monoalkylamino, dialkylamino, alkyl, haloalkyl, alkoxy, haloalkoxy, carboxyalkylcarbonylamino, carbamoylalkylcarbonylamino, cycloalkylcarbonylamino, and cycloalkylalkylamino, heteroarylalkyl, or alkoxycarbonyl-substituted heteroarylalkyl.

In one embodiment, R₃ can be hydrogen, C_1-12 alkyl, formyl, C_1-6 alkylcarbonyl, C_6-10 aryl C_1-6 alkylcarbonyl, C_1-12 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of hydroxy, tri-C_1-6alkylsilyloxy, C_1-6 alkoxy, C_1-6 alkoxycarbonyl, C_1-6 alkoxycarbonylamino, C_3-6 cycloalkyl, carboxy, amino, amidinoamino, C_1-6 alkoxycarbonyl-substituted amidinoamino, carbamoyl, and 5- to 6-membered heterocycloalkyl, C_6-10 aryl C_1-6 alkyl, C_6-10 aryl C_1-12 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, nitro, hydroxy, amino, mono-C_1-6 alkylamino, di-C_1-6 alkylamino, C_1-6 alkyl, C_1-6 haloalkyl, C_1-6 alkoxy, C_1-6 haloalkoxy, carboxy C_1-6 alkylcarbonylamino, carbamoyl C_1-6 alkylcarbonylamino, C_3-6 cycloalkylcarbonylamino, and C_3-6 cycloalkyl C_1-6 alkylamino, 5- to 10-membered heteroaryl C_1-6 alkyl, or C_1-6 alkoxycarbonyl-substituted 5- to 10-membered heteroaryl C_1-6 alkyl.

In some cases, R₃ can be hydrogen, C_1-12 alkyl, C_1-12 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of hydroxy, tri-C_1-6 alkylsilyloxy, C_1-6 alkoxy, C_1-6 alkoxycarbonyl, C_1-6 alkoxycarbonylamino, C_3-6 cycloalkyl, carboxy, amino, amidinoamino, C_1-6 alkoxycarbonyl-substituted amidinoamino, carbamoyl, and 5- to 6-membered heterocycloalkyl, C_6-10 aryl C_1-6 alkyl, C_6-10 aryl C_1-12 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, nitro, hydroxy, amino, mono-C_1-6 alkylamino, di-C_1-6 alkylamino, C_1-6 alkyl, C_1-6 haloalkyl, C_1-6 alkoxy, C_1-6 haloalkoxy, carboxy C_1-6 alkylcarbonylamino, carbamoyl C_1-6 alkylcarbonylamino, C_3-6 cycloalkylcarbonylamino, and C_3-6 cycloalkyl C_1-6 alkylamino, 5- to 10-membered heteroaryl C_1-6 alkyl, or C_1-6 alkoxycarbonyl-substituted 5- to 10-membered heteroaryl C_1-6 alkyl.

In one embodiment, R₃ can be C_1-12 alkyl, C_1-12 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of hydroxy, tri-C_1-6 alkylsilyloxy, C_1-6 alkoxy, C_1-6 alkoxycarbonyl, C_1-6 alkoxycarbonylamino, C_3-6 cycloalkyl, carboxy, amino, amidinoamino, C_1-6 alkoxycarbonyl-substituted amidinoamino, carbamoyl, and 5- to 6-membered heterocycloalkyl, C_6-10 aryl C_1-6 alkyl, or C_6-10 aryl C_1-12 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, nitro, hydroxy, amino, mono-C_1-6 alkylamino, di-C_1-6 alkylamino, C_1-6 alkyl, C_1-6 haloalkyl, C_1-6 alkoxy, C_1-6 haloalkoxy, carboxy C_1-6 alkylcarbonylamino, carbamoyl C_1-6 alkylcarbonylamino, C_3-6 cycloalkylcarbonylamino, and C_3-6 cycloalkyl C_1-6 alkylamino.

In one embodiment, R₃ is hydrogen, alkyl, alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amino, substituted amino, carboxy, substituted oxycarbonyl, carbamoyl, substituted aminocarbonyl, hydroxy, substituted oxy, cycloalkyl, and substituted cycloalkyl, arylalkyl, or arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, alkyl, substituted alkyl, carboxy, substituted oxycarbonyl, hydroxy, and substituted oxy, wherein the substituted amino, substituted oxy, substituted oxycarbonyl, substituted aminocarbonyl, substituted alkyl, substituted cycloalkyl, substituted carbonyl, and substituted oxycarbonyl in R₃ each independently have one to the maximum substitutable number of the same or different substituents selected from substituent group IV.

In one embodiment, R₃ is hydrogen, alkyl, alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amidinoamino, alkoxycarbonyl, carbamoyl, carboxy, hydroxy, trialkylsilyloxy, amino, alkoxycarbonylamino, and cycloalkyl, arylalkyl, or arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, alkyl, alkoxycarbonyl, and hydroxy.

In one embodiment, R₃ is hydrogen, C_1-12 alkyl, C_1-12 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amidinoamino, C_1-6 alkoxycarbonyl, carbamoyl, carboxy, hydroxy, tri-C_1-6 alkylsilyloxy, amino, C_1-6 alkoxycarbonylamino, and C_3-10 cycloalkyl, C_6-10 aryl C_1-6 alkyl, or C_6-10 aryl C_1-6 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, C_1-6 alkyl, C_1-6 alkoxycarbonyl, and hydroxy.

In one embodiment, R_2A and R_2B are each independently hydrogen, alkyl, alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of formyl, substituted carbonyl, hydroxy, substituted oxy, amino, substituted amino, cycloalkyl, substituted cycloalkyl, heterocycloalkyl, and substituted heterocycloalkyl, arylalkyl, arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, alkyl, substituted alkyl, hydroxy, and substituted oxy, heteroarylalkyl, substituted heteroarylalkyl, cycloalkyl, or substituted cycloalkyl, wherein the substituted carbonyl, substituted oxy, substituted amino, substituted cycloalkyl, substituted heterocycloalkyl, substituted heteroarylalkyl, and substituted alkyl in R_2A and R_2B each independently have one to the maximum substitutable number of the same or different substituents selected from substituent group IV, or R_2A and R_2B, together with the nitrogen atom to which they are attached, form a non-aryl heterocycle, wherein the non-aryl heterocycle is optionally substituted with one or up to the maximum substitutable number of the same or different substituents selected from substituent group VI.

In one embodiment, R_2A and R_2B are each independently hydrogen, alkyl, alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amidinoamino, alkoxy, alkoxycarbonyl, carbamoyl, carboxy, hydroxy, amino, alkoxycarbonylamino, cycloalkyl, and heterocycloalkyl, arylalkyl, arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, alkyl, haloalkyl, alkoxy, and hydroxy, heteroarylalkyl, alkoxycarbonyl-substituted heteroarylalkyl, or cycloalkyl, or R_2A and R_2B, together with the nitrogen atom to which they are attached, form a 5- to 6-membered non-aryl heterocycle, wherein the non-aryl heterocycle is optionally substituted with one or up to the maximum substitutable number of the same or different substituents selected from substituent group VI.

In one embodiment, R_2A and R_2B are each independently hydrogen, C_1-12 alkyl, C_1-12 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amidinoamino, C_1-6 alkoxy, C_1-6 alkoxycarbonyl, carbamoyl, carboxy, hydroxy, amino, C_1-6 alkoxycarbonylamino, C_3-10 cycloalkyl, and 5- to 10-membered heterocycloalkyl, C_6-10 aryl C_1-6 alkyl, C_6-10 aryl C_1-6 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, C_1-6 alkyl, C_1-6 haloalkyl, C_1-6 alkoxy, and hydroxy, 5- to 10-membered heteroaryl C_1-6 alkyl, C_1-6 alkoxycarbonyl-substituted 5- to 10-membered heteroaryl C_1-6 alkyl, or C_3-10 cycloalkyl, R_2A and R_2B, together with the nitrogen atom to which they are attached, form a 5- to 6-membered non-aryl heterocycle, wherein the non-aryl heterocycle is optionally substituted with one or up to the maximum substitutable number of the same or different substituents selected from substituent group VI.

In one embodiment, R_2A and R_2B are each independently hydrogen, alkyl, alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of formyl, substituted carbonyl, hydroxy, substituted oxy, substituted carbonyl, amino, substituted amino, cycloalkyl, substituted cycloalkyl, heterocycloalkyl, and substituted heterocycloalkyl, arylalkyl, arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, nitro, hydroxy, substituted oxy, amino, substituted amino, alkyl, and substituted alkyl, heteroarylalkyl, or substituted heteroarylalkyl, wherein the substituted carbonyl, substituted oxy, substituted amino, substituted cycloalkyl, substituted heterocycloalkyl, substituted alkyl, and substituted heteroarylalkyl in R_2A and R_2B each independently have one to the maximum substitutable number of the same or different substituents selected from substituent group IV, or R_2A and R_2B, together with the nitrogen atom to which they are attached, form a non-aryl heterocycle, wherein the non-aryl heterocycle is optionally substituted with one or up to the maximum substitutable number of the same or different substituents selected from substituent group VI.

In some cases, R_2A and R_2B are each independently hydrogen, alkyl, alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of hydroxy, substituted oxy, substituted carbonyl, amino, substituted amino, cycloalkyl, substituted cycloalkyl, heterocycloalkyl, and substituted heterocycloalkyl, arylalkyl, arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, nitro, hydroxy, substituted oxy, amino, substituted amino, alkyl, and substituted alkyl, heteroarylalkyl, or substituted heteroarylalkyl, wherein the substituted oxy, substituted amino, substituted cycloalkyl, substituted heterocycloalkyl, substituted alkyl, and substituted heteroarylalkyl in R_2A and R_2B each independently have one to the maximum substitutable number of the same or different substituents selected from substituent group IV, or R_2A and R_2B, together with the nitrogen atom to which they are attached, form a non-aryl heterocycle, wherein the non-aryl heterocycle is optionally substituted with one or up to the maximum substitutable number of the same or different substituents selected from substituent group VI.

In one embodiment, R_2A and R_2B are each independently hydrogen, alkyl, alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of formyl, alkylcarbonyl, arylalkylcarbonyl, hydroxy, trialkylsilyloxy, alkoxy, alkoxycarbonyl, alkoxycarbonylamino, cycloalkyl, carboxy, amino, amidinoamino, alkoxycarbonyl-substituted amidinoamino, carbamoyl, and heterocycloalkyl, arylalkyl, arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, nitro, hydroxy, amino, monoalkylamino, dialkylamino, alkyl, haloalkyl, alkoxy, carboxyalkylcarbonylamino, carbamoylalkylcarbonylamino, cycloalkylcarbonylamino, and cycloalkylalkylamino, heteroarylalkyl, or alkoxycarbonyl-substituted heteroarylalkyl, or R_2A and R_2B, together with the nitrogen atom to which they are attached, form a non-aryl heterocycle, wherein the non-aryl heterocycle is optionally substituted with one or up to the maximum substitutable number of the same or different substituents selected from substituent group VI.

In some cases, R_2A and R_2B are each independently hydrogen, alkyl, alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of hydroxy, trialkylsilyloxy, alkoxy, alkoxycarbonylamino, cycloalkyl, carboxy, amino, amidinoamino, alkoxycarbonyl-substituted amidinoamino, and heterocycloalkyl, arylalkyl, arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, nitro, hydroxy, amino, monoalkylamino, dialkylamino, alkyl, haloalkyl, alkoxy, carboxyalkylcarbonylamino, carbamoylalkylcarbonylamino, cycloalkylcarbonylamino, and cycloalkylalkylamino, heteroarylalkyl, or alkoxycarbonyl-substituted heteroarylalkyl, or R_2A and R_2B, together with the nitrogen atom to which they are attached, form a non-aryl heterocycle, wherein the non-aryl heterocycle is optionally substituted with one or up to the maximum substitutable number of the same or different substituents selected from substituent group VI.

In one embodiment, R_2A and R_2B are each independently hydrogen, C_1-12 alkyl, C_1-12 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of formyl, C_1-6 alkylcarbonyl, C_6-10 aryl C_1-6 alkylcarbonyl, hydroxy, tri-C_1-6 alkylsilyloxy, C_1-6 alkoxy, C_1-6 alkoxycarbonyl, C_1-6 alkoxycarbonylamino, C_3-10 cycloalkyl, carboxy, amino, amidinoamino, C_1-6 alkoxycarbonyl-substituted amidinoamino, carbamoyl, and 5- to 6-membered heterocycloalkyl, C_6-10 aryl C_1-12 alkyl, C_6-10 aryl C_1-12 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, nitro, hydroxy, amino, mono-C_1-6 alkylamino, di-C_1-6 alkylamino, C_1-6 alkyl, C_1-6 haloalkyl, C_1-6 alkoxy, carboxy C_1-6 alkylcarbonylamino, carbamoyl C_1-6 alkylcarbonylamino, C_3-6 cycloalkylcarbonylamino, and C_3-6 cycloalkyl C_1-6 alkylamino, 5- to 10-membered heteroaryl C_1-12 alkyl, or C_1-6 alkoxycarbonyl-substituted 5- to 10-membered heteroaryl C₁-12 alkyl, or R_2A and R_2B, together with the nitrogen atom to which they are attached, form a 5- to 6-membered non-aryl heterocycle, wherein the non-aryl heterocycle is optionally substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, nitro, hydroxy, amino, C_1-6 alkyl, C_1-6 haloalkyl, C_1-6 alkoxy, C_1-6 alkoxycarbonyl, C_3-6 cycloalkylcarbonylamino, and C_3-6 cycloalkyl C_1-6 alkylamino.

In some cases, R_2A and R_2B are each independently hydrogen, C_1-12 alkyl, C_1-12 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of hydroxy, tri-C_1-6 alkylsilyloxy, C_1-6 alkoxy, C_1-6 alkoxycarbonylamino, C_3-10 cycloalkyl, carboxy, amino, amidinoamino, C_1-6 alkoxycarbonyl-substituted amidinoamino, and 5- to 6-membered heterocycloalkyl, C_6-10 aryl C_1-12 alkyl, C_6-10 aryl C_1-12 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, nitro, hydroxy, amino, mono-C_1-6 alkylamino, di-C_1-6 alkylamino, C_1-6 alkyl, C_1-6 haloalkyl, C_1-6 alkoxy, carboxy C_1-6 alkylcarbonylamino, carbamoyl C_1-6 alkylcarbonylamino, C_3-6 cycloalkylcarbonylamino, and C_3-6 cycloalkyl C_1-6 alkylamino, 5- to 10-membered heteroaryl C_1-12 alkyl, or C_1-6 alkoxycarbonyl-substituted 5- to 10-membered heteroaryl C₁-12 alkyl, or R_2A and R_n, together with the nitrogen atom to which they are attached, form a 5- to 6-membered non-aryl heterocycle, wherein the non-aryl heterocycle is optionally substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, nitro, hydroxy, amino, C_1-6 alkyl, C_1-6 haloalkyl, C_1-6 alkoxy, C_1-6 alkoxycarbonyl, C_3-6 cycloalkylcarbonylamino, and C_3-6 cycloalkyl C_1-6 alkylamino.

In one embodiment, R_2A and R_2B are each independently hydrogen, C_1-12 alkyl, C_1-12 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of hydroxy, tri-C_1-6 alkylsilyloxy, C_1-6 alkoxy, C_1-6 alkoxycarbonyl, C_1-6 alkoxycarbonylamino, C_3-10 cycloalkyl, carboxy, amino, amidinoamino, C_1-6 alkoxycarbonyl-substituted amidinoamino, carbamoyl, and 5- to 6-membered heterocycloalkyl, C_6-10 aryl C_1-12 alkyl, C_6-10 aryl C_1-12 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, nitro, hydroxy, amino, mono-C_1-6 alkylamino, di-C_1-6 alkylamino, C_1-6 alkyl, C_1-6 haloalkyl, C_1-6 alkoxy, carboxy C_1-6 alkylcarbonylamino, carbamoyl C_1-6 alkylcarbonylamino, C_3-6 cycloalkylcarbonylamino, and C_3-6 cycloalkyl C_1-6 alkylamino, 5- to 10-membered heteroaryl C_1-12 alkyl, or C_1-6 alkoxycarbonyl-substituted 5- to 10-membered heteroaryl C_1-12 alkyl, or R_2A and R_2B, together with the nitrogen atom to which they are attached, form a 5- to 6-membered non-aryl heterocycle, wherein the non-aryl heterocycle is optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group consisting of halogen, nitro, hydroxy, amino, C_1-6 alkyl, C_1-6 haloalkyl, C_1-6 alkoxy, C_1-6 alkoxycarbonyl, C_3-6 cycloalkylcarbonylamino, and C_3-6 cycloalkyl C_1-6 alkylamino.

In one embodiment, R₁ is alkyl; alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amidinoamino, carbamoyl, carboxy, hydroxy, and cycloalkyl; arylalkyl; or arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, alkyl, haloalkyl, alkoxy, substituted amino, and hydroxy, wherein the substituted amino has one to the maximum substitutable number of the same or different substituents selected from substituent group IV. Alternatively, R₁ is alkyl; arylalkyl; or arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, alkyl, haloalkyl, alkoxy, substituted amino, and hydroxy, wherein the substituted amino has one to the maximum substitutable number of the same or different substituents selected from substituent group IV.

In one embodiment, R₁ is C_1-12 alkyl; C_1-12 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amidinoamino, carbamoyl, carboxy, hydroxy, and C_3-10 cycloalkyl; C_6-10 aryl C_1-6 alkyl; or C_6-10 aryl C_1-6 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, C_1-6 alkyl, C_1-6 haloalkyl, C_1-6 alkoxy, substituted amino, and hydroxy, wherein the substituted amino has one to the maximum substitutable number of the same or different substituents selected from substituent group IV. Alternatively, R₁ is C_1-12 alkyl; C_6-10 aryl C_1-6 alkyl; or C_6-10 aryl C_1-6 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, C_1-6 alkyl, C_1-6 haloalkyl, C_1-6 alkoxy, substituted amino, and hydroxy, wherein the substituted amino has one to the maximum substitutable number of the same or different substituents selected from substituent group IV.

In one embodiment, R_2A is hydrogen, and R_2B is alkyl; alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amidinoamino, carbamoyl, carboxy, hydroxy, and cycloalkyl; arylalkyl; arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, alkyl, haloalkyl, alkoxy, and hydroxy; or cycloalkyl. Alternatively, R_2A is hydrogen, and R_2B is alkyl; arylalkyl; arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, alkyl, haloalkyl, alkoxy, and hydroxy; or cycloalkyl.

In one embodiment, R_2A is hydrogen, and R_2B is C_1-12 alkyl; C_1-12 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amidinoamino, carbamoyl, carboxy, hydroxy, and C_3-10 cycloalkyl; C_6-10 aryl C_1-6 alkyl; C_6-10 aryl C_1-6 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, C_1-6 alkyl, C_1-6 haloalkyl, C_1-6 alkoxy, and hydroxy; or C_3-10 cycloalkyl. Alternatively, R_2A is hydrogen, and R_2B is C_1-12 alkyl; C_6-10 aryl C_1-6 alkyl; C_6-10 aryl C_1-6 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, C_1-6 alkyl, C_1-6 haloalkyl, C_1-6 alkoxy, and hydroxy; or C_3-10 cycloalkyl.

In one embodiment, R₃ is alkyl; alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amidinoamino, carbamoyl, carboxy, hydroxy, and cycloalkyl; arylalkyl; or arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of alkyl and hydroxy. Alternatively, R₃ is alkyl or arylalkyl.

In one embodiment, R₃ is C_1-12 alkyl; C_1-12 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amidinoamino, carbamoyl, carboxy, hydroxy, and C_3-10 cycloalkyl; C_6-10 aryl C_1-6 alkyl; or C_6-10 aryl C_1-6 alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of C_1-6 alkyl and hydroxy.

Alternatively, in one embodiment, R₃ is C_1-12 alkyl or C_6-10 aryl C_1-6 alkyl.

In one embodiment, R₄ is hydrogen, alkyl, alkylcarbonyl, arylalkylcarbonyl, arylalkyloxycarbonyl, alkoxycarbonyl, carbamoyl, or arylalkylcarbamoyl.

In one embodiment, R₄ is hydrogen, C_1-12 alkyl, C_1-12 alkylcarbonyl, C_6-10 aryl C_1-6 alkylcarbonyl, C_6-10 aryl C_1-6 alkyloxycarbonyl, C_1-12 alkoxycarbonyl, carbamoyl, or C_6-10 aryl C_1-6 alkylcarbamoyl.

In one embodiment, R₁ is hydrogen, methyl, ethyl, isobutyl, isopentyl, amidinoaminopropyl, tert-butoxyethyl, tert-butoxypropyl, (tert-butoxycarbonyl)ethyl, carbamoylmethyl, carboxyethyl, hydroxyethyl, hydroxypropyl, cyclopentylmethyl, cyclohexylmethyl, benzyl, phenylethyl, naphthalenylmethyl, fluorobenzyl, chlorobenzyl, dichlorobenzyl, methylbenzyl, tert-butylbenzyl, (trifluoromethyl)benzyl, methoxybenzyl, ethoxybenzyl, tert-butoxybenzyl, aminobenzyl, (cyclopentylcarbonylamino)benzyl, (cyclopentylmethylamino)benzyl, (dimethylamino)benzyl, (carbamoylethylcarbonylamino)benzyl, (carboxyethylcarbonylamino)benzyl, nitrobenzyl, hydroxybenzyl, 3-methylbutanoyl, isobutylcarbonyl, 2-phenylacetyl, isopropyloxycarbonyl, benzoyl, or phenyloxycarbonyl.

In another embodiment, R₁ is methyl, n-propyl, isobutyl, isopentyl, amidinoaminopropyl, tert-butoxycarbonyl-substituted amidinoaminopropyl, tert-butoxyethyl, tert-butoxypropyl, (tert-butoxycarbonyl)ethyl, carboxyethyl, hydroxyethyl, hydroxypropyl, aminopropyl, 2-(tert-butyl-dimethylsilyloxy)ethyl, cyclopentylmethyl, cyclohexylmethyl, benzyl, phenylethyl, naphthalenylmethyl, fluorobenzyl, chlorobenzyl, dichlorobenzyl, methylbenzyl, (tert-butyl)benzyl, methoxybenzyl, ethoxybenzyl, (tert-butoxy)benzyl, (trifluoromethoxy)benzyl, (dimethylamino)benzyl, nitrobenzyl, or hydroxybenzyl.

In one embodiment, R_2A is hydrogen, and R_2B is methyl, isopropyl, isobutyl, n-pentyl, isopentyl, n-hexyl, heptyl, amidinoaminopropyl, tert-butoxyethyl, tert-butoxycarbonylmethyl, carbamoylmethyl, carbamoylethyl, carboxyethyl, hydroxyethyl, aminobutyl, ((tert-butoxycarbonyl)amino)butyl, cyclohexylmethyl, (tetrahydro-2H-pyran-2-yl)methyl, benzyl, phenylethyl, naphthalenylmethyl, naphthalenylethyl, fluorobenzyl, chlorobenzyl, dichlorobenzyl, (fluorophenyl)ethyl, methylbenzyl, (trifluoromethyl)benzyl, methoxybenzyl, tert-butoxybenzyl, hydroxybenzyl, α-hydroxymethylphenethyl, 1-hydroxyphenethyl, pyridinylmethyl, (1H-indol-3-yl)ethyl, (1-(tert-butoxycarbonyl)-1H-indol-3-yl)ethyl, cyclopentyl, or cyclohexyl, or R_2A and R_2B, together with the nitrogen atom to which they are attached, form a pyrrolidine ring or piperidine ring.

In one embodiment, R_2A and R_2B are each independently isopropyl, isobutyl, sec-butyl, pentyl, isopentyl, n-hexyl, heptyl, amidinoaminopropyl, tert-butoxycarbonyl-substituted amidinoaminopropyl, tert-butoxyethyl, tert-butoxycarbonylmethyl, (tert-butoxycarbonyl)ethylcarbamoylethyl, carboxyethyl, hydroxyethyl, aminopropyl, aminobutyl, ((tert-butoxycarbonyl)amino)butyl, cyclopentylmethyl, cyclohexylmethyl, (1,2,3,4-tetrahydronaphthalenyl)methyl, (tetrahydro-2H-pyranyl)methyl, benzyl, phenylethyl, naphthalenylmethyl, (naphthalenyl)ethyl, β-hydroxyphenethyl, α-(hydroxymethyl)phenethyl, fluorobenzyl, chlorobenzyl, dichlorobenzyl, (fluorophenyl)ethyl, methylbenzyl, (trifluoromethyl)benzyl, methoxybenzyl, (tert-butoxy)benzyl, hydroxybenzyl, pyridinylmethyl, quinolinylethyl, (1-(tert-butoxycarbonyl)-1H-indolyl)ethyl, cyclopentyl, or cyclohexyl, or R_2A and R_2B, together with the nitrogen atom to which they are attached, form a pyrrolidine ring or piperidine ring.

In one embodiment, R₃ is n-propyl, isobutyl, isopentyl, amidinoaminopropyl, (methoxycarbonyl)ethyl, (tert-butoxycarbonyl)ethyl, carbamoylmethyl, carboxyethyl, hydroxymethyl, hydroxyethyl, (tert-butyldimethylsilyloxy)ethyl, aminobutyl, ((tert-butoxycarbonyl)amino)butyl, cyclohexylmethyl, cyclohexylethyl, benzyl, phenylethyl, phenylpropyl, phenylbutyl, naphthalenylmethyl, naphthalenylethyl, chlorobenzyl, methylbenzyl, (methylphenyl)ethyl, (isopropylphenyl)ethyl, or hydroxybenzyl.

In one embodiment, R₃ is n-propyl, isobutyl, isopentyl, amidinoaminopropyl, tert-butoxycarbonyl-substituted amidinoaminopropyl, (methoxycarbonyl)ethyl, (tert-butoxycarbonyl)ethyl, carboxyethyl, hydroxyethyl, aminopropyl, (tert-butyldimethylsilyloxy)ethyl, ((tert-butoxycarbonyl)amino)butyl, cyclopentylmethyl, cyclohexylmethyl, cyclohexylethyl, benzyl, phenylethyl, phenylpropyl, phenylbutyl, naphthalenylmethyl, naphthalenylethyl, chlorobenzyl, methylbenzyl, (methylphenyl)ethyl, (isopropylphenyl)ethyl, (tert-butoxy)benzyl, or hydroxybenzyl.

In one embodiment, R₄ is hydrogen, methyl, ethyl, isobutyl, formyl, acetyl, 3-methylbutanoyl, 2-phenylacetyl, methoxycarbonyl, ethoxycarbonyl, 2-methylpropyloxycarbonyl, tert-butoxycarbonyl, benzoyl, benzyl, benzyloxycarbonyl, aminocarbonyl, N-benzylaminocarbonyl, propylcarbamoyl, N-isobutylaminocarbonyl, or N-benzylaminocarbonyl.

In some embodiments, the compound of the present disclosure can be exemplified as a compound represented by formula IF:

or an enantiomer thereof, or a salt thereof, or a solvate thereof, wherein

R₁, R₂, and R₃ are each independently optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted arylalkyl, optionally substituted heteroarylalkyl, optionally substituted cycloalkylalkyl, or optionally substituted heterocycloalkylalkyl, and

R₄ is hydrogen, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted arylalkyl, optionally substituted heteroarylalkyl, optionally substituted cycloalkylalkyl, optionally substituted heterocycloalkylalkyl, optionally substituted alkylcarbonyl, optionally substituted alkoxycarbonyl, optionally substituted arylcarbonyl, optionally substituted heteroarylcarbonyl, or optionally substituted carbamoyl.

In one embodiment, R₁, R₂, and R₃ are each independently optionally substituted alkyl, optionally substituted arylalkyl, optionally substituted heteroarylalkyl, or optionally substituted cycloalkylalkyl.

In one embodiment, R₁, R₂, and R₃ are each independently optionally substituted C_1-6 alkyl, optionally substituted C_6-10 aryl C_1-6 alkyl, optionally substituted 5- to 10-membered heteroaryl C_1-6 alkyl, or optionally substituted C_3-6 cycloalkyl C_1-6 alkyl.

In one embodiment, R₁, R₂, and R₃ are each independently optionally substituted alkyl, optionally substituted arylalkyl, optionally substituted heteroarylalkyl, or optionally substituted cycloalkylalkyl, and R₄ is hydrogen, optionally substituted alkyl, optionally substituted alkylcarbonyl, optionally substituted arylcarbonyl, optionally substituted alkoxycarbonyl, or optionally substituted alkylcarbamoyl.

In one embodiment, R₁, R₂, and R₃ are each independently C_1-6 alkyl, hydroxy-substituted C_1-6 alkyl, carbamoyl-substituted C_1-6 alkyl, amino-substituted C_1-6 alkyl, amidinoamino-substituted C_1-6 alkyl, carboxy-substituted C_1-6 alkyl, C_6-10 aryl C_1-6 alkyl, C_1-4 alkoxycarbonyl-substituted 5- to 10-membered heteroaryl C_1-6 alkyl, C_1-4 alkyl-substituted C_6-10 aryl C_1-6 alkyl, hydroxy-substituted C_6-10 aryl C_1-6 alkyl, halogen-substituted C_6-10 aryl C_1-6 alkyl, C_1-4 alkoxy-substituted C_6-10 aryl C_1-6 alkyl, (optionally substituted amino)-C_6-10 aryl C_1-6 alkyl, C_1-4 alkoxycarbonyl-substituted C_1-6 alkyl, C_1-4 alkoxycarbonylamino-substituted C_1-6 alkyl, 5- to 6-membered heterocycloalkyl-substituted C_1-6alkyl, or C_3-6 cycloalkyl C_1-6 alkyl.

In one embodiment, R₁, R₂, and R₃ are each independently C_1-6 alkyl, hydroxy-substituted C_1-6 alkyl, carbamoyl-substituted C_1-6 alkyl, amino-substituted C_1-6 alkyl, amidinoamino-substituted C_1-6 alkyl, carboxy-substituted C_1-6 alkyl, C_6-10 aryl C_1-6 alkyl, C_1-4 alkoxycarbonyl-substituted 5- to 10-membered heteroaryl C_1-6 alkyl, C_1-4 alkyl-substituted C_6-10 aryl C_1-6 alkyl, hydroxy-substituted C_6-10 aryl C_1-6 alkyl, halogen-substituted C_6-10 aryl C_1-6 alkyl, C_1-4 alkoxy-substituted C_6-10 aryl C_1-6 alkyl, (optionally substituted amino)-C_6-10 aryl C_1-6 alkyl, C_1-4 alkoxycarbonyl-substituted C_1-6 alkyl, C_1-4 alkoxycarbonylamino-substituted C_1-6 alkyl, 5- to 6-membered heterocycloalkyl-substituted C_1-6 alkyl, or C_3-6 cycloalkyl C_1-6 alkyl.

In one embodiment, R₁, R₂, and R₃ are each independently alkyl or optionally substituted arylalkyl.

In one embodiment, R₁, R₂, and R₃ are each independently C_1-6 alkyl or optionally substituted C_6-10 aryl C_1-6 alkyl.

In one embodiment, R₁, R₂, and R₃ are each independently C_1-6 alkyl, C_6-10 aryl C_1-6 alkyl, C_1-4 alkyl-substituted C_6-10 aryl C_1-6 alkyl, halogen-substituted C_6-10 aryl C_1-6 alkyl, C_1-4 alkoxy-substituted C_6-10 aryl C_1-6 alkyl, or (optionally substituted amino)-C_6-10 aryl C_1-6 alkyl.

In one embodiment, R₁, R₂, and R₃ are each independently C_1-6 alkyl, C_6-10 aryl C_1-6 alkyl, C_1-4 alkyl-substituted C_6-10 aryl C_1-6 alkyl, chloro-substituted C_6-10 aryl C_1-6 alkyl, C_1-4 alkoxy-substituted C_6-10 aryl C_1-6 alkyl, or (optionally substituted amino)-C_6-10 aryl C_1-6 alkyl.

In one embodiment, R₁ is C_1-6 alkyl or C₆ aryl C_1-4 alkyl, R₂ is C_1-6 alkyl or C_1-4 alkyl-substituted benzyl, and R₃ is C_1-6 alkyl or C₆ aryl C_1-4 alkyl.

In one embodiment, R₁ and R₃ are each independently alkyl or optionally substituted benzyl, and R₂ is optionally substituted benzyl.

In one embodiment, R₁ and R₃ are each independently C_1-6 alkyl, benzyl, C_1-4 alkyl-substituted benzyl, chloro-substituted benzyl, C_1-4 alkoxy-substituted benzyl, or amino-substituted benzyl, and R₂ is benzyl or chloro-substituted benzyl.

In one embodiment, R₁ and R₃ are each independently isobutyl, isopentyl, 4-(dimethylamino)benzyl, 4-methylbenzyl, 4-methoxybenzyl, 3-chlorobenzyl, 4-chlorobenzyl, or 3,4-dichlorobenzyl, and R₂ is benzyl, 3-chlorobenzyl, or 3,4-dichlorobenzyl.

In one embodiment, R₁ is isobutyl, benzyl, 4-(dimethylamino)benzyl, 4-methylbenzyl, 4-tert-butylbenzyl, 4-methoxybenzyl, 3-chlorobenzyl, 4-chlorobenzyl, or 3,4-dichlorobenzyl, R₂ is isobutyl, benzyl, naphthalen-1-ylmethyl, 4-methylbenzyl, 4-chlorobenzyl, or 3,4-dichlorobenzyl, and R₃ is isobutyl, isopentyl, or benzyl.

In one embodiment, R₁ is C_1-6 alkyl, hydroxy-substituted C_1-4 alkyl, carbamoyl-substituted C_1-4 alkyl, amino-substituted C_1-6 alkyl, amidinoamino-substituted C_1-4 alkyl, carboxy-substituted C_1-4 alkyl, C_1-4 alkoxycarbonyl-substituted C_1-4 alkyl, C_6-10 aryl C_1-4 alkyl, hydroxy-substituted C_6-10 aryl C_1-4 alkyl, C_1-4 alkoxy-substituted C_6-10 aryl C_1-4 alkyl, halo-substituted C_6-10 aryl C_1-4 alkyl, or C_5-6 cycloalkyl C_1-4 alkyl.

In one embodiment, R₁ is methyl, isopropyl, isobutyl, isopentyl, n-hexyl, 3-amino-3-oxopropyl, 3-(tert-butoxy)-3-oxopropyl, benzyl, naphthalen-1-ylmethyl, 2-carboxyethyl, carbamoylmethyl, 3-(amidinoamino)propyl, 4-fluorobenzyl, 4-hydroxybenzyl, 4-(tert-butoxy)benzyl, 3,4-dichlorobenzyl, naphthalen-1-ylmethyl, phenethyl, hydroxymethyl, 2-hydroxyethyl, or cyclohexylmethyl.

In one embodiment, R₁ is methyl, isopropyl, isobutyl, isopentyl, n-hexyl, 2-hydroxyethyl, carbamoylmethyl, 3-amino-3-oxopropyl, 3-(amidinoamino)propyl, 2-carboxyethyl, benzyl, phenethyl, naphthalen-1-ylmethyl, 4-hydroxybenzyl, 4-fluorobenzyl, 3,4-dichlorobenzyl, 4-(tert-butoxy)benzyl, 3-(tert-butoxy)-3-oxopropyl, hydroxymethyl, cyclohexylmethyl, or

In one embodiment, R₁ is methyl, isobutyl, isopentyl, 3-(tert-butoxy)-3-oxopropyl, benzyl, naphthalen-1-ylmethyl, 4-hydroxybenzyl, 4-(tert-butoxy)benzyl, 3,4-dichlorobenzyl, or cyclohexylmethyl.

In one embodiment, R₁ is isopropyl, isobutyl, isopentyl, n-hexyl, cyclohexylmethyl, benzyl, phenethyl, naphthalen-1-ylmethyl, 4-hydroxybenzyl, 4-fluorobenzyl, 2-carboxyethyl, carbamoylmethyl, carbamoylethyl, 3-(amidinoamino)propyl, hydroxymethyl, or hydroxyethyl.

In one embodiment, R₁ is isobutyl, isopentyl, cyclohexylmethyl, benzyl, phenethyl, naphthalen-1-ylmethyl, 4-hydroxybenzyl, 4-fluorobenzyl, 2-carboxyethyl, carbamoylmethyl, 3-(amidinoamino)propyl, or hydroxyethyl.

In one embodiment, R₁ is isobutyl, benzyl, 4-hydroxybenzyl, 2-carboxyethyl, 3-(amidinoamino)propyl, or naphthalen-1-ylmethyl.

In one embodiment, R₁ is isobutyl, 3-(amidinoamino)propyl, 2-carboxyethyl, benzyl, naphthalen-1-ylmethyl, 4-hydroxybenzyl, 4-(tert-butoxy)benzyl, 3-(tert-butoxy)-3-oxopropyl, or

In one embodiment, R₁ is isobutyl, 3-hydroxypropyl, 3-amino-3-oxopropyl, 6-aminohexyl, 2-carboxyethyl, benzyl, naphthalen-1-ylmethyl, 4-hydroxybenzyl, or cyclohexylmethyl.

In one embodiment, R₂ is C_1-4 alkyl, hydroxy-substituted C_1-4 alkyl, carbamoyl-substituted C_1-4 alkyl, amino-substituted C_1-4 alkyl, amidinoamino-substituted C_1-4 alkyl, carboxy-substituted C_1-4 alkyl, C_6-10 aryl C_1-4 alkyl, C_1-4 alkoxycarbonyl-substituted 5- to 10-membered heteroaryl C_1-4 alkyl, C_1-4 alkyl-substituted C_6-10 aryl C_1-4 alkyl, hydroxy-substituted C_6-10 aryl C_1-4 alkyl, halogen-substituted C_6-10 aryl C_1-4 alkyl, C_1-4 alkoxy-substituted C_6-10 aryl C_1-4 alkyl, C_1-4 alkoxycarbonyl-substituted C_1-4 alkyl, C_1-4 alkoxycarbonylamino-substituted C_1-4 alkyl, 5- to 6-membered heterocycloalkyl-substituted C_1-4 alkyl, or C_5-6 cycloalkyl C_1-4 alkyl.

In one embodiment, R₂ is naphthalen-1-ylmethyl or optionally substituted benzyl.

In one embodiment, R₂ is isopropyl, 1-methylpropyl, isobutyl, isopentyl, n-hexyl, hydroxymethyl, 2-hydroxyethyl, carbamoylmethyl, 3-amino-3-oxopropyl, 3-(amidinoamino)propyl, 4-aminobutyl, 2-carboxyethyl, benzyl, phenethyl, naphthalen-1-ylmethyl, 2-(naphthalen-1-yl)ethyl, 2-(1-(tert-butoxycarbonyl)-1H-indol-3-yl)ethyl, 3-methylbenzyl, 4-methylbenzyl, 4-hydroxybenzyl, 4-fluorobenzyl, 3-chlorobenzyl, 4-chlorobenzyl, 3,4-dichlorobenzyl, 4-(tert-butoxy)benzyl, 2-(tert-butoxy)-2-oxoethyl, 4-((tert-butoxycarbonyl)amino)butyl, (tetrahydro-2H-pyran-2-yl)methyl, or cyclohexylmethyl.

In one embodiment, R₂ is isopropyl, 1-methylpropyl, isobutyl, isopentyl, n-hexyl, hydroxymethyl, 2-hydroxyethyl, carbamoylmethyl, 3-amino-3-oxopropyl, 4-aminobutyl, 3-(amidinoamino)propyl, 2-carboxyethyl, benzyl, phenethyl, naphthalen-1-ylmethyl, 2-(naphthalen-1-yl)ethyl, 2-(1-(tert-butoxycarbonyl)-1H-indol-3-yl)ethyl, 3-methylbenzyl, 4-methylbenzyl, 4-hydroxybenzyl, 4-fluorobenzyl, 3-chlorobenzyl, 4-chlorobenzyl, 3,4-dichlorobenzyl, 4-(tert-butoxy)benzyl, 2-(tert-butoxy)-2-oxoethyl, 3-(tert-butoxy)-3-oxopropyl, 4-((tert-butoxycarbonyl)amino)butyl, (tetrahydro-2H-pyran-2-yl)methyl, cyclohexylmethyl, or

In one embodiment, R₂ is isobutyl, 2-hydroxyethyl, 3-amino-3-oxopropyl, 4-aminobutyl, 2-carboxyethyl, benzyl, phenethyl, naphthalen-1-ylmethyl, 2-(naphthalen-1-yl)ethyl, 2-(1-(tert-butoxycarbonyl)-1H-indol-3-yl)ethyl, 3-methylbenzyl, 4-methylbenzyl, 4-hydroxybenzyl, 3-chlorobenzyl, 4-chlorobenzyl, 3,4-dichlorobenzyl, 4-(tert-butoxy)benzyl, 2-(tert-butoxy)-2-oxoethyl, 4-((tert-butoxycarbonyl)amino)butyl, (tetrahydro-2H-pyran-2-yl)methyl, or cyclohexylmethyl.

In one embodiment, R₂ is 1-methylpropyl, isopropyl, isobutyl, isopentyl, n-hexyl, benzyl, 4-hydroxybenzyl, 4-fluorobenzyl, 2-carboxyethyl, carbamoylmethyl, carbamoylethyl, 3-(amidinoamino)propyl, hydroxymethyl, 2-hydroxyethyl, phenethyl, naphthalen-1-ylmethyl, or cyclohexylmethyl.

In one embodiment, R₂ is isopropyl, 1-methylpropyl, isobutyl, 3-(amidinoamino)propyl, 2-carboxyethyl, benzyl, naphthalen-1-ylmethyl, 4-hydroxybenzyl, 4-(tert-butoxy)benzyl, 3-(tert-butoxy)-3-oxopropyl, or

In one embodiment, R₂ is isopropyl, isobutyl, isopentyl, benzyl, 4-hydroxybenzyl, 4-fluorobenzyl, 2-carboxyethyl, carbamoylmethyl, 3-(amidinoamino)propyl, hydroxyethyl, phenethyl, naphthalen-1-ylmethyl, or n-hexyl.

In one embodiment, R₂ is isobutyl, 2-hydroxyethyl, 3-amino-3-oxopropyl, 4-aminobutyl, 2-carboxyethyl, benzyl, phenethyl, naphthalen-1-ylmethyl, 3-methylbenzyl, 4-methylbenzyl, 4-hydroxybenzyl, cyclohexylmethyl, or 2-(1H-indol-3-yl)ethyl.

In one embodiment, R₂ is 1-methylpropyl, isopropyl, isobutyl, benzyl, 4-hydroxybenzyl, 2-carboxyethyl, 3-(amidinoamino) propyl, or naphthalen-1-ylmethyl.

In one embodiment, R₃ is C_1-4 alkyl, hydroxy-substituted C_1-4 alkyl, carbamoyl-substituted C_1-4 alkyl, C_1-4 alkoxycarbonyl-substituted C_1-4 alkyl, amino-substituted C_1-4 alkyl, amidinoamino-substituted C_1-4 alkyl, carboxy-substituted C_1-4 alkyl, C_6-10 aryl C_1-4 alkyl, C_1-4 alkyl-substituted C_6-10 aryl C_1-4 alkyl, hydroxy-substituted C_6-10 aryl C_1-4 alkyl, or C_5-6 cycloalkyl C_1-4 alkyl.

In one embodiment, R₃ is isopropyl, isobutyl, isopentyl, n-hexyl, 3-amino-3-oxopropyl, 3-methoxy-3-oxopropyl, 4-aminobutyl, 2-carboxyethyl, carbamoylmethyl, 3-(amidinoamino)propyl, benzyl, naphthalen-1-ylmethyl, phenethyl, hydroxymethyl, 2-hydroxyethyl, 4-fluorobenzyl, 3-methylbenzyl, 4-methylbenzyl, 4-hydroxybenzyl, 4-((tert-butoxycarbonyl)amino)butyl, or cyclohexylmethyl.

In one embodiment, R₃ is isopropyl, isobutyl, isopentyl, n-hexyl, hydroxymethyl, 2-hydroxyethyl, carbamoylmethyl, 3-amino-3-oxopropyl, 4-aminobutyl, 3-(amidinoamino)propyl, 2-carboxyethyl, benzyl, phenethyl, naphthalen-1-ylmethyl, 3-methylbenzyl, 4-methylbenzyl, 4-hydroxybenzyl, 4-fluorobenzyl, 4-(tert-butoxy)benzyl, 3-methoxy-3-oxopropyl, 3-(tert-butoxy)-3-oxopropyl, 4-((tert-butoxycarbonyl)amino)butyl, cyclohexylmethyl, or

In one embodiment, R₃ is isobutyl, isopentyl, 3-amino-3-oxopropyl, 3-methoxy-3-oxopropyl, 4-aminobutyl, 2-carboxyethyl, benzyl, phenethyl, 3-methylbenzyl, 4-methylbenzyl, 4-hydroxybenzyl, 4-((tert-butoxycarbonyl)amino)butyl, or cyclohexylmethyl.

In one embodiment, R₃ is isopropyl, isobutyl, isopentyl, n-hexyl, cyclohexylmethyl, benzyl, phenethyl, naphthalen-1-ylmethyl, 4-hydroxybenzyl, 4-fluorobenzyl, 2-carboxyethyl, carbamoylmethyl, carbamoylethyl, 3-(amidinoamino)propyl, hydroxymethyl, or hydroxyethyl.

In one embodiment, R₃ is isobutyl, isopentyl, benzyl, phenethyl, 4-hydroxybenzyl, 2-carboxyethyl, carbamoylmethyl, 3-(amidinoamino)propyl, hydroxymethyl, or naphthalen-1-ylmethyl.

In one embodiment, R₃ is isobutyl, benzyl, 4-hydroxybenzyl, 2-carboxyethyl, 3-(amidinoamino)propyl, or naphthalen-1-ylmethyl.

In one embodiment, R₃ is isobutyl, 2-carboxyethyl, 3-(amidinoamino)propyl, benzyl, naphthalen-1-ylmethyl, 4-hydroxybenzyl, 4-(tert-butoxy)benzyl, 3-(tert-butoxy)-3-oxopropyl, or

In one embodiment, R₃ is isobutyl, hydroxymethyl, 3-amino-3-oxopropyl, 4-aminobutyl, 2-carboxyethyl, benzyl, 2-naphthylmethyl, 4-hydroxybenzyl, or cyclohexylmethyl.

In one embodiment, R₁ is C_1-6 alkyl or C_6-10 aryl C_1-6 alkyl, and R₂ and R₃ are each independently C_1-6 alkyl or optionally substituted C_6-10 aryl C_1-6 alkyl.

In one embodiment, R₁ is isobutyl, isopentyl, or benzyl, R₂ is isobutyl, benzyl, phenethyl, 3-methylbenzyl, 4-methylbenzyl, or 3,4-dichlorobenzyl, and R₃ is isobutyl, benzyl, phenethyl, 3-methylbenzyl, or 4-methylbenzyl.

In one embodiment, R₁ is isobutyl, R₂ is benzyl, and R₃ is benzyl.

In one embodiment, R₁ is benzyl, R₂ is benzyl, and R₃ is isobutyl.

In one embodiment, R₁ is isobutyl, R₂ is benzyl, and R₃ is 3-methylbenzyl.

In one embodiment, R₁ is benzyl, R₂ is 3,4-dichlorobenzyl, and R₃ is isobutyl.

In one embodiment, R₁ is isobutyl, R₂ is 4-methylbenzyl, and R₃ is benzyl.

In one embodiment, R₁ is benzyl, R₂ is isobutyl, and R₃ is isobutyl.

In one embodiment, R₄ is hydrogen, optionally substituted alkyl, optionally substituted alkylcarbonyl, optionally substituted arylcarbonyl, or optionally substituted alkoxycarbonyl.

In one embodiment, R₄ is hydrogen, optionally substituted C_1-6 alkyl, optionally substituted C_1-6 alkylcarbonyl, optionally substituted C_6-10 arylcarbonyl, optionally substituted C_1-6 alkoxycarbonyl, or optionally substituted C_1-6 alkylcarbamoyl.

In one embodiment, R₄ is hydrogen, optionally substituted C_1-6 alkyl, optionally substituted C_1-6 alkylcarbonyl, optionally substituted C_6-10 arylcarbonyl, or optionally substituted C_1-6 alkoxycarbonyl.

In one embodiment, R₄ is hydrogen, C_1-6 alkyl, C_1-6 alkylcarbonyl, C_6-10 arylcarbonyl, C_1-6 alkoxycarbonyl, or C₁-6 alkylcarbamoyl.

In one embodiment, R₄ is hydrogen, C_1-6 alkyl, C_1-6 alkylcarbonyl, C_6-10 arylcarbonyl, or C_1-6 alkoxycarbonyl.

In one embodiment, R₄ is hydrogen, C_1-4 alkyl, C_1-4 alkylcarbonyl, C₆ arylcarbonyl, C_1-4 alkoxycarbonyl, or C_1-4 alkylcarbamoyl.

In one embodiment, R₄ is hydrogen, C_1-4 alkyl, C_1-4 alkylcarbonyl, C₆ arylcarbonyl, or C_1-4 alkoxycarbonyl.

In one embodiment, R₄ is hydrogen or alkyl.

In one embodiment, R₄ is hydrogen or C_1-6 alkyl.

In one embodiment, R₄ is hydrogen, methyl, ethyl, acetyl, benzoyl, methoxycarbonyl, tert-butoxycarbonyl, or propylcarbamoyl.

In one embodiment, R₄ is hydrogen, methyl, ethyl, acetyl, benzoyl, methoxycarbonyl, or tert-butoxycarbonyl.

In one embodiment, R₄ is hydrogen or ethyl. In a preferred embodiment, R₄ is hydrogen.

A hydroxyl group, amino group, and/or carboxyl group in R₁, R₂, R₃, and/or R₄, when present, can be independently protected with a protecting group. Such a compound is also within the scope of the present disclosure.

In some embodiments, the compound of the present disclosure can be exemplified as a compound represented by formula IB:

or an enantiomer thereof, or a salt thereof, or a solvate thereof. R₁, R₂, and R₃ in formula IB are defined the same as those in formula IF.

In some embodiments, the compound of the present disclosure can be exemplified as a compound represented by formula IIF:

or an enantiomer thereof, or a salt thereof, or a solvate thereof. R₁, R₂, and R₃ in formula IIF are defined the same as those in formula IF.

In some embodiments, the compound of the present disclosure can be exemplified as a compound represented by formula IIB:

or an enantiomer thereof, or a salt thereof, or a solvate thereof. R₁, R₂, and R₃ in formula IIB are defined the same as those in formula IF.

The compound of the present disclosure is further described hereinafter.

While the compound of the present disclosure can have enantiomers and stereoisomers such as tautomers and geometric isomers depending on the type of substituent, they are also encompassed by the present disclosure. Specifically, if there is one or more asymmetric carbon atoms in the compound of the present disclosure, there is a diastereomer or enantiomer, and a mixture of such a diastereomer and enantiomer, and isolated diastereomers and enantiomers are also encompassed by the compound of the present disclosure.

The present disclosure is also intended to encompass various hydrates, solvates, and crystalline polymorphisms.

Furthermore, the compound of the present disclosure can be substituted with an isotope (e.g., ²H (or D), ³H (or T), ¹¹C, ¹³C, ¹⁴C, ¹³N, ¹⁵N, ¹⁵O, ³⁵S, ¹⁸F, ¹²⁵I, or the like). These compounds are also encompassed by the compound of the present disclosure.

Furthermore, the scope of the present disclosure encompasses prodrugs of the compound of the present disclosure. In the present disclosure, a prodrug refers to a derivative that yields a compound represented by formula IF, IB, IIF, IIB, XXIF, XXIB, XXIIF, or XXIIB, or a related structural formula by acid hydrolysis or enzymatic degradation in the body. For example, if a compound represented by formula IF, IB, IIF, IIB, XXIF, XXIB, XXIIF, or XXIIB, or a related structural formula thereof has a functional group such as a hydroxyl group, amino group, or carboxyl group or other substituents, these groups can be modified by a conventional method to manufacture a prodrug. Prodrug technologies are described in, for example, C. G. Wermuth, “The Practice of Medicinal Chemistry”, 4^th Ed., Academic Press, (2015), Chapter 28.

Examples for compounds having a carboxy group include compound whose carboxyl group is modified to be an alkoxycarbonyl group, alkylthiocarbonyl group, or alkylaminocarbonyl group.

Examples of compounds having an amino group include compounds whose amino group is substituted with an alkanoyl group to be an alkanoylamino group, compounds substituted with an alkoxycarbonyl group to be an alkoxycarbonylamino group, compounds modified to have an alkanoyloxymethylamino group, and compounds modified to have hydroxylamine.

Examples for compounds having a hydroxyl group include compounds whose hydroxyl group is substituted with an alkanoyl group to be an alkanoyloxy group, phosphate ester, or alkanoyloxymethyloxy group.

Examples of the alkyl moiety of a group used for preparing a prodrug thereof include the alkyl group. The alkyl group is optionally substituted with, for example, an alkoxy group or the like. Preferred examples thereof include the following.

For compounds whose carboxyl group is modified to be an alkoxycarbonyl group, examples thereof include alkoxycarbonyl such as methoxycarbonyl and ethoxycarbony, and alkoxycarbonyl substituted with an alkoxy group such as methoxymethoxycarbonyl, ethoxymethoxycarbonyl, 2-methoxyethoxycarbonyl, and 2-methoxyethoxymethoxycarbonyl, or privaloyloxymethoxycarbonyl.

As used herein, “pharmaceutically acceptable salt” refers to an acid addition salt or base addition salt which is pharmaceutically acceptable for use. Specific examples of “pharmaceutically acceptable salts” include, but are not limited to, acid addition salts such as acetate, propionate, butyrate, formate, trifluoroacetate, maleate, fumarate, tartrate, citrate, stearate, succinate, ethylsuccinate, malonate, lactobionate, gluconate, glucoheptonate, benzoate, methanesulfonate, benzenesulfonate, para-toluenesulfonate (tosylate), laurylsulfate, malate, ascorbate, mandelate, saccharinate, xinafoate, pamoate, cinnamate, adipate, cysteine salt, N-acetyl cysteine salt, hydrochloride, hydrobromide, phosphate, sulfate, hydroiodide, nicotinate, oxalate, picrate, thiocyanate, undecanoate, acrylic acid polymer salt, and carboxyvinyl polymer; inorganic base addition salts such as lithium salt, sodium salt, potassium salt, and calcium salt; organic base addition salts such as morpholine and piperidine; amino acid addition salts such as aspartic acid and glutamic acid; and the like.

In one embodiment, the compound of the present disclosure can be administered directly, or as a formulation, medicament, or a pharmaceutical composition using a suitable dosage form, by oral or parenteral administration. Specific examples of such dosage forms include, but are not limited to, tablets, capsules, powdered agents, granules, liquid agents, suspension, injection agents, patch-on agents, poultice, and the like. These formulations can be manufactured by a known method using an additive that is commonly used as a pharmaceutical additive.

As these additives, an excipient, disintegrant, binding agent, fluidizer, lubricant, coating agent, solubilizing agent, solubilizing promotor, thickener, dispersant, stabilizer, sweetener, flavoring agent, or the like can be used depending on the objective. Specific examples of these additives include, but are not limited to, lactose, mannitol, crystalline cellulose, low-substituted hydroxypropyl cellulose, corn starch, partially pregelatinized starch, carmellose calcium, croscarmellose sodium, hydroxypropyl cellulose, hydroxypropyl methylcellulose, polyvinyl alcohol, magnesium stearate, sodium stearyl fumarate, polyethylene glycol, propylene glycol, titanium oxide, talc, and the like.

The dosage of the compound of the present disclosure is appropriately selected depending on the subject targeted for administration, route of administration, disease, age of subject, body weight, and symptom. For example, the dosage is 0.01 mg as the lower limit (preferably 100 mg) and 10000 mg as the upper limit (preferably 6000 mg) per day for adults for oral administration. This amount can be administered once daily, or divided into several doses.

In one embodiment, the compound of the present disclosure is a compound with an antiviral activity for a virus in the Lyssavirus genus. The virus in the Lyssavirus genus comprises a rabies virus, Lagos bat virus, mokola virus, Duvenhage virus, European bat 1 lyssavirus, European bat 2 lyssavirus, Australian bat lyssavirus, and the like. The virus in the Lyssavirus genus preferably comprises a rabies virus.

In one embodiment, the compound of the present disclosure is a compound with the ability to suppress or kill tumor or cancer. The tumor or cancer can be any tumor or cancer such as carcinoma, lymphoma, blastoma, sarcoma, or leukemia. Tumor and cancer can be squamous cell carcinoma, lung cancer such as small cell lung cancer, non-small cell lung cancer, or pulmonary adenocarcinoma, squamous cell carcinoma of the lung, peritoneal cancer, hepatoma, esophageal cancer, gastrointestinal cancer, pancreatic cancer, glioblastoma, uterine cancer such as cervical cancer, ovarian cancer, liver cancer, hepatocellular cancer, bladder cancer, hepatocellular carcinoma, breast cancer, colon cancer, colorectal cancer, epithelial or uterine carcinoma, salivary gland carcinoma, kidney cancer, liver cancer, prostate cancer, vulvar cancer, thyroid cancer, liver carcinoma, various types of head and neck cancer, blood cancer (leukemia), prostate cancer, gastric cancer, fibrous cancer, glioma, melanoma, or the like.

The timing of dosing of the compound of the present disclosure and therapeutic agents thereof is not limited. The compound and therapeutic agent can be administered concurrently or sequentially to a subject being administered therewith. The compound of the present disclosure and therapeutic agent thereof can be formulated as a combined agent. The dosage of the therapeutic agent can be appropriately selected based on the clinically used dose. The ratio of the compound of the present disclosure and therapeutic agent thereof can be appropriately selected depending on the subject of administration, route of administration, target disease, symptom, combination, or the like.

In one embodiment of the present disclosure, the compound of the present disclosure can be combined and administered concurrently or at different times upon use of a pharmaceutical composition. Such a pharmaceutical composition is also within the scope of the present disclosure.

Such a medicament, formulation, or pharmaceutical composition can be manufactured by mixing the compound of the present disclosure and/or an addition agent (e.g., anti-rabies gamma globulin formulation, antimicrobial agent, antiviral agent (e.g., ribavirin, amantadine, or the like), sedative (e.g., ketamine, midazolam, or the like) or the like) with any suitable component, together or separately, as a combined agent, or as separate agents using any technology that is known in the art. An appropriate formulation such as a tablet, capsule, powder, granule, liquid agent, suspension, injection, patch, or poultice can be formulated by using any technology that is known in the art. If the compound of the present disclosure and/or an addition agent (e.g., anti-rabies gamma globulin formulation, antimicrobial agent, antiviral agent (e.g., ribavirin, amantadine, or the like), sedative (e.g., ketamine, midazolam, or the like) or the like) are prepared as separate agents, they can be provided as a kit of two agents. The kit can provide one of the components as a single agent, with instructions (package insert or the like) instructing to combine and administer the other component (for the compound of the present disclosure, the additional agent; for the addition agent (e.g., anti-rabies gamma globulin formulation, antimicrobial agent, antiviral agent (e.g., ribavirin, amantadine, or the like), sedative (e.g., ketamine, midazolam, or the like) or the like), the compound of the present disclosure) concurrently or at different times.

If the compound of the present disclosure is used as an active ingredient of a medicament, the compound is intended for use in not just humans, but also other animals other than humans (cat, dog, cow, horse, bat, fox, mangoose, raccoon, and the like).

(Method of Manufacturing the Compound of the Present Disclosure)

Hereinafter, the method of manufacturing the compound of the present disclosure is described with examples, but the present disclosure is not limited thereto.

The compound of the present disclosure can be manufactured by, for example, the following manufacturing methods, but are not limited to such methods. These manufacturing methods can be appropriately improved upon based on the expertise of those skilled in the art of organic synthetic chemistry. Salts of the compounds used as a raw material can be used in the following manufacturing method, as long as the reaction is not affected.

In the following manufacturing methods, even if use of a protecting group is not specifically described, a functional group other than those at the reaction point can be protected as needed and deprotected after the completion of a reaction or after a series of reations to obtain a compound of interest if one of the functional groups other than those at the reaction point is altered under the reaction condition or if it is unsuitable for post-reaction processing. Common protecting groups described in the document (Peter G. M. Wuts, “Greene's Protective Groups in Organic Synthesis”, 5^th Ed., John Wiley & Sons, Inc., Hoboken, N.J. (2014)) or the like can be used as the protecting groups used in these processes. A protecting group can be introduced or removed by a method that is commonly used in organic synthetic chemistry (e.g., method described in the aforementioned document or the like) or a method in accordance thereto.

The starting material and intermediate in the following manufacturing methods can be purchased as a commercially available product or are available by synthesis in accordance with a method described in a known document or a known method from a known compound. Salts of the starting material and intermediate can also be used, as long as the reaction is not affected.

The intermediate and compound of interest in the following manufacturing methods can also be converted into another compound encompassed by the present disclosure by appropriately converting their functional groups. A functional group can be converted in doing so by a method that is commonly used in organic synthetic chemistry (e.g., method described in R. C. Larock, “Comprehensive Organic Transformations”, 2^nd Ed., John Wiley and Sons, Inc., New York (1999) or the like) or a method in accordance therewith.

An inert solvent in the following manufacturing methods refers to a solvent that does not react with a raw material, reagent, base, acid, catalyst, ligand, or the like used in the reaction (hereinafter, also referred to as “raw material or the like used in the reaction”). A solvent used in each step can be used as an inert solvent even if the solvent reacts with the raw material or the like used in the reaction, as long as the reaction of interest proceeds to result in a compound of interest.

The overview of compound synthesis related to the present disclosure is shown below. “B” and “F” following the Roman numeral compound number indicate that a 5-membered ring comprising nitrogen is located in the “back” and “front”, respectively. In other words, a —C(═O)NH—R₂ group attached to a 5-membered ring comprising nitrogen referred to as “back”, and a —C(═O)NH—R₂ that is not attached to a 5-membered ring comprising nitrogen is referred to as “front”.

Synthesis Scheme 1

Synthesis of compound III

Compound III can be manufactured by, for example, the following manufacturing method.

(1) Route 1-1 Synthesis from Compound VII and Compound VIII

(2) Route 1-2 Synthesis from Compound VII and Compound VIII Through Protection of Amine

(3) Route 1-3 Synthesis from Compound XI and Compound XII

wherein X_L represents a leaving group in a nucleophilic substitution reaction. Examples thereof include halogen (e.g., chlorine, bromine, or iodine), sulfate esters (—OSO₃H and the like), and sulfonyl-O— groups (e.g., methanesulfonyl-O—, toluenesulfonyl-O—, and the like).(4) Route 1-4 Synthesis from Compound XI and Compound XIII

(5) Route 1-5 Synthesis from Compound VII and Compound XIV

wherein if R₁ in compound III can be expressed as —CH₂—R₁′, R₁ in compound III can be replaced with —CH₂—R₁′ to express compound III as compound III′.

In the formula, R₁ is as defined in item 1 or A1 herein, and “Protect” is a protecting group of amino group. Examples of protecting groups of an amino group include an ethoxycarbonyl group, tert-butoxycarbonyl group, acetyl group, benzoyl group, trifluoroacetyl group, benzyloxycarbonyl group, 3- or 4-chlorobenzyloxycarbonyl group, triphenylmethyl group, methanesulfonyl group, p-toluenesulfonyl group, trimethylsilyl group, benzyloxycarbonyl group, 3- or 4-chlorobenzyloxycarbonyl group, benzylsulfonyl group, benzyl group, 4-nitrobenzyl group, 4-methoxybenzyl group, methyl group, ethyl group, and the like.

A compound that is commercially available or a compound manufactured by a known method can be used as a starting raw material compound.

Synthesis Scheme 2

Synthesis of Compound V

A compound of formula V can be manufactured by, for example, the following manufacturing method.

(1) Route 2-1 Synthesis from Compound XVI and Compound XVII

wherein R₈ indicates alkoxy, aryloxy, hydroxy, or halogen. Examples thereof include an ethoxy group. This synthesis is achieved by various reactions known to those skilled in the art. If R₂ is aryl, compound V can be synthesized in accordance with the method described in C. W. Cheung, M. L. Ploeger, and X. Hu, Nature Communications 2017, 8, 14878.(2) Route 2-2 Synthesis from Compound XVIII

wherein R₂ is as defined in item 1 or A1 herein. A compound that is commercially available or a compound that is manufactured by a known method can be used as the starting compound.

Synthesis Scheme 3

Synthesis of Compound VI

A compound of formula VI can be manufactured from compound III and compound IV by, for example, the following manufacturing method.

wherein R₁ and R₃ are as defined in item 1 or A1 herein.

Synthesis Scheme 4

Compound of Formula IIF and Compound of Formula IIB-Route 1

A compound of formula IIF and compound of formula IIB can be manufactured, for example, from three components through one-pot synthesis in accordance with a known method (e.g., method described in Bioorg. Med. Chem. 23 (2015) 2629-2635, Tetrahedron 63 (2007) 6004-6014, Eur. J. Org. Chem. 2009, 2185-2189, Eur. J. Org. Chem. 2011, 2354-2359 or the like).

wherein R₁, R₂, and R₃ are as defined in item 1 or A1 herein.

Synthesis Scheme 5

Compound of formula IIF and compound of formula IIB-Route 2

A compound of formula IIF and compound of formula IIB can be manufactured, for example, from two components as described below.

wherein R₁, R₂, and R₃ are as defined in item 1 or A1 herein.

Synthesis Scheme 6

Synthesis of Compound IF and Compound IB

Step 6-1

Reduction of Imine

Compound IF (i.e., compound of formula IF) or compound

IB (i.e., compound of formula IB) can be manufactured, for example, from compound IIF (i.e., compound of formula IIF) or compound IIB (i.e., compound of formula IIB) by reduction as described below. However, R₄ therein is H.

Step 6-2

Modification of Amine of Piperidine Ring

Amine of a piperidine ring of compound IF or compound IB can be modified, for example by alkylation, amidation, or the like as follows.

Synthesis Scheme 7

Synthesis of Compound V′

A compound of formula V′ can be manufactured by, for example, the following manufacturing method.

(1) Route 7-1 Synthesis from Compound XVI and Compound XVII′

A compound of formula V′ can be manufactured under the same condition as Route 2-1 of Synthesis Scheme 2. R₈ indicates alkoxy, aryloxy, hydroxy, or halogen.

(2) Route 7-2 Synthesis from Compound XVIII′

wherein R_2A and R_2B are as defined in item 1 herein. A compound that is commercially available or a compound manufactured by a known method can be used as a starting raw material compound.

Synthesis Scheme 8

Synthesis of Compound of Formula XXIIF and Compound of Formula XXIIB-Route 1

A compound of formula XXIIF and a compound of formula XXIIB can be synthesized under the same condition as Synthesis Scheme 4.

wherein R₁, R_2A, R_2B, and R₃ are as defined in item 1 herein.

Synthesis Scheme 9

Synthesis of Compound of Formula XXIIF and Compound of Formula XXIIB-Route 2

A compound of formula XXIIF and compound of formula XXIIB can be manufactured, for example, from two components as described below.

wherein R₁, R_2A, R_2B, and R₃ are as defined in item 1 herein.

Synthesis Scheme 10

Synthesis of Compound XXIF and Compound XXIB

Step 10-1

Reduction of Imine

Under the same condition as step 6-1 of Synthesis Scheme 6, compound XXIF (i.e., compound of formula XXIF) or compound XXIB (i.e., compound of formula XXIB) can be manufactured, for example, from compound XXIIF (i.e., compound of formula XXIIF) or compound XXIIB (i.e., compound of formula XXIIB) by reduction as described below. However, R₄ therein is H.

Step 10-2

Modification of Amine of Piperidine Ring

Amine of a piperidine ring in compound XXIF or compound XXIB can be modified by, for example, alkylation, amidation, or the like as follows.

R₄ in the product of this step is a group defined herein other than H.

The intermediate and compound of interest in the manufacturing methods described above can be isolated and purified by subjecting them to a purification method that is commonly used in organic synthesis chemistry (e.g., neutralization, filtration, extraction, washing, drying, concentration, recrystallization, various chromatography, or the like). Each intermediate can also be subjected to the subsequent reaction without any particular purification.

Optically active forms of the compound of the present disclosure can be manufactured by using an optically active starting material or intermediate, or by optically resolving a racemate of the final product or intermediate. Examples of optional resolution methods include, but are not limited to, separation method using an optically active column or a separation method such as fractional crystallization method. A diastereomer of the compound of the present disclosure can be manufactured by, for example, but not limited to, a separation method such as column chromatography or fractional crystallization.

A pharmaceutically acceptable salt of a compound represented by formula IF, IB, IIF, IIB, XXIF, XXIB, XXIIF, or XXIIB, or a related structural formula can be manufactured by, for example, but not limited to, mixing a compound represented by formula IF, IB, IIF, IIB, XXIF, XXIB, XXIIF, or XXIIB, or a related structural formula with a pharmaceutically acceptable acid or base in a solvent such as water, methanol, ethanol, 2-propanol, ethyl acetate, or acetone.

As used herein, “or” is used when “at least one or more” of the listed matters in the sentence can be employed. When explicitly described herein as “within the range of two values”, the range also includes the two values themselves.

Reference literatures such as scientific literatures, patents, and patent applications cited herein are incorporated herein by reference to the same extent that the entirety of each document is specifically described.

The present disclosure has been described while showing preferred embodiments to facilitate understanding. While the present disclosure is described hereinafter based on the Examples, the above descriptions and the following Examples are provided for the sole purpose of exemplification, not limitation of the present disclosure. Thus, the scope of the present disclosure is not limited to the embodiments and Examples that are specifically described herein and is limited only by the scope of claims.

EXAMPLES

The present disclosure is specifically described based on the Examples. The scope of the present disclosure is not limited to the Examples described below.

For Thin Layer Chromatography (TLC), Merck's TLC Silica gel 60 F254 (25 glass plate, 20×20 cm) and Fuji Silysia Chemical's CHROMATOREX NH-TLC Plates (20×20 cm) were used. As the developing solvent, chloroform-methanol mixed solvent system, ethyl acetate-methanol mixed solvent system, or ethyl acetate-hexane mixed solvent system was used. Spots were checked using coloring with UV irradiation, ninhydrin, iodine, or phosphomolybdic acid (ethanol solution). An organic solvent was dried using anhydrous sodium sulfate and anhydrous magnesium sulfate. For column chromatography, Fuji Silysia Chemical's cartridge column CHROMATOREX Q-PACKS 130 (SIZE 10, 20, or 60) and DNH (SIZE 20) or Shoko Science's Purif-Pack®-EX SI50 (SIZE 20 or 60) were used in accordance with the amount of raw product to be purified. Silica gel thin layer chromatography for separation (PTLC: Preparative Thin Layer Chromatography) used Merck's PLC Silica gel 60 F254 (20×20 cm; thickness: 0.5 mm; product number: 1.05744.0001; thickness: 1 mm; product number: 1.13895.0001) and Fuji Silysia Chemical's CHROMATOREX NH-PLCO5 (20×20 cm; thickness: 0.5 mm). Synthesized compounds were identified by LC/MS (Liquid Chromatography/Mass Spectrometry). Tables 1 to 4 show the retention (t_R) and m/z value [M+1]⁺. For measurement, Shimadzu's LCMS-2020 system was used, and Chemicals Evaluation and Research Institute's L-column2 ODS, 3 μm, 3.0×50 mm was used as the analysis column. The column oven was set to 40° C., and compounds were detected by using both UV absorption (220 nm, 254 nm) and mass spectrometry. Elution condition A or B shown below was used.

Elution Condition A:

Flow rate 1.5 mL/min, mobile phase a=aqueous 0.05% (v/v) trifluoroacetic acid solution, mobile phase b=0.05% (v/v) trifluoroacetic acid containing acetonitrile; 0-0.9 minutes, linear gradient, A:B (95:5)-A:B (10:90), 0.9-2 minutes

Elution Condition B:

Flow rate 1.0 mL/min, mobile phase a=aqueous 0.05% (v/v) formic acid solution, mobile phase b=0.05% (v/v) formic acid containing acetonitril; 0-0.9 minutes, linear gradient, A:B (95:5)-A:B (10:90), 0.9-2 minutes

Elution Condition B1:

Flow rate 1.0 mL/min, mobile phase a=aqueous 0.05% (v/v) formic acid solution, mobile phase b=0.05% (v/v) formic acid containing acetonitrile; 0.1-2.0 minutes, linear gradient, A:B (95:5)-A:B (60:40), 2.0-3.0 minutes, linear gradient, A:B (60:40)-A:B (10:90), 3.0-4.0 minutes

Furthermore, LC/MS measurement used the following instrument and measurement conditions.

Measurement Condition C:

Shimadzu's LCMS-2020 system was used, and Chemicals Evaluation and Research Institute's L-column2 ODS, 3 μm, 3.0×50 mm was used as the analysis column. The column oven was set to 40° C., and the compound was detected by using both UV absorption (220 nm, 254 nm) and mass spectrometry.

Elution condition: flow rate of 1.5 mL/min, mobile phase a=aqueous 0.05% (v/v) trifluoroacetic acid solution, mobile phase b=0.05% (v/v) trifluoroacetic acid containing acetonitrile

TABLE A1
           Ratio of mobile
Time (min) phase b (%)
0.0        5
0.01-0..89 5-90 linear gradient
0.9        90
2.00       90

Measurement Condition D:

The same apparatus as measurement condition C was used.

Elution condition: flow rate of 1.5 mL/min, mobile phase a=aqueous 0.05% (v/v) trifluoroacetic acid solution, mobile phase b=0.05% (v/v) trifluoroacetic acid containing acetonitrile

TABLE A2
           Ratio of mobile
Time (min) phase b (%)
0.0        0
0.5        0
0.51-1.39  0-70 linear gradient
1.4        70
1.5        90
2.00       90

Measurement Condition E:

The same apparatus as measurement condition C was used.

Elution condition: flow rate of 1.5 mL/min, mobile phase a=5 mM NH₄HCO₃ containing water/acetonitrile=900/100 (v/v), mobile phase b=5 mM NH₄HCO₃ containing water/acetonitrile=100/900 (v/v)

TABLE A3
           Ratio of mobile
Time (min) phase b (%)
0.0        0
0.5        0
0.51-1.39  0-70 linear gradient
1.4        70
1.5        90
2.00       90

Measurement Condition F:

Waters' Alliance 2695 Separation Module system was used, and YMC's YMC-Triart C18, 5 μm, 3.0×50 mm was used as the analysis column. The column oven was set to 30° C., and the compound was detected using both UV absorption (220 nm) and mass spectrometry.

Elution condition: flow rate of 1.27 mL/min, mobile phase a=aqueous 0.05% (v/v) trifluoroacetic acid solution, mobile phase b=0.05% (v/v) trifluoroacetic acid containing acetonitrile

TABLE A4
           Ratio of mobile
Time (min) phase b (%)
0.0        10
1.0        10
1.0-1.5    10-30 gradient
1.5-4.5    30-70 gradient
4.5-5.0    70-90 gradient
6.0        90

Measurement Condition G:

The same apparatus as measurement condition F was used.

Elution condition: flow rate of 1.27 mL/min, mobile phase a=aqueous 0.05% (v/v) trifluoroacetic acid solution, mobile phase b=0.05% (v/v) trifluoroacetic acid containing acetonitrile

TABLE A5
           Ratio of mobile
Time (min) phase b (%)
0.0        1
1.0        1
1.0-4.0    1-40 gradient
4.0-5.0    40-90 gradient
6.0        90

Measurement Condition H:

Waters' 2767 system was used, and YMC's YMC-Triart C18, 5 μm, 4.6×50 mm was used as the analysis column. The column oven was set to 25° C., and compound was detected using UV absorption (220 nm), mass spectrometry, and ELS (Evaporative Light Scattering).

Elution condition: flow rate of 2 mL/min, mobile phase a=aqueous 0.1% (v/v) trifluoroacetic acid solution, mobile phase b=0.1% (v/v) trifluoroacetic acid containing acetonitrile

TABLE A6
           Ratio of mobile
Time (min) phase b (%)
0.0        5
0.5        5
0.5-3.0    5-95 gradient
5.0        95

Measurement Condition I:

Waters' H-class/SQD2 system was used, and Waters' ACQUITY UPLC BEH C18 1.7 μm, 2.1×50 mm was used as the analysis column. A compound was detected using both UV absorption (220 nm) and mass spectrometry.

Elution condition: flow rate of 0.6 mL/min, mobile phase a=aqueous 0.1% (v/v) formic acid solution, mobile phase b=0.1% (v/v) formic acid containing acetonitrile

TABLE A7
           Ratio of mobile
Time (min) phase b (%)
0.0        2
2.0-2.6    2-100
2.6-3.0    100

Measurement Condition J:

The same apparatus as measurement condition F was used.

Elution condition: flow rate of 1.27 mL/min, mobile phase a=aqueous 0.05% (v/v) trifluoroacetic acid solution, mobile phase b=0.05% (v/v) trifluoroacetic acid containing acetonitrile

TABLE A8
           Ratio of mobile
Time (min) phase b (%)
0.0        10
1.0        10
1.0-2.0    10-60 gradient
2.0-5.0    60-99 gradient
5.0-6.0    99

Nuclear Magnetic Resonance (NMR) was measured using Bruker AVANCE III 400 MHz Spectrometer (resonant frequency: ¹H: 400 MHz, ¹³C: 100 MHz) and Bruker AVANCE III 300 MHz Spectrometer (resonant frequency: ¹H: 300 MHz, ¹³C: 75 MHz). For the measurement of X-ray crystal structure, Rigaku Corporation's single crystal X-ray diffractometer XtaLAB P200 was used. Cu—K_α rays monochromed with a multilayer mirror were used as the source. The structure was determined by a direct method using SIR2008. The structure was refined by the full-matrix least-squares method with respect to F2 using SHELEX-2014/7. Non-hydrogen atoms were refined with anisotropic atomic displacement parameters.

The abbreviations described above and the following abbreviations are also used in the Examples to simplify the description.

s: singletd: doublett: tripletm: multipletdd: double doubletJ: coupling constant

Hz: Hertz

δ: chemical shiftmin: minuteRT and tR: retentionCDCl₃: deuterated chloroformMe: methylEt: ethylPr: propyli-Pr: isopropyli-Bu: isobutyls-Bu and sec-Bu: secondary butyl^tBu, tBu and tert-Bu: tertiary butyli-Pnt: isopentylHxy: n-hexylAc: acetylBz: benzoylBnzl: benzyl3-Me-Bnzl: 3-methylbenzyl4-Me-Bnzl: 4-methylbenzyl3-MeO-Bnzl: 3-methoxybenzyl4-MeO-Bnzl: 4-methoxybenzyl4-OH-Bnzl: 4-hydroxybenzyl3-F-Bnzl: 3-fluorobenzyl4-F-Bnzl: 4-fluorobenzyl3-Cl-Bnzl: 3-chlorobenzyl4-Cl-Bnzl: 4-chlorobenzyl3,4-Cl₂-Bnzl: 3,4-dichlorobenzyl4-tBuO-Bnzl: 4-(tert-butoxy)benzyl4-Nt-Bnzl: 4-nitrobenzylCbx-E and 2-Cbx-Et: 2-carboxyethylCbm-M: 2-amino-2-oxoethyl or carbamoylmethylCbm-E: 3-amino-3-oxopropyl or 2-carbamoylethyltBOC-E: 2-(tert-butoxycarbonyl)ethyl or 3-(tert-butoxy)-3-oxopropylGun-Pr and 3-Gun-Pr: 3-guanidinopropylHdr-M: hydroxymethylHdr-E and 2-OH-Et: 2-hydroxyethyltBuO-E and 2-OtBu-Et: 2-(tert-butoxy)ethylPh-Et: 2-phenylethylPh-Pr: 3-phenylpropylPh-Bu: 4-phenylbutylNp-M and 1-Npm: naphthalen-1-ylmethyl2-Npm: naphthalen-2-ylmethylNp-E: 2-(naphthalen-1-yl)ethylCpm: cyclopentylmethylChm: cyclohexylmethylBoc and tBOC and tBOC: tert-butoxycarbonylTBSO-E and 2-0TBS-Et: 2-(tert-butyldimethylsilyloxy)ethyl

Example 1: Synthesis of Compound

Synthesis Example for Compound V

Synthesis of N-benzyl-1,2,4-triazine-3-carboxamide

Ethyl 1,2,4-triazine-3-carboxylate (1.53 g, 10.0 mmol) was dissolved in methanol (10.0 mL), and phenylmethaneamine (1.18 g, 11.0 mmol) was added. The mixture was then stirred for 3 hours at 50° C. Methanol was evaporated under reduced pressure, and the resulting residue was purified by column chromatography (column: Purif-Pack Si50, Size 60, eluent: ethyl acetate-methanol (gradient from 0% to 15%)). A fraction of a compound of interest was concentrated. The eluted crystal was filtered out to obtain the aforementioned compound (1.25 g, yield: 58%).

Under the same conditions as this reaction, the following compounds were synthesized. N-(naphthalen-1-ylmethyl)-1,2,4-triazine-3-carboxamide tert-butyl (4-(1,2,4-triazine-3-carboxamide)butyl)carbamate N-(4-(tert-butoxy)benzyl)-1,2,4-triazine-3-carboxamide N-isobutyl-1,2,4-triazine-3-carboxamide N-(4-methylbenzyl)-1,2,4-triazine-3-carboxamide N-phenethyl-1,2,4-triazine-3-carboxamide N-(3-methylbenzyl)-1,2,4-triazine-3-carboxamide N-(3-chlorobenzyl)-1,2,4-triazine-3-carboxamide N-(4-chlorobenzyl)-1,2,4-triazine-3-carboxamide N-(2-(naphthalen-1-yl)ethyl)-1,2,4-triazine-3-carboxamide tert-butyl 3-(2-(1,2,4-triazine-3-carboxamide)ethyl)-1H-indol-1-carboxylate N-(3,4-dichlorobenzyl)-1,2,4-triazine-3-carboxamide

Synthesis Example for Compound V

Synthesis of N-(2-hydroxyethyl)-1,2,4-triazine-3-carboxamide

Ethyl 1,2,4-triazine-3-carboxylate (76.5 mg, 0.500 mmol) was dissolved in ethanol (1.00 mL), and 2-aminoethanol (24.2 mg, 0.525 mmol) was added. The mixture was then stirred for 3 hours at room temperature. Methanol was evaporated under reduced pressure, and the resulting residue was purified by column chromatography (column: Purif-Pack Si50, Size 20, eluent: ethyl acetate-methanol (gradient from 0% to 30%)). A fraction of a compound of interest was concentrated to obtain the aforementioned compound (44.8 mg, yield: 53%).

Under the same conditions as this reaction, the following compound was synthesized. N-(cyclohexylmethyl)-1,2,4-triazine-3-carboxamide

Synthesis Example for Compound V

Synthesis of Tert-Butyl 3-(1,2,4-triazine-3-carboxamide)propanoate

Triethylamine (0.245 mL, 1.75 mmol) was added to an ethanol (2.00 mL) solution of tert-butyl 3-aminopropanoate.HCl (272 mg, 1.50 mmol). A methanol (1.00 mL) suspension of ethyl 1,2,4-triazine-3-carboxylate (76.0 mg, 0.500 mmol) was added thereto. The mixture was stirred for 4 hours at room temperature. Ethanol was evaporated under reduced pressure. The residue was dissolved in ethyl acetate. The organic layer was washed with 10% citric acid water and 5% bicarbonate aqueous solution and dried with anhydrous sodium sulfate. The solvent was evaporated. The resulting residue was purified by column chromatography (column: Purif-Pack Si50, Size 20, eluent: hexane-ethyl acetate (gradient from 60% to 100%)) to obtain the aforementioned compound (65.7 mg, yield: 52%).

Synthesis Example for Compound XV

Synthesis of 4-methylpentanal

A methylene chloride (40.0 mL) solution of acetic acid (0.0994 mL, 1.30 mmol) and 4-methylpentan-1-ol (1.49 mL, 11.8 mmol) was slowly added dropwise into a methylene chloride (45.0 mL) solution of 1,1,1-triacetoxy-1,1-dihydro-1,2-benziodoxol-3-(1H)-one (Dess-Martin periodinane) (5.25 g, 12.4 mmol) at room temperature. After completion of the addition, the mixture was stirred for another hour, and then diethyl ether (280 mL) was added. An aqueous 1.30M sodium hydroxide solution (200 mL) was added to the organic layer and stirred for 10 minutes at room temperature. The organic layer was washed with an aqueous 1.30M sodium hydroxide solution (90.0 mL) and (50.0 mL). After drying with anhydrous sodium magnesium sulfate, the solvent was carefully evaporated to obtain the aforementioned compound (1.01 g, 86%).

Under the same conditions as this reaction, the following compound was synthesized. 5-methylhexanal

Synthesis Example for Compound III

Synthesis of N-benzylprop-2-en-1-amine

(Bromomethyl)benzene (0.992 mL, 8.35 mmol) was gradually added dropwise to a suspension of anhydrous potassium carbonate (1.39 g, 10.0 mmol) and prop-2-en-1-amine (7.53 mL, 100 mmol) and then stirred for 3 hours at room temperature. The solids were filtered and washed with methylene chloride. The combined organic layer was evaporated under reduced pressure. The resulting residue was purified with CHROMATOREX Q-PACK SI30 SIZE 20 (hexane: ethyl acetate=50%:50% to 0%:100%) to obtain the aforementioned compound (934 mg, yield: 76%).

Under the same conditions as this reaction, the following compound was synthesized. N-(3,4-dichlorobenzyl)prop-2-en-1-amine

Synthesis Example for Compound III

Synthesis of N-(cyclohexylmethyl)prop-2-en-1-amine

Prop-2-en-1-amine (3.42 g, 60.0 mmol) was added dropwise to a methanol (40.0 mL) solution of cyclohexanecarbaldehyde (7.06 g, 63.0 mmol) while cooling with ice. After the completion of the addition, sodium tetrahydroborate (0.850 g, 22.0 mmol) was resolved and added while cooling with ice, and the mixture was stirred for another hour. Methanol was evaporated under reduced pressure. Ethyl ether was added to the residue. The organic layer was washed with saturated saline and dried with anhydrous sodium sulfate and then concentrated under reduce pressure. The residue was evaporated under reduced pressure to obtain the aforementioned compound (7.35 g, 80%, boiling point, 79 to 84° C./9.1 mmHg).

Under the same conditions as this reaction, the following compounds were synthesized. N-isobutylprop-2-en-1-amine N-allyl-3-methylbutan-1-amine

Synthesis Example for Compound III

Synthesis of N-(4-tert-butoxybenzyl)prop-2-en-1-amine

A methanol (2.00 mL) solution of 4-tert-butoxybenzaldehyde (468 mg, 2.63 mmol) was added dropwise to a methanol (3.00 mL) solution of prop-2-en-1-amine (143 mg, 2.50 mmol) while cooling with ice. After the completion of the addition, sodium tetrahydroborate (35.0 mg, 0.920 mmol) was resolved and added while cooling with ice, and the mixture was stirred for another hour. Methanol was evaporated under reduced pressure. Ethyl acetate was added to the residue. The organic layer was washed with saturated saline and dried with anhydrous sodium sulfate and then concentrated under reduce pressure. The resulting residue was purified by column chromatography (column: Purif-Pack Si50, Size 60, eluent: hexane-ethyl acetate (gradient from 20% to 100%) and then ethyl acetate-methanol (gradient from 0% to 15%)) to obtain the aforementioned compound (370 mg, yield: 68%).

Under the same conditions as this reaction, the following compounds were synthesized. N-(naphthalen-1-ylmethyl)prop-2-en-1-amine N-(3,4-dichlorobenzyl)prop-2-en-1-amine

Synthesis Example: IIB-1 and IIF-1

Synthesis of (3S*,3aS*,6R*,7R*,7aS*)—N,7-dibenzyl-1-isobutyl-1,2,3,6,7,7a-hexahydro-3aH-3,6-methanopyrrolo[3,2-b]pyridine-3a-carboxamide (IIB-1) and (3S*, 3aR*, 6S*, 7R*, 7aR*)—N, 7-dibenzyl-1-isobutyl-1,2,3,3a,7,7a-hexahydro-6H-3,6-methanopyrrolo[3,2-c]pyridine-6-carboxamide (IIF-1)

4A molecular sieves (850 mg), 3-phenylpropanal (0.157 mL, 1.19 mmol), and N-isobutylprop-2-en-1-amine (purity: 90%, 150 mg, 1.19 mmol) were added to a chloroform (8.50 mL) solution of N-benzyl-1,2,4-triazine-3-carboxamide (III) (170 mg, 0.794 mmol), and heated and refluxed for 10 hours. The molecular sieves were filtered and washed twice with chloroform (5.00 mL). The combined organic layer was evaporated under reduced pressure. The resulting residue was purified with CHROMATOREX Q-PACK SI30 SIZE 60 (ethyl acetate:methanol=100%: 0% to 960:40) to obtain the aforementioned compounds (IIF-1) (86.9 mg, yield: 26%, RT=1.14 minutes (B method), [M+1]⁺=416) and (IIB-1) (149 mg, yield: 45%, RT=1.19 minutes (B method), [M+1]⁺=416).

Synthesis Example: IIB-29

Synthesis of (3S*, 3aS*, 6R*, 7R*, 7aS*)—N-(4-aminobutyl)-7-benzyl-1-isobutyl-1,2,3,6,7,7a-hexahydro-3aH-3,6-methanopyrrolo[3,2-b]pyridine-3a-carboxamide (IIB-29)

Formic acid (300 μL) was added to (3S*, 3aS*, 6R*,7R*,7aS*)-7-benzyl-1-isobutyl-N-(4-((tert-butoxycarbonyl)amino)butyl)-1,2,3,6,7,7a-hexahydro-3aH-3,6-methanopyrrolo[3,2-b]pyridine-3a-carboxamide (IIB-30) (9.30 mg, 0.0187 mmol) and incubated overnight at room temperature. Formic acid was evaporated under reduced pressure to obtain a diformic acid salt of the aforementioned compound (7.70 mg, yield: 84%, RT=0.71 minutes (A method), [M+1]⁺=397).

Synthesis Example: IIF-26

Synthesis of 3-((3S*, 3aR*, 6S*, 7R*, 7aR*)-7-benzyl-1-isobutyl-1,2,3,3a, 7,7a-hexahydro-1H-3,6-methanopyrrolo[3,2-c]pyridine-6-carboxamide) propanoic acid (11-26)

Formic acid (1.00 mL) was added to (3S*, 3aR*, 6S*, 7R*, 7aR*)-7-benzyl-1-isobutyl-N— (2-(tert-butoxy)-2-oxoethyl)-1,2,3,3a, 7,7a-hexahydro-6H-3,6-methanopyrrolo[3,2-c]pyridine-6-carboxamide (IIF-27) (30.4 mg, 0.0660 mmol), and heated overnight at 50° C. Formic acid was evaporated under reduced pressure to obtain a monoformic acid salt of the aforementioned compound (29.7 mg, yield: 100%, RT=0.75 minutes (A method), [M+1]+=398).

Synthesis Example: IIB-28

Synthesis of (3S*,3aS*,6R*,7R*,7aS*)—N-(3-amino-3-oxopropyl)-7-benzyl-1-isobutyl-1,2,3,6,7,7a-hexahydro-3aH-3,6-methanopyrrolo[3,2-b]pyridine-3a-carboxamide (IIB-28)

3-((3S*,3aS*,6R*,7R*,7aS*)-7-benzyl-1-isobutyl-1,2,3,6,7,7a-hexahydro-1H-3,6-methanopyrrolo[3,2-b]pyridine-3a-carboxamide)propanoic acid (IIB-26) (15.0 mg, 0.0380 mmol) was dissolved in methanol (2.00 mL), and ammonium water (25.0 μL) and 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride (110 mg, 0.397 mmol) were resolved and added 4 times each at room temperature. The solvent was evaporated under reduced pressure. The resulting residue was purified by preparative PLC (Fuji Silysia Chemical's CHROMATOREX NH-PLCO5 (layer thickness 0.500 mm) (ethyl acetate:methanol=9:1) to obtain the aforementioned compound (7.10 mg, yield: 47%, RT=0.79 minutes (A method), [M+1]⁺=397).

Tables 1 to 4 summarize the synthesized compounds of formula IIB and compounds of IIF. The following abbreviations are used in the following tables.

INT-iBu: N-isobutyl-1,2,4-triazine-3-carboxamide

INT-Bnzl: N-benzyl-1,2,4-triazine-3-carboxamide

SM1-iBu: N-isobutylprop-2-en-1-amine

SM1-Bnzl: N-benzylprop-2-en-1-amine

SM2-Ph: 3-phenylpropanal

SM2-Pnt: 4-methylpentanal

Since samples with a blank entry under Mass in the following tables are prepared based on Mass Number in HPLC, it can be understood that the molecular weight is inferred and confirmed based on the time of retension (UV) of HPLC to identify the structure.

TABLE 1-1
Compound				Synthesis
number	R1	R2	R3	method	Intermediate	Raw material 1	Raw material 2
IIB-1	i-Bu	Bnzl	Bnzl	EX	INT-Bnzl	SM1-iBu	SM2-Ph

TABLE 1-2
IIB-	i-Bu	i-Bu	i-Bu	IIB-1,	INT-iBu	SM1-iBu	SM2-Pnt
2				IIF-1
IIB-	i-Bu	i-Bu	Bnzl	IIB-1,	INT-iBu	SM1-iBu	SM2-Ph
3				IIF-1
IIB-	Bnzl	i-Bu	i-Bu	IIB-1,	INT-iBu	SM1-Bnzl	SM2-Pnt
4				IIF-1
IIB-	i-Bu	Bnzl	i-Bu	IIB-1,	INT-Bnzl	SM1-iBu	SM2-Pnt
5				IIF-1
IIB-	Bnzl	i-Bu	Bnzl	IIB-1,	INT-iBu	SM1-Bnzl	SM2-Ph
6				IIF-1
IIB-	Bnzl	Bnzl	i-Bu	IIB-1,	INT-Bnzl	SM1-Bnzl	SM2-Pnt
7				IIF-1
IIB-	Bnzl	Bnzl	Bnzl	IIB-1,	INT-Bnzl	SM1-Bnzl	SM2-Ph
8				IIF-1
IIB-	i-Pnt	Bnzl	Bnzl	IIB-1,	INT-Bnzl	N-allyl-	SM2-Ph
9				IIF-1		3-
						methylbutan-
						1-amine
IIB-	Bnzl	Bnzl	i-Pnt	IIB-1,	INT-Bnzl	SM1-Bnzl	5-
10				IIF-1			methylhexanal
IIB-	i-Bu	Bnzl	Ph-Et	IIB-1,	INT-Bnzl	SM1-iBu	4-
11				IIF-1			phenylbutanal
IIB-	i-Bu	Ph-Et	Bnzl	IIB-1,	N-	SM1-iBu	SM2-Ph
12				IIF-1	phenethyl-
					1,2,4-
					triazine-3-
					carboxamide
IIB-	i-Bu	Bnzl	3-Me-	IIB-1,	INT-Bnzl	SM1-iBu	3-(m-tolyl)
13			Bnzl	IIF-1			propanal
IIB-	i-Bu	Bnzl	4-Me-	IIB-1,	INT-Bnzl	SM1-iBu	3-(p-tolyl)
14			Bnzl	IIF-1			propanal
IIB-	i-Bu	3-Me-	Bnzl	IIB-1,	N-(3-	SM1-iBu	SM2-Ph
15		Bnzl		IIF-1	methylbenzyl)-
					1,2,4-
					triazine-3-
					carboxamide
IIB-	i-Bu	4-Me-	Bnzl	IIB-1,	N-(4-	SM1-iBu	SM2-Ph
16		Bnzl		IIF-1	methylbenzyl)-
					1,2,4-
					triazine-3-
					carboxamide
IIB-	i-Bu	3-Cl-	Bnzl	IIB-1,	N-(3-	SM1-iBu	SM2-Ph
17		Bnzl		IIF-1	chlorobenzyl)-
					1,2,4-
					triazine-3-
					carboxamide
IIB-	i-Bu	4-Cl-	Bnzl	IIB-1,	N-(4-	SM1-iBu	SM2-Ph
18		Bnzl		IIF-1	chlorobenzyl)-
					1,2,4-
					triazine-3-
					carboxamide
IIB-	3,4-	Bnzl	i-Bu	IIB-1,	INT-Bnzl	N-(3,4-	SM2-Pnt
19	Cl2-			IIF-1		dichlorobenzyl)
	Bnzl					prop-2-en-1-
						amine
IIB-	Bnzl	3,4-Cl2-	i-Bu	IIB-1,	N-(3,4-	SM1-Bnzl	SM2-Pnt
20		Bnzl		IIF-1	dichlorobenzyl)-
					1,2,4-
					triazine-3-
					carboxamide
IIB-	Me	Np-E	Bnzl	IIB-1,	N-(2-	N-	SM2-Ph
21				IIF-1	(naphthalen-1-	methylprop-
					yl)ethyl)-	2-en-1-amine
					1,2,4-
					triazine-3-
					carboxamide

TABLE 1-3
IIB-	i-Bu	4-(tert-	Bnzl	IIB-1,	N-(4-tert-	SM1-iBu	SM2-Ph
23		butoxy)		IIF-1	butoxybenzyl)-
		benzyl			1,2,4-
					triazine-3-
					carboxamide
IIB-	i-Bu	Np-M	Bnzl	IIB-1,	N-	SM1-iBu	SM2-Ph
24				IIF-1	((naphthalen-
					1-yl)methyl)-
					1,2,4-
					triazine-3-
					carboxamide
IIB-	i-Bu	Hdr-E	Bnzl	IIB-1,	N-(2-	SM1-iBu	SM2-Ph
25				IIF-1	hydroxyethyl)-
					1,2,4-
					triazine-3-
					carboxamide
IIB-	i-Bu	Cbx-E	Bnzl	IB-40		IIB-27
26
IIB-	i-Bu	2-(tert-	Bnzl	IIB-1,	tert-butyl	SM1-iBu	SM2-Ph
27		butoxy)-		IIF-1	3-(1,2,4-
		2-			triazine-3-
		oxoethyl			carboxamide)
					propanoate
IIB-	i-Bu	Cbm-E	Bnzl	EX		IIB-26
28
IIB-	i-Bu	4-	Bnzl	EX		IIB-30
29		aminobutyl
IIB-	i-Bu	4-	Bnzl	IIB-1,	tert-butyl	SM1-iBu	SM2-Ph
30		((tert-		IIF-1	4-(1,2,4-
		butoxycarbonyl)			triazine-3-
		amino)butyl			carboxamide)
					butylcarbamate
IIB-	i-Bu	Chm	Bnzl	IIB-1,	N-	SM1-iBu	SM2-Ph
31				IIF-1	(cyclohexyl-
					methyl)-
					1,2,4-
					triazine-3-
					carboxamide
IIB-	i-Bu	(tetrahydro-	Bnzl	IIB-1,	N-	SM1-iBu	SM2-Ph
32		2H-		IIF-1	((tetrahydro-
		pyran-2-			2H-pyran-
		yl)methyl			2-yl)methyl)-
					1,2,4-
					triazine-3-
					carboxamide
IIB-	i-Bu	Bnzl	4-	IIB-1,	INT-Bnzl	SM1-iBu	tert-
34			((tert-	IIF-1			butyl
			butoxy-				5-
			carbonyl)				formyl-
			amino)				pentyl-
			butyl				carbamate
IIB-	i-Bu	Bnzl	3-	IIB-1,	INT-Bnzl	SM1-iBu	methyl
36			methoxy-	IIF-1			4-formyl-
			3-				butanoate
			oxopropyl
IIB-	i-Bu	Bnzl	Chm	IIB-1,	INT-Bnzl	SM1-iBu	3-
38				IIF-1			cyclo-
							hexylpropanal
IIB-	Chm	Bnzl	Bnzl	IIB-1,	INT-Bnzl	N-	SM2-Ph
39				IIF-1		(cyclohexylmethyl)
						prop-
						2-en-1-
						amine
IIB-	4-OH-	Bnzl	Bnzl	IB-40		IIB-41
40	Bnzl
IIB-	4-	Bnzl	Bnzl	IIB-1,	INT-Bnzl	N-(4-	SM2-Ph
41	(tert-			IIF-1		tert-
	butoxy)					butoxybenzyl)
	benzyl					prop-2-en-
						1-amine
IIB-	Np-M	Bnzl	Bnzl	IIB-1,	INT-Bnzl	N-	SM2-Ph
42				IIF-1		((naphthalen-
						1-yl)methyl)
						prop-
						2-en-1-
						amine

TABLE 1-4
IIB-	3-	Bnzl	Bnzl	IIB-1,	INT-Bnzl	N-(3-	SM2-Ph
76	(tert-			IIF-1		(tert-
	butoxy)-					butoxy)-
	3-					3-
	oxopropyl					oxopropyl)-
						prop-2-en-1-
						amine
IIB-	Bnzl	Bnzl	4-OH-	IIB-1,	INT-Bnzl	SM1-Bnzl	3-(4-
77			Bnzl	IIF-1			hydroxy-
							phenyl)
							propanal
IIB-	Me	2-(1-	Bnzl	IIB-1,	N-(2-(1-	N-	SM2-Ph
78		(tert-		IIF-1	(tert-	methyl-
		butoxycarbonyl)-			butoxycarbonyl)-	prop-2-
		1H-			1H-	en-1-
		indol-3-			indol-3-	amine
		yl)ethyl			yl)ethyl)-
					1,2,4-
					triazine-3-
					carboxamide
IIB-	Np-M	Bnzl	Pr	IIB-1,	INT-Bnzl	N-	pentanal
80				IF-1		((naphthalen-
						1-
						yl)methyl)
						prop-
						2-en-1-
						amine
IIB-	benzyl	naphthalen-	isobutyl	IIB-1,
81		1-ylmethyl		IF-1
EX: described in the Examples

TABLE 1-5
				LCMS	Mass
Compound				tR	(M +	Measurement
number	R1	R2	R3	(min)	H)+	condition
IIB-81	benzyl	naphthalen-	isobutyl	1.29	467	B
		1-ylmethyl
IIB-82	benzyl	4-(trifluoromethyl)	isobutyl	1.29	484	B
		benzyl
IIB-83	4-chlorobenzyl	benzyl	isobutyl	1.29	450	B
IIB-84	3-chlorobenzyl	benzyl	isobutyl	1.30	450	B
IIB-85	4-methoxybenzyl	benzyl	isobutyl	1.23	446	B
IIB-86	4-methylbenzyl	benzyl	isobutyl	1.27	430	B
IIB-88	isobutyl	isobutyl	4-chlorobenzyl	1.26	416	B
IIB-89	isobutyl	4-chlorobenzyl	isobutyl	1.27	416	B
IIB-90	isobutyl	benzyl	isopentyl	1.26	396	B
IIB-91	isopentyl	benzyl	isobutyl	1.26	396	B
IIB-92	isobutyl	isopentyl	benzyl	1.27	396	B
IIB-93	4-hydroxybenzyl	benzyl	isobutyl	1.19	432	B
IIB-94	4-(dimethylamino)	benzyl	isobutyl	1.27	459	B
	benzyl

TABLE 1-6
IIB-95	4-(tert-butyl)	benzyl	isobutyl	1.31	472	B
	benzyl
IIB-96	4-(trifluoro-	benzyl	isobutyl	1.32	500	B
	methoxy)benzyl
IIB-97	4-ethoxybenzyl	benzyl	isobutyl	1.25	460	B
IIB-98	isopentyl	isobutyl	benzyl	1.26	396	B
IIB-99	benzyl	4-hydroxy-	isobutyl	1.17	432	B
		benzyl
IIB-100	4-methoxybenzyl	4-hydroxy-	isobutyl	1.17	462	B
		benzyl
IIB-101	4-hydroxybenzyl	benzyl	isopentyl	1.20	446	B
IIB-102	benzyl	naphthalen-2-	isobutyl	1.27	466	B
		ylmethyl
IIB-103	isopentyl	4-chlorobenzyl	isobutyl	1.28	431	B
IIB-104	isopentyl	4-fluorobenzyl	isobutyl	1.26	414	B
IIB-105	benzyl	pyridin-4-yl	isobutyl	1.06	417	B
		methyl
IIB-106	4-methoxybenzyl	benzyl	benzyl	0.99	480	C
IIB-107	phenethyl	benzyl	2-(tert-	1.12	532	C
			butyl-
			dimethyl-
			silyloxy)
			ethyl
IIB-108	cyclopentyl-	4-hydroxy-	2-carboxy-	0.78	440	C
	methyl	benzyl	ethyl
IIB-109	4-nitrobenzyl	4-(tert-butoxy)	2-(tert-	1.03	605	C
		benzyl	butoxy-
			carbonyl)
			ethyl
IIB-110	i-Bu	i-Pr	Bnzl	3.09	368	F
IIB-111	i-Bu	i-Bu	4-tBuO-	3.95	454	F
			Bnzl
IIB-112	i-Bu	Bnzl	4-tBuO-	4.05	488	F
			Bnzl
IIB-113	i-Bu	tBOC-E	4-tBuO-	4.12	526	F
			Bnzl
IIB-114	i-Bu	s-Bu	4-tBuO-	3.93	454	F
			Bnzl
IIB-115	i-Bu	1-Npm	4-tBuO-	4.48	538	F
			Bnzl

TABLE 1-7
IIB-116	i-Bu	i-Pr	4-tBuO-	3.64	440	F
			Bnzl
IIB-117	i-Bu	1-Npm	tBOC-E	4.11	504	F
IIB-118	i-Bu	i-Pr	tBOC-E	3.18	406	F
IIB-119	i-Bu	1-Npm	1-Npm	4.39	516	F
IIB-120	i-Bu	i-Pr	1-Npm	3.52	418	F
IIB-121	Bnzl	4-tBuO-Bnzl	Bnzl	4.23	522	F
IIB-122	Bnzl	i-Bu	4-tBuO-	4.11	488	F
			Bnzl
IIB-123	Bnzl	Bnzl	4-tBuO-	4.20	522	F
			Bnzl
IIB-124	Bnzl	tBOC-E	4-tBuO-	4.27	560	F
			Bnzl
IIB-125	Bnzl	Bnzl	tBOC-E	3.72	488	F
IIB-126	Bnzl	4-tBuO-Bnzl	tBOC-E	4.22	560	F
IIB-127	Bnzl	1-Npm	tBOC-E	4.18	538	F
IIB-128	Bnzl	i-Bu	1-Npm	3.98	466	F
IIB-129	Bnzl	Bnzl	1-Npm	4.09	500	F
IIB-130	Bnzl	4-tBuO-Bnzl	1-Npm	4.55	572	F
IIB-131	Bnzl	tBOC-E	1-Npm	4.17	538	F
IIB-132	Bnzl	s-Bu	1-Npm	3.96	466	F
IIB-133	Bnzl	1-Npm	1-Npm	4.49	550	F
IIB-134	Bnzl	i-Pr	1-Npm	3.71	452	F
IIB-135	4-tBuO-Bnzl	i-Bu	Bnzl	3.92	488	F
IIB-136	4-tBuO-Bnzl	Bnzl	Bnzl	4.57	522	F
IIB-137	4-tBuO-Bnzl	1-Npm	Bnzl	5.10	572	F
IIB-138	4-tBuO-Bnzl	Bnzl	tBOC-E	3.95	560	F
IIB-139	4-tBuO-Bnzl	1-Npm	tBOC-E	4.35	610	F
IIB-140	4-tBuO-Bnzl	i-Bu	1-Npm	4.07	538	F
IIB-141	4-tBuO-Bnzl	Bnzl	1-Npm	5.00	572	F
IIB-142	4-tBuO-Bnzl	tBOC-E	1-Npm	4.14	610	F
IIB-143	4-tBuO-Bnzl	s-Bu	1-Npm	4.27	538	F
IIB-144	4-tBuO-Bnzl	1-Npm	1-Npm	5.40	622	F
IIB-145	i-Bu	4-tBuO-Bnzl	Bnzl	4.13	488	F
IIB-146	i-Bu	tBOC-E	Bnzl	3.66	454	F
IIB-147	i-Bu	s-Bu	Bnzl	3.38	382	F
IIB-148	i-Bu	i-Bu	tBOC-E	3.44	420	F
IIB-149	i-Bu	Bnzl	tBOC-E	3.63	454	F

TABLE 1-8
IIB-150	i-Bu	4-tBuO-Bnzl	tBOC-E	4.18	526	F
IIB-151	i-Bu	s-Bu	tBOC-E	3.46	420	F
IIB-152	i-Bu	i-Bu	1-Npm	3.87	432	F
IIB-153	i-Bu	Bnzl	1-Npm	3.98	466	F
IIB-154	i-Bu	4-tBuO-Bnzl	1-Npm	4.44	538	F
IIB-155	i-Bu	tBOC-E	1-Npm	4.04	504	F
IIB-156	Bnzl	tBOC-E	Bnzl	3.82	488	F
IIB-157	Bnzl	s-Bu	Bnzl	3.55	416	F
IIB-158	Bnzl	1-Npm	Bnzl	4.21	500	F
IIB-159	Bnzl	i-Pr	Bnzl	3.31	402	F
IIB-160	Bnzl	s-Bu	4-tBuO-	4.08	488	F
			Bnzl
IIB-161	Bnzl	1-Npm	4-tBuO-	4.61	572	F
			Bnzl
IIB-162	Bnzl	i-Pr	4-tBuO-	3.83	474	F
			Bnzl
IIB-163	Bnzl	s-Bu	tBOC-E	3.60	454	F
IIB-164	Bnzl	i-Pr	tBOC-E	3.28	440	F
IIB-165	4-tBuO-Bnzl	i-Pr	Bnzl	3.70	474	F
IIB-166	4-tBuO-Bnzl	i-Pr	tBOC-E	3.75	512	F
IIB-167	4-tBuO-Bnzl	i-Pr	1-Npm	4.07	524	F
IIB-168	tBOC-E	i-Bu	Bnzl	3.77	454	F
IIB-169	tBOC-E	Bnzl	Bnzl	3.86	488	F
IIB-170	tBOC-E	4-tBuO-Bnzl	Bnzl	4.34	560	F
IIB-171	tBOC-E	s-Bu	Bnzl	3.76	454	F
IIB-172	tBOC-E	1-Npm	Bnzl	4.34	538	F
IIB-173	tBOC-E	i-Bu	4-tBuO-	4.30	526	F
			Bnzl
IIB-174	tBOC-E	Bnzl	4-tBuO-	4.40	560	F
			Bnzl
IIB-175	tBOC-E	s-Bu	4-tBuO-	4.31	526	F
			Bnzl
IIB-176	tBOC-E	1-Npm	4-tBuO-	4.80	610	F
			Bnzl
IIB-177	tBOC-E	i-Pr	4-tBuO-	4.05	512	F
			Bnzl
IIB-178	tBOC-E	i-Bu	1-Npm	4.13	504	F
IIB-179	tBOC-E	4-tBuO-Bnzl	1-Npm	4.66	610	F
IIB-180	tBOC-E	s-Bu	1-Npm	4.09	504	F
IIB-181	tBOC-E	1-Npm	1-Npm	4.63	588	F
IIB-182	1-Npm	4-tBuO-Bnzl	Bnzl	4.18	572	F
IIB-183	1-Npm	s-Bu	Bnzl	3.82	466	F

TABLE 1-9
IIB-184	1-Npm	Bnzl	4-tBuO-	4.68	572	F
			Bnzl
IIB-185	1-Npm	tBOC-E	4-tBuO-	4.24	610	F
			Bnzl
IIB-186	1-Npm	s-Bu	4-tBuO-	4.84	538	F
			Bnzl
IIB-187	1-Npm	1-Npm	4-tBuO-	4.85	622	F
			Bnzl
IIB-188	1-Npm	i-Pr	4-tBuO-	4.20	524	F
			Bnzl
IIB-189	1-Npm	i-Bu	tBOC-E	3.80	504	F
IIB-190	1-Npm	Bnzl	tBOC-E	4.45	538	F
IIB-191	1-Npm	4-tBuO-Bnzl	tBOC-E	4.84	610	F
IIB-192	1-Npm	s-Bu	tBOC-E	4.29	504	F
IIB-193	1-Npm	1-Npm	tBOC-E	4.49	588	F
IIB-194	1-Npm	Bnzl	1-Npm	4.75	550	F
IIB-195	1-Npm	4-tBuO-Bnzl	1-Npm	4.74	622	F
IIB-196	1-Npm	tBOC-E	1-Npm	4.59	588	F
IIB-197	1-Npm	s-Bu	1-Npm	4.57	516	F
IIB-198	i-Bu	4-tBuO-Bnzl	i-Bu	4.04	454	F
IIB-199	i-Bu	tBOC-E	i-Bu	3.35	420	F
IIB-200	i-Bu	s-Bu	i-Bu	3.25	348	F
IIB-201	i-Bu	1-Npm	i-Bu	4.00	432	F
IIB-202	i-Bu	i-Pr	i-Bu	2.97	334	F
IIB-203	i-Bu	(tBOC)Gun-Pr	4-tBuO-	2.81	641	J
			Bnzl
IIB-204	i-Bu	1-Npm	(tBOC)Gun-	3.27	675	J
			Pr
IIB-205	i-Bu	s-Bu	1-Npm	3.85	432	F
IIB-206	Bnzl	4-tBuO-Bnzl	i-Bu	4.13	488	F
IIB-207	Bnzl	s-Bu	i-Bu	3.45	382	F
IIB-208	Bnzl	i-Pr	i-Bu	3.14	368	F
IIB-209	Bnzl	i-Bu	(tBOC)Gun-	3.22	625	J
			Pr
IIB-210	Bnzl	4-tBuO-Bnzl	(tBOC)Gun-	2.96	675	J
			Pr
IIB-211	tBOC-E	i-Bu	i-Bu	3.63	420	F
IIB-212	tBOC-E	Bnzl	i-Bu	3.83	454	F
IIB-213	tBOC-E	4-tBuO-Bnzl	i-Bu	4.35	526	F
IIB-214	tBOC-E	s-Bu	i-Bu	3.68	420	F
IIB-215	tBOC-E	1-Npm	i-Bu	4.32	504	F
IIB-216	tBOC-E	i-Pr	i-Bu	3.41	406	F
IIB-217	tBOC-E	Bnzl	1-Npm	4.19	538	F

TABLE 1-10
IIB-218	tBOC-E	i-Pr	1-Npm	3.87	490	F
IIB-219	1-Npm	Bnzl	i-Bu	3.62	466	F
IIB-220	1-Npm	i-Bu	Bnzl	3.67	466	F
IIB-221	1-Npm	(tBOC)Gun-Pr	Bnzl	3.97	709	F
IIB-222	1-Npm	i-Bu	4-tBuO-	4.18	538	F
			Bnzl
IIB-223	1-Npm	i-Pr	tBOC-E	3.62	490	F
IIB-224	1-Npm	1-Npm	(tBOC)Gun-	5.14	759	F
			Pr
IIB-225	1-Npm	i-Pr	(tBOC)Gun-	3.15	661	F
			Pr
IIB-226	1-Npm	i-Bu	1-Npm	4.07	516	F
IIB-227	1-Npm	(tBOC)Gun-Pr	1-Npm	2.99	459	F
IIB-228	1-Npm	i-Pr	1-Npm	3.90	502	F
IIB-229	i-Bu	(tBOC)Gun-Pr	i-Bu	3.10	591	J
IIB-230	i-Bu	(tBOC)Gun-Pr	Bnzl	3.03	625	J
IIB-231	i-Bu	i-Bu	(tBOC)Gun-	3.01	591	J
			Pr
IIB-232	i-Bu	Bnzl	(tBOC)Gun-	3.02	625	J
			Pr
IIB-233	i-Bu	4-tBuO-Bnzl	(tBOC)Gun-	2.84	641	J
			Pr
IIB-234	i-Bu	s-Bu	(tBOC)Gun-	2.99	591	J
			Pr
IIB-235	i-Bu	i-Pr	(tBOC)Gun-	2.90	577	J
			Pr
IIB-236	i-Bu	(tBOC)Gun-Pr	1-Npm	3.17	675	J
IIB-237	Bnzl	(tBOC)Gun-Pr	i-Bu	3.19	625	J
IIB-238	Bnzl	(tBOC)Gun-Pr	Bnzl	3.26	659	J
IIB-239	Bnzl	(tBOC)Gun-Pr	4-tBuO-	2.84	675	J
			Bnzl
IIB-240	Bnzl	i-Bu	tBOC-E	3.56	454	F
IIB-241	Bnzl	Bnzl	(tBOC)Gun-	3.28	659	J
			Pr
IIB-242	Bnzl	s-Bu	(tBOC)Gun-	3.04	625	J
			Pr
IIB-243	Bnzl	i-Pr	(tBOC)Gun-	2.99	611	J
			Pr
IIB-244	Bnzl	(tBOC)Gun-Pr	1-Npm	3.36	709	J
IIB-245	tBOC-E	i-Pr	Bnzl	3.45	440	F
IIB-246	(tBOC)Gun-Pr	1-Npm	i-Bu	3.65	657	J
IIB-247	(tBOC)Gun-Pr	i-Pr	i-Bu	3.21	577	J
IIB-248	(tBOC)Gun-Pr	1-Npm	Bnzl	3.75	709	J
IIB-249	(tBOC)Gun-Pr	i-Pr	Bnzl	3.24	611	J
IIB-250	(tBOC)Gun-Pr	1-Npm	4-tBuO-	3.30	725	J
			Bnzl
IIB-251	(tBOC)Gun-Pr	i-Pr	4-tBuO-	2.92	627	J
			Bnzl

TABLE 1-11
IIB-252	(tBOC)Gun-Pr	1-Npm	1-Npm	3.86	759	J
IIB-253	(tBOC)Gun-Pr	i-Pr	1-Npm	3.38	661	J
IIB-254	1-Npm	(tBOC)Gun-Pr	i-Bu	4.29	675	F
IIB-255	1-Npm	1-Npm	i-Bu	4.05	516	F
IIB-256	1-Npm	1-Npm	Bnzl	4.92	550	F
IIB-257	Bnzl	tBOC-E	i-Bu	3.73	454	F
IIB-258	Bnzl	1-Npm	(tBOC)Gun-	3.80	709	J
			Pr
IIB-259	4-tBuO-Bnzl	i-Bu	i-Bu	3.67	454	F
IIB-260	4-tBuO-Bnzl	Bnzl	i-Bu	3.67	488	F
IIB-261	4-tBuO-Bnzl	tBOC-E	i-Bu	3.82	526	F
IIB-262	4-tBuO-Bnzl	(tBOC)Gun-Pr	i-Bu	3.38	641	F
IIB-263	4-tBuO-Bnzl	s-Bu	i-Bu	3.75	454	F
IIB-264	4-tBuO-Bnzl	1-Npm	i-Bu	4.22	538	F
IIB-265	4-tBuO-Bnzl	i-Pr	i-Bu	3.47	440	F
IIB-266	4-tBuO-Bnzl	tBOC-E	Bnzl	3.88	560	F
IIB-267	4-tBuO-Bnzl	(tBOC)Gun-Pr	Bnzl	3.24	675	F
IIB-268	4-tBuO-Bnzl	s-Bu	Bnzl	3.85	488	F
IIB-269	4-tBuO-Bnzl	i-Bu	tBOC-E	3.88	526	F
IIB-270	4-tBuO-Bnzl	s-Bu	tBOC-E	3.79	526	F
IIB-271	4-tBuO-Bnzl	i-Bu	(tBOC)Gun-	3.45	641	F
			Pr
IIB-272	4-tBuO-Bnzl	Bnzl	(tBOC)Gun-	3.82	675	F
			Pr
IIB-273	4-tBuO-Bnzl	s-Bu	(tBOC)Gun-	3.38	641	F
			Pr
IIB-274	4-tBuO-Bnzl	1-Npm	(tBOC)Gun-	3.88	725	F
			Pr
IIB-275	4-tBuO-Bnzl	i-Pr	(tBOC)Gun-	3.27	627	F
			Pr
IIB-276	4-tBuO-Bnzl	(tBOC)Gun-Pr	1-Npm	3.74	725	F
IIB-277	(tBOC)Gun-Pr	i-Bu	i-Bu	4.52	591	F
IIB-278	(tBOC)Gun-Pr	Bnzl	i-Bu	4.25	625	F
IIB-279	(tBOC)Gun-Pr	4-tBuO-Bnzl	i-Bu	3.79	641	F
IIB-280	(tBOC)Gun-Pr	s-Bu	i-Bu	4.04	591	F
IIB-281	(tBOC)Gun-Pr	i-Bu	Bnzl	4.39	625	F
IIB-282	(tBOC)Gun-Pr	Bnzl	Bnzl	4.30	659	F
IIB-283	(tBOC)Gun-Pr	4-tBuO-Bnzl	Bnzl	3.82	675	F
IIB-284	(tBOC)Gun-Pr	s-Bu	Bnzl	4.09	625	F
IIB-285	(tBOC)Gun-Pr	i-Bu	4-tBuO-	3.80	641	F
			Bnzl

TABLE 1-12
IIB-286	(tBOC)Gun-Pr	Bnzl	1-Npm	4.57	709	F
IIB-287	(tBOC)Gun-Pr	s-Bu	1-Npm	4.49	675	F
IIB-288	1-Npm	i-Bu	i-Bu	3.65	432	F
IIB-289	1-Npm	4-tBuO-Bnzl	i-Bu	4.09	538	F
IIB-290	1-Npm	tBOC-E	i-Bu	3.77	504	F
IIB-291	1-Npm	s-Bu	i-Bu	3.71	432	F
IIB-292	1-Npm	i-Pr	i-Bu	3.54	418	F
IIB-293	1-Npm	tBOC-E	Bnzl	3.99	538	F
IIB-294	1-Npm	i-Pr	Bnzl	3.69	452	F
IIB-295	1-Npm	(tBOC)Gun-Pr	4-tBuO-	3.59	725	F
			Bnzl
IIB-296	1-Npm	i-Bu	(tBOC)Gun-	4.00	675	F
			Pr
IIB-297	1-Npm	Bnzl	(tBOC)Gun-	4.17	709	F
			Pr
IIB-298	1-Npm	4-tBuO-Bnzl	(tBOC)Gun-	3.65	725	F
			Pr
IIB-299	Bnzl	1-Npm	3-Gun-Pr	2.70	509	F
IIB-300	4-OH-Bnzl	3-Gun-Pr	i-Bu	2.47	441	F
IIB-301	4-OH-Bnzl	1-Npm	3-Gun-Pr	2.90	525	F
IIB-302	1-Npm	3-Gun-Pr	4-OH-Bnzl	2.70	525	F
IIB-303	1-Npm	i-Bu	3-Gun-Pr	2.82	475	F
IIB-304	1-Npm	Bnzl	3-Gun-Pr	2.97	509	F
IIB-305	1-Npm	4-OH-Bnzl	3-Gun-Pr	2.77	525	F
IIB-306	1-Npm	s-Bu	3-Gun-Pr	2.82	475	F
IIB-307	Bnzl	Ph-Et	i-Bu	0.97	430	C
IIB-308	Ph-Et	i-Bu	Bnzl	1.00	430	C
IIB-309	Chm	i-Bu	Bnzl	1.05	422	C
IIB-310	Bnzl	4-F-Bnzl	i-Bu	0.98	434	C
IIB-311	Chm	Bnzl	i-Bu	1.04	422	C
IIB-312	Bnzl	Hxy	i-Bu	1.08	410	C
IIB-313	Ph-Et	i-Bu	i-Bu	0.99	396	C
IIB-314	Ph-Et	i-Bu	1-Npm	1.04	480	C
IIB-315	Bnzl	i-Bu	Ph-Et	1.00	430	C
IIB-316	4-F-Bnzl	i-Bu	Bnzl	1.00	434	C
IIB-317	i-Bu	4-F-Bnzl	Bnzl	0.99	434	C
IIB-318	Ph-Et	Bnzl	i-Bu	0.98	430	C
IIB-319	Bnzl	i-Pnt	i-Bu	1.00	396	C

	TABLE 1-13
	IIB-320	i-Bu	Hxy	Bnzl	1.05	410	C
	IIB-321	4-F-Bnzl	Bnzl	Bnzl	0.99	468	C
	IIB-322	Ph-Et	Bnzl	Bnzl	1.00	464	C
	IIB-323	Bnzl	i-Bu	i-Pnt	1.03	396	C
	IIB-324	4-F-Bnzl	Bnzl	i-Bu	0.98	434	C

TABLE 1-14
Formula XXII3
Compound					LCMS	Mass	Measurement
number	R1	R2A	R2B	R3	RT (min)	(M + H)+	condition
IIB-325	2-Npm	H	Bnzl	i-Bu	2.89	466	B1
IIB-326	i-Pnt	H	3-Cl-Bnzl	Bnzl	2.85	464	B1
IIB-327	i-Pnt	H	4-Me-Bnzl	Bnzl	2.83	444	B1
IIB-328	i-Pnt	H	4-MeO-Bnzl	Bnzl	2.71	460	B1
IIB-329	Me	H	quinolin-8-ylethyl	Bnzl	2.09	439	B1
IIB-330	Me	H	quinolin-5-ylethyl	Bnzl	1.62	439	B1
IIB-331	i-Bu	H	4-Cl-Bnzl	Ph-Et	2.84	464	B1
IIB-332	i-Bu	H	3-Cl-Bnzl	Ph-Et	2.68	464	B1
IIB-333	i-Bu	H	4-MeO-Bnzl	Ph-Et	2.70	460	B1
IIB-334	i-Bu	H	4-Me-Bnzl	Ph-Et	2.83	445	B1
IIB-335	i-Bu	H	2-Npm	Ph-Et	2.92	480	B1
IIB-336	i-Bu	H	Bnzl	Ph-Pr	2.82	444	B1
IIB-337	i-Bu	H	3-Cl-Bnzl	Ph-Pr	1.29	478	B
IIB-338	i-Bu	H	3-F-Bnzl	Ph-Pr	1.33	462	B
IIB-339	Cpm	H	4-OH-Bnzl	Cbx-E	1.10	440	B
IIB-340	i-Bu	H	3-Me-Bnzl	Ph-Pr	1.33	458	B
IIB-341	i-Bu	H	3-MeO-Bnzl	Ph-Pr	1.29	474	B
IIB-342	i-Bu	H	3-Cl-Bnzl	Ph-Bu	1.33	492	B
IIB-343	i-Bu	H	3-F-Bnzl	Ph-Bu	1.29	476	B
IIB-344	i-Bu	H	3-Me-Bnzl	Ph-Bu	1.31	473	B
IIB-345	i-Bu	H	3-MeO-Bnzl	Ph-Bu	1.36	488	B
IIB-346	i-Bu	H	Bnzl	Ph-Bu	1.29	458	B
IIB-347	i-Pnt	H	3-F-Bnzl	Ph-Pr	1.25	476	B
IIB-348	1-Npm	H	pentyl	Ph-Et	1.08	494	C
IIB-349	1-Npm	pyrrolidine †	Ph-Et	0.96	478	C

TABLE 1-15
IIB-	1-Npm	H	cyclo-	Ph-Et	1.07	506	C
350			hexyl
IIB-	1-Npm	H	cyclo-	Ph-Et	1.05	492	C
351			pentyl
IIB-	1-Npm	piperidine †	Ph-Et	1.01	492	C
352
IIB-	1-Npm	H	heptyl	Ph-Et	1.14	522	C
353
IIB-	Hdr-E	H	4-	1-Npm	0.93	486	C
354			fluoro-
			phenethyl
IIB-	tBuO-E	H	4-	1-Npm	1.07	542	C
355			fluoro-
			phenethyl
IIB-	Pr	H	Chm	Bnzl	1.00	408	C
356
IIB-	1-Npm	H	Hxy	4-methyl-	1.13	522	C
357				phenethyl
IIB-	1-Npm	H	Hxy	4-	1.18	550	C
358				Isopropyl
				phenethyl
IIB-	1-Npm	H	Hxy	2-	1.15	558	C
359				(naphthalen-
				2-yl)ethyl
IIB-	1-Npm	H	Hxy	cyclohexyl-	1.19	514	C
360				ethyl
IIB-	tBuO-E	H	4-	1-Npm	1.07	545	C
361			Cl-Bnzl
IIB-	tBuO-E	H	4-	1-Npm	1.07	524	C
362			Me-Bnzl
IIB-	Pr	H	Bnzl	Chm	1.00	408	C
363
IIB-	Pr	H	2-	Bnzl	0.95	416	C
364			methyl-
			benzyl
IIB-	Pr	H	(1,2,3,4-	Bnzl	1.01	456	C
365			tetra-
			hydro-
			naphthalen-
			1-yl)methyl
IIB-	Pr	H	Cpm	Bnzl	0.96	394	C
366
IIB-	Pr	H	Bnzl	Cpm	0.95	394	C
367
IIB-	1-Npm	H	Hxy	3-	1.13	522	C
368				methyl-
				phenethyl
IIB-	4-Nt-Bnzl	H	Bnzl	Bnzl	0.96	495	C
369
IIB-	4-Nt-Bnzl	H	Hxy	Ph-Et	1.04	503	C
370
IIB-	i-Pnt	H	4-F-	Bnzl	2.73	448	B1
371			Bnzl
IIB-	i-Pnt	H	Ph-	Bnzl	2.76	444	B1
372			Et
IIB-	i-Pnt	H	1-	Bnzl	2.93	480	B1
373			Npm
IIB-	i-Bu	H	4-F-	Ph-Et	2.73	448	B1
374			Bnzl
IIB-	i-Bu	H	Ph-	Ph-Et	2.76	444	B1
375			Et
IIB-	i-Bu	H	1-	Ph-Et	2.93	480	B1
376			Npm
IIB-	4-F-Bnzl	H	1-	Bnzl	2.98	518	B1
377			Npm
IIB-	4-F-Bnzl	H	1-	i-Bu	1.30	484	B
378			Npm
IIB-	tBuO-E	H	4-F-	1-Npm	1.06	528	C
379			Bnzl
IIB-	tBOC-E	H	Bnzl	Ph-Et	1.02	502	C
380
IIB-	4-tBuO-	H	Bnzl	Ph-Et	1.06	536	C
381	Bnzl
IIB-	tBuO-E	H	Bnzl	1-Npm	1.05	510	C
382
IIB-	Chm	H	tBuO-E	1-Npm	1.07	516	C
383
IIB-	1-Npm	H	4-F-	TBSO-E	1.16	586	C
384			Bnzl
IIB-	i-Pnt	H	Bnzl	Ph-Et	1.01	444	C
385
IIB-	1-Npm	H	4-F-	Hdr-E	0.91	472	C
386			Bnzl
IIB-	Hdr-E	H	4-F-	1-Npm	0.91	472	C
387			Bnzl
IIB-	Cbx-E	H	Bnzl	Ph-Et	0.88	446	C
388
IIB-	TBSO-E	H	Ph-	1-Npm	1.07	524	C
389			Et
IIB-	Ph-Et	H	Hxy	1-Npm	1.08	508	C
390
IIB-	Ph-Et	H	i-Bu	4-tBuO-	1.06	502	C
391				Bnzl
IIB-	Ph-Et	H	i-Bu	4-OH-Bnzl	0.89	446	C
392

TABLE 1-16
IIB-393	Ph-Et	H	i-Bu	TBSO-E	1.13	498	C
IIB-394	Ph-Et	H	i-Bu	Hdr-E	0.82	384	C
IIB-395	Ph-Et	H	i-Bu	i-Pnt	1.02	410	C
IIB-396	i-Bu	H	i-Bu	4-OH-Bnzl	0.85	398	C
IIB-397	i-Bu	H	Bnzl	4-OH-Bnzl	0.87	432	C
IIB-398	i-Bu	H	2-	4-OH-Bnzl	0.69	414	C
			Cbx-Et
IIB-399	i-Bu	H	s-Bu	4-OH-Bnzl	0.85	398	C
IIB-400	i-Bu	H	1-Npm	4-OH-Bnzl	0.95	482	C
IIB-401	i-Bu	H	i-Pr	4-OH-Bnzl	0.80	384	C
IIB-402	i-Bu	H	1-Npm	2-Cbx-Et	0.89	448	C
IIB-403	i-Bu	H	i-Pr	2-Cbx-Et	0.72	350	C
IIB-404	Bnzl	H	4-	Bnzl	0.90	466	C
			OH-Bnzl
IIB-405	Bnzl	H	i-Bu	4-OH-Bnzl	0.89	432	C
IIB-406	Bnzl	H	2-Cbx-Et	4-OH-Bnzl	0.74	448	C
IIB-407	Bnzl	H	Bnzl	2-Cbx-Et	0.82	432	C
IIB-408	Bnzl	H	4-	2-Cbx-Et	0.73	448	C
			OH-Bnzl
IIB-409	Bnzl	H	1-Npm	2-Cbx-Et	0.90	482	C
IIB-410	Bnzl	H	4-	1-Npm	0.93,	516	C
*			OH-Bnzl		0.95
IIB-411	Bnzl	H	2-Cbx-Et	1-Npm	0.88	482	C
IIB-412	4-OH-Bnzl	H	i-Bu	Bnzl	0.89	432	C
IIB-413	4-OH-Bnzl	H	1-Npm	Bnzl	0.97	516	C
IIB-414	4-OH-Bnzl	H	Bnzl	2-Cbx-Et	0.76	448	C
IIB-415	4-OH-Bnzl	H	1-Npm	2-Cbx-Et	0.84	498	C
IIB-416	4-OH-Bnzl	H	i-Bu	1-Npm	0.93,	482	C
					0.94
IIB-417	4-OH-Bnzl	H	Bnzl	1-Npm	0.95	516	C
IIB-418	4-OH-Bnzl	H	2-Cbx-Et	1-Npm	0.82	498	C
IIB-419	4-OH-Bnzl	H	s-Bu	1-Npm	0.94	482	C
IIB-420	4-OH-Bnzl	H	1-Npm	1-Npm	0.98,	566	C
					1.00
IIB-421	i-Bu	H	4-	Bnzl	0.88	432	C
			OH-Bnzl
IIB-422	i-Bu	H	i-Bu	2-Cbx-Et	0.78	364	C
IIB-423	i-Bu	H	Bnzl	2-Cbx-Et	0.81	398	C
IIB-424	i-Bu	H	4-	2-Cbx-Et	0.71	414	C
			OH-Bnzl
IIB-425	i-Bu	H	s-Bu	2-Cbx-Et	0.77	364	C
IIB-426	i-Bu	H	4-	1-Npm	0.94	482	C
			OH-Bnzl
IIB-427	i-Bu	H	2-Cbx-Et	1-Npm	0.87	448	C
IIB-428	Bnzl	H	2-	Bnzl	0.83	432	C
			Cbx-Et
IIB-429	Bnzl	H	s-Bu	4-OH-Bnzl	0.88	432	C
IIB-430	Bnzl	H	1-Npm	4-OH-Bnzl	0.97	516	C
IIB-431	Bnzl	H	i-Pr	4-OH-Bnzl	0.84	418	C
IIB-432	Bnzl	H	s-Bu	2-Cbx-Et	0.79	398	C
IIB-433	Bnzl	H	i-Pr	2-Cbx-Et	0.74	384	C
IIB-434	4-OH-Bnzl	H	i-Pr	Bnzl	0.85	418	C
IIB-435	4-OH-Bnzl	H	i-Pr	2-Cbx-Et	0.68	400	C
IIB-436	4-OH-Bnzl	H	i-Pr	1-Npm	0.90	468	C
IIB-437	2-Cbx-Et	H	i-Bu	Bnzl	0.82	398	C
IIB-438	2-Cbx-Et	H	Bnzl	Bnzl	0.84	432	C
IIB-439	2-Cbx-Et	H	4-	Bnzl	0.76	448	C
			OH-Bnzl
IIB-440	2-Cbx-Et	H	s-Bu	Bnzl	0.81	398	C
IIB-441	2-Cbx-Et	H	1-Npm	Bnzl	0.91	482	C
IIB-442	2-Cbx-Et	H	i-Bu	4-OH-Bnzl	0.76	414	C

TABLE 1-17
IIB-443	2-Cbx-Et	H	Bnzl	4-OH-Bnzl	0.78	448	C
IIB-444	2-Cbx-Et	H	s-Bu	4-OH-Bnzl	0.75	414	C
IIB-445	2-Cbx-Et	H	1-Npm	4-OH-Bnzl	0.86	498	C
IIB-446	2-Cbx-Et	H	i-Pr	4-OH-Bnzl	0.71	400	C
IIB-447	2-Cbx-Et	H	i-Bu	1-Npm	0.88	448	C
IIB-448	2-Cbx-Et	H	4-OH-Bnzl	1-Npm	0.83	498	C
IIB-449	2-Cbx-Et	H	s-Bu	1-Npm	0.87	448	C
IIB-450	2-Cbx-Et	H	1-Npm	1-Npm	0.96	532	C
IIB-451	1-Npm	H	4-OH-Bnzl	Bnzl	0.95	516	C
IIB-452	1-Npm	H	Bnzl	4-OH-Bnzl	0.95	516	C
IIB-453	1-Npm	H	2-Cbx-Et	4-OH-Bnzl	0.80	498	C
IIB-454	1-Npm	H	s-Bu	4-OH-Bnzl	0.94	482	C
IIB-455	1-Npm	H	1-Npm	4-OH-Bnzl	1.01	566	C
IIB-456	1-Npm	H	i-Pr	4-OH-Bnzl	0.90	468	C
IIB-457	1-Npm	H	i-Bu	2-Cbx-Et	0.88	448	C
IIB-458	1-Npm	H	Bnzl	2-Cbx-Et	0.89	482	C
IIB-459	1-Npm	H	4-OH-Bnzl	2-Cbx-Et	0.81	498	C
IIB-460	1-Npm	H	s-Bu	2-Cbx-Et	0.88	448	C
IIB-461	1-Npm	H	1-Npm	2-Cbx-Et	0.96	532	C
IIB-462	1-Npm	H	4-OH-Bnzl	1-Npm	0.97, 1.00	566	C
*
IIB-463	1-Npm	H	2-Cbx-Et	1-Npm	0.93, 0.95	532	C
*
IIB-464	i-Bu	H	4-OH-Bnzl	i-Bu	0.86	398	C
IIB-465	i-Bu	H	2-Cbx-Et	i-Bu	0.78	364	C
IIB-466	i-Bu	H	1-Npm	3-Gun-Pr	0.78	475	C
IIB-467	Bnzl	H	i-Bu	3-Gun-Pr	0.69	425	C
IIB-468	2-Cbx-Et	H	i-Bu	i-Bu	0.81	364	C
IIB-469	2-Cbx-Et	H	Bnzl	i-Bu	0.83	398	C
IIB-470	2-Cbx-Et	H	4-OH-Bnzl	i-Bu	0.75	414	C
IIB-471	2-Cbx-Et	H	s-Bu	i-Bu	0.81	364	C
IIB-472	2-Cbx-Et	H	1-Npm	i-Bu	0.91	448	C
IIB-473	2-Cbx-Et	H	i-Pr	i-Bu	0.76	350	C
IIB-474	2-Cbx-Et	H	Bnzl	1-Npm	0.89	482	C
IIB-475	2-Cbx-Et	H	i-Pr	1-Npm	0.84	434	C
IIB-476	1-Npm	H	3-Gun-Pr	Bnzl	0.78	509	C
IIB-477	1-Npm	H	i-Bu	4-OH-Bnzl	0.94	482	C
IIB-478	1-Npm	H	i-Pr	2-Cbx-Et	0.83	434	C
IIB-479	1-Npm	H	1-Npm	3-Gun-Pr	0.84	559	C
IIB-480	1-Npm	H	i-Pr	3-Gun-Pr	0.72	461	C
IIB-481	1-Npm	H	3-Gun-Pr	1-Npm	0.83	559	C
IIB-482	i-Bu	H	3-Gun-Pr	i-Bu	0.69	391	C
IIB-483	i-Bu	H	3-Gun-Pr	Bnzl	0.70	425	C
IIB-484	i-Bu	H	i-Bu	3-Gun-Pr	0.68	391	C
IIB-485	i-Bu	H	Bnzl	3-Gun-Pr	0.71	425	C
IIB-486	i-Bu	H	s-Bu	3-Gun-Pr	0.67	391	C
IIB-487	i-Bu	H	i-Pr	3-Gun-Pr	0.63	377	C
IIB-488	i-Bu	H	3-Gun-Pr	1-Npm	0.76	475	C
IIB-489	Bnzl	H	3-Gun-Pr	i-Bu	0.71	425	C
IIB-490	Bnzl	H	3-Gun-Pr	Bnzl	0.73	459	C
IIB-491	Bnzl	H	Bnzl	3-Gun-Pr	0.71	459	C
IIB-492	Bnzl	H	s-Bu	3-Gun-Pr	0.68	425	C

TABLE 1-18
IIB-493	Bnzl	H	i-Pr	3-Gun-Pr	0.64	411	C
IIB-494	Bnzl	H	3-Gun-Pr	1-Npm	0.78	509	C
IIB-495	2-Cbx-Et	H	i-Pr	Bnzl	0.77	384	C
IIB-496	3-Gun-Pr	H	1-Npm	i-Bu	0.79	475	C
IIB-497	3-Gun-Pr	H	i-Pr	i-Bu	0.66	377	C
IIB-498	3-Gun-Pr	H	1-Npm	Bnzl	0.79	509	C
IIB-499	3-Gun-Pr	H	i-Pr	Bnzl	0.66, 0.67	411	C
IIB-500	3-Gun-Pr	H	1-Npm	1-Npm	0.82	559	C
IIB-501	3-Gun-Pr	H	i-Pr	1-Npm	0.71, 0.74	461	C
*
IIB-502	1-Npm	H	3-Gun-Pr	i-Bu	0.77	475	C
IIB-503	3-	H	4-F-	1-Npm	1.05	542	C
	tertbutoxy-		Bnzl
	propyl
IIB-504	3-	H	4-F-	1-Npm	0.9	486	C
	hydroxy-		Bnzl
	propyl
IIB-505	Hdr-E	H	4-Cl-	1-Npm	0.93	488	C
			Bnzl
IIB-506	3-	H	3-	3-	1.06	751	C
	aminopropyl		amino-	amino-
			propy	propyl
IIB-507	1-Npm	H	β-	Ph-Et	0.98	544	C
			hydroxy-
			phenethy
IIB-508	1-Npm	H	α-	Ph-Et	0.97	558	C
			(hydroxy-
			methyl)-
			phenethyl
IIB-509	1-Npm	H	α-	Ph-Et	1.00	558	C
			(hydroxy-
			methyl)-
			phenethyl
IIB-510	4-Nt-Bnzl	H	Bnzl	tBOC-E	0.96	533	C
IIB-511	2-OH-Et	H	Ph-Et	1-Npm	0.89	468.3	C
IIB-512	Chm	H	2-OH-	1-Npm	0.86	460.3	C
			Et
IIB-513	i-Bu	H	i-Pr	3-Gun-Pr	0.58	377.3	C
IIB-514	Bnzl	H	4-OH-	i-Bu	0.81	432.2	C
			Bnzl
IIB-515	Bnzl	H	i-Bu	4-OH-Bnzl	0.81	432.2	C
IIB-516	i-Bu	H	Bnzl	4-OH-Bnzl	0.81	432.3	C
IIB-517	i-Bu	H	4-OH-	Bnzl	0.81	432.3	C
			Bnzl
IIB-518	2-OH-Et	H	Bnzl	1-Npm	0.87	454.3	C
IIB-519	Ph-Et	H	1-Npm	Hxy	1.10	508.4	C
IIB-520	1-Npm	H	Ph-Et	Hxy	1.10	508.4	C
IIB-521	Hxy	H	Ph-Et	1-Npm	1.08	508.4	C
IIB-522	Hxy	H	1-Npm	Ph-Et	1.09	508.4	C
IIB-523	i-Pnt	H	i-Pr	i-Bu	3.52	348	F
IIB-524	Chm	H	i-Pr	i-Bu	3.94	374	F
IIB-525	Chm	H	i-Pr	i-Pnt	4.35	388	F
IIB-526	i-Bu	H	s-Bu	i-Pnt	3.95	362	F
IIB-527	i-Pnt	H	s-Bu	i-Bu	3.75	362	F
IIB-528	i-Pnt	H	s-Bu	Ph-Et	4.29	410	F
IIB-529	Chm	H	s-Bu	i-Bu	4.22	388	F
IIB-530	Chm	H	s-Bu	Ph-Et	4.32	436	F
IIB-531	Chm	H	s-Bu	i-Pnt	4.52	402	F
IIB-532	Chm	H	i-Pnt	i-Bu	4.7	402	F
IIB-533	i-Pnt	H	Hxy	i-Bu	4.55	390	F
IIB-534	2-Cbx-Et	H	Bnzl	2-OH-Et	2.27	386	F
IIB-535	2-Cbx-Et	H	Bnzl	i-Pnt	3.49	412	F
IIB-536	Ph-Et	H	Bnzl	2-Cbx-Et	3.02	446	F
IIB-537	4-F-Bnzl	H	Bnzl	2-Cbx-Et	3.13	450	F

TABLE 1-19
IIB-538	2-OH-Et	H	Bnzl	2-Cbx-Et	2.52	386	F
IIB-539	i-Pnt	H	Bnzl	2-Cbx-Et	3.15	412	F
IIB-540	i-Pnt	H	Bnzl	2-OH-Et	3.07	384	F
IIB-541	Chm	H	Bnzl	2-Cbx-Et	3.42	438	F
IIB-542	2-Cbx-Et	H	i-Bu	Ph-Et	3.3	412	F
IIB-543	2-Cbx-Et	H	i-Bu	i-Pnt	3.29	378	F
IIB-544	Ph-Et	H	i-Bu	2-Cbx-Et	3.13	412	F
IIB-545	4-F-Bnzl	H	i-Bu	2-Cbx-Et	2.98	416	F
IIB-546	2-OH-Et	H	i-Bu	2-Cbx-Et	3.57	352	G
IIB-547	i-Pnt	H	i-Bu	4-OH-Bnzl	3.38	412	F
IIB-548	i-Pnt	H	i-Bu	2-Cbx-Et	2.99	378	F
IIB-549	Chm	H	i-Bu	4-OH-Bnzl	3.63	438	F
IIB-550	Chm	H	i-Bu	2-Cbx-Et	3.29	404	F
IIB-551	2-Cbx-Et	H	1-Npm	Ph-Et	3.84	496	F
IIB-552	2-Cbx-Et	H	1-Npm	2-OH-Et	2.82	436	F
IIB-553	2-Cbx-Et	H	1-Npm	i-Pnt	3.92	462	F
IIB-554	Ph-Et	H	1-Npm	2-Cbx-Et	3.72	496	F
IIB-555	4-F-Bnzl	H	1-Npm	2-Cbx-Et	3.62	500	F
IIB-556	2-OH-Et	H	1-Npm	2-Cbx-Et	2.95	436	F
IIB-557	i-Pnt	H	1-Npm	2-Cbx-Et	3.65	462	F
IIB-558	Chm	H	1-Npm	2-Cbx-Et	3.94	488	F
IIB-559	4-OH-Bnzl	H	i-Pr	Ph-Et	3.3	432	F
IIB-560	4-OH-Bnzl	H	i-Pr	i-Pnt	3.1	398	F
IIB-561	2-Cbx-Et	H	i-Pr	Ph-Et	3.04	398	F
IIB-562	2-Cbx-Et	H	i-Pr	2-OH-Et	2.82	338	G
IIB-563	2-Cbx-Et	H	i-Pr	i-Pnt	3	364	F
IIB-564	Ph-Et	H	i-Pr	2-Cbx-Et	2.87	398	F
IIB-565	Ph-Et	H	i-Pr	2-OH-Et	2.82	370	F
IIB-566	4-F-Bnzl	H	i-Pr	2-OH-Et	2.77	374	F
IIB-567	2-OH-Et	H	i-Pr	Bnzl	2.77	356	F
IIB-568	2-OH-Et	H	i-Pr	1-Npm	3.24	406	F
IIB-569	2-OH-Et	H	i-Pr	4-OH-Bnzl	2.52	372	F
IIB-570	2-OH-Et	H	i-Pr	2-Cbx-Et	3.09	338	G
IIB-571	2-OH-Et	H	i-Pr	Ph-Et	3.02	370	F
IIB-572	i-Pnt	H	i-Pr	4-OH-Bnzl	3.04	398	F
IIB-573	i-Pnt	H	i-Pr	2-Cbx-Et	2.69	364	F
IIB-574	i-Pnt	H	i-Pr	2-OH-Et	2.65	336	F
IIB-575	Chm	H	i-Pr	4-OH-Bnzl	3.34	424	F
IIB-576	Chm	H	i-Pr	2-Cbx-Et	2.94	390	F
IIB-577	i-Bu	H	s-Bu	2-OH-Et	2.62	336	F
IIB-578	4-OH-Bnzl	H	s-Bu	Ph-Et	3.50	446	F
IIB-579	4-OH-Bnzl	H	s-Bu	i-Pnt	3.38	412	F
IIB-580	2-Cbx-Et	H	s-Bu	Ph-Et	3.22	412	F
IIB-581	2-Cbx-Et	H	s-Bu	i-Pnt	3.27	378	F
IIB-582	Ph-Et	H	s-Bu	2-Cbx-Et	3.10	412	F
IIB-583	4-F-Bnzl	H	s-Bu	2-Cbx-Et	2.88	416	F
IIB-584	2-OH-Et	H	s-Bu	4-OH-Bnzl	2.69	386	F
IIB-585	2-OH-Et	H	s-Bu	2-Cbx-Et	3.47	352	G
IIB-586	2-OH-Et	H	s-Bu	i-Pnt	3.24	350	F
IIB-587	i-Pnt	H	s-Bu	4-OH-Bnzl	3.34	412	F

TABLE 1-20
IIB-588	i-Pnt	H	s-Bu	2-Cbx-Et	2.90	378	F
IIB-589	i-Pnt	H	s-Bu	2-OH-Et	2.90	350	F
IIB-590	Chm	H	s-Bu	4-OH-Bnzl	3.62	438	F
IIB-591	Chm	H	s-Bu	2-Cbx-Et	3.24	404	F
IIB-592	i-Bu	H	4-OH-	i-Pnt	3.52	412	F
			Bnzl
IIB-593	2-Cbx-Et	H	4-OH-	Ph-Et	3.04	462	F
			Bnzl
IIB-594	2-Cbx-Et	H	4-OH-	i-Pnt	2.92	428	F
			Bnzl
IIB-595	Ph-Et	H	4-OH-	2-Cbx-Et	2.85	462	F
			Bnzl
IIB-596	4-F-Bnzl	H	4-OH-	2-Cbx-Et	2.77	466	F
			Bnzl
IIB-597	2-OH-Et	H	4-OH-	2-Cbx-Et	3.24	402	G
			Bnzl
IIB-598	i-Pnt	H	4-OH-	2-Cbx-Et	2.72	428	F
			Bnzl
IIB-599	Chm	H	4-OH-	2-Cbx-Et	2.97	454	F
			Bnzl
IIB-600	i-Bu	H	2-	Ph-Et	3.12	412	F
			Cbx-Et
IIB-601	i-Bu	H	2-	i-Pnt	3.12	378	F
			Cbx-Et
IIB-602	2-OH-Et	H	2-	i-Bu	3.5	352	G
			Cbx-Et
IIB-603	i-Pnt	H	2-	i-Bu	3.04	378	F
			Cbx-Et
IIB-604	i-Pnt	H	2-	4-OH-Bnzl	2.63	428	F
			Cbx-Et
IIB-605	Chm	H	2-	i-Bu	3.34	404	F
			Cbx-Et
IIB-606	Chm	H	2-	4-OH-Bnzl	2.85	454	F
			Cbx-Et
IIB-607	Chm	H	2-	i-Pnt	3.59	418	F
			Cbx-Et
IIB-608	Bnzl	H	4-F-	4-OH-Bnzl	3.63	484	F
			Bnzl
IIB-609	Bnzl	H	4-F-	2-Cbx-Et	3.12	450	F
			Bnzl
IIB-610	i-Bu	H	4-F-	4-OH-Bnzl	3.44	450	F
			Bnzl
IIB-611	i-Bu	H	4-F-	2-Cbx-Et	3.02	416	F
			Bnzl
IIB-612	1-Npm	H	4-F-	4-OH-Bnzl	3.99	534	F
			Bnzl
IIB-613	1-Npm	H	4-F-	2-Cbx-Et	3.57	500	F
			Bnzl
IIB-614	4-OH-Bnzl	H	4-F-	2-Cbx-Et	2.85	466	F
			Bnzl
IIB-615	4-OH-Bnzl	H	4-F-	Ph-Et	3.63	498	F
			Bnzl
IIB-616	4-OH-Bnzl	H	4-F-	i-Pnt	3.57	464	F
			Bnzl
IIB-617	2-Cbx-Et	H	4-F-	4-OH-Bnzl	2.95	466	F
			Bnzl
IIB-618	2-Cbx-Et	H	4-F-	Ph-Et	3.48	464	F
			Bnzl
IIB-619	2-Cbx-Et	H	4-F-	i-Pnt	3.42	430	F
			Bnzl
IIB-620	Ph-Et	H	4-F-	4-OH-Bnzl	3.67	498	F
			Bnzl
IIB-621	Ph-Et	H	4-F-	2-Cbx-Et	3.32	464	F
			Bnzl
IIB-622	2-OH-Et	H	4-F-	4-OH-Bnzl	2.95	438	F
			Bnzl
IIB-623	2-OH-Et	H	4-F-	2-Cbx-Et	2.57	404	F
			Bnzl
IIB-624	i-Pnt	H	4-F-	4-OH-Bnzl	3.54	464	F
			Bnzl
IIB-625	i-Pnt	H	4-F-	2-Cbx-Et	3.19	430	F
			Bnzl
IIB-626	Chm	H	4-F-	4-OH-Bnzl	3.80	490	F
			Bnzl
IIB-627	Chm	H	4-F-	2-Cbx-Et	3.45	456	F
			Bnzl
IIB-628	i-Bu	H	i-Pnt	2-Cbx-Et	3.05	378	F
IIB-629	4-OH-Bnzl	H	i-Pnt	2-Cbx-Et	2.80	428	F
IIB-630	2-Cbx-Et	H	i-Pnt	i-Bu	3.25	378	F
IIB-631	2-Cbx-Et	H	i-Pnt	4-OH-Bnzl	2.90	428	F
IIB-632	2-OH-Et	H	i-Pnt	i-Bu	3.20	350	F
IIB-633	2-OH-Et	H	i-Pnt	2-Cbx-Et	2.59	366	F
IIB-634	Chm	H	i-Pnt	2-Cbx-Et	3.54	418	F
IIB-635	i-Bu	H	2-OH-	i-Bu	2.69	336	F
			Et
IIB-636	i-Bu	H	2-OH-	4-OH-Bnzl	2.35	386	F
			Et
IIB-637	1-Npm	H	2-OH-	4-OH-Bnzl	2.94	470	F
			Et

TABLE 1-21
IIB-638	1-Npm	H	2-OH—Et	2-Cbx-Et	2.63	436	F
IIB-639	4-OH-Bnzl	H	2-OH—Et	Bnzl	2.67	420	F
IIB-640	4-OH-Bnzl	H	2-OH—Et	1-Npm	3.04	470	F
IIB-641	4-OH-Bnzl	H	2-OH—Et	Ph—Et	2.75	434	F
IIB-642	4-OH-Bnzl	H	2-OH—Et	i-Pnt	2.60	400	F
IIB-643	2-Cbx-Et	H	2-OH—Et	Bnzl	3.60	386	F
IIB-644	2-Cbx-Et	H	2-OH—Et	i-Bu	3.40	352	F
IIB-645	2-Cbx-Et	H	2-OH—Et	1-Npm	2.84	436	F
IIB-646	2-Cbx-Et	H	2-OH—Et	Ph—Et	2.57	400	F
IIB-647	2-Cbx-Et	H	2-OH—Et	i-Pnt	2.52	366	F
IIB-648	Ph—Et	H	2-OH—Et	2-Cbx-Et	2.37	400	F
IIB-649	4-F-Bnzl	H	2-OH—Et	2-Cbx-Et	2.12	404	F
IIB-650	i-Pnt	H	2-OH—Et	i-Bu	2.94	350	F
IIB-651	i-Pnt	H	2-OH—Et	2-Cbx-Et	3.34	366	F
IIB-652	Chm	H	2-OH—Et	1-Bu	3.17	376	F
IIB-653	Chm	H	2-OH—Et	2-Cbx-Et	2.47	392	F
IIB-654	Bnzl	H	Ph—Et	4-OH-Bnzl	3.69	480	F
IIB-655	Bnzl	H	Ph—Et	2-Cbx-Et	3.15	446	F
IIB-656	i-Bu	H	Ph—Et	4-OH-Bnzl	3.47	446	F
IIB-657	i-Bu	H	Ph—Et	2-Cbx-Et	3.05	412	F
IIB-658	1-Npm	H	Ph—Et	4-OH-Bnzl	4.02	530	F
IIB-659	1-Npm	H	Ph—Et	2-Cbx-Et	3.62	496	F
IIB-660	4-OH-Bnzl	H	Ph—Et	2-Cbx-Et	2.85	462	F
IIB-661	4-OH-Bnzl	H	Ph—Et	i-Pnt	3.74	460	F
IIB-662	2-Cbx-Et	H	Ph—Et	4-OH-Bnzl	3.02	462	F
IIB-663	2-Cbx-Et	H	Ph—Et	i-Pnt	3.55	426	F
IIB-664	4-F-Bnzl	H	Ph—Et	4-OH-Bnzl	3.69	498	F
IIB-665	4-F-Bnzl	H	Ph—Et	2-Cbx-Et	3.22	464	F
IIB-666	2-OH—Et	H	Ph—Et	4-OH-Bnzl	2.99	434	F
IIB-667	2-OH—Et	H	Ph—Et	2-Cbx-Et	2.62	400	F
IIB-668	i-Pnt	H	Ph—Et	4-OH-Bnzl	3.63	460	F
IIB-669	i-Pnt	H	Ph—Et	2-Cbx-Et	3.27	426	F
IIB-670	Chm	H	Ph—Et	4-OH-Bnzl	3.92	486	F
IIB-671	Chm	H	Ph—Et	2-Cbx-Et	3.55	452	F
IIB-672	Bnzl	H	Hxy	2-Cbx-Et	3.54	426	F
IIB-673	i-Bu	H	Hxy	2-Cbx-Et	3.42	392	F
IIB-674	1-Npm	H	Hxy	2-Cbx-Et	4	476	F
IIB-675	4-OH-Bnzl	H	Hxy	2-Cbx-Et	3.17	442	F
IIB-676	2-Cbx-Et	H	Hxy	i-Bu	3.54	392	F
IIB-677	2-Cbx-Et	H	Hxy	4-OH-Bnzl	3.25	442	F
IIB-678	2-Cbx-Et	H	Hxy	i-Pnt	3.84	406	F
IIB-679	Ph—Et	H	Hxy	2-Cbx-Et	3.75	440	F
IIB-680	4-F-Bnzl	H	Hxy	2-Cbx-Et	3.6	444	F
IIB-681	2-OH—Et	H	Hxy	i-Bu	3.6	364	F
IIB-682	2-OH—Et	H	Hxy	4-OH-Bnzl	3.29	414	F
IIB-683	2-OH—Et	H	Hxy	2-Cbx-Et	2.88	380	F
IIB-684	2-OH—Et	H	Hxy	i-Pnt	3.87	378	F
IIB-685	i-Pnt	H	Hxy	4-OH-Bnzl	3.98	440	F
IIB-686	i-Pnt	H	Hxy	2-Cbx-Et	3.59	406	F
IIB-687	i-Pnt	H	Hxy	2-OH—Et	3.52	378	F

TABLE 1-22
IIB-688	Chm	H	Hxy	4-OH-Bnzl	4.24	466	F
IIB-689	Chm	H	Hxy	2-Cbx-Et	3.88	432	F
IIB-690	tBOC-E	H	Bnzl	i-Pnt	4.47	468	F
IIB-691	Ph—Et	H	Bnzl	tBOC-E	4.34	502	F
IIB-692	4-F-Bnzl	H	Bnzl	tBOC-E	4.09	506	F
IIB-693	2-OtBu—Et	H	Bnzl	tBOC-E	4.27	498	F
IIB-694	i-Pnt	H	Bnzl	tBOC-E	4.25	468	F
IIB-695	Chm	H	Bnzl	tBOC-E	4.5	494	F
IIB-696	tBOC-E	H	i-Bu	Ph—Et	4.25	468	F
IIB-697	tBOC-E	H	i-Bu	i-Pnt	4.3	434	F
IIB-698	Ph—Et	H	i-Bu	tBOC-E	4.18	468	F
IIB-699	2-OtBu—Et	H	i-Bu	tBOC-E	4.09	464	F
IIB-700	i-Pnt	H	i-Bu	4-tBuO-	4.43	468	F
				Bnzl
IIB-701	i-Pnt	H	i-Bu	tBOC-E	3.97	434	F
IIB-702	Chm	H	i-Bu	4-tBuO-	4.67	494	F
				Bnzl
IIB-703	Chm	H	i-Bu	tBOC-E	4.43	460	F
IIB-704	tBOC-E	H	1-Npm	Ph—Et	4.78	552	F
IIB-705	tBOC-E	H	1-Npm	i-Pnt	4.89	518	F
IIB-706	Ph—Et	H	1-Npm	tBOC-E	4.72	552	F
IIB-707	4-F-Bnzl	H	1-Npm	tBOC-E	4.52	556	F
IIB-708	2-OtBu—Et	H	1-Npm	tBOC-E	5.37	548	F
IIB-709	i-Pnt	H	1-Npm	tBOC-E	4.68	518	F
IIB-710	Chm	H	1-Npm	tBOC-E	4.9	544	F
IIB-711	4-tBuO-Bnzl	H	i-Pr	Ph—Et	4.29	488	F
IIB-712	tBOC-E	H	i-Pr	Ph—Et	3.92	454	F
IIB-713	tBOC-E	H	i-Pr	i-Pnt	4	420	F
IIB-714	Ph—Et	H	i-Pr	tBOC-E	3.92	454	F
IIB-715	2-OtBu—Et	H	i-Pr	Bnzl	3.77	412	F
IIB-716	2-OtBu—Et	H	i-Pr	1-Npm	4.24	462	F
IIB-717	2-OtBu—Et	H	i-Pr	4-tBuO-	4.37	484	F
				Bnzl
IIB-718	2-OtBu—Et	H	i-Pr	tBOC-E	3.94	450	F
IIB-719	2-OtBu—Et	H	i-Pr	i-Pnt	4.04	392	F
IIB-720	i-Pnt	H	i-Pr	4-tBuO-	4.22	454	F
				Bnzl
IIB-721	i-Pnt	H	i-Pr	tBOC-E	4.82	420	F
IIB-722	Chm	H	i-Pr	4-tBuO-	4.57	480	F
				Bnzl
IIB-723	4-tBuO-Bnzl	H	s-Bu	Ph—Et	4.5	502	F
IIB-724	4-tBuO-Bnzl	H	s-Bu	i-Pnt	4.62	468	F
IIB-725	tBOC-E	H	s-Bu	Ph—Et	4.29	468	F
IIB-726	tBOC-E	H	s-Bu	i-Pnt	4.3	434	F
IIB-727	Ph—Et	H	s-Bu	tBOC-E	4.14	468	F
IIB-728	4-F-Bnzl	H	s-Bu	tBOC-E	4.52	472	F
IIB-729	2-OtBu—Et	H	s-Bu	4-tBuO-	4.68	498	F
				Bnzl
IIB-730	2-OtBu—Et	H	s-Bu	tBOC-E	4.17	464	F
IIB-731	i-Pnt	H	s-Bu	4-tBuO-	4.74	468	F
				Bnzl
IIB-732	i-Pnt	H	s-Bu	tBOC-E	4.27	434	F
IIB-733	Chm	H	s-Bu	4-tBuO-	4.74	494	F
				Bnzl
IIB-734	i-Bu	H	4-tBuO-	i-Pnt	4.57	468	F
			Bnzl
IIB-735	tBOC-E	H	4-tBuO-	Ph—Et	5.2	574	F
			Bnzl
IIB-736	tBOC-E	H	4-tBuO-	i-Pnt	4.6	540	F
			Bnzl
IIB-737	Ph—Et	H	4-tBuO-	tBOC-E	4.59	574	F
			Bnzl

TABLE 1-23
IIB-738	4-F-Bnzl	H	4-tBuO-	tBOC-E	4.5	578	F
			Bnzl
IIB-739	2-OtBu—Et	H	4-tBuO-	tBOC-E	4.79	570	F
			Bnzl
IIB-740	i-Pnt	H	4-tBuO-	tBOC-E	4.8	540	F
			Bnzl
IIB-741	Chm	H	4-tBuO-	tBOC-E	4.99	566	F
			Bnzl
IIB-742	i-Bu	H	tBOC-	Ph—Et	4.12	468	F
			E
IIB-743	i-Bu	H	tBOC-	i-Pnt	4.18	434	F
			E
IIB-744	2-OtBu—Et	H	tBOC-	i-Bu	4.1	464	F
			E
IIB-745	i-Pnt	H	tBOC-	i-Bu	4.17	434	F
			E
IIB-746	Chm	H	tBOC-	4-tBuO-	4.95	566	F
			E	Bnzl
IIB-747	Chm	H	tBOC-	i-Pnt	4.55	474	F
			E
IIB-748	Bnzl	H	4-F-	4-tBuO-	4.54	540	F
			Bnzl	Bnzl
IIB-749	Bnzl	H	4-F-	tBOC-E	4.05	506	F
			Bnzl
IIB-750	i-Bu	H	4-F-	4-tBuO-	4.39	506	F
			Bnzl	Bnzl
IIB-751	i-Bu	H	4-F-	tBOC-E	3.97	472	F
			Bnzl
IIB-752	1-Npm	H	4-F-	4-tBuO-	4.92	590	F
			Bnzl	Bnzl
IIB-753	1-Npm	H	4-F-	tBOC-E	4.57	556	F
			Bnzl
IIB-754	4-tBuO-Bnzl	H	4-F-	tBOC-E	4.62	578	F
			Bnzl
IIB-755	4-tBuO-Bnzl	H	4-F-	Ph—Et	4.6	554	F
			Bnzl
IIB-756	4-tBuO-Bnzl	H	4-F-	i-Pnt	4.47	520	F
			Bnzl
IIB-757	tBOC-E	H	4-F-	4-tBuO-	4.74	578	F
			Bnzl	Bnzl
IIB-758	tBOC-E	H	4-F-	Ph—Et	4.24	520	F
			Bnzl
IIB-759	tBOC-E	H	4-F-	i-Pnt	4.4	486	F
			Bnzl
IIB-760	Ph—Et	H	4-F-	4-tBuO-	4.59	554	F
			Bnzl	Bnzl
IIB-761	Ph—Et	H	4-F-	tBOC-E	4.4	520	F
			Bnzl
IIB-762	2-OtBu—Et	H	4-F-	4-tBuO-	4.72	550	F
			Bnzl	Bnzl
IIB-763	2-OtBu—Et	H	4-F-	tBOC-E	4.3	516	F
			Bnzl
IIB-764	i-Pnt	H	4-F-	4-tBuO-	4.57	520	F
			Bnzl	Bnzl
IIB-765	i-Pnt	H	4-F-	tBOC-E	4.22	486	F
			Bnzl
IIB-766	Chm	H	4-F-	4-tBuO-	4.89	546	F
			Bnzl	Bnzl
IIB-767	Chm	H	4-F-	tBOC-E	4.39	512	F
			Bnzl
IIB-768	i-Bu	H	i-Pnt	tBOC-E	4	434	F
IIB-769	4-tBuO-Bnzl	H	i-Pnt	tBOC-E	4.77	540	F
IIB-770	tBOC-E	H	i-Pnt	i-Bu	4.37	434	F
IIB-771	tBOC-E	H	i-Pnt	4-tBuO-	4.79	540	F
				Bnzl
IIB-772	2-OtBu—Et	H	i-Pnt	i-Bu	4.5	406	F
IIB-773	2-OtBu—Et	H	i-Pnt	tBOC-E	4.67	478	F
IIB-774	i-Bu	H	2-	i-Bu	3.49	392	F
			OtBu—Et
IIB-775	i-Bu	H	2-	4-tBuO-	4.34	498	F
			OtBu—Et	Bnzl
IIB-776	i-Bu	H	2-	tBOC-E	3.74	464	F
			OtBu—Et
IIB-777	1-Npm	H	2-	4-tBuO-	4.75	582	F
			OtBu—Et	Bnzl
IIB-778	1-Npm	H	2-	tBOC-E	4.42	548	F
			OtBu—Et
IIB-779	4-tBuO-Bnzl	H	2-	Bnzl	4.42	532	F
			OtBu—Et
IIB-780	4-tBuO-Bnzl	H	2-	1-Npm	4.82	582	F
			OtBu—Et
IIB-781	4-tBuO-Bnzl	H	2-	tBOC-E	4.4	570	F
			OtBu—Et
IIB-782	4-tBuO-Bnzl	H	2-	i-Pnt	4.64	512	F
			OtBu—Et
IIB-783	tBOC-E	H	2-	Bnzl	3.99	498	F
			OtBu—Et
IIB-784	tBOC-E	H	2-	i-Bu	4.15	464	F
			OtBu—Et
IIB-785	tBOC-E	H	2-	4-tBuO-	4.54	570	F
			OtBu—Et	Bnzl
IIB-786	tBOC-E	H	2-	i-Pnt	4.22	478	F
			OtBu—Et
IIB-787	Ph—Et	H	2-	tBOC-E	4.04	512	F
			OtBu—Et

TABLE 1-24
IIB-788	Chm	H	2-	i-Bu	4.12	432	F
			OtBu—Et
IIB-789	Chm	H	2-	tBOC-E	4.32	504	F
			OtBu—Et
IIB-790	Bnzl	H	Ph—Et	4-tBuO-	4.62	536	F
				Bnzl
IIB-791	Bnzl	H	Ph—Et	tBOC-E	4.15	502	F
IIB-792	i-Bu	H	Ph—Et	4-tBuO-	4.47	502	F
				Bnzl
IIB-793	i-Bu	H	Ph—Et	tBOC-E	4.09	468	F
IIB-794	1-Npm	H	Ph—Et	4-tBuO-	4.95	586	F
				Bnzl
IIB-795	1-Npm	H	Ph—Et	tBOC-E	4.62	552	F
IIB-796	4-tBuO-Bnzl	H	Ph—Et	tBOC-E	4.72	574	F
IIB-797	4-tBuO-Bnzl	H	Ph—Et	i-Pnt	4.74	516	F
IIB-798	tBOC-E	H	Ph—Et	i-Pnt	4.65	482	F
IIB-799	4-F-Bnzl	H	Ph—Et	4-tBuO-	4.67	554	F
				Bnzl
IIB-800	4-F-Bnzl	H	Ph—Et	tBOC-E	4.24	520	F
IIB-801	2-OtBu—Et	H	Ph—Et	4-tBuO-	4.8	546	F
				Bnzl
IIB-802	2-OtBu—Et	H	Ph—Et	tBOC-E	4.3	512	F
IIB-803	i-Pnt	H	Ph—Et	4-tBuO-	4.67	516	F
				Bnzl
IIB-804	i-Pnt	H	Ph—Et	tBOC-E	4.34	482	F
IIB-805	Chm	H	Ph—Et	4-tBuO-	4.93	542	F
				Bnzl
IIB-806	Chm	H	Ph—Et	tBOC-E	4.6	508	F
IIB-807	Bnzl	H	Hxy	tBOC-E	4.49	482	F
IIB-808	1-Npm	H	Hxy	tBOC-E	5	532	F
IIB-809	4-tBuO-Bnzl	H	Hxy	1-Npm	5.37	566	F
IIB-810	4-tBuO-Bnzl	H	Hxy	tBOC-E	5.05	554	F
IIB-811	tBOC-E	H	Hxy	i-Bu	4.75	448	F
IIB-812	tBOC-E	H	Hxy	1-Npm	4.92	532	F
IIB-813	tBOC-E	H	Hxy	4-tBuO-	5.04	554	F
				Bnzl
IIB-814	tBOC-E	H	Hxy	i-Pnt	5	462	F
IIB-815	Ph—Et	H	Hxy	tBOC-E	4.72	496	F
IIB-816	4-F-Bnzl	H	Hxy	tBOC-E	4.6	500	F
IIB-817	2-	H	Hxy	4-tBuO-	5.17	526	F
	OtBu—Et			Bnzl
IIB-818	2-	H	Hxy	tBOC-E	4.87	492	F
	OtBu—Et
IIB-819	2-	H	Hxy	i-Pnt	4.95	434	F
	OtBu—Et
IIB-820	i-Pnt	H	Hxy	4-tBuO-	5.05	496	F
				Bnzl
IIB-821	i-Pnt	H	Hxy	tBOC-E	4.7	462	F
IIB-822	Chm	H	Hxy	4-tBuO-	5.29	522	F
				Bnzl
IIB-823	i-Bu	H	i-Bu	Ph—Et	3.33	396	H
IIB-824	i-Bu	H	i-Bu	i-Pnt	3.17	362	H
IIB-825	1-Npm	H	i-Bu	i-Pnt	3.45	446	H
IIB-826	4-F-Bnzl	H	i-Bu	i-Bu	3.03	400	H
IIB-827	4-F-Bnzl	H	i-Bu	1-Npm	3.26	484	H
IIB-828	4-F-Bnzl	H	i-Bu	Ph—Et	3.15	448	H
IIB-829	4-F-Bnzl	H	i-Bu	i-Pnt	3.15	414	H
IIB-830	i-Pnt	H	i-Bu	i-Bu	3.13	362	H
IIB-831	i-Pnt	H	i-Bu	1-Npm	3.3	446	H
IIB-832	i-Pnt	H	i-Bu	Ph—Et	3.17	410	H
IIB-833	Chm	H	i-Bu	i-Bu	3.26	388	H
IIB-834	Chm	H	i-Bu	1-Npm	3.48	472	H
IIB-835	Chm	H	i-Bu	Ph—Et	3.32	436	H
IIB-836	Bnzl	H	Bnzl	Ph—Et	3.39	464	H
IIB-837	1-Npm	H	Bnzl	i-Pnt	3.37	480	H

TABLE 1-25
IIB-	Ph—Et	H	Bnzl	1-Npm	3.4	514	H
838
IIB-	Ph—Et	H	Bnzl	i-Pnt	3.26	444	H
839
IIB-	4-F-Bnzl	H	Bnzl	1-Npm	3.34	518	H
840
IIB-	4-F-Bnzl	H	Bnzl	Ph—Et	3.17	482	H
841
IIB-	4-F-Bnzl	H	Bnzl	i-Pnt	3.21	448	H
842
IIB-	i-Pnt	H	Bnzl	1-Npm	3.36	480	H
843
IIB-	Chm	H	Bnzl	1-Npm	3.47	506	H
844
IIB-	Chm	H	Bnzl	Ph—Et	3.33	470	H
845
IIB-	Chm	H	Bnzl	i-Pnt	3.37	436	H
846
IIB-	Bnzl	H	1-Npm	Ph—Et	3.39	514	H
847
IIB-	Bnzl	H	1-Npm	i-Pnt	3.44	480	H
848
IIB-	i-Bu	H	1-Npm	i-Pnt	3.3	446	H
849
IIB-	1-Npm	H	1-Npm	Ph—Et	3.56	564	H
850
IIB-	1-Npm	H	1-Npm	i-Pnt	3.59	530	H
851
IIB-	Ph—Et	H	1-Npm	Bnzl	3.41	514	H
852
IIB-	Ph—Et	H	1-Npm	i-Bu	3.38	480	H
853
IIB-	Ph—Et	H	1-Npm	1-Npm	3.53	564	H
854
IIB-	Ph—Et	H	1-Npm	i-Pnt	3.46	494	H
855
IIB-	4-F-Bnzl	H	1-Npm	1-Npm	3.48	568	H
856
IIB-	4-F-Bnzl	H	1-Npm	Ph—Et	3.39	532	H
857
IIB-	4-F-Bnzl	H	1-Npm	i-Pnt	3.4	498	H
858
IIB-	i-Pnt	H	1-Npm	i-Bu	3.42	446	H
859
IIB-	i-Pnt	H	1-Npm	1-Npm	3.51	530	H
860
IIB-	i-Pnt	H	1-Npm	Ph—Et	3.42	494	H
861
IIB-	Chm	H	1-Npm	Bnzl	3.58	506	H
862
IIB-	Chm	H	1-Npm	i-Bu	3.54	472	H
863
IIB-	Chm	H	1-Npm	1-Npm	3.67	556	H
864
IIB-	Chm	H	1-Npm	Ph—Et	3.57	520	H
865
IIB-	Chm	H	1-Npm	i-Pnt	3.59	486	H
866
IIB-	Bnzl	H	i-Pr	Ph—Et	3.16	416	H
867
IIB-	Bnzl	H	i-Pr	i-Pnt	3.17	382	H
868
IIB-	i-Bu	H	i-Pr	Ph—Et	3.12	382	H
869
IIB-	1-Npm	H	i-Pr	Ph—Et	3.34	466	H
870
IIB-	1-Npm	H	i-Pr	i-Pnt	3.38	432	H
871
IIB-	Ph—Et	H	i-Pr	Bnzl	3.15	416	H
872
IIB-	Ph—Et	H	i-Pr	i-Bu	3.12	382	H
873
IIB-	Ph—Et	H	i-Pr	1-Npm	3.34	466	H
874
IIB-	Ph—Et	H	i-Pr	i-Pnt	3.22	396	H
875
IIB-	4-F-Bnzl	H	i-Pr	Bnzl	3.11	420	H
876
IIB-	4-F-Bnzl	H	i-Pr	i-Bu	3.04	386	H
877
IIB-	4-F-Bnzl	H	i-Pr	1-Npm	3.28	470	H
878
IIB-	4-F-Bnzl	H	i-Pr	Ph—Et	3.13	434	H
879
IIB-	4-F-Bnzl	H	i-Pr	i-Pnt	3.11	400	H
880
IIB-	i-Pnt	H	i-Pr	Bnzl	3.08	382	H
881
IIB-	i-Pnt	H	i-Pr	1-Npm	3.31	432	H
882
IIB-	i-Pnt	H	i-Pr	Ph—Et	3.19	396	H
883
IIB-	Chm	H	i-Pr	Bnzl	3.27	408	H
884
IIB-	Chm	H	i-Pr	1-Npm	3.45	458	H
885
IIB-	Chm	H	i-Pr	Ph—Et	3.32	422	H
886
IIB-	Bnzl	H	s-Bu	Ph—Et	3.22	430	H
887

TABLE 1-26
IIB-	Bnzl	H	s-Bu	i-Pnt	3.25	396	H
888
IIB-	i-Bu	H	s-Bu	Ph—Et	3.19	396	H
889
IIB-	1-Npm	H	s-Bu	Ph—Et	3.41	480	H
890
IIB-	1-Npm	H	s-Bu	i-Pnt	3.42	446	H
891
IIB-	Ph—Et	H	s-Bu	Bnzl	3.24	430	H
892
IIB-	Ph—Et	H	s-Bu	i-Bu	3.22	396	H
893
IIB-	Ph—Et	H	s-Bu	1-Npm	3.39	480	H
894
IIB-	Ph—Et	H	s-Bu	i-Pnt	3.32	410	H
895
IIB-	4-F-Bnzl	H	s-Bu	Bnzl	3.25	434	H
896
IIB-	4-F-Bnzl	H	s-Bu	i-Bu	3.13	400	H
897
IIB-	4-F-Bnzl	H	s-Bu	1-Npm	3.35	484	H
898
IIB-	4-F-Bnzl	H	s-Bu	Ph—Et	3.23	448	H
899
IIB-	4-F-Bnzl	H	s-Bu	i-Pnt	3.25	414	H
900
IIB-	i-Pnt	H	s-Bu	Bnzl	3.23	396	H
901
IIB-	i-Pnt	H	s-Bu	1-Npm	3.39	446	H
902
IIB-	Chm	H	s-Bu	Bnzl	3.38	422	H
903
IIB-	Chm	H	s-Bu	1-Npm	3.51	472	H
904
IIB-	Bnzl	H	Ph—Et	Bnzl	3.24	464	H
905
IIB-	Bnzl	H	Ph—Et	1-Npm	3.43	514	H
906
IIB-	Bnzl	H	Ph—Et	i-Pnt	3.28	444	H
907
IIB-	i-Bu	H	Ph—Et	i-Bu	3.15	396	H
908
IIB-	i-Bu	H	Ph—Et	1-Npm	3.38	480	H
909
IIB-	i-Bu	H	Ph—Et	i-Pnt	4.41	410	H
910
IIB-	1-Npm	H	Ph—Et	Bnzl	3.47	514	H
911
IIB-	1-Npm	H	Ph—Et	i-Bu	3.43	480	H
912
IIB-	1-Npm	H	Ph—Et	1-Npm	3.58	564	H
913
IIB-	4-F-Bnzl	H	Ph—Et	Bnzl	3.23	482	H
914
IIB-	4-F-Bnzl	H	Ph—Et	i-Bu	3.17	448	H
915
IIB-	4-F-Bnzl	H	Ph—Et	1-Npm	3.38	532	H
916
IIB-	4-F-Bnzl	H	Ph—Et	i-Pnt	3.26	462	H
917
IIB-	i-Pnt	H	Ph—Et	i-Bu	3.24	410	H
918
IIB-	i-Pnt	H	Ph—Et	1-Npm	3.42	494	H
919
IIB-	Chm	H	Ph—Et	Bnzl	3.38	470	H
920
IIB-	Chm	H	Ph—Et	i-Bu	3.33	436	H
921
IIB-	Chm	H	Ph—Et	1-Npm	3.49	520	H
922
IIB-	Chm	H	Ph—Et	i-Pnt	3.45	450	H
923
IIB-	Bnzl	H	4-F-	Bnzl	3.2	468	H
924			Bnzl
IIB-	Bnzl	H	4-F-	1-Npm	3.34	518	H
925			Bnzl
IIB-	Bnzl	H	4-F-	Ph—Et	3.2	482	H
926			Bnzl
IIB-	Bnzl	H	4-F-	i-Pnt	3.23	448	H
927			Bnzl
IIB-	i-Bu	H	4-F-	i-Bu	3.13	400	H
928			Bnzl
IIB-	i-Bu	H	4-F-	1-Npm	3.32	484	H
929			Bnzl
IIB-	i-Bu	H	4-F-	i-Pnt	3.21	414	H
930			Bnzl
IIB-	1-Npm	H	4-F-	Bnzl	3.47	518	H
931			Bnzl
IIB-	1-Npm	H	4-F-	i-Bu	3.43	484	H
932			Bnzl
IIB-	1-Npm	H	4-F-	1-Npm	3.63	568	H
933			Bnzl
IIB-	1-Npm	H	4-F-	Ph—Et	3.48	532	H
934			Bnzl
IIB-	1-Npm	H	4-F-	i-Pnt	3.5	498	H
935			Bnzl
IIB-	Ph—Et	H	4-F-	Bnzl	3.28	482	H
936			Bnzl
IIB-	Ph—Et	H	4-F-	i-Bu	3.27	448	H
937			Bnzl

TABLE 1-27
IIB-	Ph—Et	H	4-F-	1-Npm	3.42	532	H
938			Bnzl
IIB-	Ph—Et	H	4-F-	i-Pnt	3.33	462	H
939			Bnzl
IIB-	i-Pnt	H	4-F-	1-Npm	3.33	498	H
940			Bnzl
IIB-	i-Pnt	H	4-F-	Ph—Et	3.28	462	H
941			Bnzl
IIB-	Chm	H	4-F-	Bnzl	3.31	474	H
942			Bnzl
IIB-	Chm	H	4-F-	i-Bu	3.29	440	H
943			Bnzl
IIB-	Chm	H	4-F-	1-Npm	3.47	524	H
944			Bnzl
IIB-	Chm	H	4-F-	Ph—Et	3.42	488	H
945			Bnzl
IIB-	Chm	H	4-F-	i-Pnt	3.38	454	H
946			Bnzl
IIB-	Bnzl	H	i-Pnt	Bnzl	3.27	430	H
947
IIB-	Bnzl	H	i-Pnt	1-Npm	3.42	480	H
948
IIB-	Bnzl	H	i-Pnt	Ph—Et	3.29	444	H
949
IIB-	i-Bu	H	i-Pnt	1-Npm	3.38	446	H
950
IIB-	i-Bu	H	i-Pnt	Ph—Et	3.3	410	H
951
IIB-	1-Npm	H	i-Pnt	Bnzl	3.45	480	H
952
IIB-	1-Npm	H	i-Pnt	i-Bu	3.42	446	H
953
IIB-	1-Npm	H	i-Pnt	1-Npm	3.56	530	H
954
IIB-	Ph—Et	H	i-Pnt	Bnzl	3.29	444	H
955
IIB-	Ph—Et	H	i-Pnt	i-Bu	3.28	410	H
956
IIB-	Ph—Et	H	i-Pnt	1-Npm	3.43	494	H
957
IIB-	4-F-Bnzl	H	i-Pnt	Bnzl	3.27	448	H
958
IIB-	4-F-Bnzl	H	i-Pnt	i-Bu	3.2	414	H
959
IIB-	4-F-Bnzl	H	i-Pnt	1-Npm	3.42	498	H
960
IIB-	4-F-Bnzl	H	i-Pnt	Ph—Et	3.28	462	H
961
IIB-	Chm	H	i-Pnt	Bnzl	3.44	436	H
962
IIB-	Chm	H	i-Pnt	1-Npm	3.58	486	H
963
IIB-	Chm	H	i-Pnt	Ph—Et	3.45	450	H
964
IIB-	Bnzl	H	Hxy	Bnzl	3.42	444	H
965
IIB-	Bnzl	H	Hxy	1-Npm	3.53	494	H
966
IIB-	Bnzl	H	Hxy	i-Pnt	3.43	424	H
967
IIB-	i-Bu	H	Hxy	1-Npm	3.49	460	H
968
IIB-	1-Npm	H	Hxy	1-Npm	3.67	544	H
969
IIB-	1-Npm	H	Hxy	i-Pnt	3.63	474	H
970
IIB-	Ph—Et	H	Hxy	Bnzl	3.43	458	H
971
IIB-	Ph—Et	H	Hxy	i-Bu	3.39	424	H
972
IIB-	Ph—Et	H	Hxy	i-Pnt	3.49	438	H
973
IIB-	4-F-Bnzl	H	Hxy	Bnzl	3.41	462	H
974
IIB-	4-F-Bnzl	H	Hxy	i-Bu	3.33	428	H
975
IIB-	4-F-Bnzl	H	Hxy	1-Npm	3.52	512	H
976
IIB-	4-F-Bnzl	H	Hxy	Ph—Et	3.4	476	H
977
IIB-	4-F-Bnzl	H	Hxy	i-Pnt	3.42	442	H
978
IIB-	i-Pnt	H	Hxy	Bnzl	3.41	424	H
979
IIB-	i-Pnt	H	Hxy	1-Npm	3.58	474	H
980
IIB-	Chm	H	Hxy	Bnzl	3.54	450	H
981
IIB-	Chm	H	Hxy	1-Npm	3.64	500	H
982
IIB-	2-	H	i-Bu	Bnzl	4.35	426	H
983	OtBu—Et
IIB-	2-	H	i-Bu	1-Npm	4.49	476	H
984	OtBu—Et
IIB-	2-	H	Bnzl	i-Pnt	4.48	440	H
985	OtBu—Et
IIB-	i-Pnt	H	Bnzl	4-tBuO-	3.42	502	H
986				Bnzl
IIB-	Chm	H	Bnzl	4-tBuO-	3.53	528	H
987				Bnzl

TABLE 1-28
IIB-	4-tBuO-Bnzl	H	1-Npm	Ph—Et	3.58	586	H
988
IIB-	4-tBuO-Bnzl	H	1-Npm	i-Pnt	3.58	552	H
989
IIB-	Ph—Et	H	1-Npm	4-tBuO-	3.53	586	H
990				Bnzl
IIB-	4-F-Bnzl	H	1-Npm	4-tBuO-	3.54	590	H
991				Bnzl
IIB-	2-OtBu—Et	H	1-Npm	Bnzl	4.52	510	H
992
IIB-	2-OtBu—Et	H	1-Npm	i-Bu	4.52	476	H
993
IIB-	2-OtBu—Et	H	1-Npm	1-Npm	4.6	560	H
994
IIB-	i-Pnt	H	1-Npm	4-tBuO-	3.58	552	H
995				Bnzl
IIB-	Chm	H	1-Npm	4-tBuO-	3.69	578	H
996				Bnzl
IIB-	Bnzl	H	4-tBuO-	Ph—Et	3.46	536	H
997			Bnzl
IIB-	Bnzl	H	4-tBuO-	i-Pnt	3.46	502	H
998			Bnzl
IIB-	i-Bu	H	4-tBuO-	Ph—Et	3.42	502	H
999			Bnzl
IIB-	1-Npm	H	4-tBuO-	Ph—Et	3.6	586	H
1000			Bnzl
IIB-	1-Npm	H	4-tBuO-	i-Pnt	3.61	552	H
1001			Bnzl
IIB-	Ph—Et	H	4-tBuO-	Bnzl	3.47	536	H
1002			Bnzl
IIB-	Ph—Et	H	4-tBuO-	1-Npm	3.53	586	H
1003			Bnzl
IIB-	Ph—Et	H	4-tBuO-	i-Pnt	3.53	516	H
1004			Bnzl
IIB-	4-F-Bnzl	H	4-tBuO-	Bnzl	3.39	540	H
1005			Bnzl
IIB-	4-F-Bnzl	H	4-tBuO-	1-Npm	3.53	590	H
1006			Bnzl
IIB-	4-F-Bnzl	H	4-tBuO-	Ph—Et	3.43	554	H
1007			Bnzl
IIB-	4-F-Bnzl	H	4-tBuO-	i-Pnt	3.44	520	H
1008			Bnzl
IIB-	2-OtBu—Et	H	4-tBuO-	1-Npm	3.63	582	H
1009			Bnzl
IIB-	i-Pnt	H	4-tBuO-	i-Bu	3.38	468	H
1010			Bnzl
IIB-	i-Pnt	H	4-tBuO-	1-Npm	3.58	552	H
1011			Bnzl
IIB-	i-Pnt	H	4-tBuO-	Ph—Et	3.48	516	H
1012			Bnzl
IIB-	Chm	H	4-tBuO-	Bnzl	3.54	528	H
1013			Bnzl
IIB-	Chm	H	4-tBuO-	i-Bu	3.43	494	H
1014			Bnzl
IIB-	Chm	H	4-tBuO-	1-Npm	3.66	578	H
1015			Bnzl
IIB-	Chm	H	4-tBuO-	Ph—Et	3.63	542	H
1016			Bnzl
IIB-	Chm	H	4-tBuO-	i-Pnt	3.63	508	H
1017			Bnzl
IIB-	Bnzl	H	tBOC-	Ph—Et	3.27	502	H
1018			E
IIB-	Bnzl	H	tBOC-	i-Pnt	3.25	468	H
1019			E
IIB-	1-Npm	H	tBOC-	Ph—Et	3.45	552	H
1020			E
IIB-	1-Npm	H	tBOC-	i-Pnt	3.47	518	H
1021			E
IIB-	4-tBuO-Bnzl	H	tBOC-	Ph—Et	3.48	574	H
1022			E
IIB-	4-tBuO-Bnzl	H	tBOC-	i-Pnt	3.53	540	H
1023			E
IIB-	Ph—Et	H	tBOC-	Bnzl	3.23	502	H
1024			E
IIB-	Ph—Et	H	tBOC-	i-Bu	3.29	468	H
1025			E
IIB-	Ph—Et	H	tBOC-	1-Npm	3.41	552	H
1026			E
IIB-	Ph—Et	H	tBOC-	4-tBuO-	3.47	574	H
1027			E	Bnzl
IIB-	Ph—Et	H	tBOC-	i-Pnt	3.32	482	H
1028			E
IIB-	4-F-Bnzl	H	tBOC-	Bnzl	3.26	506	H
1029			E
IIB-	4-F-Bnzl	H	tBOC-	i-Bu	3.21	472	H
1030			E
IIB-	4-F-Bnzl	H	tBOC-	1-Npm	3.42	556	H
1031			E
IIB-	4-F-Bnzl	H	tBOC-	4-tBuO-	3.44	578	H
1032			E	Bnzl
IIB-	4-F-Bnzl	H	tBOC-	Ph—Et	3.27	520	H
1033			E
IIB-	4-F-Bnzl	H	tBOC-	i-Pnt	3.29	486	H
1034			E
IIB-	2-OtBu—Et	H	tBOC-	Bnzl	3.34	498	H
1035			E
IIB-	2-OtBu—Et	H	tBOC-	1-Npm	3.46	548	H
1036			E
IIB-	2-OtBu—Et	H	tBOC-	4-tBuO-	3.52	570	H
1037			E	Bnzl

TABLE 1-29
IIB-	2-OtBu—Et	H	tBOC-	Ph—Et	3.36	512	H
1038			E
IIB-	1-Pnt	H	tBOC-	Bnzl	3.25	468	H
1039			E
IIB-	i-Pnt	H	tBOC-	1-Npm	3.38	518	H
1040			E
IIB-	1-Pnt	H	tBOC-	Ph—Et	3.27	482	H
1041			E
IIB-	Chm	H	tBOC-	Bnzl	3.39	494	H
1042			E
IIB-	Chm	H	tBOC-	1-Npm	3.54	544	H
1043			E
IIB-	Chm	H	tBOC-	Ph—Et	3.5	508	H
1044			E
IIB-	Ph—Et	H	i-Pr	4-tBuO-	3.36	488	H
1045				Bnzl
IIB-	4-F-Bnzl	H	i-Pr	4-tBuO-	3.33	492	H
1046				Bnzl
IIB-	Ph—Et	H	s-Bu	4-tBuO-	3.43	502	H
1047				Bnzl
IIB-	4-F-Bnzl	H	s-Bu	4-tBuO-	3.46	506	H
1048				Bnzl
IIB-	2-OtBu—Et	H	s-Bu	Bnzl	3.28	426	H
1049
IIB-	2-OtBu—Et	H	s-Bu	i-Bu	3.26	392	H
1050
IIB-	2-OtBu—Et	H	s-Bu	1-Npm	3.48	476	H
1051
IIB-	2-OtBu—Et	H	s-Bu	Ph—Et	3.39	440	H
1052
IIB-	4-tBuO-Bnzl	H	Ph—Et	Bnzl	3.48	536	H
1053
IIB-	4-tBuO-Bnzl	H	Ph—Et	i-Bu	3.38	502	H
1054
IIB-	4-tBuO-Bnzl	H	Ph—Et	1-Npm	3.58	586	H
1055
IIB-	tBOC-E	H	Ph—Et	Bnzl	3.3	502	H
1056
IIB-	tBOC-E	H	Ph—Et	i-Bu	3.28	468	H
1057
IIB-	tBOC-E	H	Ph—Et	1-Npm	3.47	552	H
1058
IIB-	2-OtBu—Et	H	Ph—Et	Bnzl	3.29	474	H
1059
IIB-	2-OtBu—Et	H	Ph—Et	i-Bu	3.27	440	H
1060
IIB-	2-OtBu—Et	H	Ph—Et	i-Pnt	3.36	454	H
1061
IIB-	4-tBuO-Bnzl	H	4-F-	Bnzl	3.52	540	H
1062			Bnzl
IIB-	4-tBuO-Bnzl	H	4-F-	i-Bu	3.42	506	H
1063			Bnzl
IIB-	4-tBuO-Bnzl	H	4-F-	1-Npm	3.6	590	H
1064			Bnzl
IIB-	tBOC-E	H	4-F-	Bnzl	3.27	506	H
1065			Bnzl
IIB-	tBOC-E	H	4-F-	1-Bu	3.28	472	H
1066			Bnzl
IIB-	tBOC-E	H	4-F-	1-Npm	3.45	556	H
1067			Bnzl
IIB-	2-OtBu—Et	H	4-F-	i-Bu	3.22	444	H
1068			Bnzl
IIB-	2-OtBu—Et	H	4-F-	Ph—Et	3.33	492	H
1069			Bnzl
IIB-	2-OtBu—Et	H	4-F-	i-Pnt	3.33	458	H
1070			Bnzl
IIB-	Bnzl	H	2-	Bnzl	4.32	460	H
1071			OtBu—Et
IIB-	Bnzl	H	2-	i-Bu	4.25	426	H
1072			OtBu—Et
IIB-	Bnzl	H	2-	1-Npm	4.42	510	H
1073			OtBu—Et
IIB-	Bnzl	H	2-	Ph—Et	4.31	474	H
1074			OtBu—Et
IIB-	Bnzl	H	2-	i-Pnt	4.34	440	H
1075			OtBu—Et
IIB-	i-Bu	H	2-	Bnzl	4.33	426	H
1076			OtBu—Et
IIB-	i-Bu	H	2-	1-Npm	4.42	476	H
1077			OtBu—Et
IIB-	i-Bu	H	2-	Ph—Et	4.35	440	H
1078			OtBu—Et
IIB-	1-Npm	H	2-	Bnzl	4.45	510	H
1079			OtBu—Et
IIB-	1-Npm	H	2-	i-Bu	4.48	476	H
1080			OtBu—Et
IIB-	1-Npm	H	2-	Ph—Et	4.48	524	H
1081			OtBu—Et
IIB-	1-Npm	H	2-	i-Pnt	4.53	490	H
1082			OtBu—Et
IIB-	4-tBuO-	H	2-	i-Bu	4.43	498	H
1083	Bnzl		OtBu—Et
IIB-	Ph—Et	H	2-	Bnzl	4.33	474	H
1084			OtBu—Et
IIB-	Ph—Et	H	2-	i-Bu	4.33	440	H
1085			OtBu—Et
IIB-	Ph—Et	H	2-	1-Npm	4.47	524	H
1086			OtBu—Et
IIB-	Ph—Et	H	2-	4-tBuO-	4.49	546	H
1087			OtBu—Et	Bnzl

TABLE 1-30
IIB-	Ph—Et	H	2-	i-Pnt	4.41	454	H
1088			OtBu—Et
IIB-	4-F-Bnzl	H	2-	Bnzl	4.33	478	H
1089			OtBu—Et
IIB-	4-F-Bnzl	H	2-	i-Bu	4.26	444	H
1090			OtBu—Et
IIB-	4-F-Bnzl	H	2-	1-Npm	4.43	528	H
1091			OtBu—Et
IIB-	4-F-Bnzl	H	2-	4-tBuO-	4.47	550	H
1092			OtBu—Et	Bnzl
IIB-	4-F-Bnzl	H	2-	Ph—Et	4.32	492	H
1093			OtBu—Et
IIB-	4-F-Bnzl	H	2-	i-Pnt	4.37	458	H
1094			OtBu—Et
IIB-	i-Pnt	H	2-	Bnzl	4.29	440	H
1095			OtBu—Et
IIB-	i-Pnt	H	2-	1-Npm	4.43	490	H
1096			OtBu—Et
IIB-	i-Pnt	H	2-	4-tBuO-	4.47	512	H
1097			OtBu—Et	Bnzl
IIB-	Chm	H	2-	Bnzl	4.43	466	H
1098			OtBu—Et
IIB-	Chm	H	2-	4-tBuO-	4.56	538	H
1099			OtBu—Et	Bnzl
IIB-	Chm	H	2-	Ph—Et	4.46	480	H
1100			OtBu—Et
IIB-	Bnzl	H	i-Pnt	4-tBuO-	3.43	502	H
1101				Bnzl
IIB-	Bnzl	H	i-Pnt	tBOC-E	3.23	468	H
1102
IIB-	1-Npm	H	i-Pnt	4-tBuO-	3.6	552	H
1103				Bnzl
IIB-	1-Npm	H	i-Pnt	tBOC-E	3.45	518	H
1104
IIB-	4-tBuO-Bnzl	H	i-Pnt	Bnzl	3.48	502	H
1105
IIB-	4-tBuO-Bnzl	H	i-Pnt	i-Bu	3.47	468	H
1106
IIB-	4-tBuO-Bnzl	H	i-Pnt	1-Npm	3.64	552	H
1107
IIB-	4-tBuO-Bnzl	H	i-Pnt	Ph—Et	3.53	516	H
1108
IIB-	tBOC-E	H	i-Pnt	Bnzl	3.33	468	H
1109
IIB-	tBOC-E	H	i-Pnt	1-Npm	3.49	518	H
1110
IIB-	tBOC-E	H	i-Pnt	Ph—Et	3.38	482	H
1111
IIB-	Ph—Et	H	i-Pnt	4-tBuO-	3.53	516	H
1112				Bnzl
IIB-	Ph—Et	H	i-Pnt	tBOC-E	3.34	482	H
1113
IIB-	4-F-Bnzl	H	i-Pnt	4-tBuO-	3.44	520	H
1114				Bnzl
IIB-	4-F-Bnzl	H	i-Pnt	tBOC-E	2.47	486	H
1115
IIB-	Chm	H	i-Pnt	4-tBuO-	2.82	508	H
1116				Bnzl
IIB-	Bnzl	H	Hxy	4-tBuO-	2.73	516	H
1117				Bnzl
IIB-	i-Bu	H	Hxy	4-tBuO-	2.7	482	H
1118				Bnzl
IIB-	1-Npm	H	Hxy	4-tBuO-	2.88	566	H
1119				Bnzl
IIB-	4-tBuO-Bnzl	H	Hxy	Bnzl	2.78	516	H
1120
IIB-	4-tBuO-Bnzl	H	Hxy	Ph—Et	2.83	530	H
1121
IIB-	4-tBuO-Bnzl	H	Hxy	i-Pnt	2.85	496	H
1122
IIB-	tBOC-E	H	Hxy	Bnzl	2.62	482	H
1123
IIB-	tBOC-E	H	Hxy	Ph—Et	2.68	496	H
1124
IIB-	Ph—Et	H	Hxy	4-tBuO-	2.77	530	H
1125				Bnzl
IIB-	4-F-Bnzl	H	Hxy	4-tBuO-	2.75	534	H
1126				Bnzl
IIB-	2-OtBu—Et	H	Hxy	Bnzl	2.48	454	H
1127
IIB-	2-OtBu—Et	H	Hxy	1-Npm	2.75	504	H
1128
IIB-	2-OtBu—Et	H	Hxy	Ph—Et	2.68	468	H
1129
†Ring formed together by R2A and R2B
*IIB-410, 416, 420, 462, 463, 499, and 501 are mixtures of conformational isomers.

TABLE 1-31
		LCMS
Compound		tR	Mass	Measurement	Yield
number	Name of compound	(min)	(M + H)+	condition	(%)
IIB-1	(3S*,3aS*,6R*,7R*,7aS*)-N,7-	1.19	416	B	18
	dibenzyl-1-isobutyl-1,2,3,6,7,7a-hexahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-carboxamide
IIB-2	(3S*,3aS*,6R*,7R*,7aS*)-N,1,7-	1.17	348	B	33
	triisobutyl-1,2,3,6,7,7a-hexahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-carboxamide
IIB-3	(3S*,3aS*,6R*,7R*,7aS*)-7-	1.18	382	B	26
	benzyl-N,1-diisobutyl-1,2,3,6,7,7a-hexahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-carboxamide
IIB-4	(3S*,3aS*,6R*,7R*,7aS*)-1-	1.17	382	B	40
	benzyl-N,7-diisobutyl-1,2,3,6,7,7a-hexahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-carboxamide
IIB-5	(3S*,3aS*,6R*,7R*,7aS*)-N-	1.18	382	B	36
	benzyl-1,7-diisobutyl-1,2,3,6,7,7a-hexahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-carboxamide
IIB-6	(3S*,3aS*,6R*,7R*,7aS*)-1,7-	1.19	416	B	47
	dibenzyl-N-isobutyl-1,2,3,6,7,7a-hexahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-carboxamide
IIB-7	(3S*,3aS*,6R*,7R*,7aS*)-N,1-	1.19	416	B	35
	dibenzyl-7-isobutyl-1,2,3,6,7,7a-hexahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-carboxamide
IIB-8	(3S*,3aS*,6R*,7R*,7aS*)-N,1,7-	1.21	450	B	36
	tribenzyl-1,2,3,6,7,7a-hexahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-carboxamide
IIB-9	(3S*,3aS*,6R*,7R*,7aS*)-N,7-	1.22	430	B	35
	dibenzyl-1-isopentyl-1,2,3,6,7,7a-hexahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-carboxamide
IIB-10	(3S*,3aS*,6R*,7R*,7aS*)-N,1-	1.22	430	B	27
	dibenzyl-7-isopentyl-1,2,3,6,7,7a-hexahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-carboxamide
IIB-11	(3S*,3aS*,6R*,7R*,7aS*)-N-	1.21	430	B	35
	benzyl-1-isobutyl-7-phenethyl-1,2,3,6,7,7a-hexahydro-
	3aH-3,6-methanopyrrolo[3,2-b]pyridine-3a-carboxamide
IIB-12	(3S*,3aS*,6R*,7R*,7aS*)-1-	1.21	430	B	19
	benzyl-7-isobutyl-N-phenethyl-1,2,3,6,7,7a-hexahydro-
	3aH-3,6-methanopyrrolo[3,2-b]pyridine-3a-carboxamide

TABLE 1-32
IIB-13	(3S*,3aS*,6R*,7R*,7aS*)-N-benzyl-1-	1.22	430	B	39
	isobutyl-7-(3-methylbenzyl)-1,2,3,6,7,7a-hexahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-carboxamide
IIB-14	(3S*,3aS*,6R*,7R*,7aS*)-N-benzyl-1-	1.21	430	B	37
	isobutyl-7-(4-methylbenzyl)-1,2,3,6,7,7a-hexahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-carboxamide
IIB-15	(3S*,3aS*,6R*,7R*,7aS*)-7-benzyl-1-	1.22	430	B	20
	isobutyl-N-(3-methylbenzyl)-1,2,3,6,7,7a-hexahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-carboxamide
IIB-16	(3S*,3aS*,6R*,7R*,7aS*)-7-benzyl-1-	1.23	430	B	30
	isobutyl-N-(4-methylbenzyl)-1,2,3,6,7,7a-hexahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-carboxamide
IIB-17	(3S*,3aS*,6R*,7R*,7aS*)-7-benzyl-N-	1.22	450	B	34
	(3-chlorobenzyl)-1-isobutyl-1,2,3,6,7,7a-hexahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-carboxamide
IIB-18	(3S*,3aS*,6R*,7R*,7aS*)-7-benzyl-N-	1.22	450	B	24
	(4-chlorobenzyl)-1-isobutyl-1,2,3,6,7,7a-hexahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-carboxamide
IIB-19	(3S*,3aS*,6R*,7R*,7aS*)-N-benzyl-1-	1.28	484	B	27
	(3,4-dichlorobenzyl)-7-isobutyl-1,2,3,6,7,7a-hexahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-carboxamide
IIB-20	(3S*,3aS*,6R*,7R*,7aS*)-1-benzyl-N-	1.25	484	B	31
	(3,4-dichlorobenzyl)-7-isobutyl-1,2,3,6,7,7a-hexahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-carboxamide
IIB-21	(3S*,3aS*,6R*,7R*,7aS*)-7-benzyl-1-	1.18	438	B	54
	isobutyl-N-(2-(naphthalen-1-yl)ethyl)-1,2,3,6,7,7a-hexahydro-
	3aH-3,6-methanopyrrolo[3,2-b]pyridine-3a-carboxamide
IIB-23	(3S*,3aS*,6R*,7R*,7aS*)-7-benzyl-1-	1.05	488	A	28
	isobutyl-N-(4-(tert-butoxy)benzyl)-1,2,3,6,7,7a-hexahydro-
	3aH-3,6-methanopyrrolo[3,2-b]pyridine-3a-carboxamide
IIB-24	(3S*,3aS*,6R*,7R*,7aS*)-7-benzyl-1-	1.03	466	A	30
	isobutyl-N-(naphthalen-1-ylmethyl)-1,2,3,6,7,7a-hexahydro-
	3aH-3,6-methanopyrrolo[3,2-b]pyridine-3a-carboxamide
IIB-25	(3S*,3aS*,6R*,7R*,7aS*)-7-benzyl-N-	0.79	370	A	20
	(2-hydroxyethyl)-1-isobutyl-1,2,3,6,7,7a-hexahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-carboxamide
IIB-26	3-((3S*,3aS*,6R*,7R*,7aS*)-7-benzyl-	0.80	398	A	95
	1-isobutyl-1,2,3,6,7,7a-hexahydro-1H-3,6-methanopyrrolo
	[3,2-b]pyridine-3a-carboxamide)propanoic acid
IIB-27	(3S*,3aS*,6R*,7R*,7aS*)-7-benzyl-1-	0.98	454	A	11
	isobutyl-N-(2-(tert-butoxy)-2-oxoethyl)-1,2,3,6,7,7a-hexahydro-
	3aH-3,6-methanopyrrolo[3,2-b]pyridine-3a-carboxamide
IIB-28	(3S*,3aS*,6R*,7R*,7aS*)-N-(3-amino-	0.79	397	A	80
	3-oxopropyl)-7-benzyl-1-isobutyl-1,2,3,6,7,7a-hexahydro-
	3aH-3,6-methanopyrrolo[3,2-b]pyridine-3a-carboxamide
IIB-29	(3S*,3aS*,6R*,7R*,7aS*)-N-(4-	0.71	397	A	93
	aminobutyl)-7-benzyl-1-isobutyl-1,2,3,6,7,7a-hexahydro-
	3aH-3,6-methanopyrrolo[3,2-b]pyridine-3a-carboxamide
IIB-30	(3S*,3aS*,6R*,7R*,7aS*)-7-benzyl-1-	0.97	497	A	18
	isobutyl-N-(4-((tert-butoxycarbonyl)amino)butyl)-1,2,3,6,7,7a-
	hexahydro-3aH-3,6-methanopyrrolo[3,2-b]pyridine-3a-carboxamide
IIB-31	(3S*,3aS*,6R*,7R*,7aS*)-7-benzyl-N-	1.04	422	A	5
	cyclohexylmethyl-1-isobutyl-1,2,3,6,7,7a-hexahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-carboxamide

TABLE 1-33
IIB-32	(3S*,3aS*,6R*,7R*,7aS*)-7-benzyl-	0.93	424	A	38
	1-isobutyl-N-((tetrahydro-2H-pyran-
	2-yl)methyl)-1,2,3,6,7,7a-
	hexahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-
	carboxamide
IIB-34	(3S*,3aS*,6R*,7R*,7aS*)-N-benzyl-	0.99	497	A	36
	1-isobutyl-7-(4-((tert-
	butoxycarbonyl)amino)butyl)-
	1,2,3,6,7,7a-hexahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-
	carboxamide
IIB-36	(3S*,3aS*,6R*,7R*,7aS*)-N-benzyl-	0.89	412	A	22
	1-isobutyl-7-(3-methoxy-3-
	oxopropyl)-1,2,3,6,7,7a-hexahydro-
	3aH-3,6-methanopyrrolo[3,2-
	b]pyridine-3a-carboxamide
IIB-38	(3S*,3aS*,6R*,7R*,7aS*)-N-benzyl-	1.05	422	A	59
	7-(cyclohexylmethyl)-1-isobutyl-
	1,2,3,6,7,7a-hexahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-
	carboxamide
IIB-39	(3S*,3aS*,6R*,7R*,7aS*)-N,7-	1.04	456	A	12
	dibenzyl-1-cyclohexylmethyl-
	1,2,3,6,7,7a-hexahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-
	carboxamide
IIB-40	(3S*,3aS*,6R*,7R*,7aS*)-N,7-	0.91	466	A	92
	dibenzyl-1-(4-hydroxybenzyl)-
	1,2,3,6,7,7a-hexahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-
	carboxamide
IIB-41	(3S*,3aS*,6R*,7R*,7aS*)-N,7-	1.05	522	A	10
	dibenzyl-1-(4-(tert-
	butoxy)benzyl)-1,2,3,6,7,7a-
	hexahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-
	carboxamide
IIB-42	(3S*,3aS*,6R*,7R*,7aS*)-N,7-	1.04	500	A	4
	dibenzyl-1-(naphthalen-1-
	ylmethyl)-1,2,3,6,7,7a-hexahydro-
	3aH-3,6-methanopyrrolo[3,2-
	b]pyridine-3a-carboxamide
IIB-76	tert-butyl 3-	0.83	488	B	34
	((3S*,3aS*,6R*,7R*,7aS*)-7-benzyl-
	3a-(benzylcarbamoyl)-
	2,3,3a,6,7,7a-hexahydro-1H-3,6-
	methanopyrrolo[3,2-b]pyridin-
	1-yl)propanoate
IIB-77	(3S*,3aS*,6R*,7R*,7aS*)-N,1-	0.85	466	B	34
	dibenzyl-7-(4-hydroxybenzyl)-
	1,2,3,6,7,7a-hexahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-
	carboxamide
IIB-78	tert-butyl 3-	1.00	527	B	49
	((3S*,3aS*,6R*,7R*,7aS*)-2-(7-
	benzyl-1-methyl-2,3,3a,6,7,7a-
	hexahydro-1H-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-
	carboxamide)ethyl)-1H-indole-1-
	carboxylate
IIB-80	(3S*,3aS*,6R*,7R*,7aS*)-N-benzyl-	0.95	452	A	9
	1-(naphthalen-1-ylmethyl)-7-propyl-
	1,2,3,6,7,7a-hexahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-
	carboxamide

TABLE 2-1
Compound				Synthesis		Raw	Raw
number	R1	R2	R3	method	Intermediate	material	material
						1	2

TABLE 2-2
IIF-1	i-Bu	Bnzl	Bnzl	EX	INT-Bnzl	SM1-iBu	SM2-Ph
IIF-2	i-Bu	i-Bu	i-Bu	IIB-1,	INT-iBu	SM1-iBu	SM2-Pnt
				IIF-1
IIF-3	i-Bu	i-Bu	Bnzl	IIB-1,	INT-iBu	SM1-iBu	SM2-Ph
				IIF-1
IIF-4	Bnzl	i-Bu	i-Bu	IIB-1,	INT-iBu	SM1-Bnzl	SM2-Pnt
				IIF-1
IIF-5	i-Bu	Bnzl	i-Bu	IIB-1,	INT-Bnzl	SM1-iBu	SM2-Pnt
				IIF-1
IIF-6	Bnzl	i-Bu	Bnzl	IIB-1,	INT-iBu	SM1-Bnzl	SM2-Ph
				IIF-1
IIF-7	Bnzl	Bnzl	i-Bu	IIB-1,	N-(benzyl-	SM1-Bnzl	SM2-Pnt
				IIF-1	1,2,4-triazine-
					3-carboxamide
IIF-8	Bnzl	Bnzl	Bnzl	IIB-1,	INT-Bnzl	SM1-Bnzl	SM2-Ph
				IIF-1
IIF-9	i-Pnt	Bnzl	Bnzl	IIB-1,	INT-Bnzl	N-allyl-3-	SM2-Ph
				IIF-1		methylbutan-
						1-amine
IIF-10	Bnzl	Bnzl	i-Pnt	IIB-1,	INT-Bnzl	SM1-Bnzl	5-
				IIF-1			methylhexanal
IIF-11	i-Bu	Bnzl	Ph-Et	IIB-1,	INT-Bnzl	SM1-iBu	4-
				IIF-1			phenylbutanal
IIF-12	i-Bu	Ph-Et	Bnzl	IIB-1,	N-phenethyl-	SM1-iBu	SM2-Ph
				IIF-1	1,2,4-triazine-3-
					carboxamide
IIF-13	i-Bu	Bnzl	3-Me-	IIB-1,	INT-Bnzl	SM1-iBu	3-(m-tolyl)propanal
			Bnzl	IIF-1
IIF-14	i-Bu	Bnzl	4-Me-	IIB-1,	INT-Bnzl	SM1-iBu	3-(p-tolyl)propanal
			Bnzl	IIF-1
IIF-15	i-Bu	3-Me-	Bnzl	IIB-1,	N-(3-methylbenzyl)-	SM1-iBu	SM2-Ph
		Bnzl		IIF-1	1,2,4-triazine-3-
					carboxamide
IIF-16	i-Bu	4-Me-	Bnzl	IIB-1,	N-(4-methylbenzyl)-	SM1-iBu	SM2-Ph
		Bnzl		IIF-1	1,2,4-triazine-3-
					carboxamide
IIF-17	i-Bu	3-Cl-	Bnzl	IIB-1,	N-(3-chlorobenzyl)-	SM1-iBu	SM2-Ph
		Bnzl		IIF-1	1,2,4-triazine-3-
					carboxamide
IIF-18	i-Bu	4-Cl-	Bnzl	IIB-1,	N-(4-chlorobenzyl)-	SM1-iBu	SM2-Ph
		Bnzl		IIF-1	1,2,4-triazine-3-
					carboxamide
IIF-19	3,4-	Bnzl	i-Bu	IIB-1,	INT-Bnzl	N-(3,4-	SM2-Pnt
	Cl2-			IIF-1		dichlorobenzyl)
	Bnzl					prop-2-en-1-amine
IIF-20	Bnzl	3,4-	i-Bu	IIB-1,	N-(3,4-	SM1-Bnzl	SM2-Pnt
		Cl2-		IIF-1	dichlorobenzyl)-
		Bnzl			1,2,4-triazine-3-
					carboxamide
IIF-23	i-Bu	4-	Bnzl	IIB-1,	N-(4-tert-	SM1-iBu	SM2-Ph
		(tert-		IIF-1	butoxybenzyl)-
		butoxy)			1,2,4-triazine-3-
		benzyl			carboxamide

TABLE 2-3
IIF-24	i-Bu	Np-M	Bnzl	IIB-1,	N-	SM1-iBu	SM2-Ph
				IIF-1	((naphthalen-1-yl)
					methyl)-1,2,4-triazine-
					3-carboxamide
IIF-25	i-Bu	Hdr-E	Bnzl	IIB-1,	N-(2-	SM1-iBu	SM2-Ph
				IIF-1	hydroxyethyl)-
					1,2,4-triazine-
					3-carboxamide
IIF-26	i-Bu	Cbx-E	Bnzl	EX		IIB-27
IIF-27	i-Bu	2-(tert-	Bnzl	IIB-1,	tert-butyl	SM1-iBu	SM2-Ph
		butoxy)-		IIF-1	3-(1,2,4-
		2-oxoethyl			triazine-3-
					carboxamide)
					propanoate
IIF-28	i-Bu	Cbm-E	Bnzl	IIB-28		IIF-26
IIF-29	i-Bu	4-aminobutyl	Bnzl	IIB-29		IIF-30
IIF-30	i-Bu	4-((tert-	Bnzl	IIB-1,	tert-butyl	SM1-iBu	SM2-Ph
		butoxycarbonyl)		IIF-1	4-(1,2,4-
		amino)butyl			triazine-3-
					carboxamide)
					butylcarbamate
IIF-31	i-Bu	Chm	Bnzl	IIB-1,	N-	SM1-iBu	SM2-Ph
				IIF-1	(cyclohexyl
					methyl)-
					1,2,4-triazine-
					3-carboxamide
IIF-32	i-Bu	(tetrahydro-	Bnzl	IIB-1,	N-((tetrahydro-2H-	SM1-iBu	SM2-Ph
		2H-pyran-2-yl)		IIF-1	pyran-2-yl)methyl)-
		methyl			1,2,4-triazine-
					3-carboxamide
IIF-34	i-Bu	Bnzl	4-	IIB-1,	INT-Bnzl	SM1-iBu	tert-butyl
			((tert-	IIF-1			5-
			butoxycarbonyl)				formylpentylcarbamate
			amino)butyl
IIF-36	i-Bu	Bnzl	3-methoxy-	IIB-1,	INT-Bnzl	SM1-iBu	methyl
			3-oxopropyl	IIF-1			4-formylbutanoate
IIF-38	i-Bu	Bnzl	Chm	IIB-1,	INT-Bnzl	SM1-iBu	3-cyclohexylpropanal
				IIF-1
IIF-39	Chm	Bnzl	Bnzl	IIB-1,	INT-Bnzl	N-	SM2-Ph
				IIF-1		(cyclohexylmethyl)
						prop-2-en-1-amine
IIF-40	4-OH-Bnzl	Bnzl	Bnzl	IF-40		IIF-41
IIF-41	4-(tert-	Bnzl	Bnzl	IIB-1,	INT-Bnzl	N-(4-tert-	SM2-Ph
	butoxy)			IIF-1		butoxybenzyl)
	benzyl					prop-2-en-1-amine
IIF-42	Np-M	Bnzl	Bnzl	IIB-1,	INT-Bnzl	N-	SM2-Ph
				IIF-1		((naphthalen-1-yl)
						methyl)prop-2-en-
						1-amine

TABLE 2-4
IIF-76	3-(tert-	Bnzl	Bnzl	IIB-1,	N-benzyl-	N-(3-(tert-	SM2-Ph
	butoxy)-			IIF-1	1,2,4-	butoxy)-
	3-				triazine-3-	3-oxopropyl)-
	oxopropyl				carboxamide	prop-2-en-1-
						amine
IIF-77	Bnzl	Bnzl	4-	IIB-1,	N-benzyl-	SM1-Bnzl	3-(4-
			OH-	IIF-1	1,2,4-		hydroxyphenyl)
			Bnzl		triazine-3-		propanal
					carboxamide
IIF-80	Np-M	Bnzl	Pr	IIB-1,	N-benzyl	N-	pentanal
				IIF-1	1,2,4-	((naphthalen-1-yl)
					triazine-3-	methyl)prop-2-en-
					carboxamide	1-amine

TABLE 2-5
				LCMS
Compound				t R	Mass	Measurement
number	R1	R2	R3	(min)	(M + H) +	condition
IIF-81	benzyl	naphthalen-1-	isobutyl	1.29	467	B
		ylmethyl
IIF-82	benzyl	4-(trifluoromethyl)	isobutyl	1.29	484	B
		benzyl
IIF-83	4-chlorobenzyl	benzyl	isobutyl	1.29	450	B
IIF-84	3-chlorobenzyl	benzyl	isobutyl	1.30	450	B
IIF-85	4-methoxybenzyl	benzyl	isobutyl	1.23	446	B
IIF-86	4-methylbenzyl	benzyl	isobutyl	1.24	430	B
IIF-88	isobutylbenzyl	isobutyl	4-chloro	1.26	416	B
IIF-89	isobutyl	4-chlorobenzyl	isobutyl	1.22	416	B
IIF-90	isobutyl	benzyl	isopentyl	1.23	396	B
IIF-91	isopentyl	benzyl	isobutyl	1.26	396	B
IIF-92	isobutyl	isopentyl	benzyl	1.23	396	B
IIF-93	4-hydroxybenzyl	benzyl	isobutyl	1.19	432	B
IIF-94	4-(dimethylamino)	benzyl	isobutyl	1.27	459	B
	benzyl
IIF-95	4-(tert-butyl)	benzyl	isobutyl	1.29	472	B
	benzyl
IIF-96	4-(trifluoromethoxy)	benzyl	isobutyl	1.32	500	B
	benzyl
IIF-97	4-ethoxybenzyl	benzyl	isobutyl	1.25	460	B
IIF-98	isopentyl	isobutyl	benzyl	1.22	396	B
IIF-99	benzyl	4-hydroxybenzyl	isobutyl	1.17	432	B

TABLE 2-6
IIF-100	4-methoxybenzyl	4-hydroxybenzyl	isobutyl	1.17	462	B
IIF-101	4-hydroxybenzyl	benzyl	isopentyl	1.20	446	B
IIF-102	benzyl	naphthalen-2-	isobutyl	1.27	466	B
		ylmethyl
IIF-103	isopentyl	4-chlorobenzyl	isobutyl	1.28	431	B
IIF-104	isopentyl	4-fluorobenzyl	isobutyl	1.26	414	B
IIF-105	benzyl	pyridin-4-	isobutyl	1.06	417	B
		ylmethyl
IIF-106	4-methoxybenzyl	benzyl	benzyl	0.93	480	c
IIF-107	phenethyl	benzyl	2-(tert-	1.08	532	C
			butyldimethylsilyloxy)
			ethyl
IIF-109	4-nitrobenzyl	4-(tert-butoxy)	2-(tert-	1.00	605	C
		benzyl	butoxycarbonyl)
			ethyl
IIF-110	i-Bu	i-Pr	Bnzl	2.92	368	F
IIF-111	i-Bu	i-Bu	4-tBuO-Bnzl	3.64	454	F
IIF-112	i-Bu	Bnzl	4-tBuO-Bnzl	3.75	488	F
IIF-113	i-Bu	tBOC-E	4-tBuO-Bnzl	3.73	526	F
IIF-114	i-Bu	s-Bu	4-tBuO-Bnzl	3.64	454	F
IIF-115	i-Bu	1-Npm	4-tBuO-Bnzl	4.18	538	F
IIF-116	i-Bu	i-Pr	4-tBuO-Bnzl	3.4	440	F
IIF-117	i-Bu	1-Npm	tBOC-E	3.92	504	F
IIF-118	i-Bu	1-Npm	1-Npm	4.25	516	F
IIF-119	i-Bu	i-Pr	1-Npm	3.4	418	F
IIF-120	Bnzl	4-tBuO-Bnzl	Bnzl	3.95	522	F
IIF-121	Bnzl	i-Bu	4-tBuO-Bnzl	3.79	488	F
IIF-122	Bnzl	Bnzl	4-tBuO-Bnzl	3.91	522	F
IIF-123	Bnzl	tBOC-E	4-tBuO-Bnzl	3.94	560	F
IIF-124	Bnzl	Bnzl	tBOC-E	3.47	488	F
IIF-125	Bnzl	4-tBuO-Bnzl	tBOC-E	3.98	560	F
IIF-126	Bnzl	1-Npm	tBOC-E	3.96	538	F
IIF-127	Bnzl	i-Bu	1-Npm	3.74	466	F

TABLE 2-7
IIF-128	Bnzl	Bnzl	1-Npm	3.92	500	F
IIF-129	Bnzl	4-tBuO-Bnzl	1-Npm	4.27	572	F
IIF-130	Bnzl	tBOC-E	1-Npm	3.8	538	F
IIF-131	Bnzl	s-Bu	1-Npm	3.74	466	F
IIF-132	Bnzl	1-Npm	1-Npm	4.31	550	F
IIF-133	4-tBuO-Bnzl	Bnzl	Bnzl	4.1	522	F
IIF-134	4-tBuO-Bnzl	tBOC-E	Bnzl	3.6	560	F
IIF-135	4-tBuO-Bnzl	s-Bu	Bnzl	3.47	488	F
IIF-136	4-tBuO-Bnzl	1-Npm	Bnzl	4.75	572	F
IIF-137	4-tBuO-Bnzl	Bnzl	tBOC-E	3.69	560	F
IIF-138	4-tBuO-Bnzl	1-Npm	tBOC-E	4.04	610	F
IIF-139	4-tBuO-Bnzl	i-Bu	1-Npm	3.82	538	F
IIF-140	4-tBuO-Bnzl	Bnzl	1-Npm	4.68	572	F
IIF-141	4-tBuO-Bnzl	tBOC-E	1-Npm	3.8	610	F
IIF-142	4-tBuO-Bnzl	s-Bu	1-Npm	3.92	538	F
IIF-143	4-tBuO-Bnzl	1-Npm	1-Npm	4.65	622	F
IIF-144	i-Bu	4-tBuO-Bnzl	Bnzl	3.87	488	F
IIF-145	i-Bu	tBOC-E	Bnzl	3.25	454	F
IIF-146	i-Bu	s-Bu	Bnzl	3.12	382	F
IIF-147	i-Bu	i-Bu	tBOC-E	3.19	420	F
IIF-148	i-Bu	Bnzl	tBOC-E	3.37	454	F
IIF-149	i-Bu	4-tBuO-Bnzl	tBOC-E	3.93	526	F
IIF-150	i-Bu	i-Pr	tBOC-E	2.93	406	F
IIF-151	i-Bu	i-Bu	1-Npm	3.68	432	F
IIF-152	i-Bu	Bnzl	1-Npm	3.72	466	F
IIF-153	i-Bu	4-tBuO-Bnzl	1-Npm	4.24	538	F
IIF-154	i-Bu	tBOC-E	1-Npm	3.74	504	F
IIF-155	Bnzl	tBOC-E	Bnzl	3.44	488	F
IIF-156	Bnzl	s-Bu	Bnzl	3.24	416	F
IIF-157	Bnzl	1-Npm	Bnzl	3.87	500	F
IIF-158	Bnzl	i-Pr	Bnzl	3.01	402	F
IIF-159	Bnzl	s-Bu	4-tBuO-Bnzl	3.82	488	F
IIF-160	Bnzl	1-Npm	4-tBuO-Bnzl	4.43	572	F
IIF-161	Bnzl	i-Pr	4-tBuO-Bnzl	3.51	474	F

TABLE 2-8
IIF-162	Bnzl	s-Bu	tBOC-E	3.34	454	F
IIF-163	Bnzl	i-Pr	tBOC-E	3.15	440	F
IIF-164	Bnzl	i-Pr	1-Npm	3.5	452	F
IIF-165	4-tBuO-Bnzl	i-Pr	Bnzl	3.49	474	F
IIF-166	4-tBuO-Bnzl	i-Pr	tBOC-E	3.38	512	F
IIF-167	4-tBuO-Bnzl	i-Pr	1-Npm	3.82	524	F
IIF-168	tBOC-E	i-Bu	Bnzl	3.5	454	F
IIF-169	1-Npm	i-Bu	Bnzl	3.54	466	F
IIF-170	1-Npm	4-tBuO-Bnzl	Bnzl	3.95	572	F
IIF-171	1-Npm	s-Bu	Bnzl	3.52	466	F
IIF-172	1-Npm	i-Pr	Bnzl	3.19	452	F
IIF-173	1-Npm	Bnzl	4-tBuO-Bnzl	4.3	572	F
IIF-174	1-Npm	tBOC-E	4-tBuO-Bnzl	3.95	610	F
IIF-175	1-Npm	s-Bu	4-tBuO-Bnzl	3.87	538	F
IIF-176	1-Npm	1-Npm	4-tBuO-Bnzl	4.62	622	F
IIF-177	1-Npm	i-Pr	4-tBuO-Bnzl	3.84	524	F
IIF-178	1-Npm	Bnzl	tBOC-E	3.8	538	F
IIF-179	1-Npm	4-tBuO-Bnzl	tBOC-E	4.5	610	F
IIF-180	1-Npm	s-Bu	tBOC-E	3.62	504	F
IIF-181	1-Npm	1-Npm	tBOC-E	4.15	588	F
IIF-182	1-Npm	Bnzl	1-Npm	4.3	550	F
IIF-183	1-Npm	4-tBuO-Bnzl	1-Npm	4.75	622	F
IIF-184	1-Npm	tBOC-E	1-Npm	4.02	588	F
IIF-185	1-Npm	s-Bu	1-Npm	4.25	516	F
IIF-186	i-Bu	4-tBuO-Bnzl	i-Bu	3.68	454	F
IIF-187	i-Bu	tBOC-E	i-Bu	3.05	420	F
IIF-188	i-Bu	s-Bu	i-Bu	2.84	348	F
IIF-189	i-Bu	1-Npm	i-Bu	3.71	432	F
IIF-190	i-Bu	i-Pr	i-Bu	2.66	334	F
IIF-191	i-Bu	(tBOC)Gun-Pr	4-tBuO-Bnzl	2.71	641	J
IIF-192	i-Bu	1-Npm	(tBOC)Gun-Pr	3.47	675	J
IIF-193	i-Bu	s-Bu	1-Npm	3.64	432	F
IIF-194	Bnzl	4-tBuO-Bnzl	i-Bu	3.93	488	F
IIF-195	Bnzl	i-Pr	i-Bu	3.01	368	F

TABLE 2-9
IIF-196	Bnzl	i-Bu	tBOC-E	3.32	454	F
IIF-197	tBOC-E	Bnzl	i-Bu	3.52	454	F
IIF-198	tBOC-E	4-tBuO-Bnzl	i-Bu	4.01	526	F
IIF-199	tBOC-E	s-Bu	i-Bu	3.26	420	F
IIF-200	tBOC-E	1-Npm	i-Bu	4.09	504	F
IIF-201	tBOC-E	i-Pr	i-Bu	3.03	406	F
IIF-202	tBOC-E	1-Npm	Bnzl	4.06	538	F
IIF-203	tBOC-E	Bnzl	4-tBuO-Bnzl	4.19	560	F
IIF-204	tBOC-E	1-Npm	4-tBuO-Bnzl	4.62	610	F
IIF-205	tBOC-E	i-Bu	1-Npm	3.96	504	F
IIF-206	tBOC-E	4-tBuO-Bnzl	1-Npm	4.41	610	F
IIF-207	tBOC-E	1-Npm	1-Npm	4.48	588	F
IIF-208	tBOC-E	i-Pr	1-Npm	3.71	490	F
IIF-209	1-Npm	i-Bu	i-Bu	3.32	432	F
IIF-210	1-Npm	Bnzl	i-Bu	3.38	466	F
IIF-211	1-Npm	4-tBuO-Bnzl	i-Bu	3.67	538	F
IIF-212	1-Npm	s-Bu	i-Bu	3.35	432	F
IIF-213	1-Npm	1-Npm	i-Bu	3.8	516	F
IIF-214	1-Npm	i-Pr	i-Bu	3.17	418	F
IIF-215	1-Npm	i-Bu	4-tBuO-Bnzl	3.92	538	F
IIF-216	1-Npm	i-Bu	tBOC-E	3.5	504	F
IIF-217	1-Npm	i-Pr	tBOC-E	3.34	490	F
IIF-218	1-Npm	i-Bu	1-Npm	3.79	516	F
IIF-219	1-Npm	(tBOC)Gun-Pr	1-Npm	3.82	759	F
IIF-220	1-Npm	i-Pr	1-Npm	3.65	502	F
IIF-221	i-Bu	(tBOC)Gun-Pr	i-Bu	2.89	591	J
IIF-222	i-Bu	(tBOC)Gun-Pr	Bnzl	2.96	625	J
IIF-223	i-Bu	s-Bu	tBOC-E	3.13	420	F
IIF-224	i-Bu	i-Bu	(tBOC)Gun-Pr	2.96	591	J
IIF-225	i-Bu	Bnzl	(tBOC)Gun-Pr	3	625	J
IIF-226	i-Bu	4-tBuO-Bnzl	(tBOC)Gun-Pr	2.78	641	J
IIF-227	i-Bu	s-Bu	(tBOC)Gun-Pr	2.95	591	J
IIF-228	i-Bu	i-Pr	(tBOC)Gun-Pr	2.81	577	J
IIF-229	i-Bu	(tBOC)Gun-Pr	1-Npm	3.08	675	J

TABLE 2-10
IIF-230	Bnzl	(tBOC)Gun-Pr	i-Bu	2.93	625	J
IIF-231	Bnzl	s-Bu	i-Bu	3.23	382	F
IIF-232	Bnzl	(tBOC)Gun-Pr	Bnzl	2.94	659	J
IIF-233	Bnzl	(tBOC)Gun-Pr	4-tBuO-Bnzl	2.74	675	J
IIF-234	Bnzl	i-Bu	(tBOC)Gun-Pr	3.49	698?	J
IIF-235	Bnzl	Bnzl	(tBOC)Gun-Pr	3.18	659	J
IIF-236	Bnzl	4-tBuO-Bnzl	(tBOC)Gun-Pr	2.95	675	J
IIF-237	Bnzl	s-Bu	(tBOC)Gun-Pr	3.04	625	J
IIF-238	Bnzl	1-Npm	(tBOC)Gun-Pr	4.09	709	J
IIF-239	Bnzl	(tBOC)Gun-Pr	1-Npm	3.36	709	J
IIF-240	tBOC-E	i-Bu	i-Bu	3.25	420	F
IIF-241	tBOC-E	Bnzl	Bnzl	3.62	488	F
IIF-242	tBOC-E	4-tBuO-Bnzl	Bnzl	4.1	560	F
IIF-243	tBOC-E	s-Bu	Bnzl	4.48	454	F
IIF-244	tBOC-E	i-Pr	Bnzl	3.24	440	F
IIF-245	tBOC-E	i-Bu	4-tBuO-Bnzl	4.15	526	F
IIF-246	tBOC-E	i-Pr	4-tBuO-Bnzl	3.89	512	F
IIF-247	tBOC-E	Bnzl	1-Npm	4.03	538	F
IIF-248	tBOC-E	s-Bu	1-Npm	3.96	504	F
IIF-249	(tBOC)	1-Npm	i-Bu	3.77	657	J
	Gun-Pr
IIF-250	(tBOC)	i-Pr	i-Bu	3.16	577	J
	Gun-Pr
IIF-251	(tBOC)	1-Npm	Bnzl	3.71	709	J
	Gun-Pr
IIF-252	(tBOC)	i-Pr	Bnzl	3.18	611	J
	Gun-Pr
IIF-253	(tBOC)	1-Npm	4-tBuO-Bnzl	3.39	725	J
	Gun-Pr
IIF-254	(tBOC)	i-Pr	4-tBuO-Bnzl	2.96	627	J
	Gun-Pr
IIF-255	(tBOC)	1-Npm	1-Npm	3.97	759	J
	Gun-Pr
IIF-256	(tBOC)	i-Pr	1-Npm	3.47	661	J
	Gun-Pr
IIF-257	1-Npm	1-Npm	Bnzl	4.5	550	F
IIF-258	Bnzl	tBOC-E	i-Bu	3.51	454	F
IIF-259	Bnzl	i-Pr	(tBOC)Gun-Pr	2.99	611	J
IIF-260	4-tBuO-	i-Bu	i-Bu	3.42	454	F
	Bnzl
IIF-261	4-tBuO-	Bnzl	i-Bu	3.44	488	F
	Bnzl
IIF-262	4-tBuO-	tBOC-E	i-Bu	3.5	526	F
	Bnzl
IIF-263	4-tBuO-	(tBOC)Gun-Pr	i-Bu	3.29	641	F
	Bnzl

TABLE 2-11
IIF-264	4-tBuO-Bnzl	s-Bu	i-Bu	3.45	454	F
IIF-265	4-tBuO-Bnzl	1-Npm	i-Bu	3.9	538	F
IIF-266	4-tBuO-Bnzl	i-Pr	i-Bu	3.24	440	F
IIF-267	4-tBuO-Bnzl	i-Bu	Bnzl	3.57	488	F
IIF-268	4-tBuO-Bnzl	(tBOC)Gun-Pr	Bnzl	3.1	675	F
IIF-269	4-tBuO-Bnzl	i-Bu	tBOC-E	3.6	526	F
IIF-270	4-tBuO-Bnzl	s-Bu	tBOC-E	3.59	526	F
IIF-271	4-tBuO-Bnzl	i-Bu	(tBOC)Gun-Pr	3.38	641	F
IIF-272	4-tBuO-Bnzl	Bnzl	(tBOC)Gun-Pr	3.72	675	F
IIF-273	4-tBuO-Bnzl	s-Bu	(tBOC)Gun-Pr	3.38	641	F
IIF-274	4-tBuO-Bnzl	1-Npm	(tBOC)Gun-Pr	3.79	725	F
IIF-275	4-tBuO-Bnzl	i-Pr	(tBOC)Gun-Pr	3.27	627	F
IIF-276	4-tBuO-Bnzl	(tBOC)Gun-Pr	1-Npm	3.54	725	F
IIF-277	tBOC-E	s-Bu	4-tBuO-Bnzl	4.09	526	F
IIF-278	(tBOC)Gun-Pr	i-Bu	i-Bu	4.24	591	F
IIF-279	(tBOC)Gun-Pr	Bnzl	i-Bu	3.99	625	F
IIF-280	(tBOC)Gun-Pr	4-tBuO-Bnzl	i-Bu	3.51	641	F
IIF-281	(tBOC)Gun-Pr	s-Bu	i-Bu	3.82	591	F
IIF-282	(tBOC)Gun-Pr	i-Bu	Bnzl	4.27	625	F
IIF-283	(tBOC)Gun-Pr	Bnzl	Bnzl	4.14	659	F
IIF-284	(tBOC)Gun-Pr	4-tBuO-Bnzl	Bnzl	3.72	675	F
IIF-285	(tBOC)Gun-Pr	s-Bu	Bnzl	3.99	625	F
IIF-286	(tBOC)Gun-Pr	i-Bu	4-tBuO-Bnzl	3.59	641	F
IIF-287	(tBOC)Gun-Pr	Bnzl	4-tBuO-Bnzl	4.32	675	F
IIF-288	(tBOC)Gun-Pr	Bnzl	1-Npm	4.57	709	F
IIF-289	(tBOC)Gun-Pr	s-Bu	1-Npm	4.49	675	F
IIF-290	1-Npm	tBOC-E	i-Bu	3.35	504	F
IIF-291	1-Npm	(tBOC)Gun-Pr	i-Bu	3.95	675	F
IIF-292	1-Npm	(tBOC)Gun-Pr	Bnzl	3.7	709	F
IIF-293	1-Npm	(tBOC)Gun-Pr	4-tBuO-Bnzl	3.3	725	F
IIF-294	1-Npm	i-Bu	(tBOC)Gun-Pr	3.77	675	F
IIF-295	1-Npm	Bnzl	(tBOC)Gun-Pr	3.82	709	F
IIF-296	1-Npm	4-tBuO-Bnzl	(tBOC)Gun-Pr	3.6	725	F
IIF-297	1-Npm	s-Bu	(tBOC)Gun-Pr	4.15	675	F

TABLE 2-12
IIF-298	1-Npm	1-Npm	(tBOC)Gun-Pr	4.91	759	F
IIF-299	1-Npm	i-Pr	(tBOC)Gun-Pr	3.5	661	F
IIF-300	1-Npm	tBOC-E	Bnzl	3.47	538	F
IIF-301	Bnzl	i-Pr	3-Gun-Pr	1.47	411	F
IIF-302	4-OH-Bnzl	i-Pr	3-Gun-Pr	1.37	427	F
IIF-303	1-Npm	3-Gun-Pr	i-Bu	2.75	475	F
IIF-304	1-Npm	i-Bu	3-Gun-Pr	2.6	475	F
IIF-305	1-Npm	Bnzl	3-Gun-Pr	2.69	509	F
IIF-306	1-Npm	i-Pr	3-Gun-Pr	2.49	461	F
IIF-307	Bnzl	Ph-Et	i-Bu	0.93	430	C
IIF-308	Chm	i-Bu	Bnzl	0.97	422	C
IIF-309	Bnzl	4-F-Bnzl	i-Bu	0.93	434	C
IIF-310	Chm	Bnzl	i-Bu	0.97	422	C
IIF-311	Bnzl	Hxy	i-Bu	1.02	410	C
IIF-312	Ph-Et	i-Bu	i-Bu	0.94	396	C
IIF-313	Ph-Et	i-Bu	1-Npm	1.01	480	C
IIF-314	Bnzl	i-Bu	Ph-Et	0.97	430	C
IIF-315	4-F-Bnzl	i-Bu	Bnzl	0.94	434	C
IIF-316	i-Bu	4-F-Bnzl	Bnzl	0.93	434	C
IIF-317	Ph-Et	Bnzl	i-Bu	0.94	430	C
IIF-318	Bnzl	i-Pnt	i-Bu	0.96	396	C
IIF-319	i-Bu	Hxy	Bnzl	0.98	410	C
IIF-320	4-F-Bnzl	Bnzl	Bnzl	0.94	468	C
IIF-321	Ph-Et	Bnzl	Bnzl	0.96	464	C
IIF-322	Bnzl	i-Bu	i-Pnt	0.97	396	C
IIF-323	4-F-Bnzl	Bnzl	i-Bu	0.94	434	C

TABLE 2-13
Formula XXIIF
Compound					LCMS	Mass	Measurement
number	R1	R2A	R2B	R3	RT (min)	(M + H)+	condition
IIF-324	2-Npm	H	Bnzl	i-Bu	2.89	466	B1
IIF-325	i-Pnt	H	3-Cl-Bnzl	Bnzl	2.85	464	B1
IIF-326	i-Pnt	H	4-Cl-Bnzl	Bnzl	2.85	464	B1
IIF-327	i-Pnt	H	4-F-Bnzl	Bnzl	2.73	448	B1
IIF-328	i-Pnt	H	4-Me-Bnzl	Bnzl	2.83	444	B1
IIF-329	i-Pnt	H	4-MeO-Bnzl	Bnzl	2.71	460	B1
IIF-330	i-Bu	H	4-Cl-Bnzl	Ph-Et	2.68	464	B1
IIF-331	i-Bu	H	3-Cl-Bnzl	Ph-Et	2.85	464	B1
IIF-332	i-Bu	H	4-MeO-Bnzl	Ph-Et	2.50	460	B1
IIF-333	i-Bu	H	4-Me-Bnzl	Ph-Et	2.65	444	B1
IIF-334	i-Bu	H	2-Npm	Ph-Et	2.77	480	B1
IIF-335	i-Bu	H	Bnzl	Ph-Pr	2.65	444	B1
IIF-336	i-Bu	H	3-Cl-Bnzl	Ph-Pr	1.27	478	B
IIF-337	i-Bu	H	3-F-Bnzl	Ph-Pr	1.25	462	B
IIF-338	Cpm	H	4-OH-Bnzl	Cbx-E	0.96	440	B
IIF-339	i-Bu	H	3-Me-Bnzl	Ph-Pr	1.26	458	B
IIF-340	i-Bu	H	3-MeO-Bnzl	Ph-Pr	1.25	474	B
IIF-341	i-Bu	H	3-Cl-Bnzl	Ph-Bu	1.30	492	B
IIF-342	i-Bu	H	3-F-Bnzl	Ph-Bu	1.26	476	B
IIF-343	i-Bu	H	3-Me-Bnzl	Ph-Bu	1.29	472	B
IIF-344	i-Bu	H	3-MeO-Bnzl	Ph-Bu	1.26	488	B
IIF-345	i-Bu	H	Bnzl	Ph-Bu	1.25	458	B
IIF-346	i-Pnt	H	3-F-Bnzl	Ph-Pr	1.25	476	B
IIF-347	Hdr-E	H	4-fluorophenethyl	1-Npm	0.9	486	C
IIF-348	1-Npm	H	cyclohexyl	Ph-Et	1.02	506	C
IIF-349	1-Npm	H	cyclopentyl	Ph-Et	0.99	492	C
IIF-350	1-Npm	H	pentyl	Ph-Et	1.01	494	C
IIF-351	1-Npm	H	heptyl	Ph-Et	1.08	522	C
IIF-352	propyl	H	Chm	Bnzl	0.95	408	C
IIF-353	1-Npm	H	hexyl	4-methylphenethyl	1.07	522	C
IIF-354	1-Npm	H	hexyl	2-(naphthalen-2-yl)ethyl	1.10	558	C
IIF-355	1-Npm	H	hexyl	4-isopropylphenethyl	1.12	550	C
IIF-356	1-Npm	H	hexyl	cyclohexylethyl	1.13	514	C
IIF-357	tBuO-E	H	4-fluorophenethyl	1-Npm	1.01	542	C
IIF-358	tBuO-E	H	4-Cl-Bnzl	1-Npm	1.03	545	C
IIF-359	tBuO-E	H	4-Me-Bnzl	1-Npm	1.02	524	C
IIF-360	1-Npm	piperidine †	Ph-Et	0.95	492	C

TABLE 2-14
IIF-361	1-Npm	pyrrolidine †	Ph-Et	0.93	478	C
IIF-362	propyl	H	Bnzl	Chm	0.94	408	C
IIF-363	propyl	H	2-methylbenzyl	Bnzl	0.91	416	C
IIF-364	propyl	H	(1,2,3,4-	Bnzl	0.97	456	C
			tetrahydronaphthalen-
			1-yl)methyl
IIF-365	propyl	H	Cpm	Bnzl	0.92	394	C
IIF-366	propyl	H	Bnzl	Cpm	0.91	394	C
IIF-367	1-Npm	H	Hxy	3-	1.07	522	C
				methylphenethyl
IIF-368	4-	H	Bnzl	Bnzl	0.92	495	C
	Nt-Bnzl
IIF-369	4-	H	Hxy	Ph-Et	1.01	503	C
	Nt-Bnzl
IIF-370	i-Pnt	H	Ph-Et	Bnzl	2.76	444	B1
IIF-371	i-Pnt	H	1-Npm	Bnzl	2.93	480	B1
IIF-372	i-Bu	H	4-F-Bnzl	Ph-Et	2.56	448	B1
IIF-373	i-Bu	H	Ph-Et	Ph-Et	2.60	444	B1
IIF-374	i-Bu	H	1-Npm	Ph-Et	2.79	480	B1
IIF-375	4-F-	H	1-Npm	Bnzl	2.80	518	B1
	Bnzl
IIF-376	4-F-	H	1-Npm	i-Bu	1.26	484	B
	Bnzl
IIF-377	tBuO-E	H	4-F-Bnzl	1-Npm	1.01	528	C
IIF-378	4-tBuO-	H	Bnzl	Ph-Et	1.01	536	C
	Bnzl
IIF-379	tBuO-E	H	Bnzl	1-Npm	1.00	510	C
IIF-380	Chm	H	tBuO-E	1-Npm	1.01	516	C
IIF-381	tBOC-E	H	Bnzl	Ph-Et	0.97	502	C
IIF-382	i-Pnt	H	Bnzl	Ph-Et	0.96	444	C
IIF-383	1-Npm	H	4-F-Bnzl	Hdr-E	0.83	472	C
IIF-384	Hdr-E	H	4-F-Bnzl	1-Npm	0.88	472	C
IIF-385	Cbx-E	H	Bnzl	Ph-Et	0.86	446	C
IIF-386	tBuO-E	H	Ph-Et	1-Npm	1.02	524	C
IIF-387	Ph-Et	H	Hxy	1-Npm	1.06	508	C
IIF-388	Ph-Et	H	i-Bu	TBSO-E	1.09	498	C
IIF-389	Ph-Et	H	i-Bu	Hdr-E	0.77	384	C
IIF-390	Ph-Et	H	i-Bu	i-Pnt	0.96	410	C
IIF-391	Ph-Et	H	i-Bu	4-tBuO-Bnzl	1.02	502	C
IIF-392	Ph-Et	H	i-Bu	4-OH-Bnzl	0.85	446	C
IIF-393	i-Bu	H	i-Bu	4-OH-Bnzl	0.80	398	C
IIF-394	i-Bu	H	Bnzl	4-OH-Bnzl	0.82	432	C
IIF-395	i-Bu	H	2-Cbx-Et	4-OH-Bnzl	0.63	414	C
IIF-396	i-Bu	H	s-Bu	4-OH-Bnzl	0.79	398	C
IIF-397	i-Bu	H	1-Npm	4-OH-Bnzl	0.89	482	C
IIF-398	i-Bu	H	i-Pr	4-OH-Bnzl	0.75	384	C
IIF-399	i-Bu	H	1-Npm	2-Cbx-Et	0.82	448	C
IIF-400	Bnzl	H	4-OH-Bnzl	Bnzl	0.83	466	C
IIF-401	Bnzl	H	i-Bu	4-OH-Bnzl	0.82	432	C
IIF-402	Bnzl	H	2-Cbx-Et	4-OH-Bnzl	0.67	448	C
IIF-403	Bnzl	H	Bnzl	2-Cbx-Et	0.76	432	C
IIF-404	Bnzl	H	4-OH-Bnzl	2-Cbx-Et	0.68	448	C
IIF-405	Bnzl	H	1-Npm	2-Cbx-Et	0.84	482	C
IIF-406	Bnzl	H	4-OH-Bnzl	1-Npm	0.89	516	C
IIF-407	Bnzl	H	2-Cbx-Et	1-Npm	0.83	482	C
IIF-408	4-	H	2-Cbx-Et	Bnzl	0.69	448	C
	OH-Bnzl

TABLE 2-15
IIF-409	4-OH-	H	s-Bu	Bnzl	0.84	432	C
	Bnzl
IIF-410	4-OH-	H	1-Npm	Bnzl	0.93	516	C
	Bnzl
IIF-411	4-OH-	H	Bnzl	2-Cbx-Et	0.73	448	C
	Bnzl
IIF-412	4-OH-	H	1-Npm	2-Cbx-Et	0.81	498	C
	Bnzl
IIF-413	4-OH-	H	i-Bu	1-Npm	0.91	482	C
	Bnzl
IIF-414	4-OH-	H	Bnzl	1-Npm	0.92	516	C
	Bnzl
IIF-415	4-OH-	H	2-Cbx-	1-Npm	0.76	498	C
	Bnzl		Et
IIF-416	4-OH-	H	s-Bu	1-Npm	0.91	482	C
	Bnzl
IIF-417	4-OH-	H	1-Npm	1-Npm	0.98	566	C
	Bnzl
IIF-418	i-Bu	H	4-OH-	Bnzl	0.81	432	C
			Bnzl
IIF-419	i-Bu	H	i-Bu	2-Cbx-Et	0.71	364	C
IIF-420	i-Bu	H	Bnzl	2-Cbx-Et	0.73	398	C
IIF-421	i-Bu	H	4-OH-	2-Cbx-Et	0.65	414	C
			Bnzl
IIF-422	i-Bu	H	i-Pr	2-Cbx-Et	0.65	350	C
IIF-423	i-Bu	H	4-OH-	1-Npm	0.87	482	C
			Bnzl
IIF-424	i-Bu	H	2-Cbx-	1-Npm	0.81	448	C
			Et
IIF-425	Bnzl	H	2-Cbx-	Bnzl	0.76	432	C
			Et
IIF-426	Bnzl	H	s-Bu	4-OH-Bnzl	0.81	432	C
IIF-427	Bnzl	H	1-Npm	4-OH-Bnzl	0.90	516	C
IIF-428	Bnzl	H	i-Pr	4-OH-Bnzl	0.77	418	C
IIF-429	Bnzl	H	s-Bu	2-Cbx-Et	0.73	398	C
IIF-430	Bnzl	H	i-Pr	2-Cbx-Et	0.69	384	C
IIF-431	4-OH-	H	i-Pr	Bnzl	0.8	418	C
	Bnzl
IIF-432	4-OH-	H	i-Pr	2-Cbx-Et	0.65	400	C
	Bnzl
IIF-433	4-OH-	H	i-Pr	1-Npm	0.87	468	C
	Bnzl
IIF-434	2-Cbx-	H	i-Bu	Bnzl	0.80	398	C
	Et
IIF-435	1-Npm	H	4-OH-	Bnzl	0.89	516	C
			Bnzl
IIF-436	1-Npm	H	Bnzl	4-OH-Bnzl	0.87	516	C
IIF-437	1-Npm	H	2-Cbx-	4-OH-Bnzl	0.73	498	C
			Et
IIF-438	1-Npm	H	s-Bu	4-OH-Bnzl	0.86	482	C
IIF-439	1-Npm	H	1-Npm	4-OH-Bnzl	0.94	566	C
IIF-440	1-Npm	H	i-Pr	4-OH-Bnzl	0.82	468	C
IIF-441	1-Npm	H	Bnzl	2-Cbx-Et	0.81	482	C
IIF-442	1-Npm	H	4-OH-	2-Cbx-Et	0.74	498	C
			Bnzl
IIF-443	1-Npm	H	s-Bu	2-Cbx-Et	0.79	448	C
IIF-444	1-Npm	H	1-Npm	2-Cbx-Et	0.88	532	C
IIF-445	1-Npm	H	4-OH-	1-Npm	0.96	566	C
			Bnzl
IIF-446	1-Npm	H	2-Cbx-	1-Npm	0.88	532	C
			Et
IIF-447	i-Bu	H	4-OH-	i-Bu	0.78	398	C
			Bnzl
IIF-448	i-Bu	H	2-Cbx-	i-Bu	0.70	364	C
			Et
IIF-449	i-Bu	H	1-Npm	3-Gun-Pr	0.72	475	C
IIF-450	Bnzl	H	i-Bu	2-Cbx-Et	0.73	398	C
IIF-451	2-Cbx-	H	Bnzl	i-Bu	0.80	398	C
	Et
IIF-452	2-Cbx-	H	4-OH-	i-Bu	0.70	414	C
	Et		Bnzl
IIF-453	2-Cbx-	H	s-Bu	i-Bu	0.78	364	C
	Et
IIF-454	2-Cbx-	H	1-Npm	i-Bu	0.88	448	C
	Et
IIF-455	2-Cbx-	H	i-Pr	i-Bu	0.74	350	C
	Et
IIF-456	2-Cbx-	H	1-Npm	Bnzl	0.88	482	C
	Et
IIF-457	2-Cbx-	H	Bnzl	4-OH-Bnzl	0.77	448	C
	Et
IIF-458	2-Cbx-	H	1-Npm	4-OH-Bnzl	0.84	498	C
	Et

TABLE 2-16
IIF-459	2-Cbx-	H	i-Bu	1-Npm	0.86	448	C
	Et
IIF-460	2-Cbx-	H	4-OH	1-Npm	0.77	498	C
	Et		Bnzl
IIF-461	2-Cbx-	H	1-Npm	1-Npm	0.94	532	C
	Et
IIF-462	2-Cbx-	H	i-Pr	1-Npm	0.82	434	C
	Et
IIF-463	1-Npm	H	4-OH-	i-Bu	0.87	482	C
			Bnzl
IIF-464	1-Npm	H	i-Bu	4-OH-	0.85	482	C
				Bnzl
IIF-465	1-Npm	H	i-Bu	2-Cbx-	0.78	448	C
				Et
IIF-466	1-Npm	H	i-Pr	2-Cbx-	0.75	434	C
				Et
IIF-467	1-Npm	H	3-Gun-	1-Npm	0.78	559	C
			Pr
IIF-468	i-Bu	H	3-Gun-	i-Bu	0.63	391	C
			Pr
IIF-469	i-Bu	H	3-Gun-	Bnzl	0.66	425	C
			Pr
IIF-470	i-Bu	H	s-Bu	2-Cbx-	0.70	364	C
				Et
IIF-471	i-Bu	H	i-Bu	3-Gun-	0.62	391	C
				Pr
IIF-472	i-Bu	H	Bnzl	3-Gun-	0.65	425	C
				Pr
IIF-473	i-Bu	H	s-Bu	3-Gun-	0.62	391	C
				Pr
IIF-474	i-Bu	H	i-Pr	3-Gun-	0.58	377	C
				Pr
IIF-475	i-Bu	H	3-Gun-	1-Npm	0.72	475	C
			Pr
IIF-476	Bnzl	H	3-Gun-	i-Bu	0.67	425	C
			Pr
IIF-477	Bnzl	H	3-Gun-	Bnzl	0.69	459	C
			Pr
IIF-478	Bnzl	H	i-Bu	3-Gun-	0.64	425	C
				Pr
IIF-479	Bnzl	H	Bnzl	3-Gun-	0.66	459	C
				Pr
IIF-480	Bnzl	H	s-Bu	3-Gun-	0.64	425	C
				Pr
IIF-481	Bnzl	H	1-Npm	3-Gun-	0.73	509	C
				Pr
IIF-482	Bnzl	H	3-Gun-	1-Npm	0.74	509	C
			Pr
IIF-483	2-Cbx-	H	i-Bu	i-Bu	0.79	364	C
	Et
IIF-484	2-Cbx-	H	Bnzl	Bnzl	0.81	432	C
	Et
IIF-485	2-Cbx-	H	4-OH-	Bnzl	0.72	448	C
	Et		Bnzl
IIF-486	2-Cbx-	H	s-Bu	Bnzl	0.79	398	C
	Et
IIF-487	2-Cbx-	H	i-Pr	Bnzl	0.75	384	C
	Et
IIF-488	2-Cbx-	H	i-Bu	4-OH-	0.75	414	C
	Et			Bnzl
IIF-489	2-Cbx-	H	i-Pr	4-OH-	0.70	400	C
	Et			Bnzl
IIF-490	2-Cbx-	H	Bnzl	1-Npm	0.87	482	C
	Et
IIF-491	2-Cbx-	H	s-Bu	1-Npm	0.86	448	C
	Et
IIF-492	3-Gun-	H	1-Npm	i-Bu	0.79	475	C
	Pr
IIF-493	3-Gun-	H	i-Pr	i-Bu	0.67	377	C
	Pr
IIF-494	3-Gun-	H	i-Pr	Bnzl	0.66	411	C
	Pr
IIF-495	3-Gun-	H	1-Npm	1-Npm	0.83	559	C
	Pr
IIF-496	3-Gun-	H	i-Pr	1-Npm	0.73	461	C
	Pr
IIF-497	3-	H	4-F-	1-Npm	1.00	542	C
	tert-		Bnzl
	butoxy-
	propyl
IIF-498	3-	H	4-F-	1-Npm	0.88	486	C
	hydroxy-		Bnzl
	propyl
IIF-499	3-amino-	H	3-	3-	1.02	751	C
	propyl		amino-	amino-
			propyl	propyl
IIF-500	1-Npm	H	β-	Ph—Et	0.93	544	C
			hydroxy-
			phenethyl
IIF-501	1-Npm	H	α-	Ph—Et	0.92	558	C
			(hydroxy-
			methyl)
			phenethyl
IIF-502	1-Npm	H	α-	Ph—Et	0.95	558	C
			(hydroxy-
			methyl)
			phenethyl

TABLE 2-17
IIF-503	4-Nt-	H	Bnzl	tBOC-E	0.93	533	C
	Bnzl
IIF-504	2-OH-	H	Ph—Et	1-Npm	0.89	468.3	C
	Et
IIF-505	Chm	H	2-	1-Npm	0.86	460.3	C
			OH—Et
IIF-506	2-OH—Et	H	Benzl	1-Npm	0.87	454.3	C
IIF-507	Ph—Et	H	1-Npm	Hxy	1.06	508.4	C
IIF-508	1-Npm	H	Ph—Et	Hxy	1.04	508.4	C
IIF-509	Hxy	H	Ph—Et	1-Npm	1.04	508.4	C
IIF-510	Hxy	H	1-Npm	Ph—Et	1.03	508.4	C
IIF-511	i-Pnt	H	i-Pr	i-Bu	3.25	348	F
IIF-512	Chm	H	i-Pr	i-Bu	3.49	374	F
IIF-513	Chm	H	i-Pr	i-Pnt	3.74	388	F
IIF-514	i-Bu	H	s-Bu	i-Pnt	3.55	362	F
IIF-515	i-Pnt	H	s-Bu	i-Bu	3.45	362	F
IIF-516	Chm	H	s-Bu	i-Bu	3.72	388	F
IIF-517	Chm	H	s-Bu	Ph—Et	4	436	F
IIF-518	Chm	H	s-Bu	i-Pnt	4.02	402	F
IIF-519	i-Bu	H	i-Pnt	i-Bu	3.52	362	F
IIF-520	Chm	H	i-Pnt	i-Bu	3.99	402	F
IIF-521	i-Bu	H	Hxy	i-Bu	3.88	376	F
IIF-522	Chm	H	Hxy	i-Bu	4.34	416	F
IIF-523	2-Cbx-	H	Bnzl	i-Pnt	3.3	412	F
	Et
IIF-524	Ph—Et	H	Bnzl	2-Cbx-	3.02	446	F
				Et
IIF-525	4-F-	H	Bnzl	2-Cbx-	2.85	450	F
	Bnzl			Et
IIF-526	2-	H	Bnzl	2-Cbx-	2.45	386	F
	OH—Et			Et
IIF-527	i-Pnt	H	Bnzl	2-Cbx-	2.85	412	F
				Et
IIF-528	i-Pnt	H	Bnzl	2-	2.84	384	F
				OH—Et
IIF-529	Chm	H	Bnzl	2-Cbx-	3	438	F
				Et
IIF-530	2-Cbx-	H	i-Bu	Ph—Et	3.17	412	F
	Et
IIF-531	2-Cbx-	H	i-Bu	i-Pnt	3.12	378	F
	Et
IIF-532	4-F-Bnzl	H	i-Bu	2-Cbx-	2.69	416	F
				Et
IIF-533	2-	H	i-Bu	2-Cbx-	3.49	352	G
	OH—Et			Et
IIF-534	i-Pnt	H	i-Bu	4-OH-	3.12	412	F
				Bnzl
IIF-535	Chm	H	i-Bu	2-Cbx-	2.84	404	F
				Et
IIF-536	2-	H	1-Npm	Ph—Et	3.72	496	F
	Cbx-
	Et
IIF-537	2-Cbx-	H	1-Npm	i-Pnt	3.65	462	F
	Et
IIF-538	Ph—Et	H	1-Npm	2-Cbx-	3.47	496	F
				Et
IIF-539	4-F-Bnzl	H	1-Npm	2-Cbx-	3.3	500	F
				Et
IIF-540	2-	H	1-Npm	2-Cbx-	2.87	436	F
	OH—Et			Et
IIF-541	i-Pnt	H	1-Npm	2-Cbx-	3.34	462	F
				Et
IIF-542	Chm	H	1-Npm	2-Cbx-	3.4	488	F
				Et
IIF-543	4-	H	i-Pr	Ph—Et	3.19	432	F
	OH-Bnzl
IIF-544	4-	H	i-Pr	i-Pnt	3.09	398	F
	OH-
	Bnzl
IIF-545	2-Cbx-	H	i-Pr	Ph—Et	2.92	398	F
	Et
IIF-546	2-	H	i-Pr	2-	3.02	338	G
	Cbx-Et			OH—Et
IIF-547	Ph—Et	H	i-Pr	2-Cbx-	2.65	398	F
				Et
IIF-548	Ph—Et	H	i-Pr	2-	2.62	370	F
				OH—Et
IIF-549	4-F-	H	i-Pr	2-Cbx-	2.5	402	F
	Bnzl			Et
IIF-550	4-F-	H	i-Pr	2-	2.47	374	F
	Bnzl			OH—Et
IIF-551	2-	H	i-Pr	Bnzl	2.69	356	F
	OH—Et
IIF-552	2-	H	i-Pr	i-Bu	2.57	322	F
	OH—Et

TABLE 2-18
IIF-553	2-	H	I-Pr	1-Npm	3.07	406	F
	OH—Et
IIF-554	2-	H	i-Pr	4-	2.45	372	F
	OH—Et			OH-Bnzl
IIF-555	2-	H	i-Pr	2-Cbx-	3.12	338	G
	OH—Et			Et
IIF-556	2-	H	i-Pr	Ph—Et	2.9	370	F
	OH—Et
IIF-557	2-	H	i-Pr	i-Pnt	2.82	336	F
	OH—Et
IIF-558	i-Pnt	H	i-Pr	4-	2.88	398	F
				OH-
				Bnzl
IIF-559	i-Pnt	H	i-Pr	2-Cbx-	2.49	364	F
				Et
IIF-560	i-Pnt	H	i-Pr	2-	3.67	336	G
				OH—Et
IIF-561	i-Bu	H	s-Bu	2-	3.69	336	G
				OH—Et
IIF-562	4-	H	s-Bu	Ph—Et	3.35	446	F
	OH-Bnzl
IIF-563	4-	H	s-Bu	i-Pnt	3.2	412	F
	OH-Bnzl
IIF-564	2-	H	s-Bu	i-Pnt	3.09	378	F
	Cbx-Et
IIF-565	Ph—Et	H	s-Bu	2-Cbx-	2.8	412	F
				Et
IIF-566	4-F-	H	s-Bu	2-Cbx-	2.69	416	F
	Bnzl			Et
IIF-567	2-	H	s-Bu	4-OH-	2.67	386	F
	OH—Et			Bnzl
IIF-568	2-	H	s-Bu	2-Cbx-	3.47	352	G
	OH—Et			Et
IIF-569	i-Pnt	H	s-Bu	4-OH-	3.07	412	F
				Bnzl
IIF-570	i-Pnt	H	s-Bu	2-Cbx-	2.67	378	F
				Et
IIF-571	Chm	H	s-Bu	4-	3.2	438	F
				OH-Bnzl
IIF-572	Chm	H	s-Bu	2-Cbx-	2.8	404	F
				Et
IIF-573	i-Bu	H	4-	i-Pnt	3.1	412	F
			OH-
			Bnzl
IIF-574	2-Cbx-	H	4-	Ph—Et	2.77	462	F
	Et		OH-
			Bnzl
IIF-575	2-Cbx-	H	4-	i-Pnt	2.72	428	F
	Et		OH-
			Bnzl
IIF-576	Ph—Et	H	4-	2-Cbx-	2.67	462	F
			OH-	Et
			Bnzl
IIF-577	4-F-Bnzl	H	4-	2-Cbx-	2.55	466	F
			OH-	Et
			Bnzl
IIF-578	2-OH-Et	H	4-	2-Cbx-	3.2	402	G
			OH-	Et
			Bnzl
IIF-579	i-Pnt	H	4-	2-Cbx-	2.52	428	F
			OH-	Et
			Bnzl
IIF-580	Chm	H	4-	2-Cbx-	2.67	454	F
			OH-	Et
			Bnzl
IIF-581	i-Bu	H	2-	Ph—Et	2.82	412	F
			Cbx-
			Et
IIF-582	i-Bu	H	2-	i-Pnt	2.72	378	F
			Cbx-
			Et
IIF-583	i-Pnt	H	2-	i-Bu	2.74	378	F
			Cbx-
			Et
IIF-584	i-Pnt	H	2-	4-OH-	2.45	428	F
			Cbx-	Bnzl
			Et
IIF-585	Chm	H	2-	i-Bu	2.94	404	F
			Cbx-
			Et
IIF-586	Chm	H	2-	i-Pnt	3.17	418	F
			Cbx-
			Et
IIF-587	Bnzl	H	4-F-	4-OH-	3.25	484	F
			Bnzl	Bnzl
IIF-588	Bnzl	H	4-F-	2-Cbx-	2.88	450	F
			Bnzl	Et
IIF-589	i-Bu	H	4-F-	4-OH-	3.12	450	F
			Bnzl	Bnzl
IIF-590	i-Bu	H	4-F-	2-Cbx-	2.72	416	F
			Bnzl	Et
IIF-591	1-Npm	H	4-F-	4-OH-	3.5	534	F
			Bnzl	Bnzl
IIF-592	1-Npm	H	4-F-	2-Cbx-	3.13	500	F
			Bnzl	Et
IIF-593	4-OH-	H	4-F-	2-Cbx-	2.7	466	F
	Bnzl		Bnzl	Et
IIF-594	4-OH-	H	4-F-	Ph—Et	3.5	498	F
	Bnzl		Bnzl
IIF-595	4-OH-	H	4-F-	i-Pnt	3.44	464	F
	Bnzl		Bnzl
IIF-596	2-Cbx-	H	4-F-	4-OH-	2.9	466	F
	Et		Bnzl	Bnzl
IIF-597	2-Cbx-	H	4-F-	Ph—Et	3.32	464	F
	Et		Bnzl
IIF-598	2-Cbx-	H	4-F-	i-Pnt	3.25	430	F
	Et		Bnzl
IIF-599	Ph—Et	H	4-F-	4-OH-	3.42	498	F
			Bnzl	Bnzl
IIF-600	Ph—Et	H	4-F-	2-Cbx-	3.07	464	F
			Bnzl	Et
IIF-601	2-OH-	H	4-F-	4-OH-	2.84	438	F
	Et		Bnzl	Bnzl
IIF-602	2-OH-	H	4-F-	2-Cbx-	2.52	404	F
	Et		Bnzl	Et

TABLE 2-19
IIF-603	i-	H	4-F-	4-OH-	3.27	464	F
	Pnt		Bnzl	Bnzl
IIF-604	Chm	H	4-F-	4-OH-	3.37	490	F
			Bnzl	Bnzl
IIF-605	Chm	H	4-F-	2-Cbx-	3	456	F
			Bnzl	Et
IIF-606	i-Bu	H	i-Pnt	2-Cbx-	2.72	378	F
				Et
IIF-607	4-	H	i-Pnt	2-Cbx-	2.72	428	F
	OH-			Et
	Bnzl
IIF-608	2-Cbx-	H	i-Pnt	i-Bu	3.1	378	F
	Et
IIF-609	2-Cbx-	H	i-Pnt	4-OH-	2.94	428	F
	Et			Bnzl
IIF-610	2-OH-	H	i-Pnt	i-Bu	3.04	350	F
	Et
IIF-611	Chm	H	i-Pnt	2-Cbx-	3.05	418	F
				Et
IIF-612	i-Bu	H	2-OH-	i-Bu	2.43	336	F
			Et
IIF-613	i-Bu	H	2-OH-	4-OH-	1.34	386	F
			Et	Bnzl
IIF-614	i-Bu	H	2-OH-	2-Cbx-	2.57	352	F
			Et	Et
IIF-615	1-Npm	H	2-OH-	4-OH-	2.62	470	F
			Et	Bnzl
IIF-616	1-Npm	H	2-OH-	2-Cbx-	2.45	436	F
			Et	Et
IIF-617	4-OH-	H	2-OH-	Bnzl	2.43	420	F
	Bnzl		Et
IIF-618	4-OH-	H	2-OH-	1-Npm	2.74	470	F
	Bnzl		Et
IIF-619	4-OH-	H	2-OH-	i-Pnt	2.45	400	F
	Bnzl		Et
IIF-620	2-Cbx-	H	2-OH-	Bnzl	3.32	386	F
	Et		Et
IIF-621	2-Cbx-	H	2-OH-	4-OH-	2.94	402	G
	Et		Et	Bnzl
IIF-622	2-Cbx-	H	2-OH-	i-Pnt	3.42	366	G
	Et		Et
IIF-623	Bnzl	H	Ph—Et	4-OH-	3.29	480	F
				Bnzl
IIF-624	Bnzl	H	Ph—Et	2-Cbx-	2.9	446	F
				Et
IIF-625	i-Bu	H	Ph—Et	4-OH-	3.15	446	F
				Bnzl
IIF-626	i-Bu	H	Ph—Et	2-Cbx-	2.77	412	F
				Et
IIF-627	1-Npm	H	Ph—Et	4-OH-	3.55	530	F
				Bnzl
IIF-628	4-OH-	H	Ph—Et	i-Pnt	3.57	460	F
	Bnzl
IIF-629	2-Cbx-	H	Ph—Et	4-OH-	2.95	462	F
	Et			Bnzl
IIF-630	4-F-	H	Ph—Et	4-OH-	3.3	498	F
	Bnzl			Bnzl
IIF-631	2-OH-	H	Ph—Et	4-OH-	2.88	434	F
	Et			Bnzl
IIF-632	i-Pnt	H	Ph—Et	4-OH-	3.37	460	F
				Bnzl
IIF-633	i-Pnt	H	Ph—Et	2-Cbx-	2.99	426	F
				Et
IIF-634	Chm	H	Ph—Et	4-OH-	3.47	486	F
				Bnzl
IIF-635	Chm	H	Ph—Et	2-Cbx-	3.1	452	F
				Et
IIF-636	Bnzl	H	Hxy	2-Cbx-	3.15	426	F
				Et
IIF-637	4-OH-	H	Hxy	1-Npm	4.15	510	F
	Bnzl
IIF-638	4-OH-	H	Hxy	2-Cbx-	3	442	F
	Bnzl			Et
IIF-639	2-Cbx-	H	Hxy	i-Bu	3.4	392	F
	Et
IIF-640	2-Cbx-	H	Hxy	1-Npm	3.85	476	F
	Et
IIF-641	2-Cbx-	H	Hxy	4-OH-	3.22	442	F
	Et			Bnzl
IIF-642	2-Cbx-	H	Hxy	i-Pnt	3.65	406	F
	Et
IIF-643	Ph—Et	H	Hxy	2-Cbx-	3.37	440	F
				Et
IIF-644	4-F-	H	Hxy	2-Cbx-	3.2	444	F
	Bnzl			Et
IIF-645	2-	H	Hxy	i-Bu	3.35	364	F
	OH—Et
IIF-646	2-	H	Hxy	4-OH-	3.15	414	F
	OH—Et			Bnzl
IIF-647	2-	H	Hxy	2-Cbx-	2.79	380	F
	OH—Et			Et
IIF-648	2-	H	Hxy	i-Pnt	3.55	378	F
	OH—Et
IIF-649	i-Pnt	H	Hxy	4-OH-	3.69	440	F
				Bnzl
IIF-650	i-Pnt	H	Hxy	2-Cbx-	3.24	406	F
				Et
IIF-651	i-Pnt	H	Hxy	2-	3.24	378	F
				OH—Et
IIF-652	Chm	H	Hxy	4-OH-	3.75	466	F
				Bnzl

TABLE 2-20
IIF-653	Chm	H	Hxy	2-Cbx-	3.35	432	F
				Et
IIF-654	tBOC-	H	Bnzl	i-Pnt	4.09	468	F
	E
IIF-655	Ph—Et	H	Bnzl	tBOC-	4.04	502	F
				E
IIF-656	4-F-	H	Bnzl	tBOC-	3.8	506	F
	Bnzl			E
IIF-657	tBOC-	H	i-Bu	Ph—Et	3.92	468	F
	E
IIF-658	4-F-	H	i-Bu	tBOC-	3.7	472	F
	Bnzl			E
IIF-659	i-Pnt	H	i-Bu	4-tBuO-	4.39	468	F
				Bnzl
IIF-660	Chm	H	i-Bu	4-tBuO-	4.35	494	F
				Bnzl
IIF-661	Chm	H	i-Bu	tBOC-	3.94	460	E
				E
IIF-662	tBOC-	H	1-Npm	Ph—Et	4.47	552	F
	E
IIF-663	tBOC-	H	1-Npm	i-Pnt	4.52	518	F
	E
IIF-664	Ph—Et	H	1-Npm	tBOC-	4.39	552	F
				E
IIF-665	4-F-	H	1-Npm	tBOC-	4.25	556	F
	Bnzl			E
IIF-666	2-	H	1-Npm	tBOC-	4.89	548	F
	OtBu-			E
	Et
IIF-667	i-Pnt	H	1-Npm	tBOC-	4.35	518	F
				E
IIF-668	Chm	H	1-Npm	tBOC-	4.54	544	F
				E
IIF-669	4-	H	i-Pr	i-Pnt	4.07	454	F
	tBuO-
	Bnzl
IIF-670	tBOC-	H	i-Pr	Ph—Et	3.72	454	F
	E
IIF-671	2-	H	i-Pr	1-Npm	3.87	462	F
	OtBu-
	Et
IIF-672	2-	H	i-Pr	4-tBuO-	3.9	484	F
	OtBu-			Bnzl
	Et
IIF-673	Chm	H	i-Pr	4-tBuO-	4.07	480	F
				Bnzl
IIF-674	4-	H	s-Bu	Ph—Et	4.22	502	F
	tBuO-
	Bnzl
IIF-675	4-	H	s-Bu	i-Pnt	4.07	468	F
	tBuO-
	Bnzl
IIF-676	tBOC-	H	s-Bu	i-Pnt	3.82	434	F
	E
IFF-677	Ph—Et	H	s-Bu	tBOC-	3.84	468	F
				E
IIF-678	4-F-	H	s-Bu	tBOC-	3.95	472	F
	Bnzl			E
IIF-679	2-	H	s-Bu	tBOC-	3.7	464	F
	OtBu-			E
	Et
IIF-680	i-Pnt	H	s-Bu	4-tBuO-	4.12	468	F
				Bnzl
IIF-681	i-Pnt	H	s-Bu	tBOC-	3.7	434	F
				E
IIF-682	Chm	H	s-Bu	4-tBuO-	4.35	494	F
				Bnzl
IIF-683	i-Bu	H	4-	i-Pnt	4.07	468	F
			tBuO-
			Bnzl
IIF-684	tBOC-	H	4-	Ph—Et	4.52	574	F
	E		tBuO-
			Bnzl
IIF-685	tBOC-	H	4-	i-Pnt	4.42	540	F
	E		tBuO-
			Bnzl
IIF-686	Ph—Et	H	4-	tBOC-	4.52	574	F
			tBuO-	E
			Bnzl
IIF-687	4-F-	H	4-	tBOC-	4.22	578	F
	Bnzl		tBuO-	E
			Bnzl
IIF-688	Chm	H	4-	tBOC-	4.54	566	F
			tBuO-	E
			Bnzl
IIF-689	i-Bu	H	tBOC-	i-Pnt	3.7	434	F
			E
IIF-690	Bnzl	H	4-F-	4-tBuO-	4.17	540	F
			Bnzl	Bnzl
IIF-691	i-Bu	H	4-F-	4-tBuO-	3.99	506	F
			Bnzl	Bnzl
IIF-692	i-Bu	H	4-F-	tBOC-	3.67	472	F
			Bnzl	E
IIF-693	1-Npm	H	4-F-	4-tBuO-	4.59	590	F
			Bnzl	Bnzl
IIF-694	1-Npm	H	4-F-	tBOC-	4.17	556	F
			Bnzl	E
IIF-695	4-	H	4-F-	tBOC-	4.34	578	F
	tBuO-		Bnzl	E
	Bnzl
IIF-696	4-	H	4-F-	Ph—Et	4.75	554	F
	tBuO-		Bnzl
	Bnzl
IIF-697	4-	H	4-F-	i-Pnt	4.42	520	F
	tBuO-		Bnzl
	Bnzl
IIF-698	tBOC-	H	4-F-	4-tBuO-	4.39	578	F
	E		Bnzl	Bnzl
IIF-699	tBOC-	H	4-F-	i-Pnt	4.09	486	F
	E		Bnzl
IIF-700	Ph—Et	H	4-F-	4-tBuO-	4.34	554	F
			Bnzl	Bnzl
IIF-701	2-	H	4-F-	4-tBuO-	4.32	550	F
	OtBu-		Bnzl	Bnzl
	Et

TABLE 2-21
IIF-703	Chm	H	4-F-	4-tBuO-	4.39	546	F
			Bnzl	Bnzl
IIF-704	Chm	H	4-F-	tBOC-	4.05	512	F
			Bnzl	E
IIF-705	4-	H	i-Pnt	tBOC-	4.32	540	F
	tBuO-			E
	Bnzl
IIF-706	tBOC-	H	i-Pnt	4-tBuO-	4.54	540	F
	E			Bnzl
IIF-707	i-Bu	H	2-	4-tBuO-	3.87	498	F
			OtBu-	Bnzl
			Et
IIF-708	1-Npm	H	2-	4-tBuO-	4.47	582	F
			OtBu-	Bnzl
			Et
IIF-709	1-Npm	H	2-	tBOC-	4	548	F
			OtBu-	E
			Et
IIF-710	4-	H	2-	Bnzl	4.02	532	F
	tBuO-		OtBu-
	Bnzl		Et
IIF-711	4-	H	2-	i-Pnt	4.25	512	F
	tBuO-		OtBu-
	Bnzl		Et
IIF-712	tBOC-	H	2-	Bnzl	3.67	498	F
	E		OtBu-
			Et
IIF-713	tBOC-	H	2-	4-tBuO-	4.17	570	F
	E		OtBu-	Bnzl
			Et
IIF-714	Bnzl	H	Ph—Et	4-tBuO-	4.25	536	F
				Bnzl
IIF-715	i-Bu	H	Ph—Et	4-tBuO-	4.1	502	F
				Bnzl
IIF-716	1-Npm	H	Ph—Et	4-tBuO-	4.59	586	F
				Bnzl
IIF-717	1-Npm	H	Ph—Et	tBOC-	4.2	552	F
				E
IIF-718	4-F-	H	Ph—Et	4-tBuO-	4.29	554	F
	Bnzl			Bnzl
IIF-719	2-	H	Ph—Et	4-tBuO-	4.39	546	F
	OtBu-			Bnzl
	Et
IIF-720	i-Pnt	H	Ph—Et	4-tBuO-	4.37	516	F
				Bnzl
IIF-721	Chm	H	Ph—Et	4-tBuO-	4.54	542	F
IIF-722	Chm	H	Ph—Et	tBOC-	4.05	508	F
				E
IIF-723	4-	H	Hxy	1-Npm	5.09	566	F
	tBuO-
	Bnzl
IIF-724	4-	H	Hxy	tBOC-	4.74	554	F
	tBuO-			E
	Bnzl
IIF-725	tBOC-	H	Hxy	4-tBuO-	4.8	554	F
	E			Bnzl
IIF-726	Ph—Et	H	Hxy	tBOC-	4.45	496	F
				E
IIF-727	4-F-	H	Hxy	tBOC-	4.27	500	F
	Bnzl			E
IIF-728	2-	H	Hxy	4-tBuO-	4.79	526	F
	OtBu-			Bnzl
	Et
IIF-729	2-	H	Hxy	i-Pnt	4.42	434	F
	OtBu-
	Et
IIF-730	i-Pnt	H	Hxy	4-tBuO-	4.74	496	F
				Bnzl
IIF-731	Chm	H	Hxy	4-tBuO-	4.87	522	F
				Bnzl
IIF-732	i-Bu	H	i-Bu	Ph—Et	3.11	396	H
IIF-733	i-Bu	H	i-Bu	i-Pnt	2.96	362	H
IIF-734	1-Npm	H	i-Bu	i-Pnt	3.25	446	H
IIF-735	4-F-	H	i-Bu	i-Bu	2.88	400	H
	Bnzl
IIF-736	4-F-	H	i-Bu	1-Npm	3.12	484	H
	Bnzl
IIF-737	4-F-	H	i-Bu	Ph—Et	2.98	448	H
	Bnzl
IIF-738	4-F-	H	i-Bu	i-Pnt	2.98	414	H
	Bnzl
IIF-739	i-Pnt	H	i-Bu	i-Bu	2.92	362	H
IIF-740	i-Pnt	H	i-Bu	1-Npm	3.17	446	H
IIF-741	i-Pnt	H	i-Bu	Ph—Et	2.99	410	H
IIF-742	Chm	H	i-Bu	i-Bu	2.99	388	H
IIF-743	Chm	H	i-Bu	1-Npm	3.31	472	H
IIF-744	Chm	H	i-Bu	Ph—Et	3.1	436	H
IIF-745	Chm	H	i-Bu	i-Pnt	3.13	402	H
IIF-746	Bnzl	H	Bnzl	Ph—Et	3.22	464	H
IIF-747	1-Npm	H	Bnzl	i-Pnt	3.17	480	H
IIF-748	Ph—Et	H	Bnzl	1-Npm	3.27	514	H
IIF-749	Ph—Et	H	Bnzl	i-Pnt	3.12	444	H
IIF-750	4-F-	H	Bnzl	1-Npm	3.19	518	H
	Bnzl
IIF-751	4-F-	H	Bnzl	Ph—Et	3.02	482	H
	Bnzl
IIF-752	4-F-	H	Bnzl	i-Pnt	3.05	448	H
	Bnzl

TABLE 2-22
IIF-753	i-Pnt	H	Bnzl	1-Npm	3.2	480	H
IIF-754	Chm	H	Bnzl	1-Npm	3.3	506	H
IIF-755	Chm	H	Bnzl	Ph—Et	3.12	470	H
IIF-756	Chm	H	Bnzl	i-Pnt	3.15	436	H
IIF-757	Bnzl	H	1-Npm	Ph—Et	3.22	514	H
IIF-758	Bnzl	H	1-Npm	i-Pnt	3.27	480	H
IIF-759	i-Bu	H	1-Npm	i-Pnt	3.13	446	H
IIF-760	1-Npm	H	1-Npm	Ph—Et	3.34	564	H
IIF-761	1-Npm	H	1-Npm	i-Pnt	3.38	530	H
IIF-762	Ph—Et	H	1-Npm	Bnzl	3.27	514	H
IIF-763	Ph—Et	H	1-Npm	i-Bu	3.22	480	H
IIF-764	Ph—Et	H	1-Npm	1-Npm	3.42	564	H
IIF-765	Ph—Et	H	1-Npm	i-Pnt	3.32	494	H
IIF-766	4-F-	H	1-Npm	1-Npm	3.36	568	H
	Bnzl
IIF-767	4-F-	H	1-Npm	Ph—Et	3.22	532	H
	Bnzl
IIF-768	4-F-	H	1-Npm	i-Pnt	3.24	498	H
	Bnzl
IIF-769	i-Pnt	H	1-Npm	i-Bu	3.22	446	H
IIF-770	i-Pnt	H	1-Npm	1-Npm	3.39	530	H
IIF-771	i-Pnt	H	1-Npm	Ph—Et	3.27	494	H
IIF-772	Chm	H	1-Npm	Bnzl	3.38	506	H
IIF-773	Chm	H	1-Npm	i-Bu	3.3	472	H
IIF-774	Chm	H	1-Npm	1-Npm	3.49	556	H
IIF-775	Chm	H	1-Npm	Ph—Et	3.36	520	H
IIF-776	Chm	H	1-Npm	i-Pnt	3.38	486	H
IIF-777	Bnzl	H	i-Pr	Ph—Et	3	416	H
IIF-778	Bnzl	H	i-Pr	i-Pnt	3.01	382	H
IIF-779	i-Bu	H	i-Pr	Ph—Et	2.93	382	H
IIF-780	1-Npm	H	i-Pr	Ph—Et	3.14	466	H
IIF-781	1-Npm	H	i-Pr	i-Pnt	3.17	432	H
IIF-782	Ph—Et	H	i-Pr	Bnzl	2.99	416	H
IIF-783	Ph—Et	H	i-Pr	i-Bu	2.95	382	H
IIF-784	Ph—Et	H	i-Pr	1-Npm	3.22	466	H
IIF-785	Ph—Et	H	i-Pr	i-Pnt	3.08	396	H
IIF-786	4-F-	H	i-Pr	Bnzl	2.92	420	H
	Bnzl
IIF-787	4-F-	H	i-Pr	i-Bu	2.92	386	H
	Bnzl
IIF-788	4-F-	H	i-Pr	1-Npm	3.14	470	H
	Bnzl
IIF-789	4-F-	H	i-Pr	Ph—Et	2.98	434	H
	Bnzl
IIF-790	4-F-	H	i-Pr	i-Pnt	2.97	400	H
	Bnzl
IIF-791	i-Pnt	H	i-Pr	Bnzl	2.91	382	H
IIF-792	i-Pnt	H	i-Pr	1-Npm	3.16	432	H
IIF-793	i-Pnt	H	i-Pr	Ph—Et	3.02	396	H
IIF-794	Chm	H	i-Pr	Bnzl	3.05	408	H
IIF-795	Chm	H	i-Pr	1-Npm	3.28	458	H
IIF-796	Chm	H	i-Pr	Ph—Et	3.09	422	H
IIF-797	Bnzl	H	s-Bu	Ph—Et	3.07	430	H
IIF-798	Bnzl	H	s-Bu	i-Pnt	3.07	396	H
IIF-799	i-Bu	H	s-Bu	Ph—Et	3	396	H
IIF-800	1-Npm	H	s-Bu	Ph—Et	3.21	480	H
IIF-801	1-Npm	H	s-Bu	i-Pnt	3.22	446	H
IIF-802	Ph—Et	H	s-Bu	Bnzl	3.09	430	H

TABLE 2-23
IIF-803	Ph—Et	H	s-Bu	i-Bu	3.05	396	H
IIF-804	Ph—Et	H	s-Bu	1-Npm	3.28	480	H
IIF-805	Ph—Et	H	s-Bu	i-Pnt	3.17	410	H
IIF-806	4-F-	H	s-Bu	Bnzl	3.07	434	H
	Bnzl
IIF-807	4-F-	H	s-Bu	i-Bu	2.97	400	H
	Bnzl
IIF-808	4-F-	H	s-Bu	1-Npm	3.22	484	H
	Bnzl
IIF-809	4-F-	H	s-Bu	Ph—Et	3.06	448	H
	Bnzl
IIF-810	4-F-	H	s-Bu	i-Pnt	3.1	414	H
	Bnzl
IIF-811	i-Pnt	H	s-Bu	Bnzl	3.05	396	H
IIF-812	i-Pnt	H	s-Bu	1-Npm	3.25	446	H
IIF-813	Chm	H	s-Bu	Bnzl	3.15	422	H
IIF-814	Chm	H	s-Bu	1-Npm	3.34	472	H
IIF-815	Bnzl	H	Ph—Et	Bnzl	3.07	464	H
IIF-816	Bnzl	H	Ph—Et	1-Npm	3.31	514	H
IIF-817	Bnzl	H	Ph—Et	i-Pnt	3.15	444	H
IIF-818	i-Bu	H	Ph—Et	i-Bu	2.96	396	H
IIF-819	i-Bu	H	Ph—Et	1-Npm	3.22	480	H
IIF-820	i-Bu	H	Ph—Et	i-Pnt	4.26	410	H
IIF-821	1-Npm	H	Ph—Et	Bnzl	3.29	514	H
IIF-822	1-Npm	H	Ph—Et	i-Bu	3.26	480	H
IIF-823	1-Npm	H	Ph—Et	1-Npm	3.42	564	H
IIF-824	4-F-	H	Ph—Et	Bnzl	3.08	482	H
	Bnzol
IIF-825	4-F-	H	Ph—Et	i-Bu	3.04	448	H
	Bnzl
IIF-826	4-F-	H	Ph—Et	1-Npm	3.24	532	H
	Bnzl
IIF-827	4-F-	H	Ph—Et	i-Pnt	3.13	462	H
	Bnzl
IIF-828	i-Pnt	H	Ph—Et	i-Bu	3.07	410	H
IIF-829	i-Pnt	H	Ph—Et	1-Npm	3.28	494	H
IIF-830	Chm	H	Ph—Et	Bnzl	3.19	470	H
IIF-831	Chm	H	Ph—Et	i-Bu	3.12	436	H
IIF-832	Chm	H	Ph—Et	1-Npm	3.34	520	H
IIF-833	Chm	H	Ph—Et	i-Pnt	3.24	450	H
IIF-834	Bnzl	H	4-F-	Bnzl	3.03	468	H
			Bnzl
IIF-835	Bnzl	H	4-F-	1-Npm	3.19	518	H
			Bnzl
IIF-836	Bnzl	H	4-F-	Ph—Et	3.06	482	H
			Bnzl
IIF-837	Bnzl	H	4-F-	i-Pnt	3.08	448	H
			Bnzl
IIF-838	i-Bu	H	4-F-	i-Bu	2.92	400	H
			Bnzl
IIF-839	i-Bu	H	4-F-	1-Npm	3.16	484	H
			Bnzl
IIF-840	i-Bu	H	4-F-	i-Pnt	3.03	414	H
			Bnzl
IIF-841	1-Npm	H	4-F-	Bnzl	3.31	518	H
			Bnzl
IIF-842	1-Npm	H	4-F-	i-Bu	3.23	484	H
			Bnzl
IIF-843	1-Npm	H	4-F-	1-Npm	3.47	568	H
			Bnzl
IIF-844	1-Npm	H	4-F-	Ph—Et	3.29	532	H
			Bnzl
IIF-845	1-Npm	H	4-F-	i-Pnt	3.31	498	H
			Bnzl
IIF-846	Ph—Et	H	4-F-	Bnzl	3.16	482	H
			Bnzl
IIF-847	Ph—Et	H	4-F-	i-Bu	3.11	448	H
			Bnzl
IIF-848	Ph—Et	H	4-F-	1-Npm	3.31	532	H
			Bnzl
IIF-849	Ph—Et	H	4-F-	i-Pnt	3.2	462	H
			Bnzl
IIF-850	i-Pnt	H	4-F-	Bnzl	3.05	448	H
			Bnzl
IIF-851	i-Pnt	H	4-F-	1-Npm	3.21	498	H
			Bnzl
IIF-852	i-Pnt	H	4-F-	Ph—Et	3.13	462	H
			Bnzl

TABLE 2-24
IIF-853	Chm	H	4-F-	Bnzl	3.12	474	H
			Bnzl
IIF-854	Chm	H	4-F-	i-Bu	3.09	440	H
			Bnzl
IIF-855	Chm	H	4-F-	1-Npm	3.3	524	H
			Bnzl
IIF-856	Chm	H	4-F-	Ph—Et	3.21	488	H
			Bnzl
IIF-857	Chm	H	4-F-	i-Pnt	3.17	454	H
			Bnzl
IIF-858	Bnzl	H	i-Pnt	Bnzl	3.08	430	H
IIF-859	Bnzl	H	i-Pnt	1-Npm	3.28	480	H
IIF-860	Bnzl	H	i-Pnt	Ph—Et	3.12	444	H
IIF-861	i-Bu	H	i-Pnt	1-Npm	3.23	446	H
IIF-862	i-Bu	H	i-Pnt	Ph—Et	3.11	410	H
IIF-863	1-Npm	H	i-Pnt	Bnzl	3.25	480	H
IIF-864	1-Npm	H	i-Pnt	i-Bu	3.22	446	H
IIF-865	1-Npm	H	i-Pnt	1-Npm	3.42	530	H
IIF-866	Ph—Et	H	i-Pnt	Bnzl	3.16	444	H
IIF-867	Ph—Et	H	i-Pnt	i-Bu	3.13	410	H
IIF-868	Ph—Et	H	i-Pnt	1-Npm	3.33	494	H
IIF-869	4-F-	H	i-Pnt	Bnzl	3.09	448	H
	Bnzl
IIF-870	4-F-	H	i-Pnt	i-Bu	3.05	414	H
	Bnzl
IIF-871	4-F-	H	i-Pnt	1-Npm	3.29	498	H
	Bnzl
IIF-872	4-F-	H	i-Pnt	Ph—Et	3.13	462	H
	Bnzl
IIF-873	Chm	H	i-Pnt	Bnzl	3.23	436	H
IIF-874	Chm	H	i-Pnt	1-Npm	3.42	486	H
IIF-875	Chm	H	i-Pnt	Ph—Et	3.25	450	H
IIF-876	Bnzl	H	Hxy	Bnzl	3.24	444	H
IIF-877	Bnzl	H	Hxy	1-Npm	3.39	494	H
IIF-878	Bnzl	H	Hxy	i-Pnt	3.27	424	H
IIF-879	i-Bu	H	Hxy	1-Npm	3.36	460	H
IIF-880	1-Npm	H	Hxy	1-Npm	3.54	544	H
IIF-881	1-Npm	H	Hxy	i-Pnt	3.43	474	H
IIF-882	Ph—Et	H	Hxy	Bnzl	3.3	458	H
IIF-883	Ph—Et	H	Hxy	i-Bu	3.24	424	H
IIF-884	Ph—Et	H	Hxy	i-Pnt	3.35	438	H
IIF-885	4-F-	H	Hxy	Bnzl	3.23	462	H
	Bnzl
IIF-886	4-F-	H	Hxy	i-Bu	3.17	428	H
	Bnzl
IIF-887	4-F-	H	Hxy	1-Npm	3.4	512	H
	Bnzl
IIF-888	4-F-	H	Hxy	Ph—Et	3.24	476	H
	Bnzyl
IIF-889	4-F-	H	Hxy	i-Pnt	3.28	442	H
	Bnzl
IIF-890	i-Pnt	H	Hxy	Bnzl	3.26	424	H
IIF-891	i-Pnt	H	Hxy	1-Npm	3.47	474	H
IIF-892	Chm	H	Hxy	Bnzl	3.34	450	H
IIF-893	Chm	H	Hxy	1-Npm	3.5	500	H
IIF-894	2-	H	i-Bu	Bnzl	4.15	426	H
	OtBu-
	Et
IIF-895	2-	H	i-Bu	i-Bu	4.18	392	H
	OtBu-
	Et
IIF-896	2-	H	i-Bu	1-Npm	4.31	476	H
	OtBu-
	Et
IIF-897	2-	H	i-Bu	4-	4.37	498	H
	OtBu-			tBuO-
	Et			Bnzl
IIF-898	2-	H	i-Bu	Ph—Et	4.18	440	H
	OtBu-
	Et
IIF-899	2-	H	i-Bu	i-Pnt	4.28	406	H
	OtBu-
	Et
IIF-900	2-	H	Bnzl	Bnzl	4.2	460	H
	OtBu-
	Et
IIF-901	2-	H	Bnzl	i-Bu	4.17	426	H
	OtBu-
	Et
IIF-902	2-	H	Bnzl	4-	4.32	532	H
	OtBu-			tBuO-
	Et			Bnzl

TABLE 2-25
IIF-903	2-	H	Bnzl	Ph—Et	4.29	474	H
	OtBu-
	Et
IIF-904	2-	H	Bnzl	i-Pnt	4.27	440	H
	OtBu-
	Et
IIF-905	i-Pnt	H	Bnzl	4-tBuO-Bnzl	3.26	502	H
IIF-906	Chm	H	Bnzl	4-tBuO-Bnzl	3.32	528	H
IIF-907	4-	H	1-Npm	Ph—Et	3.42	586	H
	tBuO-
	Bnzl
IIF-908	4-	H	1-Npm	i-Pnt	3.42	552	H
	tBuO-
	Bnzl
IIF-909	Ph—Et	H	1-Npm	4-tBuO-Bnzl	3.4	586	H
IIF-910	4-F-	H	1-Npm	4-tBuO-Bnzl	3.4	590	H
	Bnzl
IIF-911	2-	H	1-Npm	Bnzl	4.38	510	H
	OtBu-
	Et
IIF-912	2-	H	1-Npm	i-Bu	4.35	476	H
	OtBu-
	Et
IIF-913	2-	H	1-Npm	1-Npm	4.5	560	H
	OtBu-
	Et
IIF-914	i-Pnt	H	1-Npm	4-tBuO-Bnzl	3.43	552	H
IIF-915	Chm	H	1-Npm	4-tBuO-Bnzl	3.5	578	H
IIF-916	Bnzl	H	4-tBuO-	Ph—Et	3.31	536	H
			Bnzl
IIF-917	Bnzl	H	4-tBuO-	i-Pnt	3.29	502	H
			Bnzl
IIF-918	i-Bu	H	4-tBuO-	Ph—Et	3.22	502	H
			Bnzl
IIF-919	1-Npm	H	4-tBuO-	Ph—Et	3.41	586	H
			Bnzl
IIF-920	1-Npm	H	4-tBuO-	i-Pnt	3.41	552	H
			Bnzl
IIF-921	Ph—Et	H	4-tBuO-	Bnzl	3.32	536	H
			Bnzl
IIF-922	Ph—Et	H	4-tBuO-	1-Npm	3.43	586	H
			Bnzl
IIF-923	Ph—Et	H	4-tBuO-	i-Pnt	3.37	516	H
			Bnzl
IIF-924	4-F-	H	4-tBuO-	Bnzl	3.22	540	H
	Bnzl		Bnzl
IIF-925	4-F-	H	4-tBuO-	1-Npm	3.38	590	H
	Bnzl		Bnzl
IIF-926	4-F-	H	4-tBuO-	Ph—Et	3.28	554	H
	Bnzl		Bnzl
IIF-927	4-F-	H	4-tBuO-	i-Pnt	3.29	520	H
	Bnzl		Bnzl
IIF-928	2-	H	4-tBuO-	1-Npm	3.46	582	H
	OtBu-		Bnzl
	Et
IIF-929	i-Pnt	H	4-tBuO-	i-Bu	3.2	468	H
			Bnzl
IIF-930	i-Pnt	H	4-tBuO-	1-Npm	3.42	552	H
			Bnzl
IIF-931	i-Pnt	H	4-tBuO-	Ph—Et	3.33	516	H
			Bnzl
IIF-932	Chm	H	4-tBuO-	Bnzl	3.33	528	H
			Bnzl
IIF-933	Chm	H	4-tBuO-	i-Bu	3.24	494	H
			Bnzl
IIF-934	Chm	H	4-tBuO-	1-Npm	3.5	578	H
			Bnzl
IIF-935	Chm	H	4-tBuO-	Ph—Et	3.41	542	H
			Bnzl
IIF-936	Chm	H	4-tBuO-	i-Pnt	3.42	508	H
			Bnzl
IIF-937	Bnzl	H	tBOC-E	Ph—Et	3.08	502	H
IIF-938	Bnzl	H	tBOC-E	i-Pnt	3.08	468	H
IIF-939	1-Npm	H	tBOC-E	Ph—Et	3.25	552	H
IIF-940	1-Npm	H	tBOC-E	i-Pnt	3.26	518	H
IIF-941	4-	H	tBOC-E	Ph—Et	3.32	574	H
	tBuO-
	Bnzl
IIF-942	4-	H	tBOC-E	i-Pnt	3.34	540	H
	tBuO-
	Bnzl
IIF-943	Ph—Et	H	tBOC-E	Bnzl	3.08	502	H
IIF-944	Ph—Et	H	tBOC-E	i-Bu	3.12	468	H
IIF-945	Ph—Et	H	tBOC-E	1-Npm	3.27	552	H
IIF-946	Ph—Et	H	tBOC-E	4-tBuO-Bnzl	3.33	574	H
IIF-947	Ph—Et	H	tBOC-E	i-Pnt	3.18	482	H
IIF-948	4-F-	H	tBOC-E	Bnzl	3.06	506	H
	Bnzl
IIF-949	4-F-	H	tBOC-E	i-Bu	3.04	472	H
	Bnzl
IIF-950	4-F-	H	tBOC-E	1-Npm	3.23	556	H
	Bnzl
IIF-951	4-F-	H	tBOC-E	4-tBuO-Bnzl	3.27	578	H
	Bnzl
IIF-952	4-F-	H	tBOC-E	Ph—Et	3.12	520	H
	Bnzl

TABLE 2-26
IIF-953	4-F-	H	tBOC-E	i-Pnt	3.13	486	H
	Bnzl
IIF-954	2-	H	tBOC-E	Bnzl	3.11	498	H
	OtBu-
	Et
IIF-955	2-	H	tBOC-E	1-Npm	3.27	548	H
	OtBu-
	Et
IIF-956	2-	H	tBOC-E	4-tBuO-Bnzl	3.37	570	H
	OtBu-
	Et
IIF-957	2-	H	tBOC-E	Ph—Et	3.17	512	H
	OtBu-
	Et
IIF-958	i-Pnt	H	tBOC-E	Bnzl	3.08	468	H
IIF-959	i-Pnt	H	tBOC-E	1-Npm	3.22	518	H
IIF-960	i-Pnt	H	tBOC-E	Ph—Et	3.13	482	H
IIF-961	Chm	H	tBOC-E	Bnzl	3.17	494	H
IIF-962	Chm	H	tBOC-E	1-Npm	3.34	544	H
IIF-963	Ph—Et	H	i-Pr	4-tBuO-Bnzl	3.22	488	H
IIF-964	4-F-	H	i-Pr	4-tBuO-Bnzl	3.16	492	H
	Bnzl
IIF-965	Ph—Et	H	s-Bu	4-tBuO-Bnzl	3.29	502	H
IIF-966	4-F-	H	s-Bu	4-tBuO-Bnzl	3.29	506	H
	Bnzl
IIF-967	2-	H	s-Bu	Bnzl	3.04	426	H
	OtBu-
	Et
IIF-968	2-	H	s-Bu	i-Bu	3.03	392	H
	OtBu-
	Et
IIF-969	2-	H	s-Bu	1-Npm	3.3	476	H
	OtBu-
	Et
IIF-970	2-	H	s-Bu	Ph—Et	3.15	440	H
	OtBu-
	Et
IIF-971	4-	H	Ph—Et	Bnzl	3.33	536	H
	tBuO-
	Bnzl
IIF-972	4-	H	Ph—Et	i-Bu	3.25	502	H
	tBuO-
	Bnzl
IIF-973	4-	H	Ph—Et	1-Npm	3.47	586	H
	tBuO-
	Bnzl
IIF-974	tBOC-	H	Ph—Et	Bnzl	3.16	502	H
	E
IIF-975	tBOC-	H	Ph—Et	i-Bu	3.13	468	H
	E
IIF-976	tBOC-	H	Ph—Et	1-Npm	3.35	552	H
	E
IIF-977	2-	H	Ph—Et	Bnzl	3.1	474	H
	OtBu-
	Et
IIF-978	2-	H	Ph—Et	i-Bu	3.08	440	H
	OtBu-
	Et
IIF-979	2-	H	Ph—Et	i-Pnt	3.17	454	H
	OtBu-
	Et
IIF-980	4-	H	4-F-Bnzl	Bnzl	3.35	540	H
	tBuO-
	Bnzl
IIF-981	4-	H	4-F-Bnzl	i-Bu	3.28	506	H
	tBuO-
	Bnzl
IIF-982	4-	H	4-F-Bnzl	1-Npm	3.47	590	H
	tBuO-
	Bnzl
IIF-983	tBOC-	H	4-F-Bnzl	Bnzl	3.14	506	H
	E
IIF-984	tBOC-	H	4-F-Bnzl	i-Bu	3.11	472	H
	E
IIF-985	tBOC-	H	4-F-Bnzl	1-Npm	3.32	556	H
	E
IIF-986	2-	H	4-F-Bnzl	i-Bu	3.03	444	H
	OtBu-
	Et
IIF-987	2-	H	4-F-Bnzl	Ph—Et	3.13	492	H
	OtBu-
	Et
IIF-988	2-	H	4-F-Bnzl	i-Pnt	3.13	458	H
	OtBu-
	Et
IIF-989	Bnzl	H	2-OtBu-	Bnzl	4.08	460	H
			Et
IIF-990	Bnzl	H	2-OtBu-	i-Bu	4.07	426	H
			Et
IIF-991	Bnzl	H	2-OtBu-	1-Npm	4.26	510	H
			Et
IIF-992	Bnzl	H	2-OtBu-	Ph—Et	4.17	474	H
			Et
IIF-993	Bnzl	H	2-OtBu-	i-Pnt	4.15	440	H
			Et
IIF-994	i-Bu	H	2-OtBu-	Bnzl	4.12	426	H
			Et
IIF-995	i-Bu	H	2-OtBu-	1-Npm	4.29	476	H
			Et
IIF-996	i-Bu	H	2-OtBu-	Ph—Et	4.16	440	H
			Et
IIF-997	1-Npm	H	2-OtBu-	i-Bu	4.22	476	H
			Et
IIF-998	1-Npm	H	2-OtBu-	i-Pnt	4.33	490	H
			Et
IIF-999	4-	H	2-OtBu-	i-Bu	4.3	498	H
	tBuO-		Et
	Bnzl
IIF-1000	Ph—Et	H	2-OtBu-	Bnzl	4.2	474	H
			Et
IIF-1001	Ph—Et	H	2-OtBu-	i-Bu	4.17	440	H
			Et
IIF-1002	Ph—Et	H	2-OtBu-	1-Npm	4.35	524	H
			Et

TABLE 2-27
IIF-1003	Ph—Et	H	2-OtBu-	4-tBuO-Bnzl	4.36	546	H
			Et
IIF-1004	Ph—Et	H	2-OtBu-	i-Pnt	4.28	454	H
			Et
IIF-1005	4-F-	H	2-OtBu-	Bnzl	4.17	478	H
	Bnzl		Et
IIF-1006	4-F-	H	2-OtBu-	i-Bu	4.05	444	H
	Bnzl		Et
IIF-1007	4-F-	H	2-OtBu-	1-Npm	4.3	528	H
	Bnzl		Et
IIF-1008	4-F-	H	2-OtBu-	4-tBuO-Bnzl	4.35	550	H
	Bnzl		Et
IIF-1009	4-F-	H	2-OtBu-	Ph—Et	4.18	492	H
	Bnzl		Et
IIF-1010	4-F-	H	2-OtBu-	i-Pnt	4.18	458	H
	Bnzl		Et
IIF-1011	i-Pnt	H	2-OtBu-	Bnzl	4.15	440	H
			Et
IIF-1012	i-Pnt	H	2-OtBu-	1-Npm	4.32	490	H
			Et
IIF-1013	i-Pnt	H	2-OtBu-	4-tBuO-Bnzl	4.36	512	H
			Et
IIF-1014	i-Pnt	H	2-OtBu-	Ph—Et	4.26	454	H
			Et
IIF-1015	Chm	H	2-OtBu-	Bnzl	4.25	466	H
			Et
IIF-1016	Chm	H	2-OtBu-	4-tBuO-Bnzl	4.41	538	H
			Et
IIF-1017	Chm	H	2-OtBu-	Ph—Et	4.28	480	H
			Et
IIF-1018	Bnzl	H	i-Pnt	4-tBuO-Bnzl	3.27	502	H
IIF-1019	Bnzl	H	i-Pnt	tBOC-E	3.08	468	H
IIF-1020	1-Npm	H	i-Pnt	4-tBuO-Bnzl	3.46	552	H
IIF-1021	1-Npm	H	i-Pnt	tBOC-E	3.25	518	H
IIF-1022	4-	H	i-Pnt	Bnzl	3.32	502	H
	tBuO-
	Bnzl
IIF-1023	4-	H	i-Pnt	i-Bu	3.3	468	H
	tBuO-
	Bnzl
IIF-1024	4-	H	i-Pnt	1-Npm	3.53	552	H
	tBuO-
	Bnzl
IIF-1025	4-	H	i-Pnt	Ph—Et	3.37	516	H
	tBuO-
	Bnzl
IIF-1026	tBOC-	H	i-Pnt	Bnzl	3.18	468	H
	E
IIF-1027	tBOC-	H	i-Pnt	1-Npm	3.38	518	H
	E
IIF-1028	tBOC-	H	i-Pnt	Ph—Et	3.22	482	H
	E
IIF-1029	Ph—Et	H	i-Pnt	4-tBuO-Bnzl	3.39	516	H
IIF-1030	Ph—Et	H	i-Pnt	tBOC-E	3.22	482	H
IIF-1031	4-F-	H	i-Pnt	4-tBuO-Bnzl	3.29	520	H
	Bnzl
IIF-1032	4-F-	H	i-Pnt	tBOC-E	2.35	486	H
	Bnzl
IIF-1033	Chm	H	i-Pnt	4-tBuO-Bnzl	2.62	508	H
IIF-1034	Bnzl	H	Hxy	4-tBuO-Bnzl	2.63	516	H
IIF-1035	i-Bu	H	Hxy	4-tBuO-Bnzl	2.55	482	H
IIF-1036	1-Npm	H	Hxy	4-tBuO-Bnzl	2.88	566	H
IIF-1037	4-	H	Hxy	Bnzl	2.63	516	H
	tBuO-
	Bnzl
IIF-1038	4-	H	Hxy	i-Bu	2.6	482	H
	tBuO-
	Bnzl
IIF-1039	4-	H	Hxy	Ph—Et	2.67	530	H
	tBuO-
	Bnzl
IIF-1040	4-	H	Hxy	i-Pnt	2.7	496	H
	tBuO-
	Bnzl
IIF-1041	tBOC-	H	Hxy	Ph—Et	2.55	496	H
	E
IIF-1042	Ph—Et	H	Hxy	4-tBuO-Bnzl	2.68	530	H
IIF-1043	4-F-	H	Hxy	4-tBuO-Bnzl	2.63	534	H
	Bnzl
IIF-1044	2-	H	Hxy	Bnzl	2.47	454	H
	OtBu—Et
IIF-1045	2-	H	Hxy	1-Npm	2.63	504	H
	OtBu—Et
IIF-1046	2-	H	Hxy	Ph—Et	2.5	468	H
	OtBu—Et
IIF-1047	1-Npm	H	4-F-Bnzl	2-OTBS—Et	1.11	586.4	C
† Ring formed together by R2A and R2B

TABLE 2-28
Compound		LCMS tR	Mass	Measurement	Yield
number	Name of compound	(min)	(M + H)+	condition	(%)
IIF-1	(3S*,3aR*,6S*,7R*,7aR*)-N,7-	1.14	416	B	10
	dibenzyl-1-isobutyl-
	1,2,3,3a,7,7a-hexahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IIF-2	(3S*,3aR*,6S*,7R*,7aR*)-N,1,7-	1.11	348	B	16
	triisobutyl-1,2,3,3a,7,7a-
	hexahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IIF-3	(3S*,3aR*,6S*,7R*,7aR*)-7-benzyl-	1.14	382	B	14
	N,1-diisobutyl-1,2,3,3a,7,7a-
	hexahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IIF-4	(3S*,3aR*,6S*,7R*,7aR*)-1-benzyl-	1.14	382	B	8
	N,7-diisobutyl-1,2,3,3a,7,7a-
	hexahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IIF-5	(3S*,3aR*,6S*,7R*,7aR*)-N-benzyl-	1.13	382	B	13
	1,7-diisobutyl-1,2,3,3a,7,7a-
	hexahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IIF-6	(3S*,3aR*,6S*,7R*,7aR*)-1,7-	1.15	416	B	19
	dibenzyl-N-isobutyl-1,2,3,3a,7,7a-
	hexahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IIF-7	(3S*,3aR*,6S*,7R*,7aR*)-N,1-	1.00	416	B	22
	dibenzyl-7-isobutyl-1,2,3,3a,7,7a-
	hexahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IIF-8	(3S*,3aR*,6S*,7R*,7aR*)-N,1,7-	1.16	450	B	21
	tribenzyl-1,2,3,3a,7,7a-
	hexahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IIF-9	(3S*,3aR*,6S*,7R*,7aR*)-N,7-	1.18	430	B	20
	dibenzyl-1-isopentyl-1,2,3,3a,7,7a-
	hexahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IIF-10	(3S*,3aR*,6S*,7R*,7aR*)-N,1-	1.18	430	B	11
	dibenzyl-7-isopentyl-1,2,3,3a,7,7a-
	hexahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-
	6-carboxamide

TABLE 2-29
IIF-11	(3S*,3aR*,6S*,7R*,7aR*)-N-benzyl-	1.16	430	B	12
	1-isobutyl-7-phenethyl-
	1,2,3,3a,7,7a-hexahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IIF-12	(3S*,3aR*,6S*,7R*,7aR*)-1-benzyl-	1.16	430	B	12
	7-isobutyl-N-phenethyl-
	1,2,3,3a,7,7a-hexahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IIF-13	(3S*,3aR*,6S*,7R*,7aR*)-N-benzyl-	1.17	430	B	17
	1-isobutyl-7-(3-methylbenzyl)-
	1,2,3,3a,7,7a-hexahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-6-
	carboxamide
IIF-14	(3S*,3aR*,6S*,7R*,7aR*)-N-benzyl-	1.16	430	B	15
	1-isobutyl-7-(4-methylbenzyl)-
	1,2,3,3a,7,7a-hexahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-6-
	carboxamide
IIF-15	(3S*,3aR*,6S*,7R*,7aR*)-7-benzyl-	1.18	430	B	16
	1-isobutyl-N-(3-methylbenzyl)-
	1,2,3,3a,7,7a-hexahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-6-
	carboxamide
IIF-16	(3S*,3aR*,6S*,7R*,7aR*)-7-benzyl-	1.18	430	B	15
	1-isobutyl-N-(4-methylbenzyl)-
	1,2,3,3a,7,7a-hexahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-6-
	carboxamide
IIF-17	(3S*,3aR*,6S*,7R*,7aR*)-7-benzyl-	1.18	450	B	14
	N-(3-chlorobenzyl)-1-isobutyl-
	1,2,3,3a,7,7a-hexahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-6-
	carboxamide
IIF-18	(3S*,3aR*,6S*,7R*,7aR*)-7-benzyl-	1.17	450	B	13
	N-(4-chlorobenzyl)-1-isobutyl-
	1,2,3,3a,7,7a-hexahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-6-
	carboxamide
IIF-19	(3S*,3aR*,6S*,7R*,7aR*)-N-benzyl-	1.28	484	B	22
	1-(3,4-dichlorobenzyl)-7-isobutyl-
	1,2,3,3a,7,7a-hexahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-6-
	carboxamide
IIF-20	(3S*,3aR*,6S*,7R*,7aR*)-1-benzyl-	1.25	484	B	21
	N-(3,4-dichlorobenzyl)-7-isobutyl-
	1,2,3,3a,7,7a-hexahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-6-
	carboxamide
IIF-23	(3S*,3aR*,6S*,7R*,7aR*)-7-benzyl-	0.99	488	A	33
	1-isobutyl-N-(4-(tert-butoxy)benzyl)-
	1,2,3,3a,7,7a-hexahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-6-
	carboxamide
IIF-24	(3S*,3aR*,6S*,7R*,7aR*)-7-benzyl-	0.98	466	A	14
	1-isobutyl-N-(naphthalen-1-ylmethyl)-
	1,2,3,3a,7,7a-hexahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-6-
	carboxamide
IIF-25	(3S*,3aR*,6S*,7R*,7aR*)-7-benzyl-	0.74	370	A	5
	N-(2-hydroxyethyl)-1-isobutyl-
	1,2,3,3a,7,7a-hexahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-6-
	carboxamide
IIF-26	3-(3S*,3aR*,6S*,7R*,7aR*)-7-	0.75	398	A	100
	benzyl-1-isobutyl-1,2,3,3a,7,7a-
	hexahydro-1H-3,6-
	methanopyrrolo[3,2-c]pyridine-6-
	carboxamide)propanoic acid
IIF-27	(3S*,3aR*,6S*,7R*,7aR*)-7-benzyl-	0.92	454	A	20
	1-isobutyl-N-(2-(tert-butoxy)-2-
	oxoethyl)-1,2,3,3a,7,7a-
	hexahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IIF-28	(3S*,3aR*,6S*,7R*,7aR*)-7-benzyl-	0.72	397	A	88
	N-(3-amino-3-oxopropyl)-1-isobutyl-
	1,2,3,3a,7,7a-hexahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-6-
	carboxamide
IIF-29	(3S*,3aR*,6S*,7R*,7aR*)-N-(4-	0.67	397	A	100
	aminobutyl)-7-benzyl-1-isobutyl-
	1,2,3,3a,7,7a-hexahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-6-
	carboxamide

TABLE 2-30
IIF-30	(3S*,3aR*,6S*,7R*,7aR*)-7-	0.91	497	A	10
	benzyl-1-isobutyl-N-(4-((tert-
	butoxycarbonyl)amino)butyl)-
	1,2,3,3a,7,7a-hexahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-6-
	carboxamide
IIF-31	(3S*,3aR*,6S*,7R*,7aR*)-7-	0.98	422	A	12
	benzyl-N-cyclohexylmethyl-1-
	isobutyl-1,2,3,3a,7,7a-hexahydro-
	6H-3,6-methanopyrrolo[3,2-
	c]pyridine-6-carboxamide
IIF-32	(3S*,3aR*,6S*,7R*,7aR*)-7-	0.87	424	A	24
	benzyl-1-isobutyl-N-((tetrahydro-
	2H-pyran-2-yl)methyl)-
	1,2,3,3a,7,7a-hexahydro-6H-
	3,6-methanopyrrolo[3,2-
	c]pyridine-6-carboxamide
IIF-34	(3S*,3aR*,6S*,7R*,7aR*)-	0.93	497	A	17
	N-benzyl-1-isobutyl-7-(4-((tert-
	butoxycarbonyl)amino)butyl)-
	1,2,3,3a,7,7a-hexahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IIF-36	(3S*,3aR*,6S*,7R*,7aR*)-	0.82	412	A	5
	N-benzyl-1-isobutyl-7-(3-
	methoxy-3-oxopropyl)-
	1,2,3,3a,7,7a-hexahydro-6H-
	3,6-methanopyrrolo[3,2-
	c]pyridine-6-carboxamide
IIF-38	(3S*,3aR*,6S*,7R*,7aR*)-	0.99	422	A	23
	N-benzyl-7-(cyclohexylmethyl)-
	1-isobutyl-1,2,3,3a,7,7a-
	hexahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-6-
	carboxamide
IIF-39	(3S*,3aR*,6S*,7R*,7aR*)-N,7-	0.96	456	A	22
	dibenzyl-1-cyclohexylmethyl-
	1,2,3,3a,7,7a-hexahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IIF-40	(3S*,3aR*,6S*,7R*,7aR*)-N,7-	0.86	466	A	76
	dibenzyl-1-(4-hydroxybenzyl)-
	1,2,3,3a,7,7a-hexahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-6-
	carboxamide
IIF-41	(3S*,3aR*,6S*,7R*,7aR*)-N,7-	1.00	522	A	14
	dibenzyl-1-(4-(tert-
	butoxy)benzyl)-1,2,3,3a,7,7a-
	hexahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IIF-42	(3S*,3aR*,6S*,7R*,7aR*)-N,7-	0.97	500	A	4
	dibenzyl-1-(naphthalen-1-
	ylmethyl)-1,2,3,3a,7,7a-
	hexahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IIF-76	tert-butyl 3-	0.70	488	B	22
	(3S*,3aR*,6S*,7R*,7aR*)-7-
	benzyl-6-(benzylcarbamoyl)-
	2,3,3a,6,7,7a-hexahydro-1H-3,6-
	methanopyrrolo[3,2-c]pyridin-1-
	yl)propanoate
IIF-77	(3S*,3aR*,6S*,7R*,7aR*)-N,1-	0.80	466	B	19
	dibenzyl-7-(4-hydroxybenzyl)-
	1,2,3,3a,7,7a-hexahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-6-
	carboxamide
IIF-80	(3S*,3aR*,6S*,7R*,7aR*)-N-	1.01	452	A	6
	benzyl-1-(naphthalen-1-ylmethyl)-
	7-propyl-1,2,3,3a,7,7a-hexahydro-
	6H-3,6-methanopyrrolo[3,2-
	c]pyridine-6-carboxamide

Synthesis Example: IF-1

Synthesis of (3S*,3aS*,6S*,7R*,7aS*)—N,7-dibenzyl-1-isobutyloctahydro-6H-3,6-methanopyrrolo[3,2-c]pyridine-6-carboxamide(IF-1)

Sodium tetrahydroborate (1.86 mg, 0.0490 mmol) was added to a methanol (0.500 mL) solution of (3S*,3aR*,6S*,7R*,7aR*)—N,7-dibenzyl-1-isobutyl-1,2,3,3a,7,7a-hexahydro-6H-3,6-methanopyrrolo[3,2-c]pyridine-6-carboxamide (IIF-1) (10.2 mg, 0.0245 mmol) and stirred for 1 hour. After evaporating the solvent under reduced pressure, 5% sodium bicarbonate solution (1.00 mL) was added to the residue, which was extracted with ethyl acetate (3.00 mL). The organic layer was washed with water (1.00 mL), then dried with anhydrous sodium sulfate and filtered. The solvent was evaporated under reduced pressure. The resulting residue was purified with preparative PLC silica gel 60F254 (layer thickness 0.500 mm) (ethyl acetate:methanol=85:15) to obtain the aforementioned compound (6.37 mg, yield: 62%, RT=0.99 minutes (B method), [M+1]⁺=418).

¹H-NMR spectrum (400 MHz, CDCl₃) δ (ppm): 0.52 (3H, d), 0.58 (3H, d), 0.89-0.97 (1H, m), 1.57-1.62 (1H, m), 1.83-1.94 (3H, m), 2.01-2.07 (1H, m), 2.18-2.24 (2H, m), 2.29 (1H, d), 2.40-2.44 (1H, m), 2.71-2.75 (2H, m), 2.86-2.89 (1H, m), 3.10-3.19 (2H, m), 4.39-4.48 (2H, m), 7.24-7.38 (11H, m). ¹³C-NMR spectrum (100 MHz, CDCl₃) δ (ppm): 20.20, 26.99, 33.45, 35.79, 36.41, 39.83, 42.13, 42.79, 46.40, 56.95, 61.37, 61.78, 61.97, 125.50, 126.96, 127.39, 127.73, 128.25, 129.41, 138.20, 139.59, 175.20.

The three-dimensional structure of the molecules was studied by X-ray crystallography. FIG. 1 shows an ORTEP diagram thereof. Daicel Corporation's chiral column, CHIRALPAK IG (5 μm, 4.6×150 mm), mobile phase: methanol: diethylamine (100:0.1) was used to confirm that the molecule was a racemate through analysis. FIG. 2 shows the chromatogram thereof.

Synthesis Example: IB-1

Synthesis of (3S*, 3aS*, 6R*, 7R*, 7aS*)—N, 7-dibenzyl-1-isobutyloctahydro-3aH-3,6-methanopyrrolo[3,2-b]pyridine-3a-carboxamide (IB-1)

Sodium tetrahydroborate (3.83 mg, 0.101 mmol) was added to a methanol (1.00 mL) solution of (3S*, 3aS*, 6R*, 7R*, 7aS*)—N, 7-dibenzyl-1-isobutyl-1,2,3,6,7,7a-hexahydro-3aH-3,6-methanopyrrolo[3,2-b]pyridine-3a-carboxamide (IIB-1) (21.0 mg, 0.0506 mmol) and stirred for 1 hour. After evaporating the solvent under reduced pressure, 5% sodium bicarbonate solution (1.00 mL) was added to the residue, which was extracted with ethyl acetate (4.00 mL). The organic layer was washed with water (1.00 mL), then dried with anhydrous sodium sulfate and filtered. The solvent was evaporated under reduced pressure. The resulting residue was purified with preparative PLC silica gel 60F254 (layer thickness 0.500 mm) (ethyl acetate:methanol=90:10) to obtain the aforementioned compound (17.0 mg, yield: 81%, RT=1.21 minutes (B method), [M+1]⁺=418).

¹H-NMR spectrum (400 MHz, CDCl₃) δ (ppm): 0.48 (3H, d), 0.57 (3H, d), 1.18-1.28 (1H, m), 1.35-1.39 (1H, m), 1.55 (1H, s), 1.83-1.88 (1H, m), 2.09-2.14 (3H, m), 2.24-2.28 (1H, m), 2.45 (1H, s), 2.70-2.75 (1H, m), 2.78-2.88 (1H, m), 2.97 (1H, s), 3.20-3.27 (1H, m), 3.28-3.31 (1H, m), 4.28-4.33 (1H, m), 4.48-4.53 (1H, m), 7.21-7.27 (1H, m), 9.56 (1H, t).

¹³C-NMR spectrum (400 MHz, CDCl₃) δ (ppm): 20.20, 20.37, 25.84, 26.43, 38.09, 38.60, 39.25, 42.99, 58.19, 61.48, 62.33, 66.49, 125.58, 126.77, 127.49, 127.93, 128.07, 128.70, 138.22, 140.32, 173.83.

Synthesis Example: IB-29

Synthesis of (3S*, 3aS*, 6R*, 7R*, 7aS*)—N-(4-aminobutyl)-7-benzyl-1-isobutyloctahydro-3aH-3,6-methanopyrrolo[3,2-b]pyridine-3a-carboxamide (IB-29)

Formic acid (500 μL) was added to (3S*, 3aS*, 6R*,7R*,7aS*)-7-benzyl-1-isobutyl-N-(4-((tert-butoxycarbonyl)amino)butyl) octahydro-3aH-3,6-methanopyrrolo[3,2-b]pyridine-3a-carboxamide (IB-30) (7.70 mg, 0.0154 mmol) and incubated overnight at room temperature. The formic acid was evaporated under reduced pressure to obtain a triformic acid salt of the aforementioned compound (7.60 mg, yield: 92%, RT=0.75 minutes (A method), [M+1]⁺=399).

Synthesis Example: IB-40

Synthesis of (3S*, 3aS*, 6R*, 7R*, 7aS*)—N, 7-dibenzyl-1-(4-hydroxybenzyl)octahydro-3aH-3,6-methanopyrrolo[ 3,2-b]pyridine-3a-carboxamide (IB-40)

Formic acid (250 μL) was added to (3S*, 3aS*, 6R*, 7R*, 7aS*)—N, 7-dibenzyl-1-(4-(tert-butoxy)benzyl) octahydro-3aH-3,6-methanopyrrolo[3,2-b]pyridine-3a-carboxamide (IB-41) (7.80 mg, 0.0149 mmol) and incubated for 3 hours at room temperature. The formic acid was evaporated under reduced pressure to obtain a diformic acid salt of the aforementioned compound (6.30 mg, yield: 99%, RT=0.89 minutes (A method), [M+1]⁺=468).

Synthesis Example: IB-74

Synthesis of tert-butyl (3S*, 3aS*, 6R*, 7R*, 7aS*k)-3a-(benzylcarbamoyl)-1-isobutyl-7-(3-methoxy-3-oxopropyl)octahydro-4H-3,6-methanopyrrolo[3,2-b]pyridine-4-carboxylate (IB-74)

(3S*, 3aS*, 6R*, 7R*, 7aS*)—N-benzyl-1-isobutyl-7-(3-methoxy-3-oxopropyl)octahydro-3aH-3,6-methanopyrrolo[ 3,2-b]pyridine-3a-carboxamide (IB-36) (23.5 mg, 0.0570 mmol) was dissolved in tetrahydrofuran (0.400 mL), and a 30% tetrahydrofuran solution (140 μL, 0.140 mmol) of di-tert-butyl dicarbonate was added and heated for 2 hours at 50° C. The solvent was evaporated under reduced pressure. The resulting residue was purified by preparative PLC (Merck 1.05744.0001 (layer thickness 0.500 mm) (ethyl acetate:methanol=9:1)) to obtain the aforementioned compound (22.0 mg, yield: 75%, RT=0.97 minutes (A method), [M+1]⁺=514).

Synthesis Example: IB-73

Synthesis of tert-butyl (3S*, 3aS*, 6R*, 7R*, 7aS*)-3a-(benzylcarbamoyl)-1-isobutyl-7-(2-carboxyethyl) octahydro-4H-3,6-methanopyrrolo[3,2-b]pyridine-4-carboxylate (IB-73)

tert-butyl (3S*, 3aS*, 6R*, 7R*, 7aS*)-3a-(benzylcarbamoyl)-1-isobutyl-7-(3-methoxy-3-oxopropyl) octahydro-4H-3,6-methanopyrrolo[3,2-b]pyridine-4-carboxylate (IB-74) (22.0 mg, 0.0430 mmol) was dissolved in methanol (1.00 mL), and lithium hydroxide monohydrate (18.0 mg, 0.430 mmol) was added and stirred overnight at room temperature. Methanol was evaporated under reduced pressure. 10% citric acid solvent (450 μL) and ethyl acetate were added thereto. The organic layer was dried with anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure to obtain the aforementioned compound (21.40 mg, yield: 100%, RT=0.91 minutes (A method), [M+1]⁺=500).

Synthesis Example: IB-75

Synthesis of tert-butyl (3S*,3aS*,6R*,7R*,7aS*)-3a-(benzylcarbamoyl)-1-isobutyl-7-(3-amino-3-oxopropyl)octahydro-4H-3,6-methanopyrrolo[3,2-b]pyridine-4-carboxylate (IB-75)

tert-butyl (3S*,3aS*,6R*,7R*,7aS*)-3a-(benzylcarbamoyl)-1-isobutyl-7-(2-carboxyethyl)octahydro-4H-3,6-methanopyrrolo[3,2-b]pyridine-4-carboxylate (IB-73) (6.9 mg, 0.0130 mmol) was dissolved in tetrahydrofuran (0.200 mL), and carbonyldiimidazole (4.2 mg, 0.0260 mmol) was added and stirred overnight at room temperature. Ammonium water (13 M) (20.0 μL, 0.260 mmol) was added thereto and stirred for 1 hour. The solvent was evaporated. The resulting residue was purified by preparative PLC (Fuji Silysia Chemical's CHROMATOREX NH-TLC (layer thickness 0.200 mm) (ethyl acetate)) to obtain the aforementioned compound (1.70 mg, yield: 26%, RT=0.86 minutes (A method), [M+1]⁺=499).

Synthesis Example: IB-79

Synthesis of (3S*,3aS*,6R*,7R*,7aS*)—N^3a,7-dibenzyl-1-(cyclohexylmethyl)-N⁴-propylhexahydro-1H-3,6-methanopyrrolo[3,2-b]pyridine-3a,4-dicarboxamide (IB-79)

(3S*,3aS*,6R*,7R*,7aS*)—N,7-dibenzyl-1-cyclohexylmethyloctahydro-3aH-3,6-methanopyrrolo[3,2-b]pyridine-3a-carboxamide (IB-39) (4.6 mg, 0.0100 mmol) was dissolved in tetrahydrofuran (0.180 mL), then triethylamine (1.6 μL, 0.0120 mmol) and propylisocyanate (1.13 μL, 0.120 mmol) were added and incubated for 1 hour at room temperature. The reaction mixture was purified with preparative PLC silica gel 60F254 (layer thickness 0.250 mm) (ethyl acetate:methanol=5:1) to obtain the aforementioned compound (3.50 mg, yield: 65%, RT=1.05 minutes (A method), [M+1]⁺=543).

Synthesis of 3-((3S*,3aS*,6R*,7R*,7aS*)-3a-(benzylcarbamoyl)-1-isobutyloctahydro-1H-3,6-methanopyrrolo[3,2-b]pyridin-7-yl)propanoic Acid (IB-35)

Trifluoroacetic acid (200 μL) was added to tert-butyl (3S*, 3aS*, 6R*, 7R*, 7aS*)-3a-(benzylcarbamoyl)-1-isobutyl-7-(2-carboxyethyl)octahydro-4H-3,6-methanopyrrolo[3,2-b]pyridine-4-carboxylate (IB-73) (5.50 mg, 0.0110 mmol) and incubated overnight at room temperature. Trifluoroacetic acid was evaporated under reduced pressure to obtain a ditrifluoroacetic acid salt of the aforementioned compound (6.80 mg, yield: 100%, RT=0.83 minutes (A method), [M+1]⁺=400).

Synthesis Example: IF-26

Synthesis of ((3S*,3aS*,6S*,7R*,7aS*)-7-benzyl-1-isobutyloctahydro-1H-3,6-methanopyrrolo[3,2-c]pyridine-6-carboxamide)propanoic Acid (IF-26)

Formic acid (0.500 mL) was added to (3S*,3aS*,6S*,7R*,7aS*)-7-benzyl-1-isobutyl-N-(2-(tert-butoxy)-2-oxoethyl)octahydro-6H-3,6-methanopyrrolo[3,2-c]pyridine-6-carboxamide (IF-27) (15.0 mg, 0.0330 mmol) and heated overnight at 45° C. The formic acid was evaporated under reduced pressure to obtain a diformic acid salt of the aforementioned compound (16.2 mg, yield: 100%, RT=0.66 minutes (A method), [M+1]⁺=400).

Synthesis Example: IF-33

Synthesis of (3S*,3aS*,6S*,7R*,7aS*)-7-(4-aminobutyl)-N-benzyl-1-isobutyloctahydro-6H-3,6-methanopyrrolo[3,2-c]pyridine-6-carboxamide (IF-33)

Trifluoroacetic acid (200 μL) was added to (3S*,3aS*,6S*,7R*,7aS*)—N-benzyl-1-isobutyl-7-(4-((tert-butoxycarbonyl)amino)butyl)octahydro-6H-3,6-methanopyrrolo[3,2-c]pyridine-6-carboxamide (IF-34) (7.80 mg, 0.0156 mmol) and incubated overnight at room temperature. The trifluoroacetic acid was evaporated under reduced pressure to obtain a tritrifluoroacetic acid salt of the aforementioned compound (7.80 mg, yield: 100%, RT=0.62 minutes (A method), [M+1]+=399).

Synthesis Example: IF-41

Synthesis of (3S*,3aS*,6S*,7R*,7aS*)—N,7-dibenzyl-1-(4-(tert-butoxy)benzyl)octahydro-6H-3,6-methanopyrrolo[3,2-c]pyridine-6-carboxamide (IF-41)

9.50 mg of 10% palladium-carbon was added to a methanol (0.500 mL) solution of (3S*, 3aR*, 6S*, 7R*, 7aR*)—N, 7-dibenzyl-1-(4-(tert-butoxy)benzyl)-1,2,3,3a,7,7a-hexahydro-6H-3,6-methanopyrrolo[3,2-c]pyridine-6-carboxamide (IIF-41) (11 mg, 0.0210 mmol) and stirred for a week under a hydrogen gas atmosphere. After filtering out the palladium-carbon, the solution was concentrated. The residue was purified with preparative PLC silica gel 60F254 (layer thickness 0.500 mm) (ethyl acetate:methanol=5:1) to obtain the aforementioned compound (5.70 mg, yield: 52%, RT=0.90 minutes (A method), [M+1]⁺=524).

Synthesis Example: IF-40

Synthesis of (3S*,3aS*,6S*,7R*,7aS*)—N,7-dibenzyl-1-(4-hydroxybenzyl)octahydro-6H-3,6-methanopyrrolo[3,2-c]pyridine-6-carboxamide (IF-40)

Formic acid (250 μL) was added to (3S*,3aS*,6S*,7R*,7aS*)—N,7-dibenzyl-1-(4-(tert-butoxy)benzyl)octahydro-6H-3,6-methanopyrrolo[3,2-c]pyridine-6-carboxamide (IF-41) (5.70 mg, 10.9 mmol) and incubated for 3 hours at room temperature. The formic acid was evaporated under reduced pressure to obtain a diformic acid salt of the aforementioned compound (3.20 mg, yield: 52%, RT=0.75 minutes (A method), [M+1]⁺=468).

Synthesis Example: IF-71

Synthesis of (3S*,3aS*,6S*,7R*,7aS*)—N,7-dibenzyl-1-isobutyl-4-methyloctahydro-6H-3,6-methanopyrrolo[3,2-c]pyridine-6-carboxamide (IF-71)

A 37% formalin solution (0.06 mL, 0.736 mmol) was added to a tetrahydrofuran (2.00 mL) solution of (3S*,3aS*,6S*,7R*,7aS*)—N,7-dibenzyl-1-isobutyloctahydro-6H-3,6-methanopyrrolo[3,2-c]pyridine-6-carboxamide (IF-1) (30.8 mg, 0.0736 mmol) and stirred for 15 minutes at room temperature. Sodium triacetoxyborohydride (46.8 mg, 0.221 mmol) was added to the reaction mixture, and stirred for 1 hour at room temperature. An aqueous 5% sodium bicarbonate solution (2.00 mL) was added to the reaction mixture, and the organic phase was extracted with ethyl acetate (5.00 mL). The organic layer was washed with water (2.00 mL), then dried with anhydrous sodium sulfate and filtered. The solvent was evaporated under reduced pressure. The resulting residue was purified with preparative PLC silica gel 60F254 (layer thickness 0.500 mm) (ethyl acetate:methanol=85:15) to obtain the aforementioned compound (12.1 mg, yield: 38%, RT=1.02 minutes (B method), [M+1]⁺=432).

Synthesis Example: IF-43

Synthesis of (3S*,3aS*,6S*,7R*,7aS*)-4-acetyl-N,7-dibenzyl-1-isobutyloctahydro-6H-3,6-methanopyrrolo[3,2-c]pyridine-6-carboxamide (IF-43)

Triethylamine (0.0156 mL, 1.13 mmol) and acetyl chloride (0.00804 mL, 1.13 mmol) were added to a tetrahydrofuran (1.80 mL) solution of (3S*,3aS*,6S*,7R*,7aS*)—N,7-dibenzyl-1-isobutyloctahydro-6H-3,6-methanopyrrolo[3,2-c]pyridine-6-carboxamide (IF-1) (31.4 mg, 0.0751 mmol), and stirred for 30 minutes while cooling with ice. A 5% sodium bicarbonate solution (2.00 mL) was added to the reaction mixture, and the organic phase was extracted with ethyl acetate (5.00 mL). The organic layer was washed with water (2.00 mL), then dried with anhydrous sodium sulfate and filtered. The solvent was evaporated under reduced pressure. The resulting residue was purified with preparative PLC silica gel 60F254 (layer thickness 0.500 mm) (ethyl acetate:methanol=85:15) to obtain the aforementioned compound (17.6 mg, yield: 51%, RT=1.08 minutes (B method),[M+1]⁺=460).

Synthesis Example: IB-68

Synthesis of (3S*,3aS*,6R*,7R*,7aS*)-4-benzoyl-N,7-dibenzyl-1-isobutyloctahydro-3aH-3,6-methanopyrrolo[3,2-b]pyridine-3a-carboxamide (IB-68)

Triethylamine (0.0152 mL, 0.110 mmol) and benzoyl chloride (0.0127 mL, 1.10 mmol) were added to a tetrahydrofuran (2.00 mL) solution of (3S*,3aS*,6R*,7R*,7aS*)—N,7-dibenzyl-1-isobutyloctahydro-3aH-3,6-methanopyrrolo[3,2-b]pyridine-3a-carboxamide (IB-1) (30.6 mg, 0.0733 mmol) and stirred for 30 minutes while cooling with ice. An aqueous 5% sodium bicarbonate solution (2.00 mL) was added to the reaction mixture, and an organic phase was extracted with ethyl acetate (5.00 mL). The organic layer was washed with water (2.00 mL), then dried with anhydrous sodium sulfate and filtered. The solvent was evaporated under reduced pressure. The resulting residue was purified with preparative PLC silica gel 60F254 (layer thickness 0.500 mm) (ethyl acetate:methanol=95:5) to obtain the aforementioned compound (14.8 mg, yield: 39%, RT=1.23 minutes (B method), [M+1]⁺=522).

Synthesis Example: IB-69

Synthesis of (3S*,3aS*,6R*,7R*,7aS*)—N,7-dibenzyl-4-ethyl-1-isobutyloctahydro-3aH-3,6-methanopyrrolo[3,2-b]pyridine-3a-carboxamide (IB-69)

An acetaldehyde 2% N,N-dimethylformamide solution (0.870 mL, 0.395 mmol) was added to a tetrahydrofuran (2.00 mL) solution of (3S*,3aS*,6R*,7R*,7aS*)—N,7-dibenzyl-1-isobutyloctahydro-3aH-3,6-methanopyrrolo[3,2-b]pyridine-3a-carboxamide (IB-1) (33.0 mg, 0.790 mmol) and stirred for 15 minutes at room temperature. Sodium triacetoxyborohydride (50.2 mg, 0.273 mmol) was added to the reaction mixture, and further stirred for 2 hours at room temperature. An aqueous 5% sodium bicarbonate solution (10.0 mL) was added to the reaction mixture, and an organic phase was extracted with ethyl acetate (30.0 mL). The organic layer was washed twice with water (10.0 mL), then dried with anhydrous sodium sulfate and filtered. The solvent was evaporated under reduced pressure. The resulting residue was purified with preparative PLC silica gel 60F254 (layer thickness 0.500 mm) (ethyl acetate:methanol=95:5) to obtain the aforementioned compound (9.85 mg, yield: 28%, RT=1.24 minutes (B method), [M+1]⁺=446).

Synthesis Example: IB-70

Synthesis of (3S*,3aS*,6R*,7R*,7aS*)—N,7-dibenzyl-1-isobutyl-4-(methoxycarbonyl)octahydro-3aH-3,6-methanopyrrolo[3,2-b]pyridine-3a-carboxamide (IB-70)

Triethylamine (0.0157 mL, 0.113 mmol) and chloroformic acid methyl (0.00870 mL, 0.113 mmol) were added to a tetrahydrofuran (2.00 mL) solution of (3S*,3aS*,6R*,7R*,7aS*)—N,7-dibenzyl-1-isobutyloctahydro-3aH-3,6-methanopyrrolo[3,2-b]pyridine-3a-carboxamide (IB-1) (31.5 mg, 0.0754 mmol), and stirred for 30 minutes while cooling with ice. After stirring for 30 minutes at room temperature, a 5% sodium bicarbonate solution (2.00 mL) was added to the reaction mixture, and the organic phase was extracted with ethyl acetate (5.00 mL). The organic layer was washed with water (2.00 mL), then dried with anhydrous sodium sulfate and filtered. The solvent was evaporated under reduced pressure. The resulting residue was purified with preparative PLC silica gel 60F254 (layer thickness 0.500 mm) (ethyl acetate:methanol=95:5) to obtain the aforementioned compound (31.0 mg, yield: 87%, RT=1.18 minutes (B method), [M+1]⁺=476).

The following compounds were synthesized by the same method as the Synthesis Examples.

Compounds with a guanidinopropyl group in one of the substituents R₁, R₂, and R₃ were synthesized by the following method. Representative examples are provided below.

Synthesis of (3S*,3aS*,6R*,7R*,7aS*)-1-(3-guanidinopropyl)-7-isobutyl-N-(naphthalen-1-ylmethyl)octahydro-3aH-3,6-methanopyrrolo[3,2-b]pyridine-3a-carboxamide (IB-164) and (3S*,3aS*,6S*,7R*,7aS*)-1-(3-guanidinopropyl)-7-isobutyl-N-(naphthalen-1-ylmethyl)octahydro-6H-3,6-methanopyrrolo[3,2-c]pyridine-6-carboxamide (IF-162)

1. Synthesis of tert-butyl (3S*,3aR*,6S*,7R*,7aS*)-(3-(7-isobutyl-3a-((naphthalen-1-ylmethyl)carbamoyl)-2,3,3a, 6,7,7a-hexahydro-1H-3,6-methanopyrrolo[3,2-b]pyridin-yl)propyl) carbamate and tert-butyl (3S*, 3aR*, 6S*, 7R*, 7aR*)-(3-(7-isobutyl-6-(naphthalen-1-ylmethyl) carbamoyl)-2,3,3a, 6,7,7a-hexahydro-1H-3,6-methanopyrrolo[3,2-c]pyridin-1-yl)propyl)carbamate

N, N-dimethylformamide (1 mL) was added to 4-methylpentanal (60.1 mg, 0.6 mmol), tert-butyl (3-(allylamino)propyl)carbamate (128.6 mg, 0.6 mmol), and molecular sieve 4A (100 mg), and then N-(naphthalen-1-ylmethyl)-1,2,4-triazine-3-carboxamide (79.3 mg, 0.3 mmol) was added. The reaction mixture was heated for 16 hours at 85° C., and then filtered. The filtrate was purified by preparative HPLC (High Performance Liquid Chromatography). A fraction of the substance of interest was concentrated to obtain a mixture of the aforementioned compound.

2. Synthesis of (3S*, 3aS*, 6R*, 7R*, 7aS*)-1-(3-aminopropyl)-7-isobutyl-N-(naphthalen-1-ylmethyl)-1,2,3,6,7,7a-hexahydro-3aH-3,6-methanopyrrolo[3,2-b]pyridine-3a-carboxamide and (3S*, 3aR*, 6S*, 7R*, 7aR*)-1-(3-aminopropyl)-7-isobutyl-N-(naphthalen-1-ylmethyl)-1,2,3,3a, 7,7a-hexahydro-6H-3,6-methanopyrrolo[3,2-c]pyridine-6-carboxamide

Trifluoroacetic acid (0.3 mL) was added to the compound (mixture) obtained in 1. and stirred for 1 hour at room temperature. The trifluoroacetic acid was evaporated to obtain a trifluoroacetic acid salt of the aforementioned compound (mixture).

3. Synthesis of (3S*, 3aS*, 6R*, 7R*, 7aS*)-1-(3-(N,N′-di(tert-butoxycarbonyl)guanidino)propyl)-7-isobutyl-N-(naphthalen-1-ylmethyl)-1,2,3,6,7,7a-hexahydro-3aH-3,6-methanopyrrolo[3,2-b]pyridine-3a-carboxamide and (3S*, 3aR*, 6S*, 7R*, 7aR*)-1-(3-(N,N′-di(tert-butoxycarbonyl)guanidino)propyl)-7-isobutyl-N-(naphthalen-1-ylmethyl)-1,2,3,3a,7,7a-hexahydro-6H-3,6-methanopyrrolo[3,2-c]pyridine-6-carboxamide

1,3-di(tert-butoxycarbonyl)-2-(trifluoromethanesulfonyl)guanidine (234.8 mg, 0.6 mmol), triethylamine (60.7 mg, 0.6 mmol), and tetrahydrofuran (0.5 mL) were added to the compound (mixture) obtained in 2. and stirred for 3 hours at room temperature. The solvent was evaporated to obtain a mixture comprising the aforementioned compound. The mixture obtained in this step was used in synthesis of the next step without purification.

4. Synthesis of (3S*,3aS*,6R*,7R*,7aS*)-1-(3-(N,N′-di(tert-butoxycarbonyl)guanidino)propyl)-7-isobutyl-N-(naphthalen-1-ylmethyl)octahydro-3aH-3,6-methanopyrrolo[3,2-b]pyridine-3a-carboxamide and (3S*,3aS*,6S*,7R*,7aS*)-1-(3-(N,N′-di(tert-butoxycarbonyl)guanidino)propyl)-7-isobutyl-N-(naphthalen-1-ylmethyl)octahydro-6H-3,6-methanopyrrolo[3,2-c]pyridine-6-carboxamide

The reaction mixture obtained in 3. was dissolved in methanol (1 mL), then sodium borohydride (22.7 mg, 0.6 mmol) was added and stirred for 2 hours at room temperature. The reaction mixture was purified by preparative HPLC. Fractions of substances of interest were concentrated to obtain each of the aforementioned compounds separately.

5. Synthesis of (3S*,3aS*,6S*,7R*,7aS*)-1-(3-guanidinopropyl)-7-isobutyl-N-(naphthalen-1-ylmethyl)octahydro-6H-3,6-methanopyrrolo[3,2-c]pyridine-6-carboxamide

Trifluoroacetic acid (0.3 mL) was added to (3S*,3aS*,6S*,7R*,7aS*)-1-(3-(N,N′-di(tert-butoxycarbonyl)guanidino)propyl)-7-isobutyl-N-(naphthalen-1-ylmethyl)octahydro-6H-3,6-methanopyrrolo[3,2-c]pyridine-6-carboxamide obtained in 4. and stirred for 1 hour at room temperature. The trifluoroacetic acid was evaporated to obtain a trifluoroacetic acid salt of the aforementioned compound.

6. Synthesis of (3S*, 3aS*, 6R*, 7R*, 7aS*)-1-(3-guanidinopropyl)-7-isobutyl-N-(naphthalen-1-ylmethyl)octahydro-3aH-3,6-methanopyrrolo[3,2-b]pyridine-3a-carboxamide

A trifluoroacetic acid salt of the aforementioned compound was obtained by the same method as 5. by using (3S*, 3aS*, 6R*, 7R*, 7aS*)-1-(3-(N,N′-di(tert-butoxycarbonyl)guanidino)propyl)-7-isobutyl-N-(naphthalen-1-ylmethyl)octahydro-3aH-3,6-methanopyrrolo[3,2-b]pyridine-3a-carboxamide obtained in 4.

Synthesis of (3S*,3aS*,6R*,7R*,7aS*)—N-benzyl-7-(2-((tert-butyldimethylsilyl)oxy)ethyl)-1-phenethyl-1,2,3,6,7,7a-hexahydro-3aH-3,6-methanopyrrolo[3,2-b]pyridine-3a-carboxamide and (3S*,3aR*,6S*,7R*,7aR*)—N-benzyl-7-(2-((tert-butyldimethylsilyl)oxy)ethyl)-1-phenethyl-1,2,3,3a,7,7a-hexahydro-6H-3,6-methanopyrrolo[3,2-c]pyridine-6H-carboxamide

Chloroform (1 mL) was added to N-phenethyl prop-2-en-1-amine (58.4 mg, 0.4 mmol), 4-((tert-butyldimethylsilyl)oxy)butanal (80.0 mg, 0.4 mmol), and molecular sieve 4A (400 mg), and then N-benzyl-1,2,4-triazine-3-carboxamide (43.8 mg, 0.2 mmol) and chloroform (1 mL) were further added. The reaction mixture was heated for 48 hours at 55° C. and filtered. The filtrate was concentrated under reduced pressure. The resulting residue was purified by preparative TLC (Merck 1.13895.001, layer thickness 1 mm) (ethyl acetate:methanol=9:1) to obtain a mixture of the aforementioned compound (73.3 mg, yield 69%, RT=1.08 minutes, 1.12 minutes (C method), [M+1]+=532).

Synthesis of (3S*,3aS*,6S*,7R*,7aS*)—N-benzyl-7-(2-((tert-butyldimethylsilyl)oxy)ethyl)-1-phenethyloctahydro-3aH-3,6-methanopyrrolo[3,2-b]pyridine-3a-carboxamide and (3S*,3aS*,6S*,7R*,7aS*)—N-benzyl-7-(2-((tert-butyldimethylsilyl)oxy)ethyl)-1-phenethyloctahydro-6H-3,6-methanopyrrolo[3,2-c]pyridine-6-carboxamide

The mixture obtained in the above reaction (73.3 mg) was dissolved in methanol (1.5 mL), and sodium borohydride (9 mg, 0.24 mmol) was added and stirred for 12 hours at room temperature. Ethyl acetate was added to the reaction mixture, which was washed twice with saturated saline. The organic phase was dried with anhydrous sodium sulfate. The anhydrous sodium sulfate was filtered out. The filtrate was concentrated under reduced pressure and purified by preparative TLC (Merck 1.13895.001, layer thickness 1 mm) (ethyl acetate:methanol=4:1) to obtain (3S*,3aS*,6S*,7R*,7aS*)—N-benzyl-7-(2-((tert-butyldimethylsilyl)oxy)ethyl)-1-phenethyloctahydro-3aH-3,6-methanopyrrolo[3,2-b]pyridine-3a-carboxamide (47.6 mg, two-step yield of 43%, RT=1.13 minutes (C method), [M+1]+=534) and (3S*,3aS*,6S*,7R*,7aS*)—N-benzyl-7-(2-((tert-butyldimethylsilyl)oxy)ethyl)-1-phenethyloctahydro-6H-3,6-methanopyrrolo[3,2-c]pyridine-6-carboxamide (20.6 mg, two-step yield of 19%, RT=0.95 minutes (C method), [M+1]+=534).

Synthesis of (3S*,3aS*,6S*,7R*,7aS*)—N-benzyl-7-(2-hydroxyethyl)-1-phenethyloctahydro-3aH-3,6-methanopyrrolo[3,2-b]pyridine-3aH-carboxamide

(3S*,3aS*,6S*,7R*,7aS*)—N-benzyl-7-(2-((tert-butyldimethylsilyl)oxy)ethyl)-1-phenethyloctahydro-3aH-3,6-methanopyrrolo[3,2-b]pyridine-a-carboxamide (46.7 mg, 0.087 mmol) was dissolved in tetrahydrofuran (1 mL), and tetrabutylammonium fluoride (approximately 1 mol/L tetrahydrofuran solution, 0.1 mL) was added and stirred overnight at room temperature. The reaction mixture was concentrated and ethyl acetate was added, and then transferred to a separatory funnel and washed with saturated saline. The organic phase was dried with anhydrous sodium sulfate, concentrated under reduced pressure, and purified by preparative TLC (Merck 1.05744.001, layer thickness 0.5 mm) (ethyl acetate:methanol=4:1) to obtain the aforementioned compound (35 mg, yield of 96%, RT=0.85 minutes (C method), [M+1]+=420).

Synthesis of (3S*,3aS*,6S*,7R*,7aS*)—N-benzyl-7-(2-hydroxyethyl)-1-phenethyloctahydro-6H-3,6-methanopyrrolo[3,2-c]pyridine-6H-carboxamide

(3S*,3aS*,6S*,7R*,7aS*)—N-benzyl-7-(2-((tert-butyldimethylsilyl)oxy)ethyl)-1-phenethyloctahydro-6H-3,6-methanopyrrolo[3,2-c]pyridine-6-carboxamide (20.6 mg, 0.039 mmol) was dissolved in tetrahydrofuran (0.5 mL), and tetrabutylammonium fluoride (approximately 1 mol/L tetrahydrofuran solution, 0.05 mL) was added and stirred overnight at room temperature. The reaction mixture was concentrated, ethyl acetate was added and transferred to a separatory funnel, and washed twice with saturated saline. The organic phase was dried with anhydrous sodium sulfate, concentrated under reduced pressure, and purified by preparative TLC (Merck 105744.001, layer thickness 0.5 mm) (ethyl acetate:methanol=4:1) to obtain the aforementioned compound (16 mg, yield of 91%, RT=0.72 minutes (C method), [M+1]⁺=420).

Synthesis of (3S*,3aS*,6S*,7R*,7aS*)—N,4,7-tribenzyl-1-(naphthalen-1-ylmethyl)octahydro-3aH-3,6-methanopyrrolo[3,2-b]pyridine-3a-carboxamide

(3S*,3aS*,6S*,7R*,7aS*)—N,7-dibenzyl-1-(naphthalen-1-ylmethyl)octahydro-3aH-3,6-methanopyrrolo[3,2-b]pyridine-3a-carboxamide (compound IB-42, 5 mg, 0.01 mmol) was dissolved in tetrahydrofuran (0.2 mL), then benzaldehyde (2.1 mg, 0.02 mmol), trifluoroacetic acid (3.4 mg, 0.03 mmol), and molecular sieve 4A (40 mg) were added and heated for 18 hours at 50° C. Sodium triacetoxyborohydride (5 mg, 0.024 mmol) was added to the reaction mixture and stirred for 5 hours at room temperature. To the reaction mixture, ethyl acetate and saturated sodium bicarbonate water are added. The organic phase was washed twice with saturated saline. The organic phase was dried with anhydrous sodium sulfate, concentrated under reduced pressure, and purified by TLC (Merck 105715.001, layer thickness 0.25 mm) (hexane:ethyl acetate=2:1) to obtain the aforementioned compound (1.2 mg, yield of 20%, RT=1.14 minutes (C method), [M+1]⁺=592).

Tables 3 and 4 summarize the synthesized compounds of formula IB and compounds of IF. In the following tables, “EX” means that the synthesis method is described in the Examples.

TABLE 3-1
Compound					Synthesis
number	R1	R2	R3	R4	method	Intermediate
IB-1	i-Bu	Bnzl	Bnzl	H	EX	IIB-1
IB-2	i-Bu	i-Bu	i-Bu	H	IB-1	IIB-2
IB-3	i-Bu	i-Bu	Bnzl	H	IB-1	IIB-3
IB-4	Bnzl	i-Bu	i-Bu	H	IB-1	IIB-4
IB-5	i-Bu	Bnzl	i-Bu	H	IB-1	IIB-5
IB-6	Bnzl	i-Bu	Bnzl	H	IB-1	IIB-6
IB-7	Bnzl	Bnzl	i-Bu	H	IB-1	IIB-7
IB-8	Bnzl	Bnzl	Bnzl	H	IB-1	IIB-8
IB-9	i-Pnt	Bnzl	Bnzl	H	IB-1	IIB-9
IB-10	Bnzl	Bnzl	i-Pnt	H	IB-1	IIB-10
IB-11	i-Bu	Bnzl	Ph-Et	H	IB-1	IIB-11
IB-12	i-Bu	Ph-Et	Bnzl	H	IB-1	IIB-12
IB-13	i-Bu	Bnzl	3-Me-Bnzl	H	IB-1	IIB-13
IB-14	i-Bu	Bnzl	4-Me-Bnzl	H	IB-1	IIB-14
IB-15	i-Bu	3-Me-Bnzl	Bnzl	H	IB-1	IIB-15
IB-16	i-Bu	4-Me-Bnzl	Bnzl	H	IB-1	IIB-16
IB-17	i-Bu	3-Cl-Bnzl	Bnzl	H	IB-1	IIB-17
IB-18	i-Bu	4-Cl-Bnzl	Bnzl	H	IB-1	IIB-18
IB-19	3,4-Cl2-Bnzl	Bnzl	i-Bu	H	IB-1	IIB-19
IB-20	Bnzl	3,4-Cl2-Bnzl	i-Bu	H	IB-1	IIB-20
IB-21	Me	Np-E	Bnzl	H	IB-1	IIB-21
IB-22	i-Bu	4-OH-Bnzl	Bnzl	H	IB-40	IB-23
IB-23	i-Bu	4-(tert-butoxy)benzyl	Bnzl	H	IB-1	IIB-23
IB-24	i-Bu	Np-M	Bnzl	H	IB-1	IIB-24
IB-25	i-Bu	Hdr-E	Bnzl	H	IB-1	IIB-25
IB-26	i-Bu	Cbx-E	Bnzl	H	IF-26	IB-27
IB-27	i-Bu	2-(tert-butoxy)-2-oxoethyl	Bnzl	H	IB-1	IIB-27
IB-28	i-Bu	Cbm-E	Bnzl	H	IB-1	IIB-28
IB-29	i-Bu	4-aminobutyl	Bnzl	H	EX	IB-30
IB-30	i-Bu	4-((tert-butoxycarbonyl)amino)butyl	Bnzl	H	IB-1	IIB-30
IB-31	i-Bu	Chm	Bnzl	H	IB-1	IIB-31

TABLE 3-2
IB-32	i-Bu	(tetrahydro-	Bnzl	H	IB-1	IIB-32
		2H-
		pyran-
		2-yl)
		methyl
IB-33	i-Bu	Bnzl	4-	H	IF-33	IB-34
			aminobutyl
IB-34	i-Bu	Bnzl	4-	H	IB-1	IIB-34
			((tert-
			butoxy-
			carbonyl)
			amino)
			butyl
IB-35	i-Bu	Bnzl	Cbx-E	H	EX	IB-73
IB-36	i-Bu	Bnzl	3-	H	IB-1	IIB-36
			methoxy-
			3-
			oxopropyl
IB-37	i-Bu	Bnzl	Cbm-E	H	IF-33	IB-75
IB-38	i-Bu	Bnzl	Chm	H	IB-1	IIB-38
IB-39	Chm	Bnzl	Bnzl	H	IB-1	IIB-39
IB-40	4-OH-	Bnzl	Bnzl	H	EX	IB-41
	Bnzl
IB-41	4-	Bnzl	Bnzl	H	IB-1	IIB-41
	(tert-
	butoxy)
	benzyl
IB-42	Np-M	Bnzl	Bnzl	H	IB-1	IIB-42
IB-43	i-Bu	Bnzl	Bnzl	Ac	IE-43	IB-1
IB-44	i-Bu	i-Bu	i-Bu	Ac	IF-43	IB-2
IB-45	i-Bu	i-Bu	Bnzl	Ac	IF-43	IB-3
IB-46	Bnzl	i-Bu	i-Bu	Ac	IF-43	IB-4
IB-47	i-Bu	Bnzl	i-Bu	Ac	IF-43	IB-5
IB-49	Bnzl	Bnzl	i-Bu	Ac	IF-43	IB-7
IB-50	Bnzl	Bnzl	Bnzl	Ac	IF-43	IB-8
IB-54	i-Bu	Ph—Et	Bnzl	Ac	IF-43	IB-12
IB-57	i-Bu	3-Me-Bnzl	Bnzl	Ac	IF-43	IB-15
IB-58	i-Bu	4-Me-Bnzl	Bnzl	Ac	IF-43	IB-16
IB-64	Me	Np-E	Bnzl	Ac	IF-43	IB-21
IB-68	i-Bu	Bnzl	Bnzl	Bz	EX	IB-1
IB-69	i-Bu	Bnzl	Bnzl	Et	EX	IB-1
IB-70	i-Bu	Bnzl	Bnzl	methoxy-	EX	IB-1
				carbonyl
IB-71	i-Bu	Bnzl	Bnzl	Me	IF-71	IB-1
IB-72	Me	Np-E	Bnzl	Et	IB-69	IB-21
IB-73	i-Bu	Bnzl	Cbx-E	tBOC	EX	IB-74
IB-74	i-Bu	Bnzl	3-	tBOC	EX	IB-36
			methoxy-
			3-
			oxopropyl
IB-75	i-Bu	Bnzl	Cbm-E	tBOC	EX	IB-73
IB-76	3-	Bnzl	Bnzl	H	IB-1	IIB-76
	(tert-
	butoxy)-
	3-
	oxopropyl
IB-77	Bnzl	Bnzl	4-OH-Bnzl	H	IB-1	IIB-77
IB-78	Me	2-(1-	Bnzl	H	IB-1	IIB-78
		(tert-
		butoxy-
		carbonyl)-
		1H-indol-
		3-yl)
		ethyl
IB-79	Chm	Bnzl	Bnzl	propyl-	EX	IB-39
				carbamoyl
IB-80	Np-M	Bnzl	Pr	H	IB-1	IIB-80

TABLE 3-3
Compound		LCMS tR	Mass	Elution	Yield
number	Name of compound	(min)	(M + H)+	condition	(%)
IB-1	(3S*,3aS*,6R*,7R*,7aS*)-N,7-dibenzyl-	1.21	418	B	81
	1-isobutyloctahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-
	carboxamide
IB-2	(3S*,3aS*,6R*,7R*,7aS*)-N,1,7-	1.20	350	B	77
	triisobutyloctahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-
	carboxamide
IB-3	(3S*,3aS*,6R*,7R*,7aS*)-7-benzyl-N,1-	1.19	384	B	75
	diisobutyloctahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-
	carboxamide
IB-4	(3S*,3aS*,6R*,7R*,7aS*)-1-benzyl-N,7-	1.20	384	B	88
	diisobutyloctahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-
	carboxamide
IB-5	(3S*,3aS*,6R*,7R*,7aS*)-N-benzyl-1,7-	1.20	384	B	76
	diisobutyloctahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-
	carboxamide
IB-6	(3S*,3aS*,6R*,7R*,7aS*)-1,7-dibenzyl-	1.20	418	B	54
	N-isobutyloctahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-
	carboxamide
IB-7	(3S*,3aS*,6R*,7R*,7aS*)-N,1-dibenzyl-	1.21	418	B	81
	7-isobutyloctahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-
	carboxamide
IB-8	(3S*,3aS*,6R*,7R*,7aS*)-N,1,7-	1.21	452	B	76
	tribenzyloctahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-
	carboxamide
IB-9	(3S*,3aS*,6R*,7R*,7aS*)-N,7-dibenzyl-	1.23	432	B	81
	1-isopentyloctahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-
	carboxamide
IB-10	(3S*,3aS*,6R*,7R*,7aS*)-N,1-dibenzyl-	1.23	432	B	37
	7-isopentyloctahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-
	carboxamide
IB-11	(3S*,3aS*,6R*,7R*,7aS*)-N-benzyl-1-	1.22	432	B	63
	isobutyl-7-phenethyloctahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-
	carboxamide
IB-12	(3S*,3aS*,6R*,7R*,7aS*)-1-benzyl-7-	1.23	432	B	65
	isobutyl-N-phenethyloctahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-
	carboxamide
IB-13	(3S*,3aS*,6R*,7R*,7aS*)-N-benzyl-1-	1.24	432	B	64
	isobutyl-7-(3-methylbenzyl)octahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-
	carboxamide
IB-14	(3S*,3aS*,6R*,7R*,7aS*)-N-benzyl-1-	1.23	432	B	74
	isobutyl-7-(4-methylbenzyl)octahydro-
	3aH-3,6-methanopyrrolo[3,2-b]pyridine-
	3a-carboxamide

TABLE 3-4
IB-15	(3S*,3aS*,6R*,7R*,7aS*)-7-benzyl-1-	1.24	432	B	66
	isobutyl-N-(3-methylbenzyl)octahydro-
	3aH-3,6-methanopyrrolo[3,2-b]pyridine-
	3a-carboxamide
IB-16	(3S*,3aS*,6R*,7R*,7aS*)-7-benzyl-1-	1.25	432	B	72
	isobutyl-N-(4-methylbenzyl)octahydro-
	3aH-3,6-methanopyrrolo[3,2-b]pyridine-
	3a-carboxamide
IB-17	(3S*,3aS*,6R*,7R*,7aS*)-7-benzyl-N-(3-	1.03	452	B	85
	chlorobenzyl)-1-isobutyloctahydro-
	3aH-3,6-methanopyrrolo[3,2-b]pyridine-
	3a-carboxamide
IB-18	(3S*,3aS*,6R*,7R*,7aS*)-7-benzyl-N-(4-	1.24	452	B	79
	chlorobenzyl)-1-isobutyloctahydro-
	3aH-3,6-methanopyrrolo[3,2-b]pyridine-
	3a-carboxamide
IB-19	(3S*,3aS*,6R*,7R*,7aS*)-N-benzyl-1-	1.13	486	B	43
	(3,4-dichlorobenzyl)-7-isobutyloctahydro-
	3aH-3,6-methanopyrrolo[3,2-b]pyridine-
	3a-carboxamide
IB-20	(3S*,3aS*,6R*,7R*,7aS*)-1-benzyl-N-	1.26	486	B	84
	(3,4-dichlorobenzyl)-7-isobutyloctahydro-
	3aH-3,6-methanopyrrolo[3,2-b]pyridine-
	3a-carboxamide
IB-21	(3S*,3aS*,6R*,7R*,7aS*)-7-benzyl-1-	1.19	440	B	82
	isobutyl-N-(2-(naphthalen-1-yl)ethyl)octahydro-
	3aH-3,6-methanopyrrolo[3,2-b]pyridine-
	3a-carboxamide
IB-22	(3S*,3aS*,6R*,7R*,7aS*)-7-benzyl-N-(4-	0.89	434	A	95
	hydroxybenzyl)-1-isobutyloctahydro-
	3aH-3,6-methanopyrrolo[3,2-b]pyridine-
	3a-carboxamide
IB-23	(3S*,3aS*,6R*,7R*,7aS*)-7-benzyl-1-	1.06	490	A	88
	isobutyl-N-(4-(tert-butoxy)benzyl)octahydro-
	3aH-3,6-methanopyrrolo[3,2-b]pyridine-3a-
	carboxamide
IB-24	(3S*,3aS*,6R*,7R*,7aS*)-7-benzyl-1-	1.05	468	A	84
	isobutyl-N-(naphthalen-1-ylmethyl)octahydro-
	3aH-3,6-methanopyrrolo[3,2-b]pyridine-
	3a-carboxamide
IB-25	(3S*,3aS*,6R*,7R*,7aS*)-7-benzyl-N-(2-	0.80	372	A	77
	hydroxyethyl)-1-isobutyloctahydro-
	3aH-3,6-methanopyrrolo[3,2-b]pyridine-
	3a-carboxamide
IB-26	3-((3S*,3aS*,6R*,7R*,7aS*)-7-benzyl-1-	0.82	400	A	95
	isobutyloctahydro-1H-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-
	carboxamide)propanoic acid
IB-27	(3S*,3aS*,6R*,7R*,7aS*)-7-benzyl-1-	0.99	456	A	93
	isobutyl-N-(2-(tert-butoxy)-2-
	oxoethyl)octahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-
	3a-carboxamide
IB-28	(3S*,3aS*,6R*,7R*,7aS*)-N-(3-amino-3-	0.79	399	A	80
	oxopropyl)-7-benzyl-1-isobutyloctahydro-
	3aH-3,6-methanopyrrolo[3,2-b]pyridine-
	3a-carboxamide
IB-29	(3S*,3aS*,6R*,7R*,7aS*)-N-(4-	0.75	399	A	100
	aminobutyl)-7-benzyl-1-isobutyloctahydro-
	3aH-3,6-methanopyrrolo[3,2-b]pyridine-
	3a-carboxamide
IB-30	(3S*,3aS*,6R*,7R*,7aS*)-7-benzyl-1-	0.97	499	A	62
	isobutyl-N-(4-((tert-
	butoxycarbonyl)amino)butyl)octahydro-
	3aH-3,6-methanopyrrolo[3,2-b]pyridine-
	3a-carboxamide
IB-31	(3S*,3aS*,6R*,7R*,7aS*)-7-benzyl-N-	1.05	424	A	42
	cyclohexylmethyl-1-isobutyloctahydro-
	3aH-3,6-methanopyrrolo[3,2-b]pyridine-
	3a-carboxamide

TABLE 3-5
IB-32	(3S*,3aS*,6R*,7R*,7aS*)-7-benzyl-1-	0.96	426	A	97
	isobutyl-N-((tetrahydro-
	2H-pyran-2-yl)methyl)octahydro-
	3aH-3,6-methanopyrrolo[3,2-b]pyridine-
	3a-carboxamide
IB-33	(3S*,3aS*,6R*,7R*,7aS*)-7-(4-	0.74	399	A	100
	aminobutyl)-N-benzyl-1-
	isobutyloctahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-
	3a-carboxamide
IB-34	(3S*,3aS*,6R*,7R*,7aS*)-N-benzyl-1-	0.99	499	A	77
	isobutyl-7-(4-((tert-
	butoxycarbonyl)amino)butyl)octahydro-
	3aH-3,6-methanopyrrolo[3,2-b]pyridine-
	3a-carboxamide
IB-35	3-((3S*,3aS*,6R*,7R*,7aS*)-3a-	0.83	400	A	100
	(benzylcarbamoyl)-1-
	isobutyloctahydro-1H-3,6-
	methanopyrrolo[3,2-b]pyridin-7-
	yl)propanoic acid
IB-36	(3S*,3aS*,6R*,7R*,7aS*)-N-benzyl-1-	0.90	414	A	73
	isobutyl-7-(3-methoxy-3-
	oxopropyl)octahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-
	3a-carboxamide
IB-37	(3S*,3aS*,6R*,7R*,7aS*)-7-(3-amino-3-	0.78	399	A	100
	oxopropyl)-N-benzyl-1-isobutyloctahydro-
	3aH-3,6-methanopyrrolo[3,2-b]pyridine-
	3a-carboxamide
IB-38	(3S*,3aS*,6R*,7R*,7aS*)-N-benzyl-7-	1.07	424	A	82
	(cyclohexylmethyl)-1-isobutyloctahydro-
	3aH-3,6-methanopyrrolo[3,2-b]pyridine-
	3a-carboxamide
IB-39	(3S*,3aS*,6R*,7R*,7aS*)-N,7-dibenzyl-	1.06	458	A	78
	1-cyclohexylmethyloctahydro-
	3aH-3,6-methanopyrrolo[3,2-b]pyridine-
	3a-carboxamide
IB-40	(3S*,3aS*,6R*,7R*,7aS*)-N,7-dibenzyl-	0.89	468	A	99
	1-(4-hydroxybenzyl)octahydro-
	3aH-3,6-methanopyrrolo[3,2-b]pyridine-
	3a-carboxamide
IB-41	(3S*,3aS*,6R*,7R*,7aS*)-N,7-dibenzyl-	1.05	524	A	65
	1-(4-(tert-butoxy)benzyl)octahydro-
	3aH-3,6-methanopyrrolo[3,2-b]pyridine-
	3a-carboxamide
IB-42	(3S*,3aS*,6R*,7R*,7aS*)-N,7-dibenzyl-	1.05	502	A	63
	1-(naphthalen-1-ylmethyl)octahydro-
	3aH-3,6-methanopyrrolo[3,2-b]pyridine-
	3a-carboxamide
IB-43	(3S*,3aS*,6R*,7R*,7aS*)-4-acetyl-N,7-	1.14	460	B	86
	dibenzyl-1-isobutyloctahydro-
	3aH-3,6-methanopyrrolo[3,2-
	b]pyridine-3a-carboxamide
IB-44	(3S*,3aS*,6R*,7R*,7aS*)-4-acetyl-	1.10	392	B	86
	N,1,7-triisobutyloctahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-
	3a-carboxamide
IB-45	(3S*,3aS*,6R*,7R*,7aS*)-4-acetyl-7-	1.10	426	B	82
	benzyl-N,1-diisobutyloctahydro-3aH-
	3,6-methanopyrrolo[3,2-b]pyridine-
	3a-carboxamide
IB-46	(3S*,3aS*,6R*,7R*,7aS*)-4-acetyl-1-	1.10	426	B	91
	benzyl-N,7-diisobutyloctahydro-3aH-
	3,6-methanopyrrolo[3,2-b]pyridine-
	3a-carboxamide
IB-47	(3S*,3aS*,6R*,7R*,7aS*)-4-acetyl-N-	1.11	426	B	85
	benzyl-1,7-diisobutyloctahydro-3aH-
	3,6-methanopyrrolo[3,2-b]pyridine-
	3a-carboxamide
IB-49	(3S*,3aS*,6R*,7R*,7aS*)-4-acetyl-N,1-	1.13	460	B	86
	dibenzyl-7-isobutyloctahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-
	carboxamide

TABLE 3-6
IB-50	(3S*,3aS*,6R*,7R*,7aS*)-4-acetyl-	1.16	494	B	81
	N,1,7-tribenzyloctahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-
	3a-carboxamide
IB-54	(3S*,3aS*,6R*,7R*,7aS*)-4-acetyl-1-	1.15	474	B	82
	benzyl-7-isobutyl-N-phenethyloctahydro-
	3aH-3,6-methanopyrrolo[3,2-b]pyridine-
	3a-carboxamide
IB-57	(3S*,3aS*,6R*,7R*,7aS*)-4-acetyl-7-	1.17	474	B	87
	benzyl-1-isobutyl-N-(3-
	methylbenzyl)octahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-
	carboxamide
IB-58	(3S*,3aS*,6R*,7R*,7aS*)-4-acetyl-7-	1.17	474	B	80
	benzyl-1-isobutyl-N-(4-
	methylbenzyl)octahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-
	3a-carboxamide
IB-64	(3S*,3aS*,6R*,7R*,7aS*)-4-acetyl-7-	1.12	482	B	100
	benzyl-1-isobutyl-N-(2-(naphthalen-
	1-yl)ethyl)octahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-
	3a-carboxamide
IB-68	(3S*,3aS*,6R*,7R*,7aS*)-4-benzoyl-	1.23	522	B	39
	N,7-dibenzyl-1-isobutyloctahydro-
	3aH-3,6-methanopyrrolo[3,2-b]pyridine-
	3a-carboxamide
IB-69	(3S*,3aS*,6R*,7R*,7aS*)-N,7-dibenzyl-	1.24	446	B	28
	4-ethyl-1-isobutyloctahydro-3aH-
	3,6-methanopyrrolo[3,2-b]pyridine-
	3a-carboxamide
IB-70	(3S*,3aS*,6R*,7R*,7aS*)-N,7-dibenzyl-	1.18	476	B	85
	1-isobutyl-4-(methoxycarbonyl)octahydro-
	3aH-3,6-methanopyrrolo[3,2-b]pyridine-
	3a-carboxamide
IB-71	(3S*,3aS*,6R*,7R*,7aS*)-N,7-dibenzyl-	1.22	432	B	35
	1-isobutyl-4-methyloctahydro-3aH-
	3,6-methanopyrrolo[3,2-b]pyridine-
	3a-carboxamide
IB-72	(3S*,3aS*,6R*,7R*,7aS*)-7-benzyl-4-	1.24	468	B	70
	ethyl-1-isobutyl-N-(2-(naphthalen-
	1-yl)ethyl)octahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-
	carboxamide
IB-73	tert-butyl (3S*,3aS*,6R*,7R*,7aS*)-	0.91	500	A	100
	3a-(benzylcarbamoyl)-1-isobutyl-7-
	(2-carboxyethyl)octahydro-4H-3,6-
	methanopyrrolo[3,2-b]pyridine-4-
	carboxylate
IB-74	tert-butyl (3S*,3aS*,6R*,7R*,7aS*)-	0.97	514	A	75
	3a-(benzylcarbamoyl)-1-isobutyl-7-
	(3-methoxy-3-oxopropyl)octahydro-
	4H-3,6-methanopyrrolo[3,2-b]pyridine-
	4-carboxylate
IB-75	tert-butyl (3S*,3aS*,6R*,7R*,7aS*)-	0.86	499	A	26
	3a-(benzylcarbamoyl)-1-isobutyl-7-
	(3-amino-3-oxopropyl)octahydro-4H-
	3,6-methanopyrrolo[3,2-b]pyridine-
	4-carboxylate
IB-76	tert-butyl 3-	1.20	490	B	68
	((3S*,3aS*,6R*,7R*,7aS*)-7-benzyl-
	3a-(benzylcarbamoyl)octahydro-1H-3,6-
	methanopyrrolo[3,2-b]pyridin-1-
	yl)propanoate
IB-77	(3S*,3aS*,6R*,7R*,7aS*)-N,1-dibenzyl-	1.13	468	B	60
	7-(4-hydroxybenzyl)octahydro-
	3aH-3,6-methanopyrrolo[3,2-b]pyridine-
	3a-carboxamide
IB-78	tert-butyl 3-	1.25	529	B	71
	((3S*,3aS*,6R*,7R*,7aS*)-2-
	(7-benzyl-1-methyloctahydro-1H-3,6-
	methanopyrrolo[3,2-b]pyridine-
	3a-carboxamide)ethyl)-1H-indole-
	1-carboxylate

TABLE 3-7
IB-79	(3S*,3aS*,6R*,7R*,7aS*)-N3a,7-	1.05	543	A	65
	dibenzyl-1-(cyclohexylmethyl)-N4-
	propylhexahydro-1H-3,6-
	methanopyrrolo[3,2-b]pyridine-3a,4-
	dicarboxamide
IB-80	(3S*,3aS*,6R*,7R*,7aS*)-N-benzyl-	1.02	454	A	62
	1-(naphthalen-1-ylmethyl)-7-
	propyloctahydro-3aH-3,6-
	methanopyrrolo[3,2-b]pyridine-3a-
	carboxamide

TABLE 3-8
				Time of
Compound				retention	Mass	Measurement
number	R1	R2	R3	TR (min)	(M + H)+	condition
IB-81	Cbm-M	Np-M	i-Bu	0.79	435	C
IB-82	Cbm-M	Np-M	Bnzl	0.80	469	C
IB-83	Cbm-M	Np-M	4-OH-Bnzl	0.75	485	C
IB-84	Cbm-M	Np-M	i-Pnt	0.83	449	C
IB-85	Cbm-M	Np-M	Ph-Et	0.83	483	C
IB-86	Cbm-M	Ph-Et	i-Bu	0.74	399	C
IB-87	Cbm-M	Ph-Et	Bnzl	0.75	433	C
IB-88	Cbm-M	Ph-Et	4-OH-Bnzl	0.69	449	C
IB-89	Cbm-M	Ph-Et	i-Pnt	0.78	413	C
IB-90	Cbm-M	Np-M	Np-M	0.84	519	C
IB-91	Cbm-M	4-F-Bnzl	i-Bu	0.74	403	C
IB-92	Cbm-M	4-F-Bnzl	Bnzl	0.75	437	C
IB-93	Cbm-M	4-F-Bnzl	4-OH-Bnzl	0.69	453	C
IB-94	Cbm-M	4-F-Bnzl	i-Pnt	0.78	417	C
IB-95	Cbm-M	4-F-Bnzl	Ph-Et	0.78	451	C
IB-96	Cbm-M	4-F-Bnzl	Np-M	0.80	487	C
IB-97	Cbm-M	Ph-Et	Np-M	0.82	483	C
IB-98	Cbm-M	i-Pnt	i-Bu	0.73	365	C
IB-99	Cbm-M	i-Pnt	Bnzl	0.74	399	C
IB-100	Cbm-M	i-Pnt	4-OH-Bnzl	0.70	415	C
IB-101	Cbm-M	i-Pnt	Cbx-E	0.64	381	C
IB-102	Cbm-M	i-Pnt	Ph-Et	0.78	413	C
IB-103	Cbm-M	i-Pnt	Np-M	0.80	449	C
IB-104	Cbm-M	Hxy	i-Bu	0.78	379	C
IB-105	Cbm-M	Hxy	Bnzl	0.79	413	C
IB-106	Cbm-M	Hxy	4-OH-Bnzl	0.74	429	C
IB-107	Cbm-M	Hxy	Cbx-E	0.70	395	C

TABLE 3-9
IB-108	Cbm-M	Hxy	i-Pnt	0.82	393	C
IB-109	Cbm-M	Hxy	Ph—Et	0.82	427	C
IB-110	Cbm-M	Hxy	Np-M	0.84	463	C
IB-111	Cbm-M	i-Pr	i-Bu	0.65	337	C
IB-112	Cbm-M	i-Pr	Bnzl	0.66	371	C
IB-113	Cbm-M	i-Pr	4-OH-Bnzl	0.59	387	C
IB-114	Cbm-M	i-Pr	Cbx-E	0.98	353	D
IB-115	Cbm-M	i-Pr	i-Pnt	0.70	351	C
IB-116	Cbm-M	i-Pr	Ph—Et	0.72	385	C
IB-117	Cbm-M	i-Pr	Np-M	0.74	421	C
IB-118	Cbm-M	i-Bu	i-Bu	0.71	351	C
IB-119	Cbm-M	i-Bu	Bnzl	0.72	385	C
IB-120	Cbm-M	i-Bu	4-OH-Bnzl	0.65	401	C
IB-121	Cbm-M	i-Bu	Cbx-E	0.60	367	C
IB-122	Cbm-M	i-Bu	i-Pnt	0.76	365	C
IB-123	Cbm-M	i-Bu	Ph—Et	0.77	399	C
IB-124	Cbm-M	i-Bu	Np-M	0.79	435	C
IB-125	Cbm-M	Bnzl	i-Bu	0.74	385	C
IB-126	Cbm-M	Bnzl	Bnzl	0.75	419	C
IB-127	Cbm-M	Bnzl	4-OH-Bnzl	0.69	435	C
IB-128	Cbm-M	Bnzl	Cbx-E	0.63	401	C
IB-129	Cbm-M	Bnzl	i-Pnt	0.79	399	C
IB-130	Cbm-M	Bnzl	Ph—Et	0.80	433	C
IB-131	Cbm-M	Bnzl	Np-M	0.81	469	C
IB-132	Cbm-M	4-OH-Bnzl	i-Bu	0.67	401	C
IB-133	Cbm-M	4-OH-Bnzl	Bnzl	0.69	435	C
IB-134	Cbm-M	4-OH-Bnzl	Cbx-E	0.98	417	D
IB-135	Cbm-M	4-OH-Bnzl	i-Pnt	0.73	415	C
IB-136	Cbm-M	4-OH-Bnzl	Ph—Et	0.74	449	C
IB-137	Cbm-M	4-OH-Bnzl	Np-M	0.76	485	C
IB-138	Cbm-M	Cbx-E	i-Bu	0.61	367	C
IB-139	Cbm-M	Cbx-E	Bnzl	0.62	401	C
IB-140	Cbm-M	Cbx-E	4-OH-Bnzl	0.98	417	D
IB-141	Cbm-M	Cbx-E	i-Pnt	0.67	381	C
IB-142	Cbm-M	Cbx-E	Ph—Et	0.69	415	C
IB-143	Cbm-M	Cbx-E	Np-M	0.71	451	C
IB-144	Cbm-M	Cbm-E	i-Bu	0.59	366	C
IB-145	Cbm-M	Cbm-E	Bnzl	0.61	400	C
IB-146	Cbm-M	Cbm-E	4-OH-Bnzl	0.97	416	D
IB-147	Cbm-M	Cbm-E	Cbx-E	0.20	382	E
IB-148	Cbm-M	Cbm-E	i-Pnt	0.65	380	C
IB-149	Cbm-M	Cbm-E	Ph—Et	0.67	414	C
IB-150	Cbm-M	Cbm-E	Np-M	0.69	450	C
IB-151	Cbm-M	Gun-Pr	i-Bu	0.59	394	C
IB-152	Cbm-M	Gun-Pr	Bnzl	0.60	428	C
IB-153	Cbm-M	Gun-Pr	4-OH-Bnzl	0.91	444	D

TABLE 3-10
IB-154	Cbm-M	Gun-Pr	i-Pnt	0.63	408	C
IB-155	Cbm-M	Gun-Pr	Ph—Et	0.65	442	C
IB-156	Cbm-M	Gun-Pr	Np-M	1.15	478	D
IB-157	Cbm-M	Hdr-E	i-Bu	0.60	339	C
IB-158	Cbm-M	Hdr-E	Bnzl	0.61	373	C
IB-159	Cbm-M	Hdr-E	4-OH-Bnz1	0.98	389	D
IB-160	Cbm-M	Hdr-E	Cbx-E	0.20	355	E
IB-161	Cbm-M	Hdr-E	i-Pnt	0.65	353	C
IB-162	Cbm-M	Hdr-E	Ph—Et	0.67	387	C
IB-163	Cbm-M	Hdr-E	Np-M	0.70	423	C
IB-164	Gun-Pr	Np-M	i-Bu	1.25	477	D
IB-165	Gun-Pr	Np-M	Bnzl	0.73	511	C
IB-166	Gun-Pr	Np-M	4-OH-Bnzl	0.71	527	C
IB-167	Gun-Pr	Np-M	i-Pnt	1.30	491	D
IB-168	Gun-Pr	Np-M	Ph—Et	1.31	525	D
IB-169	Gun-Pr	Np-M	Np-M	1.31	561	D
IB-170	Gun-Pr	Hxy	i-Bu	0.74	421	C
IB-171	Gun-Pr	Hxy	Bnzl	0.74	455	C
IB-172	Gun-Pr	Hxy	4-OH-Bnzl	1.23	471	D
IB-173	Gun-Pr	Hxy	i-Pnt	0.77	435	C
IB-174	Gun-Pr	Hxy	Ph—Et	1.33	469	D
IB-175	Gun-Pr	Hxy	Np-M	1.32	505	D
IB-176	Gun-Pr	i-Pr	i-Bu	1.08	379	D
IB-177	Gun-Pr	i-Pr	4-OH-Bnzl	1.04	429	D
IB-178	Gun-Pr	i-Pr	i-Pnt	1.15	393	D
IB-179	Gun-Pr	i-Pr	Ph—Et	1.17	427	D
IB-180	Gun-Pr	i-Pr	Np-M	1.18	463	D
IB-181	Gun-Pr	4-F-Bnzl	i-Bu	1.19	445	D
IB-182	Gun-Pr	4-F-Bnzl	Bnzl	0.70	479	C
IB-183	Gun-Pr	4-F-Bnzl	4-OH-Bnzl	1.14	495	D
IB-184	Gun-Pr	4-F-Bnzl	i-Pnt	1.26	459	D
IB-185	Gun-Pr	4-F-Bnzl	Ph—Et	0.74	493	C
IB-186	Gun-Pr	4-F-Bnzl	Np-M	0.74	529	C
IB-187	i-Bu	i-Bu	Gun-Pr	3.80	393	G
IB-188	i-Bu	Bnzl	Gun-Pr	4.09	427	G
IB-189	i-Bu	4-OH-Bnzl	Gun-Pr	3.67	443	G
IB-190	i-Bu	Cbm-E	Gun-Pr	3.04	408	G
IB-191	i-Bu	Hdr-E	Gun-Pr	3.00	381	G
IB-192	i-Bu	i-Pnt	Gun-Pr	4.15	407	G
IB-193	i-Bu	Ph—Et	Gun-Pr	4.30	441	G
IB-194	i-Bu	Np-M	Gun-Pr	4.70	477	G
IB-195	i-Bu	Hxy	Gun-Pr	4.54	421	G
IB-196	i-Bu	i-Pr	Gun-Pr	3.72	379	G
IB-197	i-Bu	4-F-Bnzl	Gun-Pr	4.29	445	G
IB-198	Bnzl	i-Bu	Gun-Pr	2.65	427	F
IB-199	Bnzl	4-OH-Bnzl	Gun-Pr	3.88	477	G

TABLE 3-11
IB-200	Bnzl	Cbm-E	Gun-Pr	3.17	442	G
IB-201	Bnzl	Hdr-E	Gun-Pr	3.20	415	G
IB-202	Bnzl	i-Pr	Gun-Pr	3.82	413	F
IB-203	4-OH-Bnzl	i-Bu	Gun-Pr	3.65	443	G
IB-204	4-OH-Bnzl	i-Pnt	Gun-Pr	3.92	457	G
IB-205	4-OH-Bnzl	Ph—Et	Gun-Pr	3.95	491	G
IB-206	4-OH-Bnzl	Np-M	Gun-Pr	4.32	527	G
IB-207	4-OH-Bnzl	4-F-Bnzl	Gun-Pr	3.94	495	G
IB-208	i-Pnt	i-Bu	Gun-Pr	2.54	407	F
IB-209	i-Pnt	Bnzl	Gun-Pr	2.65	441	F
IB-210	i-Pnt	4-OH-Bnzl	Gun-Pr	2.43	457	F
IB-211	i-Pnt	Cbm-E	Gun-Pr	3.07	422	G
IB-212	i-Pnt	Hdr-E	Gun-Pr	3.07	395	G
IB-213	i-Pnt	Ph—Et	Gun-Pr	2.75	455	F
IB-214	i-Pnt	Np-M	Gun-Pr	3.07	491	F
IB-215	i-Pnt	Hxy	Gun-Pr	2.84	435	F
IB-216	i-Pnt	i-Pr	Gun-Pr	3.59	393	G
IB-217	i-Pnt	4-F-Bnzl	Gun-Pr	2.74	459	F
IB-218	Ph—Et	Hdr-E	Gun-Pr	3.63	429	G
IB-219	Np-M	i-Bu	Gun-Pr	3.02	477	F
IB-220	Np-M	Bnzl	Gun-Pr	4.80	511	G
IB-221	Np-M	4-OH-Bnzl	Gun-Pr	4.35	527	G
IB-222	Np-M	Cbm-E	Gun-Pr	3.85	492	G
IB-223	Np-M	Hdr-E	Gun-Pr	3.92	465	G
IB-224	Np-M	i-Pnt	Gun-Pr	3.22	491	F
IB-225	Np-M	Ph—Et	Gun-Pr	3.10	525	F
IB-226	Np-M	Np-M	Gun-Pr	3.24	561	F
IB-227	Np-M	Hxy	Gun-Pr	5.09	505	G
IB-228	Np-M	i-Pr	Gun-Pr	2.82	463	F
IB-229	Np-M	4-F-Bnzl	Gun-Pr	4.87	529	G
IB-230	Chm	i-Bu	Gun-Pr	2.82	433	F
IB-231	Chm	Bnzl	Gun-Pr	2.95	467	F
IB-232	Chm	4-OH-Bnzl	Gun-Pr	2.67	483	F
IB-233	Chm	Cbm-E	Gun-Pr	3.49	448	G
IB-234	Chm	Hdr-E	Gun-Pr	3.50	421	G
IB-235	Chm	i-Pnt	Gun-Pr	3.04	447	F
IB-236	Chm	Ph—Et	Gun-Pr	2.94	481	F
IB-237	Chm	Np-M	Gun-Pr	3.22	517	F
IB-238	Chm	Hxy	Gun-Pr	3.15	461	F
IB-239	Chm	i-Pr	Gun-Pr	2.69	419	F
IB-240	Chm	4-F-Bnzl	Gun-Pr	2.99	485	F
IB-241	4-F-Bnzl	4-OH-Bnzl	Gun-Pr	4.00	495	G
IB-242	4-F-Bnzl	Cbm-E	Gun-Pr	3.29	460	G
IB-243	4-F-Bnzl	Hdr-E	Gun-Pr	3.27	433	F
IB-244	4-F-Bnzl	i-Pr	Gun-Pr	3.84	431	G
IB-245	Bnzl	Bnzl	Gun-Pr	2.69	461	F

TABLE 3-12
IB-246	Bnzl	i-Pnt	Gun-Pr	2.74	441	F
IB-247	Bnzl	Ph—Et	Gun-Pr	2.77	475	F
IB-248	Bnzl	Np-M	Gun-Pr	3.07	511	F
IB-249	Bnzl	Hxy	Gun-Pr	2.97	455	F
IB-250	Bnzl	4-F-Bnzl	Gun-Pr	2.77	479	F
IB-251	Ph—Et	i-Bu	Gun-Pr	2.75	441	F
IB-252	Ph—Et	Bnzl	Gun-Pr	2.85	475	F
IB-253	Ph—Et	4-OH-Bnzl	Gun-Pr	2.60	491	F
IB-254	Ph—Et	i-Pnt	Gun-Pr	2.85	455	F
IB-255	Ph—Et	Np-M	Gun-Pr	3.25	525	F
IB-256	Ph—Et	Hxy	Gun-Pr	3.15	469	F
IB-257	Ph—Et	i-Pr	Gun-Pr	2.52	427	F
IB-258	Ph—Et	4-F-Bnzl	Gun-Pr	2.97	493	F
IB-259	4-F-Bnzl	i-Bu	Gun-Pr	2.67	445	F
IB-260	4-F-Bnzl	Bnzl	Gun-Pr	2.80	479	F
IB-261	4-F-Bnzl	i-Pnt	Gun-Pr	2.84	459	F
IB-262	4-F-Bnzl	Ph—Et	Gun-Pr	2.88	493	F
IB-263	4-F-Bnzl	Np-M	Gun-Pr	3.20	529	F
IB-264	4-F-Bnzl	Hxy	Gun-Pr	3.04	473	F
IB-265	i-Bu	Cbm-E	Cbx-E	2.06	381	H
IB-266	i-Bu	Cbm-E	i-Pnt	2.48	379	H
IB-267	i-Bu	Gun-Pr	i-Bu	2.35	393	H
IB-268	i-Bu	Gun-Pr	Bnzl	2.39	427	H
IB-269	i-Bu	Gun-Pr	4-OH-Bnzl	1.98	443	H
IB-270	i-Bu	Gun-Pr	i-Pnt	2.24	407	H
IB-271	i-Bu	Gun-Pr	Ph—Et	2.25	441	H
IB-272	i-Bu	Gun-Pr	Np-M	2.28	477	H
IB-273	Bnzl	Cbm-E	Cbx-E	1.90	415	H
IB-274	Bnzl	Cbm-E	i-Pnt	2.28	413	H
IB-275	Bnzl	Gun-Pr	i-Bu	2.17	427	H
IB-276	Bnzl	Gun-Pr	Bnzl	2.25	461	H
IB-277	Bnzl	Gun-Pr	4-OH-Bnzl	2.07	477	H
IB-278	Bnzl	Gun-Pr	i-Pnt	2.36	441	H
IB-279	Bnzl	Gun-Pr	Ph—Et	2.28	475	H
IB-280	Bnzl	Gun-Pr	Np-M	2.33	511	H
IB-281	4-OH-Bnzl	Cbm-E	Cbx-E	1.71	431	H
IB-282	4-OH-Bnzl	Cbm-E	i-Pnt	2.03	429	H
IB-283	4-OH-Bnzl	Gun-Pr	i-Bu	1.96	443	H
IB-284	4-OH-Bnzl	Gun-Pr	Bnzl	2.12	477	H
IB-285	4-OH-Bnzl	Gun-Pr	i-Pnt	2.03	457	H
IB-286	4-OH-Bnzl	Gun-Pr	Ph—Et	2.13	491	H
IB-287	4-OH-Bnzl	Gun-Pr	Np-M	2.22	527	H
IB-288	Cbx-E	Cbm-E	i-Pnt	2.10	395	H
IB-289	Gun-Pr	i-Bu	i-Bu	2.02	393	H
IB-290	Gun-Pr	i-Bu	Bnzl	2.01	427	H
IB-291	Gun-Pr	i-Bu	4-OH-Bnzl	1.95	443	H

TABLE 3-13
IB-292	Gun-Pr	i-Bu	i-Pnt	2.04	407	H
IB-293	Gun-Pr	i-Bu	Ph—Et	2.12	441	H
IB-294	Gun-Pr	i-Bu	Np-M	2.14	477	H
IB-295	Gun-Pr	Bnzl	i-Bu	2.03	427	H
IB-296	Gun-Pr	Bnzl	Bnzl	2.06	461	H
IB-297	Gun-Pr	Bnzl	4-OH-Bnzl	1.98	477	H
IB-298	Gun-Pr	Bnzl	i-Pnt	2.16	441	H
IB-299	Gun-Pr	Bnzl	Ph—Et	2.19	475	H
IB-300	Gun-Pr	Bnzl	Np-M	2.21	511	H
IB-301	Gun-Pr	4-OH-Bnzl	i-Bu	1.93	443	H
IB-302	Gun-Pr	4-OH-Bnzl	Bnzl	1.95	477	H
IB-303	Gun-Pr	4-OH-Bnzl	i-Pnt	2.05	457	H
IB-304	Gun-Pr	4-OH-Bnzl	Ph—Et	2.07	491	H
IB-305	Gun-Pr	4-OH-Bnzl	Np-M	2.11	527	H
IB-306	Gun-Pr	Cbm-E	i-Bu	1.83	408	H
IB-307	Gun-Pr	Cbm-E	Bnzl	1.85	442	H
IB-308	Gun-Pr	Cbm-E	4-OH-Bnzl	1.75	458	H
IB-309	Gun-Pr	Cbm-E	i-Pnt	1.91	422	H
IB-310	Gun-Pr	Cbm-E	Ph—Et	1.96	456	H
IB-311	Gun-Pr	Cbm-E	Np-M	1.98	492	H
IB-312	Gun-Pr	Hdr-E	i-Bu	1.81	381	H
IB-313	Gun-Pr	Hdr-E	Bnzl	1.85	415	H
IB-314	Gun-Pr	Hdr-E	4-OH-Bnzl	1.73	431	H
IB-315	Gun-Pr	Hdr-E	i-Pnt	1.92	395	H
IB-316	Gun-Pr	Hdr-E	Ph—Et	1.94	429	H
IB-317	Gun-Pr	Hdr-E	Np-M	1.98	465	H
IB-318	Gun-Pr	i-Pnt	i-Bu	2.10	407	H
IB-319	Gun-Pr	i-Pnt	Bnzl	2.11	441	H
IB-320	Gun-Pr	i-Pnt	4-OH-Bnzl	2.03	457	H
IB-321	Gun-Pr	i-Pnt	Ph—Et	2.12	455	H
IB-322	Gun-Pr	i-Pnt	Np-M	2.22	491	H
IB-323	Gun-Pr	Ph—Et	i-Bu	2.12	441	H
IB-324	Gun-Pr	Ph—Et	Bnzl	2.09	475	H
IB-325	Gun-Pr	Ph—Et	4-OH-Bnzl	2.02	491	H
IB-326	Gun-Pr	Ph—Et	i-Pnt	2.18	455	H
IB-327	Gun-Pr	Ph—Et	Np-M	2.25	525	H
IB-328	Hdr-E	Cbm-E	i-Pnt	1.98	367	H
IB-329	Hdr-E	Gun-Pr	i-Bu	1.89	381	H
IB-330	Hdr-E	Gun-Pr	Bnzl	1.96	415	H
IB-331	Hdr-E	Gun-Pr	4-OH-Bnzl	1.84	431	H
IB-332	Hdr-E	Gun-Pr	i-Pnt	2.00	395	H
IB-333	Hdr-E	Gun-Pr	Ph—Et	2.03	429	H
IB-334	Hdr-E	Gun-Pr	Np-M	1.83	465	H
IB-335	i-Pnt	Cbm-E	Cbx-E	1.85	395	H
IB-336	i-Pnt	Gun-Pr	i-Bu	2.14	408	H
IB-337	i-Pnt	Gun-Pr	Bnzl	2.17	441	H

TABLE 3-14
IB-338	i-Pnt	Gun-Pr	4-OH-Bnzl	1.92	457	H
IB-339	i-Pnt	Gun-Pr	Ph—Et	2.26	455	H
IB-340	i-Pnt	Gun-Pr	Np-M	2.31	491	H
IB-341	Ph—Et	Cbm-E	Cbx-E	2.00	429	H
IB-342	Ph—Et	Cbm-E	i-Pnt	2.39	427	H
IB-343	Ph—Et	Gun-Pr	i-Bu	2.22	441	H
IB-344	Ph—Et	Gun-Pr	Bnzl	2.27	475	H
IB-345	Ph—Et	Gun-Pr	4-OH-Bnzl	2.10	491	H
IB-346	Ph—Et	Gun-Pr	i-Pnt	2.33	455	H
IB-347	Ph—Et	Gun-Pr	Np-M	2.38	525	H
IB-348	Np-M	Cbm-E	Cbx-E	2.14	465	H
IB-349	Np-M	Cbm-E	i-Pnt	2.57	463	H
IB-350	Np-M	Gun-Pr	i-Bu	2.33	477	H
IB-351	Np-M	Gun-Pr	Bnzl	2.31	511	H
IB-352	Np-M	Gun-Pr	4-OH-Bnzl	2.18	527	H
IB-353	Np-M	Gun-Pr	i-Pnt	2.42	491	H
IB-354	Np-M	Gun-Pr	Ph—Et	2.38	525	H
IB-355	Np-M	Gun-Pr	Np-M	2.41	561	H
IB-356	Chm	Cbm-E	Cbx-E	2.00	421	H
IB-357	Chm	Cbm-E	i-Pnt	2.41	419	H
IB-358	Chm	Gun-Pr	i-Bu	2.27	433	H
IB-359	Chm	Gun-Pr	Bnzl	2.31	467	H
IB-360	Chm	Gun-Pr	4-OH-Bnzl	2.13	483	H
IB-361	Chm	Gun-Pr	i-Pnt	2.33	447	H
IB-362	Chm	Gun-Pr	Ph—Et	2.34	481	H
IB-363	Chm	Gun-Pr	Np-M	2.42	517	H
IB-364	4-F-Bnzl	Cbm-E	Cbx-E	1.93	433	H
IB-365	4-F-Bnzl	Cbm-E	i-Pnt	2.29	431	H
IB-366	4-F-Bnzl	Gun-Pr	i-Bu	2.21	445	H
IB-367	4-F-Bnzl	Gun-Pr	Bnzl	2.26	478	H
IB-368	4-F-Bnzl	Gun-Pr	4-OH-Bnzl	2.09	495	H
IB-369	4-F-Bnzl	Gun-Pr	i-Pnt	2.27	459	H
IB-370	4-F-Bnzl	Gun-Pr	Ph—Et	2.28	493	H
IB-371	4-F-Bnzl	Gun-Pr	Np-M	2.36	529	H
IB-372	Hdr-E	i-Bu	i-Pnt	1.68	352	I
IB-373	Ph—Et	i-Bu	i-Pnt	2.16	412	I
IB-374	Np-M	i-Bu	i-Pnt	2.21	448	I
IB-375	Chm	i-Bu	i-Pnt	2.28	404	I
IB-376	4-F-Bnzl	i-Bu	i-Pnt	2.09	416	I
IB-377	Bnzl	i-Bu	i-Pnt	2.09	398	I
IB-378	i-Bu	i-Bu	i-Pnt	2.06	364	I
IB-379	Hdr-E	Cbx-E	i-Bu	1.33	354	I
IB-380	Hdr-E	4-OH-Bnzl	Cbx-E	1.11	404	I
IB-381	i-Pnt	Cbx-E	Np-M	1.87	464	I
IB-382	Chm	Cbx-E	i-Bu	1.87	406	I
IB-383	Chm	4-OH-Bnzl	Cbx-E	1.68	456	I

TABLE 3-15
IB-384	4-F-Bnzl	Cbx-E	Np-M	1.90	502	I
IB-385	4-F-Bnzl	4-OH-Bnzl	Cbx-E	1.53	468	I
IB-386	i-Pnt	4-F-Bnzl	Cbx-E	1.85	432	I
IB-387	Ph—Et	Hdr-E	Cbx-E	1.37	402	I
IB-388	Np-M	Hdr-E	Cbx-E	1.54	438	I
IB-389	Chm	Np-M	Cbx-E	1.99	490	I
IB-390	4-F-Bnzl	Np-M	Cbx-E	1.86	502	I
IB-391	Cbx-E	Hdr-E	Bnzl	1.35	388	I
IB-392	Cbx-E	Np-M	i-Bu	1.80	450	I
IB-393	Cbx-E	Hxy	Bnzl	1.79	428	I
IB-394	Cbx-E	4-F-Bnzl	Bnzl	1.70	452	I
IB-395	Cbx-E	Hdr-E	i-Pnt	1.46	368	I
IB-396	Cbx-E	Hdr-E	Ph—Et	1.45	402	I
IB-397	Cbx-E	Hdr-E	Np-M	1.59	438	I
IB-398	Cbx-E	Np-M	i-Pnt	1.83	464	I
IB-399	Cbx-E	4-F-Bnzl	i-Pnt	1.82	432	I
IB-400	Cbx-E	i-Bu	Bnzl	1.53	400	I
IB-401	Cbx-E	Cbm-E	Ph—Et	1.49	429	I
IB-402	Cbx-E	4-OH-Bnzl	i-Pnt	1.60	430	I
IB-403	Bnzl	Hdr-E	Cbx-E	1.31	388	I
IB-404	Bnzl	Hxy	Cbx-E	1.88	428	I
IB-405	Bnzl	4-OH-Bnzl	Cbx-E	1.54	450	I
IB-406	i-Bu	Hxy	Cbx-E	1.88	394	I
IB-407	i-Bu	Cbx-E	i-Bu	1.62	366	I
IB-408	i-Bu	i-Bu	Cbx-E	1.71	366	I
IB-409	i-Bu	4-OH-Bnzl	Cbx-E	1.47	416	I
IB-410	4-OH-Bnzl	Cbx-E	Np-M	1.70	500	I
IB-411	Ph—Et	i-Bu	Np-M	2.32	482	I
IB-412	Ph—Et	4-OH-Bnzl	Np-M	2.02	532	I
IB-413	Np-M	i-Bu	Ph—Et	2.23	482	I
IB-414	Np-M	i-Bu	Np-M	2.25	518	I
IB-415	Np-M	i-Bu	Bnzl	2.15	468	I
IB-416	Np-M	4-OH-Bnzl	Ph—Et	2.08	532	I
IB-417	Np-M	4-OH-Bnzl	Np-M	2.11	568	I
IB-418	4-F-Bnzl	i-Bu	Np-M	2.15	486	I
IB-419	4-F-Bnzl	Ph—Et	Np-M	2.17	534	I
IB-420	Bnzl	i-Bu	Np-M	2.17	468	I
IB-421	Bnzl	4-OH-Bnzl	Ph—Et	1.92	482	I
IB-422	i-Bu	4-OH-Bnzl	Ph—Et	1.93	448	I
IB-423	4-OH-Bnzl	Ph—Et	Np-M	1.97	532	I
IB-424	4-OH-Bnzl	i-Bu	i-Pnt	1.82	414	I
IB-425	Hdr-E	Np-M	Cbx-E	1.55	438	I
IB-426	i-Pnt	Np-M	Hdr-M	1.91	422	I
IB-427	4-F-Bnzl	Np-M	Hdr-M	1.96	460	I
IB-428	Cbx-E	Ph—Et	4-OH-Bnzl	1.59	464	I
IB-429	Cbx-E	Np-M	Hdr-M	1.55	424	I

TABLE 3-16
IB-430	Cbx-E	i-Bu	Ph—Et	1.66	414	I
IB-431	Cbx-E	i-Bu	Hdr-M	1.21	340	I
IB-432	Cbx-E	i-Bu	4-OH-Bnzl	1.40	416	I
IB-433	Cbx-E	Cbm-E	Np-M	1.56	465	I
IB-434	Cbx-E	Cbm-E	Bnzl	1.41	415	I
IB-435	Cbx-E	Cbm-E	i-Bu	1.37	381	I
IB-436	Cbx-E	Cbm-E	4-OH-Bnzl	1.19	431	I
IB-437	i-Bu	Np-M	Cbx-E	1.86	450	I
IB-438	4-OH-Bnzl	Ph—Et	Cbx-E	1.60	464	I
IB-439	4-OH-Bnzl	Np-M	Cbx-E	1.69	500	I
IB-440	4-OH-Bnzl	Np-M	Hdr-M	1.70	458	I
IB-441	Hdr-E	Cbm-E	4-OH-Bnzl	1.18	403	I
IB-442	Hdr-E	4-OH-Bnzl	i-Pnt	1.58	402	I
IB-443	Hdr-E	4-OH-Bnzl	Ph—Et	1.60	436	I
IB-444	Hdr-E	4-OH-Bnzl	Bnzl	1.52	422	I
IB-445	i-Pnt	4-OH-Bnzl	Np-M	2.02	498	I
IB-446	i-Pnt	4-OH-Bnzl	i-Bu	1.90	414	I
IB-447	Ph—Et	4-OH-Bnzl	i-Pnt	2.02	462	I
IB-448	Ph—Et	4-OH-Bnzl	Bnzl	1.93	482	I
IB-449	Ph—Et	4-OH-Bnzl	i-Bu	1.90	448	I
IB-450	Np-M	4-OH-Bnzl	i-Pnt	2.08	498	I
IB-451	Np-M	4-OH-Bnzl	Bnzl	1.99	518	I
IB-452	Np-M	4-OH-Bnzl	i-Bu	2.00	484	I
IB-453	Chm	4-OH-Bnzl	i-Pnt	2.11	454	I
IB-454	Chm	4-OH-Bnzl	Ph—Et	2.08	488	I
IB-455	Chm	4-OH-Bnzl	Np-M	2.13	524	I
IB-456	Chm	4-OH-Bnzl	Bnzl	2.02	474	I
IB-457	4-F-Bnzl	4-OH-Bnzl	Np-M	2.02	536	I
IB-458	4-F-Bnzl	4-OH-Bnzl	i-Bu	1.87	452	I
IB-459	Np-M	Hdr-E	4-OH-Bnzl	1.64	472	I
IB-460	Chm	Hdr-E	Bnzl	1.94	412	I
IB-461	Ph—Et	Hdr-E	i-Pnt	1.86	400	I
IB-462	Bnzl	4-OH-Bnzl	i-Pnt	1.94	448	I
IB-463	Bnzl	4-OH-Bnzl	Bnzl	1.86	468	I
IB-464	Bnzl	4-OH-Bnzl	i-Bu	1.84	434	I
IB-465	i-Bu	4-OH-Bnzl	i-Pnt	1.96	414	I
IB-466	i-Bu	4-OH-Bnzl	Np-M	2.00	484	I
IB-467	i-Bu	4-OH-Bnzl	i-Bu	1.85	400	I
IB-468	4-OH-Bnzl	Hdr-E	i-Bu	1.40	388	I
IB-469	4-OH-Bnzl	Hdr-E	i-Pnt	1.55	402	I
IB-470	Hdr-E	4-OH-Bnzl	Np-M	1.68	472	I
IB-471	Ph—Et	i-Pr	4-OH-Bnzl	1.24	434	I
IB-472	Np-M	Bnzl	4-OH-Bnzl	1.98	518	I
IB-473	Chm	i-Pr	4-OH-Bnzl	1.20	426	I
IB-474	4-F-Bnzl	Bnzl	Np-M	2.16	520	I
IB-475	4-F-Bnzl	i-Pr	4-OH-Bnzl	1.13	428	I

TABLE 3-17
IB-476	Hdr-E	Hxy	Bnzl	1.92	400	I
IB-477	Hdr-E	Hxy	i-Bu	1.87	366	I
IB-478	Hdr-E	Hxy	4-OH-Bnzl	1.79	416	I
IB-479	Hdr-E	4-F-Bnzl	Bnzl	1.73	424	I
IB-480	i-Pnt	Hxy	4-OH-Bnzl	2.07	442	I
IB-481	i-Pnt	4-F-Bnzl	4-OH-Bnzl	1.93	466	I
IB-482	Np-M	Hxy	i-Bu	2.35		I
IB-483	Np-M	Hxy	4-OH-Bnzl	2.17	512	I
IB-484	Chm	Ph-Et	Bnzl	2.36		I
IB-485	Chm	Hxy	Bnzl	2.42		I
IB-486	Chm	Hxy	i-Bu	2.44		I
IB-487	Chm	Hxy	4-OH-Bnzl	2.18	468	I
IB-488	Chm	4-F-Bnzl	i-Bu	2.22	442	I
IB-489	4-F-Bnzl	Ph-Et	Bnzl	2.18	484	I
IB-490	Hdr-E	Hxy	i-Pnt	1.99	380	I
IB-491	Hdr-E	Hxy	Np-M	1.98	450	I
IB-492	Hdr-E	4-F-Bnzl	Ph-Et	1.80	438	I
IB-493	Np-M	Hdr-E	Np-M	1.99	506	I
IB-494	Chm	Hxy	i-Pnt	2.54		I
IB-495	i-Bu	Ph-Et	i-Bu	2.16	398	I
IB-496	i-Bu	Hxy	4-OH-Bnzl	2.04	428	I
IB-497	i-Bu	4-F-Bnzl	i-Bu	2.05	402	I
IB-498	i-Bu	4-F-Bnzl	4-OH-Bnzl	1.89	452	I
IB-499	4-OH-Bnzl	4-F-Bnzl	i-Bu	1.91	452	I
IB-500	4-OH-Bnzl	Bnzl	Np-M	1.92	518	I
IB-501	4-OH-Bnzl	i-Pr	i-Pnt	1.77	400	I
IB-502	4-OH-Bnzl	i-Pr	Np-M	1.83	470	I
IB-503	Hdr-E	Bnzl	Cbx-E	1.37	388	I
IB-504	Hdr-E	i-Bu	Cbx-E	1.28	354	I
IB-505	i-Pnt	Bnzl	Cbx-E	1.79	414	I
IB-506	i-Pnt	i-Bu	Cbx-E	1.75	380	I
IB-507	i-Pnt	4-OH-Bnzl	Cbx-E	1.49	430	I
IB-508	Ph-Et	i-Bu	Cbx-E	1.71	414	I
IB-509	Np-M	i-Bu	Cbx-E	1.93	450	I
IB-510	Chm	i-Bu	Cbx-E	1.91	406	I
IB-511	4-F-Bnzl	i-Pnt	Cbx-E	1.88	432	I
IB-512	Cbx-E	i-Pnt	4-OH-Bnzl	1.55	430	I
IB-513	Cbx-E	i-Pnt	Ph-Et	1.71	428	I
IB-514	Cbx-E	i-Pnt	Np-M	1.83	464	I
IB-515	Cbx-E	4-OH-Bnzl	Ph-Et	1.63	464	I
IB-516	Cbx-E	4-OH-Bnzl	Np-M	1.68	500	I
IB-517	i-Bu	Cbx-E	Np-M	1.81	450	I
IB-518	4-OH-Bnzl	i-Pnt	Cbx-E	1.61	430	I
IB-519	Hdr-E	Cbm-E	Np-M	1.54	437	I
IB-520	Np-M	Cbm-E	i-Bu	1.83	449	I
IB-521	Np-M	Cbm-E	4-OH-Bnzl	1.64	499	I

TABLE 3-18
IB-522	Chm	Cbm-E	Np-M	1.95	489	I
IB-523	Chm	Cbm-E	4-OH-Bnzl	1.57	455	I
IB-524	4-F-Bnzl	Cbm-E	Ph-Et	1.78	465	I
IB-525	4-F-Bnzl	Cbm-E	Np-M	1.86	501	I
IB-526	Hdr-E	Ph-Et	4-OH-Bnzl	1.53	436	I
IB-527	Hdr-E	Np-M	4-OH-Bnzl	1.69		I
IB-528	Chm	Np-M	i-Bu	2.35	474	I
IB-529	Chm	4-F-Bnzl	4-OH-Bnzl	1.99	492	I
IB-530	4-F-Bnzl	Np-M	4-OH-Bnzl	1.98	536	I
IB-531	Hdr-E	Ph-Et	i-Pnt	1.80	400	I
IB-532	4-F-Bnzl	Np-M	i-Pnt	2.24	500	I
IB-533	Bnzl	4-F-Bnzl	i-Bu	2.07	436	I
IB-534	Bnzl	4-F-Bnzl	4-OH-Bnzl	1.88	486	I
IB-535	Bnzl	Cbm-E	Ph-Et	1.73	447	I
IB-536	i-Bu	Ph-Et	4-OH-Bnzl	1.85	448	I
IB-537	i-Bu	Np-M	4-OH-Bnzl	1.99	484	I
IB-538	i-Bu	Np-M	i-Pnt	2.28	448	I
IB-539	i-Bu	Cbm-E	Ph-Et	1.71	413	I
IB-540	4-OH-Bnzl	Ph-Et	i-Bu	1.80	448	I
IB-541	4-OH-Bnzl	Np-M	i-Bu	1.94	484	I
IB-542	4-OH-Bnzl	Hxy	Bnzl	1.98	462	I
IB-543	4-OH-Bnzl	4-F-Bnzl	Bnzl	1.83	486	I
IB-544	4-OH-Bnzl	Ph-Et	i-Pnt	1.92	462	I
IB-545	4-OH-Bnzl	Cbm-E	Bnzl	1.53	449	I
IB-546	Ph-Et	Bnzl	Np-M	2.22	516	I
IB-547	4-F-Bnzl	Bnzl	Ph-Et	2.15	484	I
IB-548	4-F-Bnzl	Cbm-E	4-OH-Bnzl	1.48	467	I
IB-549	Hdr-E	4-F-Bnzl	4-OH-Bnzl	1.51	440	I
IB-550	i-Pnt	Hxy	Bnzl	2.22	426	I
IB-551	i-Pnt	Hxy	i-Bu	2.24	392	I
IB-552	i-Pnt	4-F-Bnzl	Bnzl	2.11	450	I
IB-553	i-Pnt	4-F-Bnzl	i-Bu	2.10	416	I
IB-554	Ph-Et	Hxy	Bnzl	2.27	460	I
IB-555	Ph-Et	4-F-Bnzl	Bnzl	2.13	484	I
IB-556	Ph-Et	4-F-Bnzl	i-Bu	2.12	450	I
IB-557	i-Pnt	Hxy	Ph-Et	2.31	440	I
IB-558	i-Pnt	Hxy	Np-M	2.35	476	I
IB-559	Ph-Et	4-F-Bnzl	i-Pnt	2.20	464	I
IB-560	Chm	4-F-Bnzl	Np-M	2.29	526	I
IB-561	Bnzl	i-Pnt	i-Bu	2.13	398	I
IB-562	Bnzl	Hxy	Bnzl	2.20	446	I
IB-563	Bnzl	Hxy	i-Bu	2.22	412	I
IB-564	Bnzl	4-F-Bnzl	Bnzl	2.08	470	I
IB-565	Bnzl	Hxy	i-Pnt	2.27	426	I
IB-566	Bnzl	Hxy	Ph-Et	2.24	460	I
IB-567	Bnzl	4-F-Bnzl	i-Pnt	2.13	450	I

TABLE 3-19
IB-568	Bnzl	4-F-Bnzl	Ph-Et	2.12	484	I
IB-569	Bnzl	Cbm-E	4-OH-Bnzl	1.47	449	I
IB-570	i-Bu	Hxy	i-Bu	2.22	378	I
IB-571	i-Bu	Hxy	i-Pnt	2.31	392	I
IB-572	i-Bu	Hxy	Ph-Et	2.25	426	I
IB-573	i-Bu	Hxy	Np-M	2.48	462	I
IB-574	4-OH-Bnzl	i-Pnt	Bnzl	1.90	448	I
IB-575	Cbx-E	i-Bu	Np-M	1.80	450	I
IB-576	i-Pnt	4-OH-Bnzl	Ph-Et	1.97	462	I
IB-577	i-Pnt	4-OH-Bnzl	Bnzl	1.87	448	I
IB-578	Np-M	Bnzl	Np-M	2.24	552	I
IB-579	Np-M	i-Pr	Ph-Et	2.15	468	I
IB-580	Np-M	i-Pr	Bnzl	2.05	454	I
IB-581	Chm	4-OH-Bnzl	i-Bu	2.02	440	I
IB-582	4-F-Bnzl	4-OH-Bnzl	i-Pnt	1.96	466	I
IB-583	4-F-Bnzl	4-OH-Bnzl	Bnzl	1.88	486	I
IB-584	Hdr-E	Ph-Et	Bnzl	1.75	420	I
IB-585	Hdr-E	Np-M	i-Bu	1.80	422	I
IB-586	Hdr-E	4-F-Bnzl	i-Bu	1.62	390	I
IB-587	i-Pnt	Hdr-E	4-OH-Bnzl	1.36	402	I
IB-588	Np-M	Hdr-E	Bnzl	1.89	456	I
IB-589	Np-M	Np-M	4-OH-Bnzl	2.06	568	I
IB-590	Np-M	4-F-Bnzl	i-Bu	2.16	486	I
IB-591	Chm	Hdr-E	4-OH-Bnzl	1.56	428	I
IB-592	Chm	4-F-Bnzl	Bnzl	2.23	476	I
IB-593	Ph-Et	Hdr-E	Np-M	1.88	470	I
IB-594	Ph-Et	i-Pnt	Np-M	2.24	496	I
IB-595	Ph-Et	Hxy	Np-M	2.33	510	I
IB-596	Np-M	Hdr-E	Ph-Et	1.94	470	I
IB-597	Np-M	Hxy	Ph-Et	2.34	510	I
IB-598	Np-M	Hxy	Np-M	2.36	546	I
IB-599	Np-M	4-F-Bnzl	i-Pnt	2.26	500	I
IB-600	Chm	4-F-Bnzl	i-Pnt	2.28	456	I
IB-601	Bnzl	Np-M	4-OH-Bnzl	1.98	518	I
IB-602	Bnzl	Hdr-E	Np-M	1.85	456	I
IB-603	Bnzl	i-Pnt	Np-M	2.29	482	I
IB-604	Bnzl	Hxy	Np-M	2.29	496	I
IB-605	Bnzl	i-Pr	Np-M	2.11	454	I
IB-606	Bnzl	4-OH-Bnzl	Np-M	1.96	518	I
IB-607	i-Bu	Hdr-E	4-OH-Bnzl	1.40	388	I
IB-608	i-Bu	4-F-Bnzl	Np-M	2.15	486	I
IB-609	i-Bu	Cbm-E	i-Bu	1.59	365	I
IB-610	Hdr-E	Cbx-E	Np-M	1.56	438	I
IB-611	i-Pnt	Cbx-E	i-Bu	1.68	380	I
IB-612	Np-M	Cbx-E	Bnzl	1.89	484	I
IB-613	Chm	Cbx-E	i-Pnt	1.95	420	I

TABLE 3-20
IB-614	Chm	Cbx-E	Np-M	2.02	490	I
IB-615	4-F-Bnzl	Cbx-E	4-OH-Bnzl	1.53	468	I
IB-616	Bnzl	Cbx-E	Np-M	1.85	484	I
IB-617	Hdr-E	Bnzl	i-Pnt	1.79	286	I
IB-618	Hdr-E	Bnzl	Ph-Et	1.79	420	I
IB-619	Hdr-E	Bnzl	Bnzl	1.71	406	I
IB-620	Hdr-E	i-Bu	Ph-Et	1.74	386	I
IB-621	Hdr-E	i-Bu	Np-M	1.80	422	I
IB-622	Hdr-E	i-Bu	Bnzl	1.59	372	I
IB-623	Hdr-E	i-Bu	4-OH-Bnzl	1.48	388	I
IB-624	i-Pnt	Bnzl	Ph-Et	2.17	446	I
IB-625	Ph-Et	i-Bu	4-OH-Bnzl	1.88	448	I
IB-626	Chm	Bnzl	i-Pnt	2.35		I
IB-627	Chm	Bnzl	4-OH-Bnzl	2.01	474	I
IB-628	4-F-Bnzl	Bnzl	4-OH-Bnzl	1.94	486	I
IB-629	4-F-Bnzl	i-Bu	Bnzl	2.06	436	I
IB-630	4-F-Bnzl	i-Bu	i-Bu	2.03	402	I
IB-631	4-F-Bnzl	i-Bu	4-OH-Bnzl	1.90	452	I
IB-632	Bnzl	Bnzl	Ph-Et	2.12	466	I
IB-633	i-Bu	i-Bu	Ph-Et	2.11	398	I
IB-634	4-OH-Bnzl	Bnzl	Ph-Et	1.87	482	I
IB-635	4-OH-Bnzl	i-Bu	Np-M	1.97	484	I
IB-636	i-Pnt	Cbm-E	Ph-Et	1.80	427	I
IB-637	Chm	Cbm-E	Bnzl	1.83	439	I
IB-638	i-Pnt	Hdr-E	Bnzl	1.68	386	I
IB-639	i-Pnt	Hdr-E	i-Bu	1.62	352	I
IB-640	Ph-Et	Hdr-E	Bnzl	1.77	420	I
IB-641	Ph-Et	Hdr-E	i-Bu	1.77	386	I
IB-642	Ph-Et	4-F-Bnzl	4-OH-Bnzl	1.99	500	I
IB-643	Np-M	Hdr-E	i-Bu	1.87	422	I
IB-644	Np-M	i-Pnt	i-Bu	2.27	448	I
IB-645	Np-M	i-Pnt	4-OH-Bnzl	2.06	498	I
IB-646	Chm	Hdr-E	i-Bu	1.79	378	I
IB-647	Chm	i-Pnt	Bnzl	2.32	438	I
IB-648	Chm	i-Pnt	4-OH-Bnzl	2.07	454	I
IB-649	4-F-Bnzl	Hdr-E	Bnzl	1.76	424	I
IB-650	4-F-Bnzl	Hdr-E	i-Bu	1.70	390	I
IB-651	4-F-Bnzl	i-Pnt	Bnzl	2.17	450	I
IB-652	4-F-Bnzl	i-Pnt	i-Bu	2.14	416	I
IB-653	4-F-Bnzl	Np-M	i-Bu	2.19	486	I
IB-654	4-F-Bnzl	Hxy	Bnzl	2.24	464	I
IB-655	4-F-Bnzl	Hxy	i-Bu	2.24		I
IB-656	4-F-Bnzl	Hxy	4-OH-Bnzl	2.02	480	I
IB-657	Hdr-E	4-F-Bnzl	i-Pnt	1.83	404	I
IB-658	i-Pnt	Hdr-E	Ph-Et	1.79	400	I
IB-659	i-Pnt	Hdr-E	Np-M	1.94	436	I

TABLE 3-21
IB-660	Ph-Et	Hxy	i-Pnt	2.39		I
IB-661	Np-M	Hdr-E	i-Pnt	1.98	436	I
IB-662	Np-M	Hxy	i-Pnt	2.44		I
IB-663	Chm	Hdr-E	Ph-Et	1.89	426	I
IB-664	Chm	Hdr-E	Np-M	1.98	462	I
IB-665	Chm	Hxy	Ph-Et	2.50		I
IB-666	Chm	Hxy	Np-M	2.54		I
IB-667	Chm	4-F-Bnzl	Ph-Et	2.31	490	I
IB-668	4-F-Bnzl	Hdr-E	i-Pnt	1.77	404	I
IB-669	4-F-Bnzl	Hdr-E	Ph-Et	1.78	438	I
IB-670	4-F-Bnzl	Hdr-E	Np-M	1.87	474	I
IB-671	4-F-Bnzl	i-Pnt	Ph-Et	2.21	464	I
IB-672	4-F-Bnzl	i-Pnt	Np-M	2.27	500	I
IB-673	4-F-Bnzl	Hxy	i-Pnt	2.30		I
IB-674	4-F-Bnzl	Hxy	Ph-Et	2.31		I
IB-675	4-F-Bnzl	Hxy	Np-M	2.37		I
IB-676	Bnzl	Hdr-E	Bnzl	1.70	406	I
IB-677	Bnzl	Hdr-E	i-Bu	1.66	372	I
IB-678	Bnzl	i-Pnt	4-OH-Bnzl	1.95	448	I
IB-679	Bnzl	Hxy	4-OH-Bnzl	2.02	462	I
IB-680	Bnzl	Hdr-E	i-Pnt	1.79	386	I
IB-681	Bnzl	Hdr-E	Ph-Et	1.76	420	I
IB-682	i-Bu	Hdr-E	i-Bu	1.62	338	I
IB-683	i-Bu	i-Pnt	i-Bu	2.11	364	I
IB-684	i-Bu	i-Pnt	4-OH-Bnzl	1.88	414	I
IB-685	i-Bu	Hdr-E	i-Pnt	1.71	352	I
IB-686	i-Bu	Hdr-E	Ph-Et	1.74	386	I
IB-687	i-Bu	Hdr-E	Np-M	1.82	422	I
IB-688	i-Bu	i-Pnt	Ph-Et	2.17	412	I
IB-689	i-Bu	4-F-Bnzl	i-Pnt	2.13	416	I
IB-690	i-Bu	4-F-Bnzl	Ph-Et	2.22		I
IB-691	Ph-Et	Bnzl	Cbx-E	1.84	448	I
IB-692	4-F-Bnzl	Bnzl	Cbx-E	1.79	452	I
IB-693	Np-M	i-Pnt	Cbx-E	1.99	464	I
IB-694	Cbx-E	Bnzl	i-Pnt	1.79	414	I
IB-695	Cbx-E	Bnzl	i-Bu	1.64	400	I
IB-696	Cbx-E	i-Bu	i-Pnt	1.77	380	I
IB-697	Bnzl	i-Pnt	Cbx-E	1.84	414	I
IB-698	Bnzl	Bnzl	Cbx-E	1.82	434	I
IB-699	Bnzl	i-Bu	Cbx-E	1.74	400	I
IB-700	i-Bu	i-Pnt	Cbx-E	1.81	380	I
IB-701	Hdr-E	Cbm-E	Ph-Et	1.46	401	I
IB-702	Hdr-E	Cbm-E	Bnzl	1.39	387	I
IB-703	i-Pnt	Cbm-E	Np-M	1.86	463	I
IB-704	i-Pnt	Cbm-E	Bnzl	1.71	413	I
IB-705	i-Pnt	Cbm-E	i-Bu	1.71	379	I

TABLE 3-22
IB-706	i-Pnt	Cbm-E	4-OH-Bnzl	1.38	429	I
IB-707	Ph-Et	Cbm-E	Bnzl	1.77	447	I
IB-708	Ph-Et	Cbm-E	i-Bu	1.77	413	I
IB-709	Ph-Et	Cbm-E	4-OH-Bnzl	1.55	463	I
IB-710	Chm	Cbm-E	Ph-Et	1.91	453	I
IB-711	Chm	Cbm-E	i-Bu	1.84	405	I
IB-712	4-F-Bnzl	Cbm-E	Bnzl	1.76	451	I
IB-713	4-F-Bnzl	Cbm-E	i-Bu	1.71	417	I
IB-714	Hdr-E	i-Pnt	Bnzl	1.72	386	I
IB-715	Hdr-E	i-Pnt	i-Bu	1.71	352	I
IB-716	Hdr-E	i-Pnt	4-OH-Bnzl	1.61	402	I
IB-717	Hdr-E	Ph-Et	i-Bu	1.74	386	I
IB-718	i-Pnt	Np-M	i-Bu	2.29	448	I
IB-719	i-Pnt	Np-M	4-OH-Bnzl	2.02	498	I
IB-720	Ph-Et	i-Pnt	4-OH-Bnzl	1.99	462	I
IB-721	Np-M	Ph-Et	4-OH-Bnzl	2.09	532	I
IB-722	Chm	Ph-Et	i-Bu	2.32	438	I
IB-723	Chm	Np-M	4-OH-Bnzl	2.13	524	I
IB-724	4-F-Bnzl	i-Pnt	4-OH-Bnzl	2.00	466	I
IB-725	4-F-Bnzl	Ph-Et	i-Bu	2.16	450	I
IB-726	4-F-Bnzl	Ph-Et	4-OH-Bnzl	1.96	500	I
IB-727	Hdr-E	i-Pnt	Np-M	1.88	436	I
IB-728	Np-M	i-Pnt	Ph-Et	2.33	496	I
IB-729	Np-M	Ph-Et	Np-M	2.38		I
IB-730	Chm	i-Pnt	Ph-Et	2.36		I
IB-731	Chm	Np-M	i-Pnt	2.46		I
IB-732	4-F-Bnzl	Ph-Et	i-Pnt	2.22	464	I
IB-733	Bnzl	i-Pnt	Ph-Et	2.20	446	I
IB-734	Bnzl	Cbm-E	Bnzl	1.74	433	I
IB-735	i-Bu	Np-M	i-Bu	2.25	434	I
IB-736	i-Bu	i-Pnt	Np-M	2.27	448	I
IB-737	i-Bu	Cbm-E	Np-M	1.84	449	I
IB-738	i-Bu	Cbm-E	4-OH-Bnzl	1.40	415	I
IB-739	4-OH-Bnzl	i-Pnt	i-Bu	1.84	414	I
IB-740	4-OH-Bnzl	i-Pnt	Ph-Et	1.95	462	I
IB-741	4-OH-Bnzl	i-Pnt	Np-M	2.01	498	I
IB-742	4-OH-Bnzl	Cbm-E	Ph-Et	1.59	463	I
IB-743	4-OH-Bnzl	Cbm-E	Np-M	1.75	499	I
IB-744	Hdr-E	Bnzl	i-Bu	1.67	372	I
IB-745	Hdr-E	Bnzl	4-OH-Bnzl	1.51	422	I
IB-746	Hdr-E	i-Bu	i-Bu	1.57	338	I
IB-747	i-Pnt	Bnzl	Np-M	2.21	482	I
IB-748	i-Pnt	Bnzl	i-Bu	2.10	398	I
IB-749	i-Pnt	Bnzl	4-OH-Bnzl	1.82	448	I
IB-750	i-Pnt	i-Bu	Ph-Et	2.16	412	I
IB-751	i-Pnt	i-Bu	Np-M	2.18	448	I

TABLE 3-23
IB-752	i-Pnt	i-Bu	Bnzl	2.06	398	I
IB-753	i-Pnt	i-Bu	i-Bu	2.04	364	I
IB-754	i-Pnt	i-Bu	4-OH-Bnzl	2.34		I
IB-755	Ph-Et	Bnzl	i-Pnt	2.22	446	I
IB-756	Ph-Et	Bnzl	Bnzl	2.10	466	I
IB-757	Ph-Et	Bnzl	i-Bu	2.13	432	I
IB-758	Ph-Et	Bnzl	4-OH-Bnzl	1.90	482	I
IB-759	Ph-Et	i-Bu	Bnzl	2.08	432	I
IB-760	Ph-Et	i-Bu	i-Bu	2.10	398	I
IB-761	Np-M	Bnzl	i-Bu	2.22	468	I
IB-762	Np-M	i-Bu	i-Bu	2.16	434	I
IB-763	Np-M	i-Bu	4-OH-Bnzl	1.97	484	I
IB-764	Chm	Bnzl	Ph-Et	2.31	472	I
IB-765	Chm	Bnzl	i-Bu	2.24	424	I
IB-766	Chm	i-Bu	Ph-Et	2.27	438	I
IB-767	Chm	i-Bu	Np-M	2.32	474	I
IB-768	Chm	i-Bu	Bnzl	2.19	424	I
IB-769	Chm	i-Bu	i-Bu	2.22	390	I
IB-770	Chm	i-Bu	4-OH-Bnzl	1.99	440	I
IB-771	4-F-Bnzl	Bnzl	i-Pnt	2.18	450	I
IB-772	4-F-Bnzl	Bnzl	Bnzl	2.10	470	I
IB-773	4-F-Bnzl	Bnzl	i-Bu	2.12	436	I
IB-774	4-F-Bnzl	i-Bu	Ph-Et	2.11	450	I
IB-775	Ph-Et	i-Pnt	Bnzl	2.18	446	I
IB-776	Bnzl	i-Pnt	Bnzl	2.13	432	I
IB-777	Bnzl	Bnzl	Np-M	2.20	502	I
IB-778	Bnzl	i-Bu	Ph-Et	2.14	432	I
IB-779	Bnzl	i-Bu	4-OH-Bnzl	1.85	434	I
IB-780	i-Bu	i-Pnt	Bnzl	2.15	398	I
IB-781	i-Bu	Bnzl	i-Pnt	2.19	398	I
IB-782	i-Bu	Bnzl	Np-M	2.16	468	I
IB-783	i-Bu	Bnzl	4-OH-Bnzl	1.85	434	I
IB-784	i-Bu	i-Bu	Np-M	2.19	434	I
IB-785	i-Bu	i-Bu	4-OH-Bnzl	1.81	400	I
IB-786	4-OH-Bnzl	Bnzl	i-Pnt	1.90	448	I
IB-787	4-OH-Bnzl	Bnzl	i-Bu	1.80	434	I
IB-788	Ph-Et	Cbm-E	Np-M	1.91	497	I
IB-789	Ph-Et	i-Pr	Np-M	2.19	468	I
IB-790	Np-M	Cbm-E	Bnzl	1.88	483	I
IB-791	i-Pnt	Np-M	Bnzl	2.27	483	I
IB-792	Ph-Et	Np-M	i-Bu	2.29	482	I
IB-793	Ph-Et	Np-M	4-OH-Bnzl	2.09	532	I
IB-794	Np-M	i-Pnt	Bnzl	2.29	482	I
IB-795	Np-M	Ph-Et	Bnzl	2.32	516	I
IB-796	Np-M	Np-M	i-Bu	2.37	518	I
IB-797	Np-M	4-F-Bnzl	Bnzl	2.24	520	I

TABLE 3-24
IB-798	Chm	Np-M	Bnzl	2.41	508	I
IB-799	4-F-Bnzl	Np-M	Bnzl	2.25	520	I
IB-800	Ph-Et	Np-M	i-Pnt	2.36	497	I
IB-801	Ph-Et	4-F-Bnzl	Np-M	2.27	534	I
IB-802	Np-M	i-Pnt	Np-M	2.42	532	I
IB-803	Np-M	Np-M	i-Pnt	2.41	532	I
IB-804	Np-M	Np-M	Ph-Et	2.39	566	I
IB-805	Np-M	4-F-Bnzl	Ph-Et	2.28	534	I
IB-806	Np-M	4-F-Bnzl	Np-M	2.36	570	I
IB-807	Chm	Np-M	Ph-Et	2.47	522	I
IB-808	Chm	Np-M	Np-M	2.47	558	I
IB-809	4-F-Bnzl	Np-M	Ph-Et	2.28	534	I
IB-810	4-F-Bnzl	Np-M	Np-M	2.31	570	I
IB-811	Bnzl	Np-M	i-Pnt	2.30	482	I
IB-812	Bnzl	4-F-Bnzl	Np-M	2.21	520	I
IB-813	Bnzl	Cbm-E	Np-M	1.86	483	I
IB-814	i-Bu	Np-M	Np-M	2.39	518	I
IB-815	4-OH-Bnzl	Np-M	Bnzl	2.01	518	I
IB-816	4-OH-Bnzl	Np-M	Ph-Et	2.05	532	I
IB-817	Np-M	Bnzl	Ph-Et	2.32	516	I
IB-818	Np-M	Cbm-E	Np-M	2.00	533	I
IB-819	Chm	Bnzl	Np-M	2.40	508	I
IB-820	Hdr-E	Np-M	Bnzl	1.89	456	I
IB-821	i-Pnt	Ph-Et	4-OH-Bnzl	1.94	462	I
IB-822	Ph-Et	i-Pnt	i-Bu	2.13	412	I
IB-823	Ph-Et	Np-M	Bnzl	2.33	516	I
IB-824	Ph-Et	Hxy	i-Bu	2.35	426	I
IB-825	Np-M	Np-M	Bnzl	2.39	552	I
IB-826	Chm	Ph-Et	4-OH-Bnzl	2.02	488	I
IB-827	Hdr-E	i-Pnt	Ph-Et	1.82	400	I
IB-828	Hdr-E	Np-M	i-Pnt	1.98	436	I
IB-829	Hdr-E	Np-M	Ph-Et	1.99	470	I
IB-830	Hdr-E	Np-M	Np-M	2.02	506	I
IB-831	Hdr-E	4-F-Bnzl	Np-M	1.90	474	I
IB-832	i-Pnt	Np-M	Ph-Et	2.45	496	I
IB-833	i-Pnt	Np-M	Np-M	2.45	532	I
IB-834	i-Pnt	4-F-Bnzl	Np-M	2.24	500	I
IB-835	Chm	i-Pnt	Np-M	2.46	488	I
IB-836	Bnzl	Ph-Et	4-OH-Bnzl	1.98	482	I
IB-837	Bnzl	Np-M	Bnzl	2.30	502	I
IB-838	Bnzl	Ph-Et	Np-M	2.28	516	I
IB-839	i-Bu	Hxy	Bnzl	2.24	412	I
IB-840	i-Bu	4-F-Bnzl	Bnzl	2.11	436	I
IB-841	4-OH-Bnzl	Hdr-E	Np-M	1.72	472	I
IB-842	4-OH-Bnzl	Np-M	Np-M	2.08	568	I
IB-843	4-OH-Bnzl	i-Bu	Ph-Et	1.89	448	I

TABLE 3-25
IB-844	Ph-Et	Cbx-E	i-Bu	0.85	414	C
IB-845	Ph-Et	Cbx-E	i-Pnt	0.89	428	C
IB-846	4-OH-Bnzl	Cbx-E	i-Pnt	0.73	430	C
IB-847	4-OH-Bnzl	Cbx-E	Bnzl	0.75	450	C
IB-848	4-OH-Bnzl	Cbx-E	Ph-Et	0.74		C
IB-849	Bnzl	Cbx-E	i-Bu	0.80	400	C
IB-850	Bnzl	Cbx-E	i-Pnt	0.84	414	C
IB-851	Bnzl	Cbx-E	Ph-Et	0.85	448	C
IB-852	i-Bu	Cbx-E	Ph-Et	0.84	414	C
IB-853	i-Bu	Cbx-E	4-OH-Bnzl	0.54	416	C
IB-854	i-Pnt	Cbx-E	Ph-Et	0.84	428	C
IB-855	i-Pnt	Cbx-E	4-OH-Bnzl	0.68	430	C
IB-856	Chm	Cbx-E	Ph-Et	0.91	454	C
IB-857	Chm	Cbx-E	4-OH-Bnzl	0.77	456	C
IB-858	i-Pnt	Cbx-E	Bnzl	0.80	414	C
IB-859	Chm	Cbx-E	Bnzl	0.90	440	C
IB-860	4-OH-Bnzl	Cbx-E	i-Bu	0.69	416	C

TABLE 3-26
Compound					Retention	Mass	Measurement
number	R1	R2	R3	R4	RT (min)	(M + H)+	condition
IB-861	methyl	2-(1H-indol-3-yl)ethyl	benzyl	H	1.212	429	B
IB-862	benzyl	Np-M	i-Bu	H	1.29	468	B
IB-863	benzyl	4-(trifluoromethyl)benzyl	i-Bu	H	1.298	486	B
IB-864	4-Cl-Bnzl	benzyl	i-Bu	H	1.288	452	B
IB-865	3-Cl-Bnzl	benzyl	i-Bu	H	1.293	452	B
IB-866	4-methoxybenzyl	benzyl	i-Bu	H	1.263	448	B
IB-867	4-methylbenzyl	benzyl	i-Bu	H	1.288	432	B
IB-868	i-Pnt	i-Bu	benzyl	H	1.277	398	B
IB-869	i-Bu	i-Bu	4-Cl-Bnzl	H	1.275	418	B
IB-870	i-Bu	i-Pnt	benzyl	H	1.287	398	B
IB-871	i-Bu	4-Cl-Bnzl	i-Bu	H	1.285	418	B
IB-872	4-hydroxybenzyl	benzyl	i-Bu	H	1.187	434	B

TABLE 3-27
IB-873	4-(dimethyl-	benzyl	i-Bu	H	1.255	461	B
	amino)-
	benzyl
IB-874	4-(tert-	benzyl	i-Bu	H	1.345	474	B
	butyl)-
	benzyl
IB-875	i-Bu	benzyl	i-Pnt	H	1.283	398	B
IB-876	i-Pnt	benzyl	i-Bu	H	1.067	398	B
IB-877	4-(trifluoro-	benzyl	i-Bu	H	1.29	502	B
	methyl)-
	benzyl
IB-878	4-ethoxy-	benzyl	i-Bu	H	1.275	462	B
	benzyl
IB-879	benzyl	naphthalen-	i-Bu	H	1.282	468	B
		2-ylmethyl
IB-880	4-methyl-	benzyl	i-Bu	ethyl	1.332	460	B
	benzyl
IB-881	4-methyl-	benzyl	i-Bu	i-Bu	1.495	488	B
	benzyl
IB-882	4-methyl-	benzyl	i-Bu	acetyl	1.223	474	B
	benzyl
IB-883	4-methyl-	benzyl	i-Bu	3-methyl-	1.312	516	B
	benzyl			butanoyl
IB-884	4-methyl-	benzyl	i-Bu	2-phenyl-	1.3	550	B
	benzyl			acetyl
IB-885	4-methyl-	benzyl	i-Bu	methoxy-	1.267	490	B
	benzyl			carbonyl
IB-886	4-methyl-	benzyl	i-Bu	2-methyl-	1.328	532	B
	benzyl			propoxy-
				carbonyl
IB-887	4-methyl-	benzyl	i-Bu	benzyloxy-	1.347	566	B
	benzyl			carbonyl
IB-888	4-methyl-	benzyl	i-Bu	amino-	1.173	475	B
	benzyl			carbonyl
IB-889	4-methyl-	benzyl	i-Bu	N-benzyl-	1.288	565	B
	benzyl			amino-
				carbonyl
IB-890	benzyl	pyridin-	i-Bu	H	1.11	419	B
		4-ylmethyl
IB-891	4-(dimethyl-	3-hydroxy-	i-Bu	H	1.223	477	B
	amino)-	benzyl
	benzyl
IB-892	4-(dimethyl-	4-hydroxy-	i-Bu	H	1.208	477	B
	amino)-	benzyl
	benzyl
IB-893	4-methoxy-	benzyl	benzyl	H	0.98	482	C
	benzyl
IB-894	4-methoxy-	benzyl	benzyl	tert-	1.06	582	C
	benzyl			butoxy-
				carbonyl

TABLE 3-28
IB-895	methyl	benzyl	benzyl	tert-	0.97	476	C
				butoxy-
				carbonyl
IB-896	methyl	benzyl	benzyl	H	0.84	376	C
IB-897	phenethyl	benzyl	2-(tert-	H	1.13	534	C
			butyl-
			dimethyl-
			silyloxy)-
			ethyl
IB-898	cyclo-	4-(tert-	2-(tert-	H	1.16	554	C
	pentyl-	butoxy)-	butoxy-
	methyl	benzyl	carbonyl)-
			ethyl
IB-899	cyclo-	4-(tert-	2-(tert-	methoxy-	1.04	612	C
	pentyl-	butoxy)-	butoxy-	carbonyl
	methyl	benzyl	carbonyl)-
			ethyl
IB-900	cyclo-	4-	2-carboxy-	H	0.77	442	C
	pentyl-	hydroxy-	ethyl
	methyl	benzyl
IB-901	cyclo-	4-	2-carboxy-	methoxy-	0.76	500	C
	pentyl-	hydroxy-	ethyl	carbonyl
	methyl	benzyl
IB-902	4-nitro-	4-(tert-	2-(tert-	H	1.06	607	C
	benzyl	butoxy)-	butoxy-
		benzyl	carbonyl)-
			ethyl
IB-903	phenethyl	benzyl	2-hydroxy-	H	0.85	420	C
			ethyl
IB-904	phenethyl	benzyl	2-hydroxy-	acetyl	0.81	462	C
			ethyl
IB-905	phenethyl	benzyl	2-hydroxy-	methoxy-	0.86	478	C
			ethyl	carbonyl
IB-906	phenethyl	benzyl	2-hydroxy-	ethyl	0.9	448	C
			ethyl
IB-907	4-nitro-	4-(tert-	2-(tert-	methoxy-	1.04	665	C
	benzyl	butoxy)-	butoxy-	carbonyl
		benzyl	carbonyl)-
			ethyl
IB-908	1-naphthyl-	benzyl	benzyl	benzyl	1.14	592	C
	methyl
IB-909	4-amino-	4-(tert-	2-(tert-	methoxy-	0.94	635	C
	benzyl	butoxy)-	butoxy-	carbonyl
		benzyl	carbonyl)-
			ethyl
IB-910	4-(cyclo-	4-(tert-	2-(tert-	methoxy-	1.05	731	C
	pentyl-	butoxy)-	butoxy-	carbonyl
	carbonyl-	benzyl	carbonyl)-
	amino)-		ethyl
	benzyl
IB-911	4-(2-car-	4-(tert-	2-(tert-	methoxy-	0.92	735	C
	boxyethyl-	butoxy)-	butoxy-	carbonyl
	carbonyl-	benzyl	carbonyl)-
	amino)-		ethyl
	benzyl
IB-912	4-(2-car-	4-(tert-	2-(tert-	methoxy-	0.9	734	C
	boxyethyl-	butoxy)-	butoxy-	carbonyl
	carbonyl-	benzyl	carbonyl)-
	amino)-		ethyl
	benzyl

TABLE 3-29
IB-913	4-nitro-	4-hydroxy-	2-carboxyl	H	0.76	495	C
	benzyl	benzyl	ethyl
IB-914	4-(cyclo-	4-hydroxy-	2-carboxyl	methoxy-	0.79	619	C
	pentyl-	benzyl	ethyl	carbonyl
	carbonyl-
	amino)-
	benzyl
IB-915	4-nitro-	4-(tert-	2-(tert-	tert-butoxy-	1.12	707	C
	benzyl	butoxy)-	butoxy-	carbonyl
		benzyl	carbonyl)-
			ethyl
IB-916	4-(cyclo-	4-(tert-	2-(tert-	methoxy-	1.14	717	C
	pentyl-	butoxy)-	butoxy-	carbonyl
	methyl-	benzyl	carbonyl)-
	amino)-		ethyl
	benzyl
IB-917	4-(cyclo-	4-(tert-	2-(tert-	tert-	1.14	774	C
	pentyl-	butoxy)-	butoxy-	butoxy-
	carbonyl-	benzyl	carbonyl)-	carbonyl
	amino)-		ethyl
	benzyl
IB-918	4-(cyclo-	4-(tert-	2-(tert-	tert-	1.24	760	C
	pentyl-	butoxy)-	butoxy-	butoxy-
	methyl-	benzyl	carbonyl)-	carbonyl
	amino)-		ethyl
	benzyl
IB-919	4-nitro-	4-(tert-	2-(tert-	formyl	0.98	635	C
	benzyl	butoxy)-	butoxy-
		benzyl	carbonyl)-
			ethyl
IB-920	4-(2-car-	4-hydroxy-	2-carboxyl	methoxy-	0.61	622	C
	bamoyl-	benzyl	ethyl	carbonyl
	ethyl-
	carbonyl-
	amino)-
	benzyl
IB-921	4-(cyclo-	4-hydroxy-	2-carboxyl	methoxy-	0.82	605	C
	pentyl-	benzyl	ethyl	carbonyl
	methyl-
	amino)-
	benzyl
IB-922	4-(cyclo-	4-hydroxy-	2-carboxyl	H	0.79	561	C
	pentyl-	benzyl	ethyl
	carbonyl-
	amino)-
	benzyl
IB-923	4-(cyclo-	4-hydroxy-	2-carboxyl	H	0.75	547	C
	pentyl-	benzyl	ethyl
	methyl-
	amino)-
	benzyl

TABLE 3-30
Formula XXIB
Compound						Retention	Mass	Measurement
number	R1	R2A	R2B	R3	R4	RT (min)	(M + H)+	condition
IB-924	4-Me-Bnzl	H	Bnzl	i-Bu	N-isobutyl-	2.88	531	B1
					aminocarbonyl
IB-925	i-Bu	H	4-Cl-Bnzl	Ph-Et	H	2.93	466	B1
IB-926	i-Bu	H	3-Cl-Bnzl	Ph-Et	H	2.94	466	B1
IB-927	i-Bu	H	4-MeO-Bnzl	Ph-Et	H	2.84	462	B1
IB-928	i-Bu	H	4-Me-Bnzl	Ph-Et	H	2.93	446	B1
IB-929	i-Bu	H	2-Npm	Ph-Et	H	2.97	482	B1
IB-930	i-Bu	H	Bnzl	Ph-Pr	H	1.36	446	B
IB-931	i-Bu	H	3-Cl-Bnzl	Ph-Pr	H	1.31	480	B
IB-932	i-Bu	H	3-F-Bnzl	Ph-Pr	H	1.35	464	B
IB-933	i-Bu	H	3-Me-Bnzl	Ph-Pr	H	1.38	460	B
IB-934	i-Bu	H	3-MeO-Bnzl	Ph-Pr	H	1.36	476	B
IB-935	i-Bu	H	3-Cl-Bnzl	Ph-Bu	H	1.33	494	B
IB-936	i-Bu	H	3-F-Bnzl	Ph-Bu	H	1.29	478	B
IB-937	i-Bu	H	3-Me-Bnzl	Ph-Bu	H	1.38	474	B
IB-938	i-Bu	H	3-MeO-Bnzl	Ph-Bu	H	1.31	491	B
IB-939	i-Bu	H	Bnzl	Ph-Bu	H	1.32	461	B
IB-940	i-Pnt	H	3-F-Bnzl	Ph-Pr	H	1.31	478	B
IB-941	1-Npm	H	pentyl	Ph-Et	H	1.08	496	C
IB-942	1-Npm	H	cyclohexyl	Ph-Et	H	1.08	508	C
IB-943	1-Npm	H	cyclopentyl	Ph-Et	H	1.06	494	C
IB-944	1-Npm	piperidine †	Ph-Et	H	1.04	494	C
IB-945	1-Npm	piperidine †	Ph-Et	H	1.00	480	C
IB-946	1-Npm	H	Hxy	4-methylphenethyl	H	1.14	524	C
IB-947	1-Npm	H	Hxy	2-(naphthalen-2-yl)ethyl	H	1.16	560	C
IB-948	1-Npm	H	heptyl	Ph-Et	H	1.14	524	C
IB-949	1-Npm	H	Hxy	4-isopropylphenethyl	H	1.19	552	C
IB-950	1-Npm	H	Hxy	cyclohexylethyl	H	1.19	516	C
IB-951	tBuO-E	H	4-fluorophenethyl	1-Npm	H	1.06	544	C
IB-952	H	H	4-tBuO-Bnzl	tBOC-E	methoxycarbonyl	0.93	530	C
IB-953 **	2-phenylacetyl	H	4-tBuO-Bnzl	tBOC-E	methoxycarbonyl	1.17,	648	C
						1.20

TABLE 3-31
IB-	3-	H	4-tBuO-	tBOC-	methoxy-	1.16,	614	C
954	methyl-		Bnzl	E	carbonyl	1.21
**	buta-
	noyl
IB-	2-	H	4-OH-	Cbx-E	methoxy-	0.78,	536	C
955	phenyl-		Bnzl		carbonyl	0.83
**	acetyl
IB-	3-	H	4-OH-	Cbx-E	methoxy-	0.75,	502	C
956	methyl-		Bnzl		carbonyl	0.81
**	buta-
	noyl
IB-	i-Bu	H	Ph-Et	Ph-Et	H	2.89	446	B1
957
IB-	i-Bu	H	1-Npm	Ph-Et	H	2.97	482	B1
958
IB-	Chm	H	tBuO-E	1-Npm	H	1.10	518	C
959
IB-	tBuO-	H	Ph-Et	1-Npm	H	1.06	526	C
960	E
IB-	Hdr-E	H	4-	1-Npm	H	0.90	488.3	C
961			fluoro-
			phenethyl
IB-	3-	H	4-F-Bnzl	1-Npm	H	1.04	544.4	C
962	tert-
	butoxy-
	propyl
IB-	tBuO-	H	4-Cl-Bnzl	1-Npm	H	1.07,	546.3	C
963	E					1.09
IB-	Hdr-E	H	4-Cl-Bnzl	1-Npm	H	0.92	490.3	C
964
IB-	Hdr-E	H	4-Cl-Bnzl	1-Npm	H	0.92	490.2	C
965
IB-	3-	H	4-F-Bnzl	1-Npm	H	0.87	488.3	C
966	hydroxy-
	propyl
IB-	1-Npm	H	Hxy	3-	H	1.14	524.4	C
967				methyl-
				phen-
				ethyl
IB-	1-Npm	H	β-	Ph-Et	H	1.01	546.4	C
968			hydroxy-
			phenethyl
IB-	1-Npm	H	α-	Ph-Et	H	1.01	560.4	C
969			hydroxy-
			methyl-
			phenethyl
IB-	1-Npm	H	α-	Ph-Et	H	1.03	560.4	C
970			hydroxy-
			methyl-
			phenethyl
IB-	4-Nt-	H	Bnzl	tBOC-	H	0.97	535	C
971	Bnzl			E
IB-	4-Nt-	H	Bnzl	tBOC-	ethoxy-	0.98	563	C
972	Bnzl			E	carbonyl
IB-	H	H	Bnzl	tBOC-	ethoxy-	0.87	472	C
973				E	carbonyl
IB-	phenyl-	H	Bnzl	tBOC-	ethoxy-	0.14,	590	C
974	acetyl				carbonyl	0.16
IB-	phenyl-	H	Bnzl	Cbx-E	ethoxy-	0.91,	534	C
975	acetyl				carbonyl	0.97
IB-	4-	H	Bnzl	tBOC-	ethoxy-	0.87	577	C
976	amino			E	carbonyl
	benzyl
IB-	4-	H	Bnzl	tBOC-	ethoxy-	1.09	659	C
977	(cyclo-			E	carbonyl
	pentyl-
	methyl-
	amino)-
	benzyl
IB-	4-	H	Bnzl	Cbx-E	ethoxy-	0.93	603	C
978	(cyclo-				carbonyl
	pentyl-
	methyl-
	amino)-
	benzyl
IB-	4-	H	Bnzl	tBOC-	ethoxy-	1.00	673	C
979	(cyclo-			E	carbonyl
	pentyl-
	carbonyl-
	amino)-
	benzyl
IB-	3-	H	Bnzl	tBOC-	ethoxy-	1.13,	556	C
980	methyl-			E	carbonyl	1.16
**	butanoyl

TABLE 3-32
IB-	H	H	Bnzl	Bnzl	tert-	0.93	462	C
981					butoxy-
					carbonyl
IB-	3-	H	Bnzl	Cbx-E	ethoxy-	0.89,	500	C
982	methyl-				carbonyl	0.96
**	butanoyl
IB-	iso-	H	Bnzl	Cbx-E	ethoxy-	0.94	502	C
983	propoxy-				carbonyl
	carbonyl
IB-	phenyl-	H	Bnzl	3-	ethoxy-	1.05,	562	C
984	acetyl			ethoxy-	carbonyl	1.08
**				3-oxo-
				propyl
IB-	benzoyl	H	Bnzl	Bnzl	tert-	1.22	566	C
985					butoxy-
					carbonyl
IB-	phenyl-	H	Bnzl	Bnzl	tert-	1.23	580	C
986	acetyl				butoxy-
					carbonyl
IB-	4-	H	Bnzl	Cbx-E	ethoxy-	0.87	617	C
987	(cyclo				carbonyl
	pentyl-
	carbonyl-
	amino)-
	benzyl
IB-	1-Npm	H	4-F-Bnzl	2-OH-	H	0.89	474.3	C
988				Et
IB-	2-OH-	H	Ph-Et	1-Npm	H	0.89	470.3	C
989	Et
IB-	4-	H	Bnzl	i-Bu	H	1.02	490.3	C
990	tBuO-Bnzl
IB-	4-	H	i-Bu	Bnzl	H	1.03	490.4	C
991	tBuO-Bnzl
IB-	2-	H	Bnzl	1-Npm	H	1.04	512.4	C
992	OtBu-Et
IB-	2-OH-	H	Bnzl	1-Npm	H	0.87	456.3	C
993	Et
IB-	4-OH-	H	i-Bu	Bnzl	H	0.85	434.3	C
994	Bnzl
IB-	1-Npm	H	4-F-Bnzl	2-	H	1.17	588.4	C
995				OTBS-Et
† Ring formed together by R2A and R2B
** IB-953, 954, 955, 956, 980, 982, and 984 are mixtures of cis-trans isomers. For this reason, two values are shown for the retention of LCMS.

TABLE 4-1
Compound					Synthesis
number	R1	R2	R3	R4	method	Intermediate
IF-1	i-Bu	Bnzl	Bnzl	H	EX	IIF-1
IF-2	i-Bu	i-Bu	i-Bu	H	IF-1	IIF-2
IF-3	i-Bu	i-Bu	Bnzl	H	IF-1	IIF-3
IF-4	Bnzl	i-Bu	i-Bu	H	IF-1	IIF-4
IF-5	i-Bu	Bnzl	i-Bu	H	IF-1	IIF-5
IF-6	Bnzl	i-Bu	Bnzl	H	IF-1	IIF-6
IF-7	Bnzl	Bnzl	i-Bu	H	IF-1	IIF-7
IF-8	Bnzl	Bnzl	Bnzl	H	IF-1	IIF-8
IF-9	i-Pnt	Bnzl	Bnzl	H	IF-1	IIF-9
IF-10	Bnzl	Bnzl	i-Pnt	H	IF-1	IIF-10
IF-11	i-Bu	Bnzl	Ph-Et	H	IF-1	IIF-11
IF-12	i-Bu	Ph-Et	Bnzl	H	IF-1	IIF-12
IF-13	i-Bu	Bnzl	3-Me-Bnzl	H	IF-1	IIF-13
IF-14	i-Bu	Bnzl	4-Me-Bnzl	H	IF-1	IIF-14
IF-15	i-Bu	3-Me-Bnzl	Bnzl	H	IF-1	IIF-15
IF-16	i-Bu	4-Me-Bnzl	Bnzl	H	IF-1	IIF-16
IF-17	i-Bu	3-Cl-Bnzl	Bnzl	H	IF-1	IIF-17
IF-18	i-Bu	4-Cl-Bnzl	Bnzl	H	IF-1	IIF-18
IF-19	3,4-Cl2-Bnzl	Bnzl	i-Bu	H	IF-1	IIF-19
IF-20	Bnzl	3,4-Cl2-Bnzl	i-Bu	H	IF-1	IIF-20
IF-22	i-Bu	4-OH-Bnzl	Bnzl	H	IF-40	IF-23
IF-23	i-Bu	4-(tert-butoxy)benzyl	Bnzl	H	IF-1	IIF-23
IF-24	i-Bu	Np-M	Bnzl	H	IF-1	IIF-24
IF-25	i-Bu	Hdr-E	Bnzl	H	IF-1	IIF-25
IF-26	i-Bu	Cbx-E	Bnzl	H	EX	IF-27
IF-27	i-Bu	2-(tert-butoxy)-2-oxoethyl	Bnzl	H	IF-1	IIF-27
IF-28	i-Bu	Cbm-E	Bnzl	H	IF-1	IIF-28
IF-29	i-Bu	4-aminobutyl	Bnzl	H	IB-29	IF-30
IF-30	i-Bu	4-((tert-butoxycarbonyl)amino)butyl	Bnzl	H	IF-1	IIF-30
IF-31	i-Bu	Chm	Bnzl	H	IF-1	IIF-31
IF-32	i-Bu	(tetrahydro-2H-pyran-2-yl)methyl	Bnzl	H	IF-1	IIF-32
IF-33	i-Bu	Bnzl	4-aminobutyl	H	EX	IF-34

TABLE 4-2
IF-34	i-Bu	Bnzl	4-((tert-	H	IF-1	IIF-34
			butoxy-
			carbonyl) -
			amino)butyl
IF-35	i-Bu	Bnzl	Cbx-E	H	IB-35	IF-73
IF-36	i-Bu	Bnzl	3-	H	IF-1	IIF-36
			methoxy-
			3-
			oxopropyl
IF-38	i-Bu	Bnzl	Chm	H	IF-1	IIF-38
IF-39	Chm	Bnzl	Bnzl	H	IF-1	IIF-39
IF-40	4-OH-	Bnzl	Bnzl	H	EX	IF-41
	Bnzl
IF-41	4-	Bnzl	Bnzl	H	EX	IIF-41
	(tert-
	butoxy)-
	benzyl
IF-42	Np-M	Bnzl	Bnzl	H	IF-1	IIF-42
IF-43	i-Bu	Bnzl	Bnzl	Ac	EX	IF-1
IF-44	i-Bu	i-Bu	i-Bu	Ac	IF-43	IF-2
IF-45	i-Bu	i-Bu	Bnzl	Ac	IF-43	IF-3
IF-46	Bnzl	i-Bu	i-Bu	Ac	IF-43	IF-4
IF-47	i-Bu	Bnzl	i-Bu	Ac	IF-43	IF-5
IF-49	Bnzl	Bnzl	i-Bu	Ac	IF-43	IF-7
IF-50	Bnzl	Bnzl	Bnzl	Ac	IF-43	IF-8
IF-54	i-Bu	Ph-Et	Bnzl	Ac	IF-43	IF-12
IF-57	i-Bu	3-Me-Bnzl	Bnzl	Ac	IF-43	IF-15
IF-58	i-Bu	4-Me-Bnzl	Bnzl	Ac	IF-43	IF-16
IF-68	i-Bu	Bnzl	Bnzl	Bz	IB-68	IF-1
IF-69	i-Bu	Bnzl	Bnzl	Et	IB-69	IF-1
IF-70	i-Bu	Bnzl	Bnzl	meth-	IB-70	IF-1
				oxy-
				carbonyl
IF-71	i-Bu	Bnzl	Bnzl	Me	EX	IF-1
IF-72	Bnzl	Bnzl	i-Bu	Et	IB-69	IF-7
IF-73	i-Bu	Bnzl	Cbx-E	tBOC	IB-73	IF-74
IF-74	i-Bu	Bnzl	3-	tBOC	IB-74	IF-36
			methoxy-
			3-
			oxopropyl
IF-76	3-	Bnzl	Bnzl	H	IF-1	IIF-76
	(tert-
	butoxy)-
	3-
	oxo-
	propyl
IF-77	Bnzl	Bnzl	4-OH-Bnzl	H	IF-1	IIF-77
IF-80	Np-M	Bnzl	Pr	H	IB-1	IIF-80

TABLE 4-3
Compound		LCMS tR	Mass	Elution	Yield
number	Name of compound	(min)	(M + H)+	condition	(%)
IF-1	(3S*,3aS*,6S*,7R*,7aS*)-N,7-	0.99	418	B	62
	dibenzyl-1-isobutyloctahydro-
	6H-3,6-methanopyrrolo[3,2-
	c]pyridine-6-carboxamide
IF-2	(3S*,3aS*,6S*,7R*,7aS*)-N,1,7-	0.93	350	B	73
	triisobutyloctahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-
	6-carboxamide

TABLE 4-4
IF-3	(3S*,3aS*,6S*,7R*,7aS*)-7-benzyl-N,1-	0.96	384	B	67
	diisobutyloctahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IF-4	(3S*,3aS*,6S*,7R*,7aS*)-1-benzyl-N,7-	0.97	384	B	82
	diisobutyloctahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IF-5	(3S*,3aS*,6S*,7R*,7aS*)-N-benzyl-1,7-	0.95	384	B	73
	diisobutyloctahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IF-6	(3S*,3aS*,6S*,7R*,7aS*)-1,7-dibenzyl-	1.00	418	B	68
	N-isobutyloctahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IF-7	(3S*,3aS*,6S*,7R*,7aS*)-N,1-dibenzyl-	0.99	418	B	64
	7-isobutyloctahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IF-8	(3S*,3aS*,6S*,7R*,7aS*)-N,1,7-	1.02	452	B	69
	tribenzyloctahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IF-9	(3S*,3aS*,6S*,7R*,7aS*)-N,7-dibenzyl-	1.01	432	B	47
	1-isopentyloctahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IF-10	(3S*,3aS*,6S*,7R*,7aS*)-N,1-dibenzyl-	1.02	432	B	60
	7-isopentyloctahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IF-11	(3S*,3aS*,6S*,7R*,7aS*)-N-benzyl-1-	0.99	432	B	63
	isobutyl-7-phenethyloctahydro-6H-
	3,6-methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IF-12	(3S*,3aS*,6S*,7R*,7aS*)-1-benzyl-7-	1.01	432	B	60
	isobutyl-N-phenethyloctahydro-6H-
	3,6-methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IF-13	(3S*,3aS*,6S*,7R*,7aS*)-N-benzyl-1-	1.01	432	B	55
	isobutyl-7-(3-methylbenzyl)octahydro-
	6H-3,6-methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IF-14	(3S*,3aS*,6S*,7R*,7aS*)-N-benzyl-1-	1.01	432	B	57
	isobutyl-7-(4-methylbenzyl)octahydro-
	6H-3,6-methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IF-15	(3S*,3aS*,6S*,7R*,7aS*)-7-benzyl-1-	1.02	432	B	62
	isobutyl-N-(3-methylbenzyl)octahydro-
	6H-3,6-methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IF-16	(3S*,3aS*,6S*,7R*,7aS*)-7-benzyl-1-	1.02	432	B	63
	isobutyl-N-(4-methylbenzyl)octahydro-
	6H-3,6-methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IF-17	(3S*,3aS*,6S*,7R*,7aS*)-7-benzyl-N-	1.03	452	B	69
	(3-chlorobenzyl)-1-isobutyloctahydro-
	6H-3,6-methanopyrrolo[3,2-c]pyridine-6-
	carboxamide
IF-18	(3S*,3aS*,6S*,7R*,7aS*)-7-benzyl-N-	1.03	452	B	68
	(4-chlorobenzyl)-1-isobutyloctahydro-
	6H-3,6-methanopyrrolo[3,2-c]pyridine-6-
	carboxamide
IF-19	(3S*,3aS*,6S*,7R*,7aS*)-N-benzyl-1-	1.13	486	B	38
	(3,4-dichlorobenzyl)-7-isobutyloctahydro-
	6H-3,6-methanopyrrolo[3,2-c]pyridine-6-
	carboxamide

TABLE 4-5
IF-20	(3S*,3aS*,6S*,7R*,7aS*)-1-benzyl-N-	1.06	486	B	37
	(3,4-dichlorobenzyl)-7-isobutyloctahydro-
	6H-3,6-methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IF-22	(3S*,3aS*,6S*,7R*,7aS*)-7-benzyl-N-(4-	0.71	434	A	95
	hydroxybenzyl)-1-isobutyloctahydro-
	6H-3,6-methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IF-23	(3S*,3aS*,6S*,7R*,7aS*)-7-benzyl-1-	0.87	490	A	95
	isobutyl-N-(4-(tert-butoxy)benzyl)octahydro-
	6H-3,6-methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IF-24	(3S*,3aS*,6S*,7R*,7aS*)-7-benzyl-1-	0.85	468	A	77
	isobutyl-N-(naphthalen-1-
	ylmethyl)octahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-6-
	carboxamide
IF-25	(3S*,3aS*,6S*,7R*,7aS*)-7-benzyl-N-(2-	0.65	372	A	95
	hydroxyethyl)-1-isobutyloctahydro-6H-
	3,6-methanopyrrolo[3,2-c]pyridine-6-
	carboxamide
IF-26	3-((3S*,3aS*,6S*,7R*,7aS*)-7-benzyl-1-	0.66	400	A	100
	isobutyloctahydro-1H-3,6-
	methanopyrrolo[3,2-c]pyridine-
	6-carboxamide)propanoic acid
IF-27	(3S*,3aS*,6S*,7R*,7aS*)-7-benzyl-1-	0.81	456	A	100
	isobutyl-N-(2-(tert-butoxy)-2-
	oxoethyl)octahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IF-28	(3S*,3aS*,6S*,7R*,7aS*)-7-benzyl-	0.67	399	A	53
	N-(3-amino-3-oxopropyl)-1-
	isobutyloctahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IF-29	(3S*,3aS*,6S*,7R*,7aS*)-N-(4-	0.83	399	A	100
	aminobutyl)-7-benzyl-1-
	isobutyloctahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IF-30	(3S*,3aS*,6S*,7R*,7aS*)-7-benzyl-1-	0.81	499	A	80
	isobutyl-N-(4-((tert-
	butoxycarbonyl)amino)butyl)octahydro-
	6H-3,6-methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IF-31	(3S*,3aS*,6S*,7R*,7aS*)-7-benzyl-N-	0.85	424	A	22
	cyclohexylmethyl-1-isobutyloctahydro-
	6H-3,6-methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IF-32	(3S*,3aS*,6S*,7R*,7aS*)-7-benzyl-1-	0.76,	426	A	93
	isobutyl-N-((tetrahydro-2H-pyran-2-	0.75
	yl)methyl)octahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IF-33	(3S*,3aS*,6S*,7R*,7aS*)-7-(4-	0.62	399	A	100
	aminobutyl)-N-benzyl-1-isobutyloctahydro-
	6H-3,6-methanopyrrolo[3,2-c]pyridine-6-
	carboxamide
IF-34	(3S*,3aS*,6S*,7R*,7aS*)-N-benzyl-1-	0.82	499	A	78
	isobutyl-7-(4-((tert-
	butoxycarbonyl)amino)butyl)octahydro-
	6H-3,6-methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IF-35	3-((3S*,3aS*,6S*,7R*,7aS*)-3a-	0.65	400	A	100
	(benzylcarbamoyl)-1-isobutyloctahydro-
	1H-3,6-methanopyrrolo[3,2-c]pyridin-
	7-yl)propanoic acid
IF-36	(3S*,3aS*,6S*,7R*,7aS*)-N-benzyl-1-	0.72	414	A
	isobutyl-7-(3-methoxy-3-
	oxopropyl)octahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IF-38	(3S*,3aS*,6S*,7R*,7aS*)-N-benzyl-7-	0.86	424	A	83
	(cyclohexylmethyl)-1-isobutyloctahydro-
	6H-3,6-methanopyrrolo[3,2-c]pyridine-
	6-carboxamide

TABLE 4-6
IF-39	(3S*,3aS*,6S*,7R*,7aS*)-N,7-dibenzyl-	0.86	458	A	62
	1-cyclohexylmethyloctahydro-
	6H-3,6-methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IF-40	(3S*,3aS*,6S*,7R*,7aS*)-N,7-dibenzyl-	0.75	468	A	63
	1-(4-hydroxybenzyl)octahydro-
	6H-3,6-methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IF-41	(3S*,3aS*,6S*,7R*,7aS*)-N,7-dibenzyl-	0.90	524	A	52
	1-(4-(tert-butoxy)benzyl)octahydro-
	6H-3,6-methanopyrrolo[3,2-c]pyridine-6-
	carboxamide
IF-42	(3S*,3aS*,6S*,7R*,7aS*)-N,7-dibenzyl-	0.88	502	A	65
	1-(naphthalen-1-ylmethyl)octahydro-
	6H-3,6-methanopyrrolo[3,2-c]pyridine-6-
	carboxamide
IF-43	(3S*,3aS*,6S*,7R*,7aS*)-4-acetyl-N,7-	1.08	460	B	51
	dibenzyl-1-isobutyloctahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-6-
	carboxamide
IF-44	(3S*,3aS*,6S*,7R*,7aS*)-4-acetyl-	1.04	392	B	82
	N,1,7-triisobutyloctahydro-6H-
	3,6-methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IF-45	(3S*,3aS*,6S*,7R*,7aS*)-4-acetyl-7-	1.05	426	B	83
	benzyl-N,1-diisobutyloctahydro-6H-
	3,6-methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IF-46	(3S*,3aS*,6S*,7R*,7aS*)-4-acetyl-1-	1.05	426	B	79
	benzyl-N,7-diisobutyloctahydro-6H-
	3,6-methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IF-47	(3S*,3aS*,6S*,7R*,7aS*)-4-acetyl-N-	1.06	426	B	88
	benzyl-1,7-diisobutyloctahydro-6H-
	3,6-methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IF-49	(3S*,3aS*,6S*,7R*,7aS*)-4-acetyl-N,1-	1.08	460	B	84
	dibenzyl-7-isobutyloctahydro-
	6H-3,6-methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IF-50	(3S*,3aS*,6S*,7R*,7aS*)-4-acetyl-	1.10	494	B	75
	N,1,7-tribenzyloctahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-6-
	carboxamide
IF-54	(3S*,3aS*,6S*,7R*,7aS*)-4-acetyl-1-	1.10	474	B	58
	benzyl-7-isobutyl-N-phenethyloctahydro-
	6H-3,6-methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IF-57	(3S*,3aS*,6S*,7R*,7aS*)-4-acetyl-7-	1.12	474	B	40
	benzyl-1-isobutyl-N-
	(3-methylbenzyl)octahydro-6H-
	3,6-methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IF-58	(3S*,3aS*,6S*,7R*,7aS*)-4-acetyl-7-	1.12	474	B	55
	benzyl-1-isobutyl-N-(4-
	methylbenzyl)octahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IF-68	(3S*,3aS*,6S*,7R*,7aS*)-4-benzoyl-	1.17	522	B	51
	N,7-dibenzyl-1-isobutyloctahydro-
	6H-3,6-methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IF-69	(3S*,3aS*,6S*,7R*,7aS*)-N,7-dibenzyl-	1.06	446	B	57
	4-ethyl-1-isobutyloctahydro-6H-
	3,6-methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IF-70	(3S*,3aS*,6S*,7R*,7aS*)-N,7-dibenzyl-	1.13	476	B	32
	1-isobutyl-4-
	(methoxycarbonyl)octahydro-6H-
	3,6-methanopyrrolo[3,2-c]pyridine-6-
	carboxamide

TABLE 4-7
IF-71	(3S*,3aS*,6S*,7R*,7aS*)-N,7-dibenzyl-	1.02	432	B	38
	1-isobutyl-4-methyloctahydro-6H-
	3,6-methanopyrrolo[3,2-c]pyridine-6-
	carboxamide
IF-72	(3S*,3aS*,6S*,7R*,7aS*)-N,1-dibenzyl-	1.06	446	B	45
	4-ethyl-7-isobutyloctahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-6-
	carboxamide
IF-73	tert-butyl (3S*,3aS*,6S*,7R*,7aS*)-6-	0.84	500	A	9
	(benzylcarbamoyl)-1-isobutyl-7-(2-
	carboxyethyl)octahydro-5H-3,6-
	methanopyrrolo[3,2-c]pyridine-5-
	carboxylate
IF-74	tert-butyl (3S*,3aS*,6S*,7R*,7aS*)-	0.91	514	A	71
	3a-(benzylcarbamoyl)-1-isobutyl-7-
	(3-methoxy-3-oxopropyl)octahydro-
	4H-3,6-methanopyrrolo[3,2-b]
	pyridine-4-carboxylate
IF-76	tert-butyl 3-	1.04	490	B	53
	((3S*,3aS*,6S*,7R*,7aS*)-7-benzyl-6-
	(benzylcarbamoyl)octahydro-1H-3,6-
	methanopyrrolo[3,2-c]pyridin-1-
	yl)propanoate
IF-77	(3S*,3aS*,6S*,7R*,7aS*)-N,1-dibenzyl-	0.93	468	B	60
	7-(4-hydroxybenzyl)octahydro-6H-
	3,6-methanopyrrolo[3,2-c]pyridine-
	6-carboxamide
IF-80	(3S*,3aS*,6S*,7R*,7aS*)-N-benzyl-1-	0.84	454	A	44
	(naphthalen-1-ylmethyl)-7-
	propyloctahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-6-
	carboxamide

TABLE 4-8
Compound				Retention	Mass	Measurement
number	R1	R2	R3	RT (min)	(M + H)+	condition
IF-81	Cbm-M	Np-M	i-Bu	0.71	435	C
IF-82	Cbm-M	Np-M	Bnzl	0.72	469	C
IF-83	Cbm-M	Np-M	4-OH-Bnzl	0.67	485	C
IF-84	Cbm-M	Np-M	i-Pnt	0.73	449	C
IF-85	Cbm-M	Np-M	Ph-Et	0.75	483	C
IF-86	Cbm-M	Ph-Et	i-Bu	0.66	399	C
IF-87	Cbm-M	Ph-Et	Bnzl	0.68	433	C
IF-88	Cbm-M	Ph-Et	4-OH-Bnzl	0.63	449	C
IF-89	Cbm-M	Ph-Et	i-Pnt	0.70	413	C
IF-90	Cbm-M	Ph-Et	Np-M	0.74	483	C
IF-91	Cbm-M	Np-M	Np-M	0.76	519	C
IF-92	Cbm-M	4-F-Bnzl	i-Bu	0.65	403	C
IF-93	Cbm-M	4-F-Bnzl	Bnzl	0.67	437	C

TABLE 4-9
IF-94	Cbm-M	4-F-Bnzl	4-OH-Bnzl	0.62	453	C
IF-95	Cbm-M	4-F-Bnzl	i-Pnt	0.69	417	C
IF-96	Cbm-M	4-F-Bnzl	Ph-Et	0.71	451	C
IF-97	Cbm-M	4-F-Bnzl	Np-M	0.73	487	C
IF-98	Cbm-M	i-Pnt	i-Bu	0.66	365	C
IF-99	Cbm-M	i-Pnt	Bnzl	0.67	399	C
IF-100	Cbm-M	i-Pnt	4-OH-Bnzl	0.62	415	C
IF-101	Cbm-M	i-Pnt	Cbx-E	0.58	381	C
IF-102	Cbm-M	i-Pnt	Ph-Et	0.71	413	C
IF-103	Cbm-M	i-Pnt	Np-M	0.73	449	C
IF-104	Cbm-M	Hxy	i-Bu	0.71	379	C
IF-105	Cbm-M	Hxy	Bnzl	0.72	413	C
IF-106	Cbm-M	Hxy	4-OH-Bnzl	0.67	429	C
IF-107	Cbm-M	Hxy	Cbx-E	0.63	395	C
IF-108	Cbm-M	Hxy	i-Pnt	0.73	393	C
IF-109	Cbm-M	Hxy	Ph-Et	0.75	427	C
IF-110	Cbm-M	Hxy	Np-M	0.77	463	C
IF-111	Cbm-M	i-Pr	i-Bu	1.03	337	D
IF-112	Cbm-M	i-Pr	Bnzl	0.58	371	C
IF-113	Cbm-M	i-Pr	4-OH-Bnzl	0.97	387	D
IF-114	Cbm-M	i-Pr	Cbx-E	0.22	353	E
IF-115	Cbm-M	i-Pr	i-Pnt	1.09	351	D
IF-116	Cbm-M	i-Pr	Ph-Et	0.63	385	C
IF-117	Cbm-M	i-Pr	Np-M	0.65	421	C
IF-118	Cbm-M	i-Bu	i-Bu	0.62	351	C
IF-119	Cbm-M	i-Bu	Bnzl	0.64	385	C
IF-120	Cbm-M	i-Bu	4-OH-Bnzl	0.59	401	C
IF-121	Cbm-M	i-Bu	Cbx-E	0.93	367	D
IF-122	Cbm-M	i-Bu	i-Pnt	0.66	365	C
IF-123	Cbm-M	i-Bu	Ph-Et	0.69	399	C
IF-124	Cbm-M	i-Bu	Np-M	0.71	435	C
IF-125	Cbm-M	Bnzl	i-Bu	0.65	385	C
IF-126	Cbm-M	Bnzl	Bnzl	0.67	419	C
IF-127	Cbm-M	Bnzl	4-OH-Bnzl	0.62	435	C
IF-128	Cbm-M	Bnzl	Cbx-E	0.99	401	D
IF-129	Cbm-M	Bnzl	i-Pnt	0.69	399	C
IF-130	Cbm-M	Bnzl	Ph-Et	0.71	433	C
IF-131	Cbm-M	Bnzl	Np-M	0.73	469	C
IF-132	Cbm-M	4-OH-Bnzl	i-Bu	0.57	401	C
IF-133	Cbm-M	4-OH-Bnzl	Bnzl	0.59	435	C
IF-134	Cbm-M	4-OH-Bnzl	Cbx-E	0.87	417	D
IF-135	Cbm-M	4-OH-Bnzl	i-Pnt	0.60	415	C
IF-136	Cbm-M	4-OH-Bnzl	Ph-Et	0.63	449	C
IF-137	Cbm-M	4-OH-Bnzl	Np-M	0.65	485	C
IF-138	Cbm-M	Cbx-E	Bnzl	0.94	401	D
IF-139	Cbm-M	Cbx-E	4-OH-Bnzl	0.47	417	D

TABLE 4-10
IF-140	Cbm-M	Cbx-E	Ph-Et	1.01	415	D
IF-141	Cbm-M	Cbx-E	Np-M	0.60	451	C
IF-142	Cbm-M	Cbm-E	i-Bu	0.23	366	E
IF-143	Cbm-M	Cbm-E	Bnzl	0.88	400	D
IF-144	Cbm-M	Cbm-E	4-OH-Bnzl	0.23	416	E
IF-145	Cbm-M	Cbm-E	Cbx-E	0.20	382	E
IF-146	Cbm-M	Cbm-E	i-Pnt	0.91	380	D
IF-147	Cbm-M	Cbm-E	Ph-Et	0.89	414	D
IF-148	Cbm-M	Cbm-E	Np-M	0.57	450	C
IF-149	Cbm-M	Gun-Pr	i-Bu	0.83	394	D
IF-150	Cbm-M	Gun-Pr	Bnzl	0.92	428	D
IF-151	Cbm-M	Gun-Pr	4-OH-Bnzl	0.34	442 1)	E
IF-152	Cbm-M	Gun-Pr	i-Pnt	0.93	408	D
IF-153	Cbm-M	Gun-Pr	Ph-Et	0.96	442	D
IF-154	Cbm-M	Gun-Pr	Np-M	1.01	478	D
IF-155	Cbm-M	Hdr-E	i-Bu	0.46	339	E
IF-156	Cbm-M	Hdr-E	Bnzl	0.49	373	C
IF-157	Cbm-M	Hdr-E	4-OH-Bnzl	0.35	389	E
IF-158	Cbm-M	Hdr-E	Cbx-E	0.20	355	E
IF-159	Cbm-M	Hdr-E	i-Pnt	0.93	353	D
IF-160	Cbm-M	Hdr-E	Ph-Et	0.98	387	D
IF-161	Cbm-M	Hdr-E	Np-M	0.58	423	C
IF-162	Gun-Pr	Np-M	i-Bu	1.25	477	D
IF-163	Gun-Pr	Np-M	Bnzl	0.72	511	C
IF-164	Gun-Pr	Np-M	4-OH-Bnzl	0.69	527	C
IF-165	Gun-Pr	Np-M	i-Pnt	1.28	491	D
IF-166	Gun-Pr	Np-M	Ph-Et	0.75	525	C
IF-167	Gun-Pr	Np-M	Np-M	1.31	561	D
IF-168	Gun-Pr	Hxy	i-Pnt	0.74	435	C
IF-169	Gun-Pr	Hxy	Ph-Et	1.30	469	D
IF-170	Gun-Pr	Hxy	Np-M	1.33	505	D
IF-171	Gun-Pr	i-Pr	i-Bu	1.08	379	D
IF-172	Gun-Pr	i-Pr	4-OH-Bnzl	1.04	429	D
IF-173	Gun-Pr	i-Pr	i-Pnt	1.12	393	D
IF-174	Gun-Pr	i-Pr	Ph-Et	1.15	427	D
IF-175	Gun-Pr	i-Pr	Np-M	1.17	463	D
IF-176	Gun-Pr	4-F-Bnzl	i-Bu	1.17	445	D
IF-177	Gun-Pr	4-F-Bnzl	Bnzl	0.68	479	C
IF-178	Gun-Pr	4-F-Bnzl	4-OH-Bnzl	1.13	495	D
IF-179	Gun-Pr	4-F-Bnzl	i-Pnt	1.21	459	D
IF-180	Gun-Pr	4-F-Bnzl	Ph-Et	0.71	493	C
IF-181	Gun-Pr	4-F-Bnzl	Np-M	0.72	529	C
IF-182	i-Bu	Hdr-E	Cbm-M	0.63	339	G
IF-183	i-Bu	Ph-Et	Cbm-M	3.40	399	G
IF-184	i-Bu	Np-M	Cbm-M	3.87	435	G
IF-185	i-Bu	i-Bu	Gun-Pr	3.15	393	G

TABLE 4-11
IF-186	i-Bu	Bnzl	Gun-Pr	3.42	427	G
IF-187	i-Bu	4-OH-Bnzl	Gun-Pr	3.09	443	G
IF-188	i-Bu	Hdr-E	Gun-Pr	1.17	381	G
IF-189	i-Bu	Ph-Et	Gun-Pr	3.57	441	G
IF-190	i-Bu	Np-M	Gun-Pr	3.87	477	G
IF-191	i-Bu	Hxy	Gun-Pr	3.79	421	G
IF-192	i-Bu	4-F-Bnzl	Gun-Pr	3.49	445	G
IF-193	Bnzl	Cbx-E	Cbm-M	1.82	401	G
IF-194	Bnzl	Hdr-E	Cbm-M	1.52	373	G
IF-195	Bnzl	i-Pnt	Cbm-M	3.59	399	G
IF-196	Bnzl	Ph-Et	Cbm-M	3.62	433	G
IF-197	Bnzl	i-Pr	Cbm-M	3.02	371	G
IF-198	Bnzl	4-OH-Bnzl	Gun-Pr	3.54	477	G
IF-199	Bnzl	Hdr-E	Gun-Pr	2.74	415	F
IF-200	4-OH-Bnzl	Ph-Et	Gun-Pr	3.59	491	G
IF-201	4-OH-Bnzl	Np-M	Gun-Pr	3.90	527	G
IF-202	Cbx-E	i-Pr	Cbm-M	0.95	353	G
IF-203	i-Pnt	i-Bu	Cbm-M	3.25	365	G
IF-204	i-Pnt	Bnzl	Cbm-M	3.47	399	F
IF-205	i-Pnt	4-OH-Bnzl	Cbm-M	3.13	415	G
IF-206	i-Pnt	Ph-Et	Cbm-M	2.43	413	F
IF-207	i-Pnt	Np-M	Cbm-M	2.62	449	F
IF-208	i-Pnt	Hxy	Cbm-M	3.97	393	G
IF-209	i-Pnt	i-Pr	Cbm-M	2.97	351	G
IF-210	i-Pnt	4-F-Bnzl	Cbm-M	3.60	417	G
IF-211	i-Pnt	Bnzl	Gun-Pr	3.60	441	G
IF-212	i-Pnt	Ph-Et	Gun-Pr	3.79	455	G
IF-213	i-Pnt	Np-M	Gun-Pr	2.63	491	G
IF-214	i-Pnt	i-Pr	Gun-Pr	3.25	393	G
IF-215	i-Pnt	4-F-Bnzl	Gun-Pr	3.72	459	G
IF-216	Ph-Et	Bnzl	Cbm-M	2.45	433	F
IF-217	Ph-Et	4-OH-Bnzl	Cbm-M	3.40	449	G
IF-218	Ph-Et	Cbx-E	Cbm-M	2.85	415	G
IF-219	Ph-Et	Cbm-E	Cbm-M	2.67	414	G
IF-220	Ph-Et	Gun-Pr	Cbm-M	2.94	442	G
IF-221	Ph-Et	Hdr-E	Cbm-M	2.75	387	G
IF-222	Ph-Et	i-Pnt	Cbm-M	3.87	413	G
IF-223	Ph-Et	Np-M	Cbm-M	2.75	483	F
IF-224	Ph-Et	4-F-Bnzl	Cbm-M	2.52	451	F
IF-225	Ph-Et	Hdr-E	Gun-Pr	3.05	429	G
IF-226	Np-M	i-Bu	Cbm-M	2.49	435	F
IF-227	Np-M	Bnzl	Cbm-M	2.62	469	F
IF-228	Np-M	Cbm-E	Cbm-M	3.27	450	G
IF-229	Np-M	Gun-Pr	Cbm-M	3.32	478	G
IF-230	Np-M	Hdr-E	Cbm-M	3.29	423	G
IF-231	Np-M	Ph-Et	Cbm-M	2.65	483	F

TABLE 4-12
IF-232	Np-M	Np-M	Cbm-M	2.84	519	F
IF-233	Np-M	i-Pr	Cbm-M	3.62	421	G
IF-234	Np-M	4-F-Bnzl	Cbm-M	2.65	487	F
IF-235	Np-M	i-Bu	Gun-Pr	3.70	477	G
IF-236	Np-M	Bnzl	Gun-Pr	3.88	511	G
IF-237	Np-M	4-OH-Bnzl	Gun-Pr	3.62	527	G
IF-238	Np-M	Cbm-E	Gun-Pr	3.22	492	G
IF-239	Np-M	Hdr-E	Gun-Pr	3.20	465	G
IF-240	Np-M	i-Pnt	Gun-Pr	3.95	491	G
IF-241	Np-M	Ph-Et	Gun-Pr	4.07	525	G
IF-242	Np-M	Np-M	Gun-Pr	4.27	561	G
IF-243	Np-M	Hxy	Gun-Pr	4.25	505	G
IF-244	Np-M	i-Pr	Gun-Pr	2.38	463	F
IF-245	Np-M	4-F-Bnzl	Gun-Pr	3.95	529	G
IF-246	Chm	Bnzl	Cbm-M	3.75	425	G
IF-247	Chm	4-OH-Bnzl	Cbm-M	3.40	441	G
IF-248	Chm	Cbx-E	Cbm-M	2.90	407	G
IF-249	Chm	Cbm-E	Cbm-M	2.74	406	G
IF-250	Chm	i-Pnt	Cbm-M	2.50	405	F
IF-251	Chm	Ph-Et	Cbm-M	2.52	439	F
IF-252	Chm	Np-M	Cbm-M	2.69	475	F
IF-253	Chm	Hxy	Cbm-M	4.17	419	G
IF-254	Chm	i-Pr	Cbm-M	3.29	377	F
IF-255	Chm	4-F-Bnzl	Cbm-M	2.54	443	F
IF-256	Chm	Bnzl	Gun-Pr	3.79	467	G
IF-257	Chm	i-Pnt	Gun-Pr	3.90	447	G
IF-258	Chm	Ph-Et	Gun-Pr	3.95	481	G
IF-259	Chm	Np-M	Gun-Pr	4.27	517	G
IF-260	Chm	Hxy	Gun-Pr	4.12	461	G
IF-261	Chm	4-F-Bnzl	Gun-Pr	3.95	485	G
IF-262	4-F-Bnzl	i-Bu	Cbm-M	3.34	403	G
IF-263	4-F-Bnzl	Bnzl	Cbm-M	3.57	437	G
IF-264	4-F-Bnzl	4-OH-Bnzl	Cbm-M	3.22	453	G
IF-265	4-F-Bnzl	Cbx-E	Cbm-M	2.34	419	G
IF-266	4-F-Bnzl	Cbm-E	Cbm-M	1.63	418	G
IF-267	4-F-Bnzl	Hdr-E	Cbm-M	1.79	391	G
IF-268	4-F-Bnzl	i-Pnt	Cbm-M	3.70	417	G
IF-269	4-F-Bnzl	Ph-Et	Cbm-M	2.43	451	F
IF-270	4-F-Bnzl	Np-M	Cbm-M	2.62	487	F
IF-271	4-F-Bnzl	Hxy	Cbm-M	2.60	431	F
IF-272	4-F-Bnzl	i-Pr	Cbm-M	3.10	389	G
IF-273	4-F-Bnzl	Hdr-E	Gun-Pr	2.70	433	G
IF-274	4-F-Bnzl	i-Pr	Gun-Pr	3.37	431	G
IF-275	Cbx-E	i-Bu	Cbm-M	3.20	367	G
IF-276	Cbx-E	i-Pnt	Cbm-M	3.54	381	G
IF-277	Bnzl	Bnzl	Cbm-M	2.38	419	F

TABLE 4-13
IF-278	Bnzl	Np-M	Cbm-M	4.09	469	G
IF-279	Bnzl	Hxy	Cbm-M	4.02	413	G
IF-280	Bnzl	4-F-Bnzl	Cbm-M	2.43	437	F
IF-281	Bnzl	Bnzl	Gun-Pr	2.40	461	F
IF-282	Bnzl	i-Pnt	Gun-Pr	2.47	441	F
IF-283	Bnzl	Ph-Et	Gun-Pr	2.50	475	F
IF-284	Bnzl	Np-M	Gun-Pr	2.62	511	F
IF-285	Bnzl	Hxy	Gun-Pr	2.62	455	F
IF-286	Bnzl	4-F-Bnzl	Gun-Pr	2.47	479	F
IF-287	Ph-Et	Bnzl	Gun-Pr	2.52	475	F
IF-288	Ph-Et	4-OH-Bnzl	Gun-Pr	2.38	491	F
IF-289	Ph-Et	i-Pnt	Gun-Pr	2.57	455	F
IF-290	Ph-Et	Np-M	Gun-Pr	2.72	525	F
IF-291	Ph-Et	Hxy	Gun-Pr	2.70	469	F
IF-292	Ph-Et	4-F-Bnzl	Gun-Pr	2.59	493	F
IF-293	4-F-Bnzl	i-Bu	Gun-Pr	2.34	445	F
IF-294	4-F-Bnzl	Bnzl	Gun-Pr	2.43	479	F
IF-295	4-F-Bnzl	i-Pnt	Gun-Pr	2.50	459	F
IF-296	4-F-Bnzl	Ph-Et	Gun-Pr	2.50	493	F
IF-297	4-F-Bnzl	Np-M	Gun-Pr	2.63	529	F
IF-298	4-F-Bnzl	Hxy	Gun-Pr	2.63	473	F
IF-299	i-Bu	Cbm-E	Cbx-E	1.03	381	H
IF-300	i-Bu	Cbm-E	i-Pnt	2.15	379	H
IF-301	i-Bu	Gun-Pr	i-Bu	2.13	393	H
IF-302	i-Bu	Gun-Pr	Bnzl	2.19	427	H
IF-303	i-Bu	Gun-Pr	4-OH-Bnzl	1.79	443	H
IF-304	i-Bu	Gun-Pr	i-Pnt	1.95	407	H
IF-305	i-Bu	Gun-Pr	Ph-Et	1.98	441	H
IF-306	i-Bu	Gun-Pr	Np-M	2.08	477	H
IF-307	Bnzl	Cbm-E	Cbx-E	1.76	415	H
IF-308	Bnzl	Cbm-E	i-Pnt	2.02	413	H
IF-309	Bnzl	Gun-Pr	i-Bu	1.82	427	H
IF-310	Bnzl	Gun-Pr	Bnzl	2.02	461	H
IF-311	Bnzl	Gun-Pr	4-OH-Bnzl	1.87	477	H
IF-312	Bnzl	Gun-Pr	i-Pnt	2.05	441	H
IF-313	Bnzl	Gun-Pr	Ph-Et	2.08	475	H
IF-314	Bnzl	Gun-Pr	Np-M	2.14	511	H
IF-315	4-OH-Bnzl	Cbm-E	Cbx-E	1.28	431	H
IF-316	4-OH-Bnzl	Cbm-E	i-Pnt	1.85	429	H
IF-317	4-OH-Bnzl	Gun-Pr	i-Bu	1.85	443	H
IF-318	4-OH-Bnzl	Gun-Pr	Bnzl	1.91	477	H
IF-319	4-OH-Bnzl	Gun-Pr	i-Pnt	1.89	457	H
IF-320	4-OH-Bnzl	Gun-Pr	Ph-Et	1.96	491	H
IF-321	4-OH-Bnzl	Gun-Pr	Np-M	2.00	527	H
IF-322	Cbx-E	Cbm-E	i-Pnt	1.73	395	H
IF-323	Gun-Pr	i-Bu	i-Bu	1.98	393	H

TABLE 4-14
IF-324	Gun-Pr	i-Bu	Bnzl	1.99	427	H
IF-325	Gun-Pr	i-Bu	4-OH-Bnzl	1.92	443	H
IF-326	Gun-Pr	i-Bu	i-Pnt	2.10	407	H
IF-327	Gun-Pr	i-Bu	Ph-Et	2.15	441	H
IF-328	Gun-Pr	i-Bu	Np-M	2.14	477	H
IF-329	Gun-Pr	Bnzl	i-Bu	2.06	427	H
IF-330	Gun-Pr	Bnzl	Bnzl	2.08	461	H
IF-331	Gun-Pr	Bnzl	4-OH-Bnzl	1.98	47	H
IF-332	Gun-Pr	Bnzl	i-Pnt	2.16	441	H
IF-333	Gun-Pr	Bnzl	Ph-Et	2.19	475	H
IF-334	Gun-Pr	Bnzl	Np-M	2.21	511	H
IF-335	Gun-Pr	4-OH-Bnzl	i-Bu	1.89	443	H
IF-336	Gun-Pr	4-OH-Bnzl	Bnzl	1.95	477	H
IF-337	Gun-Pr	4-OH-Bnzl	i-Pnt	1.92	457	H
IF-338	Gun-Pr	4-OH-Bnzl	Ph-Et	1.97	491	H
IF-339	Gun-Pr	4-OH-Bnzl	Np-M	2.01	527	H
IF-340	Gun-Pr	Cbm-E	i-Bu	1.64	408	H
IF-341	Gun-Pr	Cbm-E	Bnzl	1.72	442	H
IF-342	Gun-Pr	Cbm-E	4-OH-Bnzl	1.15	458	H
IF-343	Gun-Pr	Cbm-E	i-Pnt	1.73	422	H
IF-344	Gun-Pr	Cbm-E	Ph-Et	1.79	456	H
IF-345	Gun-Pr	Cbm-E	Np-M	1.84	492	H
IF-346	Gun-Pr	Hdr-E	i-Bu	1.70	381	H
IF-347	Gun-Pr	Hdr-E	Bnzl	1.73	415	H
IF-348	Gun-Pr	Hdr-E	4-OH-Bnzl	1.59	431	H
IF-349	Gun-Pr	Hdr-E	i-Pnt	1.78	395	H
IF-350	Gun-Pr	Hdr-E	Ph-Et	1.82	429	H
IF-351	Gun-Pr	Hdr-E	Np-M	1.84	465	H
IF-352	Gun-Pr	i-Pnt	i-Bu	2.07	407	H
IF-353	Gun-Pr	i-Pnt	Bnzl	2.10	441	H
IF-354	Gun-Pr	i-Pnt	4-OH-Bnzl	2.02	457	H
IF-355	Gun-Pr	i-Pnt	Ph-Et	2.12	455	H
IF-356	Gun-Pr	i-Pnt	Np-M	2.22	491	H
IF-357	Gun-Pr	Ph-Et	i-Bu	2.09	441	H
IF-358	Gun-Pr	Ph-Et	Bnzl	2.10	475	H
IF-359	Gun-Pr	Ph-Et	4-OH-Bnzl	2.02	491	H
IF-360	Gun-Pr	Ph-Et	i-Pnt	2.18	455	H
IF-361	Gun-Pr	Ph-Et	Np-M	2.19	525	H
IF-362	Hdr-E	Cbm-E	Cbx-E	0.41	369	H
IF-363	Hdr-E	Cbm-E	i-Pnt	1.71	367	H
IF-364	Hdr-E	Gun-Pr	i-Bu	1.64	381	H
IF-365	Hdr-E	Gun-Pr	Bnzl	1.76	415	H
IF-366	Hdr-E	Gun-Pr	4-OH-Bnzl	1.84	431	H
IF-367	Hdr-E	Gun-Pr	i-Pnt	1.75	395	H
IF-368	Hdr-E	Gun-Pr	Ph-Et	1.81	429	H
IF-369	Hdr-E	Gun-Pr	Np-M	1.83	465	H

TABLE 4-15
IF-370	i-Pnt	Cbm-E	Cbx-E	1.75	395	H
IF-371	i-Pnt	Gun-Pr	i-Bu	2.01	407	H
IF-372	i-Pnt	Gun-Pr	Bnzl	2.05	441	H
IF-373	i-Pnt	Gun-Pr	4-OH-Bnzl	1.91		H
IF-374	i-Pnt	Gun-Pr	Ph-Et	2.09	455	H
IF-375	i-Pnt	Gun-Pr	Np-M	2.15	491	H
IF-376	Ph-Et	Cbm-E	Cbx-E	1.85	429	H
IF-377	Ph-Et	Cbm-E	i-Pnt	2.09	427	H
IF-378	Ph-Et	Gun-Pr	i-Bu	2.05	441	H
IF-379	Ph-Et	Gun-Pr	Bnzl	2.18		H
IF-380	Ph-Et	Gun-Pr	4-OH-Bnzl	1.94	491	H
IF-381	Ph-Et	Gun-Pr	i-Pnt	2.11	455	H
IF-382	Ph-Et	Gun-Pr	Np-M	2.20	525	H
IF-383	Np-M	Cbm-E	Cbx-E	1.91	465	H
IF-384	Np-M	Cbm-E	i-Pnt	2.17	463	H
IF-385	Np-M	Gun-Pr	i-Bu	1.82	477	H
IF-386	Np-M	Gun-Pr	Bnzl	2.15	511	H
IF-387	Np-M	Gun-Pr	4-OH-Bnzl	1.97	527	H
IF-388	Np-M	Gun-Pr	i-Pnt	2.17	491	H
IF-389	Np-M	Gun-Pr	Ph-Et	2.20	525	H
IF-390	Np-M	Gun-Pr	Np-M	2.22	561	H
IF-391	Chm	Cbm-E	Cbx-E	1.83	421	H
IF-392	Chm	Cbm-E	i-Pnt	2.10	419	H
IF-393	Chm	Gun-Pr	i-Bu	2.06	433	H
IF-394	Chm	Gun-Pr	Bnzl	2.13	467	H
IF-395	Chm	Gun-Pr	4-OH-Bnzl	1.91	483	H
IF-396	Chm	Gun-Pr	i-Pnt	2.13	447	H
IF-397	Chm	Gun-Pr	Ph-Et	2.15	481	H
IF-398	Chm	Gun-Pr	Np-M	2.22	517	H
IF-399	4-F-Bnzl	Cbm-E	Cbx-E	1.78	433	H
IF-400	4-F-Bnzl	Cbm-E	i-Pnt	2.06	431	H
IF-401	4-F-Bnzl	Gun-Pr	i-Bu	2.03	445	H
IF-402	4-F-Bnzl	Gun-Pr	Bnzl	2.10	479	H
IF-403	4-F-Bnzl	Gun-Pr	4-OH-Bnzl	1.90	495	H
IF-404	4-F-Bnzl	Gun-Pr	i-Pnt	2.10	459	H
IF-405	4-F-Bnzl	Gun-Pr	Ph-Et	2.13	493	H
IF-406	4-F-Bnzl	Gun-Pr	Np-M	2.19	529	H
IF-407	Ph-Et	i-Bu	i-Pnt	1.54	412	I
IF-408	Np-M	i-Bu	i-Pnt	1.68	448	I
IF-409	Chm	i-Bu	i-Pnt	1.55	404	I
IF-410	4-F-Bnzl	i-Bu	i-Pnt	1.51	416	I
IF-411	Bnzl	i-Bu	i-Pnt	1.46	398	I
IF-412	i-Bu	i-Bu	i-Pnt	1.40	364	I
IF-413	i-Pnt	Cbx-E	Np-M	1.41	464	I
IF-414	i-Pnt	Cbx-E	i-Bu	1.15	380	I
IF-415	Chm	Cbx-E	i-Pnt	1.15	420	I

TABLE 4-16
IF-416	Chm	Cbx-E	Np-M	1.51	490	I
IF-417	4-F-Bnzl	Cbx-E	Np-M	1.46	502	I
IF-418	i-Pnt	4-F-Bnzl	Cbx-E	1.18	432	I
IF-419	Chm	Np-M	Cbx-E	1.40	490	I
IF-420	4-F-Bnzl	Np-M	Cbx-E	1.42	502	I
IF-421	Cbx-E	4-F-Bnzl	i-Bu	1.27	418	I
IF-422	Cbx-E	Np-M	i-Pnt	1.48	464	I
IF-423	Cbx-E	4-F-Bnzl	Np-M	1.47	502	I
IF-424	Cbx-E	i-Bu	Bnzl	1.20	400	I
IF-425	Cbx-E	4-OH-Bnzl	Np-M	1.28	500	I
IF-426	Bnzl	Hxy	Cbx-E	1.31	428	I
IF-427	i-Bu	Hxy	Cbx-E	1.24	394	I
IF-428	i-Bu	Cbx-E	Np-M	1.35	450	I
IF-429	i-Bu	Cbx-E	i-Bu	1.02	366	I
IF-430	Hdr-E	i-Bu	i-Pnt	1.23	352	I
IF-431	Ph-Et	i-Bu	Np-M	1.75	482	I
IF-432	Np-M	i-Bu	Ph-Et	1.75	482	I
IF-433	Np-M	i-Bu	Np-M	1.96	518	I
IF-434	Np-M	i-Bu	Bnzl	1.73	468	I
IF-435	Np-M	Cbm-E	4-OH-Bnzl	1.17	499	I
IF-436	4-F-Bnzl	i-Bu	Np-M	1.73	486	I
IF-437	i-Pnt	Ph-Et	i-Bu	1.55	412	I
IF-438	Ph-Et	Hxy	i-Bu	1.67	426	I
IF-439	Chm	Ph-Et	4-OH-Bnzl	1.43	488	I
IF-440	4-F-Bnzl	Ph-Et	Np-M	1.77	534	I
IF-441	Bnzl	i-Bu	Np-M	1.65	468	I
IF-442	4-OH-Bnzl	Hdr-E	Np-M	1.26	472	I
IF-443	4-OH-Bnzl	i-Bu	i-Pnt	1.25	414	I
IF-444	Hdr-E	Cbx-E	Np-M	1.15	438	I
IF-445	i-Pnt	4-OH-Bnzl	Cbx-E	0.97	430	I
IF-446	Chm	Cbx-E	i-Bu	1.25	406	I
IF-447	Chm	4-OH-Bnzl	Cbx-E	1.12	456	I
IF-448	Np-M	Hdr-E	Cbx-E	1.13	438	I
IF-449	Cbx-E	Np-M	i-Bu	1.43	450	I
IF-450	Cbx-E	Hxy	i-Bu	1.43	394	I
IF-451	Cbx-E	Hdr-E	Ph-Et	0.91	402	I
IF-452	Cbx-E	Hdr-E	Np-M	1.13	438	I
IF-453	Cbx-E	4-F-Bnzl	Ph-Et	1.41	466	I
IF-454	Cbx-E	i-Bu	Ph-Et	1.30	414	I
IF-455	Cbx-E	i-Bu	4-OH-Bnzl	1.11	416	I
IF-456	Cbx-E	Cbm-E	Ph-Et	0.95	429	I
IF-457	Cbx-E	Cbm-E	Np-M	1.16	465	I
IF-458	Cbx-E	4-OH-Bnzl	i-Pnt	1.13	430	I
IF-459	Bnzl	Cbx-E	Np-M	1.42	484	I
IF-460	i-Bu	Np-M	Cbx-E	1.32	450	I
IF-461	4-OH-Bnzl	Np-M	Cbx-E	1.26		I

TABLE 4-17
IF-462	Hdr-E	4-OH-Bnzl	Ph-Et	1.20		I
IF-463	Hdr-E	4-OH-Bnzl	Np-M	1.27	472	I
IF-464	i-Pnt	4-OH-Bnzl	Ph-Et	1.40	462	I
IF-465	i-Pnt	4-OH-Bnzl	Np-M	1.53	498	I
IF-466	i-Pnt	4-OH-Bnzl	Bnzl	1.37	448	I
IF-467	i-Pnt	4-OH-Bnzl	i-Bu	1.32	414	I
IF-468	Ph-Et	4-OH-Bnzl	i-Pnt	1.48	462	I
IF-469	Ph-Et	4-OH-Bnzl	Bnzl	1.46	482	I
IF-470	Ph-Et	4-OH-Bnzl	i-Bu	1.38	448	I
IF-471	Np-M	4-OH-Bnzl	i-Pnt	1.63	498	I
IF-472	Np-M	4-OH-Bnzl	Bnzl	1.58	518	I
IF-473	Np-M	4-OH-Bnzl	i-Bu	1.51	484	I
IF-474	Chm	4-OH-Bnzl	i-Pnt	1.46	454	I
IF-475	Chm	4-OH-Bnzl	Ph-Et	1.49	488	I
IF-476	Chm	4-OH-Bnzl	Np-M	1.62	524	I
IF-477	Chm	4-OH-Bnzl	Bnzl	1.43	474	I
IF-478	Chm	4-OH-Bnzl	i-Bu	1.41	440	I
IF-479	4-F-Bnzl	4-OH-Bnzl	i-Pnt	1.41	466	I
IF-480	4-F-Bnzl	4-OH-Bnzl	Np-M	1.58	536	I
IF-481	4-F-Bnzl	4-OH-Bnzl	Bnzl	1.38	486	I
IF-482	4-F-Bnzl	4-OH-Bnzl	i-Bu	1.32	452	I
IF-483	i-Pnt	Hdr-E	Bnzl	1.23	386	I
IF-484	Ph-Et	Hdr-E	Bnzl	1.30	420	I
IF-485	Np-M	Hdr-E	4-OH-Bnzl	1.17	472	I
IF-486	Chm	Hdr-E	Bnzl	1.33	412	I
IF-487	4-F-Bnzl	Hdr-E	Bnzl	1.24	424	I
IF-488	4-F-Bnzl	Hdr-E	4-OH-Bnzl	0.75	440	I
IF-489	i-Pnt	Hdr-E	Ph-Et	1.29	400	I
IF-490	4-F-Bnzl	Hdr-E	i-Pnt	1.30	404	I
IF-491	4-F-Bnzl	Hdr-E	Ph-Et	1.34	438	I
IF-492	Bnzl	Hdr-E	i-Bu	1.17	372	I
IF-493	Bnzl	4-OH-Bnzl	i-Pnt	1.40	448	I
IF-494	Bnzl	4-OH-Bnzl	Bnzl	1.37	468	I
IF-495	Bnzl	4-OH-Bnzl	i-Bu	1.29	434	I
IF-497	i-Bu	Hdr-E	i-Pnt	1.12	352	I
IF-498	i-Bu	Hdr-E	Ph-Et	1.18	386	I
IF-499	i-Bu	4-OH-Bnzl	i-Pnt	1.29	414	I
IF-500	i-Bu	4-OH-Bnzl	Np-M	1.46	484	I
IF-501	i-Bu	4-OH-Bnzl	i-Bu	1.22	400	I
IF-502	4-OH-Bnzl	Hdr-E	i-Pnt	0.99	402	I
IF-503	4-OH-Bnzl	i-Pr	i-Pnt	1.20	400	I
IF-504	4-OH-Bnzl	i-Pr	Np-M	1.39	470	I
IF-505	Np-M	Bnzl	4-OH-Bnzl	1.46	518	I
IF-506	4-F-Bnzl	Bnzl	Np-M	1.73	520	I
IF-507	Hdr-E	Hxy	i-Bu	1.43	366	I
IF-508	Hdr-E	4-F-Bnzl	Bnzl	1.31	424	I

TABLE 4-18
IF-509	i-Pnt	4-F-Bnzl	4-OH-Bnzl	1.40	466	I
IF-510	Ph-Et	Hxy	4-OH-Bnzl	1.59	476	I
IF-511	Np-M	Hxy	i-Bu	1.89	462	I
IF-512	Np-M	Hxy	4-OH-Bnzl	1.69	512	I
IF-513	Chm	Hxy	i-Bu	1.75	418	I
IF-514	Chm	Hxy	4-OH-Bnzl	1.49	468	I
IF-515	Hdr-E	4-F-Bnzl	i-Pnt	1.42	404	I
IF-516	Hdr-E	4-F-Bnzl	Ph-Et	1.41	438	I
IF-517	Ph-Et	Hxy	i-Pnt	1.83	440	I
IF-518	Np-M	Hdr-E	Ph-Et	1.46	470	I
IF-519	Np-M	Hxy	i-Pnt	1.98	476	I
IF-520	Chm	Hxy	i-Pnt	1.81	432	I
IF-521	Chm	4-F-Bnzl	Ph-Et	1.67	490	I
IF-522	4-F-Bnzl	Hxy	Ph-Et	1.85	478	I
IF-523	i-Bu	Hxy	4-OH-Bnzl	1.46	428	I
IF-524	i-Bu	4-F-Bnzl	4-OH-Bnzl	1.37	452	I
IF-525	i-Bu	4-F-Bnzl	Ph-Et	1.63	450	I
IF-526	Np-M	i-Bu	Cbx-E	1.39	450	I
IF-527	Ph-Et	i-Pnt	Cbx-E	1.35	428	I
IF-528	Cbx-E	i-Pnt	Bnzl	1.41	414	I
IF-529	Cbx-E	i-Pnt	Ph-Et	1.46	428	I
IF-530	Cbx-E	i-Bu	i-Pnt	1.30	380	I
IF-531	Hdr-E	Cbm-E	Np-M	1.10	437	I
IF-532	Hdr-E	Cbm-E	i-Bu	1.26	353	I
IF-533	Hdr-E	4-OH-Bnzl	i-Bu	1.47	388	I
IF-534	Ph-Et	4-OH-Bnzl	Np-M	1.55	532	I
IF-535	Np-M	Cbm-E	i-Bu	1.36	449	I
IF-536	Chm	Cbm-E	Np-M	1.51	489	I
IF-537	Chm	Cbm-E	4-OH-Bnzl	1.01	455	I
IF-538	4-F-Bnzl	Cbm-E	Ph-Et	1.31	465	I
IF-539	4-F-Bnzl	Cbm-E	Np-M	1.41	501	I
IF-540	Hdr-E	Ph-Et	Bnzl	1.32	420	I
IF-541	Hdr-E	Ph-Et	4-OH-Bnzl	1.25	436	I
IF-542	Hdr-E	Np-M	i-Bu	1.42	422	I
IF-543	Hdr-E	Np-M	4-OH-Bnzl	1.34		I
IF-544	Hdr-E	4-F-Bnzl	i-Bu	1.21	390	I
IF-545	i-Pnt	Ph-Et	4-OH-Bnzl	1.36	462	I
IF-546	i-Pnt	Hxy	i-Bu	1.61	392	I
IF-547	i-Pnt	4-F-Bnzl	Bnzl	1.58	450	I
IF-548	i-Pnt	4-F-Bnzl	i-Bu	1.48	416	I
IF-549	Ph-Et	4-F-Bnzl	Bnzl	1.62	484	I
IF-550	Ph-Et	4-F-Bnzl	i-Bu	1.56	450	I
IF-551	Chm	Np-M	i-Bu	1.75	474	I
IF-552	4-F-Bnzl	Np-M	4-OH-Bnzl	1.48	536	I
IF-553	Hdr-E	Ph-Et	i-Pnt	1.37	400	I
IF-554	i-Pnt	Hxy	Ph-Et	1.77	440	I

TABLE 4-19
IF-555	i-Pnt	Hxy	Np-M	1.84	476	I
IF-556	Ph-Et	4-F-Bnzl	i-Pnt	1.66	464	I
IF-557	Chm	4-F-Bnzl	i-Pnt	1.66	456	I
IF-558	4-F-Bnzl	Np-M	i-Pnt	1.73	500	I
IF-559	Bnzl	Hxy	Bnzl	1.70	446	I
IF-560	Bnzl	Hxy	i-Bu	1.63	412	I
IF-561	Bnzl	4-F-Bnzl	Bnzl	1.55	470	I
IF-562	Bnzl	Hxy	i-Pnt	1.67	426	I
IF-563	Bnzl	Hxy	Ph-Et	1.74	460	I
IF-564	Bnzl	Cbm-E	Ph-Et	1.31	447	I
IF-565	Bnzl	4-OH-Bnzl	Ph-Et	1.45	482	I
IF-566	Bnzl	4-OH-Bnzl	Np-M	1.53	518	I
IF-567	i-Bu	Ph-Et	4-OH-Bnzl	1.33	448	I
IF-568	i-Bu	Np-M	4-OH-Bnzl	1.42	484	I
IF-569	i-Bu	Hxy	i-Bu	1.53	378	I
IF-570	i-Bu	Np-M	i-Pnt	1.61	448	I
IF-571	i-Bu	Hxy	i-Pnt	1.61	392	I
IF-572	i-Bu	Hxy	Ph-Et	1.66	426	I
IF-573	i-Bu	Hxy	Np-M	1.83	462	I
IF-574	i-Bu	4-F-Bnzl	Np-M	1.67	486	I
IF-575	i-Bu	Cbm-E	Ph-Et	1.19	413	I
IF-576	i-Bu	4-OH-Bnzl	Ph-Et	1.31	448	I
IF-577	4-OH-Bnzl	Ph-Et	Bnzl	1.44	482	I
IF-578	4-OH-Bnzl	Np-M	i-Bu	1.47	484	I
IF-579	4-OH-Bnzl	Hdr-E	Ph-Et	1.59	436	I
IF-580	4-OH-Bnzl	Ph-Et	Np-M	1.61	532	I
IF-581	Np-M	4-OH-Bnzl	Ph-Et	1.64	532	I
IF-582	Np-M	4-OH-Bnzl	Np-M	1.80	568	I
IF-583	i-Pnt	Hxy	4-OH-Bnzl	1.50	442	I
IF-584	4-F-Bnzl	i-Pnt	Bnzl	1.65	450	I
IF-585	4-F-Bnzl	i-Pnt	i-Bu	1.57	416	I
IF-586	4-F-Bnzl	Ph-Et	Bnzl	1.69	484	I
IF-587	4-F-Bnzl	Hxy	Bnzl	1.79	464	I
IF-588	Chm	4-F-Bnzl	Np-M	1.79	526	I
IF-589	4-F-Bnzl	i-Pnt	Np-M	1.82	500	I
IF-590	4-OH-Bnzl	Ph-Et	i-Bu	1.40	448	I
IF-591	i-Pnt	Bnzl	Cbx-E	1.23	414	I
IF-592	Ph-Et	Bnzl	Cbx-E	1.31	448	I
IF-593	Np-M	i-Pnt	Cbx-E	1.51	464	I
IF-594	Cbx-E	i-Bu	Np-M	1.43	450	I
IF-595	Bnzl	Bnzl	Cbx-E	1.19	434	I
IF-596	Np-M	i-Pr	Np-M	1.81	504	I
IF-597	i-Pnt	Hdr-E	i-Bu	1.13	352	I
IF-598	i-Pnt	Hdr-E	4-OH-Bnzl	0.61	402	I
IF-599	i-Pnt	Hxy	Bnzl	1.67	426	I
IF-600	Ph-Et	Hdr-E	i-Bu	1.23	386	I

TABLE 4-20
IF-601	Ph-Et	Hdr-E	4-OH-Bnzl	1.01	436	I
IF-602	Ph-Et	Hxy	Bnzl	1.75	460	I
IF-603	Np-M	Hdr-E	Bnzl	1.49	456	I
IF-604	Np-M	Hdr-E	i-Bu	1.35	422	I
IF-605	Np-M	Hxy	Bnzl	1.92	496	I
IF-606	Chm	Hdr-E	i-Bu	1.23	378	I
IF-607	Chm	Hdr-E	4-OH-Bnzl	0.99	428	I
IF-608	Chm	4-F-Bnzl	Bnzl	1.61	476	I
IF-609	4-F-Bnzl	Hdr-E	i-Bu	1.17	390	I
IF-610	Hdr-E	Ph-Et	Np-M	1.48	470	I
IF-611	i-Pnt	Hdr-E	Np-M	1.45	436	I
IF-612	Ph-Et	Hdr-E	Np-M	1.44	470	I
IF-613	Np-M	Hdr-E	i-Pnt	1.43	436	I
IF-614	Np-M	Hdr-E	Np-M	1.59	506	I
IF-615	Np-M	Hxy	Ph-Et	1.96	510	I
IF-616	Np-M	Hxy	Np-M	2.10	546	I
IF-617	Chm	Hdr-E	i-Pnt	1.35	392	I
IF-618	Chm	Hdr-E	Ph-Et	1.39	426	I
IF-619	Chm	Hdr-E	Np-M	1.46	462	I
IF-620	4-F-Bnzl	Hdr-E	Np-M	1.43	474	I
IF-621	Bnzl	Hdr-E	Bnzl	1.22	406	I
IF-622	Bnzl	Hdr-E	4-OH-Bnzl	0.75	422	I
IF-623	Bnzl	Hdr-E	Ph-Et	1.31	420	I
IF-624	Bnzl	Hdr-E	Np-M	1.42	456	I
IF-625	i-Bu	Hdr-E	Np-M	1.33	422	I
IF-627	Hdr-E	Bnzl	i-Pnt	1.34	386	I
IF-628	Hdr-E	Bnzl	Bnzl	1.30	406	I
IF-629	Hdr-E	Bnzl	i-Bu	1.25	372	I
IF-630	Hdr-E	Bnzl	4-OH-Bnzl	1.22	422	I
IF-631	Hdr-E	i-Bu	i-Bu	1.15	338	I
IF-632	i-Pnt	Bnzl	Ph-Et	1.62	446	I
IF-634	i-Pnt	Bnzl	4-OH-Bnzl	1.31	448	I
IF-635	i-Pnt	i-Bu	Ph-Et	1.54	412	I
IF-636	i-Pnt	i-Bu	i-Bu	1.42	364	I
IF-637	i-Pnt	i-Bu	4-OH-Bnzl	1.30	414	I
IF-638	Ph-Et	Bnzl	i-Pnt	1.66	446	I
IF-639	Ph-Et	Bnzl	i-Bu	1.56	432	I
IF-640	Ph-Et	Bnzl	4-OH-Bnzl	1.40	482	I
IF-641	Ph-Et	i-Bu	Bnzl	1.58	432	I
IF-642	Np-M	Bnzl	i-Bu	1.73	468	I
IF-643	Chm	Bnzl	Ph-Et	1.66	472	I
IF-644	Chm	Bnzl	i-Bu	1.59	424	I
IF-645	Chm	Bnzl	4-OH-Bnzl	1.34	474	I
IF-646	Chm	i-Bu	Np-M	1.76	474	I
IF-647	Chm	i-Bu	4-OH-Bnzl	1.35	440	I
IF-648	4-F-Bnzl	Bnzl	Ph-Et	1.68	484	I

TABLE 4-21
IF-649	4-F-Bnzl	Bnzl	Bnzl	1.60	470	I
IF-650	4-F-Bnzl	Bnzl	i-Bu	1.57	436	I
IF-651	4-F-Bnzl	Bnzl	4-OH-Bnzl	1.32	486	I
IF-652	4-F-Bnzl	i-Bu	Ph-Et	1.59	450	I
IF-653	4-F-Bnzl	i-Bu	Bnzl	1.52	436	I
IF-654	4-F-Bnzl	i-Bu	i-Bu	1.48	402	I
IF-655	4-F-Bnzl	i-Bu	4-OH-Bnzl	1.29	452	I
IF-656	Hdr-E	i-Pnt	Bnzl	1.36	386	I
IF-657	Ph-Et	i-Pnt	i-Bu	1.62	412	I
IF-658	Chm	i-Pnt	Bnzl	1.65	438	I
IF-659	Chm	i-Pnt	i-Bu	2.29	404	I
IF-660	Hdr-E	i-Pnt	Np-M	1.53	436	I
IF-661	Np-M	i-Pnt	Ph-Et	1.91	496	I
IF-662	Chm	i-Pnt	Ph-Et	1.72	452	I
IF-663	Chm	i-Pnt	Np-M	1.83	488	I
IF-664	4-F-Bnzl	i-Pnt	Ph-Et	1.68	464	I
IF-665	Bnzl	i-Pnt	Bnzl	1.61	432	I
IF-666	Bnzl	i-Pnt	4-OH-Bnzl	1.36	448	I
IF-667	Bnzl	i-Pnt	Ph-Et	1.65	446	I
IF-670	Bnzl	i-Bu	Ph-Et	1.54	432	I
IF-671	i-Bu	i-Pnt	i-Bu	1.44	364	I
IF-672	i-Bu	i-Pnt	4-OH-Bnzl	1.30	414	I
IF-673	i-Bu	i-Pnt	Ph-Et	1.56	412	I
IF-674	i-Bu	i-Pnt	Np-M	1.71	448	I
IF-675	i-Bu	Bnzl	i-Pnt	1.53	398	I
IF-678	i-Bu	Bnzl	4-OH-Bnzl	1.23	434	I
IF-679	i-Bu	i-Bu	Ph-Et	1.48	398	I
IF-680	i-Bu	i-Bu	Np-M	1.59	434	I
IF-683	i-Bu	i-Bu	4-OH-Bnzl	1.23	400	I
IF-684	4-OH-Bnzl	i-Pnt	Np-M	1.62	498	I
IF-686	i-Pnt	Cbm-E	Ph-Et	1.28	427	I
IF-687	Np-M	i-Pnt	4-OH-Bnzl	1.56	498	I
IF-688	Chm	4-F-Bnzl	i-Bu	1.56	442	I
IF-689	4-F-Bnzl	Hxy	4-OH-Bnzl	1.47	480	I
IF-690	Ph-Et	Hdr-E	i-Pnt	1.30	400	I
IF-691	Bnzl	i-Pnt	i-Bu	1.54	398	I
IF-692	Bnzl	Hxy	4-OH-Bnzl	1.45	462	I
IF-693	Cbx-E	Bnzl	Bnzl	1.30	434	I
IF-694	Cbx-E	Bnzl	i-Bu	1.24	400	I
IF-695	Bnzl	i-Pnt	Cbx-E	1.26	414	I
IF-696	i-Pnt	Cbm-E	Np-M	1.46	463	I
IF-697	i-Pnt	Cbm-E	Bnzl	1.28	413	I
IF-698	Ph-Et	Cbm-E	Bnzl	1.36	447	I
IF-699	Ph-Et	Cbm-E	i-Bu	1.24	413	I
IF-700	Chm	Cbm-E	Ph-Et	1.43	453	I
IF-701	Chm	Cbm-E	Bnzl	1.36	439	I

TABLE 4-22
IF-702	4-F-Bnzl	Cbm-E	Bnzl	1.27	451	I
IF-703	4-F-Bnzl	Cbm-E	i-Bu	1.23	417	I
IF-704	Hdr-E	Ph-Et	i-Bu	1.31	386	I
IF-705	i-Pnt	Np-M	i-Bu	1.69	448	I
IF-706	i-Pnt	Np-M	4-OH-Bnzl	1.50	498	I
IF-707	Ph-Et	i-Pnt	4-OH-Bnzl	1.47	462	I
IF-708	Np-M	Ph-Et	4-OH-Bnzl	1.57	532	I
IF-709	Chm	i-Pnt	4-OH-Bnzl	1.40	454	I
IF-710	Chm	Ph-Et	Bnzl	1.72	472	I
IF-711	Chm	Ph-Et	i-Bu	1.69	438	I
IF-712	Chm	Np-M	4-OH-Bnzl	1.58	524	I
IF-713	4-F-Bnzl	i-Pnt	4-OH-Bnzl	1.38	466	I
IF-714	4-F-Bnzl	Ph-Et	i-Bu	1.62	450	I
IF-715	4-F-Bnzl	Ph-Et	4-OH-Bnzl	1.42	500	I
IF-716	4-F-Bnzl	Np-M	i-Bu	1.71	486	I
IF-717	Chm	Ph-Et	i-Pnt	1.76	452	I
IF-718	Chm	Ph-Et	Np-M	1.94	522	I
IF-719	Chm	Np-M	i-Pnt	1.81	488	I
IF-720	4-F-Bnzl	Ph-Et	i-Pnt	1.68	464	I
IF-721	Bnzl	Ph-Et	i-Bu	1.58	432	I
IF-722	Bnzl	Ph-Et	4-OH-Bnzl	1.41	482	I
IF-723	Bnzl	Ph-Et	i-Pnt	1.68	446	I
IF-724	Bnzl	Cbm-E	Bnzl	1.24	433	I
IF-725	i-Bu	Ph-Et	i-Bu	1.51	398	I
IF-726	i-Bu	Np-M	i-Bu	1.62	434	I
IF-727	i-Bu	Ph-Et	i-Pnt	1.62	412	I
IF-728	i-Bu	Cbm-E	Np-M	1.37	449	I
IF-730	4-OH-Bnzl	Np-M	i-Pnt	1.62		I
IF-731	4-OH-Bnzl	Cbm-E	Np-M	1.29	499	I
IF-732	i-Pnt	Bnzl	Np-M	1.72	482	I
IF-733	i-Pnt	Bnzl	i-Bu	1.49	398	I
IF-734	i-Pnt	i-Bu	Np-M	1.66	448	I
IF-735	i-Pnt	i-Bu	Bnzl	1.50	398	I
IF-736	Ph-Et	Bnzl	Np-M	1.76	516	I
IF-737	Ph-Et	Bnzl	Bnzl	1.61	466	I
IF-738	Ph-Et	i-Bu	i-Bu	1.49	398	I
IF-739	Np-M	i-Bu	i-Bu	1.66	434	I
IF-740	Chm	Bnzl	i-Pnt	1.69	438	I
IF-742	Chm	i-Bu	i-Bu	1.49	390	I
IF-743	4-F-Bnzl	Bnzl	i-Pnt	1.64	450	I
IF-744	Ph-Et	i-Pnt	Bnzl	1.65	446	I
IF-746	Bnzl	Bnzl	Ph-Et	1.58	466	I
IF-747	Bnzl	Bnzl	Np-M	1.72	502	I
IF-751	Bnzl	i-Bu	4-OH-Bnzl	1.26	434	I
IF-752	i-Bu	i-Pnt	Bnzl	1.50	398	I
IF-753	i-Bu	Bnzl	Np-M	1.64	468	I

TABLE 4-23
IF-755	4-OH-Bnzl	Bnzl	i-Pnt	1.42	448	I
IF-756	Ph-Et	Cbm-E	Np-M	1.48	497	I
IF-757	Ph-Et	i-Pr	Np-M	1.65	468	I
IF-758	Hdr-E	Np-M	Bnzl	1.46	456	I
IF-759	i-Pnt	Np-M	Bnzl	1.72	482	I
IF-760	Ph-Et	Np-M	i-Bu	1.71	482	I
IF-761	Ph-Et	Np-M	4-OH-Bnzl	1.57	532	I
IF-762	Np-M	i-Pnt	Bnzl	1.86	482	I
IF-763	Np-M	Np-M	i-Bu	1.95	518	I
IF-764	Chm	Np-M	Bnzl	1.77	508	I
IF-765	4-F-Bnzl	Np-M	Bnzl	1.76	520	I
IF-766	Ph-Et	Np-M	i-Pnt	1.74	497	I
IF-767	Np-M	Np-M	i-Pnt	1.96	532	I
IF-768	Np-M	4-F-Bnzl	Np-M	2.03	570	I
IF-769	Chm	Np-M	Ph-Et	1.85	522	I
IF-770	Chm	Np-M	Np-M	1.95	558	I
IF-771	4-F-Bnzl	Np-M	Ph-Et	1.80	534	I
IF-772	4-F-Bnzl	Np-M	Np-M	1.95	570	I
IF-773	Bnzl	Np-M	i-Bu	1.67	468	I
IF-774	Bnzl	Np-M	i-Pnt	1.73	482	I
IF-775	Bnzl	4-F-Bnzl	Np-M	1.75	520	I
IF-776	Bnzl	Cbm-E	Np-M	1.42	483	I
IF-777	i-Bu	Np-M	Ph-Et	1.71	482	I
IF-778	i-Bu	Np-M	Np-M	1.81	518	I
IF-779	4-OH-Bnzl	Np-M	Np-M	1.71	568	I
IF-780	Hdr-E	i-Bu	Ph-Et	1.34	386	I
IF-781	Hdr-E	i-Bu	4-OH-Bnzl	1.12	388	I
IF-782	Ph-Et	i-Bu	4-OH-Bnzl	1.44		I
IF-783	Ph-Et	Cbm-E	4-OH-Bnzl	1.03	463	I
IF-784	Np-M	Bnzl	i-Pnt	1.84	482	I
IF-785	Np-M	Bnzl	Ph-Et	1.88	516	I
IF-786	Np-M	Bnzl	Np-M	2.03	552	I
IF-787	Np-M	i-Bu	4-OH-Bnzl	1.40	484	I
IF-788	Np-M	Cbm-E	Np-M	1.65	533	I
IF-789	Np-M	i-Pr	Ph-Et	1.69	468	I
IF-790	Np-M	i-Pr	Bnzl	1.67	454	I
IF-791	Chm	Bnzl	Np-M	1.80	508	I
IF-792	Hdr-E	i-Pnt	i-Bu	1.30	352	I
IF-793	Ph-Et	Np-M	Bnzl	1.80	516	I
IF-794	Np-M	Np-M	Bnzl	2.05	552	I
IF-795	Np-M	4-F-Bnzl	Bnzl	1.89	520	I
IF-796	Hdr-E	i-Pnt	Ph-Et	1.44	400	I
IF-797	Hdr-E	Np-M	i-Pnt	1.50	436	I
IF-798	Hdr-E	Np-M	Ph-Et	1.50	470	I
IF-799	i-Pnt	Np-M	Ph-Et	1.78	496	I
IF-800	i-Pnt	4-F-Bnzl	Ph-Et	1.63	464	I

TABLE 4-24
IF-801	i-Pnt	4-F-Bnzl	Np-M	1.71	500	I
IF-802	Ph-Et	i-Pnt	Np-M	1.77	496	I
IF-803	Ph-Et	Np-M	Np-M	1.93	566	I
IF-804	Ph-Et	4-F-Bnzl	Np-M	1.84	534	I
IF-805	Bnzl	Np-M	Bnzl	1.72	502	I
IF-806	Bnzl	Np-M	4-OH-Bnzl	1.45	518	I
IF-807	Bnzl	4-F-Bnzl	i-Bu	1.55	436	I
IF-808	Bnzl	4-F-Bnzl	4-OH-Bnzl	1.39	486	I
IF-809	Bnzl	i-Pnt	Np-M	1.79	482	I
IF-810	Bnzl	Np-M	Ph-Et	1.81	516	I
IF-811	Bnzl	4-F-Bnzl	i-Pnt	1.60	450	I
IF-812	Bnzl	i-Pr	Np-M	1.54	454	I
IF-814	i-Bu	Hxy	Bnzl	1.62	412	I
IF-815	i-Bu	4-F-Bnzl	Bnzl	1.52	436	I
IF-816	4-OH-Bnzl	i-Pnt	Ph-Et	1.51	462	I
IF-817	4-OH-Bnzl	Bnzl	Ph-Et	1.43	482	I
IF-818	4-OH-Bnzl	Bnzl	i-Bu	1.32	434	I
IF-819	4-OH-Bnzl	i-Bu	i-Bu	1.25	400	I
IF-820	i-Pnt	Cbx-E	Bnzl	0.70	414	C
IF-821	Ph-Et	Cbx-E	i-Pnt	0.73	428	C
IF-822	Chm	Cbx-E	Bnzl	0.72	440	C
IF-823	4-OH-Bnzl	Cbx-E	i-Pnt	0.61	430	C
IF-824	4-OH-Bnzl	Cbx-E	Ph-Et	0.65	464	C
IF-825	Bnzl	Cbx-E	i-Bu	0.67	400	C
IF-826	Bnzl	Cbx-E	i-Pnt	0.70	414	C
IF-827	Bnzl	Cbx-E	Ph-Et	0.71	448	C
IF-828	i-Bu	Cbx-E	Ph-Et	0.67	414	C
IF-829	i-Bu	Cbx-E	4-OH-Bnzl	0.70	416	C
IF-830	i-Pnt	Cbx-E	Ph-Et	0.72	428	C
IF-831	i-Pnt	Cbx-E	4-OH-Bnzl	0.59	430	C
IF-832	Chm	Cbx-E	Ph-Et	0.74	454	C
IF-833	Chm	Cbx-E	4-OH-Bnzl	0.62	456	C
IF-835	Ph-Et	Cbx-E	i-Bu	0.69	414	C
IF-836	4-OH-Bnzl	Cbx-E	i-Bu	0.58	416	C
1) (M-H)-

TABLE 4-25
Compound					Retention	Mass	Measurement
number	R1	R2	R3	R4	RT (min)	(M + H)+	condition
IF-837	Bnzl	Np-M	i-Bu	H	1.127	468	B
IF-838	Bnzl	4-(trifluoromethyl)benzyl	i-Bu	H	1.14	486	B

TABLE 4-26
IF-839	4-Cl-Bnzl	Bnzl	i-Bu	H	1.13	452	B
IF-840	3-Cl-Bnzl	Bnzl	i-Bu	H	1.14	452	B
IF-841	4-methoxybenzyl	Bnzl	i-Bu	H	1.072	448	B
IF-842	4-methylbenzyl	Bnzl	i-Bu	H	1.097	432	B
IF-843	i-Pnt	i-Bu	Bnzl	H	1.278	398	B
IF-844	i-Bu	i-Bu	4-Cl-Bnzl	H	1.275	418	B
IF-845	i-Bu	i-Pnt	Bnzl	H	1.082	398	B
IF-846	i-Bu	4-Cl-Bnzl	i-Bu	H	1.085	418	B
IF-847	4-hydroxybenzyl	Bnzl	i-Bu	H	1.187	434	B
IF-848	4-(dimethylamino)benzyl	Bnzl	i-Bu	H	1.097	461	B
IF-849	4-(tert-butyl)benzyl	Bnzl	i-Bu	H	1.175	474	B
IF-850	i-Bu	Bnzl	i-Pnt	H	1.075	398	B
IF-851	i-Pnt	Bnzl	i-Bu	H	1.29	398	B
IF-852	4-(trifluoromethyl)benzyl	Bnzl	i-Bu	H	1.18	502	B
IF-853	4-ethoxybenzyl	Bnzl	i-Bu	H	1.112	462	B
IF-854	Bnzl	naphthalen-2-ylmethyl	i-Bu	H	1.142	468	B
IF-855	4-methylbenzyl	Bnzl	i-Bu	ethyl	1.172	460	B
IF-856	4-methylbenzyl	Bnzl	i-Bu	i-Bu	1.303	488	B
IF-857	4-methylbenzyl	Bnzl	i-Bu	acetyl	1.187	474	B
IF-858	4-methylbenzyl	Bnzl	i-Bu	3-methylbutanoyl	1.247	516	B
IF-859	4-methylbenzyl	Bnzl	i-Bu	2-phenylacetyl	1.253	550	B
IF-860	4-methylbenzyl	Bnzl	i-Bu	methoxycarbonyl	1.23	490	B
IF-861	4-methylbenzyl	Bnzl	i-Bu	2-methylpropoxycarbonyl	1.292	532	B
IF-862	4-methylbenzyl	Bnzl	i-Bu	benzyloxycarbonyl	1.297	566	B
IF-863	4-methylbenzyl	Bnzl	i-Bu	aminocarbonyl	1.157	475	B

TABLE 4-27
IF-864	4-methylbenzyl	Bnzl	i-Bu	N-benzylaminocarbonyl	1.252	565	B
IF-865	Bnzl	pyridin-4-ylmethyl	i-Bu	H	1.11	419	B
IF-866	4-(dimethylamino)benzyl	3-hydroxybenzyl	i-Bu	H	1.223	477	B
IF-867	4-(dimethylamino)benzyl	4-hydroxybenzyl	i-Bu	H	1.208	477	B
IF-868	2-hydroxyethyl	4-fluorobenzyl	Np-M	H	0.76	474	C
IF-869	4-methoxybenzyl	Bnzl	Bnzl	H	0.83	482	C
IF-870	4-methoxybenzyl	Bnzl	Bnzl	tert-butoxycarbonyl	1.01	582	C
IF-871	ethyl	Bnzl	Bnzl	tert-butoxycarbonyl	0.94	490	C
IF-872	phenethyl	Bnzl	2-(tert-butyldimethylsilyloxy)	H	0.95	534	C
			ethyl
IF-873	cyclopentylmethyl	4-(tert-butoxy)benzyl	2-(tert-butoxycarbonyl)ethyl	H	0.93	554	C
IF-874	4-nitrobenzyl	4-(tert-butoxy)	2-(tert-butoxycarbonyl)ethyl	H	0.97	607	C
		benzyl
IF-875	phenethyl	Bnzl	2-hydroxyethyl	H	0.72	420	C
IF-876	cyclopentylmethyl	4-(tert-butoxy)benzyl	2-(tert-butoxycarbonyl)ethyl	methoxycarbonyl	1.03	612	C
IF-877	cyclopentylmethyl	4-hydroxybenzyl	2-carboxyethyl	methoxycarbonyl	0.71	500	C
IF-878	cyclopentylmethyl	4-hydroxybenzyl	2-carboxyethyl	H	0.64	442	C
IF-879	phenethyl	Bnzl	2-hydroxyethyl	methoxycarbonyl	0.8	478	C
IF-880	4-aminobenzyl	4-(tert-butoxy)benzyl	2-(tert-butoxycarbonyl)ethyl	formyl	0.89	605	C
IF-881	4-(cyclopentylcarbonylamino)	4-(tert-butoxy)benzyl	2-(tert-butoxycarbonyl)ethyl	formyl	1	701	C
	benzyl
IF-882	4-(cyclopentylmethylamino)	4-(tert-butoxy)benzyl	2-(tert-butoxycarbonyl)ethyl	formyl	1.07	687	C
	benzyl

TABLE 4-28
IF-	4-(cyclopentylmethylamino)	4-	2-	H	0.81	561	C
883	benzyl	hydroxybenzyl	methoxycarbonylethyl
IF-	4-(cyclopentylmethylamino)	4-	2-	H	0.75	547	C
884	benzyl	hydroxybenzyl	carboxylethyl

TABLE 4-29
Formula XXIF
Compound						Retention	Mass	Measurement
number	R1	R2A	R2B	R3	R4	RT (min)	(M + H)+	condition
IF-885	i-Bu	H	4-Cl-Bnzl	Ph-Et	H	1.99	466	B1
IF-886	i-Bu	H	3-Cl-Bnzl	Ph-Et	H	1.98	466	B1
IF-887	i-Bu	H	4-MeO-Bnzl	Ph-Et	H	1.75	462	B1
IF-888	i-Bu	H	4-Me-Bnzl	Ph-Et	H	1.92	446	B1
IF-889	i-Bu	H	2-Npm	Ph-Et	H	2.07	482	B1
IF-890	i-Bu	H	Bnzl	Ph-Pr	H	1.89	446	B
IF-891	i-Bu	H	3-Cl-Bnzl	Ph-Pr	H	1.16	480	B
IF-892	i-Bu	H	3-F-Bnzl	Ph-Pr	H	1.14	464	B
IF-893	i-Bu	H	3-Me-Bnzl	Ph-Pr	H	1.13	460	B
IF-894	i-Bu	H	3-MeO-Bnzl	Ph-Pr	H	1.10	476	B
IF-895	i-Bu	H	3-Cl-Bnzl	Ph-Bu	H	1.16	494	B
IF-896	i-Bu	H	3-F-Bnzl	Ph-Bu	H	1.12	478	B
IF-897	i-Bu	H	3-Me-Bnzl	Ph-Bu	H	1.16	474	B
IF-898	i-Bu	H	3-MeO-Bnzl	Ph-Bu	H	1.12	491	B
IF-899	i-Bu	H	Bnzl	Ph-Bu	H	1.13	460	B
IF-900	i-Pnt	H	3-F-Bnzl	Ph-Pr	H	1.14	478	B
IF-901	1-Npm	H	pentyl	Ph-Et	H	0.92	496	C
IF-902	1-Npm	H	cyclohexyl	Ph-Et	H	0.92	508	C
IF-903	1-Npm	H	cyclopentyl	Ph-Et	H	0.90	494	C
IF-904	1-Npm	H	Hxy	4-methylphenethyl	H	0.99	524	C
IF-905	1-Npm	H	Hxy	2-(naphthalen-2-yl)ethyl	H	1.02	560	C
IF-906	1-Npm	H	heptyl	Ph-Et	H	1.00	524	C
IF-907	1-Npm	H	Hxy	4-isopropylphenethyl	H	1.05	552	C
IF-908	1-Npm	H	Hxy	cyclohexylethyl	H	1.03	516	C

TABLE 4-30
IF-909	i-Bu	H	Ph-Et	Ph-Et	H	1.87	444	B1
IF-910	Chm	H	tBuO-E	1-Npm	H	0.87	518	C
IF-911	tBuO-E	H	Ph-Et	1-Npm	H	0.88	526	C
IF-912	Ph-Et	H	Hxy	1-Npm	H	0.95	510	C
IF-913	tBuO-E	H	4-fluorophenethyl	1-Npm	H	0.89	544.4	C
IF-914	Hdr-E	H	4-fluorophenethyl	1-Npm	H	0.77	488.3	C
IF-915	3-tert-butoxypropyl	H	4-F-Bnzl	1-Npm	H	0.89	544.4	C
IF-916	tBuO-E	H	4-Cl-Bnzl	1-Npm	H	0.9	546.3	C
IF-917	3-hydroxypropyl	H	4-F-Bnzl	1-Npm	H	0.76	488.3	C
IF-918	Hdr-E	H	4-Cl-Bnzl	1-Npm	H	0.78	490.3	C
IF-919	1-Npm	H	Hxy	3-methylphenethyl	H	0.99	524.4	C
IF-920	1-Npm	H	β-hydroxyphenethyl	Ph-Et	H	0.84	546.4	C
IF-921	1-Npm	H	α-hydroxymethylphenethyl	Ph-Et	H	0.88	560.4	C
IF-922	1-Npm	H	α-hydroxymethylphenethyl	Ph-Et	H	0.85	560.4	C
IF-923	4-Nt-Bnzl	H	Bnzl	tBOC-E	H	0.86	535	C
IF-924	4-Nt-Bnzl	H	Bnzl	tBOC-E	ethoxycarbonyl	0.94	607	C
IF-925	1-Npm	H	4-F-Bnzl	2-OH-Et	H	0.73	474.3	C
IF-926	4-tBuO-Bnzl	H	Bnzl	i-Bu	H	0.91	490.4	C
IF-927	4-tBuO-Bnzl	H	i-Bu	Bnzl	H	0.88	490.4	C
IF-928	2-OtBu-Et	H	Bnzl	1-Npm	H	0.85	512.4	C
IF-929	2-OH-Et	H	Bnzl	1-Npm	H	0.74	456.3	C
IF-930	4-OH-Bnzl	H	i-Bu	Bnzl	H	0.73	434.3	C
IF-931	1-Npm	H	4-F-Bnzl	2-OTBS-Et	H	1.01	588.4	C

Example 2: Assay Method for Anti-Rabies Virus Activity

Each tested compound prepared as a 10 mM with DMSO was first diluted to 100 μM or 40 μM with 10% fetal bovine serum-supplemented Eagle's minimal essential medium (hereinafter, medium), and further diluted with the medium to the final concentration of interest. Fifty microlitter of the diluted medium was added dropwise to each well of a 96-well plate. Furthermore, 50 μL of medium comprising 4×10² infectious units of the recombinant rabies virus 1088 strain expressing Gaussia Luciferase (GLuc) (1088/GLuc) and 4×10⁴ Neuro-2a cells were added to each well. The plate was shaken for 30 seconds with a multiple microplate mixer NS-4P (AS ONE Corporation) and then cultured for 3 days at 37° C. in the presence of 5% CO₂. After incubation, 25 μL of coelenterazine, which is a substrate of the luciferase, was added dropwise to each well of the plate, and the plate was immediately loaded into a luminescent plate reader LuMate (Awareness Technology) and shaken for 10 seconds. The relative light unit (RLU) was then measured.

The synthesized compounds were tested. It was found that the compounds described in Table 5 exhibited the higher anti-rabies virus activity compared to T-705 (generic name: Favipiravir) (IC₅₀=30 μM), which is examined as an anti-rabies antiviral drug.

The compounds are classified as A if IC_H is 5 μM or less, B if greater than 5 μM and less than or equal to 10 μM, and C if greater than 10 μM and less than 30 μM. The ‘na’ indicates not applicable.

TABLE 5-1
Compound		IC50
number	Name of compound	(μM)
IB-3	(3S*,3aS*,6R*,7R*,7aS*)-7-benzyl-N,1-	19.6
	diisobutyloctahydro-3aH-3,6-methanopyrrolo[3,2-
	b]pyridine-3a-carboxamide
IB-4	(3S*,3aS*,6R*,7R*,7aS*)-1-benzyl-N,7-	19.2
	diisobutyloctahydro-3aH-3,6-methanopyrrolo[3,2-
	b]pyridine-3a-carboxamide
IB-5	(3S*,3aS*,6R*,7R*,7aS*)-N-benzyl-1,7-	18.2
	diisobutyloctahydro-3aH-3,6-methanopyrrolo[3,2-
	b]pyridine-3a-carboxamide
IB-9	(3S*,3aS*,6R*,7R*,7aS*)-N,7-dibenzyl-1-	17.0
	isopentyloctahydro-3aH-3,6-methanopyrrolo[3,2-
	b]pyridine-3a-carboxamide
IB-12	(3S*,3aS*,6R*,7R*,7aS*)-1-benzyl-7-isobutyl-N-	15.5
	phenethyloctahydro-3aH-3,6-methanopyrrolo[3,2-
	b]pyridine-3a-carboxamide
IB-13	(3S*,3aS*,6R*,7R*,7aS*)-N-benzyl-1-isobutyl-7-(3-	14.3
	methylbenzyl)octahydro-3aH-3,6-methanopyrrolo[3,2-
	b]pyridine-3a-carboxamide
IB-15	(3S*,3aS*,6R*,7R*,7aS*)-7-benzyl-1-isobutyl-N-(3-	15.9
	methylbenzyl)octahydro-3aH-3,6-methanopyrrolo[3,2-
	b]pyridine-3a-carboxamide

TABLE 5-2
IF-1	(3S*,3aS*,6S*,7R*,7aS*)-N,7-dibenzyl-1-	12.6
	isobutyloctahydro-6H-3,6-methanopyrrolo[3,2-
	c]pyridine-6-carboxamide
IF-6	(3S*,3aS*,6S*,7R*,7aS*)-1,7-dibenzyl-N-	16.3
	isobutyloctahydro-6H-3,6-methanopyrrolo[3,2-
	c]pyridine-6-carboxamide
IF-7	(3S*,3aS*,6S*,7R*,7aS*)-N,1-dibenzyl-7-	8.5
	isobutyloctahydro-6H-3,6-methanopyrrolo[3,2-
	c]pyridine-6-carboxamide
IF-9	(3S*,3aS*,6S*,7R*,7aS*)-N,7-dibenzyl-1-	15.6
	isopentyloctahydro-6H-3,6-methanopyrrolo[3,2-
	c]pyridine-6-carboxamide
IF-11	(3S*,3aS*,6S*,7R*,7aS*)-N-benzyl-1-isobutyl-7-	17.5
	phenethyloctahydro-6H-3,6-methanopyrrolo[3,2-
	c]pyridine-6-carboxamide
IF-13	(3S*,3aS*,6S*,7R*,7aS*)-N-benzyl-1-isobutyl-7-(3-	13.1
	methylbenzyl)octahydro-6H-3,6-methanopyrrolo[3,2-
	c]pyridine-6-carboxamide
IF-14	(3S*,3aS*,6S*,7R*,7aS*)-N-benzyl-1-isobutyl-7-(4-	14.1
	methylbenzyl)octahydro-6H-3,6-methanopyrrolo[3,2-
	c]pyridine-6-carboxamide
IF-15	(3S*,3aS*,6S*,7R*,7aS*)-7-benzyl-1-isobutyl-N-(3-	17.1
	methylbenzyl)octahydro-6H-3,6-methanopyrrolo[3,2-
	c]pyridine-6-carboxamide
IF-20	(3S*,3aS*,6S*,7R*,7aS*)-1-benzyl-N-(3,4-	11.6
	dichlorobenzyl)-7-isobutyloctahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-6-carboxamide
IF-69	(3S*,3aS*,6S*,7R*,7aS*)-N,7-dibenzyl-4-ethyl-1-	16.5
	isobutyloctahydro-6H-3,6-methanopyrrolo[3,2-
	c]pyridine-6-carboxamide
IIB-4	(3S*,3aS*,6R*,7R*,7aS*)-1-benzyl-N,7-dilsobutyl-	8.9
	1,2,3,6,7,7a-hexahydro-3aH-3,6-methanopyrrolo[3,2-
	b]pyridine-3a-carboxamide
IIF-16	(3S*,3aR*,6S*,7R*,7aR*)-7-benzyl-1-isobutyl-N-(4-	28.7
	methylbenzyl)-1,2,3,3a,7,7a-hexahydro-6H-3,6-
	methanopyrrolo[3,2-c]pyridine-6-carboxamide

TABLE 5-3
Table. Anti-rabies activity of compound of formula IB
Compound					Anti-rabies
number	R1	R2	R3	R4	activity
IB-3	i-Bu	i-Bu	Bnzl	H	C
IB-4	Bnzl	i-Bu	i-Bu	H	C
IB-5	i-Bu	Bnzl	i-Bu	H	C
IB-9	i-Pnt	Bnzl	Bnzl	H	C
IB-12	i-Bu	phenethyl	Bnzl	H	C
IB-13	i-Bu	Bnzl	3-methylbenzyl	H	C
IB-15	i-Bu	3-methylbenzyl	Bnzl	H	C
IB-42	Np-M	Bnzl	Bnzl	H	C
IB-81	carbamoylmethyl	1-naphthylmethyl	i-Bu	H	C
IB-82	carbamoylmethyl	1-naphthylmethyl	Bnzl	H	C
IB-83	carbamoylmethyl	1-naphthylmethyl	4-hydroxybenzyl	H	C
IB-84	carbamoylmethyl	1-naphthylmethyl	i-Pnt	H	C
IB-86	carbamoylmethyl	2-phenylethyl	i-Bu	H	C
IB-87	carbamoylmethyl	2-phenylethyl	Bnzl	H	A
IB-89	carbamoylmethyl	2-phenylethyl	i-Pnt	H	A
(A: IC50 ≤ 5 μM,B: 5 μM < IC50 ≤ 10 μM,C: 10 μM < IC50 < 30 μM)

TABLE 5-4
IB-90	carbamoylmethyl	1-naphthylmethyl	1-naphthylmethyl	H	A
IB-92	carbamoylmethyl	4-fluorobenzyl	Bnzl	H	C
IB-95	carbamoylmethyl	4-fluorobenzyl	2-phenylethyl	H	A
IB-96	carbamoylmethyl	4-fluorobenzyl	1-naphthylmethyl	H	C
IB-97	carbamoylmethyl	2-phenylethyl	1-naphthylmethyl	H	A
IB-102	carbamoylmethyl	i-Pnt	2phenylethyl-	H	A
IB-103	carbamoylmethyl	i-Pnt	1-naphthylmethyl	H	C
IB-105	carbamoylmethyl	hexyl	Bnzl	H	C
IB-108	carbamoylmethyl	hexyl	i-Pnt	H	C
IB-109	carbamoylmethyl	hexyl	2-phenylethyl	H	C
IB-110	carbamoylmethyl	hexyl	1-naphthylmethyl	H	A
IB-130	carbamoylmethyl	Bnzl	2-phenylethyl	H	C
IB-164	3-guanidinopropyl	1-naphthylmethyl	i-Bu	H	A
IB-174	3-guanidinopropyl	hexyl	2-phenylethyl	H	C
IB-176	3-guanidinopropyl	isopropyl	i-Bu	H	C
IB-179	3-guanidinopropyl	isopropyl	2-phenylethyl	H	C
IB-182	3-guanidinopropyl	4-fluorobenzyl	Bnzl	H	C
IB-187	i-Bu	i-Bu	3-guanidinopropyl	H	C
IB-192	i-Bu	i-Pnt	3-guanidinopropyl	H	A
IB-198	Bnzl	i-Bu	3-guanidinopropyl	H	C
IB-203	4-hydroxybenzyl	i-Bu	3-guanidinopropyl	H	C
IB-207	4-hydroxybenzyl	4-fluorobenzyl	3-guanidinopropyl	H	C
IB-247	Bnzl	phenethyl	3-guanidinopropyl	H	C
IB-249	Bnzl	hexyl	3-guanidinopropyl	H	C
IB-250	Bnzl	4-fluorobenzyl	3-guanidinopropyl	H	C
IB-256	phenethyl	hexyl	3-guanidinopropyl	H	C
IB-260	4-fluorobenzyl	Bnzl	3-guanidinopropyl	H	C
IB-262	4-fluorobenzyl	phenethyl	3-guanidinopropyl	H	C
IB-274	Bnzl	3-amino-3-oxopropyl	i-Pnt	H	C

TABLE 5-5
IB-276	Bnzl	3-	Bnzl	H	C
		guanidinopropyl
IB-279	Bnzl	3-	phenethyl	H	C
		guanidinopropyl
IB-280	Bnzl	3-	Np-M	H	C
		guanidinopropyl
IB-300	3-	Bnzl	Np-M	H	C
	guanidinopropyl
IB-327	3-	phenethyl	Np-M	H	C
	guanidinopropyl
IB-342	phenethyl	3-amino-3-	i-Pnt	H	C
		oxopropyl
IB-344	phenethyl	3-	Bnzl	H	C
		guanidinopropyl
IB-346	phenethyl	3-	i-Pnt	H	C
		guanidinopropyl
IB-347	phenethyl	3-	Np-M	H	C
		guanidinopropyl
IB-349	Np-M	3-amino-3-	i-Pnt	H	A
		oxopropyl
IB-350	Np-M	3-	i-Bu	H	C
		guanidinopropyl
IB-351	Np-M	3-	Bnzl	H	C
		guanidinopropyl
IB-353	Np-M	3-	i-Pnt	H	A
		guanidinopropyl
IB-354	Np-M	3-	phenethyl	H	A
		guanidinopropyl
IB-357	cyclohexylmethyl	3-amino-3-	i-Pnt	H	C
		oxopropyl
IB-361	cyclohexylmethyl	3-	i-Pnt	H	C
		guanidinopropyl
IB-362	cyclohexylmethyl	3-	phenethyl	H	A
		guanidinopropyl
IB-365	4-	3-amino-3-	i-Pnt	H	C
	fluorobenzyl	oxopropyl
IB-369	4-	3-	i-Pnt	H	C
	fluorobenzyl	guanidinopropyl
IB-372	2-	i-Bu	i-Pnt	H	C
	hydroxyethyl
IB-378	i-Bu	i-Bu	i-Pnt	H	A
IB-381	i-Pnt	2-	Np-M	H	C
		carboxyethyl
IB-384	4-	2-	Np-M	H	C
	fluorobenzyl	carboxyethyl
IB-386	i-Pnt	4-	2-	H	C
		fluorobenzyl	carboxyethyl
IB-389	cyclohexylmethyl	Np-M	2-	H	C
			carboxyethyl

TABLE 5-6
IB-390	4-	Np-M	2-	H	C
	fluorobenzyl		carboxyethyl
IB-392	2-	Np-M	i-Bu	H	C
	carboxyethyl
IB-394	2-	4-	Bnzl	H	C
	carboxyethyl	fluorobenzyl
IB-398	2-	Np-M	i-Pnt	H	C
	carboxyethyl
IB-399	2-	4-	i-Pnt	H	C
	carboxyethyl	fluorobenzyl
IB-402	2-	4-	i-Pnt	H	C
	carboxyethyl	hydroxybenzyl
IB-410	4-	2-	Np-M	H	C
	hydroxybenzyl	carboxyethyl
IB-417	Np-M	4-	Np-M	H	C
		hydroxybenzyl
IB-425	2-	Np-M	2-	H	C
	hydroxyethyl		carboxyethyl
IB-426	i-Pnt	Np-M	hydroxymethyl	H	A
IB-430	2-	i-Bu	phenethyl	H	A
	carboxyethyl
IB-431	2-	i-Bu	hydroxymethyl	H	C
	carboxyethyl
IB-449	phenethyl	4-	i-Bu	H	C
		hydroxybenzyl
IB-458	4-	4-	i-Bu	H	C
	fluorobenzyl	hydroxybenzyl
IB-459	Np-M	2-	4-	H	C
		hydroxyethyl	hydroxybenzyl
IB-461	phenethyl	2-	i-Pnt	H	C
		hydroxyethyl
IB-464	Bnzl	4-	i-Bu	H	A
		hydroxybenzyl
IB-465	i-Bu	4-	i-Pnt	H	C
		hydroxybenzyl
IB-470	2-	4-	Np-M	H	C
	hydroxyethyl	hydroxybenzyl
IB-476	2-	hexyl	Bnzl	H	A
	hydroxyethyl
IB-477	2-	hexyl	i-Bu	H	A
	hydroxyethyl
IB-478	2-	hexyl	4-	H	C
	hydroxyethyl		hydroxybenzyl
IB-479	2-	4-	Bnzl	H	C
	hydroxyethyl	fluorobenzyl
IB-481	i-Pnt	4-	4-	H	A
		fluorobenzyl	hydroxybenzyl
IB-484	cyclohexylmethyl	phenethyl	Bnzl	H	A
IB-490	2-	hexyl	i-Pnt	H	A
	hydroxyethyl
IB-492	2-	4-	phenethyl	H	A
	hydroxyethyl	fluorobenzyl

TABLE 5-7
IB-495	i-Bu	phenethyl	i-Bu	H	A
IB-498	i-Bu	4-	4-	H	A
		fluorobenzyl	hydroxybenzyl
IB-499	4-	4-	i-Bu	H	A
	hydroxybenzyl	fluorobenzyl
IB-501	4-	isopropyl	i-Pnt	H	A
	hydroxybenzyl
IB-502	4-	isopropyl	Np-M	H	A
	hydroxybenzyl
IB-505	i-Pnt	Bnzl	2-	H	C
			carboxyethyl
IB-508	phenethyl	i-Bu	2-	H	C
			carboxyethyl
IB-510	cyclohexylmethyl	i-Bu	2-	H	C
			carboxyethyl
IB-515	2-	4-	phenethyl	H	C
	carboxyethyl	hydroxybenzyl
IB-516	2-	4-	Np-M	H	C
	carboxyethyl	hydroxybenzyl
IB-520	Np-M	3-amino-3-	i-Bu	H	A
		oxopropyl
IB-521	Np-M	3-amino-3-	4-	H	C
		oxopropyl	hydroxybenzyl
IB-522	cyclohexylmethyl	3-amino-3-	Np-M	H	C
		oxopropyl
IB-525	4-	3-amino-3-	Np-M	H	C
	fluorobenzyl	oxopropyl
IB-527	2-	Np-M	4-	H	C
	hydroxyethyl		hydroxybenzyl
IB-531	2-	phenethyl	i-Pnt	H	C
	hydroxyethyl
IB-535	Bnzl	3-amino-3-	phenethyl	H	C
		oxopropyl
IB-536	i-Bu	phenethyl	4-	H	C
			hydroxybenzyl
IB-539	i-Bu	3-amino-3-	phenethyl	H	C
		oxopropyl
IB-540	4-	phenethyl	i-Bu	H	C
	hydroxybenzyl
IB-541	4-	Np-M	i-Bu	H	A
	hydroxybenzyl
IB-544	4-	phenethyl	i-Pnt	H	C
	hydroxybenzyl
IB-549	2-	4-	4-	H	C
	hydroxyethyl	fluorobenzyl	hydroxybenzyl
IB-551	i-Pnt	hexyl	i-Bu	H	A
IB-553	i-Pnt	4-	i-Bu	H	A
		fluorobenzyl
IB-562	Bnzl	hexyl	Bnzl	H	C
IB-568	Bnzl	4-	phenethyl	H	C
		fluorobenzyl
IB-574	4-	i-Pnt	Bnzl	H	C
	hydroxybenzyl

TABLE 5-8
IB-575	2-	i-Bu	Np-M	H	C
	carboxyethyl
IB-576	i-Pnt	4-	phenethyl	H	C
		hydroxybenzyl
IB-577	i-Pnt	4-	Bnzl	H	C
		hydroxybenzyl
IB-581	cyclohexylmethyl	4-	i-Bu	H	C
		hydroxybenzyl
IB-582	4-	4-	i-Pnt	H	C
	fluorobenzyl	hydroxybenzyl
IB-583	4-	4-	Bnzl	H	C
	fluorobenzyl	hydroxybenzyl
IB-585	2-	Np-M	i-Bu	H	C
	hydroxyethyl
IB-588	Np-M	2-	Bnzl	H	A
		hydroxyethyl
IB-593	phenethyl	2-	Np-M	H	C
		hydroxyethyl
IB-602	Bnzl	2-	Np-M	H	C
		hydroxyethyl
IB-610	2-	2-	Np-M	H	C
	hydroxyethyl	carboxyethyl
IB-611	i-Pnt	2-	i-Bu	H	C
		carboxyethyl
IB-613	cyclohexylmethyl	2-	i-Pnt	H	C
		carboxyethyl
IB-614	cyclohexylmetyl	2-	Np-M	H	C
		carboxyethyl
IB-616	Bnzl	2-	Np-M	H	C
		carboxyethyl
IB-618	2-	Bnzl	phenethyl	H	A
	hydroxyethyl
IB-619	2-	Bnzl	Bnzl	H	C
	hydroxyethyl
IB-621	2-	i-Bu	Np-M	H	A
	hydroxyethyl
IB-625	phenethyl	i-Bu	4-	H	C
			hydroxybenzyl
IB-630	4-	i-Bu	i-Bu	H	A
	fluorobenzyl
IB-631	4-	i-Bu	4-	H	C
	fluorobenzyl		hydroxybenzyl
IB-633	i-Bu	i-Bu	phenethyl	H	A
IB-636	i-Pnt	3-amino-3-	phenethyl	H	C
		oxopropyl
IB-637	cyclohexylmethyl	3-amino-3-	Bnzl	H	A
		oxopropyl
IB-640	phenethyl	2-	Bnzl	H	A
		hydroxyethyl
IB-641	phenethyl	2-	i-Bu	H	C
		hydroxyethyl

TABLE 5-9
IB-642	phenethyl	4-	4-	H	A
		fluorobenzyl	hydroxybenzyl
IB-643	Np-M	2-	i-Bu	H	C
		hydroxyethyl
IB-646	cyclohexylmethyl	2-	i-Bu	H	C
		hydroxyethyl
IB-648	cyclohexylmethyl	i-Pnt	4-	H	C
			hydroxybenzyl
IB-649	4-	2-	Bnzl	H	C
	fluorobenzyl	hydroxyethyl
IB-650	4-	2-	i-Bu	H	C
	fluorobenzyl	hydroxyethyl
IB-656	4-	hexyl	4-	H	A
	fluorobenzyl		hydroxybenzyl
IB-657	2-	4-	i-Pnt	H	C
	hydroxyethyl	fluorobenzyl
IB-658	i-Pnt	2-	phenethyl	H	C
	hydroxyethyl
IB-659	i-Pnt	2-	Np-M	H	A
		hydroxyethyl
IB-663	cyclohexylmethyl	2-	phenethyl	H	A
		hydroxyethyl
IB-668	4-	2-	i-Pnt	H	A
	fluorobenzyl	hydroxyethyl
IB-669	4-	2-	phenethyl	H	C
	fluorobenzyl	hydroxyethyl
IB-676	Bnzl	2-	Bnzl	H	C
		hydroxyethyl
IB-678	Bnzl	i-Pnt	4-	H	A
			hydroxybenzyl
IB-680	Bnzl	2-	i-Pnt	H	C
		hydroxyethyl
IB-681	Bnzl	2-	phenethyl	H	C
		hydroxyethyl
IB-684	i-Bu	i-Pnt	4-	H	C
			hydroxybenzyl
IB-687	i-Bu	2-	Np-M	H	C
		hydroxyethyl
IB-688	i-Bu	i-Pnt	phenethyl	H	A
IB-694	2-	Bnzl	i-Pnt	H	C
	carboxyethyl
IB-703	i-Pnt	3-amino-3-	Np-M	H	A
		oxopropyl
IB-707	phenethyl	3-amino-3-	Bnzl	H	A
		oxopropyl
IB-708	phenethyl	3-amino-3-	i-Bu	H	A
		oxopropyl
IB-710	cyclohexylmethyl	3-amino-3-	phenethyl	H	A
		oxopropyl

TABLE 5-10
IB-712	4-	3-amino-3-	Bnzl	H	A
	fluorobenzyl	oxopropyl
IB-714	2-	i-Pnt	Bnzl	H	A
	hydroxyethyl
IB-725	4-	phenethyl	i-Bu	H	A
	fluorobenzyl
IB-727	2-	i-Pnt	Np-M	H	A
	hydroxyethyl
IB-729	Np-M	phenethyl	Np-M	H	A
IB-734	Bnzl	3-amino-3-	Bnzl	H	C
		oxopropyl
IB-737	i-Bu	3-amino-3-	Np-M	H	C
		oxopropyl
IB-739	4-	i-Pnt	i-Bu	H	C
	hydroxybenzyl
IB-743	4-	3-amino-3-	Np-M	H	A
	hydroxybenzyl	oxopropyl
IB-749	i-Pnt	Bnzl	4-	H	C
			hydroxybenzyl
IB-753	i-Pnt	i-Bu	i-Bu	H	A
IB-757	phenethyl	Bnzl	i-Bu	H	A
IB-759	phenethyl	i-Bu	Bnzl	H	A
IB-760	phenethyl	i-Bu	i-Bu	H	A
IB-762	Np-M	i-Bu	i-Bu	H	A
IB-763	Np-M	i-Bu	4-	H	C
			hydroxybenzyl
IB-770	cyclohexylmethyl	i-Bu	4-	H	C
			hydroxybenzyl
IB-772	4-	Bnzl	Bnzl	H	A
	fluorobenzyl
IB-773	4-	Bnzl	i-Bu	H	A
	fluorobenzyl
IB-774	4-	i-Bu	phenethyl	H	A
	fluorobenzyl
IB-777	Bnzl	Bnzl	Np-M	H	A
IB-780	i-Bu	i-Pnt	Bnzl	H	A
IB-783	i-Bu	Bnzl	4-	H	C
			hydroxybenzyl
IB-786	4-	Bnzl	i-Pnt	H	C
	hydroxybenzyl
IB-787	4-	Bnzl	i-Bu	H	C
	hydroxybenzyl
IB-804	Np-M	Np-M	phenethyl	H	A
IB-813	Bnzl	3-amino-3-	Np-M	H	A
		oxopropyl
IB-831	2-	4-	Np-M	H	A
	hydroxyethyl	fluorobenzyl
IB-864	4-C1-Bnzl	Bnzl	i-Bu	H	B
IB-865	3-C1-Bnzl	Bnzl	i-Bu	H	B
IB-866	4-	Bnzl	i-Bu	H	B
	methoxybenzyl

TABLE 5-11
IB-867	4-	Bnzl	i-Bu	H	B
	methylbenzyl
IB-870	i-Bu	i-Pnt	Bnzl	H	C
IB-871	i-Bu	4-Cl-Bnzl	i-Bu	H	C
IB-873	4-	Bnzl	i-Bu	H	B
	(dimethylamino)-
	benzyl
IB-874	4-(tert-	Bnzl	i-Bu	H	B
	butyl)benzyl
IB-875	i-Bu	Bnzl	i-Pnt	H	C
IB-876	i-Pnt	Bnzl	i-Bu	H	C
IB-877	4-	Bnzl	i-Bu	H	B
	(trifluoromethyl)-
	benzyl
IB-878	4-	Bnzl	i-Bu	H	C
	ethoxybenzyl
IB-879	Bnzl	naphthalen-	i-Bu	H	A
		2-ylmethyl
IB-880	4-	Bnzl	i-Bu	ethyl	A
	methylbenzyl
IB-881	4-	Bnzl	i-Bu	i-Bu	A
	methylbenzyl
IB-883	4-	Bnzl	i-Bu	3-	A
	methylbenzyl			methylbutanoyl
IB-884	4-	Bnzl	i-Bu	2-	A
	methylbenzyl			phenylacetyl
IB-885	4-	Bnzl	i-Bu	methoxy-	B
	methylbenzyl			carbonyl
IB-886	4-	Bnzl	i-Bu	2-	B
	methylbenzyl			methylpropoxy-
				carbonyl
IB-887	4-	Bnzl	i-Bu	benzyloxy-	B
	methylbenzyl			carbonyl
IB-888	4-	Bnzl	i-Bu	aminocarbonyl	C
	methylbenzyl
IB-889	4-	Bnzl	i-Bu	N-	B
	methylbenzyl			benzylamino-
				carbonyl
IB-891	4-	3-	i-Bu	H	C
	(dimethylamino)-	hydroxybenzyl
	benzyl
IB-892	4-	4-	i-Bu	H	C
	(dimethylamino)-	hydroxybenzyl
	benzyl

TABLE 5-12
Anti-rabies activity of compounds of formula XXIB
Compound						Anti-rabies
number	R1	R2A	R2B	R3	R4	activity
IB-924	4-Me-	H	Bnzl	i-Bu	N-isobutylamino-	na
	Bnzl				carbonyl
IB-925	i-Bu	H	4-Cl-Bnzl	Ph-Et	H	A
IB-926	i-Bu	H	3-Cl-Bnzl	Ph-Et	H	A
IB-927	i-Bu	H	4-MeO-Bnzl	Ph-Et	H	A
IB-928	i-Bu	H	4-Me-Bnzl	Ph-Et	H	A
IB-929	i-Bu	H	2-Npm	Ph-Et	H	A
IB-930	i-Bu	H	Bnzl	Ph-Pr	H	A
IB-931	i-Bu	H	3-Cl-Bnzl	Ph-Pr	H	A
IB-932	i-Bu	H	3-F-Bnzl	Ph-Pr	H	A
IB-933	i-Bu	H	3-Me-Bnzl	Ph-Pr	H	A
IB-934	i-Bu	H	3-MeO-Bnzl	Ph-Pr	H	A
IB-935	i-Bu	H	3-Cl-Bnzl	Ph-Bu	H	A
IB-936	i-Bu	H	3-F-Bnzl	Ph-Bu	H	A
IB-937	i-Bu	H	3-Me-Bnzl	Ph-Bu	H	A
IB-938	i-Bu	H	3-MeO-Bnzl	Ph-Bu	H	A
IB-939	i-Bu	H	Bnzl	Ph-Bu	H	A
IB-940	i-Pnt	H	3-F-Bnzl	Ph-Pr	H	A
IB-957	i-Bu	H	Ph-Et	Ph-Et	H	A
IB-958	i-Bu	H	1-Npm	Ph-Et	H	A

TABLE 5-13
Table. Anti-rabies activity of compounds of formula IF
Compound					Anti-rabies
number	R1	R2	R3	R4	activity
IF-1	i-Bu	Bnzl	Bnzl	H	C
IF-6	Bnzl	i-Bu	Bnzl	H	C
IF-7	Bnzl	Bnzl	i-Bu	H	B
IF-9	i-Pnt	Bnzl	Bnzl	H	C
IF-11	i-Bu	Bnzl	phenethyl	H	C
IF-13	i-Bu	Bnzl	3-methylbenzyl	H	C
IF-14	i-Bu	Bnzl	4-methylbenzyl	H	C
(A: IC50 ≤ 5 μM,B: 5 μM < IC50 ≤ 10 μM,C: 10 μM < IC50 < 30 μM)

TABLE 5-14
IF-15	i-Bu	3-	Bnzl	H	C
		methylbenzyl
IF-20	Bnzl	3,4-	i-Bu	H	C
		dichlorobenzyl
IF-38	i-Bu	Bnzl	cyclohexylmethyl	H	C
IF-42	Np-M	Bnzl	Bnzl	H	C
IF-69	i-Bu	Bnzl	Bnzl	ethyl	C
IF-81	2-amino-2-	Np-M	i-Bu	H	C
	oxoethyl
IF-82	2-amino-2-	Np-M	Bnzl	H	C
	oxoethyl
IF-84	2-amino-2-	Np-M	i-Pnt	H	C
	oxoethyl
IF-85	2-amino-2-	Np-M	phenethyl	H	C
	oxoethyl
IF-90	2-amino-2-	phenethyl	Np-M	H	C
	oxoethyl
IF-91	2-amino-2-	Np-M	Np-M	H	A
	oxoethyl
IF-95	2-amino-2-	4-	i-Pnt	H	C
	oxoethyl	fluorobenzyl
IF-97	2-amino-2-	4-	Np-M	H	C
	oxoethyl	fluorobenzyl
IF-109	2-amino-2-	hexyl	phenethyl	H	C
	oxoethyl
IF-110	2-amino-2-	hexyl	Np-M	H	A
	oxoethyl
IF-137	2-amino-2-	4-	Np-M	H	A
	oxoethyl	hydroxybenzyl
IF-214	i-Pnt	isopropyl	3-	H	C
			guanidinopropyl
IF-219	phenethyl	3-amino-	2-amino-2-	H	C
		3-oxopropyl	oxoethyl
IF-223	phenethyl	Np-M	2-amino-2-	H	C
			oxoethyl
IF-226	Np-M	i-Bu	2-amino-2-	H	C
			oxoethyl
IF-230	Np-M	2-	2-amino-2-	H	C
		hydroxyethyl	oxoethyl
IF-235	Np-M	i-Bu	3-	H	C
			guanidinopropyl
IF-236	Np-M	Bnzl	3-	H	C
			guanidinopropyl
IF-239	Np-M	2-	3-	H	C
		hydroxyethyl	guanidinopropyl
IF-243	Np-M	hexyl	3-	H	A
			guanidinopropyl
IF-244	Np-M	isopropyl	3-	H	A
			guanidinopropyl

TABLE 5-15
IF-245	Np-M	4-	3-	H	A
		fluoro-	guanidinopropyl
		benzyl
IF-246	cyclohexyl-	Bnzl	2-amino-2-	H	C
	methyl		oxoethyl
IF-247	cyclohexyl-	4-	2-amino-2-	H	C
	methyl	hydroxy-	oxoethyl
		benzyl
IF-251	cyclohexyl-	phenethyl	2-amino-2-	H	C
	methyl		oxoethyl
IF-260	cyclohexyl-	hexyl	3-	H	C
	methyl		guanidinopropyl
IF-262	4-	i-Bu	2-amino-2-	H	A
	fluorobenzyl		oxoethyl
IF-269	4-	phenethyl	2-amino-2-	H	C
	fluorobenzyl		oxoethyl
IF-274	4-	isopropyl	3-	H	C
	fluorobenzyl		guanidinopropyl
IF-284	Bnzl	Np-M	3-	H	C
			guanidinopropyl
IF-285	Bnzl	hexyl	3-	H	C
			guanidinopropyl
IF-297	4-	Np-M	3-	H	C
	fluorobenzyl		guanidinopropyl
IF-298	4-	hexyl	3-	H	C
	fluorobenzyl		guanidinopropyl
IF-300	i-Bu	3-	i-Pnt	H	C
		amino-
		3-
		oxopropyl
IF-356	3-	i-Pnt	Np-M	H	C
	guanidino-
	propyl
IF-359	3-	phenethyl	4-hydroxybenzyl	H	C
	guanidino-
	propyl
IF-384	Np-M	3-	i-Pnt	H	C
		amino-
		3-
		oxopropyl
IF-386	Np-M	3-	Bnzl	H	C
		guanidino-
		propyl
IF-389	Np-M	3-	phenethyl	H	A
		guanidino-
		propyl
IF-390	Np-M	3-	Np-M	H	C
		guanidino-
		propyl
IF-411	Bnzl	i-Bu	i-Pnt	H	A
IF-412	i-Bu	i-Bu	i-Pnt	H	A
IF-413	i-Pnt	2-	Np-M	H	C
		carboxy-
		ethyl
IF-416	cyclohexyl-	2-	Np-M	H	C
	methyl	carboxy-
		ethyl
IF-417	4-	2-	Np-M	H	C
	fluorobenzyl	carboxy-
		ethyl
IF-419	cyclohexyl-	Np-M	2-carboxyethyl	H	C
	methyl
IF-422	2-	Np-M	i-Pnt	H	C
	carboxyethyl
IF-428	i-Bu	2-	Np-M	H	C
		carboxy-
		ethyl
IF-435	Np-M	3-	4-hydroxybenzyl	H	A
		amino-
		3-
		oxopropyl
IF-437	i-Pnt	phenethyl	i-Bu	H	C

TABLE 5-16
IF-439	cyclohexyl-	phenethyl	4-hydroxybenzyl	H	A
	methyl
IF-444	2-	2-	Np-M	H	C
	hydroxyethyl	carboxy-
		ethyl
IF-445	i-Pnt	4-	2-carboxyethyl	H	C
		hydroxy-
		benzyl
IF-447	cyclohexyl-	4-	2-carboxyethyl	H	C
	methyl	hydroxy-
		benzyl
IF-452	2-	2-	Np-M	H	C
	carboxyethyl	hydroxy-
		ethyl
IF-454	2-	i-Bu	phenethyl	H	C
	carboxyethyl
IF-455	2-	i-Bu	4-hydroxybenzyl	H	C
	carboxyethyl
IF-458	2-	4-	i-Pnt	H	C
	carboxyethyl	hydroxy-
		benzyl
IF-464	i-Pnt	4-	phenethyl	H	C
		hydroxy-
		benzyl
IF-465	i-Pnt	4-	Np-M	H	C
		hydroxy-
		benzyl
IF-466	i-Pnt	4-	Bnzl	H	C
		hydroxy-
		benzyl
IF-468	phenethyl	4-	i-Pnt	H	C
		hydroxy-
		benzyl
IF-469	phenethyl	4-	Bnzl	H	C
		hydroxy-
		benzyl
IF-470	phenethyl	4-	i-Bu	H	C
		hydroxy-
		benzyl
IF-472	Np-M	4-	Bnzl	H	A
		hydroxy-
		benzyl
IF-473	Np-M	4-	i-Bu	H	A
		hydroxy-
		benzyl
IF-474	cyclohexyl-	4-	i-Pnt	H	A
	methyl	hydroxy-
		benzyl
IF-475	cyclohexyl-	4-	phenethyl	H	C
	methyl	hydroxy-
		benzyl
IF-477	cyclohexyl-	4-	Bnzl	H	A
	methyl	hydroxy-
		benzyl
IF-478	cyclohexyl-	4-	i-Bu	H	A
	methyl	hydroxy-
		benzyl
IF-479	4-	4-	i-Pnt	H	A
	fluorobenzyl	hydroxy-
		benzyl
IF-481	4-	4-	Bnzl	H	C
	fluorobenzyl	hydroxy-
		benzyl
IF-482	4-	4-	i-Bu	H	C
	fluorobenzyl	hydroxy-
		benzyl
IF-486	cyclohexyl-	2-	Bnzl	H	C
	methyl	hydroxy-
		ethyl

TABLE 5-17
IF-490	4-	2-	i-Pnt	H	C
	fluorobenzyl	hydroxyethyl
IF-493	Bnzl	4-	i-Pnt	H	A
		hydroxybenzyl
IF-494	Bnzl	4-	Bnzl	H	C
		hydroxybenzyl
IF-500	i-Bu	4-	Np-M	H	C
		hydroxybenzyl
IF-503	4-	isopropyl	i-Pnt	H	A
	hydroxybenzyl
IF-504	4-	isopropyl	Np-M	H	C
	hydroxybenzyl
IF-505	Np-M	Bnzl	4-hydroxybenzyl	H	A
IF-508	2-	4-	Bnzl	H	C
	hydroxyethyl	fluorobenzyl
IF-514	cyclohexyl-	hexyl	4-hydroxybenzyl	H	A
	methyl
IF-516	2-	4-	phenethyl	H	A
	hydroxyethyl	fluorobenzyl
IF-525	i-Bu	4-	phenethyl	H	C
		fluorobenzyl
IF-536	cyclohexyl-	3-amino-	Np-M	H	A
	methyl	3-
		oxopropyl
IF-539	4-	3-amino-	Np-M	H	A
	fluorobenzyl	3-
		oxopropyl
IF-542	2-	Np-M	i-Bu	H	A
	hydroxyethyl
IF-543	2-	Np-M	4-hydroxybenzyl	H	C
	hydroxyethyl
IF-545	i-Pnt	phenethyl	4-hydroxybenzyl	H	C
IF-546	i-Pnt	hexyl	i-Bu	H	C
IF-547	i-Pnt	4-	Bnzl	H	A
		fluorobenzyl
IF-548	i-Pnt	4-	i-Bu	H	C
		fluorobenzyl
IF-560	Bnzl	hexyl	i-Bu	H	A
IF-561	Bnzl	4-	Bnzl	H	A
		fluorobenzyl
IF-565	Bnzl	4-	phenethyl	H	A
		hydroxybenzyl
IF-567	i-Bu	phenethyl	4-hydroxybenzyl	H	C
IF-568	i-Bu	Np-M	4-hydroxybenzyl	H	A
IF-569	i-Bu	hexyl	i-Bu	H	C
IF-576	i-Bu	4-	phenethyl	H	C
		hydroxybenzyl
IF-578	4-	Np-M	i-Bu	H	A
	hydroxybenzyl
IF-580	4-	phenethyl	Np-M	H	C
	hydroxybenzyl

TABLE 5-18
IF-583	i-Pnt	hexyl	4-hydroxybenzyl	H	A
IF-584	4-	i-Pnt	Bnzl	H	A
	fluorobenzyl
IF-585	4-	i-Pnt	i-Bu	H	A
	fluorobenzyl
IF-586	4-	phenethyl	Bnzl	H	C
	fluorobenzyl
IF-596	Np-M	isopropyl	Np-M	H	C
IF-599	i-Pnt	hexyl	Bnzl	H	C
IF-602	phenethyl	hexyl	Bnzl	H	C
IF-603	Np-M	2-	Bnzl	H	C
		hydroxy-
		ethyl
IF-604	Np-M	2-	i-Bu	H	C
		hydroxy-
		ethyl
IF-606	cyclohexyl-	2-	i-Bu	H	C
	methyl	hydroxy-
		ethyl
IF-610	2-	phenethyl	Np-M	H	C
	hydroxyethyl
IF-611	i-Pnt	2-	Np-M	H	C
		hydroxy-
		ethyl
IF-612	phenethyl	2-	Np-M	H	C
		hydroxy-
		ethyl
IF-613	Np-M	2-	i-Pnt	H	C
		hydroxy-
		ethyl
IF-614	Np-M	2-	Np-M	H	C
		hydroxy-
		ethyl
IF-619	cyclohexyl-	2-	Np-M	H	C
	methyl	hydroxy-
		ethyl
IF-620	4-	2-	Np-M	H	A
	fluorobenzyl	hydroxy-
		ethyl
IF-624	Bnzl	2-	Np-M	H	C
		hydroxy-
		ethyl
IF-635	i-Pnt	i-Bu	phenethyl	H	C
IF-639	phenethyl	Bnzl	i-Bu	H	A
IF-640	phenethyl	Bnzl	4-hydroxybenzyl	H	C
IF-641	phenethyl	i-Bu	Bnzl	H	A
IF-644	cyclohexyl-	Bnzl	i-Bu	H	A
	methyl
IF-645	cyclohexyl-	Bnzl	4-hydroxybenzyl	H	C
	methyl
IF-646	cyclohexyl-	i-Bu	Np-M	H	A
	methyl
IF-649	4-	Bnzl	Bnzl	H	A
	fluorobenzyl
IF-650	4-	Bnzl	i-Bu	H	A
	fluorobenzyl
IF-652	4-	i-Bu	phenethyl	H	A
	fluorobenzyl
IF-653	4-	i-Bu	Bnzl	H	C
	fluorobenzyl
IF-654	4-	i-Bu	i-Bu	H	A
	fluorobenzyl

TABLE 5-19
IF-656	2-	i-Pnt	Bnzl	H	C
	hydroxyethyl
IF-657	phenethyl	i-Pnt	i-Bu	H	A
IF-658	cyclohexyl-	i-Pnt	Bnzl	H	A
	methyl
IF-659	cyclohexyl-	i-Pnt	i-Bu	H	C
	methyl
IF-660	2-	i-Pnt	Np-M	H	C
	hydroxyethyl
IF-665	Bnzl	i-Pnt	Bnzl	H	A
IF-670	Bnzl	i-Bu	phenethyl	H	A
IF-673	i-Bu	i-Pnt	phenethyl	H	A
IF-674	i-Bu	i-Pnt	Np-M	H	C
IF-675	i-Bu	Bnzl	i-Pnt	H	A
IF-679	i-Bu	i-Bu	phenethyl	H	A
IF-680	i-Bu	i-Bu	Np-M	H	C
IF-684	4-	i-Pnt	Np-M	H	C
	hydroxybenzyl
IF-691	benzyl	i-Pnt	i-Bu	H	C
IF-692	Bnzl	hexyl	4-hydroxybenzyl	H	A
IF-699	phenethyl	3-	i-Bu	H	C
		amino-
		3-
		oxopropyl
IF-705	i-Pnt	Np-M	i-Bu	H	A
IF-706	i-Pnt	Np-M	4-hydroxybenzyl	H	A
IF-707	phenethyl	i-Pnt	4-hydroxybenzyl	H	A
IF-708	Np-M	phenethyl	4-hydroxybenzyl	H	A
IF-709	cyclohexyl-	i-Pnt	4-hydroxybenzyl	H	C
	methyl
IF-710	cyclohexyl-	phenethyl	Bnzl	H	A
	methyl
IF-711	cyclohexyl-	phenethyl	i-Bu	H	C
	methyl
IF-714	4-	phenethyl	i-Bu	H	A
	fluorobenzyl
IF-715	4-	phenethyl	4-hydroxybenzyl	H	A
	fluorobenzyl
IF-717	cyclohexyl-	phenethyl	i-Pnt	H	A
	methyl
IF-718	cyclohexyl-	phenethyl	Np-M	H	A
	methyl
IF-721	Bnzl	phenethyl	i-Bu	H	A
IF-722	Bnzl	phenethyl	4-hydroxybenzyl	H	A
IF-723	Bnzl	phenethyl	i-Pnt	H	C
IF-725	i-Bu	phenethyl	i-Bu	H	C
IF-726	i-Bu	Np-M	i-Bu	H	C
IF-727	i-Bu	phenethyl	i-Pnt	H	A
IF-730	4-	Np-M	i-Pnt	H	C
	hydroxybenzyl

TABLE 5-20
IF-733	i-Pnt	Bnzl	i-Bu	H	A
IF-734	i-Pnt	i-Bu	Np-M	H	A
IF-735	i-Pnt	i-Bu	Bnzl	H	C
IF-738	phenethyl	i-Bu	i-Bu	H	C
IF-739	Np-M	i-Bu	i-Bu	H	A
IF-740	cyclohexyl-	Bnzl	i-Pnt	H	C
	methyl
IF-742	cyclohexyl-	i-Bu	i-Bu	H	C
	methyl
IF-743	4-	Bnzl	i-Pnt	H	C
	fluorobenzyl
IF-744	phenethyl	i-Pnt	Bnzl	H	A
IF-753	i-Bu	Bnzl	Np-M	H	C
IF-758	2-	Np-M	Bnzl	H	A
	hydroxyethyl
IF-778	i-Bu	Np-M	Np-M	H	A
IF-779	4-	Np-M	Np-M	H	C
	hydroxybenzyl
IF-789	Np-M	isopropyl	phenethyl	H	C
IF-805	Bnzl	Np-M	Bnzl	H	C
IF-807	Bnzl	4-	i-Bu	H	A
		fluorobenzyl
IF-815	i-Bu	4-	Bnzl	H	A
		fluorobenzyl
IF-830	i-Pnt	2-	phenethyl	H	C
		carboxy-
		ethyl
IF-837	Bnzl	Np-M	i-Bu	H	B
IF-838	Bnzl	4-	i-Bu	H	C
		(trifluoro-
		methyl)-
		benzyl
IF-839	4-Cl-Bnzl	Bnzl	i-Bu	H	B
IF-840	3-Cl-Bnzl	Bnzl	i-Bu	H	B
IF-841	4-	Bnzl	i-Bu	H	B
	methoxybenzyl
IF-842	4-	Bnzl	i-Bu	H	A
	methylbenzyl
IF-845	i-Bu	i-Pnt	Bnzl	H	C
IF-846	i-Bu	4-Cl-	i-Bu	H	C
		Bnzl
IF-848	4-	Bnzl	i-Bu	H	B
	(dimethylamino)-
	benzyl
IF-849	4-(tert-	Bnzl	i-Bu	H	B
	butyl)benzyl
IF-850	i-Bu	Bnzl	i-Pnt	H	B
IF-851	i-Pnt	Bnzl	i-Bu	H	C
IF-852	4-	Bnzl	i-Bu	H	B
	(trifluoro-
	methyl)benzyl

TABLE 5-21
IF-853	4-	Bnzl	i-Bu	H	B
	ethoxybenzyl
IF-854	Bnzl	naphthalen-	i-Bu	H	B
		2-
		ylmethyl
IF-855	4-	Bnzl	i-Bu	ethyl	B
	methylbenzyl
IF-856	4-	Bnzl	i-Bu	i-Bu	A
	methylbenzyl
IF-859	4-	Bnzl	i-Bu	2-	B
	methylbenzyl			phenylacetyl
IF-860	4-	Bnzl	i-Bu	methoxy-	C
	methylbenzyl			carbonyl
IF-861	4-	Bnzl	i-Bu	2-	B
	methylbenzyl			methyl-
				propoxy-
				carbonyl
IF-862	4-	Bnzl	i-Bu	benzyloxy-	B
	methylbenzyl			carbonyl
IF-864	4-	Bnzl	i-Bu	N-	C
	methylbenzyl			benzyl-
				amino-
				carbonyl
IF-866	4-	3-	i-Bu	H	C
	(dimethyl-	hydroxy-
	amino)benzyl	benzyl
IF-867	4-	4-	i-Bu	H	C
	(dimethyl-	hydroxy-
	amino)benzyl	benzyl

TABLE 5-22
Anti-rabies activity of compounds of formula XXIF
Compound						Anti-rabies
number	R1	R2A	R2B	R3	R4	activity
IF-885	i-Bu	H	4-Cl-Bnzl	Ph-Et	H	A
IF-886	i-Bu	H	3-Cl-Bnzl	Ph-Et	H	A
IF-887	i-Bu	H	4-MeO-Bnzl	Ph-Et	H	A
IF-888	i-Bu	H	4-Me-Bnzl	Ph-Et	H	A
IF-889	i-Bu	H	2-Npm	Ph-Et	H	A
IF-890	i-Bu	H	Bnzl	Ph-Pr	H	B
IF-891	i-Bu	H	3-Cl-Bnzl	Ph-Pr	H	A
IF-892	i-Bu	H	3-F-Bnzl	Ph-Pr	H	A
IF-893	i-Bu	H	3-Me-Bnzl	Ph-Pr	H	B
IF-894	i-Bu	H	3-MeO-Bnzl	Ph-Pr	H	A
IF-895	i-Bu	H	3-Cl-Bnzl	Ph-Bu	H	A
IF-896	i-Bu	H	3-F-Bnzl	Ph-Bu	H	A
IF-897	i-Bu	H	3-Me-Bnzl	Ph-Bu	H	A
IF-898	i-Bu	H	3-MeO-Bnzl	Ph-Bu	H	B
IF-899	i-Bu	H	Bnzl	Ph-Bu	H	B
IF-900	i-Pnt	H	3-F-Bnzl	Ph-Pr	H	A
IF-909	i-Bu	H	Ph-Et	Ph-Et	H	A

TABLE 5-23
Anti-rabies activity of compounds of formula IIB
(A: IC50 ≤ 5 μM, B: 5 μM < IC50 ≤ 10 μM, C: 10 μM < IC50 < 30 μM)
				Anti-
Compound				rabies
number	R1	R2	R3	activity
IIB-4	Bnzl	i-Bu	i-Bu	B
IIB-83	4-Cl-Bnzl	Bnzl	i-Bu	A
IIB-84	3-Cl-Bnzl	Bnzl	i-Bu	A
IIB-85	4-methoxybenzyl	Bnzl	i-Bu	B
IIB-86	4-methylbenzyl	Bnzl	i-Bu	B
IIB-94	4-(dimethylamino)benzyl	Bnzl	i-Bu	B
IIB-95	4-(tert-butyl)benzyl	Bnzl	i-Bu	B
IIB-96	4-(trifluoromethoxy)benzyl	Bnzl	i-Bu	B
IIB-97	4-ethoxybenzyl	Bnzl	i-Bu	C
IIB-101	4-hydroxybenzyl	Bnzl	i-Pnt	B
IIB-102	Bnzl	naphthalen-2-	i-Bu	A
		ylmethyl
IIB-103	i-Pnt	4-Cl-Bnzl	i-Bu	B
IIB-104	i-Pnt	4-fluorobenzyl	i-Bu	B

TABLE 5-24
Anti-rabies activity of compounds of formula XXIIB
					Anti-
Compound					rabies
number	R1	R2A	R2B	R3	activity
IIF-325	i-Pnt	H	3-Cl-Bnzl	Bnzl	A
IIF-328	i-Pnt	H	4-Me-Bnzl	Bnzl	A
IIF-329	i-Pnt	H	4-MeO-Bnzl	Bnzl	A
IIB-329	Me	H	quinolin-8-ylethyl	Bnzl	A
IIB-330	Me	H	quinolin-5-ylethyl	Bnzl	A
IIB-331	i-Bu	H	4-Cl-Bnzl	Ph-Et	A
IIB-332	i-Bu	H	3-Cl-Bnzl	Ph-Et	A
IIB-333	i-Bu	H	4-MeO-Bnzl	Ph-Et	A
IIB-334	i-Bu	H	4-Me-Bnzl	Ph-Et	A
IIB-335	i-Bu	H	2-Npm	Ph-Et	A
IIB-336	i-Bu	H	Bnzl	Ph-Pr	A
IIB-337	i-Bu	H	3-Cl-Bnzl	Ph-Pr	A
IIB-338	i-Bu	H	3-F-Bnzl	Ph-Pr	A
IIB-339	Cpm	H	4-OH-Bnzl	2-Cbx-Et	na
IIB-340	i-Bu	H	3-Me-Bnzl	Ph-Pr	A
IIB-341	i-Bu	H	3-MeO-Bnzl	Ph-Pr	A
IIB-342	i-Bu	H	3-Cl-Bnzl	Ph-Bu	B
IIB-343	i-Bu	H	3-F-Bnzl	Ph-Bu	A
IIB-344	i-Bu	H	3-Me-Bnzl	Ph-Bu	A
IIB-345	i-Bu	H	3-MeO-Bnzl	Ph-Bu	A
IIB-346	i-Bu	H	Bnzl	Ph-Bu	A
IIB-347	i-Pnt	H	3-F-Bnzl	Ph-Pr	A
IIF-327	i-Pnt	H	4-F-Bnzl	Bnzl	A
IIF-370	i-Pnt	H	Ph-Et	Bnzl	A
IIF-371	i-Pnt	H	1-Npm	Bnzl	A
IIB-374	i-Bu	H	4-F-Bnzl	Ph-Et	A
IIB-375	i-Bu	H	Ph-Et	Ph-Et	A
IIB-376	i-Bu	H	1-Npm	Ph-Et	A
IIB-378	4-F-Bnzl	H	1-Npm	i-Bu	A

TABLE 5-25
Anti-rabies activity of compounds of formula IIF
(A: IC50 ≤ 5 μM, B: 5 μM < IC50 ≤ 10 μM, C: 10 μM < IC50 < 30 μM)
				Anti-
Compound				rabies
number	R1	R2	R3	activity
IIF-16	i-Bu	4-Me-Bnzl	Bnzl	C
IIF-83	4-Cl-Bnzl	Bnzl	i-Bu	A
IIF-84	3-Cl-Bnzl	Bnzl	i-Bu	B
IIF-85	4-methoxybenzyl	Bnzl	i-Bu	B
IIF-86	4-methylbenzyl	Bnzl	i-Bu	A
IIF-94	4-(dimethylamino)benzyl	Bnzl	i-Bu	B
IIF-95	4-(tert-butyl)benzyl	Bnzl	i-Bu	A
IIF-96	4-(trifluoromethoxy)benzyl	Bnzl	i-Bu	B
IIF-97	4-ethoxybenzyl	Bnzl	i-Bu	C
IIF-101	4-hydroxybenzyl	Bnzl	i-Pnt	B
IIF-102	Bnzl	naphthalen-2-	i-Bu	A
		ylmethyl
IIF-103	i-Pnt	4-Cl-Bnzl	i-Bu	B
IIF-104	i-Pnt	4-fluorobenzyl	i-Bu	B

TABLE 5-26
Anti-rabies activity of compounds of formula XXIIF
Compound					Anti-rabies
number	R1	R2A	R2B	R3	activity
IIF-325	i-Pnt	H	3-Cl-Bnzl	Bnzl	A
IIF-326	i-Pnt	H	4-Cl-Bnzl	Bnzl	A
IIF-327	i-Pnt	H	4-F-Bnzl	Bnzl	A
IIF-328	i-Pnt	H	4-Me-Bnzl	Bnzl	A
IIF-329	i-Pnt	H	4-MeO-Bnzl	Bnzl	A
IIF-330	i-Bu	H	4-Cl-Bnzl	Ph-Et	A
IIF-331	i-Bu	H	3-Cl-Bnzl	Ph-Et	A
IIF-332	i-Bu	H	4-MeO-Bnzl	Ph-Et	A
IIF-333	i-Bu	H	4-Me-Bnzl	Ph-Et	A
IIF-334	i-Bu	H	2-Npm	Ph-Et	A
IIF-335	i-Bu	H	Bnzl	Ph-Pr	A
IIF-336	i-Bu	H	3-Cl-Bnzl	Ph-Pr	A
IIF-337	i-Bu	H	3-F-Bnzl	Ph-Pr	A
IIF-338	Cpm	H	4-OH-Bnzl	2-Cbx-Et	na
IIF-339	i-Bu	H	3-Me-Bnzl	Ph-Pr	A
IIF-340	i-Bu	H	3-MeO-Bnzl	Ph-Pr	A
IIF-341	i-Bu	H	3-Cl-Bnzl	Ph-Bu	A
IIF-342	i-Bu	H	3-F-Bnzl	Ph-Bu	A
IIF-343	i-Bu	H	3-Me-Bnzl	Ph-Bu	A
IIF-344	i-Bu	H	3-MeO-Bnzl	Ph-Bu	A
IIF-345	i-Bu	H	Bnzl	Ph-Bu	A
IIF-346	i-Pnt	H	3-F-Bnzl	Ph-Pr	A
IIF-370	i-Pnt	H	Ph-Et	Bnzl	A
IIF-371	i-Pnt	H	1-Npm	Bnzl	A
IIF-372	i-Bu	H	4-F-Bnzl	Ph-Et	A
IIF-373	i-Bu	H	Ph-Et	Ph-Et	A
IIF-374	i-Bu	H	1-Npm	Ph-Et	A
IIF-376	4-F-Bnzl	H	1-Npm	i-Bu	A

Example 3: Efficacy in a Mouse Model of Rabies

In this example, it was tested whether the compound of the present disclosure is effective in a rabies mouse model.

(Materials and Methods)

Recombinant rabies virus 1088 strain expressing Red Firefly Luciferase (RFLuc) (1088/RFLuc) was generated by replacing the E2Cr gene of the recombinant virus 1088/E2Cr with the RFLuc gene (Isomura M, Yamada K, Noguchi K, Nishizono A. Near-infrared fluorescent protein iRFP720 is optimal for in vivo fluorescence imaging of rabies virus infection. J Gen Virol. 2017, 98(11): 2689-2698. doi: 10.1099/jgv.0.000950.). Hairless mice (Hos: HR-1, 6-week old, female; Hoshino Laboratory Animals) were inoculated with 1×10⁵ infectious units of 1088/RFLuc intramuscularly into the right hindlimb and administered the test compound intraperitoneally for 6 days (Day 0 to Day 6), beginning 1 hour after inoculation. Actually, 0.5 mL of the solution (2% DMSO, 2% Solutol HS 15, and penicillin/streptomycin-added Dulbecco's phosphate buffered saline, available from Nacalai tesque, Sigma-Aldrich, etc.) supplemented with/without the compound (25 mg/kgBW) was administered twice daily with a 6-hour interval between doses. The inoculated mice were monitored for clinical signs and weighed everyday. The viral dynamics in the treated mice were observed longitudinally using in vivo imaging as follows; mice were administered D-Luciferin solution (150 mg/kgBW; Wako Pure Chemical Industry) intraperitoneally and then imaged (exposure time of 2 minutes and electron-multiplying gain of 300) with the Lumazone imaging system (Nippon Roper) under 2% isoflurane inhalation anesthesia after 15 minutes of substrate injection. The obtained images (16-bit TIFF) were processed and analysed using the ImageJ software. The compounds listed in Table 5 that were evaluated in Example 2 were tested as the test compounds.

(Results)

On days 6 and 8 after virus inoculation, the viral dynamics and the effect of the test compounds were observed in the mice, where the virus-driven luciferase luminescence served as an indicator. It was observed that the viral propagation and dissemination in the brain and spinal cord were significantly suppressed in three of four infected mice that were given the test compound at 50 mg/kgBW/day for 6 days (Days 0 to 5) compared to the solvent administered group, indicating that the antiviral effect of the test compounds on rabies virus was also confirmed in the infected mouse model. In other words, the compounds listed in Table 5 that were evaluated in Example 2 were confirmed to attain a significant therapeutic/prophylactic effect. For the nucleic acid analog drug favipiravir (product name: Avigan tablet/Toyama Chemical), which was confirmed to be effective on rabies virus, a significant prophylactic effect was confirmed in ddY mice given in a dose of 300 mg/kgBW/day, but not 100 mg/kgBW/day, for 7 days immediately after viral inoculation (Yamada K, Noguchi K, Komeno T, Furuta Y, Nishizono A. Efficacy of Favipiravir (T-705) in Rabies Postexposure Prophylaxis. J Infect Dis. 2016, 213(8): 1253-1261.doi:10.1093/infdis/jiv586.). Therefore, the present compound can be provided as a novel and highly effective rabies therapeutic agent that has a different mechanism of action from favipiravir.

Example 4: Anti-Cancer Cell Activity Evaluation Method

The minimum inhibitory concentration (MIC) with respect to cells was evaluated for compounds in Example 2 with which cell death of the host, i.e., mouse neuroblastoma cell strain Neuro-2A, was observed.

Each tested compound prepared as a 10 mM with DMSO was first diluted to 100 μM or 40 μM with 10% fetal bovine serum-supplemented medium, and further diluted with the medium to the final concentration of interest. Fifty microlitter of the diluted medium was added dropwise to each well of a 96-well plate. Furthermore, 50 μL of medium comprising 4×10² infectious units of 1088/GLuc and 4×10⁴ Neuro-2a cells were added to each well. The plate was shaken for 30 seconds with the microplate mixer NS-4P and then cultured for 3 days at 37° C. in the presence of 5% CO₂. After incubation, 25 μL of coelenterazine was added dropwise to each well of the plate, and the plate was immediately loaded into the luminescent plate reader LuMate and shaken for 10 seconds. The relative light unit (RLU) was then measured, and entries in which a cell death caused due to virus infection were excluded.

The following tables show the results of evaluating the compounds. Some compounds were evaluated as a mixture as shown in the following tables. The compounds are classified as a if the minimum inhibitory concentration (MIC) is 10 μM or less, b if greater than 10 μM and less than or equal to 20 μM, and c if greater than 20 μM and less than or equal to 40 μM. The ‘na’ indicates not applicable.

TABLE 6-1
Anti-cancer cell activity of compounds of formula XXIB
Compound						Anti-cancer
number	R1	R2A	R2B	R3	R4	cell activity
IB-924	4-Me-	H	Bnzl	i-Bu	N-isobutyl-	na
	Bnzl				aminocarbonyl
IB-925	i-Bu	H	4-Cl-Bnzl	Ph-Et	H	c
IB-926	i-Bu	H	3-Cl-Bnzl	Ph-Et	H	b
IB-927	i-Bu	H	4-MeO-Bnzl	Ph-Et	H	c
IB-928	i-Bu	H	4-Me-Bnzl	Ph-Et	H	c
IB-929	i-Bu	H	2-Npm	Ph-Et	H	b
IB-930	i-Bu	H	Bnzl	Ph-Pr	H	c
IB-931	i-Bu	H	3-Cl-Bnzl	Ph-Pr	H	c
IB-932	i-Bu	H	3-F-Bnzl	Ph-Pr	H	c
IB-933	i-Bu	H	3-Me-Bnzl	Ph-Pr	H	b
IB-934	i-Bu	H	3-MeO-Bnzl	Ph-Pr	H	b
IB-935	i-Bu	H	3-Cl-Bnzl	Ph-Bu	H	c
IB-936	i-Bu	H	3-F-Bnzl	Ph-Bu	H	b
IB-937	i-Bu	H	3-Me-Bnzl	Ph-Bu	H	c
IB-938	i-Bu	H	3-MeO-Bnzl	Ph-Bu	H	c
IB-939	i-Bu	H	Bnzl	Ph-Bu	H	c
IB-940	i-Pnt	H	3-F-Bnzl	Ph-Pr	H	c
IB-957	i-Bu	H	Ph-Et	Ph-Et	H	c
IB-958	i-Bu	H	1-Npm	Ph-Et	H	b
(a: MIC ≤ 10 μM,
b: 10 μM < MIC ≤ 20 μM,
c: 20 μM < MIC ≤ 40 μM)

TABLE 6-2
Anti-cancer cell activity of compounds of formula XXIF
Compound						Anti-cancer
number	R1	R2A	R2B	R3	R4	cell activity
IF-885	i-Bu	H	4-Cl-Bnzl	Ph-Et	H	c
IF-886	i-Bu	H	3-Cl-Bnzl	Ph-Et	H	c
IF-887	i-Bu	H	4-MeO-Bnzl	Ph-Et	H	c
IF-888	i-Bu	H	4-Me-Bnzl	Ph-Et	H	na
IF-889	i-Bu	H	2-Npm	Ph-Et	H	b
IF-890	i-Bu	H	Bnzl	Ph-Pr	H	c
IF-891	i-Bu	H	3-Cl-Bnzl	Ph-Pr	H	b
IF-892	i-Bu	H	3-F-Bnzl	Ph-Pr	H	c
IF-893	i-Bu	H	3-Me-Bnzl	Ph-Pr	H	c
IF-894	i-Bu	H	3-MeO-Bnzl	Ph-Pr	H	c
IF-895	i-Bu	H	3-Cl-Bnzl	Ph-Bu	H	b
IF-896	i-Bu	H	3-F-Bnzl	Ph-Bu	H	b
IF-897	i-Bu	H	3-Me-Bnzl	Ph-Bu	H	b
IF-898	i-Bu	H	3-MeO-Bnzl	Ph-Bu	H	c
IF-899	i-Bu	H	Bnzl	Ph-Bu	H	c
IF-900	i-Pnt	H	3-F-Bnzl	Ph-Pr	H	c
IF-909	i-Bu	H	Ph-Et	Ph-Et	H	na

TABLE 6-3
Anti-cancer cell activity of compounds of formula XXIIB and
formula XXIIF
Compound					Anti-cancer
number	R1	R2A	R2B	R3	cell activity
Mixture of	i-Pnt	H	3-Cl-Bnzl	Bnzl	c
IIB-326 and
IIF-325
Mixture of	i-Pnt	H	4-Me-Bnzl	Bnzl	c
IIB-327 and
IIF-328
Mixture of	i-Pnt	H	4-MeO-Bnzl	Bnzl	na
IIB-328 and
IIF-329
IIB-329	Me	H	quinolin-8-	Bnzl	na
			ylethyl
IIB-330	Me	H	quinolin-5-	Bnzl	na
			ylethyl
IIB-331	i-Bu	H	4-Cl-Bnzl	Ph-Et	c
IIB-332	i-Bu	H	3-Cl-Bnzl	Ph-Et	b
IIB-333	i-Bu	H	4-MeO-Bnzl	Ph-Et	na
IIB-334	i-Bu	H	4-Me-Bnzl	Ph-Et	c
IIB-335	i-Bu	H	2-Npm	Ph-Et	c
IIB-336	i-Bu	H	Bnzl	Ph-Pr	c
IIB-337	i-Bu	H	3-Cl-Bnzl	Ph-Pr	c
IIB-338	i-Bu	H	3-F-Bnzl	Ph-Pr	c
IIB-339	Cpm	H	4-OH-Bnzl	2-Cbx-Et	na
IIB-340	i-Bu	H	3-Me-Bnzl	Ph-Pr	c
IIB-341	i-Bu	H	3-MeO-Bnzl	Ph-Pr	c
IIB-342	i-Bu	H	3-Cl-Bnzl	Ph-Bu	b
IIB-343	i-Bu	H	3-F-Bnzl	Ph-Bu	c
IIB-344	i-Bu	H	3-Me-Bnzl	Ph-Bu	b
IIB-345	i-Bu	H	3-MeO-Bnzl	Ph-Bu	c
IIB-346	i-Bu	H	Bnzl	Ph-Bu	b
IIB-347	i-Pnt	H	3-F-Bnzl	Ph-Pr	c
Mixture of	i-Pnt	H	4-F-Bnzl	Bnzl	b
IIB-371 and
IIF-327
Mixture of	i-Pnt	H	Ph-Et	Bnzl	na
IIB-372 and
IIF-370
Mixture of	i-Pnt	H	1-Npm	Bnzl	c
IIB-373 and
IIF-371
IIB-374	i-Bu	H	4-F-Bnzl	Ph-Et	c
IIB-375	i-Bu	H	Ph-Et	Ph-Et	na
IIB-376	i-Bu	H	1-Npm	Ph-Et	c
IIB-378	4-F-Bnzl	H	1-Npm	i-Bu	b

TABLE 6-4
(continuation)
Compound					Anti-cancer
number	R1	R2A	R2B	R3	cell activity
IIF-326	i-Pnt	H	4-Cl-Bnzl	Bnzl	b
IIF-330	i-Bu	H	4-Cl-Bnzl	Ph-Et	c
IIF-331	i-Bu	H	3-Cl-Bnzl	Ph-Et	c
IIF-332	i-Bu	H	4-MeO-Bnzl	Ph-Et	na
IIF-333	i-Bu	H	4-Me-Bnzl	Ph-Et	c
IIF-334	i-Bu	H	2-Npm	Ph-Et	c
IIF-335	i-Bu	H	Bnzl	Ph-Pr	na
IIF-336	i-Bu	H	3-Cl-Bnzl	Ph-Pr	c
IIF-337	i-Bu	H	3-F-Bnzl	Ph-Pr	b
IIF-338	Cpm	H	4-OH-Bnzl	2-Cbx-Et	na
IIF-339	i-Bu	H	3-Me-Bnzl	Ph-Pr	c
IIF-340	i-Bu	H	3-MeO-Bnzl	Ph-Pr	na
IIF-341	i-Bu	H	3-Cl-Bnzl	Ph-Bu	b
IIF-342	i-Bu	H	3-F-Bnzl	Ph-Bu	c
IIF-343	i-Bu	H	3-Me-Bnzl	Ph-Bu	c
IIF-344	i-Bu	H	3-MeO-Bnzl	Ph-Bu	c
IIF-345	i-Bu	H	Bnzl	Ph-Bu	c
IIF-346	i-Pnt	H	3-F-Bnzl	Ph-Pr	c
IIF-372	i-Bu	H	4-F-Bnzl	Ph-Et	c
IIF-373	i-Bu	H	Ph-Et	Ph-Et	c
IIF-374	i-Bu	H	1-Npm	Ph-Et	c
IIF-376	4-F-Bnzl	H	1-Npm	i-Bu	c

[Note]

As disclosed above, the present disclosure is exemplified by the use of its preferred embodiments. However, it is understood that the scope of the present disclosure should be interpreted based solely on the Claims. It is also understood that any patent, any patent application, and any other references cited herein should be incorporated herein by reference in the same manner as the contents are specifically described herein. The present application is a continuation-in-part application that claims priority to Japanese Patent Application No. 2018-153227 filed on Aug. 16, 2018 and International Publication No. PCT/JP2019/032032 filed on Aug. 15, 2019 with the Japan Patent Office. The entire content thereof is incorporated herein by reference.

INDUSTRIAL APPLICABILITY

The present disclosure is useful in the field of rabies and cancer treatment and prophylaxis.

Claims

1. A compound represented by formula XXIF:

2. A compound represented by formula XXIB:

3. The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to claim 1, wherein the alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, and carbonyl of R1, R3, and R4 are each independently and optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group I, andthe alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, and carbonyl of R2A and R2B, and the non-aryl heterocycle and the heteroaryl ring are each independently and optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group I.

4. The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to claim 1, (1) wherein R1, R3, and R4 are each independently, hydrogen,optionally substituted alkyl,optionally substituted cycloalkyl,optionally substituted heterocycloalkyl,optionally substituted aryl,optionally substituted heteroaryl, oroptionally substituted carbonyl,R2A and R2B are each independently, hydrogen,optionally substituted alkyl,optionally substituted cycloalkyl,optionally substituted heterocycloalkyl,optionally substituted aryl,optionally substituted heteroaryl, oroptionally substituted carbonyl, orR2A and R2B, together with the nitrogen atom to which they are attached, form a non-aryl heterocycle or heteroaryl ring, wherein the non-aryl heterocycle and the heteroaryl ring are each independently and optionally substituted-, or(2) wherein(2) wherein R1, R3, and R4 are each independently, hydrogen,optionally substituted alkyl,optionally substituted arylalkyl,optionally substituted cycloalkyl,optionally substituted heterocycloalkyl,formyl,optionally substituted alkylcarbonyl,optionally substituted alkoxycarbonyl,optionally substituted arylcarbonyl,optionally substituted aryloxycarbonyl,optionally substituted heteroarylcarbonyl,optionally substituted heteroaryloxycarbonyl,optionally substituted cycloalkylcarbonyl,optionally substituted cycloalkyloxycarbonyl,optionally substituted heterocycloalkylcarbonyl,optionally substituted heterocycloalkyloxycarbonyl,carbamoyl,optionally substituted alkylcarbamoyl,optionally substituted alkoxycarbamoyl,optionally substituted arylcarbamoyl,optionally substituted heteroarylcarbamoyl,optionally substituted cycloalkylcarbamoyl, oroptionally substituted heterocycloalkylcarbamoyl,wherein the groups of R1, R3, and R4 are optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group II,R2A and R2B are each independently, hydrogen,optionally substituted alkyl,optionally substituted arylalkyl,optionally substituted cycloalkyl,optionally substituted heterocycloalkyl,formyl,optionally substituted alkylcarbonyl,optionally substituted alkoxycarbonyl,optionally substituted arylcarbonyl,optionally substituted aryloxycarbonyl,optionally substituted heteroarylcarbonyl,optionally substituted heteroaryloxycarbonyl,optionally substituted cycloalkylcarbonyl,optionally substituted cycloalkyloxycarbonyl,optionally substituted heterocycloalkylcarbonyl,optionally substituted heterocycloalkyloxycarbonyl,carbamoyl,optionally substituted alkylcarbamoyl,optionally substituted alkoxycarbamoyl,optionally substituted arylcarbamoyl,optionally substituted heteroarylcarbamoyl,optionally substituted cycloalkylcarbamoyl, oroptionally substituted heterocycloalkylcarbamoyl,wherein the groups of R2A and R2B are optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group II, orR2A and R2B together with the nitrogen atom to which they are attached, form a 5- to 6-membered non-aryl heterocycle or heteroaryl ring, wherein the non-aryl heterocycle and the heteroaryl ring are optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group II.

5. (canceled)

6. The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to claim 1, (1) wherein R1 and R4 are each independently, hydrogen,optionally substituted alkyl,optionally substituted arylalkyl,optionally substituted cycloalkyl,formyl,optionally substituted alkylcarbonyl,optionally substituted alkoxycarbonyl,optionally substituted arylcarbonyl,optionally substituted aryloxycarbonyl,optionally substituted cycloalkylcarbonyl,optionally substituted cycloalkyloxycarbonyl,optionally substituted heterocycloalkylcarbonyl,optionally substituted heterocycloalkyloxycarbonyl,carbamoyl,optionally substituted alkylcarbamoyl,optionally substituted alkoxycarbamoyl,optionally substituted arylcarbamoyl,optionally substituted heteroarylcarbamoyl,optionally substituted cycloalkylcarbamoyl, oroptionally substituted heterocycloalkylcarbamoyl, wherein the groups of R1 and R4 are optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group III; or(2) wherein R1 and R4 are each independently, hydrogen,optionally substituted alkyl,optionally substituted arylalkyl,formyl,optionally substituted alkylcarbonyl,optionally substituted alkoxycarbonyl,optionally substituted arylcarbonyl,optionally substituted aryloxycarbonyl,carbamoyl, oroptionally alkylcarbamoyl,wherein the croups of R1 and R4 are optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group III; or(3) wherein R1 and R4 are each independently, hydrogen,alkyl,alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amino, substituted amino, substituted oxy, substituted carbonyl, cycloalkyl, and substituted cycloalkyl,arylalkyl,arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, alkyl, substituted alkyl, hydroxy, substituted oxy, amino, substituted amino, and nitro,formyl,substituted carbonyl, orsubstituted oxycarbonyl,wherein the substituted amino, substituted oxy, substituted alkyl, substituted, carbonyl, substituted cycloalkyl, substituted carbonyl, and substituted oxycarbonyl in R1 and R4 each independently have one to the maximum substitutable number of the same or different substituents selected from substituent group IV; or(4) wherein R1 and R4 are each independently, hydrogen,alkyl,alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amidinoamino, alkoxy, alkoxycarbonyl, carbamoyl, carboxy, hydroxy, trialkylsilyloxy, and cycloalkyl,arylalkyl,arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, alkyl, haloalkyl, alkoxy, haloalkoxy, amino, substituted amino, nitro, and hydroxy,formyl,alkylcarbonyl,arylalkylcarbonyl,arylalkyloxycarbonyl,alkoxycarbonyl,arylcarbonyl,carbamoyl,alkylcarbamoyl, orarylalkylcarbamoyl,wherein the substituted aminos each independently have one to the maximum substitutable number of the same or different substituents selected from substituent group IV.

7-9. (canceled)

10. The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to claim 1, (1) wherein R3 is hydrogen,alkyl,alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amino, substituted amino, carboxy, substituted oxycarbonyl, carbamoyl, substituted aminocarbonyl, hydroxy, substituted oxy, cycloalkyl, and substituted cycloalkyl,arylalkyl, orarylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, alkyl, substituted alkyl, carboxy, substituted oxycarbonyl, hydroxy, and substituted oxy,wherein the substituted amino, substituted oxy, substituted oxycarbonyl, substituted aminocarbonyl, substituted alkyl, substituted cycloalkyl, substituted carbonyl, and substituted oxycarbonyl in R3 each independently have one to the maximum substitutable number of the same or different substituents selected from substituent group IV; or(2) wherein R3 is hydrogen, alkyl,alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consist of amidinoamino, alkoxycarbonyl, carbamoyl, carboxy, hydroxy, trialkylsilyloxy, amino, alkoxycarbonylamino, and cycloalkyl,arylalkyl, orarylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, alkyl, alkoxycarbonyl, and hydroxy, or(3) wherein R3 is alkyl, alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amidinoamino, carbamoyl, carboxy, hydroxy, and cycloalkyl,arylalkyl, orarylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of alkyl and hydroxy.

11. (canceled)

12. The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to claim 1, (1) wherein R2A and R2B are each independently, hydrogen,alkyl,alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of formyl, substituted carbonyl, hydroxy, substituted oxy, amino, substituted amino, cycloalkyl, substituted cycloalkyl, heterocycloalkyl, and substituted heterocycloalkyl,arylalkyl,arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, alkyl, substituted alkyl, hydroxy, and substituted oxy,heteroarylalkyl,substituted heteroarylalkyl,cycloalkyl, orsubstituted cycloalkyl,wherein the substituted carbonyl, substituted oxy, substituted amino, substituted cycloalkyl, substituted heterocycloalkyl, substituted heteroarylalkyl, and substituted alkyl in R2A and R2B each independently have one to the maximum substitutable number of the same or different substituents selected from substituent group IV, orR2A and R2B, together with the nitrogen atom to which they are attached, form a non-aryl heterocycle, wherein the non-aryl heterocycle is optionally substituted with one or up to the maximum substitutable number of the same or different substituents selected from substituent group VI; or(2) wherein R2A and R2B are each independently, hydrogen,alkyl,alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amidinoamino, alkoxy, alkoxycarbonyl, carbamoyl, carboxy, hydroxy, amino, alkoxycarbonylamino, cycloalkyl, and heterocycloalkyl,arylalkyl,arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, alkyl, haloalkyl, alkoxy, and hydroxy,heteroarylalkyl,alkoxycarbonyl-substituted heteroarylalkyl, orcycloalkyl, orR2A and R2B, together with the nitrogen atom to which they are attached, form a 5- to 6-membered non-aryl heterocycle, wherein the non-aryl heterocycle is optionally substituted with one or up to the maximum substitutable number of the same or different substituents selected from substituent group VI, or(3) wherein R2A is hydrogen,R2B is alkyl, alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amidinoamino, carbamoyl, carboxy, hydroxy, and cycloalkyl,arylalkyl,arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, alkyl haloalkyl, alkoxy, and hydroxy, orcycloalkyl.

13. (canceled)

14. The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to claim wherein R1 is alkyl,alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amidinoamino, carbamoyl, carboxy, hydroxy, and cycloalkyl,arylalkyl, orarylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, alkyl, haloalkyl, alkoxy, substituted amino, and hydroxy,wherein the substituted amino has one to the maximum substitutable number of the same or different substituents selected from substituent group IV.

15.-16. (canceled)

17. The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to claim 1, wherein R4 is hydrogen,alkyl,alkylcarbonyl,arylalkylcarbonyl,arylalkyloxycarbonyl,alkoxycarbonyl,carbamoyl, orarylalkylcarbamoyl.

18.-40. (canceled)

41. A method for the prophylaxis or treatment of rabies, comprising administering a therapeutically effective amount of the compound according to claim 1, or a pharmaceutically acceptable salt thereof, to a subject in need thereof.

42. A method for the prophylaxis or treatment of cancer, comprising administering a therapeutically effective amount of the compound according to claim 1, or a pharmaceutically acceptable salt thereof, to a subject in need thereof.

43. The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to claim 2, wherein the alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, and carbonyl of R1, R3, and R4 are each independently and optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group I, andthe alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, and carbonyl of R2A and R2B, and the non-aryl heterocycle and the heteroaryl ring are each independently and optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group I.

44. The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to claim 2, (1) wherein R1, R3, and R4 are each independently, hydrogen,optionally substituted alkyl,optionally substituted cycloalkyl,optionally substituted heterocycloalkyl,optionally substituted aryl,optionally substituted heteroaryl, oroptionally substituted carbonyl,R2A and R2B are each independently, hydrogen,optionally substituted alkyl,optionally substituted cycloalkyl,optionally substituted heterocycloalkyl,optionally substituted aryl,optionally substituted heteroaryl, oroptionally substituted carbonyl, orR2A and R2B, together with the nitrogen atom to which they are attached, form a non-aryl heterocycle or heteroaryl ring, wherein the non-aryl heterocycle and the heteroaryl ring are each independently and optionally substituted, or(2) wherein R1, R3, and R4 are each independently, hydrogen,optionally substituted alkyl,optionally substituted arylalkyl,optionally substituted cycloalkyl,optionally substituted heterocycloalkyl,formyl,optionally substituted alkylcarbonyl,optionally substituted alkoxycarbonyl,optionally substituted arylcarbonyl,optionally substituted aryloxycarbonyl,optionally substituted heteroarylcarbonyl,optionally substituted heteroaryloxycarbonyl,optionally substituted cycloalkylcarbonyl,optionally substituted cycloalkyloxycarbonyl,optionally substituted heterocycloalkylcarbonyl,optionally substituted heterocycloalkyloxycarbonyl,carbamoyl,optionally substituted alkylcarbamoyl,optionally substituted alkoxycarbamoyl,optionally substituted arylcarbamoyl,optionally substituted heteroarylcarbamoyl,optionally substituted cycloalkylcarbamoyl, oroptionally substituted heterocycloalkylcarbamoyl, wherein the groups of R1, R3, and R4 are optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group II,R2A and R2B are each independently, hydrogen,optionally substituted alkyl,optionally substituted arylalkyl,optionally substituted cycloalkyl,optionally substituted heterocycloalkyl,formyl,optionally substituted alkylcarbonyl,optionally substituted alkoxycarbonyl,optionally substituted arylcarbonyl,optionally substituted aryloxycarbonyl,optionally substituted heteroarylcarbonyl,optionally substituted heteroaryloxycarbonyl,optionally substituted cycloalkylcarbonyl,optionally substituted cycloalkyloxycarbonyl,optionally substituted heterocycloalkylcarbonyl,optionally substituted heterocycloalkyloxycarbonyl,carbamoyl, optionally substituted alkylcarbamoyl,optionally substituted alkoxycarbamoyl,optionally substituted arylcarbamoyl,optionally substituted heteroarylcarbamoyl,optionally substituted cycloalkylcarbamoyl, oroptionally substituted heterocycloalkylcarbamoyl, wherein the groups of R2A and R2B are optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group II, orR2A and R2B, together with the nitrogen atom to which they are attached, form a 5- to 6-membered non-aryl heterocycle or heteroaryl ring, wherein the non-aryl heterocycle and the heteroaryl ring are optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group II.

45. The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to claim 2, (1) wherein R1 and R4 are each independently, hydrogen,optionally substituted alkyl,optionally substituted arylalkyl,optionally substituted cycloalkyl,formyl,optionally substituted alkylcarbonyl,optionally substituted alkoxycarbonyl,optionally substituted arylcarbonyl,optionally substituted aryloxycarbonyl,optionally substituted cycloalkylcarbonyl,optionally substituted cycloalkyloxycarbonyl,optionally substituted heterocycloalkylcarbonyl,optionally substituted heterocycloalkyloxycarbonyl,carbamoyl,optionally substituted alkylcarbamoyl,optionally substituted alkoxycarbamoyl,optionally substituted arylcarbamoyl,optionally substituted heteroarylcarbamoyl,optionally substituted cycloalkylcarbamoyl, oroptionally substituted heterocycloalkylcarbamoyl, wherein the groups of R1 and R4 are optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group III, or(2) wherein R1 and R4 are each independently, hydrogen,optionally substituted alkyl,optionally substituted arylalkyl,formyl,optionally substituted alkylcarbonyl,optionally substituted alkoxycarbonyl,optionally substituted arylcarbonyl,optionally substituted aryloxycarbonyl,carbamoyl, oroptionally substituted alkylcarbamoyl,wherein the groups of R1 and R4 are optionally substituted with one to the maximum substitutable number of the same or different substituents selected from substituent group III, or(3) wherein R1 and R4 are each independently, hydrogen,alkyl,alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amino, substituted amino, substituted oxy, substituted carbonyl, cycloalkyl, and substituted cycloalkyl,arylalkyl,arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, alkyl, substituted alkyl, hydroxy, substituted oxy, amino, substituted amino, and nitro,formyl,substituted carbonyl, orsubstituted oxycarbonyl,wherein the substituted amino, substituted oxy, substituted alkyl, substituted carbonyl, substituted cycloalkyl, substituted carbonyl, and substituted oxycarbonyl in R1 and R4 each independently have one to the maximum substitutable number of the same or different substituents selected from substituent group IV, or(4) wherein R1 and R4 are each independently, hydrogen,alkyl,alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amidinoamino, alkoxy, alkoxycarbonyl, carbamoyl, carboxy, hydroxy, trialkylsilyloxy, and cycloalkyl,arylalkyl,arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, alkyl, haloalkyl, alkoxy, haloalkoxy, amino, substituted amino, nitro, and hydroxy,formyl,alkylcarbonyl,arylalkylcarbonyl,arylalkyloxycarbonyl,alkoxycarbonyl,arylcarbonyl,aryloxycarbonyl,carbamoyl,alkylcarbamoyl, orarylalkylcarbamoyl,wherein the substituted aminos each independently have one to the maximum substitutable number of the same or different substituents selected from substituent group IV.

46. The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to claim 2, (1) wherein R3 is hydrogen, alkyl,alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amino, substituted amino, carboxy, substituted oxycarbonyl, carbamoyl, substituted aminocarbonyl, hydroxy, substituted oxy, cycloalkyl, and substituted cycloalkyl,arylalkyl, orarylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, alkyl, substituted alkyl, carboxy, substituted oxycarbonyl, hydroxy, and substituted oxy,wherein the substituted amino, substituted oxy, substituted oxycarbonyl, substituted aminocarbonyl, substituted alkyl, substituted cycloalkyl, substituted carbonyl, and substituted oxycarbonyl in R3 each independently have one to the maximum substitutable number of the same or different substituents selected from substituent group IV, or(2) wherein R3 is hydrogen, alkyl,alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amidinoamino, alkoxycarbonyl, carbamoyl, carboxy, hydroxy, trialkylsilyloxy, amino, alkoxycarbonylamino, and cycloalkyl,arylalkyl, orarylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, alkyl, alkoxycarbonyl, and hydroxy, or(3) wherein R3 is alkyl, alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amidinoamino, carbamoyl, carboxy, hydroxy, and cycloalkyl,arylalkyl, orarylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of alkyl and hydroxy.

47. The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to claim 2, (1) wherein R2A and R2B are each independently, hydrogen,alkyl,alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of formyl, substituted carbonyl, hydroxy, substituted oxy, amino, substituted amino, cycloalkyl, substituted cycloalkyl, heterocycloalkyl, and substituted heterocycloalkyl,arylalkyl,arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, alkyl, substituted alkyl, hydroxy, and substituted oxy,heteroarylalkyl,substituted heteroarylalkyl,cycloalkyl, orsubstituted cycloalkyl,wherein the substituted carbonyl, substituted oxy, substituted amino, substituted cycloalkyl, substituted heterocycloalkyl, substituted heteroarylalkyl, and substituted alkyl in R2A and R2B each independently have one to the maximum substitutable number of the same or different substituents selected from substituent group IV, orR2A and R2B, together with the nitrogen atom to which they are attached, form a non-aryl heterocycle, wherein the non-aryl heterocycle is optionally substituted with one or up to the maximum substitutable number of the same or different substituents selected from substituent group VI, or(2) wherein R2A and R2B are each independently, hydrogen,alkyl,alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amidinoamino, alkoxy, alkoxycarbonyl, carbamoyl, carboxy, hydroxy, amino, alkoxycarbonylamino, cycloalkyl, and heterocycloalkyl,arylalkyl,arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, alkyl, haloalkyl, alkoxy, and hydroxy,heteroarylalkyl,alkoxycarbonyl-substituted heteroarylalkyl, orcycloalkyl, orR2A and R2B, together with the nitrogen atom to which they are attached, form a 5- to 6-membered non-aryl heterocycle, wherein the non-aryl heterocycle is optionally substituted with one or up to the maximum substitutable number of the same or different substituents selected from substituent group VI, or(3) wherein R2A is hydrogen,R2B is alkyl, alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amidinoamino, carbamoyl, carboxy, hydroxy, and cycloalkyl,arylalkyl,arylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, alkyl, haloalkyl, alkoxy, and hydroxy, orcycloalkyl.

48. The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to claim 2, wherein R1 is alkyl, alkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of amidinoamino, carbamoyl, carboxy, hydroxy, and cycloalkyl,arylalkyl, orarylalkyl substituted with one to the maximum substitutable number of the same or different substituents selected from the group consisting of halogen, alkyl, haloalkyl, alkoxy, substituted amino, and hydroxy,wherein the substituted amino has one to the maximum substitutable number of the same or different substituents selected from substituent group IV.

49. The compound or an enantiomer thereof, or a salt thereof, or a solvate thereof according to claim 2, wherein R4 is hydrogen, alkyl,alkylcarbonyl,arylalkylcarbonyl,arylalkyloxycarbonyl,alkoxycarbonyl,carbamoyl, orarylalkylcarbamoyl.

50. A method for the prophylaxis or treatment of rabies, comprising administering a therapeutically effective amount of the compound according to claim 2, or a pharmaceutically acceptable salt thereof, to a subject in need thereof.

51. A method for the prophylaxis or treatment of cancer, comprising administering a therapeutically effective amount of the compound according to claim 2 or a pharmaceutically acceptable salt thereof, to a subject in need thereof.