Patent Application
20240408216
The present application claims the priority to the following applications:
The present invention relates to the technical field of pharmaceutics, and particularly, to a PROTAC molecule targeting ALK, ROS1 and EGFR protein and mutein thereof, a pharmaceutical composition, and pharmaceutical use thereof.
PROTAC (proteolysis targeting chimera) has been an emerging hot spot in the research field in recent years. PROTAC molecules can be generally divided into three parts: a war head that binds to a specific target protein, an E3 ligase ligand having ubiquitination functionality, and a linker that connects the two. PROTAC molecules utilize the ubiquitin-proteasome pathway in cells to selectively degrade target proteins. Specifically, since the two ends of PROTAC molecules are ligand fragments of the target protein and E3 ligase, the PROTAC molecule can simultaneously bind to the target protein and E3 ligase, thus promoting ubiquitination of the target protein, such that the target protein is recognized and degraded by a proteasome.
Lung cancer is a serious disease threatening human health, and ranks the first among all malignant tumors in mortality. In patients with non-small cell lung cancer, the proportions of activated mutations of EGFR (epidermal growth factor receptor), ALK (anaplastic lymphoma kinase), and ROS1 (ROS proto-oncogene 1 receptor tyrosine kinase) are approximately 30%, 8% and 2%, respectively.
International Patents Nos. WO2020249048, WO2019113071, WO2019042444, WO2017204445, WO2020069106, WO2019114770, etc., design PROTAC molecules targeting ALK.
Further development of PROTAC molecules having higher efficacy and/or selectivity for diseases resistant to existing EGFR inhibitors, ALK inhibitors, and ROS1 inhibitors may have great research value and potential practical value.
The present invention is intended to develop novel compounds that inhibit and induce EGFR degradation.
The present invention provides a compound of formula (I), or a pharmaceutically acceptable salt, an enantiomer, a diastereomer, a racemate, a solvate, a hydrate, a polymorph, a prodrug or an isotopic variant thereof, and a mixture thereof,
PIN-Linker-E (I)
The present invention further provides a compound of formula (I), or a pharmaceutically acceptable salt, an enantiomer, a diastereomer, a racemate, a solvate, a hydrate, a polymorph, a prodrug or an isotopic variant thereof, and a mixture thereof,
PIN-Linker-E (I)
In one aspect, the present invention provides a compound of formula (I), or a pharmaceutically acceptable salt, an enantiomer, a diastereomer, a racemate, a solvate, a hydrate, a polymorph, a prodrug or an isotopic variant thereof, and a mixture thereof,
PIN-Linker-E (I)
Linker is an all-carbon chain system, W contains no heteroatoms, and Linker is not methylene, ethylene and propylene.
Rk1 and Rk2 are each independently hydrogen, F, Cl, Br, I, amino, hydroxy, cyano, acetyl, C1-5 alkyl, C1-5 haloalkyl, C1-5 alkoxy, C1-3 alkylene-OC1-3 alkyl, C3-6 cycloalkyl, or C3-6 heterocycloalkyl; preferably, Rk2 is hydrogen, methyl, ethyl, propyl, isopropyl, methoxy, ethoxy, propoxy, isopropoxy, cyclopropyl, cyclobutyl, or —O-oxetanyl; preferably, Rk2 and Rk4 are each independently selected from hydrogen, deuterium, halogen, cyano, acylamino, C1-5 alkyl, C1-5 haloalkyl, C1-5 alkoxy, C1-3 alkylene-OC1-3 alkyl, C3-6 cycloalkyl, or C3-6 heterocycloalkyl, wherein the C1-5 alkyl, C1-5 haloalkyl, C1-5 alkoxy, C1-3 alkylene-OC1-3 alkyl, C3-6 cycloalkyl, or C3-6 heterocycloalkyl is optionally substituted with 0, 1, 2, 3, or more substituents selected from deuterium, hydroxy, cyano, C1-5 alkyl, C1-5 haloalkyl, or C1-5 alkoxy; preferably RK4 is selected from hydrogen, deuterium, acylamino, cyano, or C1-5 alkyl, preferably methyl, ethyl, propyl, isopropyl, C1-5 haloalkyl, and C1-5 alkoxy.
In some embodiments, the pharmaceutically acceptable salt may be a hydrochloride, a formate, or a trifluoroacetate.
In some embodiments, Rk1 and Rk2 are each independently hydrogen, F, Cl, Br, I, amino, hydroxy, cyano, acetyl, C1-5 alkyl, C1-5 haloalkyl, —CONH2, C1-5 alkoxy, C1-3 alkylene-OC1-3 alkyl, C3-6 cycloalkyl, or C3-6 heterocycloalkyl; preferably, Rk2 is hydrogen, methyl, ethyl, propyl, isopropyl, methoxy, ethoxy, propoxy, isopropoxy, cyclopropyl, cyclobutyl, or —O-oxetanyl; preferably, Rk2 and Rk4 are each independently selected from hydrogen, deuterium, halogen, cyano, acylamino, C1-5 alkyl, C1-5 haloalkyl, C1-5 alkoxy, C1-3 alkylene-OC1-3 alkyl, C3-6 cycloalkyl, and C3-6 heterocycloalkyl, wherein the C1-5 alkyl, C1-5 haloalkyl, C1-5 alkoxy, C1-3 alkylene-OC1-3 alkyl, C3-6 cycloalkyl, or C3-6 heterocycloalkyl is optionally substituted with 0, 1, 2, 3, or more substituents selected from deuterium, halogen, hydroxy, cyano, C1-5 alkyl, C1-5 haloalkyl, and C1-5 alkoxy;
In some embodiments, Rk2 is hydrogen, cyano, F, Cl, Br, I, C1-5 alkyl, —CONH2, C1-5 haloalkyl, or C1-5 alkoxy, wherein the C1-5 alkyl or C1-5 alkoxy is optionally substituted with 1, 2, 3, 4, or more groups selected from the following B2 groups, and the B2 group is selected from deuterium, halo, hydroxy, cyano, C1-5 alkyl, C1-5 haloalkyl, and C1-5 alkoxy.
In some embodiments, Rk2 is hydrogen, F, Cl, Br, I, C1-5 alkyl, —CONH2, C1-5 haloalkoxy, or C1-5 alkoxy. In some embodiments, Rk4 is hydrogen, F, Cl, Br, I, cyano, acetyl, or C1-5 alkoxy, preferably hydrogen or C1-5 alkoxy.
In some embodiments, Rk2 is —CONH2.
In some embodiments, X1 is selected from O, S, NR00, —C(O)—, —S(O)—, SO2, —C(O)NR00—, —NR00C(O)—, —SO2NR00—, —NR00SO2—, —NR00C(O)NR00—, —NR00C(O)O—, —OC(O)O—, —CH═CH—, —C≡C—, C1-5 alkylene, C3-6 cycloalkylene, 3- to 6-membered heterocycloalkylene, phenylene, 5- to 6-membered heteroarylene, and 8- to 10-membered bicyclic heteroarylene, wherein R00 is selected from hydrogen or C1-3 alkyl (preferably methyl, ethyl, or propyl; preferably hydrogen or methyl).
In some embodiments, X1 is —(CRx1Rx2)x—,
Preferably, the hydrogen of the compound of formula (I) described above is optionally substituted by deuterium.
In some embodiments, Rx is hydrogen, cyano, hydroxy, acetyl, halogen, amino, C1-5 alkyl, C1-5 haloalkyl, C1-5 alkoxy, C2-10 alkenyl, C2-10 alkynyl, C3-6 cycloalkyl, 3- to 6-membered heterocycloalkyl, benzene, 5- to 6-membered heteroaryl, or 8- to 10-membered bicyclic heteroaryl.
In some embodiments, Rk3 is selected from F, Cl, Br, I, hydroxy, cyano, formyl, nitro, carboxy, acetyl, SOC1-5 alkyl, SO2C1-5 alkyl, C1-5 alkyl, C1-5 haloalkyl, C1-5 alkoxy, C1-5 alkylene-OC1-5 alkyl, C3-6 cycloalkyl, 3- to 6-membered heterocycloalkyl, —O—C3-6 cycloalkyl, and —O-3- to 6-membered heterocycloalkyl;
Preferably, Rk3 is a C1-6 alkyl, C1-6 haloalkyl, C1-6 alkoxy, C1-5 alkylene-OC1-5 alkyl, C3-6 cycloalkyl, 3- to 6-membered heterocycloalkyl, —O—C3-6 cycloalkyl, or —O-3- to 6-membered heterocycloalkyl, wherein the C1-6 alkyl, C1-6 haloalkyl, C1-6 alkoxy, C1-5 alkylene, C1-5 alkyl, C3-6 cycloalkyl, or 3- to 6-membered heterocycloalkyl is optionally substituted with 0, 1, 2, 3, 4, or 5 substituents selected from deuterium, halogen, hydroxy, cyano, C1-3 alkyl, C1-3 haloalkyl, and C1-3 alkoxy; preferably C1-6 alkyl; more preferably C1-3 alkyl;
In some embodiments, Rk3 represents —X1—Rx,
In some embodiments, X1 is a 5- to 6-membered heteroarylene or 8- to 10-membered bicyclic heteroarylene, and
In some embodiments, Rk3 is selected from:
Preferably, Rk3 is a 5- or 6-membered heterocyclyl substituted with 0, 1, or 2 substituents selected from Rb, wherein Rb is selected from hydrogen, deuterium, halogen, cyano, C1-5 alkyl, C1-5 haloalkyl, and C1-5 alkoxy.
Preferably, Rk3 is selected from
Preferably, Rk3 is selected from
F, Cl, Br, I, cyano, acetyl, ethyl, C1-5 alkylene-OC1-5 alkyl, and C3-6 cycloalkyl, wherein the C1-5 alkyl is optionally substituted with 0, 1, 2, 3, 4, or 5 substituents selected from deuterium, hydroxy, cyano, C1-3 alkyl, and C1-3 alkoxy; Ra is H, methyl, ethyl, propyl, or isopropyl; Rb is H, methyl, ethyl, propyl, isopropyl, methoxy, ethoxy, propoxy, isopropoxy, cyclopropyl, cyclobutyl, oxetanyl, fluoromethyl, difluoromethyl, trifluoromethyl, —CH2CH2F, —CHFCH3, —CH2CHF2, —CF2CH3, —CHFCH2F, —CH2CF3, —CF2CH2F, or —CHFCHF2.
Preferably, Rk3 is selected from
F, Cl, Br, I, cyano, acetyl, ethyl, C1-5 alkylene-OC1-5 alkyl, and C3-6 cycloalkyl, wherein the C1-5 alkyl is optionally substituted with 0, 1, 2, or 3 substituents selected from deuterium, hydroxy, cyano, C1-3 alkyl, and C1-3 alkoxy; Ra is H, methyl, ethyl, propyl, or isopropyl; Rb is H, methyl, ethyl, propyl or isopropyl.
In some embodiments, Rk1 and Rk4 are hydrogen.
In some embodiments, R4 is hydroxy, cyano, acetyl, carboxy, nitro, halogen, amino, C1-6 alkyl, C1-6 haloalkyl, C1-6 alkoxy, C1-6 alkylthio, C2-6 alkenyl, C2-6 alkynyl, NRaRb, C3-8 cycloalkyl, 3- to 8-membered heterocyclyl, C6-10 aryl, or 5- to 14-membered heteroaryl, wherein the C1-6 alkyl, C1-6 haloalkyl, C1-6 alkoxy, C1-6 alkylthio, C2-6 alkenyl, C2-6 alkynyl, C3-8 cycloalkyl, 3- to 8-membered heterocyclyl, C6-10 aryl, or 5- to 14-membered heteroaryl is optionally substituted with 0, 1, 2, or 3 R41s;
In some embodiments, R4 is hydrogen, hydroxy, cyano, C(O)NRaRb, halogen, C1-10 alkyl substituted with 0, 1, or 2 R41s, or 5- to 6-membered heteroaryl substituted with 0, 1, or 2 R41s; the heteroatom of the 5- to 6-membered heteroaryl is selected from one or more of nitrogen, oxygen, and sulfur, and the number of the heteroatom is 1, 2, or 3;
In some embodiments, R4 is hydrogen, halogen, or 5- to 6-membered heteroaryl; the heteroatom of the 5- to 6-membered heteroaryl is nitrogen, and the number of the heteroatom is 1, 2, or 3;
In some embodiments, ring A is a 3- to 8-membered monocyclic heterocyclylene, 7- to 16-membered spiroheterocyclylene, 7- to 14-membered fused heterocyclylene, 7- to 10-membered bridged heterocyclylene, phenylene, 5- or 6-membered monocyclic heteroarylene, or 8- to 10-membered bicyclic heteroarylene;
In some embodiments, ring A is a 3- to 8-membered monocyclic heterocyclylene or 7- to 16-membered spiroheterocyclylene; the heteroatom of the monocyclic heterocyclylene is selected from one or more of nitrogen, oxygen, and sulfur, and the number of the heteroatom is 1, 2, or 3; the heteroatom of the spiroheterocyclylene is selected from one or more of nitrogen, oxygen, and sulfur, and the number of the heteroatom is 1, 2, or 3.
In some embodiments, ring A is a 3- to 6-membered monocyclic heterocyclylene or 7- to 11-membered spiroheterocyclylene; the heteroatom of the monocyclic heterocyclylene is nitrogen, oxygen, or sulfur, and the number of the heteroatom is 1, 2, or 3; the heteroatom of the spiroheterocyclylene is nitrogen, oxygen, or sulfur, and the number of the heteroatom is 1, 2, or 3.
In some embodiments, ring A is a 3- to 8-membered monocyclic heterocyclylene or 7- to 11-membered spiroheterocyclylene; the heteroatom of the monocyclic heterocyclylene is N, and the number of the heteroatom is 1 or 2; the heteroatom of the spiroheterocyclylene is N, and the number of the heteroatom is 1 or 2.
In some embodiments, R is a bond, or a 7- to 11-membered mono-spiroheterocyclylene, 3- to 8-membered monocyclic heterocyclylene, and 8- to 10-membered bicyclic heteroarylene substituted with 0, 1, 2, or 3 R0s, wherein R0 is selected from hydrogen, deuterium, halogen, ═O, C1-6 alkyl, C1-6 haloalkyl, C1-6 alkoxy, C3-8 cycloalkyl, and 3- to 8-membered heterocyclyl, or two R0s, together with the C atom to which they are attached, form a 3- to 6-membered cycloalkyl; the heteroatom of the mono-spiroheterocyclylene is selected from one or more of nitrogen, oxygen, and sulfur, and the number of the heteroatom is 1, 2, or 3; the heteroatom of the bicyclic heteroarylene is selected from one or more of nitrogen, oxygen, and sulfur, and the number of the heteroatom is 1, 2, or 3; the heteroatom of the monocyclic heterocyclylene is selected from one or more of nitrogen, oxygen, and sulfur, and the number of the heteroatom is 1, 2, or 3; the heteroatom of the 3- to 8-membered heterocyclyl is selected from one or more of nitrogen, oxygen, and sulfur, and the number of the heteroatom is 1, 2, or 3.
In some embodiments, R is a bond, or a 7- to 11-membered mono-spiroheterocyclylene, 3- to 8-membered monocyclic heterocyclylene, and 8- to 10-membered bicyclic heteroarylene substituted with 0, 1, 2, or 3 R0s, wherein R0 is selected from hydrogen, ═O, and C1-6 alkyl, or two R0s, together with the C atom to which they are attached, form a 3- to 6-membered cycloalkyl; the heteroatom of the bicyclic heteroarylene is nitrogen, oxygen, or sulfur, and the number of the heteroatom is 1, 2, or 3; the heteroatom of the spiroheterocyclylene is nitrogen, oxygen, or sulfur, and the number of the heteroatom is 1, 2, or 3; the heteroatom of the monocyclic heterocyclylene is nitrogen, oxygen, or sulfur, and the number of the heteroatom is 1, 2, or 3.
In some embodiments, R is a bond, or a 7- to 11-membered mono-spiroheterocyclylene, 5- or 6-membered monocyclic heterocyclylene, and 8- to 10-membered bicyclic heteroarylene substituted with 0, 1, 2, or 3 R0s, wherein R0 is selected from hydrogen, ═O, and C1-6 alkyl, or two R0s, together with the C atom to which they are attached, form a 3- to 6-membered cycloalkyl; the heteroatom of the mono-spiroheterocyclylene is N, and the number of the heteroatom is 1 or 2; the heteroatom of the bicyclic heteroarylene is N, and the number of the heteroatom is 1 or 2; the heteroatom of the 6-membered monocyclic heterocyclylene is N, and the number of the heteroatom is 1 or 2.
In one aspect, the present invention provides a compound of formula (I), or a pharmaceutically acceptable salt, an enantiomer, a diastereomer, a racemate, a solvate, a hydrate, a polymorph, a prodrug or an isotopic variant thereof, and a mixture thereof,
PIN-Linker-E (I)
In one aspect, the present invention provides a compound of formula (I), or a pharmaceutically acceptable salt, an enantiomer, a diastereomer, a racemate, a solvate, a hydrate, a polymorph, a prodrug or an isotopic variant thereof, and a mixture thereof,
PIN-Linker-E (I)
In one aspect, the present invention provides a compound of formula (I), or a pharmaceutically acceptable salt, an enantiomer, a diastereomer, a racemate, a solvate, a hydrate, a polymorph, a prodrug or an isotopic variant thereof, and a mixture thereof,
PIN-Linker-E (I)
In some embodiments, ring A represents:
In some embodiments, ring A is selected from:
In some embodiments, R is a bond, or R is a 3- to 8-membered monocyclic heterocyclylene, 7- to 16-membered spiro heterocyclylene, 7- to 10-membered bicyclic fused heterocyclylene, 7- to 10-membered bridged heterocyclylene, 5- or 6-membered heteroarylene, or 8- to 10-membered bicyclic heteroarylene; preferably, R is a bond; preferably, R is a 5- to 7-membered monocyclic heterocyclylene; preferably, R is a 7- to 11-membered mono-spiroheterocyclylene or 8- to 10-membered bicyclic heteroarylene.
In some embodiments, R represents:
In some embodiments, ring C1 is selected from furan, thiophene, pyrrole, pyrazole, imidazole, thiazole, isothiazole, oxazole, isoxazole, triazole, benzene, pyridine, pyrimidine, pyrazine, or pyridazine; ring C2 is selected from cyclopentane, tetrahydrofuran, tetrahydrothiophene, tetrahydropyrrole, furan, thiophene, pyrrole, pyrazole, imidazole, thiazole, isothiazole, oxazole, isoxazole, triazole, cyclohexane, oxacyclohexane, piperidine, piperazine, morpholine, benzene, pyridine, pyrimidine, pyrazine, and pyridazine.
In some embodiments, R is
In some embodiments, R is selected from
preferably, R is selected from
is connected with Linker while the other end is connected with ring A, or
is connected with ring A while the other end is connected with Linker.
In some embodiments, L1, L2, L3, and L4 are each independently selected from —RL1—(CH2)n5—RL2—(CH2)n6—, wherein RL1 and RL2 are each independently O, S, NR00, —C(O)—, —C(O)NR00—, —NR00C(O)—, —SO2NR00—, —NR00SO2—, —NR00C(O)NR00—, —NR00C(O)O—, —OC(O)—, —C(O)O—, —OC(O)O—, and (CH2)r4; n5, n6, and r4 are each independently 0, 1, 2, 3, or 4,
Preferably, RL1 and RL2 are each independently selected from a bond, 5- or 6-membered heteroarylene, phenylene, C3-8 cycloalkylene, C3-8 heterocyclylene, CH2, CH2CH2, OCH2CH2, CH2CH2O, CH2CH2CH2, ethenylene, ethynylene,
In some embodiments, L1 is (CR21R22)n3, wherein R21 and R22 are each independently hydrogen, methyl, ethyl, propyl, isopropyl, cyclopropyl, cyclobutyl, oxetanyl, methoxy, ethoxy, or propoxy, and n3 is 0, 1, 2, or 3;
In some embodiments, L1 is a C3-6 cycloalkylene, 4- to 7-membered heterocyclylene, phenylene, or 5- or 6-membered heteroarylene (preferably cyclopropylene, cyclobutylene, cyclopentylene, azacyclopentylene, cyclohexylene, piperidinylene, piperazinylene, or 1,4-phenylene, more preferably 1,3-cyclobutylene, even more preferably 1,4-piperidylene or 1,4-piperazinylene).
In some embodiments, L2 is (CR21R22)n3, wherein R21 and R22 are each independently hydrogen, methyl, ethyl, propyl, isopropyl, cyclopropyl, cyclobutyl, oxetanyl, methoxy, ethoxy, or propoxy, and n3 is 0, 1, 2, or 3;
In some embodiments, L3 is (CR21R22)n3, wherein R21 and R22 are each independently hydrogen, methyl, ethyl, propyl, isopropyl, cyclopropyl, cyclobutyl, oxetanyl, methoxy, ethoxy, or propoxy, and n3 is 0, 1, 2, or 3;
In some embodiments, L4 is (CR21R22)n3, wherein R21 and R22 are each independently hydrogen, methyl, ethyl, propyl, isopropyl, cyclopropyl, cyclobutyl, oxetanyl, methoxy, ethoxy, or propoxy, and n3 is 0, 1, 2, or 3;
In some embodiments, L4 is a C3-6 cycloalkylene, 4- to 7-membered heterocyclylene, phenylene, or 5- or 6-membered heteroarylene (preferably cyclopropylene, cyclobutylene, cyclopentylene, azacyclopentylene, cyclohexylene, piperidinylene, piperazinylene, or 1,4-phenylene, more preferably 1,3-cyclobutylene, even more preferably 1,4-piperidylene or 1,4-piperazinylene).
In some embodiments, Linker represents:
RL1 and RL3 are each independently O, S, CO, SO, SO2, N(R00), or (CR21R22)r; R21 and R22 are hydrogen, acetyl, halogen, amino, C1-10 alkyl, C1-10 haloalkyl, C1-10 alkoxy, C2-10 alkenyl, C2-10 alkynyl, C3-8 cycloalkyl, 3- to 8-membered heterocycloalkyl, C6-10 aryl, or 5- to 14-membered heteroaryl; or, R21 and R22, together with the C atom to which they are attached, form a 3- to 8-membered cycloalkyl or 3- to 8-membered heterocycloalkyl;
In some embodiments, Linker represents:
In some embodiments, Linker represents:
or cyclopropylene
In some embodiments, Linker represents:
In some embodiments, RL1 is a bond, O, S, CO, SO, SO2, NH, N(CH3), CONH, NHCO, methylene,
In some embodiments, W is a bond, O, S, NR00, —C(O)—, —S(O)—, SO2, —C(O)NR00—, —NR00C(O)—, —NR00C(O)NR00—, —SO2NR00—, —NR00SO2—, —NR00C(O)O—, —C(O)O—, —OC(O)—, —OC(O)O—, —CH═CH—, —C≡C—, —(CR43R44)n8—, C3-6 cycloalkylene, 3- to 6-membered heterocycloalkylene, phenylene, 5- to 6-membered heteroarylene, or 8- to 10-membered arylene or heteroarylene, wherein R00, R43, and R44 are each independently hydrogen, methyl, ethyl, propyl, isopropyl, methoxy, ethoxy, isopropoxy, cyclopentyl, or cyclohexyl, or R43 and R44, together with the C atom to which they are attached, form cyclopropyl, cyclobutyl, cyclopentyl, or oxetanyl, and n8 is 0, 1, 2, or 3;
In some embodiments, ring B is selected from a 3- to 8-membered saturated or unsaturated cycloalkyl, 3- to 8-membered saturated or unsaturated heterocycloalkyl, 6- to 10-membered aryl, or 5- to 14-membered heteroaryl; preferably, ring B is a 5- to 7-membered saturated monocyclic heterocyclyl, benzene, or 5- to 6-membered heteroaryl; preferably, ring B is benzene or 5- to 6-membered heteroaryl; preferably, ring B is a 5- to 7-membered saturated monoheterocyclyl; preferably, ring B is cyclopentane, tetrahydropyrrole, 1,3-dioxolane, oxolane, 1,4-dioxane, furan, thiophene, thiazole, isothiazole, oxazole, isoxazole, pyrrole, imidazole, pyrazole, piperidine, piperazine, benzene, pyridine, pyridazine, or pyrimidine; preferably, ring B is 1,3-dioxolane, oxolane, 1,4-dioxane, imidazole, benzene, or pyrimidine; preferably, ring B is a 5- to 6-membered heteroaryl; preferably, ring B is 1,4-dioxane or 1,3-dioxolane.
In some embodiments, ring B is selected from
In some embodiments, V1 and V2 are both N, V3 is CR3, and V4 is CR4, wherein R3 is hydrogen, and R4 is hydrogen, halogen, amino, cyano, acetyl, C1-3 alkyl, C1-3 alkoxy, or C1-3 haloalkyl (preferably fluorine or chlorine);
In some embodiments, L5 and L6 are each independently selected from a bond, NH, CONH, NHCO, C1-3 alkylene (preferably methylene or ethylene), C2-6 alkenylene, or C2-6 alkynylene.
In some embodiments, E further represents:
wherein
In some embodiments, G1 is N, G2 is CRG2, G3 is CRG3, and G4 is CRG4; preferably, G1 is CRG1, G2 is N, G3 is CRG3, and G4 is CRG4; preferably, G1 is CRG1, G2 is CRG2, G3 is N, and G4 is CRG4; preferably, G1 is CRG1, G2 is CRG2, G3 is CRG3, and G4 is N; preferably, G1 is N, G2 is N, G3 is CRG3, and G4 is CRG4; preferably, G1 is N, G2 is CRG2, G3 is N, and G4 is CRG4; preferably, G1 is N, G2 is CRG2, G3 is CRG3, and G4 is N; preferably, G1 is CRG1, G2 is N, G3 is N, and G4 is CRG4; preferably, G1 is CRG1, G2 is N, G3 is CRG3, and G4 is N;
In some embodiments, one of RG1, RG2, RG3, and RG4 is attached to W, the others are each independently selected from hydrogen, hydroxy, cyano, acetyl, fluorine, chlorine, bromine, amino, methyl, ethyl, propyl, isopropyl, methoxy, ethoxy, fluoromethyl, difluoromethyl, trifluoromethyl, —CH2CH2F, —CHFCH3, —CH2CHF2, —CF2CH3, —CHFCH2F, —CH2CF3, —CF2CH2F, or —CHFCHF2; preferably, RG1, RG2, RG3, and RG4 are each independently hydrogen, halogen (preferably F), C1-3 alkyl, or C1-3 haloalkyl.
In some embodiments, Z1 is N, and Z2 is CH2 or C(O).
In some embodiments, E is further selected from
Preferably, RG1, RG2, RG3, RG4, and R0 are each independently hydrogen, deuterium, cyano, halogen (preferably F), C1-3 alkyl, or C1-3 haloalkyl (preferably methyl or trifluoromethyl).
In some embodiments, J1 is N, J2 is CRJ2, J3 is CRJ3, and J4 is CRJ4; preferably, J1 is CRJ1, J2 is N, J3 is CRJ3, and J4 is CRJ4; preferably, J1 is CRJ1, J2 is CRJ2, J3 is N, and J4 is CRJ4; preferably, J1 is CRJ1, J2 is CRJ2, J3 is CRJ3, and J4 is N; preferably, J1 is N, J2 is N, J3 is CRJ3, and J4 is CRJ4; preferably, J1 is N, J2 is CRJ2, J3 is N, and J4 is CRJ4; preferably, J1 is N, J2 is CRJ2, J3 is CRJ3, and J4 is N; preferably, J1 is CRJ1, J2 is N, J3 is N, and J4 is CRJ4; preferably, J1 is CRJ1, J2 is N, J3 is CRJ3, and J4 is N; preferably, J1 is CRJ1, J2 is CRJ2, J3 is N, and J4 is N; RJ1, RJ2, RJ3, and RJ4 are defined in any one of the above items.
R0 is selected from hydrogen, halogen (preferably F), C1-3 alkyl, or C1-3 haloalkyl, preferably F, methyl, trifluoromethyl, cyano, or difluoromethyl.
In some embodiments, RJ1, RJ2, RJ3, and RJ4 are each independently selected from H, F, Cl, Br, I, methyl, ethyl, propyl, isopropyl, methoxy, ethoxy, propoxy, isopropoxy, cyclopropyl, cyclobutyl, oxetanyl, fluoromethyl, difluoromethyl, trifluoromethyl, —CH2CH2F, —CHFCH3, —CH2CHF2, —CF2CH3, —CHFCH2F, —CH2CF3, —CF2CH2F, or —CHFCHF2;
In some embodiments, RJ1, RJ2, and RJ4 are hydrogen, and RJ3 and Rk3 are connected to form a bond, which is a single, double or triple bond (preferably a C—C single bond).
In some embodiments, Q is C(Rq1)3, C(O)Rq1, S(O)Rq1, SO2Rq1, P(O)Rq1Rq2, or NRq1Rq2, wherein Rq1 and Rq2 are each independently selected from methyl, ethyl, propyl, isopropyl, amino, acetyl, methylsulfonyl, acylamino, and aminoacyl. Preferably, Rq1 and Rq2 are each independently C1-6 alkyl or C1-6 alkoxy.
In some embodiments, Q is P(O)Rq1Rq2, wherein Rq1 and Rq2 are each independently C1-6 alkyl or C1-6 alkoxy.
In some embodiments, J2 is N or CH.
In some embodiments, J3 is N or CH.
In some embodiments, J4 is N or CH.
In some embodiments, V1 is N or CH.
In some embodiments, V2 is N or CH.
In some embodiments, V3 is N or CR3, R3 is hydrogen, or R3 and R4, together with the atoms to which they are attached, form a 5- to 6-membered heteroaryl or benzene substituted with 0, 1, or 2 R41s; the heteroatom of the 5- to 6-membered heteroaryl is nitrogen, and the number of the heteroatom is 1, 2, or 3.
In some embodiments, K1 is N or CH.
In some embodiments, K2 is N or CRk2.
In some embodiments, L5 is NH.
In some embodiments, L6 is NH.
In some embodiments,
In some embodiments, W is O or —C≡C—.
In some embodiments, Q is P(O)Rq1Rq2, wherein Rq1 and Rq2 are each independently C1-6 alkyl or C1-6 alkoxy;
In some embodiments, Q is P(O)Rq1Rq2, wherein Rq1 and Rq2 are each independently C1-5 alkyl or C1-5 alkoxy;
In some embodiments, Q is P(O)Rq1Rq2, wherein Rq1 and Rq2 are each independently C1-5 alkyl or C1-5 alkoxy;
In some embodiments, PIN further represents:
In some embodiments, it further represents the following formulas:
Rk3 is halogen, acetyl, cyano, C1-5 alkyl, C3-6 cycloalkyl, C1-5 haloalkyl, or C1-5 alkoxy;
Further, in the above formula (III-1-1) or (III-1-2),
In some embodiments, the compound of formula (I), or the pharmaceutically acceptable salt, the enantiomer, the diastereomer, the racemate, the solvate, the hydrate, the polymorph, the prodrug or the isotopic variant thereof, and the mixture thereof are further represented by formula (III-2-1):
In some embodiments, the compound of formula (I), or the pharmaceutically acceptable salt, the enantiomer, the diastereomer, the racemate, the solvate, the hydrate, the polymorph, the prodrug or the isotopic variant thereof, and the mixture thereof are further represented by formula (III-2-2) or (III-2-3):
In some embodiments, the compound of formula (I), or the pharmaceutically acceptable salt, the enantiomer, the diastereomer, the racemate, the solvate, the hydrate, the polymorph, the prodrug or the isotopic variant thereof, and the mixture thereof are further represented by formula (Ib-1) or (Ib-2):
In some embodiments, the compound of formula (I), or the pharmaceutically acceptable salt, the enantiomer, the diastereomer, the racemate, the solvate, the hydrate, the polymorph, the prodrug or the isotopic variant thereof, and the mixture thereof are further represented by formula (IV) or (IV-1):
In some embodiments, the compound of formula (I), or the pharmaceutically acceptable salt, the enantiomer, the diastereomer, the racemate, the solvate, the hydrate, the polymorph, the prodrug or the isotopic variant thereof, and the mixture thereof are further represented by formula (VIII):
In some embodiments, T is O, S, or C, preferably, T is O or N. In some embodiments, M is O, S, or C, preferably, M is O or N. In some embodiments, U is C or N.
In some embodiments, m2 is 0 or 1; R0 is selected from hydrogen, fluorine, chlorine, bromine, iodine, cyano, acetyl, C1-5 alkyl, C1-5 alkoxy, C1-5 haloalkyl, C3-6 cycloalkyl, or 3- to 6-membered heterocycloalkyl;
In some embodiments, the compound of formula (V), or the pharmaceutically acceptable salt, the enantiomer, the diastereomer, the racemate, the solvate, the hydrate, the polymorph, the prodrug or the isotopic variant thereof, and the mixture thereof are further represented by (V-1) or (V-2):
In some embodiments, E further represents (II-i-1):
In some embodiments, E is selected from:
In some embodiments, L5 is a bond or NH; ring Cy1 is selected from phenyl,
Rcy is selected from: hydrogen, deuterium, halogen, C1-6 alkyl, C1-6 haloalkyl, C1-6 alkoxy, C1-6 haloalkoxy, C1-6 hydroxyalkoxy, cyano, amino, —P(O)(CH3)2, —N(CH3)S(O)2CH3, or —S(O)2(CH)(CH3)2.
In some embodiments, the compound is selected from Table 1, and the pharmaceutically acceptable salt of the compound of formula I is selected from a hydrochloride or formate salt of a compound in Table 1:
In another aspect, the present invention provides a compound of (1c-1), (1e-1), (1c-1-1), (1e-1-1), (1c-1-2), or
In another aspect, the present invention further provides a preparation method for a compound of formula (X-1) or (X-2):
Specifically, the preparation method comprises: subjecting —NH in formula (1c-1) or (1c-2) to a nucleophilic substitution reaction with a leaving group of formula (1d-1) to obtain the compound of formula (X-1) or (X-2), wherein LG is the leaving group, and RJ1, RJ2, Q, R4, Rk2, Rk3, ring A, R, Linker, W, G1, G2, G3, G4, Z1, and Z2 are defined in any one of the above items. —NH in formula (1c-1) or (1c-2) may be NH on ring R, or NH attached to R. In some embodiments, R is a bond, and then the leaving group reacts with NH of ring A.
The leaving group is preferably halogen (chlorine, bromine, or iodine), —OMs (mesylate), —OTf (triflate), —OTs (p-methylbenzenesulfonate), or the like. The nucleophilic substitution reaction is preferably conducted with a polar solvent in an alkaline system. Specifically, the polar solvent is preferably one or more of DMF, DMSO, NMP, acetonitrile, THF, and toluene, and the alkaline system includes: triethylamine, DIEA, sodium bicarbonate, potassium carbonate, sodium carbonate, cesium carbonate, cesium fluoride, and the like. In some embodiments, an alkali metal catalyst, such as NaI, KI, and CuI, may also be added as a catalyst.
In another aspect, the present invention further provides another preparation method for the compound of formula (X-1) or (X-2),
Specifically, the preparation method comprises: subjecting —C═O of formula (1e-1) or (1e-2) to a reductive amination reaction with NH of R in formula (1f) to obtain the compound of formula (X-1) or (X-2), wherein ring B, Q, R4, Rk2, Rk3, ring A, R, Linker, W, G1, G2, G3, G4, Z1, and Z2 are defined in any one of the above items.
Preferably, the reducing agent is sodium cyanoborohydride or NaBH(OAc)3, and the reaction is preferably conducted in a solvent, wherein the solvent is selected from 1,2-dichloroethane, dichloromethane, DMF, and the like.
In another aspect, the present invention provides a pharmaceutical composition comprising the compound of the present invention, and optionally a pharmaceutically acceptable excipient.
In another aspect, the present invention provides a pharmaceutical composition comprising the compound of the present invention and a pharmaceutically acceptable excipient, wherein the pharmaceutical composition further comprises an additional therapeutic agent.
In another aspect, the present invention provides use of the above compound or pharmaceutical composition in preparing a protein inhibitor or degrading agent, wherein the protein of the protein inhibitor or degrading agent is selected from at least one of EGFR, ROS1, or ALK.
In another aspect, the present invention provides a kit comprising the compound of the present invention, an additional therapeutic agent, and a pharmaceutically acceptable carrier, adjuvant or vehicle.
In another aspect, the present invention provides use of the compound of the present invention in preparing a medicament for treating and/or preventing a cancer.
In another aspect, the present invention provides a method for treating and/or preventing a cancer in a subject, comprising administering to the subject the compound of the present invention or the composition of the present invention.
In another aspect, the present invention provides the compound of the present invention or the composition of the present invention for use in the treatment and/or prevention of a cancer.
In a specific embodiment, the cancer is selected from lung cancer; lymphoma; inflammatory myofibroblastoma; colorectal cancer; cerebral glioma; astroblastoma; ovarian cancer; bone marrow cancer; transplantation-related cancer; neutropenia; leukemia; Wagner-Unverricht syndrome; bronchial carcinoma; prostate cancer; breast cancer; thyroid cancer; pancreatic cancer; neuroblastoma; extramedullary plasmacytoma; plasmacytoma; gastric cancer; gastrointestinal stromal tumor; esophageal cancer; large intestine adenocarcinoma; esophageal squamous cell carcinoma; liver cancer; renal cell carcinoma; bladder cancer; endometrial cancer; melanoma; brain cancer; oral cancer; sarcoma; a tumor resistant to targeted therapies; or a tumor or disease dependent on ALK, ROS1 or EGFR, or any mutein thereof.
In another specific embodiment, the cancer is selected from small cell lung cancer; non-small cell lung cancer; diffuse large B-cell lymphoma; non-Hodgkin's lymphoma; anaplastic lymphoma; anaplastic large cell lymphoma; CD20-positive lymphoma; primary lymphoma; B cell lymphoma; recurrent B-cell non-Hodgkin's lymphoma; recurrent diffuse large B-cell lymphoma; recurrent mediastinal (thymic) large B-cell lymphoma; primary mediastinal (thymic) large B-cell lymphoma; recurrent transformed non-Hodgkin's lymphoma; refractory B-cell non-Hodgkin's lymphoma; refractory diffuse large B-cell lymphoma; refractory primary mediastinal (thymic) large B-cell lymphoma; refractory transformed non-Hodgkin's lymphoma; multiple myeloma; myelodysplastic syndrome (MDS); previously treated myelodysplastic syndrome; plasma cell myeloma; smoldering myeloma; smoldering multiple myeloma; myelofibrosis; acute myeloid leukemia (AML); leukemia-associated anemia; chronic granulocytic leukemia; B cell chronic lymphocytic leukemia; Wagner-Unverricht syndrome; bronchial carcinoma; prostate cancer; triple-negative breast cancer; sporadic breast cancer; a patient with Cowden disease; thyroid cancer; pancreatic cancer; neuroblastoma; extramedullary plasmacytoma; plasmacytoma; gastric cancer; gastrointestinal stromal tumor; esophageal cancer; large intestine adenocarcinoma; esophageal squamous cell carcinoma; liver cancer; renal cell carcinoma; bladder cancer; endometrial cancer; melanoma; brain cancer; oral cancer; rhabdomyosarcoma; various adipose-derived tumors; Ewing sarcoma/primitive neuroectodermal tumor (Ewing/PNET); leiomyosarcoma; or a tumor resistant to EGFR-, ROS1- or ALK-targeted therapies.
In another specific embodiment, the cancer is selected from anaplastic lymphoma kinase (ALK) mutation-positive non-small cell lung cancer (NSCLC); ROS1-positive non-small cell lung cancer; EGFR mutant non-small cell lung cancer; lung adenocarcinoma; lung cancer resistant to EGFR-, ROS1-, or ALK-targeted therapies; lymphoma resistant to ALK-targeted therapies; or the following tumor, cancer or disease dependent on a protein selected from ALK, ROS1 or EGFR, or any mutein thereof: lung cancer, lymphoma, inflammatory myofibroblastoma, colorectal cancer, cerebral glioma, astroblastoma, ovarian cancer, leukemia, breast cancer, thyroid cancer, neuroblastoma, extramedullary plasmacytoma, plasmacytoma, esophageal squamous cell carcinoma, renal cell carcinoma, bronchial carcinoma, prostate cancer, breast cancer, thyroid cancer, pancreatic cancer, neuroblastoma, extramedullary plasmacytoma, plasmacytoma, gastric cancer, gastrointestinal stromal tumor, esophageal cancer, large intestine adenocarcinoma, esophageal squamous cell carcinoma, liver cancer, renal cell carcinoma, bladder cancer, endometrial cancer, melanoma, brain cancer, oral cancer, or sarcoma.
Other objects and advantages of the present invention will be apparent to those skilled in the art from the subsequent specific embodiments, examples, and claims.
In another aspect, the present invention further provides a compound, which is any one of the compounds in Table 2 or a salt thereof:
Definitions of specific functional groups and chemical terms are described in more detail below.
Definitions of specific functional groups and chemical terms are described in more detail below.
Where a numerical range is given, it is intended to include each value and every sub-range within itself. For example, “C1-5 alkyl” includes C1, C2, C3, C4, C5, C1-5, C1-4, C1-3, C1-2, C2-5, C2-4, C2-3, C3-5, C3-4 and C4-5 alkyl.
“Alkyl” refers to linear and branched saturated aliphatic alkyl, and C1-10 alkyl is alkyl containing 1 to 10 carbon atoms, preferably C1-8 alkyl, more preferably C1-5 alkyl, and even more preferably C1-3 alkyl. Non-limiting examples of C1-10 alkyl include: methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, sec-butyl, n-pentyl, 1,1-dimethylpropyl, 1,2-dimethylpropyl, 2,2-dimethylpropyl, 1-ethylpropyl, 2-methylbutyl, 3-methylbutyl, n-hexyl, 1-ethyl-2-methylpropyl, 1,1,2-trimethylpropyl, 1,1-dimethylbutyl, 1,2-dimethylbutyl, 2,2-dimethylbutyl, 1,3-dimethylbutyl, 2-ethylbutyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl, 2,3-dimethylbutyl, n-heptyl, 2-methylhexyl, 3-methylhexyl, 4-methylhexyl, 5-methylhexyl, 2,3-dimethylpentyl, 2,4-dimethylpentyl, 2,2-dimethylpentyl, 3,3-dimethylpentyl, 2-ethylpentyl, 3-ethylpentyl, n-octyl, 2,3-dimethylhexyl, 2,4-dimethylhexyl, 2,5-dimethylhexyl, 2,2-dimethylhexyl, 3,3-dimethylhexyl, 4,4-dimethylhexyl, 2-ethylhexyl, 3-ethylhexyl, 4-ethylhexyl, 2-methyl-2-ethylpentyl, 2-methyl-3-ethylpentyl, n-nonyl, 2-methyl-2-ethylhexyl, 2-methyl-3-ethylhexyl, 2,2-diethylpentyl, n-decyl, 3,3-diethylhexyl, 2,2-diethylhexyl, and various branched isomers thereof, and the like.
“Alkylene” means a divalent group formed by the removal of another hydrogen from the above “alkyl” and may be substituted or unsubstituted. C1-10 alkylene is preferred, C1-5 alkylene is more preferred, and C1-3 alkylene is even more preferred. Exemplary alkylene groups include, but are not limited to, methylene, ethylene, propylene, butylene, and the like.
“C2-10 alkenyl” refers to a linear or branched hydrocarbon group having 2 to 10 carbon atoms and at least one carbon-carbon double bond. In some embodiments, C2-6 alkenyl is preferred; in some embodiments, C2-4 alkenyl is preferred. Examples of C2-10 alkenyl include: ethenyl (C2), 1-propenyl (C3), 2-propenyl (C3), 1-butenyl (C4), 2-butenyl (C4), butadienyl (C4), pentenyl (C5), pentadienyl (C5), hexenyl (C6), heptenyl (C7), octenyl (C8), and the like. The term “C2-10 alkenyl” also encompasses heteroalkenyl where one or more (e.g., 1, 2, 3, or 4) carbon atoms are replaced with heteroatoms (e.g., oxygen, sulfur, nitrogen, boron, silicon, or phosphorus). An alkenyl group may optionally be substituted with one or more substituents, for example, 1 to substituents, 1 to 3 substituents, or 1 substituent.
“C2-10 alkynyl” refers to a linear or branched hydrocarbon group having 2 to 10 carbon atoms and at least one carbon-carbon triple bond. In some embodiments, C2-6 alkynyl is preferred; in some embodiments, C2-4 alkynyl is preferred. Examples of C2-10 alkynyl include, but are not limited to: ethynyl (C2), 1-propynyl (C3), 2-propynyl (C3), 1-butynyl (C4), 2-butynyl (C4), pentynyl (C5), hexynyl (C6), heptynyl (C7), octynyl (C8), and the like. The term “C2-10 alkynyl” also encompasses heteroalkynyl where one or more (e.g., 1, 2, 3, or 4) carbon atoms are replaced with heteroatoms (e.g., oxygen, sulfur, nitrogen, boron, silicon, or phosphorus). An alkynyl group may optionally be substituted with one or more substituents, for example, 1 to 5 substituents, 1 to 3 substituents, or 1 substituent.
“Halo” or “halogen” refers to fluorine (F), chlorine (Cl), bromine (Br), and iodine (I).
Accordingly, “C1-5 haloalkyl” refers to the above “C1-5 alkyl”, which is substituted with one or more halogen groups. In some embodiments, C1-4 haloalkyl is particularly preferred, and C1-2 haloalkyl is more preferred. Examples of the haloalkyl include, but are not limited to: —CF3, —CH2F, —CHF2, —CHFCH2F, —CH2CHF2, —CF2CF3, —CCl3, —CH2Cl, —CHCl2, 2,2,2-trifluoro-1,1-dimethyl-ethyl, and the like. A haloalkyl group may be substituted at any accessible point of attachment with, for example, 1 to 5 substituents, 1 to 3 substituents, or 1 substituent.
“C3-8 cycloalkyl” refers to a non-aromatic cyclic hydrocarbon group having 3 to 8 ring carbon atoms and zero heteroatoms. In some embodiments, C3-6 cycloalkyl and C3-5 cycloalkyl are particularly preferred. Cycloalkyl also includes ring systems where the cycloalkyl ring described above is fused with one or more aryl or heteroaryl groups, wherein the point of attachment is on the cycloalkyl ring, and in such instances, the number of carbons continues to represent the number of carbons in the cycloalkyl system. Examples of the cycloalkyl include, but are not limited to: cyclopropyl (C3), cyclopropenyl (C3), cyclobutyl (C4), cyclobutenyl (C4), cyclopentyl (C5), cyclopentenyl (C5), cyclohexyl (C6), cyclohexenyl (C6), cyclohexadienyl (C6), cycloheptyl (C7), cycloheptenyl (C7), cycloheptadienyl (C7), cycloheptatrienyl (C7), and the like. A cycloalkyl group may optionally be substituted with one or more substituents, for example, 1 to 5 substituents, 1 to 3 substituents, or 1 substituent.
“3- to 8-membered heterocycloalkyl” refers to a radical of a 3- to 8-membered non-aromatic ring system having ring carbon atoms and 1 to 5 ring heteroatoms, wherein each of the heteroatoms is independently selected from nitrogen, oxygen, sulfur, boron, phosphorus, and silicon, and the heteroatoms are independently preferably nitrogen and/or oxygen, e.g., nitrogen; the number of the heteroatom is preferably 1 or 2. In a heterocyclyl group containing one or more nitrogen atoms, the point of attachment may be a carbon atom or a nitrogen atom, so long as valence permits. 3- to 7-membered heterocyclyl is preferred, 3- to 6-membered heterocyclyl is preferred, 4- to 8-membered heterocyclyl is preferred, and 5- to 6-membered heterocyclyl is more preferred, which is a 5- to 6-membered non-aromatic ring system having ring carbon atoms and 1 to 3 ring heteroatoms. Exemplary 3- to 8-membered heterocycloalkyl groups include, but are not limited to: aziridinyl, oxiranyl, thiorenyl\azetidinyl, oxetanyl, thietanyl, tetrahydrofuranyl, dihydrofuranyl, tetrahydrothienyl, dihydrothienyl, pyrrolidinyl, dihydropyrrolyl, pyrrolyl-2,5-dione, dioxolanyl, oxasulfuranyl, disulfuranyl, oxazolidin-2-one, triazolinyl, oxadiazolinyl, thiadiazolinyl, piperidinyl, tetrahydropyranyl, dihydropyridinyl, thianyl, piperazinyl, morpholinyl, dithianyl, dioxanyl, and the like.
As used herein, “cycloalkyl” and “cycloalkyl ring” are used interchangeably.
“C6-10 aryl” refers to a radical of a monocyclic or polycyclic (e.g., bicyclic) 4n+2 aromatic ring system (e.g., having 6 or 10 π electrons shared in a cyclic arrangement) having 6-10 ring carbon atoms and zero heteroatoms. In some embodiments, an aryl group has six ring carbon atoms (“C6 aryl”; e.g., phenyl). In some embodiments, an aryl group has ten ring carbon atoms (“C10 aryl”; e.g., naphthyl such as 1-naphthyl and 2-naphthyl). Aryl further includes ring systems where the aryl ring described above is fused with one or more cycloalkyl or heterocyclyl groups, wherein the point of attachment is on the aryl ring, and in such instances, the number of carbon atoms continues to represent the number of carbon atoms in the aryl ring system. An aryl group may optionally be substituted with one or more substituents, for example, 1 to 5 substituents, 1 to 3 substituents, or 1 substituent.
“5- to 14-membered heteroaryl” refers to a group having a 5- to 14-membered monocyclic or bicyclic 4n+2 aromatic ring system (e.g., having 6, 10, or 14 π electrons shared in a cyclic arrangement) having ring carbon atoms and 1-4 ring heteroatoms, wherein each of the heteroatoms is independently selected from nitrogen, oxygen, and sulfur; in the 5- to 14-membered heteroaryl, the heteroatoms are independently preferably nitrogen and/or oxygen, e.g., nitrogen; the number of the heteroatom is preferably 1, 2, or 3. In a heteroaryl group containing one or more nitrogen atoms, the point of attachment may be a carbon atom or a nitrogen atom, so long as valence permits. Heteroaryl bicyclic ring systems may include one or more heteroatoms in one or both rings. Heteroaryl further includes ring systems where the heteroaryl ring described above is fused with one or more cycloalkyl or heterocyclyl groups, wherein the point of attachment is on the heteroaryl ring, and in such instances, the number of carbon atoms continues to represent the number of carbon atoms in the heteroaryl ring system. 5- to 10-membered heteroaryl is preferred, and 5- to 6-membered heteroaryl is more preferred. Exemplary 5- to 6-membered heteroaryl groups include, but are not limited to: pyrrolyl, furanyl, thienyl, imidazolyl, pyrazolyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, triazolyl, oxadiazolyl (e.g., 1,2,4-oxadiazolyl), thiadiazolyl, tetrazolyl, pyridyl, pyridazinyl, pyrimidinyl, pyrazinyl, triazinyl, tetrazinyl, azepinyl, oxepinyl, and thiepinyl. Exemplary 5,6-bicyclic heteroaryl groups include, but are not limited to: indolyl, isoindolyl, indazolyl, benzotriazolyl, benzothiophenyl, isobenzothiophenyl, benzofuranyl, benzoisofuranyl, benzimidazolyl, benzoxazolyl, benzisoxazolyl, benzoxadiazolyl, benzthiazolyl, benzisothiazolyl, benzthiadiazolyl, indolizinyl, and purinyl. Exemplary 6,6-bicyclic heteroaryl groups include, but are not limited to: naphthyridinyl, pteridinyl, quinolyl, isoquinolyl, cinnolinyl, quinoxalinyl, phthalazinyl, and quinazolinyl. A heteroaryl group may optionally be substituted with one or more substituents, for example, 1 to 5 substituents, 1 to 3 substituents, or 1 substituent.
“C6-10 arylene” and “5- to 14-membered heteroarylene” refer to divalent groups formed by the removal of another hydrogen from the above “C6-10 aryl” and “5- to 14-membered heteroaryl”, respectively, and may be substituted or unsubstituted. C6-10 arylene and 5- to 10-membered heteroarylene are preferred. Representative C6-10 arylene groups include 1,2-phenylene, 1,3-phenylene, 1,4-phenylene, 1,2-naphthylene, 1,3-naphthylene, 1,4-naphthylene, 1,5-naphthylene, 1,6-naphthylene, 1,7-naphthylene, 1,8-naphthylene, 2,3-naphthylene, 2,5-naphthylene, 2,6-naphthylene, and 2,7-naphthylene. Representative 5- to 10-membered heteroarylene groups include 1,2-pyrrolylene, 1,3-pyrrolylene, 2,3-pyrrolylene, 2,4-pyrrolylene, 2,5-pyrrolylene, 3,4-pyrrolylene, 2,3-furanylene, 2,4-furanylene, 2,5-furanylene, 3,4-furanylene, 2,3-thienylene, 2,4-thienylene, 2,5-thienylene, 3,4-thienylene, 1,2-imidazolylene, 1,4-imidazolylene, 1,5-imidazolylene, 2,4-imidazolylene, 2,5-imidazolylene, 4,5-imidazolylene, 1,3-pyrazolylene, 1,4-pyrazolylene, 1,5-pyrazolylene, 3,4-pyrazolylene, 3,5-pyrazolylene, 4,5-pyrazolylene, 2,4-oxazolylene, 2,5-oxazolylene, 4,5-oxazolylene, 3,4-isoxazolylene, 3,5-isoxazolylene, 4,5-isoxazolylene, 2,4-thiazolylene, 2,5-thiazolylene, 4,5-thiazolylene, 3,4-isothiazolylene, 3,5-isothiazolylene, 4,5-isothiazolylene, 1,4-triazolylene, 1,5-triazolylene, 4,5-triazolylene, 1,2,4-oxadiazol-3,5-ylene, 1,2,3-oxadiazol-4,5-ylene, 1,2,4-thiadiazol-3,5-ylene, 1,2,3-thiadiazol-4,5-ylene, 2,3-pyridinylene, 2,4-pyridinylene, 2,5-pyridinylene, 2,6-pyridinylene, 3,4-pyridinylene, 3,5-pyridinylene, 3,4-pyridazinylene, 3,5-pyridazinylene, 3,6-pyridazinylene, 4,5-pyridazinylene, 2,4-pyrimidinylene, 2,5-pyrimidinylene, 4,5-pyrimidinylene, 4,6-pyrimidinylene, 2,3-pyrazinylene, 2,5-pyrazinylene, 2,6-pyrazinylene, 1,2,3-triazinyl-4,5-ylene, 1,2,3-triazinyl-4,6-ylene, 1,2,4-triazinyl-3,5-ylene, 1,2,4-triazinyl-3,6-ylene, 1,2,5-triazinyl-3,4-ylene, 1,2,5-triazinyl-3,6-ylene, 1,2,5-triazinyl-4,6-ylene, 1,3,5-triazinyl-2,4-ylene, 1,2,3,4-tetrazinyl-5,6-ylene, 1,2,3,5-tetrazinyl-4,6-ylene, 1,2,4,6-tetrazinyl-3,5-ylene, and the like.
“Heteroaryl ring” and “heteroaryl group” are used interchangeably and refer to a monocyclic or fused polycyclic (i.e., rings that share a pair of adjacent carbon atoms or heteroatoms) group containing 1 to 4 heteroatoms, having 5 to 14 ring atoms, preferably 5 to 10 ring atoms, more preferably 5, 6, 8, 9, or 10 ring atoms, wherein the heteroatoms are selected from oxygen, sulfur, and nitrogen, wherein the nitrogen and sulfur atoms may optionally be oxidized, and the nitrogen atoms may optionally be quaternized; in the “heteroaryl ring” and “heteroaryl”, the heteroatoms are independently preferably nitrogen and/or oxygen, e.g., nitrogen; the number of the heteroatom is preferably 1, 2, or 3. The heteroaryl has 6, 10, or 14 π electrons shared in a ring system. At least one ring of the ring system is aromatic. In the present invention, the C5-14 heteroaryl includes 5- or 6-membered monocyclic heteroaryl, 8- to 10-membered bicyclic heteroaryl, 11- to 14-membered tricyclic heteroaryl, a heteroaryl group formed by the fusion of a 5- or 6-membered monocyclic heteroaryl ring with a 5- to 6-membered saturated or unsaturated monoheterocycle, a heteroaryl group formed by the fusion of a 5- or 6-membered monocyclic heteroaryl ring with a 5- to 6-membered saturated or unsaturated monocycle, and a heteroaryl group formed by the fusion of a benzene ring with a 5- to 6-membered saturated or unsaturated monoheterocycle.
“5- to 6-membered heteroaryl” refers to a monocyclic heteroaryl ring containing 5 to 6 ring atoms, for example, including (but not limited to): thiophene, furan, thiazole, isothiazole, imidazole, oxazole, pyrrole, pyrazole, triazole, 1,2,3-triazole, 1,2,4-triazole, 1,2,5-triazole, 1,3,4-triazole, tetrazole, isoxazole, oxadiazole, 1,2,3-oxadiazole, 1,2,4-oxadiazole, 1,2,5-oxadiazole, 1,3,4-oxadiazole, thiadiazole, pyridine, pyridazine, pyrimidine or pyrazine, etc.; in the 5- to 6-membered heteroaryl, the heteroatoms are independently preferably nitrogen and/or oxygen, e.g., nitrogen; the number of the heteroatom is preferably 1, 2, or 3.
“8- to 10-membered bicyclic heteroaryl” refers to a 9- or 10-membered bicyclic heteroaryl formed by the fusion of a benzene ring with a 5- or 6-membered monocyclic heteroaryl, or an 8- to 10-membered bicyclic heteroaryl formed by the fusion of a 5- or 6-membered monocyclic heteroaryl with a 5- or 6-membered monocyclic heteroaryl; wherein the 5- or 6-membered monocyclic heteroaryl is selected from: thiophene, furan, thiazole, isothiazole, imidazole, oxazole, pyrrole, pyrazole, triazole, 1,2,3-triazole, 1,2,4-triazole, 1,2,5-triazole, 1,3,4-triazole, tetrazole, isoxazole, oxadiazole, 1,2,3-oxadiazole, 1,2,4-oxadiazole, 1,2,5-oxadiazole, 1,3,4-oxadiazole, thiadiazole, pyridine, pyridazine, pyrimidine, or pyrazine. In the 8- to 10-membered bicyclic heteroaryl, the heteroatoms are independently preferably nitrogen and/or oxygen, e.g., nitrogen; the number of the heteroatom is preferably 1, 2, or 3.
As used herein, “saturated or unsaturated monocycle” and “saturated or unsaturated monocycloalkyl” are used interchangeably and refer to a saturated or unsaturated all-carbon monocyclic ring system, wherein “unsaturated” refers to a cyclic moiety comprising at least one double or triple bond. 3- to 6-membered is preferred, 4- to 6-membered is more preferred, and 5- to 6-membered is more preferred.
“Saturated or unsaturated monoheterocycle”, “saturated or unsaturated monocyclic heterocycle”, and “monocyclic heterocyclyl” are used interchangeably and refer to a saturated or unsaturated monocycle in which 1, 2, or 3 ring carbon atoms are replaced by a heteroatom selected from nitrogen, oxygen or S(O)t (where t is an integer of 0 to 2), but which excludes a cyclic moiety of —O—O—, —O—S—, or —S—S—, with the remaining ring atoms being carbon. It is preferably 3- to 6-membered, more preferably 4- to 6-membered, and more preferably 5- to 6-membered. In the “saturated or unsaturated monoheterocycle”, “saturated or unsaturated monocyclic heterocycle”, and “monocyclic heterocyclyl”, the heteroatoms are independently preferably nitrogen and/or oxygen, e.g., nitrogen; the number of the heteroatom is preferably 1, 2, or 3.
“3- to 8-membered monocyclic heterocyclyl” refers to a monocyclic heterocyclic system group containing 3 to 8 ring atoms, the heteroatoms being nitrogen, oxygen, sulfur, etc.; 5- to 7-membered monocyclic heterocycle is preferred, for example, including (but not limited to): oxolane, azacyclopentane, thiolane, 1,3-dioxolane, piperidine, piperazine, morpholine, and the like. In the “3- to 8-membered monocyclic heterocyclyl”, the heteroatoms are independently preferably nitrogen and/or oxygen, e.g., nitrogen; the number of the heteroatom is preferably 1, 2, or 3.
“Polycycle” and “polycycloalkyl” are used interchangeably and refer to a saturated or unsaturated bicyclic, tricyclic, or higher polycyclic all-carbon cyclic hydrocarbon system, wherein the bicyclic system includes spiro rings and fused rings, and the tricyclic system includes bridged rings. Fused rings and spiro rings are preferred.
“Polycyclic heterocycle” and “polycyclic heteroalkyl” are used interchangeably and refer to a saturated or unsaturated polycycle in which 1, 2, 3, or 4 ring carbon atoms are replaced by a heteroatom selected from nitrogen, oxygen, or S(O)t (where t is an integer of 0 to 2), but which excludes a cyclic moiety of —O—O—, —O—S—, or —S—S—, with the remaining ring atoms being carbon. Spiro heterocycle (also known as spiroheterocyclyl) or bicyclic fused heterocyclyl is preferred, and 7- to 16-membered spiroheterocyclyl and 7- to 10-membered bicyclic fused heterocyclyl are more preferred. “5- or 6-membered monocyclic heteroaryl ring” and “5- or 6-membered monocyclic heteroaryl” are used interchangeably and both refer to a monocyclic heteroaryl ring containing 5 or 6 ring atoms, for example, including (but not limited to): a thiophene ring, a N-alkylcyclopyrrole ring, a furan ring, a thiazole ring, an imidazole ring, an oxazole ring, a pyrrole ring, a pyrazole ring, a triazole ring, a 1,2,3-triazole ring, a 1,2,4-triazole ring, a 1,2,5-triazole ring, a 1,3,4-triazole ring, a tetrazole ring, an isoxazole ring, an oxadiazole ring, a 1,2,3-oxadiazole ring, a 1,2,4-oxadiazole ring, a 1,2,5-oxadiazole ring, a 1,3,4-oxadiazole ring, a thiadiazole ring, a pyridine ring, a pyridazine ring, a pyrimidine ring, a pyrazine ring, and the like. In the “polycyclic heterocycle” and “polycyclic heteroalkyl”, the heteroatoms are independently preferably nitrogen and/or oxygen, e.g., nitrogen; the number of the heteroatom is preferably 1, 2, or 3.
“8- to 10-membered bicyclic heteroaryl ring” and “8- to 10-membered bicyclic heteroaryl” are used interchangeably and both refer to a bicyclic heteroaryl ring containing 8 to 10 ring atoms, for example, including (but not limited to): benzofuran, benzothiophene, indole, isoindole, quinoline, isoquinoline, indazole, benzothiazole, benzimidazole, quinazoline, quinoxaline, cinnoline, phthalazine, pyrido[3,2-d]pyrimidine, pyrido[2,3-d]pyrimidine, pyrido[3,4-d]pyrimidine, pyrido[4,3-d]pyrimidine, 1,8-naphthyridine, 1,7-naphthyridine, 1,6-naphthyridine, and 1,5-naphthyridine. In the “8- to 10-membered bicyclic heteroaryl ring” and “8- to 10-membered bicyclic heteroaryl”, the heteroatoms are independently preferably nitrogen and/or oxygen, e.g., nitrogen; the number of the heteroatom is preferably 1, 2, or 3.
The term “spirocycloalkyl” refers to a 5- to 20-membered polycyclic group in which monocyclic rings share one carbon atom (referred to as the spiro atom). It may contain one or more double bonds, but none of the rings has a fully conjugated π-electron system. It is preferably 6- to 14-membered, and more preferably 7- to 14-membered. According to the number of spiro atoms shared among the rings, spirocycloalkyl may be monospirocycloalkyl, bispirocycloalkyl, or polyspirocycloalkyl. Monospirocycloalkyl and bispirocycloalkyl are preferred. 4-membered/4-membered, 4-membered/5-membered, 4-membered/6-membered, 5-membered/5-membered or 5-membered/6-membered monospirocycloalkyl is more preferred. Non-limiting examples of spirocycloalkyl include:
“Fused cycloalkyl” refers to a 5- to 20-membered all-carbon polycyclic group in which each ring in the system shares a pair of adjacent carbon atoms with other rings in the system, wherein one or more of the rings may contain one or more double bonds, but none of the rings has a fully conjugated π-electron system. It is preferably 6- to 14-membered, and more preferably 7- to 14-membered. According to the number of the formed rings, the fused cycloalkyl may include bicyclic, tricyclic, tetracyclic, or polycyclic fused cycloalkyl, and is preferably bicyclic. Non-limiting examples of fused cycloalkyl include:
“Bridged cycloalkyl” refers to a 5- to 20-membered all-carbon polycyclic group in which any two rings share two carbon atoms that are not directly connected to each other. It may contain one or more double bonds, but none of the rings has a fully conjugated π-electron system. It is preferably 6- to 14-membered, more preferably 7- to 14-membered, and most preferably 7- to 9-membered. According to the number of the formed rings, the bridged cycloalkyl may include bicyclic, tricyclic, tetracyclic, or polycyclic, and is preferably bicyclic, tricyclic, or tetracyclic, and more preferably bicyclic or tricyclic. Non-limiting examples of bridged cycloalkyl include:
“Spiroheterocyclyl” refers to a 5- to 20-membered polycyclic heterocyclyl group in which monocyclic rings share one atom (referred to as the spiro atom), wherein one or more of the ring atoms are heteroatoms selected from nitrogen, oxygen, and S(O)g (where g is an integer of 0 to 2), and the remaining ring atoms are carbon atoms. It may contain one or more double bonds, but none of the rings has a fully conjugated π-electron system.
In the “spiroheterocyclyl”, the heteroatoms are independently preferably nitrogen and/or oxygen, e.g., nitrogen; the number of the heteroatom is preferably 1, 2, or 3.
According to the number of spiro atoms shared among the rings, spiroheterocyclyl may include monospiroheterocyclyl, bispiroheterocyclyl, or polyspiroheterocyclyl. Monospiroheterocyclyl and bispiroheterocyclyl are preferred. 4-membered/4-membered, 4-membered/5-membered, 4-membered/6-membered, 5-membered/5-membered, 5-membered/6-membered, or 6-membered/6-membered monospiroheterocyclyl or bispiroheterocyclyl is more preferred. Non-limiting examples of spiroheterocyclyl include:
The term “fused heterocyclyl” refers to a 5- to 20-membered polycyclic heterocyclyl group in which each ring shares a pair of adjacent atoms with the other rings in the system, wherein one or more of the rings may contain one or more double bonds, but none of the rings has a fully conjugated π-electron system, and one or more of the ring atoms are heteroatoms selected from nitrogen, oxygen, and S(O)g (where g is an integer of 0 to 2), and the remaining ring atoms are carbon atoms. 7- to 14-membered fused heterocyclyl is preferred, and 7- to 10-membered (e.g., 7-, 8- or 9-membered) fused heterocyclyl is more preferred. According to the number of the formed rings, fused heterocyclyl may include bicyclic, tricyclic, tetracyclic, or polycyclic fused heterocyclyl, and is preferably bicyclic or tricyclic, and more preferably 5-membered/5-membered or 5-membered/6-membered bicyclic fused heterocyclyl. In the “fused heterocyclyl”, the heteroatoms are independently preferably nitrogen and/or oxygen, e.g., nitrogen; the number of the heteroatom is preferably 1, 2, or 3.
Unless otherwise defined, the “substituents each independently selected from . . . ” as used herein means that when one or more hydrogen atoms on a group are substituted with substituents, the substituents may be of the same or different types, and the substituents from which the selection is made are of their respective independent types. As used herein, it should be noted that the “C3-8 cycloalkylene”, “3- to 8-membered heterocycloalkylene”, “monocyclic alkylene”, “monocyclic heterocyclylene”, “polycyclic alkylene”, “polycyclic heterocyclylene”, “5- to 6-membered heteroarylene”, “8- to 10-membered bicyclic heteroarylene”, “mono-spiroheterocyclylene”, and the like refer to divalent groups formed by removing another hydrogen from the above-mentioned “C3-8 cycloalkyl”, “3- to 8-membered heterocycloalkyl”, “monocycloalkyl”, “monocyclic heterocyclyl”, “polycycloalkyl”, “polycyclic heterocyclyl”, “5- to 6-membered heteroaryl”, “8- to 10-membered bicyclic heteroaryl”, “monospiroheterocyclyl”, and the like, respectively, and may be substituted or unsubstituted.
Alkyl, alkylene, alkenyl, alkynyl, cycloalkyl, cycloalkylene, heterocycloalkyl, heterocycloalkylene, aryl, arylene, heteroaryl, heteroarylene, and the like, as defined herein, are optionally substituted groups.
Exemplary substituents on carbon atoms include, but are not limited to: halogen, —CN, —NO2, —N3, —SO2H, —SO3H, —OH, —ORaa, —ON(Rbb)2, —N(Rbb)2, —N(Rbb)3+X−, —N(ORcc)Rbb, —SH, —SRaa, —SSRcc, —C(═O)Raa, —CO2H, —CHO, —C(ORcc)2, —CO2Raa, —OC(═O)Raa, —OCO2Raa, —C(═O)N(Rbb)2, —OC(═O)N(Rbb)2, —NRbbC(═O)Raa, —NRbbCO2Raa, —NRbbC(═O)N(Rbb)2, —C(═NRbb)Raa, —C(═NRbb)ORaa, —OC(═NRbb)Raa, —OC(═NRbb)ORaa, —C(═NR(Rbb)Nbb)2, —OC(═NRbb)N(Rbb)2, —NRbbC(═NRbb)N(Rbb)2, —C(═O)NRbbSO2Raa, —NRbbSO2Raa, —SO2N(Rbb)2, —SO2Raa, —SO2ORaa, —OSO2Raa, —S(═O)Raa, —OS(═O)Raa, —Si(Raa)3, —OSi(Raa)3, —C(═S)N(Rbb)2, —C(═O)SRaa, —C(═S)SRaa, —SC(═S)SRaa, —SC(═O)SRaa, —OC(═O)SRaa, —SC(═O)ORaa, —SC(═O)Raa, —P(═O)2Raa, —OP(═O)2Raa, —P(═O)(Raa)2, —OP(═O)(Raa)2, —OP(═O)(ORcc)2, —P(═O)2N(Rbb)2, —OP(═O)2N(Rbb)2, —P(═O)(NRbb)2, —OP(═O)(NRbb)2, —NRbbP(═O)(ORcc)2, —NRbbp(═O)(NRbb)2, —P(Rcc)2, —P(Rcc)3, —OP(Rbb)2, —OP(Rcc)3, —B(Raa)2, —B(ORcc)2, —BRaa(ORcc), alkyl, haloalkyl, alkenyl, alkynyl, cycloalkyl, heterocyclyl, aryl, and heteroaryl, wherein each alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclyl, aryl, and heteroaryl is independently substituted with 0, 1, 2, 3, 4, or 5 Rdd groups;
The term “treat” or “treating” used herein relates to reversing, alleviating, or inhibiting the progression of the disorders or conditions to which the term applies, or one or more symptoms of such disorders or conditions. The noun “treatment” used herein relates to the action of the verb “treat”, the latter being as just defined.
The term “pharmaceutically acceptable salt” used herein denotes those carboxylate salts and amino acid addition salts of the compounds of the present invention, which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of a patient without undue toxicity, irritation, allergic response, and the like. They are commensurate with a reasonable benefit/risk ratio, and are effective for their intended use. The term includes, if possible, the zwitterionic forms of the compounds of the present invention. The salts may be prepared from inorganic acids, which include sulfate, pyrosulfate, bisulfate, sulfite, bisulfite, nitrate, and the like, and representative salts include: hydrobromide, hydrochloride, sulfate, bisulfate, acetate, oxalate, palmitate, benzoate, lactate, phosphate, tosylate, citrate, maleate, fumarate, succinate, tartrate, mesylate, and the like. The salts may also be prepared from organic acids, which include acetate, propionate, octanoate, isobutyrate, oxalate, and the like. Also included are cations based on alkali metals and alkaline earth metals, such as sodium, lithium, potassium, calcium, magnesium, and the like, as well as non-toxic ammonium, quaternary ammonium, and amine cations, including, but not limited to, ammonium, tetramethylammonium, tetraethylammonium, methylamine, dimethylamine, trimethylamine, triethylamine, ethylamine, and the like.
The “subject” to which the compound is administered includes, but is not limited to: a human (i.e., a male or female of any age group, e.g., a pediatric subject (e.g., an infant, a child, or an adolescent) or an adult subject (e.g., a young adult, a middle-aged adult, or an older adult)) and/or a non-human animal, e.g., a mammal, such as a primate (e.g., a cynomolgus monkey or a rhesus monkey), a cow, a pig, a horse, a sheep, a goat, a rodent, a cat, and/or a dog. In some embodiments, the subject is a human. In some embodiments, the subject is a non human animal. The terms “human”, “patient”, and “subject” are used interchangeably herein.
The terms “disease”, “disorder”, and “condition” are used interchangeably herein.
As used herein, unless otherwise specified, the term “treatment” includes the effect on a subject who is suffering from a particular disease, disorder or condition, which reduces the severity of the disease, disorder or condition, or delays or slows the progression of the disease, disorder or condition (“therapeutic treatment”). The term also includes the effect that occurs before the subject begins to suffer from a particular disease, disorder or condition (“prophylactic treatment”).
Generally, the “effective amount” of a compound refers to an amount sufficient to elicit a target biological response. As will be appreciated by those of ordinary skill in the art, the effective amount of the compound of the present invention may vary depending on, for example, the following factors: the biological target, the pharmacokinetics of the compound, the disease being treated, the mode of administration, and the age, health status and symptoms of the subject. The effective amount includes a therapeutically effective amount and a prophylactically effective amount.
The present invention also includes isotopically-labeled compounds (isotopic variants) which are equivalent to those described in formula (I), except that one or more atoms are replaced by an atom having an atomic mass or mass number different from the atomic mass or mass number usually found in nature. Examples of isotopes that can be incorporated into the compounds of the present invention include isotopes of hydrogen, carbon, nitrogen, oxygen, phosphorus, sulfur, fluorine, and chlorine, such as 2H, 3H, 13C, 11C, 14C, 15N, 18O, 17O, 31P, 32P, 35S, 18F, and 36Cl, respectively. The compounds of the present invention containing the above isotopes and/or other isotopes of other atoms, prodrugs thereof, and pharmaceutically acceptable salts of the compounds or prodrugs are all within the scope of the present invention. Certain isotopically-labeled compounds of the present invention, such as those into which radioisotope (e.g., 3H and 14C) are incorporated, are useful in drug and/or substrate tissue distribution assays. Tritium (i.e., 3H) and carbon-14 (i.e., 14C) isotopes are particularly preferred for their ease of preparation and detectability. Furthermore, substitution with heavier isotopes such as deuterium (i.e., 2H) may afford therapeutic benefits (e.g., increased in vivo half-life or reduced dose) resulting from greater metabolic stability and hence may be preferred in some circumstances. Isotopically labeled compounds of formula (I) of the present invention and prodrugs thereof can generally be prepared by using readily available isotopically-labeled reagents to replace non-isotopically-labeled reagents in the following schemes and/or the procedures disclosed in the examples and preparation examples.
The positive and progressive effects of the present invention are as follows: the compounds of the present invention have good inhibitory effects in the proliferation activity test of BaF3 cells with GFR mutants. The compounds of the present invention have good selectivity in the proliferation activity test of BaF3 cells with GFR mutants.
Step 1: Compound 1-ethyl-2-fluoro-4-methoxy-5-nitrobenzene (2 g, 10 mmol) and tert-butyl 4-(piperidin-4-yl)piperazine-1-carboxylate (4 g, 15 mmol) were added to a reaction flask before DMF (100 mL) and K2CO3 (4.1 g, 30 mmol) were added, and the system was stirred at 110° C. for 24 h. The reaction solution was concentrated, and then water was added. The mixture was extracted with dichloromethane and washed with water. The organic phase was concentrated and separated and purified by normal-phase column chromatography (dichloromethane:methanol=10:1) to give compound 3a-1. MS m/z (ESI): 449.5 [M+H]+.
Step 2: Compound 3a-1 (2.3 g, 5.13 mmol) was added to a reaction flask before a mixture of MeOH:EA=1:1 (150 mL) was added. Then Pd/C (1.14 g, 1.07 mmol) was added, and then the system was stirred at room temperature for 2 h in a H2 atmosphere, filtered, and concentrated to give compound 3a. MS m/z (ESI): 419.9 [M+H]+.
Step 1: Compound 1-chloro-2-fluoro-4-methoxy-5-nitrobenzene (0.5 g, 2.43 mmol) and compound tert-butyl 3,9-diazaspiro[5.5]undecane-3-carboxylate (680 mg, 2.68 mmol) were dissolved in DMF (10 mL). K2CO3 (672 mg, 4.86 mmol) was added with stirring, and the reaction mixture was stirred at 60° C. for 2 h. After the reaction was completed, the reaction mixture was cooled to room temperature and poured into ice water, and a solid was precipitated. The solid was then collected by filtration and dried under vacuum to give compound 7a-1, which was directly used in the next step. MS m/z (ESI): 440.4 [M+H]+.
Step 2: Compound 7a-1 (1 g, 2.27 mmol) was added to a mixed solution of ethanol (30 mL) and water (10 mL), and then iron powder (762 mg, 13.64 mmol) and ammonium chloride (1.22 g, 22.73 mmol) were added. In a nitrogen atmosphere, the reaction system was stirred at 90° C. for 2 h. After the reaction was completed, the reaction solution was cooled to 25° C. and filtered through celite. The filtrate was concentrated at reduced pressure to remove the ethanol, and then the aqueous phase was extracted with EA. The organic layers were combined, dried over anhydrous sodium sulfate, and then filtered. The filtrate was concentrated to give compound 7a, which was directly used in the next step. MS m/z (ESI): 411.2 [M+H]+.
Step 1: 2-Chloro-1-fluoro-4-nitrobenzene (0.76 g, 4.33 mmol) was added to a solution of acetonitrile (10 mL), and then tert-butyl 7-azaspiro[3.5]nonan-2-ylcarbamate (1.04 g, 4.34 mmol) and N,N-diisopropylethylamine (1.4 g, 10.82 mmol, 1.89 mL) were added. The reaction system was stirred in a nitrogen atmosphere at 85° C. for 5 h. After the reaction was completed, the reaction solution was directly concentrated at reduced pressure to remove the acetonitrile, diluted with water, and then extracted with ethyl acetate. The organic layers were combined, dried over anhydrous sodium sulfate, filtered, and concentrated to give compound 8a-1, which was directly used in the next step. MS m/z (ESI): 396.0 [M+H]+.
Step 2: Compound 8a-1 (1.6 g, 4.04 mmol, 1 eq) was added to a solution of tetrahydrofuran (16 mL), and the system was cooled to 0° C. Sodium hydride (0.64 g, 16.16 mmol, 60% purity) was added to the reaction system, and then the reaction system was stirred in a nitrogen atmosphere at 0-25° C. for 1 h. Methyl iodide (40.42 mmol, 2.51 mL) was added, and then the reaction system was stirred for another 1 h. After the reaction was completed, a saturated aqueous ammonium chloride solution was added, and the mixture was extracted with dichloromethane. The organic layers were combined, dried over anhydrous sodium sulfate, and then filtered. The filtrate was concentrated to give compound 8a-2 as a yellow solid. MS m/z (ESI): 410.2 [M+H]+.
Step 3: Compound 8a-2 (900 mg, 2.2 mmol) was added to a mixed solution of ethanol (18 mL) and water (18 mL), and then iron powder (306.54 mg, 5.49 mmol) and ammonium chloride (234.89 mg, 4.39 mmol) were added. In a nitrogen atmosphere, the reaction system was stirred at 80° C. for 1 h. After the reaction was completed, the reaction solution was cooled to 25° C. and filtered through celite. The filter cake was washed twice with ethanol, and the filtrate was collected, concentrated at reduced pressure to remove the ethanol, and extracted with ethyl acetate. The organic layers were combined, dried over anhydrous sodium sulfate, and then filtered. The filtrate was concentrated to give compound 8a, which was directly used in the next step. MS m/z (ESI): 380.2 [M+H]+.
Step 1: Compound 46a-1 was prepared with reference to step 1 for intermediate 8a. MS m/z (ESI): 503.2 [M+H]+.
Step 2: Compound 46a-2 was prepared with reference to the method for intermediate 5d. MS m/z (ESI): 451.3 [M+H]+.
Step 3: Compound 46a-2 (500 mg, 1.11 mmol) was added to a reaction flask before a mixture of MeOH:THF=1:1 (20 mL) was added. Then Rh(PPh3)Cl (0.1 g, 0.11 mmol) was added, and the system was stirred at room temperature for 2 h in a H2 atmosphere, filtered, and concentrated to give compound 46a-3 (brown solid, 400 mg). MS m/z (ESI): 453.3 [M+H]+.
Step 4: Compound 46a was prepared with reference to step 2 for intermediate 7a. MS m/z (ESI): 423.2 [M+H]+.
Step 1: Compound 39a-1 (1 g, 4.6 mmol) was dissolved in HOAc (6 mL). In an ice bath, concentrated HNO3 (1.4 g, 5.0 mmol) was slowly added. The system was then stirred at 0° C. for 2 h in a nitrogen atmosphere.
After the reaction was completed, the reaction solution was poured into ice water, and a solid was precipitated. The solid was then collected by filtration to give 98a-1 (yellow solid, 800 mg). MS m/z (ESI): 262.0 [M+H]+.
Step 2: Compound 98a-2 was prepared with reference to the method for intermediate 5d. MS m/z (ESI): 365.2 [M+H]+.
Step 3: Compound 98a was prepared with reference to step 2 for intermediate 3a. MS m/z (ESI): 337.4 [M+H]+.
Step 1: Compound 165c (170 mg, 0.23 mmol), pyrazole (31 mg, 0.46 mmol), CuI (19 mg, 0.1 mmol), N1,N2-dimethylcyclohexane-1,2-diamine (14 mg, 0.1 mmol), Cs2CO3 (223 mg, 0.69 mmol), and DMF (6 mL) were added to a reaction flask. The system was purged with nitrogen for 1 min and microwaved at 150° C. for reaction for 1 h. After the reaction was completed, the reaction solution was filtered, concentrated, and subjected to normal-phase column chromatography (MeOH/DCM=0-5%) to give compound 165a-1. MS m/z (ESI): 730.8 [M+H]+.
Step 2: Compound 165a-1 (60 mg, 0.08 mmol) and DCM (4 mL) were added to a reaction flask, and then TFA (2 mL) was added. The system was stirred at 20° C. for 1 h in a nitrogen atmosphere. After the reaction was completed, the reaction solution was concentrated, diluted with DCM, washed with saturated sodium bicarbonate until pH=7-8, and then extracted with DCM. The organic phase was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated to give compound 165a. MS m/z (ESI): 630.6 [M+H]+.
Step 1: Compound 165c (200 mg, 0.27 mmol), 166a.1 (139 mg, 0.41 mmol), catalyst Pd(PPh3)4 (22.3 mg, 0.02 mmol), and 1,4-dioxane (6 mL) were added to a microwave tube. The system was purged with nitrogen for 1 min and microwaved at 150° C. for reaction for 1 h. After the reaction was completed, a saturated KF solution was added, and the mixture was stirred at room temperature for 0.5 h, subjected to liquid separation, and extracted with DCM. The organic phases were combined, dried over anhydrous sodium sulfate, filtered, concentrated, and then subjected to normal-phase column chromatography (MeOH/DCM=0-5%) to give compound 166a-1 (yellow oil, 120 mg). MS m/z (ESI): 731.7 [M+H]+.
Step 2: Compound 166a was prepared with reference to step 2 for intermediate 3b. MS m/z (ESI): 631.5 [M+H]+.
Step 1: Compound 165c (200 mg, 0.27 mmol), 1-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (112 mg, 0.54 mmol), catalyst Pd(PPh3)4 (16 mg, 0.014 mmol), K2CO3 (112 mg, 0.81 mmol), 1,4-dioxane/H2O (v/v=6/1, 7 mL) were added to a microwave tube. The system was then purged with nitrogen for 1 min and microwaved at 130° C. for reaction for 1 h. After the reaction was completed, water was added for liquid separation, and the mixture was extracted with DCM. The organic phases were combined, dried over anhydrous sodium sulfate, filtered, concentrated, and then subjected to normal-phase column chromatography (DCM/MeOH=0-5%) to give compound 176a-1. MS m/z (ESI): 744.8 [M+H]+.
Step 2: Compound 176a-1 (50 mg, 0.067 mmol) and solvent DCM (4 mL) were added to a reaction flask, and then TFA (2 mL) was added. The system was stirred at 20° C. for 1 h in a nitrogen atmosphere. After the reaction was completed, the reaction solution was concentrated, diluted with DCM, washed with saturated sodium bicarbonate until pH=7-8, and then extracted with DCM. The organic phase was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated to give compound 176a. MS m/z (ESI): 644.5 [M+H]+.
Step 1: Compound 132c-3 (200 mg, 0.28 mmol), hydrazine hydrate (33 mg, 0.56 mmol), and DCM (6 mL) were added to a three-necked flask. In a N2 atmosphere and in an ice bath, CDI (48.6 mg, 0.3 mmol) was added, and the system was allowed to react at 20° C. for 1 h. After the reaction was completed, water was added, and the mixture was extracted with DCM. The organic phases were combined, dried over anhydrous sodium sulfate, filtered, concentrated, and then subjected to normal-phase column chromatography (DCM/MeOH=0-5%) to give compound 177a-1 (yellow solid, 120 mg). MS m/z (ESI): 722.5 [M+H]+.
Step 2: Compound 177a-1 (70 mg, 0.09 mmol), triethyl orthoacetate (73 mg, 0.45 mmol), and solvent NMP (3 mL) were added to a reaction flask, and the system was stirred at 150° C. for 1 h in an air atmosphere. After the reaction was completed, the reaction solution was concentrated and subjected to normal-phase column chromatography (DCM/MeOH=0-5%) to give compound 177a-2 (yellow oil, 60 mg). MS m/z (ESI): 746.7 [M+H]+.
Step 3: Compound 177a was prepared with reference to step 2 for intermediate 3b. MS m/z (ESI): 646.5 [M+H]+.
Step 1: Compound 165c (550 mg, 0.74 mmol), 193a.1 (431 mg, 1.11 mmol), catalyst Pd(PPh3)4 (45 mg, 0.04 mmol), and DMF (8 mL) were added to a microwave tube. The system was purged with nitrogen for 1 min and microwaved at 150° C. for reaction for 1 h. After the reaction was completed, a saturated KF solution was added, and the mixture was stirred at room temperature for 0.5 h, subjected to liquid separation, and extracted with DCM. The organic phases were combined, dried over anhydrous sodium sulfate, filtered, and then concentrated. K2CO3 and methanol were added, and the mixture was stirred at room temperature for 0.5 h, filtered, concentrated, and then subjected to normal-phase column chromatography (DCM/MeOH=0-5%) to give compound 193a-1 (yellow solid, 230 mg). MS m/z (ESI): 688.5 [M+H]+.
Step 2: Compound 193a-1 (150 mg, 0.22 mmol), TMSN3 (34 mg, 0.264 mmol), CuSO4 (3 mg, 0.02 mmol), sodium ascorbate (4 mg, 0.02 mmol), and solvents DMF, water, and t-BuOH (3 mL, v/v/v=1/1/1) were added to a reaction flask. In an air atmosphere, the system was stirred at 20° C. for 2 h. After the reaction was completed, the reaction solution was filtered. DCM and water were added, and the mixture was subjected to liquid separation and extracted with DCM. The organic phase was washed with saturated brine, dried over anhydrous sodium sulfate, concentrated, and then subjected to normal-phase column chromatography (MeOH/DCM=0-5%) to give compound 193a-2 (yellow solid, 130 mg). MS m/z (ESI): 817.8. [M+H]+.
Step 3: Compound 193a-2 (130 mg, 0.16 mmol), solvent THF (2 mL), and one drop of water were added to a reaction flask. In an ice bath, a 1.0 M solution of TBAF (1 mL, 1 mmol) in THF was dropwise added. In a nitrogen atmosphere, the system was stirred at room temperature for 1 h. After the reaction was completed, DCM and H2O were added, and the mixture was subjected to liquid separation, extracted with DCM, dried, concentrated, and then subjected to normal-phase column chromatography (DCM/MeOH=0-5%) to give compound 193a-3 (yellow oil, 80 mg). MS m/z (ESI): 746.1 [M+H]+.
Step 4: Compound 193a was prepared with reference to step 2 for 165a. MS m/z (ESI): 645.9 [M+H]+.
Step 1: Compound 165c (400 mg, 0.54 mmol), trimethyl((tributylstannyl)ethynyl)silane (313 mg, 0.81 mmol), and catalyst Pd(PPh3)4, and DMF (8 mL) were added to a 20 mL microwave tube. The system was then purged with nitrogen for 1 min and microwaved at 150° C. for reaction for 1 h. After the reaction was completed, a saturated KF solution was added, and the mixture was stirred at room temperature for half an hour, subjected to liquid separation, and extracted with DCM. The organic phases were combined, dried over anhydrous sodium sulfate, filtered, concentrated, and then subjected to normal-phase column chromatography (DCM/MeOH=0-5%) to give compound 210a-1 (yellow solid, 250 mg). MS m/z (ESI): 761.2. [M+H]+.
Step 2: Compound 210a-1 (190 mg, 0.25 mmol), PMBN3 (49 mg, 0.3 mmol), and toluene were added to a reaction flask. In an air atmosphere, the system was stirred at 130° C. for 16 h. After the reaction was completed, the reaction solution was concentrated and subjected to normal-phase column chromatography (MeOH/DCM=0-5%) to give compound 210a-2 (yellow solid, 200 mg). MS m/z (ESI): 923.4 [M+H]+.
Step 3: Compound 210a-2 (200 mg, 0.22 mmol) and solvent DCM were added to a reaction flask. In an ice bath, TFA was dropwise added, and the system was stirred at 65° C. for 2 h. After the reaction was completed, the reaction solution was concentrated, diluted with DCM, washed with saturated sodium bicarbonate until pH=7-8, and then extracted with DCM. The organic phase was washed with saturated brine, dried over anhydrous sodium sulfate, concentrated, and then separated and purified by prep-HPLC to give 210a-3 (pale yellow solid, 90 mg, hydrochloride). MS m/z (ESI): 704.1 [M+H]+.
Step 4: Compound 210a-3 (80 mg, 0.11 mmol), K2CO3 (45.5 mg, 0.33 mmol), and solvent MeOH were added to a reaction flask. In an air atmosphere, the system was stirred at 65° C. for 2 h. After the reaction was completed, the reaction solution was filtered, concentrated, and subjected to normal-phase column chromatography (DCM/MeOH=0-20%) to give compound 210a. MS m/z (ESI): 631.8 [M+H]+.
With reference to the method shown in any one of compounds 3a-46a, intermediate compounds of formula (a) were prepared from suitable substituted nitrobenzenes and amines as starting materials, as shown in Table 3 below.
Step 1: Compound 1 (5.0 g, 15.5 mmol), but-3-yn-1-ol (3.25 g, 46.5 mmol), Pd(PPh3)2Cl2 (0.22 g, 0.31 mmol), cuprous iodide (0.12 g, 0.62 mmol) were added to a reaction flask before anhydrous DMF (60 mL) and triethylamine (10 mL) were added. In a nitrogen atmosphere, the system was slowly heated to 90° C. and stirred for 16 h. After the reaction was completed, the reaction solution was filtered, and the filtrate was concentrated at reduced pressure to dryness. The residue was then triturated with ethyl acetate and petroleum ether, and the triturate was filtered at reduced pressure. The filter cake was dissolved in a mixed solution of dichloromethane and methanol, and the crude product was separated and purified by normal-phase column chromatography to give compound 1b-1 (pale yellow solid, 6.0 g). MS m/z (ESI): 313.2 [M+H]+.
Step 2: Compound 1b-1 (5.7 g, 18.2 mmol), triethylamine (9.2 g, 91 mmol), and anhydrous dichloromethane (1600 mL) were added in a reaction flask before methanesulfonyl chloride (6.0 g, 54.6 mmol) was slowly and dropwise added in an ice-water bath. After the dropwise addition, the system was stirred for 1 h in the ice-water bath. After the reaction was completed, water was added to quench the reaction. The mixture was extracted with dichloromethane, and the organic phases were combined, washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was removed at reduced pressure, and the crude product was triturated with petroleum ether and ethyl acetate. The triturate was filtered to give the target compound 1b (pale yellow solid, 4.5 g), which was used directly in the next step. MS m/z (ESI): 391.2 [M+H]+.
Step 1: At 25° C., compound tert-butyl 3-(4-hydroxy-1-oxoisoindolin-2-yl)-2,6-dioxopiperidine-1-carboxylate (350 mg, 971.25 μmol) was added to a solution of tert-butyl 8-hydroxy-2-azaspiro[4.5]decane-2-carboxylate (248.01 mg, 971.25 μmol) in THE (10 mL), and then azodicarbonamide (83.62 mg, 485.62 μmol) and tributylphosphine (98.25 mg, 485.62 μmol, 119.82 μL) were slowly added in a nitrogen atmosphere. The reaction system was stirred at room temperature for 8 h. After the reaction was completed, the reaction solution was concentrated at reduced pressure to give a crude product, which was purified by column chromatography to give compound 3b-. MS m/z (ESI): 398.2 [M+H-200]+.
Step 2: At 25° C., trifluoroacetic acid (2.70 mmol, 0.2 mL) was added to a solution of compound 3b-1 (100 mg, 167.31 μmol) in dichloromethane (1 mL), and then the reaction system was stirred for 1 h. The reaction solution was concentrated at reduced pressure to give compound 3b. The crude product was directly used in the next step. MS m/z (ESI): 398.2 [M+H]+.
Step 1: Compound 3d (500 mg, 1.47 mmol) and compound pent-4-yn-1-ol (247 mg, 2.93 mmol) were dissolved in DMF (6 ML). Et3N (1.06 mL, 7.33 mmol), CuI (56 mg, 0.29 mmol), and Pd(PPh3)2Cl2 (103 mg, 0.15 mmol) were separately added with stirring. In a nitrogen atmosphere, the reaction system was stirred at 100° C. for 16 h. After the reaction was completed, the reaction solution was poured into ice water, and then the aqueous phase was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, filtered, and concentrated. The filter cake was dissolved and subjected to column chromatography (methanol/dichloromethane: 5%-10%) to give the title compound 4b-1 (white solid, 400 mg). MS m/z (ESI): 345.3 [M+H]+.
Step 2: Compound 4b-1 (200 mg, 0.58 mmol) was dissolved in EtOH/EA/MeOH (1:1:0.5, 25 mL). In a nitrogen atmosphere, wet Pd/C (40 mg) was added with stirring. In a hydrogen atmosphere, the system was stirred at 60° C. for 16 h. After the reaction was completed, the reaction system was filtered, and the filtrate was concentrated to give compound 4b-2 (white solid, 202 mg), which was directly used in the next step. MS m/z (ESI): 349.3 [M+H]+.
Step 3: Compound 4b-2 (200 mg, 0.574 mmol) was dissolved in a solution of DCM (10 mL) and THE (20 mL). Et3N (0.5 mL, 3.44 mmol) and MsCl (197 mg, 0.14 mL, 1.72 mmol) were added with stirring, and the reaction system was stirred at room temperature for 2 h. After the reaction was completed, the reaction mixture was diluted with water to quench the reaction and then extracted with DCM. The organic layers were combined, washed with brine, dried over anhydrous sodium sulfate, filtered, and concentrated. The resulting solid was triturated with PE:EA=10:1 (20 mL), and the triturate was filtered. The filter cake was dried under vacuum to give compound 4b. MS m/z (ESI): 427.2 [M+H]+.
Compound 5b was prepared with reference to the method for intermediate 4b. MS m/z (ESI): 427.5 [M+H]+.
Compound 27b was prepared with reference to compound 21c. MS m/z (ESI): 540.3 [M+H]+.
Compound 43b was prepared with reference to the method for intermediate 21c. M/S M/Z (ESI): 616.1, 618.1 [M+H]+.
Compound 44b was prepared with reference to step 4 for intermediate 21c. MS m/z (ESI): 542.2 [M+H]+.
Step 1: Tetrabutylammonium hydrogen sulfate (100 mg, 294.52 μmol) and sodium hydride (1.84 g, 45.97 mmol, 60% purity) were added to a solution of 5-nitro-1H-indazole (3 g, 18.39 mmol) in anhydrous tetrahydrofuran (30 mL). The system was stirred at 25° C. for 1 h, and then benzenesulfonyl chloride (3.57 g, 20.23 mmol, 2.59 mL) was added. The reaction system was stirred at 25° C. for 11 h. After the reaction was completed, the reaction was quenched with an aqueous ammonium chloride solution at 0° C. The reaction mixture was extracted with water and ethyl acetate and separated into layers. The organic layer was washed with brine, dried over anhydrous sodium sulfate, filtered, and concentrated at reduced pressure to give compound Sib-1 (brown solid, 3 g). MS m/z (ESI): 304.0 [M+H]+.
Step 2: Compound 51b-2 was prepared with reference to step 3 for 45c. MS m/z (ESI): 273.8 [M+H]+.
Step 3: NIS (1.98 g, 8.78 mmol) was added to a solution of 51b-2 (2 g, 7.32 mmol) in acetonitrile (8 mL), and then the reaction system was stirred at 25° C. for 1 h. After the reaction was completed, the reaction solution was directly filtered and concentrated at reduced pressure to give compound 51b-3. MS m/z (ESI): 399.8 [M+H]+.
Steps 4-5: Compound 51b-5 was prepared with reference to steps 1-2 for 12c. MS m/z (ESI): 495.8 [M+H]+.
Steps 6-7: Compound 51b-7 was prepared with reference to steps 3-4 for 21c. MS m/z (ESI): 708.1 [M+H]+.
Step 8: Sodium hydroxide (18.07 mg, 451.87 μmol) was added to a mixture of 51b-7 (160 mg, 225.94 μmol) in anhydrous tetrahydrofuran (5 mL) and water (1 mL), and then the system was stirred at 80° C. for 5 h. After the reaction was completed, the reaction mixture was directly concentrated at reduced pressure to give a crude product. The crude product was purified by normal-phase column chromatography to give compound 51b. MS m/z (ESI): 568.2 [M+H]+.
Step 1: 103c-1 (6.39 g, 17.12 mmol) and CuCN (7.67 g, 85.61 mmol, 18.70 mL) were added to DMF (50 mL), and the reaction system was stirred in an autoclave at 140° C. for 72 h. After the reaction was completed, the reaction mixture was diluted with water and then extracted with ethyl acetate. The organic layers were combined, dried over anhydrous sodium sulfate, filtered, concentrated, and separated and purified by column chromatography (PE/EA=5/1-2/1) to give compound 52b-1 (yellow solid, 2.80 g). MS m/z (ESI): 320.1 [M+H]+.
Step 2: Compound 52b-2 was prepared with reference to step 3 for 45c. MS m/z (ESI): 290.2 [M+H]+.
Step 3: 52b-2 and 2 were added to a solution of tetrahydrofuran (25 mL), and then sodium tert-butoxide (1.46 g, 15.21 mmol) and tBuXPhos Pd G3 (604.02 mg, 760.38 μmol) were added. The reaction system was stirred at 65° C. for 12 h. After the reaction was completed, the reaction mixture was diluted with water and then extracted with dichloromethane. The organic layers were combined, dried over anhydrous sodium sulfate, filtered, and concentrated to give a crude product. The crude product was separated and purified by silica gel column chromatography (PE/EA=100/1-25/1) to give compound 52b-3. MS m/z (ESI): 569.2 [M+H]+.
Step 4: Compound 52b was prepared with reference to step 4 for intermediate 21c. MS m/z (ESI): 525.0 [M+H]+.
Step 1: 2,2,6,6-Tetramethylpiperidine (1.7 g, 12 mmol) and anhydrous THF (50 mL) were added in a 250 mL three-necked flask. In a nitrogen atmosphere, the reaction system was cooled to −45° C., and n-butyllithium (4.8 mL, 12 mmol, 2.5 M) was slowly and dropwise added. After the dropwise addition, the system was stirred at −45° C. for 1 h. A solution of 3-bromo-4-fluorobenzoic acid (2.2 g, 10 mmol) in THF (10 mL) was then slowly and dropwise added. The system was then stirred at that temperature for another 5 h. Finally, CH31 (0.79 mL, 12 mmol) was slowly and dropwise added, and the reaction system was allowed to gradually warm to room temperature and react at room temperature overnight. After the reaction was completed, at 0° C., the reaction system was diluted with 3 N HCl to quench the reaction and then extracted with EA. The organic layers were combined, washed with brine, dried over anhydrous sodium sulfate, filtered, and concentrated. The crude product was purified by column chromatography (MeOH/DCM=0-10%) to give compound 54d 1. MS m/z (ESI): 233.1 [M+H]+.
Step 2: Compound 54d-1 (1500 mg, 6.44 mmol) was dissolved in a single-necked flask with 20 mL of anhydrous MeOH. In an ice-water bath, SOCl2 (920 mg, 1.29 mmol) was then slowly and dropwise added. After the dropwise addition, the system was slowly warmed to reflux and stirred for 2 h. After the reaction was completed, the system was cooled to room temperature. The reaction solution was concentrated at reduced pressure, and the crude product was separated by column chromatography (EA/PE=0-5%) to give compound 54d-2. MS m/z (ESI): 247.1 [M+H]+
Steps 3-4: Compound 54d was prepared with reference to steps 2-3 for intermediate 3d. MS m/z (ESI): 341.2 [M+H]+.
Steps 5-6: Compound 54b was prepared with reference to steps 1-2 for intermediate 1b. MS m/z (ESI): 409.1 [M+H]+.
Compound 56b was prepared with reference to step 3 and step 4 for intermediate 21c. MIS M/Z (ESI): 630.2, 632.2 [M+H]+.
Step 1: 52b-3 (900 mg, 1.58 mmol) was added to a mixed solution of dimethyl sulfoxide (3 mL), ethanol (6 mL), and water (0.6 mL). An aqueous sodium hydroxide solution (2 M, 3.95 mL) and hydrogen peroxide (31.63 mmol, 3.04 mL, 30% purity) were added at 0° C., and then the reaction system was stirred at 25° C. for 72 h. After the reaction was completed, sodium thiosulfate was added to the reaction mixture to quench the reaction, and then the mixture was extracted with dichloromethane. The organic layers were combined, dried over anhydrous sodium sulfate, filtered, and concentrated to give compound 61b-1. MS m/z (ESI): 587.1 [M+H]+.
Step 2: Compound 61b was prepared with reference to step 4 for intermediate 21c. MS m/z (ESI): 543.1 [M+H]+.
Step 1: Compound 6-bromo-1H-indazol-3-amine (1.0 g, 4.74 mmol) was dissolved in DMF. The system was cooled to 0° C., and then NaH (284 mg, 7.1 mmol) was added. The system was allowed to react at 0° C. for 20 min, and then methyl iodide (1007 mg, 7.1 mmol) was added. The reaction system was allowed to react at 25° C. for 16 h. Water was added to the reaction solution, and the mixture was extracted with ethyl acetate. The organic phase was washed with brine, dried over anhydrous sodium sulfate, concentrated, and purified by column chromatography (MeOH/DCM=˜10%) to give compound 65b-1. MS m/z (ESI): 226.1 [M+H]+.
Step 2: Compound 65b-1 (575 mg, 1.47 mmol) was dissolved in acetic acid (5 mL) and water (5 mL), and acrylic acid (212 mg, 2.94 mmol) was added. The system was heated to 105° C. for reaction for 4 h, then adjusted to pH 5 with a saturated aqueous sodium bicarbonate solution, and extracted with DCM. The organic phase was dried over anhydrous sodium sulfate, concentrated, and purified by column chromatography (MeOH/DCM=˜10%) to give 65b-2. MS m/z (ESI): 299.1 [M+H]+.
Step 3: Compound 65b-2 (290 mg, 0.97 mmol) was dissolved in acetic acid (5 mL), and urea (30.5 mg, 1.95 mmol) was added. The system was heated to 120° C. for reaction for 4 h, and then concentrated hydrochloric acid was added. The reaction system was heated to reflux for 30 min. The solvent was removed by rotary evaporation, and a saturated aqueous sodium bicarbonate solution was added to adjust the pH to 7. The mixture was extracted with DCM, and the organic phase was dried over anhydrous sodium sulfate, concentrated, and purified by column chromatography (MeOH/DCM=˜10%) to give compound 65b-3. MS m/z (ESI): 323.1 [M+H]+.
Steps 4-6: Compound 65b was prepared with reference to steps 1-3 for intermediate 4b. MS m/z (ESI): 409.2 [M+H]+.
Compound 73b was prepared with reference to step 1 for compound 3d as step 1 and with reference to step 2 for compound 1b as step 2. MS m/z (ESI): 405.1 [M+H]+.
Step 1: Compound 77b-1 was prepared with reference to step 1 for intermediate 8a. MS m/z (ESI): 377.1 [M+H]+.
Step 2: Compound 77b-2 was prepared with reference to the preparation of intermediate 5d. MS m/z (ESI): 325.1 [M+H]+.
Step 3: Compound 77b-3 was prepared with reference to step 3 for intermediate 46a. MS m/z (ESI): 327.1 [M+H]+.
Step 4: Compound 77b-4 was prepared with reference to step 2 for intermediate 7a. MS m/z (ESI): 297.1 [M+H]+.
Steps 5-6: Compound 77b was prepared with reference to steps 3-4 for intermediate 21c. MS m/z (ESI): 532.2 [M+H]+.
Step 1: Ammonium chloride (1.22 g, 22.73 mmol), diisopropylethylamine (2.94 g, 22.73 mmol, 3.96 mL), and HATU (4.32 g, 11.36 mmol) were added to a solution of 79d (2 g, 7.58 mmol) in DMF (20 mL), and then the reaction system was stirred at 25° C. for 4 h. After the reaction was completed, the reaction solution was concentrated and purified by column chromatography (PE/EA=10/1-1/1) to give the title compound 79b-1 (yellow solid, 1.80 g). MS m/z (ESI): 263.1 [M+H]+.
Step 2: At 0° C., triethylamine (9.12 mmol, 1.27 mL) was added to a solution of 79b-1 (1.6 g, 6.08 mmol) in anhydrous tetrahydrofuran (50 mL). Trifluoroacetic anhydride (9.12 mmol, 1.27 mL) was then added slowly, and the reaction system was stirred at 25° C. for 2 h. After the reaction was completed, the reaction mixture was extracted with water and ethyl acetate and separated into layers. The organic layer was washed with brine, dried over anhydrous sodium sulfate, filtered, and concentrated at reduced pressure to give the title compound 79b-2 (yellow solid, 1.5 g, crude product). MS m/z (ESI): 245.1 [M+H]+.
Step 3: Diisopropylethylamine (422.01 mg, 3.27 mmol, 568.75 μL) and 1,4-dioxa-8-azaspiro[4.5]decane (467.53 mg, 3.27 mmol, 417.43 μL) were added to a solution of 79b-2 (800 mg, 3.27 mmol) in isopropanol (10 mL), and then the reaction system was stirred at 100° C. for 1 h. After the reaction was completed, the reaction solution was concentrated at reduced pressure to give the title compound 79b-3 (yellow solid, 1.00 g, crude product). MS m/z (ESI): 367.9 [M+H]+.
Step 4: Compound 79b-4 was prepared with reference to the method for intermediate 5d. MS m/z (ESI): 316.1 [M+H]+.
Step 5: Compound 79b-5 was prepared with reference to step 4 for intermediate 94c. MS m/z (ESI): 288.1 [M+H]+.
Step 6: 2,5-Dichloro-N-(2-dimethylphosphorylphenyl)pyrimidin-4-amine (242.02 mg, 765.60 μmol), 79b-5 (220 mg, 765.60 μmol), tris(dibenzylideneacetone)dipalladium (70.11 mg, 76.56 μmol), 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (44.3 mg, 76.56 μmol), and cesium carbonate (498.89 mg, 1.53 mmol) were added to a solution of 1,4-dioxane (2 mL), and then the reaction system was stirred at 100° C. for 8 h in a nitrogen atmosphere. After the reaction was completed, the system was extracted with water and ethyl acetate and separated into layers. The organic layer was washed with brine, dried over anhydrous sodium sulfate, filtered, concentrated at reduced pressure, and purified by thin-layer chromatography (DCM/MeOH=10/1) to give the title compound 79b-6. MS m/z (ESI): 567.2 [M+H]+.
Compound 79b was prepared with reference to step 4 for intermediate 21c as step 7. MS m/z (ESI): 523.1 [M+H]+.
Step 1: Compound tert-butyl piperazine-1-carboxylate (1 g, 5.37 mmol) and compound 4-bromobut-1-yne (785 mg, 5.91 mmol) were dissolved in CH3CN (20 mL), and then K2CO3 (1.11 g, 8.05 mmol) was added. The reaction system was stirred at 60° C. for 8 h. After the reaction was completed, the reaction system was concentrated. EA and H2O were added to the residue, and the aqueous phase was extracted with EA, dried over anhydrous sodium sulfate, filtered, concentrated, and purified by column chromatography (EA/PE: ˜20%) to give compound 80b-1 (colorless oily liquid, 950 mg).
Step 2: Compound 80b-2 was prepared with reference to step 1 for intermediate 1b. MS m/z (ESI): 481.5 [M+H]+.
Step 3: Compound 80b was prepared with reference to step 2 for intermediate 3b. MS m/z (ESI): 381.5 [M+H]+.
Step 1: NBS (5.29 g, 29.74 mmol) was added to a solution of 2-methoxy-4-nitroaniline (5 g, 29.74 mmol) in dichloromethane (50 mL) at 0° C., and then the reaction system was stirred at 25° C. for 4 h. After the reaction was completed, the reaction solution was concentrated at reduced pressure and then separated and purified by normal-phase column chromatography (PE/EA=1:0-5:1) to give the title compound 93b-1 (yellow solid, 3 g). 1H NMR (400 MHz, DMSO-d6) δ=7.97 (d, J 2.1 Hz, 1H), 8.20-7.88 (m, 1H), 7.58 (d, J 2.0 Hz, 1H), 6.41 (br s, 2H), 4.18-3.70 (m, 3H). MS m/z (ESI): 247.1 [M+H]+.
Step 2: At 0° C., 93b-1 (2 g, 8.10 mmol) and sodium nitrite (1.40 g, 20.24 mmol) were dissolved in hydrochloric acid (40 mL), and then cuprous chloride (1.60 g, 16.19 mmol, 387.18 μL) was added. The reaction system was warmed to 25° C. and stirred for 5 h in a nitrogen atmosphere. After the reaction was completed, the reaction solution was diluted with water, extracted with ethyl acetate, and separated and purified by normal-phase column chromatography (PE/EA=1:0-10:1) to give the title compound 93b-2 (white solid, 2 g). MS m/z (ESI): 266.1 [M+H]+.
Step 3: N,N-Diisopropylethylamine (2.91 g, 22.52 mmol) was added to a solution of 93b-2 (2 g, 7.51 mmol) and 1,4-dioxa-8-azaspiro[4.5]decane (2.15 g, 15.01 mmol) in dimethyl sulfoxide (20 mL), and then the reaction system was stirred at 80° C. for 1 h. After the reaction was completed, the reaction solution was diluted with water, extracted with EA, and separated and purified by normal-phase column chromatography (PE/EA=1:0-5:1) to give the title compound 93b-3 (yellow solid, 2.3 g). MS m/z (ESI): 373.1 [M+H]+.
Step 4: Compound 93b-4 was prepared with reference to the method for intermediate 5d. MS m/z (ESI): 321.1 [M+H]+.
Step 5: Compound 93b-5 was prepared with reference to step 2 for intermediate 3a. MS m/z (ESI): 293.1 [M+H]+.
Steps 6-7: Compound 93b was prepared with reference to steps 3-4 for 21c. MS m/z (ESI): 528.4[M+H]+.
Compound 97b was prepared with reference to step 2 for intermediate 1b. MS m/z (ESI): 405.2 [M+H]+.
Step 1: Compound 106b-1 was prepared with reference to the synthesis for compound C-1. MS m/z (ESI): 318.1 [M+H]+.
Step 2: Compound 106b was prepared with reference to step 2 for intermediate 1b. MS m/z (ESI): 396.8 [M+H]+.
Step 1: Compound 109b-1 was prepared with reference to step 1 for intermediate 114d. MS m/z (ESI): 331.2 [M+H]+.
Step 2: Compound 109b-2 was prepared with reference to step 2 for intermediate 3a. MS m/z (ESI): 333.1 [M+H]+.
Step 3: Compound 109b was prepared with reference to step 2 for intermediate 1b. MS m/z (ESI): 411.2 [M+H]+.
Step 1: Compound tert-butyl 9-oxo-3-azaspiro[5.5]undecane-3-carboxylate (3000 mg, 11.22 mmol) and anhydrous THE (30 mL) were added in a three-necked reaction flask. In a nitrogen atmosphere and in an ice-water bath, NaBH4 (849 mg, 22.44 mmol) was added in portions. After the addition, the system was warmed to room temperature and stirred overnight. After the reaction was completed, anhydrous Na2SO4 was added to the reaction solution, and water was slowly and dropwise added to quench the reaction. The mixture was filtered at reduced pressure and washed with DCM, and the filtrate was concentrated to give crude product 111a-1 (pale yellow oil, 3000 mg). The crude product was directly used in the next step.
Step 2: Compound 111a-2 was prepared with reference to step 1 for intermediate 110d.
Step 3: Compound 111a-3 was prepared with reference to step 2 for intermediate 3b.
Step 4: Compound 111a-4 was prepared with reference to step 1 for intermediate 3a. MS m/z (ESI): 499.6 [M+H]+.
Step 5: Compound 111a-5 was prepared with reference to the method for intermediate 5d. MS m/z (ESI): 447.8 [M+H]+.
Step 6: Compound IIIa was prepared with reference to step 2 for intermediate 3a. MS m/z (ESI): 419.7 [M+H]+.
Step 7: Compound nib-1 was prepared with reference to step 1 for intermediate 4c. MS m/z (ESI): 699.0 [M+H]+.
Step 8: Compound 111b-2 was prepared with reference to step 2 for intermediate 110d. MS m/z (ESI): 656.2 [M+H]+.
Step 9: Compound 111b was prepared with reference to step 2 for intermediate 1b. MS m/z (ESI): 734.3 [M+H]+.
Compound 145b was prepared with reference to the method for intermediate 65b. MS m/z (ESI): 391.2 [M+H]+.
Compound 155b was prepared with reference to the method for intermediate 4b. MS m/z (ESI): 409.2 [M+H]+.
Step 1: 3-(Benzyloxy)cyclobutan-1-one (4.73 g, 26.84 mmol) and tert-butyl piperazine-1-carboxylate (5 g, 26.84 mmol) were dissolved in a solution of MeOH (150 mL), and AcOH (8.06 g, 134.21 mmol) was added. The system was stirred at room temperature for 0.5 h. NaBH3CN (5.06 g, 80.53 mmol) was then added, and the reaction system was stirred at room temperature for 3.5 h. After the reaction was completed, a saturated aqueous NaHCO3 solution was added to quench the reaction. The mixture was extracted with DCM and separated into layers. The organic layer was washed with brine, dried over anhydrous sodium sulfate, filtered, concentrated at reduced pressure, and purified by column chromatography (PE/EA=5/1-3/1) to give compound 159b-1 (colorless oil, 6.5 g). 1H NMR (500 MHz, CDCl3) δ 7.38-7.30 (m, 5H), 4.42 (s, 2H), 3.83-3.73 (m, 1H), 3.47-3.37 (m, 4H), 2.44-2.40 (m, 2H), 2.33-2.22 (m, 5H), 2.18-2.14 (m, 1H), 1.90-1.82 (m, 2H), 1.72 (br s, 1H), 1.45 (s, 9H). MS m/z (ESI): 257.2 [M+H]+.
Step 2: Compound 159b-1 (6.5 g, 18.76 mmol) was dissolved in a solution of methanol (80 mL). In a nitrogen atmosphere, catalytic amounts of acetic acid (0.5 mL), Pd/C (2 g) and Pd(OH)2/C (1 g) were added. The reaction system was purged with hydrogen and stirred at 45° C. for 48 h in the hydrogen atmosphere. After the reaction was completed, the reaction mixture was filtered. The filtrate was concentrated at reduced pressure and then purified by column chromatography (MeOH/DCM: ˜3%-10%) to give compound 159b-2 (colorless oil, 3 g). MS m/z (ESI): 409.2 [M+H]+.
Step 3: Compound 159b-2 (95 mg, 0.36 mmol) and compound 3 (80 mg, 0.3 mmol) were dissolved in THE (10 mL), and then PPh3 (242 mg, 0.9 mmol) and DIAD (187 mg, 0.9 mmol) were added. In a nitrogen atmosphere, the reaction system was stirred at room temperature for 16 h. After the reaction was completed, the reaction mixture was extracted with water and EA, and the organic phase was dried and concentrated at reduced pressure to give a crude product. The crude product was purified by prep-TLC (DCM:MeOH=15:1) to give compound 159b-3 (pale yellow solid, 75 mg). MS m/z (ESI): 499.2 [M+H]+.
Step 4: Compound 159b was prepared with reference to step 2 for intermediate 3b. MS m/z (ESI): 399.2 [M+H]+.
Step 1: 3-(4-Amino-1-oxoisoindolin-2-yl)piperidine-2,6-dione (300 mg, 1.16 mmol) was added to a reaction flask. NMP (mL) was added, and then DIEA (0.5 mL) and 1,2-dibromoethane (1007 mg, 5.8 mmol) were added. The system was heated to 80° C. and stirred for 16 h. Water was added to the reaction solution, and the mixture was extracted with DCM, dried over anhydrous sodium sulfate, and concentrated. The reaction mixture was concentrated and then purified by column chromatography (dichloromethane:methanol=20:1) to give compound 163b-1 (white solid, 200 mg). MS m/z (ESI): 366.2, 368.2 [M+H]+.
Step 2: Compound 163b-1 (100 mg, 0.27 mmol) was dissolved in acetonitrile (5 mL) and water (0.1 mL), and a 37% aqueous formaldehyde solution (0.5 mL, 6.1 mmol) was added. The system was stirred at 20° C. for 2 h, then NaCNBH3 (80 mg, 1.4 mmol) was added, and the system was stirred at 20° C. for another 16 h. After the reaction was completed, water was added to quench the reaction. The mixture was extracted with DCM, and the organic phase was dried over anhydrous sodium sulfate and concentrated. The reaction mixture was concentrated and then purified by column chromatography (dichloromethane:methanol=10:1) to give 163b (white solid, 45 mg). MS m/z (ESI): 382.0 [M+H]+.
Step 1: Compound 4c (400 mg, 0.67 mmol) was dissolved in DMF (8 mL) before methyl 2-bromo-2-methylpropionate (145 mg, 0.80 mmol) and K2CO3 (185 mg, 1.34 mmol) were separately added. The system was then heated to 80° C. and stirred for 16 h. After the reaction was completed, as detected by LCMS, the reaction solution was filtered at reduced pressure, and the filtrate was concentrated by rotary evaporation at reduced pressure. The crude product was separated by normal-phase column chromatography (MeOH/DCM=0-5%) to give crude compound 207b-1 (pale yellow solid, 300 mg, yield: 63%). MS m/z (ESI): 697.3 [M+H]+.
Step 2: Title compound 207b-2 (pale yellow oil, 130 mg, yield: 45%) was prepared with reference to the synthesis method of step 2 for compound 110d. The crude product was directly used in the next step without further purification. MS m/z (ESI): 669.3 [M+H]+.
Step 3: Title compound 207b (130 mg, yield: 90%) was prepared with reference to the synthesis method of step 2 for compound 1b. MS m/z (ESI): 747.3 [M+H]+.
Step 1: Compound 3-(4-amino-1-oxoisoindolin-2-yl)piperidine-2,6-dione (1000 mg, 3.80 mmol), bis(pinacolato)diboron (1100 mg, 4.10 mmol), and anhydrous acetonitrile (20 mL) were added in a single-necked flask, and tert-butyl nitrite (600 mg, 5.70 mmol) was added slowly with stirring. After the addition, the system was stirred at room temperature for 5 h. After the reaction was completed, the reaction solution was directly evaporated to dryness at reduced pressure, and the residue was stirred with silica gel. The crude product was separated by normal-phase column chromatography to give compound 209b-1 (pale yellow solid, 700 mg). MS m/z (ESI): 371.2 [M+H]+.
Step 2: Compound 209b-1 (500 mg, 1.40 mmol), tetrahydrofuran (8 mL), and water (2 mL) were added to a single-necked flask before sodium periodate (870 mg, 4.20 mmol) was added slowly with thorough stirring. After the addition, the system was stirred at room temperature for 2 h, and then a 1 N diluted HCl solution (2 mL) was added. The system was then stirred at room temperature overnight. After the reaction was completed, the reaction solution was evaporated to dryness at reduced pressure before dichloromethane and water were added. The system was stirred at room temperature for 1 h, filtered at reduced pressure, washed with water, and lyophilized to give compound 209b (pale yellow solid, 320 mg). 1H NMR (500 MHz, DMSO-d6) δ 10.97 (s, 1H), 8.33 (s, 2H), 8.03 (d, J=7.3 Hz, 1H), 7.76 (d, J=7.3 Hz, 1H), 7.50 (t, J=7.4 Hz, 1H), 5.13 (dd, J=13.3, 5.1 Hz, 1H), 4.54 (d, J=18.1 Hz, 1H), 4.45 (d, J=18.1 Hz, 1H), 2.94-2.86 (m, 1H), 2.62-2.56 (m, 1H), 2.45-2.37 (m, 1H), 2.04-1.98 (m, 1H). MS m/z (ESI): 289.5 [M+H]+
Steps 1 and 2: Compound 223b-2 was prepared with reference to steps 2 and 3 for intermediate 3d. MS m/z (ESI): 290.2 [M+H]+.
Step 3: Compound 223b-3 was prepared with reference to step 2 for intermediate 3a. MS m/z (ESI): 260.2 [M+H]+.
Steps 4 and 5: Compound 223b was prepared with reference to steps 1 and 2 for intermediate 163b. MS m/z (ESI): 382.2 [M+H]+.
Preparation of Compounds of Formula (a-2)
With reference to the method in any one of compounds 1b, 3b, 4b, and 5b-223b, intermediate compounds of formula (a-2) were prepared from suitable lenalidomide derivatives, as shown in Table 4 below.
Step 1: Compound 13a (300 mg, 0.80 mmol) was added to a reaction flask before compound 2 (252 mg, 0.80 mmol), Pd(OAc)2 (18 mg, 0.08 mmol), Xant-phos (48 mg, 0.08 mmol), anhydrous Cs2CO3 (781 mg, 2.40 mmol), and anhydrous DMF (8 mL) were separately added. After the addition, the reaction system was purged 3 times with argon, then heated to 105° C., and stirred for 16 h. After the reaction was completed, the reaction mixture was filtered and concentrated. The crude product was purified by column chromatography (dichloromethane:methanol=30:1) and concentrated by rotary evaporation to give compound 1c-1. MS m/z (ESI): 655.3 [M+H]+.
Step 2: Compound 1c-1 (350 mg, 0.53 mmol) was added to a single-necked flask before anhydrous dichloromethane (15 mL) and TFA (3 mL) were separately added. After the addition, the system was stirred at room temperature for 2 h. After the reaction was completed, the solvent was removed from the reaction mixture at reduced pressure. The crude product was dissolved in dichloromethane and methanol before a saturated NaHCO3 solution was slowly added to the system to adjust the pH to 8-9. The mixture was then extracted with dichloromethane and methanol (10:1), and the organic phases were combined, dried over anhydrous sodium sulfate, and concentrated at reduced pressure to remove the solvent, thus giving compound 1c. MS m/z: 555.7 [M+H]+.
Compound 3c as a brown solid was prepared with reference to the method for intermediate 21c. MS m/z (ESI): 500.3 [M+H]+.
Step 1: Compound 3a (500 mg, 1.2 mmol), compound 2 (628.5 mg, 1.5 mmol), and p-toluenesulfonic acid monohydrate (412 mg, 2.4 mmol) were added to a reaction flask before i-PrOH (50 mL) was added. The reaction solution was stirred at 80° C. for 16 h and concentrated, and then a 5% NaOH solution was added. The mixture was extracted with dichloromethane, concentrated, and separated and purified by normal-phase column chromatography (dichloromethane:methanol=10:1) to give compound 4c-1 (white solid, 500 mg). MS m/z (ESI): 698.6 [M+H]+.
Step 2: Compound 4c-1 (1.4 g, 20 mmol) was added to a reaction flask before DCM (30 mL) was added. TFA (6 mL) was then added, and the reaction mixture was stirred at room temperature for 0.5 h and concentrated. A saturated sodium bicarbonate solution was added, and the mixture was extracted with dichloromethane and concentrated to give compound 4c (white solid, 1 g). MS m/z (ESI): 598.7 [M+H]+.
Compound 1d (200 mg, 0.55 mmol) and compound 5a (344 mg, 0.83 mmol) were added to a single-necked reaction flask before TsOH H2O (477 mg, 2.77 mmol) and n-BuOH (10 mL) were added. The system was purged 3 times with argon, then heated to 140° C., and stirred for 16 h. After the reaction was completed, the reaction mixture was concentrated. The crude product was purified by column chromatography and concentrated by rotary evaporation to give compound 7c (pale yellow solid, 0.2 g). MS (ESI) m/z: 628.3 [M+H]+.
Compound 9c (brown solid, 140 mg) was prepared with reference to the method for intermediate 4c. MS m/z (ESI): 568.7 [M+H]+.
Compound 10c was prepared with reference to the method for intermediate 4c. MS m/z (ESI): 605.4 [M+H]+.
Step 1: Dimethylphosphine oxide (2.90 g, 37.16 mmol), 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (4.30 g, 7.43 mmol), palladium acetate (835.00 mg, 3.72 mmol), and potassium phosphate (15.80 g, 74.43 mmol) were added to a solution of 1-iodonaphthalen-2-amine (10 g, 37.16 mmol) in 1,4-dioxane (100 mL), and the reaction system was stirred at 100° C. for 10 h. After the reaction was completed, the reaction mixture was extracted with water (80 mL) and dichloromethane and separated into layers. The organic layer was washed with brine, dried over anhydrous sodium sulfate, filtered, and concentrated at reduced pressure to give a crude product. The crude product was purified by column chromatography to give compound 12c-1 (brown solid, 5.6 g). MS m/z (ESI): 220.3 [M+H]+.
Step 2: 5-Bromo-2,4-dichloropyrimidine (5.02 g, 22.03 mmol, 2.82 mL) and N,N-diisopropylethylamine (3.54 g, 27.39 mmol, 4.77 mL) were added to a solution of compound 12c-1 (3 g, 13.68 mmol) in n-butanol (30 mL), and the reaction system was stirred at 120° C. for 8 h. After the reaction was completed, the reaction mixture was filtered and washed with ethanol to give the title compound 12c-2 (white solid, 3.27 g). MS m/z (ESI): 409.9 [M+H]+.
Step 3: p-Toluenesulfonic acid monohydrate (231.61 mg, 1.22 mmol) was added to a solution of compound 12c-2 (500 mg, 1.22 mmol) and compound 11a in isopropanol (5 mL), and then the reaction system was stirred for 6 h at 100° C. in a nitrogen atmosphere. After the reaction was completed, the reaction solution was adjusted to pH 9 with a sodium bicarbonate solution, and then extracted with water and dichloromethane and separated into layers. The organic layer was dried over anhydrous sodium sulfate, filtered, and concentrated at reduced pressure to give compound 12c. MS m/z (ESI): 663.3 [M+H]+.
Compound 13c was prepared with reference to the method for intermediate 4c. MS m/z (ESI): 610.2 [M+H]+.
Compound 14c was prepared with reference to the method for intermediate 4c. MS m/z (ESI): 559.1 [M+H]+.
Compound 15c was prepared with reference to the method for intermediate 4c. MS m/z (ESI): 584.1 [M+H]+.
Compound 17c was prepared with reference to the method for intermediate 4c. MS m/z (ESI): 574.3 [M+H]+.
Compound 18c was prepared with reference to the method for intermediate 4c. MS m/z (ESI): MS m/z: 559.6 [M+H]+.
Step 1: 1-Ethyl-2-fluoro-4-methoxy-5-nitro-benzene (1 g, 5.02 mmol) and 1,4-dioxa-8-azaspiro[4.5]decane (1.44 g, 10.04 mmol, 1.28 mL) were added to a solution of DMSO (10 mL), and then Cs2CO3 (4.91 g, 15.06 mmol) was added. The reaction system was stirred at 110° C. for 12 h. After the reaction was completed, the reaction mixture was diluted with water and extracted with ethyl acetate. The organic layers were combined, dried over anhydrous sodium sulfate, filtered, and concentrated to give a crude product. The crude product was separated and purified by column chromatography (PE:EA=25:1-1:1) to give compound 21c-1 (yellow oil, 1.34 g). MS m/z (ESI): 323.2 [M+H]+.
Step 2: Compound 21c-1 (1.2 g, 3.72 mmol) was added to a solution of ethanol (30 mL), and then wet Pd/C (200 mg, 10% purity) was added. The reaction system was stirred at 40° C. for 2 h in a hydrogen atmosphere. After the reaction was completed, the mixture was filtered, and the filtrate was concentrated to give compound 21c-2 (1.02 g, crude product), which was directly used in the next step. MS m/z (ESI): 293.2 [M+H]+.
Step 3: Compound 21c-2 (300 mg, 1.03 mmol) and compound 2 (324.37 mg, 1.03 mmol) were added to a solution of ethylene glycol (10 mL), and then p-toluenesulfonic acid monohydrate (292.77 mg, 1.54 mmol) was added. The reaction system was stirred at 90° C. for 12 h. After the reaction was completed, the reaction mixture was neutralized with a saturated aqueous sodium bicarbonate solution and extracted with ethyl acetate. The organic layers were combined, dried over anhydrous sodium sulfate, filtered, and concentrated to give a crude product. The crude product was separated and purified by a silica gel plate (dichloromethane:methanol=15:1) to give compound 21c-3 (black solid, 100 mg), which was directly used in the next step. MS m/z (ESI): 572.3 [M+H]+.
Step 4: Compound 21c-3 (90 mg, 157.33 μmol) was added to a mixed solution of water (4.5 mL) and acetic acid (4.5 mL), and the reaction system was stirred at 90° C. for 2 h. After the reaction was completed, the reaction mixture was neutralized with a saturated aqueous sodium bicarbonate solution and extracted with DCM. The organic layers were combined, dried over anhydrous sodium sulfate, filtered, and concentrated to give compound 21c, which was directly used in the next step. MS m/z (ESI): 528.3 [M+H]+.
Compound 22c was prepared with reference to step 3 and step 4 for intermediate 21c. MS m/z (ESI): 630.2 [M+H]+.
Compound 23c was prepared with reference to the method for intermediate 4c. MS m/z (ESI): 570.3 [M+H]+.
Compound 28c was prepared with reference to the method for intermediate 4c. LCMS: m/z (ESI): 685.0, 687.0 [M+H]+.
Step 1: DIEA and (Boc)2O (5.59 g, 25.61 mmol) were added to a solution of 2,3,4,5-tetrahydro-1H-benzo[d]azepine (2.9 g, 19.70 mmol) in dichloromethane (150 mL), and then the reaction system was stirred at 25° C. for 2 h. After the reaction was completed, the reaction mixture was diluted with ethyl acetate (100 mL), washed twice with hydrochloric acid, and then washed with saturated brine. The organic phase was dried over anhydrous sodium sulfate and concentrated to give compound 34c-1. MS m/z (ESI): 192.0 [M−55]+.
Step 2: At 25° C., silver trifluoroacetate and iodine (4.69 g, 18.48 mmol) were added to a solution of 34c-1 (4.57 g, 18.48 mmol) in dichloromethane (50 mL). The reaction was completed after the reaction system was stirred at 25° C. for 16 h. The reaction solution was concentrated to give crude compound 34c-2 (brown oil, 0.7 g). MS m/z (ESI): 318.0 [M−55]+.
Step 3: Cuprous oxide (67.09 mg, 468.88 μmol), N,N-dimethylethanolamine (1.25 g, 14.07 mmol), and potassium hydroxide (789.27 mg, 14.07 mmol) were added to a mixed solution of 34c-2 (1.75 g, 4.69 mmol) in dimethyl sulfoxide (15 mL) and water (7.5 mL), and then the reaction system was stirred at 100° C. for 12 h. After the reaction was completed, the reaction solution was extracted with water and EA and separated into layers. The organic layer was washed with brine, dried over anhydrous sodium sulfate, filtered, and concentrated at reduced pressure to give a crude product. The crude product was purified by silica gel column chromatography (PE:EA=100:1-10:1) to give the title compound 34c-3. MS m/z (ESI): 208.1 [M−55]+.
Steps 4-7: Compound 34c was prepared with reference to steps 2-5 for intermediate 120c. MS m/z (ESI): 406.3 [M+H]+.
Compound 36c was prepared with reference to step 2 for intermediate 4c. MS m/z (ESI): 394.1 [M+H]+.
Step 1: Compound 42c-1 was prepared with reference to the synthesis method for intermediate 1d. MS m/z (ESI): 347.3 [M+H]+.
Steps 2-3: Compound 42c was prepared with reference to steps 1-2 for intermediate 4c. MS m/z (ESI): 629.9 [M+H]+.
Step 1: Potassium tert-butoxide (1.99 g, 17.76 mmol) was added to a solution of methyl triphenyl phosphonium bromide (6.35 g, 17.76 mmol) in anhydrous tetrahydrofuran (60 mL) at −20° C., and then the system was warmed to 0° C. and stirred for 0.5 h. In a nitrogen atmosphere, a solution of 45d (3 g, 11.84 mmol) in anhydrous tetrahydrofuran (30 mL) was dropwise added, and the reaction system was stirred at 25° C. for 3 h. After the reaction was completed, the reaction was quenched with an aqueous ammonium chloride solution. The reaction mixture was extracted with water and ethyl acetate and separated into layers, dried over anhydrous sodium sulfate, filtered, concentrated at reduced pressure, and purified by column chromatography (PE/EA=10/1-5/1) to give compound 45c-1 (white oil, 2.38 g).
Step 2: 45c-1 (1.1 g, 4.38 mmol), compound 1 (1.56 g, 4.81 mmol), potassium chloride (326.25 mg, 4.38 mmol), tetrabutylammonium acetate (2.64 g, 8.75 mmol, 2.67 mL), palladium acetate (392.99 mg, 1.75 mmol), and potassium carbonate (1.21 g, 8.75 mmol) were added to a solution of DMF (10 mL). The reaction system was stirred at 100° C. for 5 h in a N2 atmosphere. After the reaction was completed, the reaction solution was directly filtered and concentrated at reduced pressure to give a crude product. The crude product was separated and purified by reverse-phase chromatography (formic acid system) to give 45c-2 (yellow solid, 1 g). MS m/z (ESI): 494.2 [M+H]+.
Step 3: Wet palladium on carbon (100 mg) was added to a solution of 45c-2 (100 mg, 202.60 μmol) in anhydrous tetrahydrofuran (2 mL), and then the reaction system was stirred at 25° C. for 1 h in a hydrogen atmosphere. After the reaction was completed, the mixture was filtered through celite and concentrated at reduced pressure to give compound 45c-2 (white solid, 92 mg). MS m/z (ESI): 396.1 [M+H-100]+.
Step 4: Compound 45c (off-white solid, 73 mg) was prepared with reference to step 2 for 3b. MS m/z (ESI): 396.1 [M+H]+.
Compound 46c was prepared with reference to the method for intermediate 4c. MS m/z (ESI): 602.3 [M+H]+.
Step 1: Compound 49c-1 (790 mg, 3.3 mmol) was dissolved in DMF (8 mL), and potassium carbonate (1.15 g, mmol) and iodoethane (1.3 g, 8.37 mmol) were added. The system was then heated to 80° C. and stirred for 16 h. After the reaction was completed, water was added to quench the reaction. The precipitated solid was collected by filtration at reduced pressure and dried to give compound 49c-1 (pale yellow solid, 610 mg). MS m/z (ESI): 266.4 [M+H]+.
Step 2: Compound 49c-2 was prepared with reference to step 1 for intermediate 8a. MS m/z (ESI): 515.5 [M+H]+.
Step 3: Compound 49c-3 was prepared with reference to the preparation of intermediate 5d. MS m/z (ESI): 461.9 [M+H]+.
Step 4: Compound 49c-4 was prepared with reference to step 2 for intermediate 3a. MS m/z (ESI): 433.2 [M+H]+.
Steps 5-6: Compound 49c was prepared with reference to steps 1-2 for intermediate 1c. MS m/z (ESI): 612.2 [M+H]+.
Step 1: Compound 55c-1 was separated with reference to the method for intermediate 5d. MS m/z (ESI): 212.2 [M+H]+.
Step 2: Compound 55c-2 was prepared with reference to step 1 for intermediate 21c. MS m/z (ESI): 335.5 [M+H]+.
Step 3: Compound 55c-3 was prepared with reference to step 2 for intermediate 3a. MS m/z (ESI): 307.2 [M+H]+.
Steps 4-5: Compound 55c was prepared with reference to steps 3-4 for intermediate 21c. MS m/z (ESI): 542.7 [M+H]+.
Step 1: Diisopropylethylamine (343.36 g, 2.66 mol), N-benzyl-2-chloro-N-(2-chloroethyl)ethan-1-amine hydrochloride (44 g, 265.67 mmol), and sodium iodide (79.65 g, 531.34 mmol) were added to a solution of compound ethyl 1-aminocyclopropane-1-carboxylate (71.36 g, 265.67 mmol) in ethanol (100 mL), and then the reaction system was stirred at 78° C. for 10 h. After the reaction was completed, the reaction mixture was concentrated at reduced pressure, diluted with ethyl acetate, washed with water, dried over anhydrous sodium sulfate, concentrated at reduced pressure, and then purified by silica gel column chromatography (PE:EA=100:1-5:1) to give 57c-1 (brown oil, 49 g). MS m/z (ESI): 289.0 [M+H]+.
Step 2: Palladium on carbon (10 g, 169.91 mmol, 10% purity) and (Boc)2O (41.17 g, 188.64 mmol) were added to a solution of 57c-1 (49 g, 169.91 mmol) in methanol (800 mL), and then the reaction system was stirred at 25° C. for 10 h in a hydrogen atmosphere. After the reaction was completed, the reaction solution was filtered through celite, and the filtrate was concentrated to give a crude product, which was purified by silica gel column chromatography (PE:EA=100:1-20:1) to give 57c-2 (brown oil, 34 g, crude product). MS m/z (ESI): 299.2 [M+H]+.
Step 3: A solution of 57c-2 (30 g, 100.54 mmol) in tetrahydrofuran (300 mL) was cooled to −78° C., and lithium aluminum hydride (11.45 g, 301.63 mmol) was added slowly in portions while maintaining this temperature. The reaction system was then stirred at 0° C. for 2 h. Then the reaction was quenched with sodium sulfate decahydrate, and the reaction solution was filtered and concentrated to give the title compound 57c-3 (white solid, 20.0 g). MS m/z (ESI): 257.2 [M+H]+.
Step 4: Oxalyl chloride (1.49 g, 11.70 mmol) was added to a solution of dimethyl sulfoxide (2.00 g, 25.60 mmol) in dichloromethane (15 mL), and the reaction system was stirred at −78° C. for 20 min. Then a solution of 57c-3 (0.5 g, 1.95 mmol) in dichloromethane (3 mL) was added, and the system was stirred at −78° C. for 1 h. Then triethylamine (1.18 g, 11.70 mmol) was added, and the system was stirred for 10 min. After the reaction was completed, the reaction was quenched with a saturated ammonium chloride solution, and then the mixture was diluted with dichloromethane, washed with water, dried over anhydrous sodium sulfate, and concentrated at reduced pressure to give the title compound 57c-4 (colorless oil, 0.5 g, crude product).
Step 5: At 0° C., potassium tert-butoxide (6.62 g, 120.4 mmol) was added to a solution of (methoxymethyl)triphenylphosphonium chloride (13.48 g, 39.32 mmol) in tetrahydrofuran (80 mL). The system was stirred for 0.5 h, and then 57c-4 (5.00 g, 19.66 mmol) was added. The reaction system was stirred at 25° C. for 16 h in a nitrogen atmosphere. After the reaction was completed, the reaction solution was directly concentrated at reduced pressure, then diluted with ethyl acetate, washed with water, and dried over anhydrous sodium sulfate. The organic phase was concentrated to give a crude product, which was purified by silica gel column chromatography (PE/EA=100/1-5/1) to give compound 57c-5 (brown oil, 0.8 g).
Step 6: A diluted hydrochloric acid solution (0.1 M, 28.33 mL) was added to a solution of 57c-5 (0.4 g, 1.42 mmol) in acetone (4 mL), and the system was stirred at 25° C. for 16 h. After the reaction was completed, the reaction solution was directly concentrated at reduced pressure to give a crude product (0.4 g). The crude product was dissolved in methanol (5 mL), and then potassium carbonate (412.03 mg, 2.98 mmol) was added. The system was cooled to 0° C., and then dimethyl (1-diazo-2-oxopropyl)phosphonate (572.71 mg, 2.98 mmol) was added. Then the system was warmed to room temperature for reaction for another 16 h. After the reaction was completed, the reaction solution was directly concentrated at reduced pressure, then diluted with ethyl acetate, washed three times with water, and dried over anhydrous sodium sulfate. The organic phase was concentrated to give a crude product,
Step 7: Compound 57c was prepared with reference to step 1 for intermediate 4b. MS m/z (ESI): 407.2 [M+H]+.
Compound 60c was prepared with reference to step 1 for intermediate 4c. MS m/z (ESI): 583.2[M+H]+.
Compound 62c was prepared with reference to steps 1-2 for intermediate 8a as steps 1-2 and with reference to steps 1-2 for intermediate 4c as steps 3-4. MS m/z (ESI): 595.2[M+H]+.
Step 1: 2,3-Dimethyl-6-nitroaniline (5 g, 30.09 mmol), methanesulfonic acid (5.78 g, 60.18 mmol, 4.28 mL), tert-butyl nitrite (7.76 g, 75.22 mmol, 8.95 mL), and tetrabutylammonium iodide (16.67 g, 45.13 mmol) were added to acetonitrile (50 mL) at 0° C. in a nitrogen atmosphere, and the reaction system was heated to 25° C. and stirred for 4 h. After the reaction was completed, the reaction system was concentrated at reduced pressure and separated and purified by normal-phase column chromatography (PE/EA=I/O-5/1) to give compound 63c-1 (brown solid, 2 g). MS m/z (ESI): 278.2[M+H]+.
Step 2: Compound 63c-2 was prepared with reference to step 2 for 7a. MS m/z (ESI): 248.2[M+H]+.
Step 3: 63c-3 was prepared with reference to step 1 for 12c. MS m/z (ESI): 198.2[M+H]+.
Step 4: 63c-3 (1 g, 5.07 mmol), 2,4,5-trichloropyrimidine (930.07 mg, 5.07 mmol), and N,N-diisopropylethylamine (1.97 g, 15.21 mmol, 2.65 mL) were dissolved in tetrahydrofuran (10 mL), and the reaction system was stirred at 65° C. for 8 h. After the reaction was completed, the reaction solution was concentrated at reduced pressure and separated and purified by reverse-phase chromatography (formic acid system) to give the title compound 63c-4 (pale yellow solid, 300 mg). MS m/z (ESI): 344.1 [M+H]+.
Step 5: 63c-5 was prepared with reference to step 3 for 52b. MS m/z (ESI): 726.2 [M+H]+.
Step 6: 63c was prepared with reference to step 2 for 3b. MS m/z (ESI): 626.1 [M+H]+.
Compound 68c was prepared with reference to the method for intermediate 165a. MS m/z (ESI): 644.3 [M+H]+.
Step 1: Compound 69c-1 was prepared with reference to step 3 for intermediate Id. MS m/z (ESI): 615.2 [M+H]+.
Step 2: Compound 69c-2 was prepared with reference to the method for intermediate 5d. MS m/z (ESI): 618.2 [M+H]+.
Step 3: Compound 69c was prepared with reference to step 4 for intermediate 21c. MS m/z (ESI): 574.2 [M+H]+.
Steps 1-2: Compound 71c-2 was prepared with reference to steps 1-2 for intermediate 3a. MS m/z (ESI): 392.0 [M+H]+.
Steps 3-4: Compound 71c was prepared with reference to steps 1-2 for intermediate 4c. MS m/z (ESI): 571.2 [M+H]+.
75c was prepared with reference to steps 2-5 for intermediate 120c. MS m/z (ESI): 392.2 [M+H]+.
Step 1: 1,1-Bis(diphenylphosphino)ferrocene palladium(II) chloride (585.92 mg, 800.76 μmol), potassium acetate (1.57 g, 16.02 mmol), and bis(pinacolato)diboron (3.05 g, 12.01 mmol) were added to a solution of 76d (2.5 g, 8.01 mmol) in 1,4-dioxane (50 mL), and then the reaction system was stirred at 100° C. for 5 h. After the reaction was completed, the reaction mixture was directly concentrated at reduced pressure to give compound 76c-1 (yellow solid, 5.00 g, crude product). MS m/z (ESI): 304.0 [M−55]+.
Step 2: At 25° C., hydrogen peroxide (15.78 g, 139.17 mmol) was added to a solution of 76c-1 (2.5 g, 6.96 mmol) in dichloromethane (50 mL), and then an aqueous solution (50 mL) of sodium hydroxide (2.78 g, 69.59 mmol) was added. The reaction system was stirred at 25° C. for 15 h. After the reaction was completed, the reaction solution was diluted with water, and then the reaction was quenched with saturated sodium thiosulfate. The mixture was then extracted with EA and dried over anhydrous sodium sulfate, and the organic phase was directly concentrated at reduced pressure to give a crude product. The crude product was purified by column chromatography (PE/EA=100/1-10/1) to give the title compound 76c-2 (yellow solid, 0.7 g). MS m/z (ESI): 194.1 [M−55]+.
Steps 3-6: Compound 76c was prepared with reference to steps 2-5 for 120c. MS m/z (ESI): 392.3 [M+H]+.
Step 1: 57c-3 (0.4 g, 1.56 mmol), tert-butyl 3-(4-hydroxy-1-oxoisoindolin-2-yl)-2,6-dioxopiperidine-1-carboxylate (562.32 mg, 1.56 mmol), azodicarbonamide (806.05 mg, 4.68 mmol), tributylphosphine (947.10 mg, 4.68 mmol) were dissolved in tetrahydrofuran (5 mL), and the reaction system was stirred at 25° C. for 2 h. After the reaction was completed, the reaction mixture was concentrated at reduced pressure, separated and purified by high performance liquid chromatography (hydrochloric acid system), and lyophilized to give 78c 1 (colorless liquid, 400 mg). MS m/z (ESI): 599.2 [M+H]+.
Step 2: 78c was prepared with reference to step 2 for 3b. MS m/z (ESI): 399.1 [M+H]+.
Compound 80c as a yellowish brown solid was prepared with reference to steps 3-4 for intermediate 21c. MS m/z (ESI): 531.7 [M+H]+.
Step 1: At 0° C., potassium carbonate (434.74 mg, 3.15 mmol) was added to a solution of 57c-4 (0.4 g, 1.57 mmol) in methanol (5 mL), and then dimethyl(1-diazo-2-oxopropyl)phosphonate (604.30 mg, 3.15 mmol) was added. The reaction system was stirred at 25° C. for 16 h in a nitrogen atmosphere. After the reaction was completed, the reaction solution was directly concentrated at reduced pressure, diluted with EA, washed with water, dried over anhydrous sodium sulfate, and concentrated to give a crude product, which was purified by silica gel column chromatography (PE/EA=100/1-20/1) to give the title compound 84c-1 (brown oil, 0.3 g).
Step 2: 84c-2 was prepared with reference to step 1 for 4b. MS m/z (ESI): 493.2 [M+H]+.
Step 3: 84c was prepared with reference to step 2 for 3b. MS m/z (ESI): 393.2 [M+H]+.
Step 1: At room temperature, HOAc (13 mg, 220 μmol) was added to a solution of compound 81d (50 mg, 110 μmol) and tert-butyl 4-oxopiperidine-1-carboxylate (44 mg, 220 μmol) in DCM (5 mL) before TEA (44 mg, 440 μmol) was added. The reaction system was adjusted to a weakly alkaline pH, stirred for 1 h before sodium triacetoxyborohydride (93 mg, 440 μmol) was added, and then stirred for another 12 h for reaction. After the reaction was completed, DCM and H2O were added to the reaction solution, and the mixture was extracted with DCM. The organic phase was washed with saturated brine and dried over anhydrous sodium sulfate. The crude product was purified by silica gel column chromatography (DCM/MeOH=100/1-20/1) to give compound 86c-1. MS m/z (ESI): 641.1 [M+H]+.
Step 2: Compound 86c-1 (50 mg, 0.08 mmol) and solvent DCM (4 mL) were added to a 25 mL reaction flask, and then TFA (2 mL) was added. The system was stirred at 20° C. for 1 h in a nitrogen atmosphere. After the reaction was completed, the reaction solution was concentrated, diluted with DCM, washed with saturated sodium bicarbonate until pH=7-8, and then extracted with DCM. The organic phase was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated to give compound 86c. MS m/z (ESI): 541.1 [M+H]+.
Step 1: tert-Butyl (4-hydroxyphenyl)carbamate (1000 mg, 4.78 mmol), 1,4-dibromobutane (2064 mg, 9.56 mmol), K2CO3 (1321 mg, 9.56 mmol), and anhydrous CH3CN (30 mL) were added to a single-necked flask. In a nitrogen atmosphere, the reaction system was heated to 90° C. and stirred for 16 h. After the reaction was completed, water was added to quench the reaction. The mixture was extracted with EA, and the organic phases were combined, then washed with saturated brine, and dried over anhydrous sodium sulfate. The crude product was subjected to normal-phase column chromatography (EA/PE=0-20%) to give compound 89c-1 (pale yellow solid, 1300 mg). MS m/z (ESI): 344.1 [M+H]+.
Step 2: Compound 89c-1 (50 mg, 0.15 mmol), compound 15c (85 mg, 0.15 mmol), K2CO3 (41 mg, 0.30 mmol), NaI (22 mg, 0.15 mmol), and anhydrous DMF (3 mL) were added to the reaction flask, and then the system was heated to 60° C. and stirred for 16 h. After the reaction was completed, the reaction mixture was filtered. The filtrate was concentrated at reduced pressure, and then the crude product was separated by normal-phase column chromatography (MeOH/DCM=0-5%) to give intermediate 89c-2 (pale yellow solid, 45 mg). MS m/z (ESI): 846.1 [M+H]+.
Step 3: Crude compound 89c was prepared with reference to step 2 for intermediate 3b. MS m/z (EST): 746 2 [M+H]+.
Step 1: Compound 2-fluoro-4-methoxybenzaldehyde (1 g, 6.5 mmol) was dissolved in concentrated sulfuric acid (5 mL). The system was cooled to 0° C., and concentrated nitric acid (441 mg, 7 mmol) was dropwise added. The mixture was then stirred at 20° C. for 2 h and poured into ice water, and a large amount of solid was precipitated. The solid was then collected by filtration at reduced pressure and dried to give compound 91c-1 (pale yellow solid, 600 mg). MS m/z (ESI): 200.1 [M+H]+.
Step 2: Compound 91c-1 (300 mg, 1.5 mmol) was dissolved in DMF (10 mL), and compound al (300 mg, 2 mmol) and potassium carbonate (414 mg, 3 mmol) were sequentially added. The system was then stirred at 85° C. for 16 h. After the reaction was completed, water was added to quench the reaction. The precipitated solid was collected by filtration at reduced pressure and dried to give compound 91c-2 (pale yellow solid, 320 mg). MS m/z (EST): 323.2 [M+H]+.
Step 3: Compound 91c-2 (320 mg, 0.98 mmol) was dissolved in MeOH (10 mL), and the system was cooled to 0° C. Sodium borohydride (137.8 mg, 4.9 mmol) was added, and then the system was warmed to room temperature and stirred for 3 h. After the reaction was completed, water was added to quench the reaction, and the mixture was extracted with dichloromethane, dried over anhydrous sodium sulfate, filtered, and then concentrated at reduced pressure to give compound 91c-3 (yellow oil, 265 mg). MS m/z (EST): 325.1 [M+H]+.
Step 4: Compound 91c-3 (265 mg, 0.82 mmol) and imidazole (111 mg, 1.63 mmol) were dissolved in DCM (mL), and the system was cooled to 0° C. TBS-Cl (244.5 mg, 1.63 mmol) was added, and then the system was warmed to room temperature and stirred for 3 h. After the reaction was completed, water was added to quench the reaction, and the mixture was extracted with dichloromethane, dried over anhydrous sodium sulfate, filtered, then concentrated at reduced pressure, and purified by normal-phase column chromatography (dichloromethane:methanol=10:1) to give compound 91c-4 (yellow oil, 330 mg). MS m/z (ESI): 439.4 [M+H]+.
Step 5: Compound 91c-5 was prepared with reference to step 2 for intermediate 3a. MS m/z (ESI): 409.1 [M+H]+.
Step 6: Compound 91c-6 was prepared with reference to step 1 for intermediate 1c. MS m/z (ESI): 688.3 [M+H]+.
Step 7: Compound 91c-6 (100 mg, 0.15 mmol) was dissolved in THE (2 mL), and 6 N HCl (0.25 mL, 1.5 mmol) was added. The reaction system was heated to 70° C., stirred for 3 h, cooled to room temperature, adjusted to pH 7 by adding a saturated aqueous sodium carbonate solution, and extracted with dichloromethane. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, filtered, and concentrated by rotary evaporation. The crude product was purified by normal-phase column chromatography (dichloromethane:methanol=10:1) to give compound 91c (yellow oil). MS m/z (ESI): 530.3 [M+H]+.
Step 1: 2-Amino-3-bromo-5-nitrobenzonitrile (10 g, 41.32 mmol) and sodium nitrite (7.13 g, 103.29 mmol) were added to hydrochloric acid (100 mL) at 0° C., and the system was purged 3 times with nitrogen. After 1 h, cuprous chloride (6.14 g, 61.98 mmol) was added, and the reaction system was stirred at 0-25° C. for 11 h. After the reaction was completed, the reaction mixture was diluted with water and extracted with ethyl acetate. The organic layers were combined, washed with saturated brine, dried over anhydrous sodium sulfate, filtered, and concentrated to give compound 94c-1 (yellow solid, 10.0 g).
Step 2: Compound 94c-2 was prepared with reference to step 1 for intermediate 21c. MS m/z (ESI): 368.1 [M+H]+.
Step 3: Compound 94c-3 was prepared with reference to the method for intermediate 5d. MS m/z (ESI): 316.0 [M+H]+.
Step 4: 94c-3 (600 mg, 1.90 mmol) was added to tetrahydrofuran (6 mL), and then wet palladium on carbon (300 mg, 10% purity) was added. The reaction system was stirred at 25° C. for 0.5 h in a hydrogen atmosphere.
After the reaction was completed, the reaction mixture was filtered and concentrated to give the title compound 94c-4 (yellow solid, 300 mg), which was directly used in the next step. MS m/z (ESI): 288.0 [M+H]+.
Steps 5-6: Compound 94c was prepared with reference to steps 3-4 for intermediate 21c. MS m/z (ESI): 523.0 [M+H]+.
Compound 98c was prepared with reference to the method for intermediate 4c as step 1 and step 3 and with reference to the method for compound E67 as step 2. MS m/z (ESI): 599.9 [M+H]+.
Step 1: Compound (50 mg, 0.155 mmol) was dissolved in MeOH (6 mL). In an ice bath, concentrated NaOMe (50 mg, 0.155 mmol) was added slowly. The system was then stirred at 0° C. for 12 h in a nitrogen atmosphere. After the reaction was completed, the reaction solution was concentrated. Water was added to quench the reaction, and the mixture was extracted with ethyl acetate. The organic phase was washed with saturated brine, dried over anhydrous sodium sulfate, concentrated, and subjected to normal-phase column chromatography (PE/EtOAc=0-20%) to give compound 90c-1 (yellow solid, 60 mg). MS m/z (ESI): 263.2 [M+H]+.
Step 2: Compound 99c-2 was prepared with reference to step 1 for intermediate 7a. MS m/z (ESI): 452.1 [M+H]+.
Step 3: Compound 99c-3 was prepared with reference to step 2 for intermediate 3a. MS m/z (ESI): 422.2 [M+H]+.
Steps 4-5: Compound 99c was prepared with reference to steps 1-2 for intermediate 4c. MS m/z (ESI): 601.9 [M+H]+.
Step 1: Potassium carbonate (3.32 g, 24.00 mmol, 2 eq) and 1,4-dioxa-8-azaspiro[4.5]decane (1.89 g, 13.20 mmol, 1.69 mL) were added to a solution of 1-bromo-2-fluoro-4-methoxy-5-nitrobenzene (3 g, 12.00 mmol) in DMF (20 mL), and then the reaction system was stirred at 60° C. for 1 h. After the reaction was completed, the reaction solution was added to 300 mL of ice water at 0° C., and a solid was precipitated. The solid was then collected by filtration and dried to give compound 103c-1 (yellow solid, 4.00 g, crude product). MS m/z (ESI): 372.8 [M+H]+.
Step 2: 103c-1 (6.39 g, 17.12 mmol) and cuprous cyanide (7.67 g, 85.61 mmol, 18.70 mL) were added to DMF (50 mL), and the reaction system was stirred in an autoclave at 140° C. for 72 h. After the reaction was completed, the reaction mixture was diluted with water and then extracted with ethyl acetate. The organic layers were combined and dried over anhydrous sodium sulfate. The crude product was then filtered, concentrated, and separated and purified by silica gel column chromatography (PE:EA=5:1-2:1) to give the title compound 103c-2 (yellow solid, 2.80). MS m/z (ESI): 320.1 [M+H]+.
Step 3: Compound 103c-3 was prepared with reference to step 2 for intermediate 3a. MS m/z (ESI): 290.1 [M+H]+.
Steps 4-5: Compound 103c-5 was prepared with reference to steps 3-4 for intermediate 21c. MS m/z (ESI): 525.1 [M+H]+.
Step 6: Compound 103c-6 was prepared with reference to the method for reference compound C-6. MS m/z (ESI): 695.3 [M+H]+.
Step 7: Compound 103c was prepared with reference to step 2 for intermediate 3b. MS m/z (ESI): 595.3 [M+H]+.
Compound 105c was prepared with reference to the method for intermediate 1d as step 1 and with reference to the method for intermediate 4c as steps 2-3. MS m/z (ESI): 650.3 [M+H]+.
Compound 108c was prepared with reference to the method for intermediate 86c. MS m/z (ESI): 626.4 [M+H]+.
Step 1: Compound 2,6-dibromo-3-nitropyridine (3000 mg, 10.64 mmol) and anhydrous MeOH (30 mL) were added to a three-necked reaction flask. In a nitrogen atmosphere and in an ice-water bath, NaH (468 mg, 11.70 mmol, 60% wt) was added in portions. After the addition, the system was stirred in the ice-water bath for another 0.5 h before CH3ONa (575 mg, 10.64 mmol) was added in portions. The system was then stirred in the ice-water bath for another 3 h. After the reaction was completed, saturated NH4Cl was added to the reaction solution to quench the reaction. The mixture was then extracted with EA, and the organic phases were combined, washed with water, washed with saturated brine, dried over anhydrous Na2SO4, and concentrated by rotary evaporation at reduced pressure. The crude product was separated by normal-phase column chromatography (EA/PE=0-15%) to give product 115c-1 (pale yellow solid, 2200 mg). MS m/z (ESI): 233.1 [M+H]+.
Step 2: Compound 115c-1 (2200 mg, 9.44 mmol) and anhydrous TFA (20 mL) were added to a single-necked flask before dibromohydantoin (3240 mg, 11.33 mmol) was added. After the addition, the system was stirred at room temperature for 16 h. After the reaction was completed, the reaction solvent was removed at reduced pressure, and the crude product was triturated with PE/EA (50:1). The triturate was filtered at reduced pressure and washed with PE. The filter cake was dried by rotary evaporation at reduced pressure to give crude compound 115c-2 (pale yellow solid, 2100 mg), which was directly used in the next step. MS m/z (ESI): 311.1 [M+H]+.
Step 3: Crude compound 115c-3 was prepared with reference to step 1 for intermediate 21c. MS m/z (ESI): 374.3 [M+H]+.
Step 4: Crude compound 115c-4 was prepared with reference to the method for intermediate 5d. MS m/z (ESI): 322.5 [M+H]+.
Step 5: Crude compound 115c-5 was prepared with reference to step 2 for intermediate 3a. MS m/z (ESI): 294.5 [M+H]+.
Step 6: Compound 115c-6 was prepared with reference to step 1 for intermediate 1c. MS m/z (ESI): 573.8 [M+H]+.
Step 7: Compound 115c-7 was prepared with reference to step 4 for intermediate 21c. MS m/z (ESI): 529.8 [M+H]+.
Step 8: Product 115c-8 was prepared with reference to compound E67. MS m/z (ESI): 700.0 [M+H]+.
Step 9: Crude compound 115c was prepared with reference to step 2 for intermediate 3b. MS m/z (ESI): 599.8 [M+H]+.
Step 1: Compound 116c-1 was prepared with reference to the method of step 1 for intermediate 3a. MS m/z (ESI): 444.1 [M+H]+.
Step 2: Compound 116c-2 was prepared with reference to the method for intermediate 5d. MS m/z (ESI): 392.1 [M+H]+.
Step 3: Compound 116c-3 was prepared with reference to the method of step 2 for intermediate 3a. MS m/z (ESI): 364.3 [M+H]+.
Steps 4-5: Compound 116c was prepared with reference to the methods of steps 1-2 for intermediate 1c. MS m/z (ESI): 543.7 [M+H]+.
Step 1: Acetic acid (3.79 mL, 1 M in DCM) and TEA (1.1 mL, 7.58 mmol) were added to a solution of compound 21c (1 g, 1.89 mmol) and tert-butyl(2-aminoethyl)carbamate (607 mg, 3.79 mmol) in DCE (5 mL), and the reaction solution was stirred at 25° C. for 2 h. Then sodium triacetoxyborohydride (1.61 g, 7.58 mmol) was added, and the reaction system was stirred at 25° C. for 16 h. Saturated NaHCO3 was added, and the mixture was extracted with DCM, dried, concentrated, and subjected to column chromatography (MeOH/DCM=˜10%) to give compound 118c-1 (white solid, 1.2 g). MS m/z (ESI): 673.4 [M+H]+.
Step 2: Compound 118c-1 (1.3 g, 1.93 mmol) was dissolved in DCM (50 mL), and then Et3N (0.84 mL, 5.8 mmol) and chloroacetyl chloride (262 mg, 2.32 mmol) were added. The reaction system was stirred at room temperature for 16 h. After the reaction was completed, the reaction was quenched with a saturated sodium bicarbonate solution, and the mixture was extracted with DCM. The organic phase was washed with brine, dried, filtered, and concentrated to give a crude product. The crude product was dissolved in DMF (20 mL), and NaH (387 mg, 9.67 mmol) was added in portions at room temperature. The reaction system was stirred at room temperature for 16 h. After the reaction was completed, the reaction was quenched with a saturated sodium bicarbonate solution. The mixture was extracted with DCM, washed with brine, dried, filtered, and concentrated to give a crude product, which was purified by column chromatography (MeOH/DCM=˜8%) to give compound 118c-2 (white solid, 0.65 g). MS m/z (ESI): 713.3 Step 3: Compound 118c was prepared with reference to step 2 for intermediate 3b. MS m/z (ESI): 613.2 [M+H]+.
Step 1: Methanesulfonato(2-di-tert-butylphosphino-2,4,6-triisopropyl-1,1-biphenyl)(2-amino-1,1-biphenyl-2-yl)palladium (II) (0.52 g, 0.65 mmol) and potassium hydroxide (0.92 g, 16.42 mmol) were added to a mixed solution of tert-butyl 5-bromoisoindoline-2-carboxylate (2.5 g, 8.43 mmol) in 1,4-dioxane (50 mL) and water (20 mL), and then the reaction system was stirred at 80° C. for 18 h. After the reaction was completed, the reaction mixture was diluted with ethyl acetate and washed with water, and then the organic phase was dried over anhydrous sodium sulfate and concentrated at reduced pressure to give compound 120c-1 (yellow solid, 1.6 g, crude product). MS m/z (ESI): 180.0 [M−55]+.
Step 2: Potassium carbonate (822.38 mg, 5.95 mmol) and 2-bromo-6-fluorobenzaldehyde (603.99 mg, 2.98 mmol) were added to a solution of 120c-1 (0.7 g, 2.98 mmol) in DMF (4 mL), and then the reaction system was stirred at 60° C. for 2 h. After the reaction was completed, the reaction solution was extracted with water and ethyl acetate and separated into layers. The organic layer was washed with brine, dried over anhydrous sodium sulfate, filtered, and concentrated at reduced pressure to give compound 120c-2 (brown oil, 0.9 g, crude product). MS m/z (ESI): 362.3 [M−55]+.
Step 3: Triethylamine (302.40 mg, 2.99 mmol) was added to a solution of 120c-2 (0.5 g, 1.20 mmol) in methanol (5 mL), and then the reaction system was stirred at 25° C. for 0.5 h. Acetic acid (100.49 mg, 1.67 mmol) and 3-aminopiperidine-2,6-dione (196.75 mg, 1.20 mmol) were then added, and the system was stirred at 25° C. for another 2 h. Sodium cyanoborohydride (225.35 mg, 3.59 mmol) was then added, and the system was stirred at 25° C. for another 1 h. The reaction solution was concentrated at reduced pressure and then separated and purified by a silica gel plate (dichloromethane:methanol=10:1) to give the title compound 120-3 (colorless oil, 0.6 g, crude product), which was used directly in the next step. MS m/z (ESI): 530.3 [M+H]+.
Step 4: 120c-3 (0.5 g, 942.67 μmol) and 1,3-bis(dicyclohexylphosphonium)propane bis(tetrafluoroborate) (57.72 mg, 94.27 μmol) were dissolved in DMF (20 mL), and then palladium acetate (21.16 mg, 94.27 μmol) and potassium carbonate (195.43 mg, 1.41 mmol) were added. In a carbon monoxide atmosphere, the reaction system was stirred at 80° C. for 24 h. After the reaction was completed, the reaction mixture was extracted with water and ethyl acetate, and the organic phase was dried and concentrated at reduced pressure to give the title compound 120c-4 (green solid, 600 mg, crude product), which was used directly in the next step. MS m/z (ESI): 378.1 [M+H-100]+.
Step 5: A solution of 120c-4 (290.83 mg, 609.06 μmol) in hydrogen chloride in ethyl acetate (4 M, 10 mL) was stirred at 25° C. for reaction for 2 h. After the reaction was completed, the reaction solution was directly concentrated to give the title compound 120c (green solid, 200 mg, HCl salt). MS m/z (ESI): 378.3 [M+H]+.
Step 1: In a nitrogen atmosphere, ethyl 3-hydroxy-propionate (90.78 mg, 768.51 μmol) was added to a solution of compound 3 (100 mg, 384.25 μmol), azodicarbonamide (198.49 mg, 1.15 mmol), and tributylphosphine (233.22 mg, 1.15 mmol, 284.42 μL) in tetrahydrofuran (3 mL), and then the reaction system was stirred at 25° C. for 10 h. After the reaction was completed, the reaction mixture was directly concentrated at reduced pressure to give a crude product. The crude product was separated and purified by thin-layer chromatography to give compound 121c-1 (white solid, 46 mg). MS m/z (ESI): 361.2 [M+H]+.
Step 2: A solution of hydrogen chloride in dioxane (4 M, 2 mL) was added to a solution of 121c-1 (40 mg, 111.00 μmol) in water (0.1 mL), and then the reaction system was stirred at 80° C. for 8 h. After the reaction was completed, the reaction mixture was directly concentrated at reduced pressure to give compound 121c (white solid, 24 mg). MS m/z (ESI): 333.1 [M+H]+.
Compound 124c was prepared with reference to step 1 for intermediate ii 4d as step 1, with reference to the method for intermediate id as step 2, and with reference to the method for intermediate 4c as steps 3-4. MS m/z (ESI): 616.2 [M+H]+.
Step 1: Compound 125c-1 was prepared with reference to compound C-6. MS m/z (ESI): 601.1 [M+H]+.
Step 2: Compound 125c-1 (100 mg, 0.19 mmol) was dissolved in methanol (4 mL), and 4 M HCl/1,4-dioxane (0.5 mL, 2 mmol) was added. The system was heated to reflux for reaction for 4 h, then adjusted to pH 7 with a saturated aqueous sodium bicarbonate solution, and extracted with DCM. The organic phase was dried over anhydrous sodium sulfate, concentrated, and purified by column chromatography (MeOH/DCM=˜10%) to give 125c (white solid, 60 mg). MS m/z (ESI): 614.1 [M+H]+.
Compound 127c was prepared with reference to step 2 for intermediate 3b. MS m/z (ESI): 600.2 [M+H]+.
Compound 129c was prepared with reference to the method for E67 as step 1 and with reference to step 2 for intermediate 15c as step 2. MS m/z (ESI): 626.9 [M+H]+.
Step 1: Compound 131c-1 was prepared with reference to step 1 for intermediate 7a. MS m/z (ESI): 459.1 [M+H]+.
Step 2: 131c-1 (2.0 g, 4.35 mmol) was added to a mixed solution of methanol (6 mL) and 1,4-dioxane (30 mL), and then sodium methoxide (2.35 g, 43.54 mmol) and cuprous iodide (829.19 mg, 4.35 mmol) were added. The reaction system was stirred at 100° C. for 2 h in a nitrogen atmosphere. After the reaction was completed, the reaction mixture was diluted with water and then extracted with dichloromethane. The organic layers were combined, dried over anhydrous sodium sulfate, filtered, and concentrated to give a crude product. The crude product was separated and purified by silica gel column chromatography (PE/EA=10:1-1:1) to give the title compound 131c-2. MS m/z (ESI): 451.1 [M+H]+.
Step 3: Compound 131c-3 was prepared with reference to step 2 for intermediate 3a. MS m/z (ESI): 421.1 [M+H]+.
Step 4: Compound 131c-4 was prepared with reference to step 1 for intermediate 4c. MS m/z (ESI): 700.3 [M+H]+.
Step 5: Compound 131c was prepared with reference to step 2 for intermediate 3b. MS m/z (ESI): 600.3 [M+H]+.
Step 1: Compound 132c-1 was prepared with reference to the method for intermediate 1d. MS m/z (ESI): 340.1 [M+H]+.
Step 2: Compound 132c-2 was prepared with reference to step 1 for intermediate 4c. MS m/z (ESI): 722.4 [M+H]+.
Step 3: Lithium hydroxide monohydrate (348.78 mg, 8.31 mmol) was added to a mixed solution of 132c-2 (1.5 g, 2.08 mmol) in tetrahydrofuran (15 mL), methanol (15 mL), and water (1.5 mL), and then the reaction system was stirred at 25° C. for 16 h in a nitrogen atmosphere. After the reaction was completed, the reaction solution was concentrated to remove the solvent. The residue was adjusted to pH 3-5 with a 1 M aqueous hydrochloric acid solution, and then the mixture was extracted with dichloromethane and separated into layers. The organic layers were combined, dried over anhydrous sodium sulfate, and concentrated at reduced pressure to give compound 132c-3 (blackish brown solid, 1.0 g). MS m/z (ESI): 708.3 [M+H]+.
Step 4: HATU (128.93 mg, 339.08 μmol), DIEA (109.56 mg, 847.70 μmol), and ammonium chloride (109.56 mg, 847.70 μmol) were added sequentially to a solution of 132c-3 (200 mg, 282.57 μmol) in DMF (5 mL), and then the reaction system was stirred at 25° C. for 3 h in a nitrogen atmosphere. After the reaction was completed, the reaction mixture was filtered to give a crude product. The crude product was separated and purified by reverse-phase chromatography to give the title compound 132C-4 (yellow solid, 100 mg). MS m/z (ESI): 707.4 [M+H]+.
Step 5: Compound 132c was prepared with reference to step 2 for intermediate 3b. MS m/z (ESI): 607.4 [M+H]+.
Step 1: Compound 132c-3 (150 mg, 0.22 mmol) and DMF (2 mL) were added to a single-necked flask, then HATU (120.87 mg, 0.32 mmol) and DIPEA (164.34 mg, 1.27 mmol) were added, and finally methylamine hydrochloride (42.93 mg, 0.64 mmol) was added. The reaction system was stirred at 25° C. for 12 h. After the reaction was completed, the reaction mixture was diluted with water and then extracted with DCM. The organic layers were combined, dried over anhydrous sodium sulfate, filtered, and concentrated. The crude product was separated and purified by a silica gel plate (dichloromethane:methanol=10:1) to give the title compound 133c-1 (123 mg, crude product). MS m/z (ESI): 721.4 [M+H]+.
Step 2: Compound 133c was prepared with reference to step 2 for intermediate 1c. MS m/z (ESI): 621.4 [M+H]+.
Compound 134c was prepared with reference to the method for intermediate 133c. MS m/z (ESI): 635.4 [M+H]+.
Compound 135c was prepared with reference to the method for intermediate 133c. MS m/z (ESI): 649.4 [M+H]+.
Compound 28c was prepared with reference to the method for intermediate 4c. LCMS: m/z (ESI): 598.3 [M+H]+.
Compound 137c was prepared with reference to the method for intermediate 86c. MS m/z (ESI): 610.9 [M+H]+.
Title compound 140c was prepared with reference to steps 5 and 6 for intermediate 154c. MS m/z (ESI): 587.2 [M+H]+.
Compound 141c was prepared with reference to steps 5-6 for intermediate 154c. MS m/z (ESI): 603.3 [M+H]+.
Step 1: Compound 142c-1 was prepared with reference to step 5 for intermediate 154c. MS m/z (ESI): 861.3 [M+H]+.
Step 2: Compound 142c-1 (650 mg, 0.75 mmol) and anhydrous THE (10 mL) were added to a three-necked flask. In a nitrogen atmosphere and in an ice-water bath, methylmagnesium bromide (1 M, 8 mL) was slowly and dropwise added. After the dropwise addition, the reaction solution was stirred at 0° C. for 0.5 h, and then warmed to room temperature and stirred for 6 h. After the reaction was completed, water was added to the reaction solution to quench the reaction. The mixture was extracted with ethyl acetate, and the organic phase was dried over anhydrous sodium sulfate, filtered, and concentrated by rotary evaporation. The crude product was separated by column chromatography to give compound 142c-2 (pale yellow solid, 630 mg). MS m/z (ESI): 861.7 [M+H]+.
Step 3: Compound 142c was prepared with reference to step 6 for intermediate 154c. MS m/z (ESI): 653.6 [M+Na]+.
Compound 144c was prepared with reference to the method for intermediate 86c. MS m/z (ESI): 624.8 [M+H]+.
Compound 146c was prepared with reference to step 1 for intermediate 3a as step 1, with reference to the method for 5d as step 2, with reference to step 2 for 3a as step 3, and with reference to steps 1-2 for intermediate 1c as steps 4-5. MS m/z (ESI): 650.3 [M+H]+.
Compound 147c was prepared with reference to the method for intermediate 176a. MS m/z (ESI): 644.7 [M+H]+.
Compound 148c was prepared with reference to step 1 for intermediate 133c as step 1 and with reference to step 2 for intermediate 1c as step 2. MS m/z (ESI): 661.6 [M+H]+.
Step 1: Compound 132c-3 (200 mg, 0.28 mmol) was dissolved in THE (50 mL), and then CDI (115 mg, 0.71 mmol) was added. The reaction system was stirred at room temperature for 16 h. (Z)—N-hydroxyacetimide (52 mg, 0.71 mmol) was then added, and the reaction system was stirred at room temperature for 16 h. After the reaction was completed, the reaction mixture was diluted with EA and poured into ice water. The mixture was extracted with EA, and the organic phase was washed with brine, dried over anhydrous sodium sulfate, filtered, and concentrated to give crude compound 149c-1 (white solid, 250 mg, crude product). MS m/z (ESI): 763.4 [M+H]+.
Step 2: Compound 149c-1 (215 mg, 0.28 mmol) was dissolved in DMSO (50 mL), and then KOH (47 mg, 0.84 mmol) was added. The reaction system was stirred at room temperature for 16 h. After the reaction was completed, the reaction solution was directly concentrated and purified by column chromatography (80 g, MeOH/DCM=˜8%) to give the title compound 149c-2 (white solid, 170 mg). MS m/z (ESI): 746.4 [M+H]+.
Step 3: Compound 149c was prepared with reference to step 2 for intermediate 3b. MS m/z (ESI): 646.5 [M+H]+.
Step 1: Compound 4-bromo-5-fluoro-2-nitrophenol (0.5 g, 2.12 mmol) was dissolved in anhydrous DMF (10 mL), and then sodium difluorochloroacetate (1.13 g, 7.42 mmol) and potassium carbonate (351.38 mg, 2.54 mmol) were separately added. After the addition, the reaction solution was stirred at 90° C. for 16 h. After the reaction was completed, water was added to the reaction solution to quench the reaction. The mixture was extracted with EA, and the organic phases were combined, washed with saturated brine, dried over anhydrous sodium sulfate, filtered, and concentrated by rotary evaporation. The crude product was separated by column chromatography to give compound 151a-1 (yellow oil, 510 mg). MS m/z (ESI): 386.2 [M+H]+.
Step 2: Compound 151a-2 (yellow solid, 1.84 g) was prepared with reference to step 1 for intermediate 3a. MS m/z (ESI): 535.3 [M+H]+.
Step 3: Compound 151a-3 (yellow oil, 1.2 g) was prepared with reference to the method for intermediate 5d. MS m/z (ESI): 483.4 [M+H]+.
Step 4: Compound 151a (red oil, 950 mg) was prepared with reference to step 2 for intermediate 3a. MS m/z (ESI): 455.3 [M+H]+.
Step 5: Compound 151a (500 mg, 1.10 mmol), compound 2 (500 mg, 1.58 mmol), sodium tert-butoxide (250 mg, 2.60 mmol), and anhydrous THE (10 mL) were dissolved in a single-necked flask. The system was purged three times with nitrogen before t-Bu Xphos (100 mg, 0.24 mmol) and t-Bu Xphos G3 (90 mg, 0.11 mmol) were separately added. After the addition, the reaction solution was stirred at 65° C. for 18 h in a nitrogen atmosphere. After the reaction was completed, the reaction solution was diluted with EA and then filtered. The filtrate was concentrated by rotary evaporation. The crude product was separated by column chromatography (EA/PE: 0-100%) to give compound 151c-1 (pale red solid, 100 mg). MS m/z (ESI): 734.3 [M+H]+.
Step 6: Crude compound 151c was prepared with reference to step 2 for intermediate 3b. MS m/z (ESI): 634.6
Step 1: Compound 1-bromo-2-fluoro-4-trifluoromethoxybenzene (2.5 g, 9.65 mmol) was dissolved in acetonitrile (37.5 mL), and then nitronium tetrafluoroborate (1.13 g, 7.42 mmol) was added at 0° C. The reaction solution was stirred at 25° C. for 4 h, then diluted with water, and extracted three times with ethyl acetate. The organic phases were combined, washed with saturated brine, dried over anhydrous sodium sulfate, filtered, and concentrated by rotary evaporation. The crude product was separated by column chromatography (0-2% ethyl acetate/petroleum ether) to give compound 152c-1 (yellow oily liquid, 1.5 g). MS m/z (ESI): 303.9 [M+H]+.
Step 2: Compound 152c-2 was prepared with reference to step 1 for intermediate 3a. MS m/z (ESI): 553.2 [M+H]+.
Step 3: Compound 152c-3 was prepared with reference to the preparation of intermediate 5d. MS m/z (ESI): 501.4 [M+H]+.
Step 4: Compound 152-4 was prepared with reference to step 2 for intermediate 3a. MS m/z (ESI): 473.3 [M+H]+.
Step 5: Compound 152c-5 was prepared with reference to step 5 for intermediate 151c. MS m/z (ESI): 753.2 [M+H]+.
Step 6: Compound 152c was prepared with reference to step 2 for intermediate 3b. MS m/z (ESI): 652.3 [M+H]+.
Compound 153c was prepared with reference to steps 1 and 2 for intermediate 3a as steps 1 and 3, with reference to the method for 5d as step 2, and with reference to steps 5 and 6 for intermediate 154c as steps 4 and 5. MS m/z (ESI): 601.3 [M+H]+.
Step 1: At 20° C., 1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione (6.8 g, 23.78 mmol) was added to a solution of 4-fluoro-1-nitro-2-trifluoromethylbenzene (5.97 g, 28.54 mmol) in concentrated sulfuric acid (30 mL). The reaction solution was stirred at 20° C. for 6 h, then poured into ice water, and extracted with EA. The organic phase was washed with saturated brine, dried, and concentrated by rotary evaporation to give compound 154c-1 (pale yellow oil, 6.55 g, crude product). MS m/z (ESI): 288.3 [M+H]+.
Step 2: Compound 154c-2 was prepared with reference to step 1 for intermediate 3a. MS m/z (ESI): 537.3 [M+H]+.
Step 3: Compound 154c-3 was prepared with reference to the method for intermediate 5d. MS m/z (ESI): 485.5 [M+H]+.
Step 4: Compound 154c-4 was prepared with reference to step 2 for intermediate 3a. MS m/z (ESI): 457.3 [M+H]+.
Step 5: Compound 154c-4 (1 g, 2.19 mmol), compound 142d (1.14 g, 2.52 mmol), potassium phosphate (1.86 g, 8.76 mmol) were added to a mixture of t-Bu Xphos (400 mg, 941.97 μmol) and t-Bu Xphos Pd G3 (350 mg, 440.60 μmol) in dioxane (12 mL) and DMF (3 mL), and the reaction system was stirred at 95° C. for 16 h in a nitrogen atmosphere. After the reaction was completed, water (100 mL) was added to the reaction solution, and the mixture was extracted with EA. The organic phases were combined, washed with saturated ammonium chloride and brine, dried over sodium sulfate, filtered, and concentrated at reduced pressure. The crude product was separated by column chromatography to give compound 154c-5 (yellow solid, 510 mg). MS m/z (ESI): 871.4 [M+H]+.
Step 6: A solution of compound 154c-5 (510 mg, 351.30 μmol) and trifluoroacetic acid (2.90 g, 25.44 mmol) in dichloromethane (5 mL) was stirred at 20° C. for 3 h. The reaction solution was concentrated. The crude product was dissolved in dichloromethane (3 mL), and ethylenediamine (72.49 mmol, 4.85 mL) was added. The reaction solution was stirred at 20° C. for 16 h. After the reaction was completed, the reaction solution was concentrated. The residue was dissolved in DCM, washed with brine, dried over sodium sulfate, filtered, and concentrated at reduced pressure to give compound 154c (pale yellow solid, 118 mg, crude product). MS m/z (ESI): 641.4 [M+H]+.
Step 1: Compound N-Boc piperazine (1 g, 5.37 mmol) was dissolved in THE (mL), and TEA (5 mL) and CuCl (60 mg, 0.6 mmol) were added. In a nitrogen atmosphere, 3-chloro-3-methyl-1-butyne (551 mg, 5.40 mmol) was added, and the system was stirred at room temperature for 30 min. Water was added to quench the reaction, and the mixture was extracted with dichloromethane, dried over anhydrous sodium sulfate, concentrated, and then purified by column chromatography (PE/EA=1:1) to give compound 156c-1 (white solid, 400 mg, crude product).
Step 2: Compound 156c-2 was prepared with reference to step 1 for intermediate 1b. MS m/z (ESI): 495.3 [M+H]+.
Step 3: Compound 156c was prepared with reference to step 2 for intermediate 3b. MS m/z (ESI): 395.3 [M+H]+.
Compound 158c was prepared with reference to the method for intermediate 176a. MS m/z (ESI): 643.4 [M+H]+.
Step 1: 4,6-Dichloropyrazolo[3,4-d]pyrimidine (2.9 g, 15.34 mmol) and (2-aminophenyl)dimethylphosphine oxide (1.30 g, 7.67 mmol) were added to tert-amyl alcohol (180 mL), and then DIEA (9.92 g, 76.72 mmol, 13.36 mL) was added. The reaction system was stirred at 100° C. for 12 h. After the reaction was completed, the reaction mixture was diluted with water and then extracted with dichloromethane/methanol. The organic layers were combined and dried over anhydrous sodium sulfate. The crude product was then filtered, concentrated, and subjected to preparative reverse-phase chromatography (hydrochloric acid system) to give compound 161c-1 (pale yellow solid, 525 mg). MS m/z (ESI): 322.0 [M+H]+.
Step 2: Compound 3a (2.19 g, 3.82 mmol) and compound 161c-1 (1.23 g, 3.82 mmol) were added to ethylene glycol (80 mL), and then TsOH-H2O (581.69 mg, 3.06 mmol) was added. The reaction system was stirred at 80° C. for 12 h. After the reaction was completed, the reaction mixture was adjusted to pH 7-8 with a saturated aqueous sodium bicarbonate solution and then extracted with dichloromethane/methanol. The organic layers were combined and dried over anhydrous sodium sulfate. The crude product was then filtered, concentrated, and subjected to preparative reverse-phase chromatography (hydrochloric acid system) to give compound 161c-2 (brown solid, 1.04 g). MS m/z (ESI): 704.4 [M+H]+.
Step 3: Compound 161c was prepared with reference to step 2 for intermediate 3b. MS m/z (ESI): 604.4 [M+H]+.
Step 1: Compound 162c-1 was prepared with reference to the method of step 1 for intermediate 3a. MS m/z (ESI): 459.2 [M+H]+.
Step 2: Compound 162c-1 (2.0 g, 4.35 mmol) was added to a mixed solution of methanol (6 mL) and 1,4-dioxane (30 mL), and then sodium methoxide (2.35 g, 43.54 mmol) and cuprous iodide (829.19 mg, 4.35 mmol) were added. The reaction system was stirred at 100° C. for 2 h in a nitrogen atmosphere. After the reaction was completed, the reaction mixture was diluted with water and then extracted with dichloromethane. The organic layers were combined, dried over anhydrous sodium sulfate, filtered, and concentrated to give a crude product. The crude product was separated and purified by silica gel column chromatography to give the title compound 162c-2 (yellow solid, 220 mg). MS m/z (ESI): 455.2 [M+H]+.
Step 3: Compound 162c-3 was prepared with reference to the method for intermediate 5d. MS m/z (ESI): 447.2 [M+H]+.
Step 4: Compound 162c-4 was prepared with reference to the method of step 2 for intermediate 3a. MS m/z (ESI): 419.3 [M+H]+.
Steps 5-6: Compound 162c was prepared with reference to the method for intermediate 4c. MS m/z (ESI): 598.4 [M+H]+.
Compound 165c was prepared with reference to the method for intermediate 1d. MS m/z (ESI): 742.3, 744.3 [M+H]+.
Compound 167c was prepared with reference to the method for intermediate 176a. MS m/z (ESI): 630.5 [M+H]+.
Compound 170c was prepared with reference to the method for intermediate 165a. MS m/z (ESI): 630.5 [M+H]+.
Compound 171c was prepared with reference to the method for intermediate 165a. MS m/z (ESI): 631.5 [M+H]+.
Compound 173c was prepared with reference to the method for intermediate 1c. MS m/z (ESI): 394.1 [M+H]+.
Compound 174c was prepared with reference to the method for intermediate 165a. MS m/z (ESI): 630.6 [M+H]+.
Compound 175c was prepared with reference to the method for intermediate 165a. MS m/z (ESI): 644.6 [M+H]+.
Step 1: Compound 146c-1 (3.8 g, 7.61 mmol), compound 146c.1 (1.78 g, 9.13 mmol), potassium fluoride (1 30.44 mL), and Pd(dppf)Cl2·CH2Cl2 (621.39 mg, 0.76 mmol) were added to dimethyl sulfoxide (150 mL), and the reaction system was stirred at 100° C. for 10 h in a nitrogen atmosphere. After the reaction was completed, the reaction mixture was diluted with water and then extracted with ethyl acetate. The organic phase was washed with water, and the organic layers were combined, dried over anhydrous sodium sulfate, filtered, and concentrated to give a crude product. The crude product was subjected to column chromatography to give compound 179c-1 (blackish brown solid, 1.7 g). MS m/z (ESI): 488.2 [M+H]+.
Step 2: 179c-1 (1.7 g, 3.49 mmol) and potassium fluoride (1 M, 10.46 mL) were added to a solution of methanol (25 mL), and the reaction system was stirred at 90° C. for 10 h in a nitrogen atmosphere. After the reaction was completed, the reaction mixture was concentrated to remove the methanol, and the aqueous phase was extracted with dichloromethane/methanol. The organic phase was washed with saturated brine, and the organic layers were combined, dried over anhydrous sodium sulfate, filtered, and concentrated to give compound 179c-2 (blackish brown solid, 1.3 g). MS m/z (ESI): 460.2 [M+H]+.
Step 3: Compound 179c-3 (blackish brown solid, 363 mg) was prepared with reference to step 2 for intermediate 7a. MS m/z (ESI): 430.2 [M+H]+.
Step 4: Compound 179c-3 (360 mg, 0.84 mmol) and compound 2 (264.94 mg, 0.84 mmol) were added to a solution of tetrahydrofuran (15 mL), and then sodium tert-butoxide (161.08 mg, 1.68 mmol) and tBuXPhos Pd G3 (66.57 mg, 83.81 μmol) were added. The reaction system was stirred at 65° C. for 12 h in a nitrogen atmosphere. After the reaction was completed, the reaction mixture was filtered. The filter cake was washed with dichloromethane/methanol, and the filtrate was concentrated to give a crude product. The crude product was purified by a silica gel plate to give compound 179c-4 (blackish brown solid, 360 mg, crude product). MS m/z (ESI): 709.4 [M+H]+.
Step 5: Compound 179c was prepared with reference to step 2 for intermediate 1c. MS m/z (ESI): 609.1 [M+H]+.
Step 1: At −20° C., 2-fluoro-4-methoxyacetophenone (5 g, 29.73 mmol) was added to sulfuric acid (31.28 g, 318.93 mmol, 17 mL), and then nitric acid (3.75 g, 59.47 mmol, 2.68 mL) was slowly and dropwise added. The reaction system was then stirred at −20° C. for 30 min. The reaction solution was added to ice water, and the mixture was stirred for 30 min and then filtered. The filter cake was washed with water to give a pale yellow solid, which was dried to give compound 185c-1 (pale yellow solid, 6 g). MS m/z (ESI): 214.1 [M+H]+.
Step 2: Compound 185c-2 was prepared with reference to step 1 for intermediate 8a. MS m/z (ESI): 433.3 [M+H]+.
Step 3: Compound 185c-2 (300 mg, 693.55 μmol), compound 2 (250 mg, 790.83 μmol), and sodium tert-butoxide (150 mg, 1.56 mmol) were dissolved in tetrahydrofuran (8 mL), and t-Bu Xphos (65 mg, 153.07 μmol) and t-Bu Xphos Pd G3 (70 mg, 88.12 μmol) were added. The reaction solution was stirred at 65° C. for 18 h in a nitrogen atmosphere. The reaction solution was diluted with EA, filtered through celite, and concentrated by rotary evaporation. The crude product was separated by column chromatography to give 185c 3 (yellow oil, 200 mg). MS m/z (ESI): 712.5 [M+H]+.
Step 4: Compound 185c was prepared with reference to step 2 for intermediate 3b. MS m/z (ESI): 612.4 [M+H]+.
Compound 190c was prepared with reference to the method for intermediate 176a. MS m/z (ESI): 630.3 [M+H]+.
Compound 192c was prepared with reference to the method for intermediate 176a. MS m/z (ESI): 644.3 [M+H]+.
Compound 196c was prepared with reference to the method for intermediate 120c. MS m/z (ESI): 378.0 [M+H]+.
Compound 198c was prepared with reference to step 1 for intermediate 166a as step 1 and with reference to step 2 for intermediate 3b as step 2. MS m/z (ESI): 648.0 [M+H]+.
Step 1: Compound 201c-1 was prepared with reference to step 1 for intermediate 4c. MS m/z (ESI): 728.2 [M+H]+.
Steps 2-3: Compound 201c was prepared with reference to the method for intermediate 176a. MS m/z (ESI): 630.2 [M+H]+.
Step 1: A solution of compound 158c (0.7 g, 923.75 μmol) and potassium carbonate (1.66 g, 12.01 mmol) in acetonitrile (10 mL) was stirred at 20° C. for 1 h. Methyl 2-bromo-2-methylpropionate (1 g, 5.52 mmol) was then added. The reaction system was stirred at 80° C. for 15 h and concentrated at reduced pressure. The crude product was separated by column chromatography to give compound 212c-1 (brown solid, 440 mg). MS m/z (ESI): 744.6 [M+H]+.
Step 2: LAH (90 mg, 2.37 mmol) was added to a solution of compound 212c-1 (440 mg, 591.50 μmol) in THE (10 mL). The reaction system was stirred at 20° C. for 30 min. Water, a sodium hydroxide solution, and water were added to the reaction solution, and then the reaction solution was concentrated at reduced pressure. The crude product was subjected to column chromatography to give compound 212c (white solid, 170 mg). MS m/z (ESI): 716.6 [M+H]+.
Steps 1-2: Compound 213c-2 was prepared with reference to the method for intermediate 3a. MS m/z (ESI): 419.5 [M+H]+.
Step 3: Compound 213c-3 was prepared with reference to the method for intermediate 165c. MS m/z (ESI): 742.2 [M+H]+.
Step 4 and step 5: Compound 213c-5 was prepared with reference to the method for intermediate 176a. MS m/z (ESI): 644.2 [M+H]+.
Step 6 and step 7: Compound 213c was prepared with reference to the method for intermediate 212c. MS m/z (ESI): 716.6 [M+H]+.
Compound 214c was prepared with reference to the method for intermediate 165a. MS m/z (ESI): 644.6 [M+H]+.
Compound 215c was prepared with reference to the method for intermediate 176a. MS m/z (ESI): 658.4 [M+H]+.
Compound 216c was prepared with reference to the method for intermediate 5d as step 4 and with reference to the method for intermediate 124c as step 1, step 2, step 3, and step 5. MS m/z (ESI): 588.3 [M+H]+.
Compound 218c was prepared with reference to the method for intermediate 219c. MS m/z (ESI): 645.4 [M+H]+.
Step 1: A solution of compound 165c (850 mg, 1.14 mmol), 4-methyltriazole (300 mg, 3.61 mmol), cuprous iodide (68.00 mg, 357.05 μmol), L-proline (42.50 mg, 369.15 μmol), and cesium carbonate (1.87 g, 5.74 mmol) in DMSO (5 mL) was microwaved at 140° C. for reaction for 3 h. The reaction solution was diluted with ethyl acetate, washed with saturated brine, dried over anhydrous sodium sulfate, filtered, and concentrated by rotary evaporation. The crude product was separated by column chromatography and then subjected to prep-HPLC (FA) to give compound 219c-1. MS m/z (ESI): 745.5 [M+H]+.
Step 2: Compound 219c-1 (20 mg, 26.85 μmol) was dissolved in DCM (2 mL), and then TFA (1 mL) was added. The reaction system was stirred at 20° C. for 1 h. The reaction solution was concentrated by rotary evaporation to give compound 219c. MS m/z (ESI): 645.5 [M+H]+.
Compound 220c was prepared with reference to the synthesis method for intermediate 219c. MS m/z (ESI): 631.3 [M+H]+.
Step 1: A solution of compound 146c-1 (1 g, 2.00 mmol), ethynyltrimethylsilane (1.97 g, 20.02 mmol), cuprous iodide (50 mg, 262.54 μmol), Pd(PPh3)2Cl2 (210 mg, 299.19 μmol), and TEA (1.22 g, 12.01 mmol) in DMF (10 mL) were allowed to react at 85° C. for 16 h in a nitrogen atmosphere. The reaction solution was diluted with EA, washed with saturated brine, dried over anhydrous sodium sulfate, filtered, and concentrated by rotary evaporation. The crude product was separated by column chromatography to give compound 221c-1. MS m/z (ESI): 517.4 [M+H]+.
Step 2: A solution of compound 221c-1 (1.82 g, 3.52 mmol) and potassium carbonate (1 g, 7.24 mmol) in methanol (20 mL) was stirred at 20° C. for 2 h. The reaction solution was concentrated. The crude product was separated by column chromatography to give compound 221c-2. MS m/z (ESI): 445.4 [M+H]+.
Step 3: Deuterium water (95.61 mmol, 2 mL) was added to a solution of compound 221c-2 (850 mg, 1.91 mmol) and potassium carbonate (550 mg, 3.98 mmol) in acetonitrile (8 mL). The reaction solution was allowed to react at 20° C. for 48 h, diluted with EA, and filtered. The filtrate was concentrated at reduced pressure to give compound 221c-3. MS m/z (ESI): 446.4 [M+H]+.
Step 4: Compound 221c-3 (750 mg, 1.68 mmol) was dissolved in deuterated methanol (100 mL) and EA (50 mL). The system was purged three times with nitrogen before palladium on carbon (200 mg, 10% purity) was added. The reaction system was stirred at 20° C. for 24 h in a deuterium atmosphere. The reaction solution was filtered through celite and then concentrated by rotary evaporation. The crude product was separated by column chromatography to give compound 221c-4. MS m/z (ESI): 424.4 [M+H]+.
Step 5: Compound 221c-5 was prepared with reference to step 3 for intermediate 185c. MS m/z (ESI): 703.2 [M+H]+.
Step 6: Compound 221c was prepared with reference to the method of step 2 for intermediate 219c. MS m/z (ESI): 603.2 [M+H]+.
Compound 225c was prepared with reference to step 1 for intermediate 176a as step 1 and with reference to step 6 for intermediate 154c as step 2. MS m/z (ESI): 644.2 [M+H]+.
(2-Aminophenyl)dimethylphosphine oxide (1.480 g, 8.8 mmol) and 5-bromo-2,4-dichloropyrimidine (1 g, 4.4 mmol) were added to a reaction flask before DIEA (2.88 g, 22 mmol) and n-BuOH (10 mL) were added. The reaction system was stirred at 140° C. for 16 h in an argon atmosphere. After the reaction was completed, the reaction mixture was concentrated. The crude product was purified by column chromatography (DCM:MeOH=20:1) and concentrated by rotary evaporation to give compound 1d (pale yellow solid, 1.1 g). MS m/z (ESI): 362.1 [M+H]+.
1-Bromo-2-fluoro-4-methoxy-5-nitrobenzene (1 g, 4.00 mmol), cyclopropylboronic acid (343.56 mg, 4.00 mmol), Pd(dppf)Cl2 (585.31 mg, 799.93 μmol), and cesium carbonate (3.91 g, 12.00 mmol) were added to a mixture of ethylene glycol dimethyl ether (2 mL) and water (0.5 mL), and the reaction system was stirred at 90° C. for 12 h in a nitrogen atmosphere. After the reaction was completed, the reaction mixture was directly concentrated at reduced pressure to give a crude product. The crude product was purified by column chromatography to give compound 2d (white solid, 0.5 g). MS m/z (ESI): 212.2 [M+H]+.
Step 1: Compound 4-bromo-5-fluoro-2-methylbenzoic acid (3 g, 12.87 mmol) was dissolved in DMF (50 mL). NaHCO3 (3.24 g, 38.62 mmol) and MeI (1.2 mL, 19.31 mmol) were added with stirring, and then the reaction system was stirred at room temperature for 3 h. After the reaction was completed, the reaction system was cooled to room temperature and poured into ice water. The aqueous phase was then extracted with ethyl acetate, and the organic layer was washed with brine, dried over anhydrous sodium sulfate, filtered, concentrated, and subjected to column chromatography (EA/PE=0-5%) to give compound 3d-1 (colorless oil, 3 g). MS m/z (ESI): 247.1 [M+H]+.
Step 2: At 25° C., compound 3d-1 (2.7 g, 10.93 mmol) was added to a solution of DCE (30 mL), and NBS (2.14 g, 12.02 mmol) and AIBN (180 mg, 1.1 mmol) were added with stirring. The reaction system was stirred at 85° C. for 16 h. After the reaction was completed, the reaction mixture was diluted with water and then extracted with dichloromethane. The organic layers were combined, dried over anhydrous sodium sulfate, filtered, and concentrated to give a crude product. The crude product was separated and purified by silica gel column chromatography (PE:EA=20:1-10:1) to give compound 3d-2 (pale yellow oil, 2 g). MS m/z (ESI): 324.8 [M+H]+.
Step 3: Compound 3d-2 (2 g, 6.14 mmol) was added to a solution of DMF (25 mL), and then 3-aminopiperidine-2,6-dione (1.51 g, 9.2 mmol, hydrochloride) and N,N-diisopropylethylamine (5.66 mL, 30.68 mol) were added. The reaction system was stirred at 85° C. for 16 h. After the reaction was completed, the reaction solution was poured into ice water, and a solid was precipitated. The mixture was filtered, and the filter cake was triturated with MTBE and dried under vacuum to give compound 3d (grey solid, 1.6 g). MS m/z (ESI): 341.2 [M+H]+.
Step 1: 2,2,6,6-Tetramethylpiperidine (8.05 g, 9.61 mL, 57 mmol) was dissolved in THE (150 mL), and the system was stirred. In a nitrogen atmosphere at 0° C., n-butyllithium (21.87 mL, 54.7 mmol, 2.5 M) was added. The reaction system was stirred at 0° C. for 1 h. The reaction system was then cooled to −45° C., and at that temperature, a solution of 4-bromo-3-fluorobenzoic acid (4.99 g, 22.8 mmol) in THE (15 mL) was added. The system was then stirred at that temperature for another 5 h. DMF (2.65 mL, 34.2 mmol) was slowly and dropwise added to the reaction solution. The reaction system was then gradually warmed to room temperature and allowed to react overnight at room temperature. After the reaction was completed, at 0° C., the reaction system was diluted with 3 N HCl to quench the reaction and then extracted with EA. The organic layers were combined, washed with brine (50 mL), dried over anhydrous sodium sulfate, filtered, and concentrated. The crude product was purified by column chromatography (EA/PE=50%-100%) to give compound 4d-1 (white solid, 3.6 g). MS m/z (ESI): 247.1 [M+H]+.
Compound 4d was prepared with reference to step 3 for intermediate 3d as step 2. MS m/z (ESI): 341.2 [M+H]+.
Compound 2-bromo-1-fluoro-4-nitrobenzene (1.5 g, 6.8 mmol) and compound (3-(4-(tert-butoxycarbonyl)piperazin-1-yl)phenyl)boronic acid (1.4 mg, 17.6 mmol) were added to a reaction flask, and dioxane (30 mL), water (10 mL), potassium carbonate (2.8 g, 20.4 mmol), and Pd(dppf)Cl2 (250 mg, 0.34 mmol) were added sequentially. The system was then stirred at 80° C. for 16 h in a nitrogen atmosphere. After the reaction was completed, water was added to quench the reaction. The mixture was extracted with ethyl acetate, and the organic phase was washed with saturated brine, dried over anhydrous sodium sulfate, concentrated, and subjected to column chromatography (PE/EA=0-10%) to give compound 5d (pale yellow solid, 900 mg). MS m/z (ESI): 168.1 [M+H]+.
Step 1: Compound 6d-1 was prepared with reference to step 1 for intermediate 1c. MS m/z (ESI): 582.4 [M+H]+.
Step 2: Compound 6d-2 was prepared with reference to step 2 for intermediate 3b. MS m/z (ESI): 482.4 [M+H]+.
Step 2: Compound 6d-2 (200 mg, 0.415 mmol) and compound 1b (178 mg, 0.456 mmol) were dissolved in CH3CN/CHCl3 (1:1, 20 mL). K2CO3 (172 mg, 1.25 mmol) was added with stirring. In a nitrogen atmosphere, the system was stirred at 65° C. for 48 h. After the reaction was completed, H2O was added to the reaction system. The mixture was extracted with DCM, and the organic phase was dried over anhydrous sodium sulfate, filtered, concentrated, purified by normal-phase column chromatography, and then subjected to prep-HPLC to give compound 6d (white solid, 75 mg, hydrochloride). MS m/z (ESI): 776.6 [M+H]+.
Step 1: N-Bromosuccinimide (52.62 g, 295.62 mmol) was added to a solution of 2-methoxy-5-nitrophenol (50 g, 295.62 mmol) in dichloromethane (300 mL), and the reaction system was stirred at 25° C. for 2 h. After the reaction was completed, the reaction mixture was directly concentrated at reduced pressure to give a crude product. The crude product was separated and purified by reverse-phase chromatography (formic acid system) and lyophilized to give the title compound 22d-1 (yellow solid, 20 g). MS m/z (ESI): 248.3 [M+H]+.
Step 2: At −75° C., boron tribromide (80.64 mmol, 7.77 mL) was added to a solution of 22d-1 (10 g, 40.32 mmol) in dichloromethane (100 mL). The reaction system was stirred at −75° C. for 2 h, and then warmed to 25° C. and stirred for 4 h. After the reaction was completed, at 0° C., methanol was added to the reaction solution to quench the reaction. The mixture was directly concentrated at reduced pressure to give a crude product. The crude product was purified by column chromatography to give compound 22d-2 (yellow solid, 9 g). MS m/z (ESI): 234.3 [M+H]+.
Step 3: Potassium carbonate (12.40 g, 89.74 mmol) and 1,2-dibromoethane (16.86 g, 89.74 mmol, 6.77 mL) were added to a solution of 22d-2 (7 g, 29.91 mmol) in DMF (40 mL), and then the reaction system was stirred at 90° C. for 4 h. After the reaction was completed, the reaction solution was extracted with water and ethyl acetate and separated into layers. The organic layer was washed with brine, dried over anhydrous sodium sulfate, filtered, and concentrated at reduced pressure to give a crude product. The crude product was purified by column chromatography (PE/EA=10:1-5:1) to give compound 22d-3 (yellow solid, 3.8 g). MS m/z (ESI): 257.3 [M+H]+.
Step 4: Compound 22d-4 was prepared with reference to step 2 for intermediate 7a. MS m/z (ESI): 230.4 [M+H]+.
Step 5: 22d-4 (500 mg, 2.17 mmol), dimethylphosphine oxide (169.63 mg, 2.17 mmol), 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (251.51 mg, 434.67 μmol), palladium acetate (48.79 mg, 217.34 μmol), and potassium phosphate (922.66 mg, 4.35 mmol) were added to a solution of DMF (5 mL), and then the reaction system was microwaved with stirring at 145° C. for 8 h in a nitrogen atmosphere. After the reaction was completed, the reaction mixture was filtered and concentrated at reduced pressure to give a crude product. The crude product was separated and purified by reverse-phase chromatography (formic acid system) to give compound 22d-5 (off-white solid, 140 mg). MS m/z (ESI): 228.3 [M+H]+.
Compound 22d was prepared with reference to the method for intermediate 1 d as step 6. MS m/z (ESI): 418.4 [M+H]+.
Step 1: Compound 35d-1 was prepared with reference to the method for reference compound C-1. MS m/z (ESI): 501.8 [M+H]+.
Step 2: Compound 35d was prepared with reference to step 2 for intermediate 3b. MS m/z (ESI): 401.6 [M+H]+.
Compound 4 (200 mg, 0.77 mmol) and compound 1,4-dibromobutane (830 mg, 3.84 mmol) were dissolved in DMF (10 mL). K2CO3 (106.2 mg, 0.77 mmol) was added with stirring. In a nitrogen atmosphere, the system was stirred at 70° C. for 48 h. After the reaction was completed, H2O was added to the reaction system. The mixture was extracted with DCM, and the organic phase was dried over anhydrous sodium sulfate, filtered, concentrated, and purified by normal-phase column chromatography (methanol/dichloromethane: ˜8%) to give compound 48d (white solid, 50 mg). MS m/z (ESI): 395.4 [M+H]+.
Compound 2b-1 (50 mg, 0.15 mmol) and acetone (5 mL) were added to a single-necked flask before Jones reagent (1 mL) was slowly and dropwise added in an ice-water bath. After the dropwise addition, the reaction system was stirred in the ice-water bath for 4 h. After the reaction was completed, the reaction solution was concentrated at reduced pressure, and then the crude product was directly subjected to pre-HPLC to give product 50d (white solid, 15 mg). MS m/z (ESI): 341.4 [M+H]+.
Compound 58d was prepared with reference to the method for intermediate 50d. MS m/z (ESI): 327.1 [M+H]+.
Compound 59d was prepared with reference to steps 1, 2 and 5 for intermediate 189d as steps 1, 2 and 5, with reference to step 1 for intermediate 3d as step 3, with reference to step 2 for intermediate 3a as step 4, with reference to steps 2-3 for intermediate 211 d as steps 6-7, and with reference to the method for intermediate 48d as step 8. MS m/z (ESI): 413.4 [M+H]+.
Step 1: Compound 66d-1 was prepared with reference to step 2 for intermediate 3a. MS m/z (ESI): 184.2 [M+H]+.
Step 2: Compound 66d-1 (10 g, 54.59 mmol) was dissolved in concentrated sulfuric acid (300.25 mmol, 16.33 mL, 98% purity) diluted with water (270 mL). A solution of sodium nitrite (4.14 g, 60.05 mmol) in water (75 mL) was slowly and dropwise added at 0° C. (over about 1 h). The reaction system was slowly warmed to 20° C. and stirred for 1 h. Concentrated sulfuric acid (136.59 g, 1.36 mol, 98% purity) and water (130 mL) were added. The reaction system was stirred at 100° C. for 2 h, then extracted with ethyl acetate, washed with saturated brine, dried over anhydrous sodium sulfate, filtered, and concentrated at reduced pressure. The crude product was purified by column chromatography to give compound 66d-2 (pale yellow solid, 8.0 g). MS m/z (ESI): 185.2 [M+H]+.
Step 3: DIAD (2.89 g, 16.22 mmol) was added to a solution of compound 66d-2 (2 g, 10.86 mmol), 2-[tert-butyl(dimethyl)silyl]oxyethanol (2.11 g, 11.95 mmol), and PPh3 (4.84 g, 18.46 mmol) in THE (10 mL). The reaction system was stirred at 50° C. for 16 h in a nitrogen atmosphere. After the reaction was completed, the reaction solution was concentrated and purified by column chromatography to give compound 66d-3 (white solid, 3.7 g). MS m/z (ESI): 343.2 [M+H]+.
Step 4: NBS (2.89 g, 16.22 mmol) and AIBN (0.7 g, 4.26 mmol) were added to a solution of compound 66d 3 (3.7 g, 10.80 mmol) in carbon tetrachloride (10 mL). The reaction system was stirred at 80° C. for 6 h in a nitrogen atmosphere. After the reaction was completed, the reaction solution was concentrated and then purified by column chromatography to give compound 66d-4 (white solid, 2.7 g). MS m/z (ESI): 307.2 [M+H]+.
Step 5: DIEA (2.84 g, 21.98 mmol) was added to a solution of compound 66d-4 (2.7 g, 8.79 mmol) and 3-aminopiperidine-2,6-dione hydrochloride (1.52 g, 9.23 mmol) in acetonitrile (30 mL). The reaction system was stirred at 45° C. for 16 h. After the reaction was completed, the reaction solution was concentrated and then purified by column chromatography to give compound 66d-5 (white solid, 1.2 g). MS m/z (ESI): 323.3 [M+H]+.
Step 6: At 0° C., carbon tetrabromide (1.73 g, 5.21 mmol) was slowly added to a solution of compound 66d-5 (1.2 g, 3.72 mmol) and PPh3 (1.76 g, 6.70 mmol) in dichloromethane (200 mL). The reaction system was stirred at 20° C. for 2 h. After the reaction was completed, the reaction solution was concentrated and then purified by column chromatography to give compound 66d (white solid, 1 g). MS m/z (ESI): 385.2 [M+H]+.
Compound 67d was prepared with reference to step 2 for intermediate 122d as step 1 and with reference to step 2 for intermediate 3b as step 2. MS m/z (ESI): 417.2 [M+H]+.
Step 1: Compound 69d-2 was prepared with reference to step 2 for intermediate 70d. 1H NMR (400 MHz, CD3OD) δ 4.32-4.26 (m, 1H), 3.41 (brs, 4H), 3.01-2.97 (m, 1H), 2.34-2.31 (m, 4H), 2.23-2.20 (m, 2H), 2.03-1.97 (m, 2H), 1.42 (s, 9H). MS m/z (ESI): 257.2 [M+H]+.
Step 2: Compound 69d-2 was prepared with reference to step 1 for intermediate 3a. MS m/z (ESI): 335.2 [M+H]+.
Step 3: Compound 69d-3 was prepared with reference to the method of step 2 for intermediate 122d. MS m/z (ESI): 499.2 [M+H]+.
Step 4: Compound 69d was prepared with reference to step 5 for intermediate 70d. MS m/z (ESI): 399.5 [M+H]+.
Step 1: Acetic acid (50.40 g, 839.27 mmol) was added to a solution of 3-benzyloxycyclobutanone (30 g, 170.25 mmol) and tert-butyl piperazine-1-carboxylate (33 g, 177.18 mmol) in methanol (400 mL). After the reaction system was stirred for 10 min, sodium cyanoborohydride (33.00 g, 525.13 mmol) was added at 0° C. The reaction was stirred at 18° C. for 2 h, until the completion of the reaction was indicated by TLC (dichloromethane:methanol=10:1). The reaction solution was concentrated by rotary evaporation, diluted with water, and extracted with ethyl acetate. The organic phases were combined and washed successively with sodium hydroxide solution and saturated brine, dried over anhydrous sodium sulfate, filtered, and concentrated by rotary evaporation. The crude product was separated by column chromatography to give compound 70d-1 (yellow oil, 4 g). MS m/z (ESI): 347.2 [M+H]+.
Step 2: Compound 70d-1 (40 g, 115.45 mmol) was dissolved in methanol (500 mL). The system was purged with nitrogen three times, and palladium hydroxide (3.0 g, 2.14 mmol, 10% purity), palladium on carbon (3 g, 10% purity), and acetic acid (525.00 mg, 8.74 mmol, 500.00 μL) were added. The reaction system was stirred in a hydrogen atmosphere at 45° C. for 36 h. The reaction solution was filtered through celite and then concentrated by rotary evaporation. The crude product was purified by column chromatography (dichloromethane:methanol=10:1) to give compound 70d-2 (white solid, 18.2 g). 1H NMR (400 MHz, CD3OD) δ 3.95-3.85 (m, 1H), 3.41-3.35 (m, 4H), 2.47-2.44 (m, 2H), 2.35-2.31 (m, 5H), 1.76-1.73 (m, 2H), 1.45 (s, 9H). MS m/z (ESI): 257.2 [M+H]+.
Step 3: Compound 70d-3 was prepared with reference to step 1 for intermediate 3a. MS m/z (ESI): 335.2 [M+H]+.
Step 4: Compound 70d-4 was prepared with reference to step 2 for intermediate 122d. MS m/z (ESI): 499.2 [M+H]+.
Step 5: Compound 70d-4 (450 mg, 0.9 mmol) was dissolved in DCM (10 mL) before TFA (2 mL) was added.
The reaction system was stirred at room temperature for 2 h. After the reaction was completed, the reaction solution was directly concentrated, and the residue was lyophilized with water to give crude compound 70d. MS m/z (ESI): 399.2 [M+H]+.
Steps 1-2: Crude compound 72d-2 was prepared with reference to steps 2-3 for intermediate 3d. MS m/z (ESI): 371.2 [M+H]+.
Step 3: Compound 72d-2 (200 mg, 0.54 mmol), tert-butyl 6-hydroxy-3,4-dihydroisoquinoline-2(1H)-carboxylate (202 mg, 0.81 mmol), CuI (21 mg, 0.11 mmol), L-proline (12 mg, 0.11 mmol), and K2CO3 (224 mg, 1.62 mmol) were added to a single-necked flask containing 10 mL of anhydrous DMSO. The mixture was heated to 110° C. in a nitrogen atmosphere and stirred for 16 h. After the reaction was completed, the solution was filtered at reduced pressure. A saturated NH4Cl solution was added to the filtrate. The mixture was extracted with EA. The organic phase was washed with water and saturated brine, dried over anhydrous sodium sulfate, and subjected to normal-phase column chromatography (DCM/MeOH=0-5%) to give compound 72d-3 (pale yellow solid, 45 mg). MS m/z (ESI): 492.5 [M+H]+.
Step 4: Crude compound 72d was prepared with reference to step 2 for intermediate 3b. MS m/z (ESI): 392.4 [M+H]+.
Compound 80d was prepared with reference to the method for intermediate 1d. MS m/z (ESI): 319.2 [M+H]+.
Step 1: 2-(4-Methoxyphenyl)ethan-1-amine (2 g, 13.2 mmol) and solvent MeOH were added to a reaction flask. 2,2,2-trifluoroacetic acid ethyl ester (2.8 g, 19.8 mmol) was then slowly and dropwise added. After the addition, the system was stirred for 3 h at 20° C. in a nitrogen atmosphere. After the reaction was completed, the solution was concentrated, quenched by adding a saturated aqueous NaHCO3 solution, and extracted with DCM. The organic phase was washed with saturated brine, dried over anhydrous sodium sulfate, concentrated, and subjected to normal-phase column chromatography (PE/EA=0-50%) to give compound 81d-1 (pale yellow solid, 2.2 g). MS m/z (ESI): 246.3 [M−H]+.
Step 2: Compound 81d-1 (2.2 g, 8.9 mmol) was dissolved in concentrated sulfuric acid (10 mL). In an ice bath, concentrated nitric acid (558 mg, 9.0 mmol) was slowly and dropwise added, and the system was stirred at 0° C. for 2 h in a nitrogen atmosphere. The reaction solution was poured into ice water after the reaction was completed, a saturated aqueous NaHCO3 solution was to neutralize the pH to 8-9. A solid was precipitated, and the mixture was filtered to give a filter cake. Water and DCM were added to dissolve the filter cake. The mixture was extracted with DCM, and the organic phase was washed with saturated brine, dried over anhydrous sodium sulfate, and subjected to normal-phase column chromatography (DCM/MeOH=0-5%) to give compound 81d-2 (pale yellow solid, 2 g). MS m/z (ESI): 293.3 [M+H]+.
Step 3: Compound 81d-2 (2 g, 6.8 mmol) was dissolved in HOAc (5 mL) and concentrated sulfuric acid (5 mL). Paraformaldehyde (1 g, 34.1 mmol) was slowly and dropwise added. The mixture was stirred for 5 h in a nitrogen atmosphere at 40° C., After the reaction was completed, the reaction solution was concentrated, and neutralized to pH 8-9 by adding a saturated aqueous NaHCO3 solution. Water and DCM were added, and the mixture was extracted with DCM. The organic phase was washed with saturated brine, dried over anhydrous sodium sulfate, and subjected to normal-phase column chromatography (DCM/MeOH=0-5%) to give compound 81d-3 (pale yellow solid, 1 g). MS m/z (ESI): 305.4 [M+H]+.
Step 4: Compound 81d-4 was prepared with reference to step 2 for intermediate 3a. MS m/z (ESI): 275.1 [M+H]+.
Step 5: Compound 81d-5 was prepared with reference to step 3 for intermediate 21c. MS m/z (ESI): 554.7 [M+H]+.
Step 6: Compound 81d-5 (50 mg, 0.155 mmol) was dissolved in MeOH and water. NaOH (50 mg, 0.155 mmol) was added and the system was stirred at 20° C. for 1 h. After the reaction was completed, the solution was concentrated and extracted with DCM. The organic phase was washed with saturated brine, dried over anhydrous sodium sulfate, and subjected to normal-phase column chromatography (DCM/MeOH=0-5%) to give compound 81d (pale yellow solid, 60 mg). MS m/z (ESI): 458.6 [M+H]+.
Compound 82d was prepared with reference to the method for intermediate 88d. MS m/z (ESI): 319.2 [M+H]+.
Compound 86d was prepared with reference to the method for intermediate 48d. MS m/z (ESI): 395.2 [M+H]+.
Step 1: Benzyl 3-oxopiperazine-1-carboxylate (1 g, 4.27 mmol) was dissolved in DMF (15 mL). NaH (342 mg, 8.54 mmol) was slowly added. The system was reacted at room temperature for 1 h. 1,4-Dibromobutane (4.5 g, 21.0114 mmol) was added and the system was stirred at 50° C. in a nitrogen atmosphere for 16 h. After the reaction was completed, the solution was concentrated and quenched with water. The reaction mixture was concentrated, and separated and purified by prep-HPLC to give compound 87d-1 (white solid, 1 g, hydrochloride). MS m/z (ESI): 369.1 [M+H]+.
Step 2: Compound 87d-1 (500 mg, 1.35 mmol), tert-butyl 3-(4-hydroxy-1-oxoisoindolin-2-yl)-2,6-dioxopiperidine-1-carboxylate (390 mg, 1.08 mmol), and solvent DMF (6 mL) were added to a reaction flask. K2CO3 (100.6 mg, 0.310 mmol) was then added and stirred at 80° C. for 2 h in a nitrogen atmosphere. After the reaction was completed, the reaction solution was filtered, concentrated, and separated and purified by prep-HPLC to give compound 87d-2 (white solid, 50 mg, hydrochloride). MS m/z (ESI): 549.7 [M+H]+.
Step 3: Compound 87d was prepared with reference to step 2 for intermediate 3a. MS m/z (ESI): 415.6 [M+H]+.
Compound 3 (100 mg, 0.38 mmol), tert-butyl 4-bromobutyrate (170 mg, 0.76 mmol), KI (63 mg, 0.38 mmol), NaHCO3 (96 mg, 1.04 mmol), and anhydrous DMF (5 mL) were added in a single-necked flask. The system was heated to 60° C. and stirred for 16 h. After the reaction was completed, the reaction solution was filtered, and the filtrate was directly subjected to pre-HPLC to give compound 88d (white solid, 15 mg). MS m/z (ESI): 347.3 [M+H]+.
Compound 92d was prepared with reference to the method for intermediate 48d. MS m/z (ESI): 413.4 [M+H]+.
Step 1: Compound 102d-1 was prepared with reference to compound C-1. MS m/z (ESI): 402.9 [M+H]+.
Step 2: Compound 102d was prepared with reference to step 2 for intermediate 112d. MS m/z (ESI): 346.2 [M+H]+.
Step 1: Compound 107d-1 was prepared with reference to step 1 for intermediate 87d. MS m/z (ESI): 275.2. [M+H]+.
Step 2: Compound 107d-2 was prepared with reference to step 1 for intermediate 114d. MS m/z (ESI): 517.2. [M+H]+.
Step 3: Compound 107d was prepared with reference to step 2 for intermediate 3a. MS m/z (ESI): 385.9 [M+H]+.
Compound 86d was prepared with reference to the method for intermediate 48d. MS m/z (ESI): 367.2 [M+H]+.
Step 1: tert-Butyl 4-hydroxypiperidine-1-carboxylate (3000 mg, 14.90 mmol), ethyl acrylate (2983 mg, 29.80 mmol), KOH (1672 mg, 29.80 mmol), and anhydrous THF (50 mL) were added to a single-necked flask. The reaction system was stirred at room temperature in a nitrogen atmosphere for 24 h. After the reaction was completed, water was added to quench the reaction. The mixture was extracted with EA, and the organic phase was washed with saturated brine and dried over anhydrous sodium sulfate. The crude product was subjected to normal-phase column chromatography (EA/PE=0-15%) to give compound 110d-1 (pale yellow oil, 2100 mg).
Step 2: Compound 110d-1 (500 mg, 1.66 mmol) and anhydrous THF (10 mL) were added to a three-necked flask. In a nitrogen atmosphere, LiAlH4 (75 mg, 1.99 mmol) was added in portions in an ice-water bath. After the reaction was completed, anhydrous Na2SO4 was added to the reaction solution, and water was slowly and dropwise added to quench the reaction. The mixture was filtered at reduced pressure, the residue was washed with DCM, and the filtrate was concentrated to give crude product 110d-2 (pale yellow oil, 410 mg). The crude product was directly used in the next step.
Step 3: Compound 110d-2 (400 mg, 1.54 mmol), compound 3 (400 mg, 1.54 mmol), PPh3 (606 mg, 2.31 mmol), and anhydrous THE (10 mL) were added in a three-necked reaction flask. In a nitrogen atmosphere, DIAD (467 mg, 2.31 mmol) was slowly and dropwise added. After the reaction was completed, water was added to the reaction solution to quench the reaction. The mixture was extracted with DCM, and the organic phases were combined, washed with saturated brine, dried over anhydrous Na2SO4, and concentrated at reduced pressure. The crude product was subjected to normal-phase column chromatography (MeOH/DCM=0-5%) to give product 110d-3 (pale yellow oil, 120 mg). MS m/z (ESI): 502.6 [M+H]+.
Step 4: Crude compound 110d was prepared with reference to step 2 for intermediate 3b. MS m/z (ESI): 402.7 [M+H]+.
Step 1: 2-(2,6-Dioxopiperidin-3-yl)-4-fluoroisoindoline-1,3-dione (1000 mg, 3.62 mmol), DIEA (930 mg, 7.24 mmol), and NMP (10 mL) were added in a three-necked reaction flask. tert-Butyl glycinate (570 mg, 4.34 mmol) was then added, and the system was heated to 110° C. and stirred overnight. After the reaction was completed, water was added to the reaction solution, and the mixture was extracted with EA. The organic phases were combined, washed with saturated brine, dried over anhydrous sodium sulfate, and dried at reduced pressure. The crude product was purified by normal-phase column chromatography (EA/PE=0-60%) to give product 112d-1 (pale yellow oil, 600 mg). MS m/z (ESI): 388.5 [M+H]+.
Step 2: Compound 112d-1 (600 mg, 1.55 mmol) was dissolved in DCM (10 mL) before TFA (2 mL) was added. The system was then stirred at room temperature for 1 h. After the reaction was completed, the solvent was removed at reduced pressure. Water and acetonitrile were added to the crude product, and the mixture was lyophilized to give crude compound 112d (pale yellow solid, 450 mg). MS m/z (ESI): 332.4 [M+H]+.
Step 1: Lenalidomide (1000 mg, 3.85 mmol) and NMP (10 mL) were added in a three-necked reaction flask. tert-Butyl bromoacetate (900 mg, 4.62 mmol) and DIPEA (995 mg, 7.70 mmol) were then separately added before the mixture was heated to 110° C. and stirred overnight. After the reaction was completed, water was added to the reaction solution. The mixture was extracted with EA. The organic phases were combined, washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated by rotary evaporation at reduced pressure. The crude product was purified by normal-phase column chromatography (EA/PE=0-70%) to give product 113d-1 (pale yellow oil, 700 mg). MS m/z (ESI): 374.4 [M+H]+.
Step 2: Compound 113d was prepared with reference to step 2 for intermediate 112d. MS m/z (ESI): 318.4 [M+H]+.
Step 1: Compound 1 (1000 mg, 3.09 mmol), tert-butyl acrylate (475 mg, 3.71 mmol), Pd2(dba)3 (282 mg, 0.31 mmol), t-Bu3PBF4 (90 mg, 0.31 mmol), dicyclohexylamine (1120 mg, 6.18 mmol), and anhydrous 1,4-dioxane (15 mL) were added in a single-necked flask. In a nitrogen atmosphere, the system was slowly heated to 60° C. and stirred overnight. After the reaction was completed, the reaction solution was filtered at reduced pressure. The filtrate was then concentrated at reduced pressure, and the crude product was isolated by normal-phase column chromatography (EA/PE=0-30%) to give compound 114d-1 (pale yellow solid, 700 mg). MS m/z (ESI): 371.5 [M+H]+.
Step 2: Compound 114d-2 was prepared with reference to step 2 for intermediate 3a. MS m/z (ESI): 373.5 [M+H]+.
Step 3: Compound 114d was prepared with reference to step 2 of the synthesis method for intermediate 112d. MS m/z (ESI): 317.7 [M+H]+.
3-(4-mercapto-1-oxoisoindolin-2-yl)piperidine-2,6-dione (1000 mg, 3.62 mmol) and anhydrous DMF (10 mL) were added in a single-necked reaction flask before K2CO3 (600 mg, 4.34 mmol) and 1,4-dibromobutane (860 mg, 3.98 mmol) were separately added. The reaction system was stirred at room temperature for 0.5 h. After the reaction was completed, the reaction solution was filtered at reduced pressure, and then a saturated NH4Cl solution was added to the filtrate. The mixture was extracted with EA, and the organic phases were combined, washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated at reduced pressure. The crude product was purified by normal-phase column chromatography (EA/PE=0-60%) to give product 117d (khaki solid, 500 mg). MS m/z (ESI): 411.3 [M+H]+.
Step 1: Lenalidomide (300 mg, 1.16 mmol) was dissolved in NMP (10 mL) before DIEA (0.64 mL, 3.47 mmol) and 1,4-dibromobutene (297 mg, 1.39 mmol) were added. The reaction system was stirred at room temperature for 16 h. After the reaction was completed, the reaction solution was diluted with EA and washed with water. The organic phase was dried over anhydrous sodium sulfate, filtered, concentrated, and purified by column chromatography (80 g, MeOH/DCM=−8%) to give compound 119d-1 (white solid, 150 mg). MS m/z (ESI): 392.7 [M+H]+.
Step 2: Compound 119d was prepared with reference to the method for compound C-1. MS m/z (ESI): 909.5 [M+H]+.
Step 1: Compound 122d-1 was prepared with reference to step 2 for intermediate 1b. M/Z (ESI): 250.1 [M+H−56]+.
Step 2: Cesium carbonate (1.25 g, 3.84 mmol) and compound 3 (0.50 g, 1.92 mmol) were added to a solution of compound 122d-1 (704 mg, 2.31 mmol) in DMF (10.0 mL). The reaction system was stirred at 80° C. for 16 h. After the reaction was completed, the reaction mixture was diluted with dichloromethane. The organic phase was washed with water, dried, and concentrated to give compound 122d-2 (colorless oily liquid, 0.60 g). MS m/z (ESI): 414.1 [M+H-56]+.
Step 3: Compound 122d was prepared with reference to step 2 for intermediate 3b. MS m/z (ESI): 370.1 [M+H]+.
Step 1: Compound 139d-1 was prepared with reference to compound E67. MS m/z (ESI): 693.3 [M+H]+.
Step 2: Compound 139c-2 (1.5 g, 2.16 mmol) was added to a mixture of concentrated sulfuric acid (2.5 mL) and water (5 mL). The reaction system was purged with nitrogen 3 times, heated to 120° C., and stirred for 3 h. After the reaction was completed, the reaction mixture was adjusted to a neutral system pH with solid NaOH, diluted with water, filtered, and concentrated to give a crude product. The crude product was subjected to reverse-phase preparative chromatography (trifluoroacetic acid system) to give compound 139d-2 (yellow solid, 1.3 g). MS m/z (ESI): 612.0 [M+H]+.
Step 3: Compound 139d was prepared with reference to the method for compound C-1. MS m/z (ESI): 926.3 [M+H]+.
Compound 141d was prepared with reference to steps 3-6 for compound 66d. MS m/z (ESI): 413.1 [M+H]+.
Step 1: Compound 142d-1 (10 g, 53.2 mmol), DMF (30 mL), and THE (90 mL) were added to a single-necked flask before NaH (2.34 g, 58.5 mmol, 60%) was added in portions in an ice-water bath. The system was stirred at 0° C. for 0.5 h and at 20° C. for 0.5 h. The system was then cooled to 0° C. before SEMCl (9.31 g, 55.9 mmol) was slowly and dropwise added, and stirred at 20° C. for 1.5 h. After the reaction was completed, the reaction solution was diluted with EA. The organic phase was washed with a saturated ammonium chloride solution and a saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate, filtered, and concentrated by rotary evaporation. The crude product was separated by column chromatography (eluent: EA/PE=0-15%) to give compound 142d-2. 1H NMR (400 MHz, CDCl3) δ 7.38 (d, J=3.7 Hz, 1H), 6.67 (d, J=3.7 Hz, 1H), 5.61 (s, 2H), 3.54 (dd, J=8.7, 7.6 Hz, 2H), 0.98-0.89 (m, 2H), −0.03 (s, 9H). MS m/z (ESI): 318.1 [M+H]+.
Step 2: 2-Dimethylphosphorylaniline (3.5 g, 20.7 mmol) and compound 142d-2 (6.6 g, 20.7 mmol) were dissolved in DMF (40 mL) before K2CO3 (3.43 g, 24.9 mmol) and DIPEA (3.2 g, 24.8 mmol, 4.3 mL) were separately added. The reaction system was then stirred at 60° C. for 16 h. After the reaction was completed, the reaction solution was diluted with ethyl acetate. The organic phase was washed twice with a saturated ammonium chloride solution, washed with a saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate, filtered, and concentrated by rotary evaporation. The crude product was separated by column chromatography (EA/PE=0-77%) to give compound 142d. MS m/z (ESI): 451.6 [M+H]+.
Compound 150d was prepared with reference to step 1 for intermediate 3d. MS m/z (ESI): 381.0 [M+H]+.
Compound 3 (150 mg, 0.58 mmol) was dissolved in DMF (5 mL) before 2-bromo-2-methylpropionaldehyde (105 mg, 0.69 mmol), KHCO3 (116 mg, 1.16 mmol), and NaI (110 mg, 0.58 mmol) were separately added. The reaction system was heated to 80° C. and stirred for 16 h. After the reaction was completed, the reaction solution was filtered at reduced pressure. The filtrate was concentrated by rotary evaporation at reduced pressure, and the crude product was separated by normal-phase column chromatography (MeOH/DCM=0-5%) to give crude compound 157d. MS m/z (EST): 331.1 [M+H]+.
Compound 168d was prepared with reference to the method for intermediate 48d. MS m/z (EST): 367.1, 369.1 [M+H]+.
Step 1: At 0° C., nitronium tetrafluoroborate (6.84 g, 58.59 mmol) was added to methyl 3-amino-5-bromo-2-methylbenzoate (11 g, 45.07 mmol) in DCM (100 mL). The reaction system was stirred at 0° C. in a nitrogen atmosphere for 1 h. o-Xylene (250 mL) was then added and the system was stirred at 80° C. for 1 h. Dichloromethane was removed and the system was stirred at 130° C. for 3 h. H2O was added and the reaction mixture was then extracted with EA. The combined organic phases were washed with saturated brine, dried over sodium sulfate, filtered, and concentrated at reduced pressure. The crude product was separated by column chromatography to give compound 186d-1. MS m/z (ESI): 247.1 [M+H]+.
Step 2: NBS (9.37 g, 52.62 mmol) and AIBN (1.33 g, 8.10 mmol) were added to a solution of compound 186d 2 (10 g, 40.48 mmol) in carbon tetrachloride (100 mL). The reaction system was stirred at 80° C. for 16 h. The reaction solution was concentrated at reduced pressure. The crude product was separated by column chromatography to give compound 186d-2. MS m/z (ESI): 325.1 [M+H]+.
Step 3: Compound 186d-2 (8.5 g, 26.08 mmol) was added to a solution of NH3/MeOH (7 M, 76.50 mL) in MeOH (10 mL), and the reaction system was stirred for 16 h at 20° C. The reaction solution was concentrated at reduced pressure to give a crude product. The crude product was dissolved in THE (100 mL). DMAP (547.18 mg, 4.48 mmol) and Boc2O (8.25 g, 37.82 mmol) were added. The reaction system was stirred at room temperature for 16 h. The reaction solution was concentrated by rotary evaporation. The crude product was separated by column chromatography to give compound 186d-3. MS m/z (ESI): 330.1 [M+H]+.
Step 4: BH3·Me2S (10 M, 12.12 mL) was added to a solution of compound 186d-3 (4.00 g, 12.12 mmol) in THE (100 mL) at 0° C. The reaction system was stirred for reaction for 1 h at 0° C., for 1 h at 20° C., and for 14 h at 65° C. Methanol and water were added to the reaction solution at 0° C. The reaction solution was extracted with EA. The organic phase was dried over sodium sulfate, filtered, and concentrated at reduced pressure. The crude product was subjected to column chromatography to give compound 186d-4. MS m/z (ESI): 316.1 [M+H]+.
Step 5: A mixture of compound 186d-4 (2 g, 6.33 mmol), palladium acetate (150.00 mg, 668.13 μmol), boric acid (584 mg, 9.44 mmol), cesium carbonate (4.12 g, 12.65 mmol) and t-BuBrettPhos (600 mg, 1.24 mmol) in NMP (30 mL) was stirred at 90° C. for 16 h in a nitrogen atmosphere. Water was added to the reaction solution, and the mixture was extracted with EA. The organic phases were combined, washed with brine, dried over anhydrous sodium sulfate, filtered, and concentrated by rotary evaporation. The crude product was subjected to column chromatography to give compound 186d-5. MS m/z (ESI): 254.1 [M+H]+.
Steps 6-9: Compound 186d was prepared with reference to steps 2-5 for intermediate 120c. MS m/z (ESI): 396.1 [M+H]+.
Step 1: tert-Butyl 2-hydroxy-6-azaspiro[3.4]octane-6-carboxylate (500 mg, 2.20 mmol) and TEA (334.42 mg, 3.30 mmol) were dissolved in DCM (20 mL) before 4-toluenesulfonyl chloride (630 mg, 3.30 mmol) was added. The reaction system was reacted at 25° C. for 18 h. The reaction solution was diluted with water and extracted with EA. The organic phases were combined, washed once with a 1 N hydrochloric acid solution, washed twice with saturated brine, dried over anhydrous sodium sulfate, filtered, and concentrated by rotary evaporation. The crude product was subjected to column chromatography to give compound 187d-1. MS m/z (ESI): 382.1 [M+H]+.
Step 2: Compound 4 (220 mg, 845.36 mmol), compound 187d-1 (600 mg, 1.57 mmol), and cesium carbonate (700 mg, 2.15 mmol) were dissolved in DMF (10 mL) before NaI (150 mg, 1.00 mmol) was added. The reaction system was stirred at 80° C. for 18 h. The reaction solution was diluted with water and extracted twice with DCM. The organic phases were combined, dried over anhydrous sodium sulfate, filtered, and concentrated by rotary evaporation. The crude product was subjected to column chromatography to give compound 187d-2. MS m/z (ESI): 470.2 [M+H]+.
Step 3: Compound 187d was prepared with reference to step 5 for intermediate 70d. MS m/z (EST): 370.1 [M+H]+.
Step 1: NBS (12 g, 67.47 mmol) was added to 4-fluoro-2-methylbenzoic acid (10 g, 64.88 mmol) in sulfuric acid (100 mL) at 0° C. The reaction system was stirred at 0° C. for 1 h. After the reaction was completed, the reaction solution was added to 2 L of ice water. The mixture was filtered and washed with water. The solid was dried to give compound 188d-1 (15.1 g, white solid). MS m/z (ESI): 233.2 [M+H]+.
Step 2: Methyl iodide (27.59 g, 194.39 mmol) was added to compound 188d-1 (15.1 g, 64.80 mmol) and potassium carbonate (26.87 g, 194.39 mmol) in DMF (60 mL) at 0° C. The reaction system was stirred at 20° C. for 16 h, until the completion of the reaction was indicated by TLC (PE/EA=1:1). The reaction solution was diluted with 200 mL of ethyl acetate, washed with saturated brine (100 mL×3), dried over anhydrous sodium sulfate, filtered, and concentrated by rotary evaporation to give compound 188d-2. MS m/z (ESI): 247.2 [M+H]+.
Steps 3-10: Compound 188d was prepared with reference to steps 2-9 for intermediate 186d. MS m/z (ESI): 396.2 [M+H]+.
Step 1: BnBr (2.98 mL, 24.4 mmol) was added to a solution of 4,5-difluoro-2-methylbenzoic acid (3.5 g, 20.33 mmol) and K2CO3 (5.62 g, 40.66 mmol) in DMF (15 mL) at 0° C. with stirring. The reaction system was stirred at 25° C. for 16 h. After the reaction was completed, a saturated aqueous sodium bicarbonate solution was added. The reaction solution was concentrated to give a crude product. The crude product was separated and purified by silica gel column chromatography (PE:EA=20:1-10:1) to give compound 189d-1. MS m/z (ESI): 263.2 [M+H]+.
Step 2: Compound 189d-1 (5.33 g, 20.32 mmol) was dissolved in THE (15 mL) at 0° C. t-BuOK (6.84 g, 60.97 mmol) was added in portions with stirring. The reaction system was then stirred at 25° C. for 16 h. After the reaction was completed, a saturated sodium bicarbonate was added. The reaction solution was concentrated to give a crude product. The crude product was separated and purified by silica gel column chromatography (PE:EA=20:1-10:1) to give compound 189d-2. MS m/z (ESI): 261.2 [M+H]+.
Step 3: Compound 189d-3 was prepared with reference to step 1 for intermediate 3d. MS m/z (ESI): 275.2 [M+H]+.
Step 4: Compound 114d-2 was prepared with reference to step 2 for intermediate 3a. MS m/z (ESI): 185.2 [M+H]+.
Step 5: Compound 189d-4 (0.7 g, 3.8 mmol) and imidazole (1.04 g, 15.2 mmol) were dissolved in DMF (15 mL) at 25° C. TBSCl (1.15 g, 7.6 mmol) was added in portions with stirring. The reaction system was then stirred at 25° C. for 16 h. After the reaction was completed, a saturated sodium bicarbonate was added. The reaction solution was concentrated to give a crude product. The crude product was separated and purified by silica gel column chromatography (PE/EA=20:1-10:1) to give compound 189d-5. MS m/z (ESI): 299.2 [M+H]+.
Steps 6-7: Compound 189d-7 was prepared with reference to steps 2-3 for intermediate 211d. MS m/z (ESI): 279.2 [M+H]+.
Step 8: Compound 189d was prepared with reference to the method for intermediate 48d. 1H NMR (500 MHz, DMSO-d6) δ 10.98 (s, 1H), 7.55 (d, J=9.9 Hz, 1H), 7.46 (d, J=7.3 Hz, 1H), 5.09 (dd, J=13.3, 5.1 Hz, 1H), 4.49 (dd, J=6.3, 4.8 Hz, 2H), 4.39 (d, J=17.2 Hz, 1H), 4.27 (d, J=17.2 Hz, 1H), 3.88 (t, J=5.4 Hz, 2H), 2.95-2.86 (m, 1H), 2.59 (d, J=16.6 Hz, 1H), 2.44-2.35 (m, 1H), 2.04-1.93 (m, 1H). MS m/z (ESI): 385.5 [M+H]+.
Compound 191 d was prepared with reference to step 2 for intermediate 122d as step 1 and with reference to step 2 for intermediate 3b as step 2. MS m/z (ESI): 399.1 [M+H]+.
Step 1: 2-Methyl-5-trifluoromethylbenzoic acid (300 mg, 1.38 mmol) and NBS (196.58 mg, 687.53 μmol) were added to sulfuric acid (3 mL). The reaction system was stirred at 25° C. for 12 h. After the reaction was completed, the reaction mixture was diluted with ice water and extracted with EA. The organic layers were combined, washed with saturated brine, dried over anhydrous sodium sulfate, filtered, and concentrated to give a crude product. The crude product was separated and purified by a silica gel plate to give compound 195d-1 (colorless oil, 110 mg). MS m/z (ESI): 283.1 [M+H]+.
Step 2: Compound 195d-1 (5.33 g, 18.83 mmol) was added to methanol (50 mL) before sulfuric acid (37.66 mmol, 2.05 mL) was added. The reaction system was stirred at 65° C. for 12 h. After the reaction was completed, the reaction mixture was diluted with ice water and extracted with dichloroethane. The organic layers were combined, washed with saturated brine, dried over anhydrous sodium sulfate, filtered, and concentrated to give compound 195d-2 (yellow oil, 5.5 g), which was directly used in the next step. MS m/z (ESI): 297.1 [M+H]+.
Step 3: Compound 195d-2 (4 g, 13.46 mmol), bis(pinacolato)diboron (5.13 g, 20.20 mmol), potassium acetate (3.96 g, 40.39 mmol), Pd(dppf)Cl2 (985.24 mg, 1.35 mmol) were added to dioxane (30 mL). The reaction system was stirred at 80° C. for 1 h in a nitrogen atmosphere. After the reaction was completed, the reaction mixture was filtered and concentrated to give compound 195d-3 (brown solid, 4.5 g), which was directly used in the next step. MS m/z (ESI): 345.1 [M+H]+.
Step 4: Compound 195d-3 (4 g, 11.62 mmol) and m-CPBA (2.01 g, 11.62 mmol) were added to a mixed solution of water (2 mL) and ethanol (4 mL). The reaction system was stirred at 25° C. for 1 h in a nitrogen atmosphere. After the reaction was completed, the reaction solution was quenched with a sodium sulfite solution, diluted with water, and extracted with ethyl acetate. The organic layers were combined, washed with saturated brine, dried over anhydrous sodium sulfate, filtered, and concentrated to give a crude product. The crude product was purified by column chromatography to give compound 195d-4 (white solid, 2.5 g). MS m/z (ESI): 235.1 [M+H]+.
Step 5: Compound 195d-5 was prepared with reference to step 5 for intermediate 189d. MS m/z (ESI): 349.1 [M+H]+.
Step 6: Compound 195d-5 (2.5 g, 7.18 mmol), NBS (1.40 g, 7.89 mmol), and BPO (173.80 mg, 717.50 μmol) were added to CCl4 (30 mL). The reaction system was stirred at 80° C. for 2 h in a nitrogen atmosphere. After the reaction was completed, the mixture was filtered and concentrated to give compound 195d-6 (yellow oil, 3.0 g), which was directly used in the next step. MS m/z (ESI): 427.1 [M+H]+.
Step 7: Compound 195d-6 (3 g, 7.02 mmol), 3-aminopiperidine-2,6-dione (989.46 mg, 7.72 mmol, hydrochloride), and DIEA (2.72 g, 21.06 mmol, 3.67 mL) were added to acetonitrile (30 mL). The reaction system was stirred at 25° C. for 2 h in a nitrogen atmosphere. After the reaction was completed, the reaction solution was filtered and concentrated to give compound 195d-7 (blue solid, 1.4 g), which was directly used in the next step. MS m/z (ESI): 329.0 [M+H]+.
Step 8: Compound 195d (yellow solid, 180 mg) was prepared with reference to the synthesis method for intermediate 48d. 1H NMR (500 MHz, DMSO-d6) δ 11.00 (s, 1H), 7.62 (d, J=6.0 Hz, 2H), 5.15 (dd, J=13.3, 5.1 Hz, 1H), 4.61 (td, J=5.0, 2.6 Hz, 2H), 4.53-4.46 (m, 1H), 4.39-4.35 (m, 1H), 3.85 (t, J=5.3 Hz, 2H), 2.95-2.90 (m, 1H), 2.55 (d, J=20.0 Hz, 1H), 2.49-2.47 (m, 1H), 2.05-1.98 (m, 1H). MS m/z (ESI): 435.3 [M+H]+.
Compound 197d was prepared with reference to the method for intermediate 70d. MS m/z (ESI): 399.7 [M+H]+.
Compound 205d was prepared with reference to step 2 for intermediate 1b as step 1, with reference to step 2 for intermediate 122d as step 2, and with reference to step 2 for intermediate 3b as step 3. MS m/z (ESI): 417.7 [M+H]+.
Step 1: Methyl 3,4-dimethylbenzoate (2000 mg, 12.18 mmol) and DCE (30 mL) were added together in a single-necked reaction flask before AIBN (200 mg, 1.22 mmol) and NBS (4770 mg, 26.80 mmol) were separately added. In a nitrogen atmosphere, the reaction system was stirred at 80° C. for 16 h. After the reaction was completed, the reaction solution was cooled to room temperature, adjusted to pH 8-9 with a saturated NaHCO3 solution, and extracted with DCM. The organic phases were combined, dried over anhydrous Na2SO4, and concentrated at reduced pressure. The crude product was purified by normal-phase column chromatography to give product 209d-1 (yellowish brown solid, 3500 mg). MS m/z (ESI): 321.1 [M+H]+.
Step 2: Compound 209d-1 (1500 mg, 4.66 mmol) and 2,4-dimethoxybenzylamine (779 mg, 4.66 mmol) were added to a single-necked reaction flask before TEA (1416 mg, 13.98 mmol) and anhydrous THE (20 mL) were added. In a nitrogen atmosphere, the system was stirred at room temperature for 5 h. After the reaction was completed, water was added to the reaction solution, and the mixture was extracted with EA. The organic phases were combined, dried over anhydrous Na2SO4, and concentrated at reduced pressure. The crude product was purified by normal-phase column chromatography to give product 209d-2 (reddish brown solid, 1000 mg). MS m/z (ESI): 328.6 [M+H]+.
Step 3: Compound 209d-2 (200 mg, 0.61 mmol) and TFA (4 mL) were added to a microwave tube. The system was heated to 140° C. by microwave and stirred for 0.5 h. After the reaction was completed, the reaction solution was concentrated at reduced pressure to give crude product 209d-3 (reddish brown oil, 150 mg), which was used directly in the next step. MS m/z (ESI): 177.9 [M+H]+.
Step 4: Compound 209d-3 (150 mg, 0.85 mmol), anhydrous DCM (10 mL), and TEA (430 mg, 4.25 mmol) were added in a single-necked reaction flask before (Boc)2O (1416 mg, 13.98 mmol) was slowly added. In a nitrogen atmosphere, the system was stirred at room temperature for 2 h. After the reaction was completed, water was added to the reaction solution to quench the reaction, and the mixture was extracted with DCM. The organic phases were combined, dried over anhydrous Na2SO4, and concentrated at reduced pressure. The crude product was purified by normal-phase column chromatography to give product 209d-4 (pale yellow solid, 200 mg). MS m/z (ESI): 278.1 [M+H]+.
Step 5: Compound 209d-5 was prepared with reference to step 8 for intermediate 111b.
Step 6: Compound 209d-5 (150 mg, 0.60 mmol), anhydrous DCM (10 mL), and PPh3 (190 mg, 0.72 mmol) were added in a single-necked reaction flask before CBr4 (238 mg, 0.72 mmol) was slowly added. In a nitrogen atmosphere, the system was stirred at room temperature for 5 h. After the reaction was completed, water was added to the reaction solution to quench the reaction, and the mixture was extracted with DCM. The organic phases were combined, dried over anhydrous Na2SO4, and concentrated at reduced pressure. The crude product was purified by normal-phase column chromatography to give product 209d-6 (pale yellow solid, 80 mg).
Step 7: Compound 209d-6 (50 mg, 0.16 mmol), compound 209b (46 mg, 0.16 mmol), Pd(PPh3)4 (18 mg, 0.02 mmol), CsF (73 mg, 0.48 mmol), and dioxane/H2O (4.5 mL, V1:V2=8:1) were added to a single-necked flask. In a nitrogen atmosphere, the system was slowly heated to 85° C. and stirred for 16 h. After the reaction was completed, the reaction solution was filtered. The filtrate was directly concentrated at reduced pressure, and the crude product was isolated by normal-phase column chromatography (MeOH/DCM=0-5%) to give compound 209d-7 (yellowish brown solid, 60 mg). 1H NMR (500 MHz, CD3OD) δ 7.69 (dd, J=7.2, 1.1 Hz, 1H), 7.51-7.43 (m, 2H), 7.22 (dd, J=13.8, 7.8 Hz, 1H), 7.18-7.11 (m, 2H), 5.12 (dd, J=13.3, 5.2 Hz, 1H), 4.65-4.57 (m, 4H), 4.38 (q, J=17.0 Hz, 2H), 4.10 (s, 2H), 2.94-2.84 (m, 1H), 2.81-2.73 (m, 1H), 2.48 (qd, J=13.3, 4.7 Hz, 1H), 2.18-2.10 (m, 1H), 1.51 (s, 9H). MS m/z (ESI): 376.6 [M-99]+.
Step 8: Compound 209d was prepared with reference to the method of step 2 for intermediate 1c. MS m/z (ESI): 376.6 [M+H]+.
Step 1: In a nitrogen atmosphere, tert-butylchlorodiphenylsilane (19.85 g, 72.21 mmol, 18.55 mL) was added to a solution of methyl 4-hydroxy-2-methylbenzoate (8 g, 48.14 mmol) and imidazole (8.19 g, 120.36 mmol) in DMF (80 mL). The reaction system was then stirred at 50° C. for 10 h. After the reaction was completed, the reaction mixture was poured into water and extracted with DCM. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, filtered, concentrated, and subjected to column chromatography to give compound 221d-1 (yellow oily liquid, 14 g) (400 MHz, DMSO-d6: δ 10.38 (s, 1H), 7.55 (d, J=8.9 Hz, 1H), 7.13 (d, J=9.0 Hz, 1H), 3.93 (s, 3H)). MS m/z (ESI): 405.5 [M+H]+.
Step 2: In a nitrogen atmosphere, azobisisobutyronitrile (284.12 mg, 1.73 mmol) and NBS (6.77 g, 38.06 mmol) were added to a solution of 211d-1 (14 g, 34.60 mmol) in carbon tetrachloride (200 mL). The mixture was stirred at 70° C. for 3 h. After the reaction was completed, the solvent was removed at reduced pressure, and the residue was subjected to column chromatography (PE/EA=20:1 to 10:1) to give compound 211d-2 (colorless oily liquid, 12 g). MS m/z (ESI): 483.2 [M+H]+.
Step 3: In a nitrogen atmosphere, DIEA (8.02 g, 62.05 mmol, 10.81 mL) was added to a solution of compound 211d-2 (10 g, 20.68 mmol) and tert-butyl 4-aminopiperidine-1-carboxylate (4.56 g, 22.75 mmol) in acetonitrile (100 mL). The reaction system was stirred at 60° C. for 12 h. The solvent was removed at reduced pressure to give compound 211d-3 (yellow oil, 12 g, crude). MS m/z (ESI): 515.1 [M+H-56]+.
Step 4: Compound 211 d-4 was prepared with reference to step 2 for intermediate 3b. MS m/z (ESI): 471.1 [M+H]+.
Step 5: In a nitrogen atmosphere, DIEA (4.12 g, 31.87 mmol, 5.55 mL) was added to a solution of compound 211d-4 (7.5 g, 15.93 mmol) and 1-bromo-2-fluoro-4-methoxy-5-nitrobenzene (4.78 g, 19.12 mmol) in ethanol (50 mL). The reaction system was stirred at 80° C. for 12 h. After the reaction was completed, the solvent was removed at reduced pressure. The residue was dissolved in water and extracted with ethyl acetate. The organic phase was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was removed by rotary evaporation to give compound 211d-5 (yellow solid, 12.5 g). MS m/z (ESI): 463.3 [M+H]+.
Step 6: Compound 221d-6 was prepared with reference to the method for intermediate 5d. MS m/z (ESI): 410.0 [M+H]+.
Steps 7-9: Compound 211d-9 was prepared with reference to steps 2-4 for intermediate 120c. MS m/z (ESI): 622.2 [M+H]+.
Step 10: Wet palladium on carbon (200 mg, 10 wt %) was added to a solution of compound 3211d-9 in THE (20 mL). The system was reacted for 12 h in an H2 atmosphere and filtered. The filter cake was rinsed with ethyl acetate and the filtrate was concentrated by rotary evaporation to give the title compound 211 d (yellow solid, 56 mg, crude). MS m/z (ESI): 624.3 [M+H]+.
Compound 214c was prepared with reference to the method for intermediate 165a. MS m/z (ESI): 343.2 [M+H]+.
Compound 222d was prepared with reference to step 5 for intermediate 189d as step 1 and with reference to steps 6 and 7 for intermediate 195d as steps 2 and 3. MS m/z (ESI): 279.3 [M+H]+.
Compound 1c (10 mg, 0.018 mmol) and compound 2b (7.6 mg, 0.018 mmol) were added to a reaction flask before NMP (2 mL), sodium iodide (5.4 mg, 0.036 mmol), and DIPEA (11.6 mg, 0.09 mmol) were added. In a nitrogen atmosphere, the reaction system was heated to 80° C. and stirred for 16 h. After the reaction was completed, the reaction mixture was filtered, and the filtrate was directly separated by preparative reverse-phase column chromatography (acetonitrile/(water+0.05% HCl)) to give compound C-1 (white solid, 6.0 mg, hydrochloride). 1H NMR (500 MHz, CD3OD) δ 8.29 (s, 1H), 8.15 (s, 1H), 7.81-7.75 (m, 3H), 7.71 (dd, J=16.4, 7.7 Hz, 2H), 7.61 (d, J=2.3 Hz, 1H), 7.54 (q, J=7.4 Hz, 2H), 7.32 (dd, J=8.7, 2.3 Hz, 1H), 5.23 (dd, J=13.3, 5.2 Hz, 1H), 4.58 (dd, J=42.8, 17.5 Hz, 2H), 4.04 (s, 3H), 3.80-3.70 (m, 4H), 3.60 (d, J=12.8 Hz, 2H), 3.42-3.36 (m, 2H), 3.27 (t, J=13.1 Hz, 2H), 3.00-2.92 (m, 1H), 2.86-2.78 (m, 1H), 2.72 (t, J=6.8 Hz, 2H), 2.64-2.54 (m, 1H), 2.41-2.04 (m, 9H), 1.94-1.90 (m, 2H), 1.90 (s, 3H), 1.88 (s, 3H). MS m/z (ESI): 863.6 [M+H]+.
Reference compound C-2 (pale yellow solid, 4.0 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.20 (s, 2H), 7.80 (d, J=6.9 Hz, 1H), 7.76-7.70 (m, 2H), 7.69-7.58 (m, 2H), 7.51 (dt, J=24.8, 7.5 Hz, 2H), 7.35 (s, 1H), 7.08 (d, J=8.2 Hz, 1H), 5.21 (dd, J=13.3, 5.2 Hz, 1H), 4.60 (dd, J=49.4, 17.6 Hz, 2H), 3.89 (d, J=62.8 Hz, 14H), 3.63 (dd, J=16.8, 9.9 Hz, 4H), 3.17 (dd, J=8.9, 4.8 Hz, 2H), 2.99-2.86 (m, 1H), 2.86-2.75 (m, 1H), 2.65-2.56 (m, 1H), 2.52 (d, J=11.4 Hz, 2H), 2.39 (d, J=10.9 Hz, 2H), 2.24-2.16 (m, 1H), 1.87 (d, J=13.6 Hz, 6H). MS m/z (ESI): 864.4 [M+H]+.
Reference compound C-3 (white solid, 0.32 g, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (800 MHz, CD3OD) δ 8.21 (s, 2H), 7.86 (d, J=7.6 Hz, 1H), 7.82 (dd, J=7.6, 0.6 Hz, 1H), 7.77-7.69 (m, 1H), 7.69-7.55 (m, 3H), 7.49 (t, J=7.4 Hz, 1H), 7.37 (s, 1H), 7.10 (d, J=7.6 Hz, 1H), 5.21 (dd, J=13.4, 5.2 Hz, 1H), 4.70 (dd, J=105.7, 17.7 Hz, 2H), 4.47 (s, 2H), 3.95 (d, J=12.4 Hz, 5H), 3.84 (d, J=39.4 Hz, 9H), 3.61 (d, J=49.5 Hz, 2H), 2.93 (ddd, J=17.8, 13.7, 5.4 Hz, 1H), 2.79 (ddd, J=17.6, 4.4, 2.3 Hz, 1H), 2.64 (qd, J=13.3, 4.5 Hz, 1H), 2.54 (d, J=12.1 Hz, 2H), 2.42 (d, J=10.3 Hz, 2H), 2.23-2.16 (m, 1H), 1.87 (d, J=13.5 Hz, 6H). MS m/z (ESI): 850.3 [M+H]+.
Reference compound C-4 (white solid, 0.58 g, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.24 (s, 1H), 8.16 (s, 1H), 7.77-7.67 (m, 2H), 7.63 (t, J=7.9 Hz, 1H), 7.60-7.44 (m, 4H), 7.19 (s, 1H), 6.95 (d, J=8.1 Hz, 1H), 5.19 (dd, J=13.3, 5.2 Hz, 1H), 4.58 (dd, J=49.1, 17.1 Hz, 2H), 3.99-3.56 (m, 14H), 3.38 (dd, J=20.4, 12.4 Hz, 4H), 2.98-2.75 (m, 4H), 2.57 (qd, J=13.3, 4.6 Hz, 1H), 2.44 (d, J=11.9 Hz, 2H), 2.31-2.16 (m, 5H), 1.87 (d, J=13.6 Hz, 6H). MS m/z (ESI): 854.3 [M+H]+.
Reference compound C-5 (white solid, 0.45 g, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.09 (s, 2H), 7.63 (ddd, J=10.8, 7.7, 2.1 Hz, 2H), 7.55 (t, J=7.9 Hz, 1H), 7.49 (d, J=8.0 Hz, 1H), 7.42-7.35 (m, 2H), 7.30 (d, J=8.0 Hz, 1H), 7.22 (s, 1H), 6.96 (d, J=7.6 Hz, 1H), 5.05 (dd, J=13.3, 5.2 Hz, 1H), 4.38 (q, J=17.0 Hz, 2H), 3.85 (s, 7H), 3.59 (dd, J=78.6, 37.9 Hz, 9H), 3.20-3.14 (m, 2H), 2.88-2.66 (m, 4H), 2.46-2.34 (m, 3H), 2.26 (d, J=10.6 Hz, 2H), 2.08 (dtd, J=12.8, 5.3, 2.4 Hz, 1H), 1.79 (s, 3H), 1.77-1.72 (m, 5H), 1.69 (dt, J=15.2, 7.7 Hz, 2H), 1.42-1.33 (m, 2H). MS m/z (ESI): 882.3 [M+H]+
Triethylamine (22.91 mg, 226.43 μmol, 31.52 μL) was added to a solution of compound 3b (90 mg, 226.43 μmol) in 1,2-dichloroethane (3 mL) at 25° C. The mixture was adjusted to a weakly alkaline pH before glacial acetic acid (13.60 mg, 226.43 μmol, 12.95 μL) was added, and adjusted to a weakly acidic pH before compound 3c (113.20 mg, 226.43 μmol). The reaction system was stirred for 1 h before sodium triacetoxyborohydride (95.98 mg, 452.87 μmol) was added, and was then stirred for another 2 h. After the reaction was completed, the reaction solution was subjected to reverse-phase preparative chromatography (formic acid system) and lyophilized to give compound C-6 (yellow solid, 8.88 mg, formate). 1H NMR (400 MHz, DMSO-d6) δ 11.12-11.24 (m, 1H), 10.81-11.06 (m, 1H), 8.38-8.58 (m, 1H), 7.93-8.18 (m, 2H), 7.42-7.62 (m, 2H), 7.21-7.41 (m, 4H), 7.00-7.17 (m, 1H), 6.57-6.70 (m, 1H), 6.44-6.54 (m, 1H), 5.06-5.18 (m, 1H), 4.47-4.62 (m, 1H), 4.30-4.43 (m, 1H), 4.14-4.28 (m, 1H), 3.76 (s, 3H), 3.62 (d, J=11.76 Hz, 3H), 2.86-2.95 (m, 1H), 2.73-2.81 (m, 2H), 2.58-2.70 (m, 4H), 2.12-2.23 (m, 1H), 1.84-2.05 (m, 6H), 1.76 (d, J=13.63 Hz, 6H), 1.65-1.72 (m, 2H), 1.52-1.63 (m, 6H), 1.38-1.48 (m, 2H). MS m/z (ESI): 881.2 [M+H]+.
Compound 6d (20 mg, 0.026 mmol) was dissolved in EtOH (3 mL) and THE (3 mL) before Pd/CaCO3 (20 mg) and quinoline (2 drops) were sequentially added. The reaction system was then stirred at room temperature for 1 h in a hydrogen atmosphere. The reaction mixture was filtered, and separated and purified by prep-HPLC (eluent (v/v):acetonitrile/(water+0.05% HCl)=10%-50%) to give title compound E1 (pale yellow solid, 4.5 mg, hydrochloride). 1H NMR (500 MHz, CD3OD) δ 8.43 (d, J=8.2 Hz, 1H), 8.22 (s, 1H), 7.89 (s, 1H), 7.83-7.77 (m, 1H), 7.68-7.60 (m, 2H), 7.58 (dd, J=8.2, 1.2 Hz, 1H), 7.43 (s, 1H), 6.78 (d, J=11.5 Hz, 1H), 5.93 (dt, J=11.6, 7.2 Hz, 1H), 5.22 (dd, J=13.4, 5.2 Hz, 1H), 4.54 (d, J=17.4 Hz, 1H), 4.45 (d, J=17.3 Hz, 1H), 4.06-3.51 (m, 9H), 3.45 (dt, J=22.8, 4.8 Hz, 4H), 2.96 (ddd, J=18.7, 11.9, 4.9 Hz, 3H), 2.90-2.76 (m, 5H), 2.62-2.47 (m, 1H), 2.35 (d, J=11.1 Hz, 2H), 2.26-2.17 (m, 1H), 2.13-2.00 (m, 2H), 1.82 (s, 6H), 1.37 (dd, J=9.5, 5.5 Hz, 3H). MS m/z (ESI): 778.6 [M+H]+.
Title compound E3 (pale yellow solid, 13.6 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.18 (s, 1H), 7.82 (d, J=7.5 Hz, 1H), 7.75 (q, J=6.7 Hz, 2H), 7.66-7.58 (m, 1H), 7.56 (dd, J=14.2, 6.5 Hz, 1H), 7.47 (t, J=7.2 Hz, 1H), 7.41 (s, 1H), 7.08 (s, 1H), 5.23 (dt, J=11.8, 5.9 Hz, 1H), 4.62 (dd, J=49.4, 17.6 Hz, 2H), 3.93 (s, 11H), 3.80-3.64 (m, 4H), 3.56 (d, J=10.5 Hz, 2H), 3.26 (s, 1H), 3.20 (t, J=7.0 Hz, 2H), 2.96 (ddd, J=18.6, 13.6, 5.4 Hz, 1H), 2.88-2.77 (m, 1H), 2.62 (qd, J=13.4, 4.7 Hz, 1H), 2.47 (d, J=11.6 Hz, 2H), 2.38-2.19 (m, 7H), 1.92 (s, 3H), 1.89 (s, 3H). MS m/z (ESI): 878.5 [M+H]+.
Compound 4a (1.1 g, 1.84 mmol) and compound 1b (1 g, 2.76 mmol) were added to a reaction flask before DMF (60 mL) was added. In a nitrogen atmosphere, sodium bicarbonate (1.5 g, 27.6 mmol) was added and the system was stirred at 65° C. for 24 h. The reaction mixture was concentrated and sequentially purified by normal-phase column chromatography and reverse-phase column chromatography to give title compound E4 (white solid, 0.31 g, hydrochloride). 1H NMR (500 MHz, CD3OD) δ 8.23 (d, J=53.6 Hz, 1H), 8.16 (s, 1H), 7.81 (t, J=7.7 Hz, 1H), 7.73 (dd, J=10.6, 7.7 Hz, 2H), 7.63-7.53 (m, 2H), 7.44 (dd, J=18.8, 11.3 Hz, 2H), 7.08 (s, 1H), 5.28-5.17 (m, 1H), 4.62 (dd, J=49.1, 17.7 Hz, 2H), 3.92 (s, 11H), 3.70 (dd, J=25.6, 18.8 Hz, 4H), 3.46 (dd, J=3.3, 1.6 Hz, 2H), 3.20 (t, J=6.9 Hz, 3H), 3.02-2.89 (m, 1H), 2.82 (ddd, J=17.6, 4.4, 2.3 Hz, 1H), 2.73-2.55 (m, 3H), 2.44 (d, J=10.8 Hz, 2H), 2.30-2.15 (m, 3H), 1.90 (d, J=13.6 Hz, 6H), 1.14 (t, J=10.8, 3H). MS m/z (ESI): 892.5 [M+H]+.
Compound E4 was isolated by chiral normal-phase chromatography (system: SHIMADZU LC-20AP; column: Chiralpak IC-column (250×50 mm, 10 μm particle size); mobile phase: A for Hexane (0.1% IPAm) and B for IPA+ACN (0.1% IPAm); gradient: B %=70% isocratic; flow rate: 100 mL/min; column temperature: room temperature; wavelength: 220 and 254 nm) and prep-HPLC (system: SHIMADZU LC-20AP; column: Luna C18 (250×70 mm, 10 μm particle size); mobile phase: A for 0.05% HCl in H2O and B for acetonitrile; gradient: phase B from 0% to 30% in 30 min; flow rate: 140 mL/min; column temperature: room temperature; wavelength: 220 and 254 nm) to give compound E5 (pale yellow solid, 1.1 g, hydrochloride, retention time: 3.224 min) and compound E6 (pale yellow solid, 1.1 g, hydrochloride, retention time: 5.300 min).
E5: 1H NMR (400 MHz, DMSO-d6) δ 12.42 (br s, 1H), 12.09 (s, 1H), 11.02 (s, 1H), 8.30 (br s, 2H), 7.74 (dd, J=11.8, 7.5 Hz, 2H), 7.68-7.63 (m, 1H), 7.56 (t, J=7.6 Hz, 1H), 7.35 (s, 2H), 7.27 (t, J=7.5 Hz, 1H), 6.86 (s, 1H), 5.17 (dd, J=13.3, 5.1 Hz, 1H), 4.58-4.35 (m, 2H), 3.79-3.44 (m, 14H), 3.20-3.11 (m, 4H), 3.00-2.74 (m, 3H), 2.66-2.54 (m, 3H), 2.47-2.40 (m, 1H), 2.24 (d, J=11.1 Hz, 2H), 2.08-1.88 (m, 3H), 1.82 (s, 3H), 1.78 (s, 3H), 1.07 (t, J=7.4 Hz, 3H). MS m/z (ESI): 892.3 [M+H]+.
E6: 1H NMR (400 MHz, DMSO-d6) δ 12.49 (s, 1H), 12.10 (s, 1H), 11.02 (s, 1H), 8.47-8.15 (m, 2H), 7.74 (dd, J=11.3, 7.6 Hz, 2H), 7.69-7.62 (m, 1H), 7.55 (t, J=7.6 Hz, 1H), 7.35 (s, 2H), 7.27 (t, J=7.5 Hz, 1H), 6.86 (s, 1H), 5.17 (dd, J=13.3, 5.1 Hz, 1H), 4.58-4.35 (m, 2H), 3.80-3.44 (m, 14H), 3.20-3.12 (m, 4H), 3.01-2.75 (m, 3H), 2.63-2.53 (m, 3H), 2.48-2.41 (m, 1H), 2.30-2.18 (m, 2H), 2.11-1.90 (m, 3H), 1.82 (s, 3H), 1.78 (s, 3H), 1.07 (t, J=7.5 Hz, 3H). MS m/z (ESI): 892.4 [M+H]+.
Title compound E7 (pale yellow solid, 9.2 mg, hydrochloride) was prepared with reference to the method for compound E4.
1H NMR (500 MHz, CD3OD) δ 8.25-8.09 (m, 2H), 7.71 (d, J=7.6 Hz, 1H), 7.66-7.59 (m, 2H), 7.45 (t, J=7.7 Hz, 2H), 7.34 (t, J=7.2 Hz, 1H), 7.19 (s, 1H), 6.78 (s, 1H), 5.12 (dd, J=13.3, 5.2 Hz, 1H), 4.49 (dd, J=45.0, 17.6 Hz, 2H), 3.80-3.50 (m, 10H), 3.43 (s, 3H), 3.28 (d, J=10.7 Hz, 2H), 3.01 (t, J=6.4 Hz, 2H), 2.84 (ddd, J=18.7, 13.6, 5.4 Hz, 3H), 2.74-2.65 (m, 1H), 2.47 (tt, J=13.4, 6.7 Hz, 1H), 2.24 (d, J=11.5 Hz, 2H), 2.14-2.06 (m, 4H), 1.98 (d, J=10.5 Hz, 2H), 1.80 (s, 3H), 1.77 (s, 3H). MS m/z (ESI): 922.0 [M+H]+.
Title compound E9 (white solid, 4.4 mg, hydrochloride) was prepared with reference to the method for compound E4.
1H NMR (500 MHz, CD3OD) δ 8.14 (s, 1H), 8.05 (s, 1H), 7.70 (d, J=7.1 Hz, 1H), 7.66-7.57 (m, 2H), 7.44 (t, J=7.7 Hz, 2H), 7.34 (t, J=7.1 Hz, 1H), 7.25-7.15 (m, 3H), 5.11 (dd, J=13.3, 5.1 Hz, 1H), 4.51 (dd, J=49.8, 17.7 Hz, 2H), 3.74 (d, J=67.1 Hz, 8H), 3.56 (t, J=6.8 Hz, 3H), 3.31 (d, J=10.5 Hz, 2H), 3.07 (dd, J=18.2, 11.6 Hz, 4H), 2.88-2.76 (m, 1H), 2.74-2.62 (m, 3H), 2.50 (tt, J=13.4, 6.6 Hz, 1H), 2.31 (d, J=11.2 Hz, 2H), 2.19-2.04 (m, 3H), 1.78 (d, J=13.6 Hz, 6H), 1.13-1.05 (m, 3H). MS m/z (ESI): 862.5 [M+H]+.
Title compound E10 (pale yellow solid, 6 mg, hydrochloride) was prepared with reference to the method for compound C-1 or E4.
1H NMR (500 MHz, CD3OD) δ 8.18 (br s, 2H), 7.78 (d, J=7.5 Hz, 1H), 7.73-7.66 (m, 2H), 7.62-7.55 (m, 2H), 7.52 (t, J=7.7 Hz, 1H), 7.42 (t, J=7.3 Hz, 1H), 6.87 (s, 1H), 5.19 (dd, J=13.3, 5.1 Hz, 1H), 4.66-4.52 (m, 2H), 4.13-3.76 (m, 11H), 3.68-3.53 (m, 5H), 3.18 (t, J=6.8 Hz, 2H), 2.95-2.75 (m, 4H), 2.63-2.55 (m, 1H), 2.36 (d, J=10.9 Hz, 2H), 2.24-2.15 (m, 1H), 2.14-2.03 (m, 2H), 1.89 (s, 3H), 1.86 (s, 3H). MS m/z (ESI): 898.7 [M+H]+.
Title compound E11 (pale yellow solid, 7.2 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, DMSO-d6) δ 12.01 (s, 1H), 11.01 (s, 1H), 10.84 (s, 1H), 8.38-8.31 (m, 2H), 7.73 (d, J=7.6 Hz, 1H), 7.71-7.62 (m, 3H), 7.56-7.53 (m, 1H), 7.45 (t, J=7.8 Hz, 1H), 7.27 (t, J=7.4 Hz, 1H), 6.93 (s, 1H), 5.17 (dd, J=13.2, 5.2 Hz, 1H), 4.58 (d, J=17.7 Hz, 1H), 4.37 (d, J=17.7 Hz, 1H), 3.84 (s, 3H), 3.35 (t, J=11.8 Hz, 2H), 3.24-3.15 (m, 2H), 3.13-2.86 (m, 7H), 2.64-2.52 (m, 3H), 2.13-2.05 (m, 2H), 2.04-2.00 (m, 1H), 1.94-1.86 (m, 2H), 1.85-1.74 (m, 11H), 1.56 (br s, 2H). MS m/z (ESI): 897.8 [M+H]+.
Title compound E12 (off-white solid, 5 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (400 MHz, DMSO-d6) δ 12.24 (s, 1H), 11.03 (s, 1H), 8.27-8.11 (m, 2H), 8.09-8.03 (m, 1H), 7.98-7.86 (m, 3H), 7.75-7.63 (m, 2H), 7.59-7.46 (m, 3H), 7.41 (s, 1H), 6.77 (s, 1H), 5.17 (dd, J=5.1, 13.3 Hz, 1H), 4.52-4.42 (m, 1H), 4.36-4.24 (m, 1H), 3.85-3.74 (m, 3H), 2.98-2.89 (m, 1H), 2.76 (s, 4H), 2.64-2.56 (m, 9H), 2.46-2.35 (m, 2H), 2.07-1.92 (m, 9H), 1.84-1.75 (m, 2H), 1.57 (s, 8H). MS m/z (ESI): 971.2, 973.2 [M+H]+.
Title compound E13 (off-white solid, 5.32 mg, hydrochloride) was prepared with reference to the method for compound E4.
1H NMR (400 MHz, DMSO-d6) δ 11.25-11.15 (m, 1H), 11.08-10.98 (m, 1H), 8.53-8.36 (m, 1H), 8.21-8.12 (m, 1H), 8.10-8.06 (m, 1H), 7.76-7.70 (m, 1H), 7.68-7.62 (m, 1H), 7.60-7.48 (m, 2H), 7.35-7.20 (m, 1H), 7.15-7.01 (m, 1H), 6.95-6.82 (m, 1H), 6.79-6.58 (m, 1H), 5.32-4.99 (m, 1H), 4.55-4.42 (m, 1H), 4.40-4.25 (m, 1H), 3.78-3.66 (m, 3H), 3.00-2.91 (m, 1H), 2.53 (s, 13H), 2.49-2.38 (m, 4H), 2.36-2.25 (m, 2H), 2.18-2.04 (m, 2H), 1.95-1.86 (m, 2H), 1.82-1.73 (m, 6H), 1.68-1.56 (m, 2H), 0.92-0.80 (m, 2H), 0.56-0.43 (m, 2H); MS m/z (ESI): 904.4 [M+H]+.
Title compound E14 (white solid, 6 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (400 MHz, DMSO-d6) δ 11.17 (s, 1H), 11.00 (s, 1H), 9.43 (s, 1H), 8.66-8.46 (m, 1H), 8.20 (s, 1H), 7.81 (d, J=2.3 Hz, 1H), 7.71 (d, J=7.0 Hz, 1H), 7.64 (d, J=7.6 Hz, 1H), 7.61-7.55 (m, 1H), 7.54 (s, 1H), 7.52 (s, 1H), 7.44 (dd, J=2.3, 8.8 Hz, 1H), 7.21-7.14 (m, 1H), 6.99 (d, J=8.8 Hz, 1H), 5.20-5.10 (m, 1H), 4.49-4.42 (m, 1H), 4.35-4.28 (m, 1H), 2.89 (dd, J=4.4, 12.8 Hz, 2H), 2.85-2.78 (m, 3H), 2.75-2.68 (m, 3H), 2.60 (s, 2H), 2.46-2.41 (m, 2H), 2.06 (s, 3H), 2.03-1.96 (m, 3H), 1.80 (s, 3H), 1.77 (s, 3H), 1.73-1.65 (m, 4H), 1.63-1.54 (m, 4H); MS m/z (ESI): 867.3 [M+H]+.
Title compound E15 (white solid, 9.0 mg) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.18 (s, 1H), 8.01 (s, 1H), 7.69-7.53 (m, 5H), 7.43-7.39 (m, 3H), 5.10 (dd, J=5.0, 10.0 Hz, 1H), 4.50 (q, J=15.0 Hz, 2H), 3.94 (s, 3H), 3.66-3.62 (m, 3H), 3.47 (d, J=10.0 Hz, 2H), 3.29-3.25 (m, 2H), 3.17-3.15 (m, 2H), 2.86-2.77 (m, 1H), 2.72-2.67 (m, 1H), 2.61-2.57 (m, 4H), 2.52-2.41 (m, 2H), 2.32-2.22 (m, 2H), 2.12-2.02 (m, 4H), 1.88-1.82 (m, 4H), 1.81 (s, 3H), 1.76 (s, 3H), 0.99-0.96 (m, 4H). MS m/z (ESI): 891.5 [M+H]+.
Title compound E16 (white solid, 5.0 mg) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.11 (s, 1H), 8.09 (s, 1H), 7.66-7.62 (m, 2H), 7.55-7.46 (m, 4H), 7.36 (t, J=7.5 Hz, 1H), 7.19 (s, 1H), 5.04 (dd, J=5.0, 10.0 Hz, 1H), 4.38 (q, J=15.0 Hz, 2H), 3.89 (s, 3H), 3.49-3.31 (m, 6H), 3.28-3.25 (m, 2H), 3.18-3.13 (m, 2H), 2.86-2.77 (m, 1H), 2.72-2.66 (m, 1H), 2.58-2.55 (m, 4H), 2.44-2.35 (m, 1H), 2.17-2.10 (m, 7H), 1.91-1.83 (m, 2H), 1.81 (s, 3H), 1.76 (s, 3H), 1.75-1.71 (m, 2H), 0.99-0.96 (m, 3H). MS m/z (ESI): 891.4 [M+H]+.
Title compound E17 (white solid, 4.0 mg, hydrochloride) was prepared with reference to the method for compound E4.
1H NMR (500 MHz, CD3OD) δ 8.21 (d, J=17.2 Hz, 2H), 7.82 (d, J=7.6 Hz, 1H), 7.73 (dd, J=18.2, 7.5 Hz, 2H), 7.62-7.54 (m, 3H), 7.44 (t, J=7.4 Hz, 1H), 7.31-7.26 (m, 1H), 7.21 (d, J=8.6 Hz, 1H), 5.23 (dd, J=13.3, 5.0 Hz, 1H), 4.67 (d, J=17.6 Hz, 1H), 4.57 (d, J=17.6 Hz, 1H), 4.11-3.74 (m, 8H), 3.64 (dd, J=17.1, 10.3 Hz, 3H), 3.57 (d, J=11.9 Hz, 2H), 3.19 (t, J=6.8 Hz, 2H), 3.00-2.91 (m, 1H), 2.90-2.80 (m, 3H), 2.68-2.55 (m, 1H), 2.37 (d, J=11.2 Hz, 2H), 2.27-2.20 (m, 1H), 2.15-2.05 (m, 2H), 1.91 (s, 3H), 1.88 (s, 3H). MS m/z (ESI): 868.7 [M+H]+.
Compound E18 (white solid, 10 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.28 (s, 1H), 8.14 (d, J=4.5 Hz, 1H), 7.83-7.75 (m, 3H), 7.69 (dd, J=15.6, 8.1 Hz, 3H), 7.56 (t, J=7.6 Hz, 1H), 7.51 (t, J=7.1 Hz, 1H), 7.45 (dd, J=8.8, 2.1 Hz, 1H), 5.23 (dd, J=13.3, 5.1 Hz, 1H), 4.58 (dd, J=36.6, 17.5 Hz, 2H), 3.568-3.50 (m, 10H), 3.00-2.91 (m, 1H), 2.82 (d, J=16.1 Hz, 1H), 2.76-2.69 (m, 2H), 2.62-2.52 (m, 1H), 2.26-2.15 (m, 4H), 2.12-2.01 (m, 7H), 1.91 (s, 3H), 1.89 (s, 3H). MS m/z (ESI): 867.6 [M+H]+.
Title compound E19 (36 mg, hydrochloride) was prepared with reference to the method for compound C-1 or E4.
1H NMR (500 MHz, DMSO-d6) δ 12.02-11.76 (m, 2H), 11.00 (s, 1H), 8.30-8.26 (m, 2H), 7.69-7.54 (m, 2H), 7.48 (d, J=8.8 Hz, 1H), 7.35 (s, 2H), 7.24 (s, 1H), 6.83 (s, 1H), 5.11 (dd, J=13.3, 5.1 Hz, 1H), 4.44-4.28 (m, 2H), 3.85-3.73 (m, 9H), 3.15 (br s, 4H), 2.95-2.87 (m, 1H), 2.84-2.73 (m, 4H), 2.62-2.58 (m, 5H), 2.45-2.36 (m, 1H), 2.22 (br s, 2H), 2.04-1.89 (m, 3H), 1.83-1.74 (m, 9H), 1.68-1.59 (m, 2H), 1.43-1.32 (m, 2H), 1.07 (t, J=7.3 Hz, 3H). MS m/z (ESI): 928.3 [M+H]+.
Title compound E20 (30 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, DMSO-d6) δ 11.90 (br s, 2H), 11.00 (s, 1H), 8.41-8.18 (m, 2H), 7.63 (d, J=13.7 Hz, 1H), 7.55-7.46 (m, 2H), 7.36 (s, 2H), 7.24 (s, 1H), 6.83 (s, 1H), 5.11 (dd, J=13.3, 5.1 Hz, 1H), 4.57-4.36 (m, 2H), 3.85-3.76 (m, 9H), 3.19-3.12 (m, 4H), 2.96-2.88 (m, 1H), 2.83-2.73 (m, 4H), 2.63-2.53 (m, 5H), 2.45-2.37 (m, 1H), 2.21 (s, 2H), 2.01 (s, 1H), 1.93 (s, 2H), 1.83-1.73 (m, 9H), 1.69-1.60 (m, 2H), 1.37 (d, J=7.3 Hz, 2H), 1.07 (t, J=7.4 Hz, 3H). MS m/z (ESI): 928.3 [M+H]+.
Title compound E21 (13.52 mg, formate) was prepared with reference to the method for compound C-6.
1H NMR (400 MHz, DMSO-d6) δ 11.22-11.06 (m, 1H), 11.0-10.86 (m, 1H), 8.57-8.38 (m, 1H), 8.15-8.03 (m, 2H), 7.60-7.51 (m, 1H), 7.50-7.39 (m, 2H), 7.36-7.22 (m, 3H), 7.15-7.00 (m, 1H), 6.86-6.61 (m, 1H), 5.16-5.05 (m, 1H), 4.64-4.48 (m, 1H), 4.41-4.30 (m, 1H), 4.27-4.16 (m, 1H), 3.81-3.71 (m, 3H), 3.07-2.80 (m, 4H), 2.76-2.65 (m, 4H), 2.63-2.52 (m, 4H), 2.31-2.14 (m, 2H), 2.09-1.85 (m, 4H), 1.82-1.74 (m, 6H), 1.46 (s, 10H), 1.11-1.02 (m, 3H). MS m/z (ESI): 909.3 [M+H]+.
Title compound E22 (2.5 mg, formate) was prepared with reference to the method for compound C-6.
1H NMR (400 MHz, CDCl3) δ 11.56-11.23 (m, 1H), 8.34-8.26 (m, 1H), 8.12 (s, 1H), 8.08-7.91 (m, 2H), 7.83 (d, J=7.5 Hz, 1H), 7.57 (d, J=7.3 Hz, 1H), 7.49-7.40 (m, 1H), 6.99-6.88 (m, 1H), 6.60 (s, 1H), 5.26 (dd, J=4.9, 13.1 Hz, 1H), 4.61-4.49 (m, 1H), 4.46-4.39 (m, 1H), 4.36-4.27 (m, 4H), 3.83 (s, 3H), 3.48 (d, J=15.9 Hz, 2H), 3.26 (s, 2H), 3.21-3.08 (m, 5H), 3.00-2.88 (m, 3H), 2.87-2.75 (m, 3H), 2.74-2.60 (m, 2H), 2.56 (q, J=7.4 Hz, 2H), 2.35-2.21 (m, 3H), 2.06-2.00 (m, 2H), 1.89 (d, J=13.9 Hz, 6H), 1.39-1.15 (m, 4H), 1.11-0.99 (m, 3H), 0.93-0.80 (m, 1H). MS m/z (ESI): 498.6 [M/2+H]+.
Title compound E23 (8.2 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.44 (s, 1H), 8.30 (s, 1H), 7.95-7.90 (m, 2H), 7.86 (s, 1H), 7.80-7.66 (m, 2H), 7.61 (s, 1H), 5.40 (dd, J=5.0, 10.0 Hz, 1H), 4.70 (q, J=15.0 Hz, 2H), 4.21 (s, 3H), 4.01-3.81 (m, 3H), 3.71 (d, J=10 Hz, 1H), 3.48-3.35 (m, 5H), 3.14-3.03 (m, 1H), 3.01-2.92 (m, 1H), 2.88-2.84 (m, 2H), 2.82-2.79 (m, 3H), 2.56-2.51 (m, 2H), 2.40-2.35 (m, 2H), 2.25-2.18 (m, 3H), 2.17 (s, 3H), 2.15 (s, 3H), 1.91-1.89 (m, 2H), 1.25-1.12 (m, 3H). MS m/z (ESI): 905.5 [M+H]+.
Title compound E24 (white solid, 4 mg, hydrochloride) was prepared with reference to the method for compound E4.
1H NMR (500 MHz, CD3OD) δ 8.42 (t, J=39.3 Hz, 2H), 8.03 (d, J=7.9 Hz, 1H), 8.00-7.94 (m, 2H), 7.89 (d, J=7.9 Hz, 1H), 7.82 (s, 1H), 7.67 (dd, J=22.9, 15.6 Hz, 2H), 7.30 (s, 1H), 5.42 (dd, J=13.3, 5.1 Hz, 1H), 4.76 (q, J=17.3 Hz, 2H), 4.17 (d, J=13.9 Hz, 11H), 3.92 (dd, J=17.7, 11.4 Hz, 4H), 3.67 (d, J=9.6 Hz, 2H), 3.42 (t, J=6.9 Hz, 3H), 3.15 (dd, J=13.4, 5.2 Hz, 1H), 3.06 (dd, J=10.0, 7.6 Hz, 1H), 2.90 (d, J=7.4 Hz, 2H), 2.80-2.62 (m, 3H), 2.52-2.42 (m, 3H), 2.14 (d, J=13.5 Hz, 6H), 1.38 (t, J=10.8, 3H). MS m/z (ESI): 892.5 [M+H]+.
Title compound E25 (6 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.21 (d, J=71.9 Hz, 2H), 7.93-7.82 (m, 2H), 7.75-7.67 (m, 1H), 7.66-7.51 (m, 2H), 7.43 (dd, J=24.8, 17.3 Hz, 2H), 7.03 (s, 1H), 5.23 (dd, J=13.4, 5.2 Hz, 1H), 4.83-4.61 (m, 2H), 4.49 (s, 2H), 3.99-3.72 (m, 10H), 3.64 (s, 1H), 3.38 (t, J=13.8 Hz, 2H), 3.12 (s, 2H), 2.96 (ddd, J=19.6, 12.5, 5.6 Hz, 1H), 2.87-2.76 (m, 1H), 2.71-2.60 (m, 3H), 2.46 (dd, J=39.4, 20.0 Hz, 3H), 2.30-2.13 (m, 3H), 1.90 (d, J=13.6 Hz, 6H), 1.14 (s, 3H). MS m/z (ESI): 878.5 [M+H]+.
Title compound E26 (white solid, 4 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.12 (dd, J=54.9, 30.2 Hz, 2H), 7.79-7.68 (m, 2H), 7.60 (d, J=7.1 Hz, 2H), 7.54 (t, J=7.5 Hz, 1H), 7.49-7.42 (m, 2H), 7.15 (s, 1H), 5.21 (dd, J=13.3, 5.1 Hz, 1H), 4.59 (dt, J=45.0, 15.5 Hz, 2H), 4.16-3.56 (m, 13H), 3.57-3.35 (m, 5H), 2.90 (qdd, J=17.6, 14.5, 3.7 Hz, 4H), 2.75-2.55 (m, 3H), 2.45 (t, J=16.3 Hz, 2H), 2.40-2.17 (m, 5H), 1.90 (d, J=13.6 Hz, 6H), 1.13 (s, 3H). MS m/z (ESI): 882.5 [M+H]+.
Title compound E27 (yellow solid, 12.93 mg, hydrochloride) was prepared with reference to the method for compound C-6.
1H NMR (400 MHz, DMSO-d6) δ 11.19 (s, 1H), 10.98 (s, 1H), 8.43 (d, J=4.8 Hz, 2H), 8.27 (s, 1H), 8.16 (s, 1H), 8.07 (s, 1H), 7.55-7.45 (m, 2H), 7.31-7.28 (m, 3H), 7.08 (d, J=7.2 Hz, 2H), 6.90 (s, 1H), 6.71 (s, 1H), 5.11 (dd, J=17.0, 5.2 Hz, 1H), 4.56 (d, J=4.4 Hz, 1H), 4.38-4.24 (m, 2H), 3.74 (s, 4H), 3.38-3.24 (m, 4H), 2.95-2.85 (m, 1H), 2.75-2.60 (m, 4H), 2.50-2.40 (m, 2H), 2.20-2.10 (m, 2H), 2.00-1.85 (m, 5H), 1.79 (s, 3H), 1.75 (s, 3H), 1.62-1.58 (m, 6H), 1.49-1.42 (m, 2H), 0.85 (d, J=8.8 Hz, 2H), 0.48 (t, J=11.0 Hz, 2H). MS m/z (ESI): 921.4 [M+H]+.
Title compound E28 (white solid, 20 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (400 MHz, DMSO-d6) δ 11.57 (s, 1H), 11.03 (s, 1H), 8.10 (s, 1H), 7.99-7.85 (m, 2H), 7.73 (d, J=7.2 Hz, 1H), 7.68-7.62 (m, 1H), 7.57-7.51 (m, 1H), 7.45 (s, 1H), 6.84 (s, 1H), 6.77 (d, J=8.8 Hz, 1H), 5.17 (dd, J=13.6, 4.8 Hz, 1H), 4.53-4.43 (m, 1H), 4.35-4.21 (m, 5H), 3.77 (s, 3H), 3.01-2.88 (m, 2H), 2.79 (s, 4H), 2.63 (d, J=5.2 Hz, 4H), 2.41 (s, 7H), 2.12-1.97 (m, 2H), 1.84-1.74 (m, 8H), 1.69-1.51 (m, 7H), 1.04 (t, J=7.2 Hz, 3H). MS m/z (ESI): 993.2 [M+H]+.
Title compound E29 (white solid, 15 mg, hydrochloride) was prepared with reference to the method for compound C-6.
1H NMR (500 MHz, CD3OD) δ 8.42-8.04 (m, 2H), 7.69 (dd, J=13.8, 7.9 Hz, 1H), 7.59-7.45 (m, 2H), 7.42-7.38 (m, 2H), 7.31 (br s, 1H), 7.24 ((d, J=10.0 Hz, 1H), 6.99-6.89 (m, 1H), 5.15 (dd, J=13.4, 4.9 Hz, 1H), 4.62-4.58 (m, 1H), 4.48-4.30 (m, 2H), 4.09-3.98 (m, 4H), 3.86 (s, 3H), 3.46-3.36 (m, 1H), 3.27-3.18 (m, 2H), 2.93-2.87 (m, 3H), 2.82-2.72 (m, 1H), 2.61-2.57 (m, 2H), 2.54-2.45 (m, 1H), 2.23-2.16 (m, 4H), 2.10-2.00 (m, 2H), 1.96-1.65 (m, 13H), 1.11 (t, J=9.0 Hz, 3H). MS m/z (ESI): 896.0 [M+H]+.
Compound E30 (pale yellow solid, 24 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.33 (s, 1H), 8.10 (s, 1H), 7.72 (dd, J=13.4, 8.3 Hz, 1H), 7.64-7.49 (m, 2H), 7.44-7.41 (m, 2H), 7.33 (s, 1H), 7.26 (d, J=8.1 Hz, 1H), 6.93 (s, 1H), 5.20 (dd, J=13.4, 5.2 Hz, 1H), 4.57-4.45 (m, 2H), 4.26 (t, J=5.7 Hz, 2H), 4.02-3.39 (m, 14H), 3.30-3.26 (m, 2H), 2.99-2.91 (m, 3H), 2.84-2.79 (m, 1H), 2.67-2.51 (m, 3H), 2.31 (d, J=11.3 Hz, 2H), 2.24-2.19 (m, 1H), 2.12-2.02 (m, 4H), 2.01-1.96 (m, 2H), 1.92 (s, 3H), 1.89 (s, 3H), 1.15 (br s, 3H). MS m/z (ESI): 913.3 [M+H]+.
Title compound E34 (white solid, 8 mg, hydrochloride) was prepared with reference to the method for compound C-6.
1H NMR (400 MHz, CD3OD) δ ppm 8.25 (dd, J=8.4 Hz, 1H), 8.06 (s, 1H), 7.68 (s, 1H), 7.63 (dd, J=13.6, 7.6 Hz, 1H) 7.58-7.54 (m, 1H), 7.50 (td, J=7.6, 4.8 Hz, 2H), 7.27 (brt, J=8.0 Hz, 1H) 7.15 (d, J=8.0 Hz, 1H), 7.10 (d, J=7.6 Hz, 1H), 6.88 (d, J=2.0 Hz, 1H), 6.82 (dd, J=8.0, 2.4 Hz, 1H), 6.77 (s, 1H), 5.14 (dd, J=13.6, 5.2 Hz, 1H), 4.48-4.35 (m, 2H), 3.84 (s, 3H), 3.07 (br d, J=11.26 Hz, 2H), 3.00-2.82 (m, 9H), 2.81-2.69 (m, 4H), 2.58-2.41 (m, 3H), 2.21-2.13 (m, 1H), 1.95-1.75 (m, 10H), 1.00 (t, J=7.6 Hz, 3H). MS m/z (ESI): 459.5[M/2+H]+.
Title compound E35 (pale yellow solid, 45 mg, hydrochloride) was prepared with reference to the method for compound C-6.
1H NMR (500 MHz, CD3OD) δ 8.29 (s, 1H), 8.08 (s, 1H), 7.67 (dd, J=14.0, 7.9 Hz, 1H), 7.56-7.47 (m, 2H), 7.41-7.35 (m, 2H), 7.23 (d, J=8.1 Hz, 1H), 7.01 (s, 1H), 6.96 (s, 1H), 5.16 (dd, J=13.3, 5.1 Hz, 1H), 4.56-4.44 (m, 2H), 4.23 (t, J=5.6 Hz, 2H), 4.08-3.65 (m, 14H), 3.43-3.37 (m, 2H), 3.24-3.12 (m, 2H), 2.95-2.88 (m, 1H), 2.82-2.75 (m, 1H), 2.63-2.55 (m, 1H), 2.43 (d, J=10.7 Hz, 2H), 2.32-2.15 (m, 4H), 2.12-2.06 (m, 2H), 1.99-1.93 (m, 2H), 1.90 (s, 3H), 1.87 (s, 3H), 0.96 (d, J=7.6 Hz, 2H), 0.56 (s, 2H). MS m/z (ESI): 925.1 [M+H]+.
Title compound E36 (white solid, 27.82 mg, formate) was prepared with reference to the method for compound C-6.
1H NMR (400 MHz, DMSO-d6) δ 11.19 (s, 1H), 10.99 (s, 1H), 8.48-8.36 (m, 1H), 8.16 (s, 1H), 8.07 (s, 1H), 7.62-7.40 (m, 4H), 7.33-7.22 (m, 1H), 7.07 (t, J=7.6 Hz, 1H), 6.90 (s, 1H), 6.73-6.66 (m, 1H), 6.26 (s, 1H), 5.18-5.08 (m, 1H), 4.43-4.17 (m, 2H), 3.73 (s, 3H), 3.28-3.20 (m, 3H), 2.97-2.86 (m, 1H), 2.77-2.68 (m, 4H), 2.61 (s, 3H), 2.30 (d, J=3.6 Hz, 2H), 2.16-2.09 (m, 1H), 2.05-1.88 (m, 5H), 1.76 (d, J=13.5 Hz, 6H), 1.69-1.46 (m, 8H), 1.26-1.12 (m, 1H), 0.84 (d, J=8.3 Hz, 2H), 0.48 (d, J=4.0 Hz, 2H). MS m/z (ESI): 917.2 [M+H]+.
By-product E37 (50 mg, hydrochloride) was prepared with reference to the method for compound C-6.
1H NMR (500 MHz, CD3OD) δ 8.23 (br s, 1H), 8.13 (br s, 1H), 7.78-7.68 (m, 2H), 7.66-7.50 (m, 3H), 7.44-7.41 (m, 1H), 7.38 (br s, 1H), 7.06 (s, 1H), 6.74 (d, J=11.4 Hz, 1H), 5.92-5.87 (m, 1H), 5.18 (dd, J=13.4, 5.2 Hz, 1H), 4.53-4.42 (m, 2H), 3.97-3.60 (m, 12H), 3.46-3.38 (m, 4H), 3.24-3.15 (m, 2H), 2.96-2.74 (m, 4H), 2.63 (q, J=7.2 Hz, 2H), 2.58-2.49 (m, 1H), 2.39 (d, J=10.6 Hz, 2H), 2.30-2.15 (m, 3H), 1.89 (s, 3H), 1.86 (s, 3H), 1.10 (br s, 3H). MS m/z (ESI): 895.3 [M+H]+.
Title compound E38 (white solid, 30 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.12 (s, 2H), 7.81-7.67 (m, 2H), 7.49 (s, 1H), 7.49 (s, 1H), 7.42 (d, J=8.0 Hz, 2H), 7.33 (s, 1H), 6.94 (s, 1H), 5.17 (dd, J=13.3, 5.2 Hz, 1H), 4.50 (q, J=17.0 Hz, 2H), 3.74 (dd, J=143.3, 21.1 Hz, 13H), 3.32-3.23 (m, 3H), 3.11-2.74 (m, 6H), 2.64 (s, 2H), 2.56-2.46 (m, 1H), 2.37 (s, 2H), 2.20 (ddd, J=10.3, 5.2, 2.8 Hz, 3H), 1.95-1.73 (m, 10H), 1.54-1.46 (m, 2H), 1.15 (s, 3H). MS m/z (ESI): 910.5 [M+H]+.
Title compound E39 (white solid, 14 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.18 (s, 1H), 7.74 (dt, J=8.9, 3.5 Hz, 1H), 7.67 (td, J=7.3, 2.3 Hz, 1H), 7.59 (s, 1H), 7.49 (ddd, J=28.7, 14.2, 7.1 Hz, 5H), 7.14 (s, 1H), 5.30-5.13 (m, 1H), 4.56 (d, J=19.6 Hz, 2H), 3.96 (d, J=26.9 Hz, 6H), 3.85-3.74 (m, 4H), 3.50 (t, J=12.9 Hz, 2H), 3.00-2.90 (m, 2H), 2.85-2.77 (m, 4H), 2.72 (s, 5H), 2.70-2.57 (m, 3H), 2.47 (d, J=12.4 Hz, 2H), 2.34 (s, 2H), 2.26-2.18 (m, 1H), 1.92 (s, 3H), 1.89 (s, 3H), 1.80 (dd, J=14.9, 7.2 Hz, 2H), 1.56-1.43 (m, 3H), 1.10 (d, J=26.7 Hz, 3H). MS m/z (ESI): 910.4 [M+H]+.
Title compound E40 (50 mg, formate) was prepared with reference to the method for compound C-6.
1H NMR (400 MHz, DMSO-d6) δ 11.15 (s, 1H), 10.99 (s, 1H), 8.42 (d, J=4.8 Hz, 1H), 8.21 (s, 1H), 8.13-8.07 (m, 2H), 7.62-7.40 (m, 5H), 7.31 (t, J=7.3 Hz, 1H), 6.76 (d, J=3.9 Hz, 1H), 6.25 (s, 1H), 5.19-5.10 (m, 1H), 4.46-4.17 (m, 2H), 3.75 (s, 3H), 3.00-2.87 (m, 3H), 2.74-2.68 (m, 1H), 2.65-2.53 (m, 5H), 2.45-2.36 (m, 4H), 2.29 (s, 2H), 2.18-2.11 (m, 1H), 2.05-1.85 (m, 5H), 1.76 (d, J=13.5 Hz, 7H), 1.65-1.48 (m, 7H), 1.06 (m, 3H). MS m/z (ESI): 453.3 [M/2+H]+.
Title compound E41 (pale yellow solid, 4.2 mg, hydrochloride) was prepared with reference to the method for compound E4.
1H NMR (500 MHz, CD3OD) δ 8.05 (s, 1H), 8.04 (s, 1H), 7.70 (d, J=7.6 Hz, 1H), 7.64-7.56 (m, 2H), 7.51 (s, 1H), 7.43 (t, J=7.6 Hz, 2H), 7.33 (t, J=7.2 Hz, 1H), 5.10 (dd, J=13.3, 4.9 Hz, 1H), 4.53 (d, J=17.6 Hz, 1H), 4.44 (d, J=17.6 Hz, 1H), 3.94-3.50 (m, 15H), 3.51-3.43 (m, 3H), 3.03 (t, J=6.5 Hz, 2H), 2.92 (t, J=12.5 Hz, 2H), 2.87-2.78 (m, 1H), 2.70 (d, J=16.3 Hz, 1H), 2.53-2.41 (m, 3H), 2.20 (d, J=10.7 Hz, 2H), 2.14-2.08 (m, 1H), 1.97 (dd, J=21.1, 11.3 Hz, 2H), 1.78 (d, J=13.5 Hz, 6H), 1.03 (t, J=7.2 Hz, 3H). MS m/z (ESI): 893.4 [M+H]+.
Title compound E42 (pale yellow solid, 11 mg, hydrochloride) was prepared with reference to the method for compound E4.
1H NMR (500 MHz, CD3OD) δ 8.10 (s, 1H), 7.87 (s, 1H), 7.79 (d, J=7.0 Hz, 1H), 7.72-7.69 (m, 1H), 7.67-7.63 (m, 1H), 7.53 (t, J=7.7 Hz, 1H), 7.48-7.38 (m, 2H), 7.31 (s, 1H), 6.89 (s, 1H), 5.20 (dd, J=13.3, 5.2 Hz, 1H), 4.62 (d, J=17.6 Hz, 1H), 4.53 (d, J=17.6 Hz, 1H), 4.04-3.58 (m, 11H), 3.53 (s, 3H), 3.28-3.20 (m, 2H), 3.11 (t, J=6.9 Hz, 2H), 3.00 (s, 3H), 2.98-2.86 (m, 3H), 2.82-2.76 (m, 1H), 2.62-2.49 (m, 3H), 2.32 (d, J=10.1 Hz, 2H), 2.24-2.17 (m, 1H), 2.10-2.00 (m, 2H), 1.06 (t, J=7.1 Hz, 3H). MS m/z (ESI): 924.1 [M+H]+.
Title compound E43 (yellow solid, 5.04 mg, formate) was prepared with reference to the method for compound C-6.
1H NMR (400 MHz, DMSO-d6) δ 11.61 (s, 1H), 11.07-10.97 (m, 1H), 8.44-8.32 (m, 1H), 8.10 (s, 1H), 7.97-7.88 (m, 2H), 7.79-7.70 (m, 3H), 7.64 (d, J=7.0 Hz, 1H), 7.58-7.48 (m, 1H), 7.44 (s, 1H), 6.81 (d, J=9.3 Hz, 1H), 6.71 (s, 1H), 5.20-5.10 (m, 1H), 4.50-4.40 (m, 1H), 4.36-4.21 (m, 5H), 3.76 (s, 3H), 3.14 (d, J=14.5 Hz, 2H), 3.08 (d, J=10.9 Hz, 2H), 3.00-2.86 (m, 2H), 2.62 (dd, J=5.8, 15.0 Hz, 6H), 2.57-2.54 (m, 3H), 2.42 (d, J=4.3 Hz, 2H), 2.31-2.19 (m, 2H), 2.13 (s, 3H), 2.09-1.96 (m, 2H), 1.91-1.83 (m, 2H), 1.80 (d, J=14.0 Hz, 6H), 1.64-1.50 (m, 2H). MS M/Z (ESI): 980.4 [M+H]+.
Title compound E44 (yellow solid, 8.18 mg) was prepared with reference to the method for compound C-6.
1H NMR (400 MHz, DMSO-d6) δ 11.17-11.09 (m, 1H), 11.08-10.99 (m, 1H), 8.48-8.37 (m, 1H), 8.14-8.04 (m, 2H), 7.76-7.69 (m, 1H), 7.67-7.61 (m, 1H), 7.60-7.50 (m, 2H), 7.46-7.42 (m, 1H), 7.37-7.29 (m, 1H), 7.16-7.09 (m, 1H), 6.82-6.77 (m, 1H), 5.21-5.12 (m, 1H), 4.50-4.42 (m, 1H), 4.38-4.26 (m, 1H), 3.80-3.72 (m, 3H), 3.02-2.85 (m, 3H), 2.74-2.57 (m, 10H), 2.53 (m, 3H), 2.46 (m, 4H), 2.37-2.21 (m, 2H), 2.10-2.01 (m, 1H), 1.93-1.84 (m, 2H), 1.80-1.73 (m, 6H), 1.59-1.41 (m, 4H), 0.90-0.81 (m, 3H). MS m/z (ESI): 906.4 [M+H]+.
Title compound E45 (white solid, 58.4 mg, formate) was prepared with reference to the method for compound C-6.
1H NMR (400 MHz, DMSO-d6) δ 11.14 (s, 1H), 11.00 (s, 1H), 8.42 (s, 1H), 8.19 (s, 1H), 8.15-8.05 (m, 2H), 7.61-7.37 (m, 5H), 7.31 (s, 1H), 7.15-7.06 (m, 1H), 6.76 (d, J=8.0 Hz, 1H), 5.13 (dd, J=12.8, 4.8 Hz, 1H), 4.51-4.39 (m, 1H), 4.35-4.24 (m, 1H), 3.75 (d, J=4.8 Hz, 4H), 3.05-2.85 (m, 4H), 2.76-2.65 (m, 4H), 2.55 (s, 4H), 2.40 (s, 2H), 2.31-2.16 (m, 1H), 2.05-1.90 (m, 3H), 1.78 (s, 3H), 1.75 (s, 3H), 1.67-1.49 (m, 9H), 1.24 (m, 2H), 1.13-1.00 (m, 5H). MS m/z (ESI): 907.5 (M+H)+.
Title compound E46 (white solid, 4 mg, hydrochloride) was prepared with reference to the method for compound E4.
1H NMR (500 MHz, CD3OD) δ 8.18 (s, 1H), 8.17 (s, 1H), 7.83 (d, J=7.6 Hz, 1H), 7.75 (d, J=7.0 Hz, 1H), 7.68 (dd, J=14.0, 8.2 Hz, 1H), 7.56 (t, J=7.7 Hz, 1H), 7.48-7.35 (m, 3H), 7.34 (s, 1H), 5.23 (dd, J=13.3, 5.2 Hz, 1H), 4.62 (dd, J=49.2, 17.6 Hz, 2H), 4.30-3.47 (m, 12H), 3.29 (s, 1H), 3.19 (dd, J=9.1, 4.3 Hz, 2H), 3.00-2.79 (m, 4H), 2.72 (q, J=7.5 Hz, 2H), 2.61 (qd, J=13.3, 4.7 Hz, 1H), 2.38 (d, J=10.7 Hz, 2H), 2.28-2.16 (m, 1H), 2.10 (dt, J=20.2, 10.1 Hz, 2H), 1.90 (d, J=13.6 Hz, 6H), 1.20 (t, J=7.4 Hz, 3H); MS m/z (ESI): 896.4 [M+H]+.
Title compound E47 (5 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.35-8.13 (m, 2H), 7.91 (d, J=10.0 Hz, 1H), 7.76-7.56 (m, 5H), 7.40 (d, J=10.0 Hz, 2H), 5.35 (dd, J=10.0, 5.0 Hz, 1H), 4.60 (q, J=15.0 Hz, 2H), 4.58 (t, J=10.0 Hz, 2H), 4.12 (s, 3H), 3.76-3.27 (m, 8H), 3.18-2.65 (m, 5H), 2.69-2.56 (m, 3H), 2.48-2.15 (m, 9H), 2.08-2.03 (m, 4H), 1.93 (s, 3H), 1.90 (s, 3H), 1.27-1.25 (m, 3H). MS m/z (ESI): 897.4 [M+H]+
Title compound E48 (white solid, 3.5 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.18 (s, 1H), 8.17 (s, 1H), 7.83 (d, J=7.6 Hz, 1H), 7.75 (d, J=7.0 Hz, 1H), 7.68 (dd, J=14.0, 8.2 Hz, 1H), 7.56 (t, J=7.7 Hz, 1H), 7.48-7.35 (m, 3H), 7.34 (s, 1H), 5.23 (dd, J=13.3, 5.2 Hz, 1H), 4.62 (dd, J=49.2, 17.6 Hz, 2H), 4.30-3.47 (m, 12H), 3.29 (s, 1H), 3.19 (dd, J=9.1, 4.3 Hz, 2H), 3.00-2.79 (m, 4H), 2.72 (q, J=7.5 Hz, 2H), 2.61 (qd, J=13.3, 4.7 Hz, 1H), 2.38 (d, J=10.7 Hz, 2H), 2.28-2.16 (m, 1H), 2.10 (dt, J=20.2, 10.1 Hz, 2H), 1.90 (d, J=13.6 Hz, 6H), 1.20 (t, J=7.4 Hz, 3H); MS m/z (ESI): 912.6 [M+H]+.
Title compound E49 (white solid, 2 mg, hydrochloride) was prepared with reference to the method for compound E4.
1H NMR (500 MHz, CD3OD) δ 8.24-8.20 (m, 2H), 7.78 (d, J=5.0 Hz, 1H), 7.75-7.68 (m, 2H), 7.61 (t, J=7.5 Hz, 1H), 7.55-7.52 (m, 2H), 7.45 (t, J=7.5 Hz, 1H), 7.35 (s, 1H), 5.23 (dd, J=10.0, 5.0 Hz, 1H), 4.57 (q, J=15.0 Hz, 2H), 4.03 (s, 3H), 3.90-3.85 (m, 4H), 3.61-3.59 (m, 2H), 3.41-3.21 (m, 5H), 2.98-2.61 (m, 5H), 2.38-2.17 (m, 11H), 1.93 (s, 3H), 1.90 (s, 3H), 1.05 (d, J=5.0 Hz, 2H), 0.96 (s, 2H). MS m/z (ESI): 906.5 [M+H]+.
Title compound E50 (white solid, 6.7 mg, hydrochloride) was prepared with reference to the synthesis method for compound E88.
1H NMR (500 MHz, CD3OD) δ 8.30-7.94 (m, 2H), 7.66 (d, J=7.5 Hz, 1H), 7.61 (dd, J=14.1, 7.6 Hz, 1H), 7.54 (d, J=7.5 Hz, 1H), 7.50-7.40 (m, 2H), 7.33 (t, J=7.1 Hz, 1H), 7.26 (s, 1H), 6.92 (s, 1H), 5.13-5.07 (m, 1H), 4.41 (dd, J=38.1, 17.7 Hz, 2H), 3.79 (s, 3H), 3.67-3.51 (m, 3H), 3.43-3.23 (m, 4H), 3.16-2.92 (m, 5H), 2.90-2.59 (m, 7H), 2.56-2.41 (m, 3H), 2.23-1.97 (m, 5H), 1.78 (d, J=13.6 Hz, 6H), 1.01 (s, J=7.0 Hz, 3H). MS m/z (ESI): 921.2 [M+H]+.
Title compound E51 (white solid, 4.22 mg, formate) was prepared with reference to the method for compound C-6.
1H NMR (400 MHz, DMSO-d6) δ 13.34 (s, 1H), 11.02 (d, J=3.6 Hz, 2H), 8.33 (s, 1H), 8.16-8.05 (m, 2H), 7.84 (s, 1H), 7.71 (d, J=7.6 Hz, 1H), 7.66-7.49 (m, 3H), 7.44 (s, 1H), 6.74 (s, 1H), 5.17 (dd, J=13.2, 4.8 Hz, 1H), 4.51-4.41 (m, 1H), 4.36-4.26 (m, 1H), 3.76 (s, 3H), 3.00-2.87 (m, 4H), 2.62 (m, 10H), 2.47-2.36 (m, 4H), 2.31-2.22 (m, 3H), 2.12-1.98 (m, 2H), 1.86 (d, J=13.6 Hz, 8H), 1.59-1.46 (m, 2H), 0.81 (t, J=7.3 Hz, 3H). MS m/z (ESI): 932.4 [M+H]+.
Title compound E52 (yellow solid, 46.7 mg, formate) was prepared with reference to the method for compound C-6.
1H NMR (400 MHz, CD3OD) δ 8.23 (m, 1H), 8.18 (s, 1H), 8.12 (s, 1H), 7.76 (d, J=7.6 Hz, 1H), 7.72-7.61 (m, 3H), 7.55-7.47 (m, 1H), 7.31 (t, J=7.6 Hz, 1H), 6.74 (d, J=3.3 Hz, 1H), 5.19 (dd, J=5.1, 13.4 Hz, 1H), 4.51 (d, J=9.5 Hz, 6H), 3.97 (s, 3H), 3.58 (d, J=10.1 Hz, 2H), 2.91-2.71 (m, 12H), 2.60-2.48 (m, 2H), 2.25-2.15 (m, 1H), 2.09 (d, J=10.6 Hz, 2H), 1.90-1.81 (m, 6H), 1.78 (dd, J=3.5, 11.9 Hz, 2H). MS m/z (ESI): 889.7 [M+H]+.
Title compound E53 (pale yellow solid, 90 mg, hydrochloride) was prepared with reference to the method of Example 21.
1H NMR (500 MHz, CD3OD) δ 8.48-7.90 (m, 2H), 7.70 (dd, J=13.5, 6.6 Hz, 1H), 7.57 (s, 1H), 7.48-7.32 (m, 3H), 7.28 (d, J=7.4 Hz, 1H), 7.21-6.95 (m, 2H), 5.16-5.05 (m, 2H), 4.46-4.18 (m, 6H), 3.90 (d, J=17.6 Hz, 3H), 3.58-3.37 (m, 3H), 3.17-3.01 (m, 1H), 2.98-2.78 (m, 5H), 2.69-2.57 (m, 3H), 2.53-2.43 (m, 1H), 2.29-2.14 (m, 3H), 2.07-1.64 (m, 9H), 1.08 (br s, 3H). MS m/z (ESI): 868.0 [M+H]+.
Title compound E54 (pale yellow solid, 5.2 mg, hydrochloride) was prepared with reference to the method for compound E4.
1H NMR (500 MHz, CD3OD) δ 8.17 (s, 2H), 7.83 (dd, J=8.4, 4.5 Hz, 1H), 7.74 (dd, J=13.6, 7.2 Hz, 1H), 7.59 (s, 1H), 7.47-7.34 (m, 3H), 7.09 (s, 1H), 5.21 (d, J=8.9 Hz, 1H), 4.70 (d, J=17.8 Hz, 1H), 4.59 (d, J=18.0 Hz, 1H), 4.05-3.87 (m, 11H), 3.79-3.65 (m, 4H), 3.48-3.42 (m, 2H), 3.25 (t, J=5.5 Hz, 3H), 2.98-2.91 (m, 1H), 2.82 (d, J=17.2 Hz, 1H), 2.71-2.59 (m, 3H), 2.50-2.40 (m, 2H), 2.34-2.19 (m, 3H), 1.92 (s, 3H), 1.89 (s, 3H), 1.14 (t, J=7.0 Hz, 3H). MS m/z (ESI): 910.9 [M+H]+.
Title compound E55 (pale yellow solid, 10.2 mg, hydrochloride) was prepared with reference to the method for compound C-6.
1H NMR (500 MHz, CD3OD) δ 8.33 (s, 1H), 8.10 (s, 1H), 7.82 (d, J=7.6 Hz, 1H), 7.75-7.66 (m, 2H), 7.56 (t, J=7.6 Hz, 2H), 7.44-7.36 (m, 1H), 7.35-7.27 (m, 1H), 7.10-7.02 (m, 1H), 5.23 (dd, J=13.1, 4.7 Hz, 1H), 4.67 (d, J=17.6 Hz, 1H), 4.57 (d, J=17.6 Hz, 1H), 4.10-3.84 (m, 10H), 3.75-3.63 (m, 3H), 3.48-3.34 (m, 3H), 3.24-3.08 (m, 4H), 3.00-2.90 (m, 1H), 2.83 (d, J=16.8 Hz, 1H), 2.70-2.56 (m, 1H), 2.48-2.38 (m, 2H), 2.30-2.14 (m, 3H), 1.91 (d, J=13.5 Hz, 6H), 1.17 (d, J=5.7 Hz, 6H). MS m/z (ESI): 906.9 [M+H]+.
Title compound E57 (2 mg, formate) was prepared with reference to the method for compound C-6.
1H NMR (400 MHz, CD3OD) δ ppm 8.26-8.16 (m, 1H), 8.10-7.99 (m, 1H), 7.82-7.72 (m, 1H), 7.68-7.59 (m, 3H), 7.55-7.49 (m, 2H), 7.31-7.22 (m, 1H), 6.82-6.69 (m, 1H), 5.19 (m, 1H), 4.46 (m, 2H), 4.28-4.28 (m, 1H), 3.84 (s, 2H), 3.09-3.07 (m, 2H), 3.02-2.98 (m, 3H), 2.84-2.82 (m, 10H), 2.50 (br d, J=7.88 Hz, 3H), 2.16-2.27 (m, 1H), 2.12-2.00 (m, 3H), 1.84 (d, J=13.6 Hz, 6H), 1.79-1.66 (m, 2H), 1.35-1.25 (m, 2H), 0.99 (t, J=7.2 Hz, 3H), 0.85-0.68 (m, 4H). MS m/z (ESI): 918.5 [M+H]+.
Title compound E58 (white solid, 12 mg, hydrochloride) was prepared with reference to the method for compound E88.
1H NMR (500 MHz, CD3OD) δ 8.40-8.06 (m, 1H), 7.81 (t, J=11.5 Hz, 1H), 7.72 (dd, J=14.5, 7.6 Hz, 2H), 7.63 (t, J=8.0 Hz, 1H), 7.60-7.50 (m, 2H), 7.43 (t, J=7.2 Hz, 1H), 7.33 (s, 1H), 6.95 (s, 1H), 5.21 (dd, J=13.3, 5.3 Hz, 1H), 4.81-4.72 (m, 1H), 4.68-4.52 (m, 1H), 3.92-3.61 (m, 8H), 3.56-3.46 (m, 1H), 3.34-3.20 (m, 7H), 3.02-2.91 (m, 3H), 2.87-2.78 (m, 1H), 2.67-2.53 (m, 3H), 2.39-2.31 (m, 2H), 2.27-2.20 (m, 1H), 2.11-2.01 (m, 2H), 1.92 (s, 3H), 1.89 (s, 3H), 1.14 (t, J=7.0 Hz, 3H). MS m/z (ESI): 906.6 [M+H]+.
Compound E59 (pale yellow solid, 2.1 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.26 (br s, 1H), 8.10 (br s, 1H), 7.69 (dd, J=14.1, 7.9 Hz, 1H), 7.59 (d, J=8.3 Hz, 1H), 7.57-7.48 (m, 1H), 7.41 (t, J=7.7 Hz, 1H), 7.32 (t, J=7.8 Hz, 2H), 6.96 (s, 1H), 5.11 (dd, J=13.4, 5.1 Hz, 1H), 4.59-4.47 (m, 2H), 4.26 (t, J=5.8 Hz, 2H), 3.97-3.60 (m, 12H), 3.47-3.41 (m, 2H), 3.10-2.97 (m, 2H), 2.95-2.83 (m, 1H), 2.80-2.75 (m, 1H), 2.62 (d, J=7.2 Hz, 2H), 2.54-2.45 (m, 1H), 2.37 (d, J=10.2 Hz, 2H), 2.20-2.06 (m, 5H), 2.02 (s, 2H), 1.92-1.84 (m, 8H), 1.11 (br s, 3H). MS m/z (ESI): 931.1 [M+H]+.
Title compound E60 (white solid, 5 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.73-8.64 (m, 1H), 8.60-8.45 (m, 1H), 8.23-8.02 (m, 5H), 7.98-7.91 (m, 2H), 7.80-7.70 (m, 1H), 5.23 (dd, J=10.0, 5.0 Hz, 1H), 5.03-4.95 (m, 2H), 4.44-4.36 (m, 4H), 4.16-3.78 (m, 5H), 3.75-3.48 (m, 6H), 3.39-2.91 (m, 5H), 2.83-2.46 (m, 10H), 2.34 (s, 3H), 2.32 (s, 3H), 1.49-1.30 (m, 3H). MS m/z (ESI): 891.5 [M+H]+.
Title compound E61 (yellow solid, 7.28 mg) was prepared with reference to the method for compound C-6.
1H NMR (400 MHz, CD3OD) δ 8.43-8.33 (m, 2H), 8.08 (s, 1H), 7.77 (d, J=7.6 Hz, 1H), 7.64 (d, J=7.3 Hz, 1H), 7.60-7.46 (m, 3H), 7.24-7.15 (m, 1H), 6.96-6.86 (m, 1H), 5.21 (dd, J=5.2, 13.2 Hz, 1H), 4.66-4.55 (m, 2H), 4.53-4.47 (m, 2H), 3.93 (s, 3H), 3.17-3.01 (m, 3H), 2.99-2.72 (m, 12H), 2.68 (t, J=5.8 Hz, 1H), 2.59-2.41 (m, 1H), 2.26-2.16 (m, 3H), 1.84 (d, J=13.4 Hz, 9H). MS m/z (ESI): 907.5 [M+H]+.
Title compound E62 (white solid, 6 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.24-8.20 (m, 2H), 7.78 (d, J=5.0 Hz, 1H), 7.75-7.68 (m, 2H), 7.61 (t, J=7.5 Hz, 1H), 7.55-7.52 (m, 2H), 7.45 (t, J=7.5 Hz, 1H), 7.35 (s, 1H), 5.23 (dd, J=10.0, 5.0 Hz, 1H), 4.57 (q, J=15.0 Hz, 2H), 4.03 (s, 3H), 3.90-3.85 (m, 4H), 3.61-3.59 (m, 2H), 3.41-3.21 (m, 5H), 2.98-2.61 (m, 5H), 2.38-2.17 (m, 11H), 1.93 (s, 3H), 1.90 (s, 3H), 1.05 (d, J=5.0 Hz, 2H), 0.96 (s, 2H). MS m/z (ESI): 903.3 [M+H]+.
Title compound E63 (yellow solid, 34.46 mg) was prepared with reference to the method for compound C-1.
1H NMR (400 MHz, CD3OD) δ=8.17-7.58 (m, 2H), 7.53-7.46 (m, 1H), 7.43-7.26 (m, 3H), 7.24 (d, J=8.0 Hz, 1H), 6.89 (s, 1H), 5.20-5.13 (m, 1H), 4.59-4.41 (m, 2H), 4.29-4.18 (m, 2H), 4.00-3.80 (m, 6H), 3.76-3.59 (m, 4H), 3.54-3.45 (m, 1H), 3.40-3.33 (m, 2H), 3.28-3.21 (m, 2H), 3.02-2.74 (m, 5H), 2.66-2.49 (m, 3H), 2.47-2.40 (m, 3H), 2.38-2.26 (m, 5H), 2.25-2.15 (m, 1H), 2.12-2.02 (m, 4H), 2.00 (s, 3H), 1.98-1.92 (m, 5H), 1.15-0.98 (m, 3H) MS m/z (ESI): 940.5[M+H]+.
Title compound E64 (3.5 mg, white solid, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.38 (s, 1H), 7.67 (dd, J=10.0, 5.0 Hz, 1H), 7.52-7.49 (m, 2H), 7.43 (t, J=7.5 Hz, 1H), 7.35-7.25 (m, 3H), 7.05 (d, J=5.0 Hz, 1H), 6.86 (s, 1H), 6.48 (s, 1H), 5.08 (dd, J=10.0, 5.0 Hz, 1H), 4.35 (q, J=15.0 Hz, 2H), 4.16 (s, 2H), 3.52-3.16 (m, 8H), 3.27-3.16 (m, 7H), 2.88-2.81 (m, 3H), 2.64-2.55 (m, 4H), 2.22-2.20 (m, 2H), 2.05-2.01 (m, 1H), 1.91-1.86 (m, 7H), 1.81 (s, 3H), 1.78 (s, 3H), 1.09 (t, J=5.0 Hz, 3H). MS m/z (ESI): 917.5 [M+H]+.
Title compound E65 (4.8 mg, white solid, 5.5 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.28-8.14 (m, 2H), 7.73 (dd, J=10.0, 5.0 Hz, 1H), 7.63-7.57 (m, 2H), 7.44 (t, J=7.50 Hz, 1H), 7.39-7.37 (m, 2H), 7.09 (d, J=10.0 Hz, 1H), 7.01 (s, 1H), 4.03 (s, 3H), 3.90 (s, 3H), 3.75-3.66 (m, 5H), 3.39-3.28 (m, 9H), 3.13-3.06 (m, 2H), 2.91-2.85 (m, 3H), 2.69-2.63 (m, 2H), 2.40-2.38 (m, 2H), 2.20-2.07 (m, 3H), 1.93 (s, 3H), 1.90 (s, 3H), 1.89-1.81 (m, 5H), 1.55-1.48 (m, 2H), 1.17-1.11 (m, 3H). MS m/z (ESI): 910.6 [M+H]+.
Title compound E66 (white solid, 64.76 mg) was prepared with reference to the method for compound C-1.
1H NMR (400 MHz, DMSO-d6) δ ppm 12.04 (s, 1H), 11.04 (s, 1H), 9.60 (s, 1H), 8.32 (s, 2H), 7.65 (dd, J=13.2, 7.6 Hz, 1H), 7.41-7.22 (m, 4H), 7.17 (m, 1H), 6.84 (s, 1H), 5.13 (dd, J=13.2, 5.2 Hz, 1H), 4.65-4.52 (m, 3H), 4.32 (m, 1H), 3.87 (s, 4H), 3.79 (s, 9H), 3.18 (m, 2H), 3.02-2.76 (m, 3H), 2.68-2.54 (m, 3H), 2.38 (m, 2H), 2.24 (m, 2H), 2.08-1.89 (m, 3H), 1.80 (d, J=13.6 Hz, 6H), 1.07 (t, J=7.2 Hz, 3H); MS m/z (ESI): 902.6 [M+H]+.
HOAc (6.7 mg, 112 μmol) was added to a solution of compound 67d (30 mg, 72.1 μmol) and compound 21c (30 mg, 56 μmol) in DCM (20 mL) at room temperature before TEA (22.5 mg, 224 μmol) was added. The reaction system was adjusted to a weakly alkaline pH, stirred for 1 h before sodium triacetoxyborohydride (47.5 mg, 224 μmol) was added, and then stirred for another 12 h for reaction. After the reaction was completed, the reaction solution was subjected to reverse-phase preparative chromatography (formic acid system) to give compound E67 (yellow solid, 6.5 mg, hydrochloride). 1H NMR (500 MHz, CD3OD) δ 8.13 (s, 2H), 7.73 (dd, J=13.4, 8.4 Hz, 1H), 7.54 (d, J=9.6 Hz, 2H), 7.44 (t, J=7.0 Hz, 1H), 7.35 (s, 1H), 7.28 (d, J=7.0 Hz, 1H), 7.00 (s, 1H), 5.14 (dd, J=13.4, 5.2 Hz, 1H), 4.81-4.73 (m, 1H), 4.47 (q, J=17.0 Hz, 2H), 4.00-3.57 (m, 14H), 3.38 (s, 1H), 3.21-2.99 (m, 4H), 2.93 (ddd, J=18.7, 13.5, 5.3 Hz, 1H), 2.84-2.76 (m, 1H), 2.67 (dd, J=16.9, 8.2 Hz, 4H), 2.50 (qd, J=13.3, 4.7 Hz, 1H), 2.39 (d, J=11.7 Hz, 2H), 2.23-2.12 (m, 3H), 1.92 (s, 3H), 1.89 (s, 3H), 1.15 (s, 3H). MS m/z (ESI): 928.5 [M+H]+.
Title compound E68 (white solid, 4 mg, hydrochloride) was prepared with reference to the synthesis method for reference compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.21-7.77 (m, 2H), 7.74 (s, 1H), 7.71-7.64 (m, 2H), 7.59 (s, 1H), 7.56-7.46 (m, 1H), 7.37 (t, J=7.3 Hz, 1H), 7.31-7.15 (m, 2H), 7.11 (dd, J=8.5, 2.1 Hz, 1H), 6.81 (s, 1H), 5.07-5.01 (m, 1H), 4.53-4.43 (m, 2H), 4.43-4.33 (m, 2H), 3.91-3.53 (m, 13H), 3.48-3.38 (m, 1H), 3.17 (d, J=11.1 Hz, 2H), 2.90-2.64 (m, 4H), 2.54-2.32 (m, 3H), 2.23 (d, J=10.6 Hz, 2H), 2.12-2.04 (m, 4H), 2.02-1.90 (m, 2H), 1.70 (d, J=13.5 Hz, 6H), 0.98 (t, J=7.0 Hz, 3H). MS m/z (ESI): 931.0 [M+H]+.
Title compound E69 (white solid, 3.5 mg, hydrochloride) was prepared with reference to the method for compound E67.
1H NMR (500 MHz, CD3OD) δ 8.00 (s, 1H), 7.81 (s, 2H), 7.57 (s, 1H), 7.52 (dd, J=12.5, 7.7 Hz, 2H), 7.44 (t, J=7.8 Hz, 1H), 7.38 (t, J=7.8 Hz, 1H), 7.31 (d, J=7.5 Hz, 1H), 7.21 (t, J=7.3 Hz, 1H), 7.00 (d, J=8.1 Hz, 1H), 6.71 (s, 1H), 5.06 (dd, J=13.3, 5.1 Hz, 1H), 4.60 (s, 2H), 4.32 (q, J=17.3 Hz, 2H), 3.86 (s, 3H), 3.77 (s, 3H), 3.52 (s, 2H), 3.13-2.99 (m, 5H), 2.90-2.67 (m, 7H), 2.39 (dd, J=15.0, 7.2 Hz, 4H), 2.34-1.89 (m, 7H), 1.86-1.71 (m, 2H), 1.68 (d, J=13.5 Hz, 6H), 0.93 (d, J=21.1 Hz, 3H); MS m/z (ESI): 956.6 [M+H]+.
Title compound E70 (white solid, 10 mg, hydrochloride) was prepared with reference to the method for compound E67.
1H NMR (500 MHz, DMSO-d6) δ 11.21 (s, 1H), 10.99 (s, 1H), 8.27-7.90 (m, 3H), 7.67 (s, 1H), 7.61 (dd, J=13.3, 8.3 Hz, 1H), 7.49 (t, J=7.8 Hz, 1H), 7.42-7.33 (m, 3H), 7.27 (t, J=7.3 Hz, 1H), 7.05 (d, J=8.1 Hz, 1H), 6.83 (s, 1H), 5.13 (dd, J=13.2, 5.1 Hz, 2H), 4.42 (d, J=17.4 Hz, 1H), 4.27 (d, J=17.3 Hz, 1H), 4.01-3.68 (m, 14H), 3.49-3.35 (m, 6H), 3.15 (d, J=9.7 Hz, 2H), 2.98-2.90 (m, 2H), 2.77 (t, J=10.8 Hz, 2H), 2.67-2.55 (m, 2H), 2.44 (dd, J=13.0, 4.3 Hz, 2H), 2.21 (s, 2H), 2.05-1.84 (m, 3H), 1.72 (d, J=13.6 Hz, 6H), 1.03 (s, 3H). MS m/z (ESI): 957.2 [M+H]+.
Title compound E71 (white solid, 4 mg, formate) was prepared with reference to the method for compound E4.
1H NMR (400 M, DMSO-d6) δ 11.19 (s, 1H), 11.03 (s, 1H), 8.41-8.29 (m, 1H), 8.28-8.03 (m, 1H), 7.88 (s, 1H), 7.02 (s, 1H), 7.62 (d, J=7.2 Hz, 1H), 7.51 (d, J=7.2 Hz, 1H), 7.47-7.25 (m, 2H), 7.06 (br, 1H), 7.04 (t, J=7.2 Hz, 1H), 6.45 (s, 1H), 5.16 (dd, J=13.2, 5.2 Hz, 1H), 4.45 (d, J=17.2 Hz, 1H), 4.35-4.28 (m, 3H), 3.78 (s, 3H), 3.02 (s, 1H), (m, 3H), 2.67-2.63 (m, 2H), 2.62 (t, J=6.0 Hz, 2H), 2.59-2.58 (m, 4H), 2.41-2.33 (m, 3H), 2.06-1.95 (m, 1H), 1.84-1.81 (m, 2H), 1.76 (d, J=13.6 Hz, 6H), 1.39-1.36 (m, 2H). MS m/z (ESI): 865.3 [M+H]+.
Title product E72 (white solid, 5.2 mg, hydrochloride) was prepared with reference to the method for compound C-6.
1H NMR (500 MHz, CD3OD) δ 8.22 (d, J=74.0 Hz, 2H), 7.81 (d, J=8.4 Hz, 1H), 7.73 (dd, J=13.7, 7.7 Hz, 1H), 7.59 (s, 1H), 7.45 (t, J=7.0 Hz, 1H), 7.37 (d, J=8.3 Hz, 2H), 7.22 (d, J=1.5 Hz, 1H), 7.15 (dd, J=8.4, 1.9 Hz, 1H), 7.09-7.03 (m, 3H), 5.16 (dd, J=13.4, 5.1 Hz, 1H), 4.68 (d, J=15.3 Hz, 1H), 4.59 (d, J=15.1 Hz, 1H), 4.49 (q, J=17.2 Hz, 2H), 4.00-3.94 (m, 1H), 3.92 (s, 3H), 3.75 (s, 1H), 3.58-3.50 (m, 1H), 3.41 (s, 2H), 3.26-3.14 (m, 3H), 2.99-2.88 (m, 1H), 2.83-2.78 (m, 1H), 2.69 (dd, J=14.5, 7.2 Hz, 2H), 2.56-2.40 (m, 3H), 2.31-2.17 (m, 3H), 1.91 (d, J=13.5 Hz, 6H), 1.36-1.29 (m, 3H), 1.16 (t, J=7.5 Hz, 3H). MS m/z (ESI): 904.1 [M+H]+.
Title compound E73 (white solid, 20 mg, hydrochloride) was prepared with reference to the method for compound E4.
1H NMR (500 MHz, CD3OD) δ 8.14 (t, J=70.0 Hz, 2H), 7.83 (d, J=7.6 Hz, 1H), 7.73 (ddd, J=14.0, 8.3, 1.0 Hz, 2H), 7.57 (t, J=7.7 Hz, 2H), 7.44 (t, J=7.1 Hz, 1H), 7.36 (s, 1H), 7.01 (s, 1H), 5.25 (dd, J=13.5, 5.1 Hz, 1H), 4.61 (dd, J=40.5, 17.6 Hz, 2H), 3.90 (s, 10H), 3.67 (t, J=6.8 Hz, 3H), 3.39 (d, J=10.2 Hz, 2H), 3.22-3.16 (m, 6H), 3.09 (s, 2H), 2.98 (ddd, J=9.3, 8.0, 5.5 Hz, 2H), 2.63 (ddd, J=19.1, 18.4, 11.2 Hz, 3H), 2.40 (d, J=11.2 Hz, 2H), 2.27-2.12 (m, 3H), 1.90 (d, J=13.6 Hz, 6H), 1.14 (s, 3H). MS m/z (ESI): 907.1 [M+H]+.
Title compound E74 (white solid, 15 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.27 (s, 1H), 8.16 (s, 1H), 7.85-7.75 (m, 2H), 7.66 (dd, J=15.3, 7.2 Hz, 2H), 7.51 (t, J=7.1 Hz, 1H), 7.37 (dd, J=19.8, 10.3 Hz, 2H), 5.20 (dd, J=13.3, 5.2 Hz, 1H), 4.64 (d, J=17.8 Hz, 1H), 4.54 (d, J=17.7 Hz, 1H), 4.04 (s, 3H), 3.80-3.52 (m, 6H), 3.42-3.36 (m, 2H), 3.33-3.24 (m, 6H), 3.00-2.91 (m, 1H), 2.84-2.79 (m, 1H), 2.76 (t, J=6.8 Hz, 2H), 2.69 (q, J=7.2 Hz, 2H), 2.64-2.53 (m, 1H), 2.38-2.14 (m, 6H), 2.04 (s, 1H), 1.91 (s, 3H), 1.88 (s, 3H), 1.10 (t, J=7.0 Hz, 3H). MS m/z (ESI): 909.4 [M+H]+.
Title compound E75 (brown solid, 4.85 mg) was prepared with reference to the method for compound C-6.
1H NMR (400 MHz, DMSO-d6) δ 11.19 (s, 1H), 10.98 (s, 1H), 8.45 (s, 1H), 8.15 (s, 1H), 8.07 (s, 1H), 7.58-7.47 (m, 3H), 7.29 (m, 1H), 7.18-7.03 (m, 3H), 6.94-6.82 (m, 3H), 6.73 (s, 1H), 5.12 (dd, J=4.8, 13.2 Hz, 1H), 4.46-4.42 (m, 1H), 4.30-4.26 (m, 1H), 3.76 (s, 2H), 3.74 (s, 3H), 2.97-2.85 (m, 1H), 2.84-2.76 (m, 5H), 2.75-2.70 (m, 2H), 2.67 (d, J=1.8 Hz, 1H), 2.60 (s, 2H), 2.21-2.10 (m, 2H), 2.05-1.89 (m, 4H), 1.77 (d, J=10.8 Hz, 9H), 0.92-0.81 (m, 2H), 0.49 (m, 2H). MS m/z (ESI): 915.7 [M+H]+.
Title compound E76 (white solid, 10 mg) was prepared with reference to the method for compound C-6.
1H NMR (400 MHz, CD3OD) δ ppm 8.29 (1H, d, J=4.4 Hz), 8.08 (1H, s), 7.72 (1H, s), 7.66 (1H, m), 7.56-7.61 (1H, m), 7.52 (2H, m), 7.26-7.33 (1H, m), 7.21 (1H, m), 7.11 (1H, m), 6.92 (1H, d, J=8.4 Hz), 6.88 (1H, s), 6.80 (1H, s), 5.16 (1H, dd, J=13.2, 4.8 Hz), 4.39-4.52 (2H, m), 3.82-3.92 (5H, m), 3.12 (2H, d, J=11.2 Hz), 3.00 (4H, d, J=8.8 Hz), 2.90 (1H, m), 2.74-2.84 (3H, m), 2.62-2.72 (1H, m), 2.47-2.60 (3H, m), 2.14-2.26 (1H, m), 2.10 (2H, d, J=11.2 Hz), 1.78-1.93 (8H, m), 1.03 (3H, t, J=7.2 Hz). MS m/z (ESI): 903.8 [M+H]+.
Title compound E77 (white solid, 6.6 mg) was prepared with reference to the method for compound C-6.
1H NMR (400 MHz, DMSO-d6) δ 11.16 (s, 1H), 11.01 (s, 1H), 9.46 (s, 1H), 8.55 (d, J=4.0 Hz, 1H), 8.22 (s, 1H), 7.71 (d, J=7.4 Hz, 1H), 7.68-7.46 (m, 5H), 7.32 (d, J=2.4 Hz, 1H), 7.19 (t, J=7.7 Hz, 1H), 6.28-5.21 (m, 1H), 5.16 (dd, J=5.1, 13.3 Hz, 1H), 4.52-4.38 (m, 1H), 4.36-4.27 (m, 1H), 2.99-2.89 (m, 1H), 2.89-2.88 (m, 1H), 2.89 (d, J=5.6 Hz, 1H), 2.79 (d, J=10.5 Hz, 2H), 2.71-2.56 (m, 6H), 2.71-2.55 (m, 1H), 2.71-2.55 (m, 1H), 2.70-2.55 (m, 1H), 2.71-2.54 (m, 1H), 2.42 (d, J=4.4 Hz, 2H), 2.37-2.30 (m, 1H), 2.23 (t, J=11.5 Hz, 2H), 2.11-1.98 (m, 2H), 1.84-1.75 (m, 1H), 1.78 (d, J=13.6 Hz, 8H), 1.55-1.40 (m, 2H), 1.09 (t, J=7.6 Hz, 3H), MS m/z (ESI): 896.5 [M+H]+.
Title compound E78 (white solid, 12 mg, formate) was prepared with reference to the method for compound C-6.
1H NMR (400 MHz, CD3OD) δ 8.25 (br s, 1H), 8.06 (s, 1H), 7.69 (s, 1H), 7.67-7.60 (m, 1H), 7.56-7.45 (m, 1H), 7.42-7.20 (m, 3H), 7.02 (br d, J=7.63 Hz, 1H), 6.76 (s, 1H), 5.16-5.08 (m, 1H), 4.54-4.32 (m, 2H), 4.15-3.91 (m, 2H), 3.90-3.77 (m, 3H), 3.15 (br d, J=2.25 Hz, 4H), 3.05 (br s, 2H), 2.94 (br d, J=3.38 Hz, 2H), 2.85-2.61 (m, 6H), 2.55-2.46 (m, 4H), 2.27-2.10 (m, 1H), 2.07-1.93 (m, 2H), 1.85 (s, 3H), 1.82 (s, 3H), 1.74-1.64 (m, 2H), 1.05-0.94 (m, 3H), 0.63 (br s, 4H). MS m/z (ESI): 910.8 [M+H]+.
Title compound E79 (yellow solid, 5.37 mg) was prepared with reference to the method for compound C-6.
1H NMR (400 MHz, CD3OD) δ 9.05-8.89 (m, 1H), 7.90-7.82 (m, 1H), 7.80-7.75 (m, 1H), 7.74-7.62 (m, 3H), 7.57-7.31 (m, 4H), 5.24-5.17 (m, 1H), 4.53 (m, 2H), 3.28-3.22 (m, 3H), 2.99-2.92 (m, 4H), 2.85-2.74 (m, 11H), 2.59-2.48 (m, 2H), 2.26-2.20 (m, 1H), 2.17-2.09 (m, 2H), 2.07-2.01 (m, 1H), 1.95-1.88 (m, 6H), 1.87-1.75 (m, 3H), 1.36-1.29 (m, 3H). MS m/z (ESI): 887.3 [M+H]+.
Title compound E80 (white solid, 5 mg, hydrochloride) was prepared with reference to the method for compound E67.
1H NMR (500 MHz, CD3OD) δ 8.16 (s, 2H), 8.07 (dd, J=8.0, 1.4 Hz, 1H), 7.82 (d, J=7.2 Hz, 1H), 7.73 (d, J=7.5 Hz, 1H), 7.56 (t, J=7.7 Hz, 2H), 7.47 (t, J=7.7 Hz, 1H), 7.33 (s, 1H), 6.94 (s, 1H), 5.23 (dd, J=13.3, 5.1 Hz, 1H), 4.60 (dd, J=45.4, 17.6 Hz, 2H), 3.83 (d, J=50.1 Hz, 11H), 3.49 (dd, J=22.3, 20.6 Hz, 4H), 3.30 (s, 1H), 3.14 (d, J=4.9 Hz, 2H), 2.96 (ddd, J=18.8, 13.5, 5.5 Hz, 3H), 2.83 (dd, J=10.1, 7.7 Hz, 1H), 2.68-2.52 (m, 3H), 2.35 (d, J=11.1 Hz, 2H), 2.26-2.17 (m, 1H), 2.09 (d, J=11.3 Hz, 2H), 1.14 (s, 3H). MS m/z (ESI): 895.6 [M+H]+.
Title compound E81 (white solid, 28 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.27 (dd, J=8.2, 4.6 Hz, 1H), 8.12 (s, 1H), 7.74 (s, 1H), 7.71-7.56 (m, 2H), 7.50 (t, J=7.8 Hz, 1H), 7.41 (d, J=7.4 Hz, 1H), 7.32 (t, J=6.7 Hz, 1H), 7.25 (d, J=8.0 Hz, 1H), 6.70 (s, 1H), 5.16 (dd, J=13.3, 5.1 Hz, 1H), 4.60 (s, 4H), 4.46 (q, J=17.2 Hz, 2H), 4.23 (t, J=5.9 Hz, 2H), 3.87 (s, 3H), 3.66 (s, 2H), 2.97-2.88 (m, 1H), 2.83-2.74 (m, 3H), 2.69-2.64 (m, 3H), 2.52 (ddd, J=26.4, 13.3, 4.6 Hz, 1H), 2.19 (dd, J=9.0, 3.8 Hz, 1H), 1.93-1.90 (m, 1H), 1.88 (s, 3H), 1.85 (s, 3H). MS m/z (ESI): 772.9 [M+H]+.
Title compound E82 (white solid, 7 mg, hydrochloride) was prepared with reference to the method of Example 88.
1H NMR (500 MHz, CD3OD) δ 8.20 (s, 1H), 8.17 (s, 1H), 7.74 (dd, J=14.0, 7.8 Hz, 1H), 7.60 (s, 1H), 7.53 (t, J=7.8 Hz, 1H), 7.49-7.40 (m, 3H), 7.26 (d, J=8.0 Hz, 1H), 7.15 (d, J=21.6 Hz, 1H), 5.19 (dd, J=13.3, 5.1 Hz, 1H), 5.16-5.02 (m, 2H), 4.56 (dd, J=35.9, 17.4 Hz, 2H), 3.93 (s, 3H), 3.83-3.35 (m, 8H), 3.32-3.14 (m, 5H), 3.00-2.90 (m, 1H), 2.85-2.79 (m, 1H), 2.72-2.64 (m, 2H), 2.62-2.52 (m, 1H), 2.45-2.19 (m, 5H), 1.92 (s, 3H), 1.89 (s, 3H), 1.14 (t, J=7.0 Hz, 3H). MS m/z (ESI): 898.3 [M+H]+.
Target product E83 (15 mg, hydrochloride) was prepared with reference to the method for compound E67.
1H NMR (500 MHz, CD3OD) δ 8.25 (s, 1H), 8.16 (s, 1H), 7.77 (dd, J=13.5, 7.6 Hz, 1H), 7.63 (s, 1H), 7.57 (s, 1H), 7.49 (dd, J=10.5, 4.8 Hz, 2H), 7.40 (d, J=7.6 Hz, 1H), 7.37 (d, J=4.2 Hz, 1H), 7.11 (dd, J=8.0, 3.0 Hz, 1H), 5.16 (dd, J=13.3, 5.1 Hz, 1H), 4.52-4.39 (m, 2H), 3.99 (d, J=5.3 Hz, 3H), 3.91-3.55 (m, 7H), 3.52-3.40 (m, 2H), 2.90-2.69 (m, 6H), 2.69-2.17 (m, 11H), 1.92 (d, J=1.8 Hz, 3H), 1.89 (d, J=1.8 Hz, 3H), 1.10 (t, J=7.0 Hz, 3H). MS m/z (ESI): 882.2 [M+H]+.
Title compound E84 (white solid, 4 mg) was prepared with reference to the method for compound C-6.
1H NMR (400 MHz, CD3OD) δ ppm 8.26-8.24 (m, 1H) 8.06 (s, 1H) 7.77 (d, J=7.2 Hz, 1H), 7.72-7.59 (m, 3H), 7.54-7.51 (m, 2H), 7.27 (t, J=7.6 Hz, 1H), 6.77 (s, 1H), 5.16 (dd, J=13.6, 5.6 Hz, 1H), 4.56 (m, 2H), 3.84 (s, 3H), 3.06 (d, J=10.8 Hz, 2H), 2.93-2.85 (5H, m), 2.83-2.56 (m, 8H), 2.51 (m, 2H), 2.37 (m, 1H), 2.27-2.15 (m, 1H), 2.06-1.93 (m, 2H), 1.86 (s, 3H), 1.83 (s, 3H), 1.78-1.60 (m, 2H), 1.12-1.06 (m, 2H), 1.05-0.96 (m, 5H). MS m/z (ESI): 904.8 [M+H]+.
Title compound E85 (white solid, 2 mg) was prepared with reference to the method for compound C-6.
1H NMR (400 MHz, CD3OD) δ ppm 8.29-8.26 (m, 1H) 8.09 (s, 1H) 7.76-7.64 (m, 4H) 7.57-7.51 (m, 2H) 7.35-7.29 (m, 1H) 6.79 (s, 1H), 6.59 (d, J=12.0 Hz, 1H), 5.98 (d, J=12.0 Hz, 1H) 5.21 (dd, J=13.2, 5.2 Hz, 1H) 4.41-4.44 (m, 2H) 3.84 (s, 3H) 3.05 (m, 2H) 2.90 (m, 1H) 2.80 (m, 2H) 2.65-2.73 (4H, m) 2.56-2.46 (m, 4H) 2.42 (brs, 3H) 2.30-2.12 (m, 3H) 2.05-2.02 (m, 1H) 1.92-1.80 (m, 8H) 1.67-1.58 (m, 2H) 1.37-1.27 (m, 3H) 1.03 (t, J=7.2 Hz, 3H). MS m/z (ESI): 906.8 [M+H]+.
Title compound E86 (white solid, 6.7 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.23 (d, J=31.1 Hz, 2H), 7.77 (d, J=35.3 Hz, 2H), 7.52 (dd, J=16.4, 8.6 Hz, 3H), 7.43 (d, J=7.2 Hz, 1H), 7.27 (d, J=7.8 Hz, 1H), 7.06 (s, 1H), 5.19 (s, 1H), 4.57 (d, J=16.7 Hz, 2H), 4.26 (s, 2H), 3.90 (d, J=29.7 Hz, 8H), 2.88 (dd, J=54.5, 14.0 Hz, 4H), 2.59 (s, 3H), 2.40 (s, 2H), 2.22 (s, 2H), 2.09 (s, 2H), 1.98 (s, 4H), 1.90 (d, J=13.3 Hz, 6H), 1.38 (d, J=6.5 Hz, 3H). MS m/z (ESI): 856.0 [M+H]+.
Title compound E87 (white solid, 5 mg, hydrochloride) was prepared with reference to the method for compound E67.
1H NMR (500 MHz, CD3OD) δ 8.15 (s, 2H), 7.77-7.65 (m, 1H), 7.54 (t, J=7.9 Hz, 2H), 7.44 (dd, J=12.9, 7.3 Hz, 2H), 7.34 (s, 1H), 7.27 (d, J=8.1 Hz, 1H), 6.93 (s, 1H), 5.16 (dd, J=13.3, 5.2 Hz, 1H), 4.48 (dd, J=42.6, 17.4 Hz, 2H), 4.23 (t, J=5.6 Hz, 2H), 4.05 (d, J=16.7 Hz, 2H), 3.87 (s, 3H), 3.80 (d, J=5.0 Hz, 2H), 3.75 (s, 2H), 3.59 (dd, J=14.2, 9.1 Hz, 3H), 3.32-3.21 (m, 2H), 3.04-2.80 (m, 4H), 2.65-2.48 (m, 3H), 2.35 (d, J=10.9 Hz, 2H), 2.28-2.19 (m, 1H), 2.05 (dt, J=20.3, 10.0 Hz, 2H), 1.91 (s, 3H), 1.88 (s, 6H), 1.10 (s, 3H). MS m/z (ESI): 926.6 [M+H]+.
Compound 88d (12 mg, 0.03 mmol), compound 4c (18 mg, 0.03 mmol), HATU (22.8 mg, 0.06), DIPEA (11 mg, 0.09 mmol), and DMF (2 mL) were added together to a reaction flask, The system was stirred at room temperature for 1 h. After the reaction was completed, the reaction solution was filtered and subjected to pre-HPLC to give target product E88 (white solid, 20 mg, hydrochloride). 1H NMR (500 MHz, CD3OD) δ 8.21 (s, 2H), 7.75 (dd, J=13.7, 7.6 Hz, 1H), 7.61 (t, J=7.4 Hz, 1H), 7.55-7.44 (m, 3H), 7.40 (t, J=12.8 Hz, 1H), 7.34-7.21 (m, 2H), 5.18 (dd, J=13.2, 5.0 Hz, 1H), 4.49 (dd, J=37.5, 17.4 Hz, 2H), 4.25 (t, J=5.9 Hz, 2H), 3.99-3.83 (m, 4H), 3.80-3.60 (m, 4H), 3.63-3.37 (m, 5H), 3.19 (s, 3H), 2.99-2.91 (m, 1H), 2.82 (d, J=15.7 Hz, 1H), 2.70 (dd, J=14.6, 7.2 Hz, 4H), 2.61-2.52 (m, 1H), 2.48-2.34 (m, 4H), 2.26-2.14 (m, 3H), 1.92 (s, 3H), 1.89 (s, 3H), 1.12 (t, J=7.0 Hz, 3H). MS m/z (ESI): 927.2 [M+H]+.
Compound 89c (25 mg, 0.03 mmol), 3-bromopiperidine-2,6-dione (6 mg, 0.03 mmol), and EtOH (3 mL) were added at room temperature to a microwave tube. The system was purged with nitrogen, heated to 140° C. by microwave, and stirred for 1 h. After the reaction was completed, the solvent was removed at reduced pressure, and the residue was subjected to prep-HPLC to give target product E89 (pale yellow solid, 12 mg, hydrochloride). 1H NMR (500 MHz, CD3OD) δ 8.28 (s, 1H), 8.15 (s, 1H), 7.78 (ddd, J=13.8, 7.7, 1.2 Hz, 1H), 7.67 (dd, J=17.8, 10.1 Hz, 2H), 7.53-7.42 (m, 4H), 7.21-7.15 (m, 2H), 4.76-4.72 (m, 1H), 4.15 (t, J=5.9 Hz, 2H), 4.05 (s, 3H), 3.80-3.65 (m, 3H), 3.58 (d, J=12.9 Hz, 2H), 3.33-3.20 (m, 6H), 2.78-2.67 (m, 4H), 2.40-2.38 (m, 2H), 2.13-2.00 (m, 6H), 1.98-1.87 (m, 11H), 1.10 (t, J=7.2 Hz, 3H). MS m/z (ESI): 858.2 [M+H]+.
Title compound E90 (white solid, 20 mg) was prepared with reference to the synthesis method for compound E88.
1H NMR (500 MHz, CD3OD) δ 8.30 (s, 1H), 8.11 (s, 1H), 7.79 (dd, J=13.1, 7.2 Hz, 1H), 7.74 (s, 1H), 7.66 (t, J=7.8 Hz, 1H), 7.52 (t, J=7.8 Hz, 2H), 7.41 (d, J=7.3 Hz, 1H), 7.37 (s, 1H), 7.26 (d, J=8.1 Hz, 1H), 5.18 (dd, J=13.3, 5.1 Hz, 1H), 4.53 (d, J=17.4 Hz, 1H), 4.47-4.42 (m, 1H), 4.28-4.22 (m, 1H), 4.22-4.15 (m, 1H), 4.04 (s, 3H), 3.88-3.48 (m, 8H), 3.00-2.90 (m, 1H), 2.85-2.72 (m, 2H), 2.66 (dd, J=14.3, 6.9 Hz, 2H), 2.61-2.51 (m, 2H), 2.27-2.02 (m, 7H), 1.90 (d, J=13.5 Hz, 6H), 1.78-1.44 (m, 4H), 1.08 (t, J=7.1 Hz, 3H). MS m/z (ESI): 912.2 [M+H]+.
Title compound E91 (gray solid, 5 mg) was prepared with reference to the method for compound E67.
1H NMR (500 MHz, CD3OD) δ 8.49 (dd, J=10.0, 5.0 Hz, 1H), 8.23 (s, 1H), 8.03 (s, 1H), 7.93 (d, J=10.0 Hz, 1H), 7.81-7.67 (m, 5H), 7.46-7.42 (m, 1H), 7.01 (s, 1H), 5.37 (dd, J=10.0, 5.0 Hz, 1H), 4.75-4.67 (m, 5H), 4.63 (q, J=15.0 Hz, 2H), 4.01 (s, 3H), 3.42-3.39 (m, 2H), 3.14-3.09 (m, 4H), 2.99-2.89 (m, 10H), 2.73-2.64 (m, 1H), 2.39-2.37 (m, 1H), 2.28-2.25 (m, 2H), 2.03 (s, 3H), 2.00 (s, 3H), 1.95-1.92 (m, 2H). MS m/z (ESI): 894.6 [M+H]+.
Compound E92 (pale yellow solid, 50 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, DMSO-d6) δ 11.55 (s, 1H), 10.98 (s, 1H), 8.89-8.61 (m, 1H), 8.39 (s, 1H), 8.19 (s, 1H), 7.60 (dd, J=14.1, 8.0 Hz, 1H), 7.54 (d, J=9.9 Hz, 1H), 7.45 (d, J=7.3 Hz, 1H), 7.41 (s, 1H), 7.35 (s, 1H), 7.21-7.15 (m, 1H), 6.81 (s, 1H), 5.09 (dd, J=13.3, 5.0 Hz, 1H), 4.40 (d, J=17.4 Hz, 1H), 4.28 (d, J=17.2 Hz, 1H), 4.20 (s, 2H), 3.78 (s, 8H), 3.28-3.22 (m, 4H), 3.14 (d, J=10.1 Hz, 4H), 2.94-2.87 (m, 1H), 2.79 (d, J=12.8 Hz, 2H), 2.61 (s, 1H), 2.39 (dd, J=12.8, 4.5 Hz, 1H), 2.25-2.15 (m, 2H), 2.02-1.96 (m, 1H), 1.95-1.82 (m, 8H), 1.80 (s, 3H), 1.77 (s, 3H), 1.07 (t, J=7.6 Hz, 3H). MS m/z (ESI): 931.2 [M+H]+.
Title compound E93 (11 mg, formate) was prepared with reference to the method for compound C-6.
1H NMR (400 MHz, CD3OD) δ 8.32 (s, 1H), 8.12 (s, 1H), 7.84-7.76 (m, 1H), 7.75-7.65 (m, 2H), 7.54-7.52 (m, 2H), 7.45-7.36 (m, 1H), 6.87 (d, J=7.6 Hz, 2H), 5.25-5.17 (m, 1H), 4.68-4.50 (m, 3H), 4.10-3.75 (m, 8H), 3.74-3.46 (m, 9H), 3.19-3.13 (m, 2H), 3.03-2.53 (m, 8H), 2.29-2.17 (m, 3H), 2.04-1.94 (m, 2H), 1.90 (s, 3H), 1.87 (s, 3H), 1.15 (t, J=7.2 Hz, 3H). MS m/z (ESI): 892.4 [M+H]+.
Title compound E94 (5 mg, hydrochloride) was prepared with reference to the method for compound E67.
1H NMR (400 MHz, CD3OD) δ 8.31-8.22 (m, 1H), 8.19-8.14 (m, 1H), 7.90-7.80 (m, 1H), 7.80-7.73 (m, 1H), 7.72-7.60 (m, 3H), 7.58-7.45 (m, 2H), 7.37-7.30 (m, 1H), 5.20 (dd, J=13.3, 5.1 Hz, 1H), 5.24-5.15 (m, 1H), 4.60-4.46 (m, 1H), 4.60-4.46 (m, 1H), 3.92-3.34 (m, 6H), 3.23-2.74 (m, 11H), 2.73-2.61 (m, 2H), 2.61-2.47 (m, 1H), 2.28-2.16 (m, 3H), 2.06-1.90 (m, 2H), 1.86 (d, J=13.5 Hz, 6H), 1.41-1.26 (m, 1H), 1.17 (t, J=7.5 Hz, 2H), 1.22-1.11 (m, 1H). MS m/z (ESI): 887.3 [M+H]+.
Title compound E95 (white solid, 5 mg, hydrochloride) was prepared with reference to the method for compound E67.
1H NMR (400 MHz, CD3OD) δ 8.41-8.18 (m, 1H), 8.09 (t, J=11.9 Hz, 1H), 7.75-7.66 (m, 1H), 7.59-7.51 (m, 2H), 7.51-7.45 (m, 1H), 7.44-7.37 (m, 1H), 7.31 (d, J=7.6 Hz, 2H), 6.95 (s, 1H), 5.18 (dd, J=5.1, 13.2 Hz, 1H), 4.74-4.49 (m, 4H), 4.03-3.78 (m, 13H), 3.67-3.52 (m, 2H), 3.06-2.86 (m, 3H), 2.85-2.74 (m, 1H), 2.69-2.49 (m, 3H), 2.36 (d, J=10.5 Hz, 2H), 2.27-2.01 (m, 4H), 1.91-1.85 (m, 6H), 1.20-1.07 (m, 3H). MS m/z (ESI): 884.7 [M+H]+.
Title compound E97 (white solid, 3 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.22-8.20 (m, 2H), 7.78-7.74 (m, 1H), 7.69-7.62 (m, 3H), 7.50-7.47 (m, 2H), 7.22-7.20 (m, 2H), 4.08-3.86 (m, 16H), 3.61-3.47 (m, 6H), 2.91-2.89 (m, 2H), 2.74-2.69 (m, 4H), 2.54-2.51 (m, 4H), 2.44-2.21 (m, 2H), 1.93 (s, 3H), 1.90 (s, 3H), 1.16-1.13 (m, 3H). MS m/z (ESI): 906.7 [M+H]+.
Title compound E98 (white solid, 30 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.27 (d, J=70.1 Hz, 1H), 8.12 (d, J=41.9 Hz, 1H), 7.72 (dd, J=13.7, 8.1 Hz, 1H), 7.53 (t, J=7.8 Hz, 2H), 7.44 (d, J=7.4 Hz, 2H), 7.27 (d, J=8.1 Hz, 1H), 7.14 (s, 1H), 7.06 (s, 1H), 5.20 (dd, J=13.3, 5.1 Hz, 1H), 4.60-4.38 (m, 2H), 4.26 (t, J=5.7 Hz, 2H), 3.95-3.82 (m, 5H), 3.70 (dd, J=62.8, 30.1 Hz, 6H), 3.50-3.37 (m, 2H), 3.33-3.16 (m, 5H), 3.02-2.90 (m, 1H), 2.83 (d, J=15.6 Hz, 1H), 2.66-2.49 (m, 3H), 2.31 (dd, J=23.6, 11.9 Hz, 4H), 2.26-2.13 (m, 3H), 2.12-2.02 (m, 2H), 2.01-1.95 (m, 2H), 1.92 (d, J=13.6 Hz, 6H). MS m/z (ESI): 913.5 [M+H]+.
Title compound E99 (white solid, 30 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.33 (s, 1H), 8.10 (s, 1H), 7.72 (s, 1H), 7.60 (ddd, J=14.1, 7.7, 1.4 Hz, 1H), 7.52-7.35 (m, 3H), 7.24 (dd, J=9.5, 4.5 Hz, 2H), 5.17 (dd, J=13.4, 5.2 Hz, 1H), 4.60 (s, 3H), 4.45 (q, J=17.2 Hz, 2H), 4.20 (t, J=6.1 Hz, 2H), 3.95 (d, J=6.4 Hz, 3H), 3.58 (s, 3H), 3.39 (t, J=15.7 Hz, 2H), 2.99-2.78 (m, 5H), 2.70 (s, 5H), 2.53-2.45 (m, 3H), 2.43 (d, J=11.6 Hz, 1H), 2.20 (ddt, J=12.8, 5.3, 2.7 Hz, 1H), 1.94 (d, J=14.2 Hz, 2H), 1.88 (s, 4H), 1.86 (s, 3H), 1.76 (dt, J=14.3, 7.2 Hz, 2H), 1.64 (dt, J=12.1, 8.6 Hz, 2H); MS m/z (ESI): 915.6 [M+H]+.
Title compound E100 (white solid, 5 mg, hydrochloride) was prepared with reference to the method for compound E88.
1H NMR (500 MHz, CD3OD) δ 8.24 (d, J=21.8 Hz, 1H), 8.18 (s, 1H), 7.80 (dd, J=13.4, 7.7 Hz, 1H), 7.71 (t, J=7.5 Hz, 1H), 7.58-7.45 (m, 4H), 7.29-7.20 (m, 1H), 7.05-6.95 (m, 1H), 5.24-5.10 (m, 3H), 5.03 (t, J=13.4 Hz, 2H), 4.61-4.13 (m, 3H), 3.93 (s, 3H), 3.82 (ddd, J=15.8, 9.8, 6.8 Hz, 1H), 3.74 (d, J=6.7 Hz, 1H), 3.47-3.34 (m, 2H), 3.30-3.17 (m, 2H), 3.12 (s, 1H), 2.98-2.88 (m, 1H), 2.87-2.72 (m, 3H), 2.55 (d, J=11.7 Hz, 1H), 2.25 (dd, J=38.0, 30.7 Hz, 3H), 1.89 (d, J=13.5 Hz, 6H), 1.82-1.54 (m, 1H). MS m/z (ESI): 841.6 [M+H]+.
Compound E101 (pale yellow solid, 18 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, DMSO-d6) δ 11.80 (br s, 1H), 11.47 (br s, 1H), 10.99 (s, 1H), 8.36 (s, 1H), 8.24 (s, 1H), 7.62 (dd, J=13.7, 8.2 Hz, 1H), 7.50 (t, J=7.8 Hz, 1H), 7.42-7.32 (m, 3H), 7.28-7.19 (m, 2H), 6.93 (br s, 1H), 5.12 (dd, J=13.3, 5.1 Hz, 1H), 4.44 (d, J=17.3 Hz, 1H), 4.26 (d, J=17.4 Hz, 1H), 4.19-4.14 (m, 1H), 3.95 (d, J=15.8 Hz, 1H), 3.86-3.56 (m, 12H), 3.24-3.07 (m, 5H), 2.95-2.89 (m, 1H), 2.62-2.55 (m, 3H), 2.44-2.40 (m, 1H), 2.04-1.88 (m, 4H), 1.85-1.75 (m, 8H), 1.77-1.60 (m, 2H), 1.08 (t, J=7.4 Hz, 3H). MS m/z (ESI): 927.6 [M+H]+.
Title compound E102 (pale yellow solid, 45 mg, hydrochloride) was prepared with reference to the method for compound E88.
1H NMR (500 MHz, CD3OD) δ 8.16 (br s, 2H), 7.76-7.68 (m, 2H), 7.66 (t, J=7.7 Hz, 1H), 7.58 (d, J=7.7 Hz, 2H), 7.44 (t, J=7.0 Hz, 2H), 7.14 (s, 1H), 5.21 (dd, J=13.3, 5.2 Hz, 1H), 4.74-4.62 (m, 3H), 4.23 (br s, 1H), 3.91 (s, 3H), 3.75-3.44 (m, 9H), 3.37-3.34 (m, 2H), 3.25-3.09 (m, 3H), 2.97-2.90 (m, 1H), 2.83-2.78 (m, 1H), 2.66 (dd, J=14.6, 7.3 Hz, 3H), 2.60-2.51 (m, 1H), 2.39 (d, J=11.0 Hz, 2H), 2.34-2.20 (m, 3H), 2.12-2.07 (m, 2H), 1.89 (s, 3H), 1.86 (s, 3H), 1.10 (t, J=7.5 Hz, 3H). MS m/z (ESI): 926.7 [M+H]+.
Title compound E103 (white solid, 14.48 mg, formate) was prepared with reference to the method for compound C-1.
1H NMR (400 MHz, DMSO-d6) δ 11.22 (s, 1H), 10.97 (s, 1H), 8.51-8.36 (m, 1H), 8.25 (s, 1H), 8.18-8.10 (m, 1H), 7.94 (s, 1H), 7.60-7.51 (m, 1H), 7.51-7.42 (m, 2H), 7.31 (d, J=7.4 Hz, 1H), 7.25 (d, J=8.1 Hz, 1H), 7.14 (t, J=7.0 Hz, 1H), 6.74 (s, 1H), 5.11 (dd, J=5.1, 13.3 Hz, 1H), 4.43-4.32 (m, 1H), 4.28-4.19 (m, 1H), 4.15 (t, J=6.3 Hz, 2H), 3.88 (s, 3H), 3.55 (d, J=11.1 Hz, 2H), 2.97-2.88 (m, 1H), 2.83 (t, J=11.6 Hz, 2H), 2.63-2.53 (m, 6H), 2.46-2.36 (m, 7H), 2.03-1.97 (m, 1H), 1.94-1.88 (m, 2H), 1.77 (d, J=13.6 Hz, 8H), 1.65-1.55 (m, 4H). MS m/z (ESI): 909.4 [M+H]+.
Title compound E100 (white solid, 5 mg, hydrochloride) was prepared with reference to the method for compound E88.
1H NMR (400 MHz, DMSO-d6) δ 11.75-11.34 (m, 1H), 10.98 (s, 1H), 8.46-8.33 (m, 1H), 8.19 (s, 1H), 7.60 (dd, J=7.5, 14.3 Hz, 1H), 7.54-7.22 (m, 4H), 7.22-7.14 (m, 2H), 6.98-6.82 (m, 1H), 5.12 (dd, J=5.3, 12.9 Hz, 1H), 5.06-4.97 (m, 2H), 4.44-4.36 (m, 1H), 4.32-4.23 (m, 1H), 3.86-3.75 (m, 3H), 3.46 (s, 6H), 2.99-2.83 (m, 4H), 2.64-2.56 (m, 3H), 2.04-1.98 (m, 1H), 1.78 (d, J=13.6 Hz, 7H), 1.73-1.63 (m, 3H), 1.62-1.48 (m, 4H), 1.07 (t, J=7.4 Hz, 3H); MS m/z (ESI): 883.6[M+H]+.
Title compound E105 (white solid, 30 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 7.79 (dd, J=11.8, 7.7 Hz, 1H), 7.60 (s, 1H), 7.57-7.50 (m, 2H), 7.42-7.30 (m, 2H), 7.29 (d, J=7.2 Hz, 1H), 7.12 (d, J=7.9 Hz, 1H), 6.62 (s, 1H), 5.21-5.12 (m, 1H), 5.06 (dd, J=13.3, 5.2 Hz, 1H), 4.34 (q, J=17.3 Hz, 2H), 4.09 (t, J=6.1 Hz, 2H), 3.74 (s, 3H), 2.92 (d, J=10.9 Hz, 2H), 2.72 (dddd, J=57.5, 55.3, 17.5, 9.7 Hz, 10H), 2.41 (dt, J=13.3, 6.6 Hz, 4H), 2.26 (d, J=44.4 Hz, 3H), 2.11-2.01 (m, 1H), 1.89 (d, J=11.3 Hz, 2H), 1.76 (dd, J=14.0, 6.6 Hz, 2H), 1.68 (t, J=13.2 Hz, 9H), 1.61-1.51 (m, 2H), 1.29 (d, J=6.3 Hz, 6H), 0.81-0.71 (m, 3H). MS m/z (ESI): 964.9 [M+H]+.
Title compound E106 (white solid, 3 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 78.00 (s, 1H), 7.58 (ddd, J=15.7, 11.3, 7.6 Hz, 2H), 7.42 (d, J=34.1 Hz, 1H), 7.28 (ddd, J=29.0, 18.1, 10.6 Hz, 3H), 7.15 (d, J=8.6 Hz, 1H), 7.08 (d, J=7.1 Hz, 1H), 6.87 (s, 1H), 4.99 (dd, J=12.6, 5.4 Hz, 2H), 3.84-3.65 (m, 10H), 3.45 (dd, J=27.0, 21.5 Hz, 4H), 2.92 (s, 2H), 2.82-2.72 (m, 1H), 2.69-2.58 (m, 2H), 2.53 (d, J=6.5 Hz, 2H), 2.27 (d, J=11.2 Hz, 2H), 2.02 (d, J=4.8 Hz, 3H), 1.79 (d, J=13.5 Hz, 6H), 1.32-1.17 (m, 3H), 1.03 (s, 3H). MS m/z (ESI): 897.8 [M+H]+.
Title compound E107 (white solid, 8 mg, hydrochloride) was prepared with reference to the method for compound E67.
1H NMR (500 MHz, CD3OD) δ 8.13 (s, 1H), 7.78-7.67 (m, 3H), 7.64-7.47 (m, 3H), 7.41 (dd, J=37.4, 30.3 Hz, 2H), 6.94 (s, 1H), 5.22 (dd, J=13.4, 5.1 Hz, 1H), 4.58 (dd, J=56.5, 17.2 Hz, 2H), 4.05 (s, 2H), 3.88 (s, 4H), 3.83-3.50 (m, 6H), 3.00-2.90 (m, 3H), 2.86-2.78 (m, 3H), 2.61 (ddd, J=26.6, 13.1, 4.4 Hz, 3H), 2.24 (ddd, J=20.8, 16.7, 9.6 Hz, 3H), 2.06 (dd, J=11.6, 6.7 Hz, 5H), 1.91 (d, J=13.6 Hz, 6H), 1.57-1.34 (m, 1H), 1.19 (d, J=41.1 Hz, 3H); MS m/z (ESI): 897.0 [M+H]+.
Title compound E108 (white solid, 10 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.11 (s, 2H), 7.64 (dd, J=13.8, 7.7 Hz, 1H), 7.49 (dd, J=18.1, 10.5 Hz, 1H), 7.43 (t, J=7.8 Hz, 2H), 7.37 (t, J=5.5 Hz, 2H), 7.20 (d, J=8.1 Hz, 1H), 7.14 (s, 1H), 5.07 (dd, J=13.3, 5.1 Hz, 1H), 4.66-4.35 (m, 4H), 4.23-3.54 (m, 12H), 3.50 (d, J=4.0 Hz, 4H), 2.87-2.66 (m, 2H), 2.59 (q, J=7.2 Hz, 2H), 2.50-2.32 (m, 5H), 2.10 (dd, J=9.0, 3.7 Hz, 1H), 1.78 (d, J=13.6 Hz, 6H), 1.69 (s, 6H), 1.00 (s, 3H). MS m/z (ESI): 912.9 [M+H]+.
Title compound E109 (white solid, 5 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.25-8.19 (m, 2H), 7.77-7.73 (m, 2H), 7.64-7.56 (m, 3H), 7.47 (t, J=5.0 Hz, 2H), 7.19-7.16 (m, 1H), 5.22 (dd, J=10.0, 5.0 Hz, 1H), 4.65 (q, J=15.0 Hz, 2H), 3.96 (s, 3H), 3.94-3.50 (m, 20H), 3.37-3.35 (m, 1H), 3.11-2.81 (m, 3H), 2.71-2.59 (m, 1H), 2.50-2.24 (m, 6H), 1.92 (s, 3H), 1.88 (s, 3H), 1.16-1.10 (m, 3H). MS m/z (ESI): 912.5 [M+H]+.
Title product E110 (pale yellow solid, 15 mg, hydrochloride) was prepared with reference to the synthesis method for compound E67.
1H NMR (500 MHz, CD3OD) δ 8.08 (s, 2H), 7.63 (dd, J=13.9, 7.7 Hz, 1H), 7.53-7.45 (m, 1H), 7.46-7.40 (m, 1H), 7.40-7.30 (m, 2H), 7.29 (d, J=7.5 Hz, 1H), 7.21 (d, J=8.1 Hz, 1H), 7.05 (d, J=21.5 Hz, 1H), 5.06 (dd, J=13.4, 5.1 Hz, 1H), 4.45-4.29 (m, 2H), 4.27-4.19 (m, 1H), 3.83 (d, J=9.2 Hz, 3H), 3.71-3.62 (m, 2H), 3.58-3.52 (m, 2H), 3.43-3.24 (m, 4H), 3.19-3.05 (m, 2H), 3.02-2.88 (m, 1H), 2.87-2.78 (m, 1H), 2.76-2.68 (m, 1H), 2.62-2.41 (m, 3H), 2.30-2.18 (m, 1H), 2.16-1.88 (m, 11H), 1.80 (s, 3H), 1.77 (s, 3H), 0.99 (t, J=7.2 Hz, 3H). MS m/z (ESI): 914.1 [M+H]+.
Compound 111b (20 mg, 0.03 mmol), compound 3 (7 mg, 0.03 mmol), NaI (6 mg, 0.03), KHCO3 (6 mg, 0.06 mmol), and DMF (2 mL) were added in a reaction flask. The system was heated to 90° C. and stirred for 16 h. After the reaction was completed, the reaction solution was filtered and subjected to pre-HPLC to give title product E111 (white solid, 1.3 mg). 1H NMR (500 MHz, CDCl3) δ 8.39 (dd, J=8.0, 4.2 Hz, 1H), 8.03 (d, J=76.6 Hz, 2H), 7.49-7.42 (m, 2H), 7.33-7.27 (m, 1H), 7.21 (d, J=7.1 Hz, 3H), 7.09-7.04 (m, 1H), 5.46-5.26 (m, 1H), 5.25-5.19 (m, 1H), 4.42 (d, J=16.3 Hz, 1H), 4.30 (d, J=16.4 Hz, 1H), 4.19 (t, J=6.0 Hz, 2H), 3.89 (s, 3H), 3.66-3.56 (m, 2H), 3.41-3.23 (m, 2H), 2.96-2.53 (m, 6H), 2.42-2.32 (m, 1H), 2.30-2.16 (m, 2H), 2.10-1.96 (m, 3H), 1.86 (s, 3H), 1.83 (s, 3H), 1.34-1.23 (m, 10H), 1.07 (t, J=7.1 Hz, 3H). MS m/z (ESI): 898.5 [M+H]+.
Compound E112 (white solid, 20 mg) was prepared with reference to the method for compound E88.
1H NMR (500 MHz, CD3OD) δ 8.13 (s, 1H), 8.11 (s, 1H), 7.72 (dd, J=14.0, 9.0 Hz, 1H), 7.60 (t, J=7.8 Hz, 2H), 7.43 (t, J=6.9 Hz, 1H), 7.33 (s, 1H), 7.14 (d, J=7.0 Hz, 1H), 7.06 (d, J=8.4 Hz, 1H), 6.94 (s, 1H), 5.11 (dd, J=12.5, 5.5 Hz, 1H), 4.42-4.22 (m, 3H), 3.88 (s, 3H), 3.80-3.66 (m, 3H), 3.56-3.48 (m, 1H), 3.43-3.35 (m, 2H), 3.32-3.20 (m, 4H), 3.02-2.92 (m, 2H), 2.92-2.85 (m, 1H), 2.82-2.72 (m, 2H), 2.71-2.57 (m, 2H), 2.34 (d, J=10.4 Hz, 2H), 2.18-2.12 (m, 1H), 2.12-2.02 (m, 2H), 1.92 (s, 3H), 1.89 (s, 3H), 1.16 (t, J=7.2 Hz, 3H). MS m/z (ESI): 911.5 [M+H]+.
Compound E113 (white solid, 12 mg, hydrochloride) was prepared with reference to the method for compound E88.
1H NMR (500 MHz, CD3OD) δ 8.24 (d, J=54.0 Hz, 1H), 8.15 (s, 1H), 7.73 (dd, J=14.0, 7.7 Hz, 1H), 7.58 (s, 1H), 7.47-7.35 (m, 3H), 7.25 (d, J=7.4 Hz, 1H), 7.05 (s, 1H), 6.97 (d, J=8.0 Hz, 1H), 5.20 (dd, J=13.3, 5.1 Hz, 1H), 4.51-4.21 (m, 5H), 3.91 (s, 3H), 3.81-3.65 (m, 3H), 3.65-3.55 (m, 1H), 3.37 (d, J=30.7 Hz, 4H), 3.32-3.08 (m, 4H), 2.99-2.89 (m, 1H), 2.86-2.79 (m, 1H), 2.67 (dd, J=14.5, 7.4 Hz, 2H), 2.60-2.50 (m, 1H), 2.38 (d, J=10.5 Hz, 2H), 2.27-2.12 (m, 3H), 1.92 (s, 3H), 1.89 (s, 3H), 1.14 (t, J=7.2 Hz, 3H). MS m/z (ESI): 897.4 [M+H]+.
Compound E114 (white solid, 13 mg, hydrochloride) was prepared with reference to the method for compound E88.
1H NMR (500 MHz, CD3OD) δ 8.16 (s, 2H), 7.72 (dd, J=13.4, 7.6 Hz, 2H), 7.58 (s, 3H), 7.48-7.40 (m, 2H), 7.12 (s, 1H), 5.26-5.04 (m, 1H), 4.79-4.39 (m, 4H), 4.20-4.00 (m, 1H), 3.91 (s, 3H), 3.73-3.33 (m, 8H), 3.14-3.04 (m, 3H), 3.01-2.88 (m, 3H), 2.85-2.75 (m, 2H), 2.67 (dd, J=14.5, 7.1 Hz, 2H), 2.61-2.51 (m, 1H), 2.35-2.15 (m, 5H), 1.89 (s, 3H), 1.87 (s, 3H), 1.11 (t, J=7.2 Hz, 3H). MS m/z (ESI): 896.6 [M+H]+.
Title compound E115 (pale yellow solid, 40 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.30 (s, 2H), 7.87 (dd, J=14.0, 7.7 Hz, 1H), 7.82-7.64 (m, 3H), 7.62-7.54 (m, 2H), 7.40 (d, J=8.0 Hz, 1H), 5.34 (dd, J=13.4, 5.1 Hz, 1H), 4.71 (d, J=17.4 Hz, 1H), 4.62 (d, J=17.4 Hz, 1H), 4.40 (t, J=5.5 Hz, 2H), 4.15-3.96 (m, 7H), 3.86-3.50 (m, 9H), 3.17 (t, J=11.9 Hz, 2H), 3.12-3.03 (m, 1H), 3.00-2.92 (m, 1H), 2.80-2.69 (m, 3H), 2.44 (d, J=10.6 Hz, 2H), 2.39-2.32 (m, 1H), 2.28-2.18 (m, 4H), 2.15-2.09 (m, 2H), 2.05 (d, J=13.6 Hz, 6H), 1.29 (t, J=7.2 Hz, 3H). MS m/z (ESI): 914.1 [M+H]+.
Title compound E116 (pale yellow solid, 15 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.03 (s, 2H), 7.62 (dd, J=14.0, 8.7 Hz, 1H), 7.42 (t, J=7.8 Hz, 2H), 7.32 (t, J=8.4 Hz, 2H), 7.21 (d, J=28.4 Hz, 1H), 7.16 (d, J=8.1 Hz, 1H), 6.87 (s, 1H), 5.08 (dd, J=13.4, 5.1 Hz, 1H), 4.44-4.30 (m, 2H), 4.16 (t, J=5.5 Hz, 2H), 3.78 (d, J=1.9 Hz, 3H), 3.52-3.40 (m, 1H), 3.35-3.27 (m, 1H), 3.20-3.13 (m, 4H), 3.00-2.90 (m, 1H), 2.84 (s, 3H), 2.82-2.76 (m, 1H), 2.68-2.61 (m, 1H), 2.58-2.48 (m, 2H), 2.46-2.36 (m, 1H), 2.17-2.00 (m, 4H), 2.00-1.85 (m, 5H), 1.79 (d, J=13.6 Hz, 6H), 1.02 (t, J=7.2 Hz, 3H). MS m/z (ESI): 858.1 [M+H]+.
Title compound E117 (white solid, 25 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.40-7.90 (m, 2H), 7.64-7.60 (m, 2H), 7.60-7.56 (m, 1H), 7.47 (t, J=7.7 Hz, 2H), 7.32 (t, J=7.2 Hz, 1H), 7.21 (s, 1H), 6.85 (s, 1H), 5.09 (ddd, J=13.3, 5.1, 2.5 Hz, 1H), 4.38 (dt, J=33.3, 9.5 Hz, 2H), 3.77 (s, 3H), 3.46-3.36 (m, 1H), 3.13-3.01 (m, 4H), 2.98-2.76 (m, 7H), 2.71-2.65 (m, 1H), 2.56-2.48 (m, 2H), 2.46-2.39 (m, 1H), 2.11-2.05 (m, 3H), 2.02-1.81 (m, 5H), 1.80 (s, 3H), 1.78 (s, 3H), 1.73-1.65 (m, 2H), 1.02 (t, J=7.2 Hz, 3H). MS m/z (ESI): 874.1 [M+H]+.
Compound E118 (pale yellow solid, 5 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.24 (dd, J=8.2, 4.3 Hz, 1H), 8.05 (s, 1H), 7.69 (s, 1H), 7.63 (ddd, J=13.9, 7.7, 1.4 Hz, 1H), 7.50 (t, J=7.9 Hz, 2H), 7.41 (d, J=7.1 Hz, 1H), 7.29-7.22 (m, 2H), 6.79 (s, 1H), 5.15 (dd, J=13.4, 5.2 Hz, 1H), 4.57 (br s, 1H), 4.52-4.42 (m, 2H), 4.32 (t, J=5.1 Hz, 2H), 3.84 (s, 3H), 3.44-3.38 (m, 2H), 3.34 (s, 2H), 3.06 (d, J=11.7 Hz, 2H), 2.96-2.74 (m, 8H), 2.58-2.48 (m, 3H), 2.20-2.16 (m, 1H), 2.02-1.94 (m, 2H), 1.85 (s, 3H), 1.82 (s, 3H), 1.70 (d, J=11.9 Hz, 2H), 1.00 (t, J=7.5 Hz, 3H). MS m/z (ESI): 899.5 [M+H]+.
Compound 119d (60 mg, 0.065 mmol) was dissolved in methanol (80 mL). In a nitrogen atmosphere, Pd/C (2 g) and Pd(OH)2/C (1 g) were added. The reaction system was purged with hydrogen and stirred at 45° C. for 48 h in the hydrogen atmosphere. After the reaction was completed, the reaction solution was filtered, and the filtrate was concentrated at reduced pressure and subjected to prep-HPLC to give compound E119 (pale yellow solid, 10 mg, hydrochloride). 1H NMR (500 MHz, DMSO-d6) δ 12.41 (br s, 1H), 12.11 (br s, 1H), 11.01 (s, 1H), 8.34 (br s, 2H), 7.66 (dd, J=13.7, 8.4 Hz, 1H), 7.38-7.26 (m, 4H), 6.98 (d, J=7.4 Hz, 1H), 6.88-6.79 (m, 2H), 5.12 (dd, J=13.3, 5.1 Hz, 1H), 4.30 (d, J=17.2 Hz, 1H), 4.17 (d, J=17.2 Hz, 1H), 3.88-3.71 (m, 12H), 3.26-3.14 (m, 6H), 2.97-2.78 (m, 3H), 2.66-2.53 (m, 3H), 2.37-2.21 (m, 3H), 2.10-1.91 (m, 3H), 1.89-1.74 (m, 8H), 1.70-1.61 (m, 2H), 1.07 (t, J=7.3 Hz, 3H). MS m/z (ESI): 912.5 [M+H]+.
Title compound E120 (white solid, 8 mg, hydrochloride) was prepared with reference to the method for compound E67.
1H NMR (500 MHz, CD3OD) δ ppm 8.26 (br dd, J=7.94, 4.19 Hz, 1H), 8.07 (s, 1H), 7.72 (s, 1H), 7.67-7.52 (m, 2H), 7.52 (br t, J=7.75 Hz, 2H), 7.36 (d, J=8.13 Hz, 1H), 7.28 (br t, J=7.07 Hz, 1H), 7.12 (d, J=7.75 Hz, 1H), 7.08-6.99 (m, 2H), 6.80 (s, 1H), 5.15 (dd, J=13.38, 5.13 Hz, 1H), 4.58 (br d, J=1.25 Hz, 1H) 4.44 (d, J=13.38 Hz, 2H), 4.26 (s, 3H), 3.85 (s, 3H), 3.10 (br d, J=10.88 Hz, 2H), 2.96-2.72 (m, 6H), 2.58-2.45 (m, 3H), 2.24-2.11 (m, 3H), 1.91-1.76 (m, 7H), 1.01 (t, J=7.50 Hz, 3H). MS m/z (ESI): 889.6 [M+H]+.
Title compound E121 (white solid, 5 mg, hydrochloride) was prepared with reference to the method for compound E88.
1H NMR (400 MHz, DMSO-d6) δ 11.99-11.62 (m, 1H), 10.43-10.04 (m, 1H), 8.42-8.21 (m, 2H), 7.64 (dd, J=7.3, 11.7 Hz, 1H), 7.56-7.12 (m, 6H), 7.11-6.96 (m, 2H), 5.21-5.09 (m, 1H), 4.38-4.29 (m, 1H), 4.24-4.16 (m, 1H), 3.83 (s, 3H), 3.26-2.90 (m, 9H), 2.70-2.55 (m, 4H), 2.11-1.92 (m, 2H), 1.79 (d, J=13.4 Hz, 9H), 1.64-1.40 (m, 6H), 1.38-1.20 (m, 2H), 1.05 (s, 3H); MS m/z (ESI): 897.6 [M+H]+
Title compounds E122 (white solid, 50 mg, hydrochloride) and E123 (white solid, 40 mg, hydrochloride) were prepared with reference to the method for compound E88.
1H NMR (400 MHz, CD3OD) δ 8.26 (m, 1H), 8.06 (s, 1H), 7.71 (d, J=2.1 Hz, 1H), 7.65-7.62 (m, 1H), 7.51-7.47 (m, 2H), 7.41-7.39 (m, 1H), 7.28-7.26 (m, 1H), 7.09-7.07 (m, 1H), 6.76 (s, 1H), 5.16 (dd, J=5.4, 12.9 Hz, 1H), 4.51-4.49 (m, 1H), 4.48-4.37 (m, 2H), 3.84 (s, 3H), 3.43-3.41 (m, 3H), 3.23-3.20 (m, 2H), 3.07-3.06 (m, 2H), 2.80-2.78 (m, 1H), 2.69-2.65 (m, 3H), 2.63-2.61 (m, 2H), 2.51-2.49 (m, 2H), 2.47-2.17 (m, 8H), 1.85-1.75 (m, 8H), 1.02-0.98 (m, 3H). MS m/z (ESI): 881.7 [M+H]+.
1H NMR (400 MHz, CD3OD) δ ppm 8.28 (dt, J=5.82, 3.47 Hz, 1H) 8.09 (s, 1H) 7.75 (s, 1H), 7.72-7.62 (m, 1H), 7.58-7.45 (m, 2H), 7.42 (br d, J=7.13 Hz, 1H), 7.30 (br t, J=6.88 Hz, 1H), 7.08 (br d, J=7.13 Hz, 1H), 6.79 (s, 1H), 5.21-5.13 (m, 1H) 4.60-4.38 (m, 3H), 3.87 (s, 3H), 3.24 (s, 4H) 3.17-3.01 (m, 4H), 2.95-2.80 (m, 1H), 2.84-2.70 (m, 5H) 2.60-2.45 (m, 3H) 2.40-2.07 (m, 8H), 1.96-1.43 (m, 6H), 1.01-0.92 (m, 3H). MS m/z (ESI): 881.7 [M+H]+.
Title compound E124 (white solid, 9 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.14 (s, 2H), 7.62-7.53 (m, 2H), 7.50 (d, J=7.2 Hz, 1H), 7.35 (t, J=12.8 Hz, 3H), 7.01 (s, 1H), 5.20 (dd, J=13.4, 5.2 Hz, 1H), 4.76-4.53 (m, 4H), 4.09-3.89 (m, 13H), 3.67 (t, J=6.1 Hz, 1H), 3.38 (d, J=12.5 Hz, 2H), 3.10 (s, 2H), 2.95 (ddd, J=18.8, 13.6, 5.4 Hz, 1H), 2.82 (ddd, J=17.6, 4.5, 2.4 Hz, 1H), 2.70-2.57 (m, 3H), 2.41 (d, J=10.5 Hz, 2H), 2.22 (ddd, J=19.1, 9.5, 7.0 Hz, 3H), 1.90 (d, J=13.6 Hz, 6H), 1.14 (s, 3H). MS m/z (ESI): 903.0 [M+H]+.
Title compound E125 (white solid, 1.5 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.14-8.07 (m, 2H), 7.63 (dd, J=10.0, 5.0 Hz, 1H), 7.51-7.48 (m, 1H), 7.42-7.31 (m, 3H), 7.30 (d, J=10.0 Hz, 1H), 7.14 (d, J=10.0 Hz, 1H), 7.04 (s, 1H), 5.07 (dd, J=10.0, 5.0 Hz, 1H), 4.42 (q, J=15.0 Hz, 2H), 4.35 (s, 2H), 4.14 (t, J=5.0 Hz, 2H), 3.94-3.62 (m, 13H), 3.48-3.46 (m, 2H), 3.34 (s, 3H), 3.31-3.30 (m, 1H), 3.21-3.19 (m, 2H), 2.86-2.79 (m, 1H), 2.72-2.67 (m, 1H), 2.55-2.46 (m, 1H), 2.35-2.33 (m, 2H), 2.18-1.97 (m, 5H), 1.89-1.82 (m, 2H), 1.80 (s, 3H), 1.76 (s, 3H). MS m/z (ESI): 929.0 [M+H]+.
Title compound E126 (white solid, 10 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.28-8.16 (m, 1H), 7.69-7.61 (m, 2H), 7.52-7.42 (m, 2H), 7.38 (d, J=10 Hz, 1H), 7.36-7.30 (m, 1H), 7.21 (d, J=10.0 Hz, 1H), 6.96-6.54 (m, 2H), 6.55-6.42 (m, 1H), 5.08 (dd, J=10.0, 5.0 Hz, 1H), 4.54 (q, J=15.0 Hz, 2H), 4.53 (t, J=5.0 Hz, 2H), 3.95-3.73 (m, 10H), 3.63-3.57 (m, 2H), 3.41-3.31 (m, 2H), 3.16-3.08 (m, 2H), 2.87-2.80 (m, 1H), 2.74-2.63 (m, 2H), 2.62-2.45 (m, 3H), 2.33-2.25 (m, 2H), 2.18-2.09 (m, 3H), 1.97-1.91 (m, 1H), 1.92 (s, 3H), 1.88 (s, 3H), 1.09-1.06 (m, 3H). MS m/z (ESI): 889.6 [M+H]+.
Title compound E127 (white solid, 5 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.25-8.23 (m, 2H), 7.77 (dd, J=10.0, 5.0 Hz, 1H), 7.66 (t, J=10.0 Hz, 1H), 7.56-7.49 (m, 3H), 7.42 (d, J=10.0 Hz, 1H), 7.33 (s, 1H), 7.25 (d, J=10.0 Hz, 1H), 5.19 (dd, J=10.0, 5.0 Hz, 1H), 4.72 (s, 2H), 4.53 (q, J=15.0 Hz, 2H), 4.25 (t, J=5.0 Hz, 2H), 4.04-3.65 (m, 14H), 3.63-3.50 (m, 2H), 3.44-3.41 (m, 2H), 2.98-2.79 (m, 1H), 2.84-2.79 (m, 1H), 2.66-2.52 (m, 3H), 2.34-2.19 (m, 3H), 2.14-2.08 (m, 2H), 2.01-1.96 (m, 2H), 1.90 (s, 3H), 1.88 (s, 3H). MS m/z (ESI): 915.0 [M+H]+.
Compound E128 (pale yellow solid, 30 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, DMSO-d6) δ 12.37 (s, 1H), 12.24-11.97 (m, 1H), 11.78 (br s, 1H), 10.64 (s, 1H), 8.44-8.19 (m, 3H), 7.63 (s, 1H), 7.41 (d, J=8.8 Hz, 2H), 7.37 (s, 2H), 7.23 (s, 1H), 6.92 (d, J=8.7 Hz, 2H), 6.87 (d, J=8.2 Hz, 1H), 6.82 (s, 1H), 6.39 (d, J=7.8 Hz, 1H), 3.91-3.65 (m, 12H), 3.21-3.09 (m, 4H), 3.07-2.96 (m, 2H), 2.84-2.75 (m, 2H), 2.64 (s, 3H), 2.56 (d, J=7.4 Hz, 2H), 2.21 (d, J=9.5 Hz, 2H), 1.97-1.86 (m, 2H), 1.83-1.75 (m, 8H), 1.34-1.24 (m, 2H), 1.07 (t, J=7.4 Hz, 3H). MS m/z (ESI): 979.8 [M+H]+.
Compound E129 (pale yellow solid, 5 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.46 (br s, 1H), 8.33 (br s, 1H), 7.94-7.87 (m, 1H), 7.78-7.66 (m, 2H), 7.64-7.59 (m, 2H), 7.57 (s, 1H), 7.46 (d, J=8.0 Hz, 1H), 7.24 (s, 1H), 5.36 (dd, J=13.3, 5.2 Hz, 1H), 4.72 (dd, J=38.8, 17.5 Hz, 2H), 4.52-4.36 (m, 4H), 4.15 (t, J=11.8 Hz, 2H), 4.08 (s, 3H), 3.87-3.78 (m, 3H), 3.73 (s, 2H), 3.65-3.57 (m, 2H), 3.41-3.25 (m, 2H), 3.19-3.05 (m, 1H), 3.02-2.95 (m, 1H), 2.92-2.79 (m, 3H), 2.62 (d, J=10.5 Hz, 2H), 2.49-2.35 (m, 3H), 2.26-2.15 (m, 4H), 2.09 (s, 3H), 2.06 (s, 3H), 1.73 (dd, J=11.2, 6.5 Hz, 6H), 1.31 (br s, 3H). MS m/z (ESI): 941.5 [M+H]+.
Compound E130 (pale yellow solid, 10 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.26 (br s, 1H), 8.14 (br s, 1H), 7.77-7.67 (m, 1H), 7.55 (t, J=7.7 Hz, 2H), 7.48 (d, J=7.6 Hz, 1H), 7.45-7.30 (m, 3H), 6.98 (s, 1H), 5.15 (dd, J=13.3, 5.1 Hz, 1H), 4.69 (d, J=17.0 Hz, 1H), 4.60 (s, 2H), 4.52 (d, J=17.3 Hz, 1H), 4.35 (d, J=29.5 Hz, 2H), 4.11-3.94 (m, 4H), 3.88 (d, J=12.9 Hz, 3H), 3.77-3.57 (m, 3H), 3.54-3.34 (m, 2H), 3.25-3.01 (m, 2H), 2.97-2.85 (m, 1H), 2.78 (d, J=17.7 Hz, 1H), 2.69-2.52 (m, 3H), 2.50-2.12 (m, 5H), 1.89 (s, 3H), 1.86 (s, 3H), 1.73-1.62 (m, 6H), 1.10 (br s, 3H); MS m/z (ESI): 913.5 [M+H]+.
Title compound E131 (6.99 mg, formate) was prepared with reference to the method for compound C-1.
1H NMR (400 MHz, CD3OD) δ 8.48 (s, 1H), 7.92 (s, 1H), 7.72 (d, J=8.0, 1H), 7.39-7.27 (m, 2H), 7.23-7.21 (m, 2H), 7.10-7.08 (m, 1H), 6.31 (s, 2H), 5.18-5.15 (m, 1H), 4.21-4.19 (m, 2H), 3.85-3.83 (m, 2H), 3.31 (s, 6H), 2.90-2.77 (m, 12H), 2.68-2.66 (m, 4H), 2.48-2.42 (m, 1H), 2.36-2.32 (m, 1H), 2.16-2.10 (m, 2H), 1.89-1.85 (m, 11H), 1.75-1.72 (m, 2H). MS m/z (ESI): 914.7 [M+H]+.
Title compound E132 (white solid, 19.31 mg, formate) was prepared with reference to the method for compound C-1.
1H NMR (400 MHz, DMSO-d6) δ 12.46-11.92 (m, 1H), 11.84-11.64 (m, 1H), 11.06-10.84 (m, 1H), 9.76-9.38 (m, 1H), 8.95-8.64 (m, 1H), 8.47-8.21 (m, 1H), 7.81 (br dd, J=7.8, 11.8 Hz, 2H), 7.68-7.59 (m, 1H), 7.59-7.57 (m, 1H), 7.55-7.21 (m, 4H), 6.77 (s, 1H), 5.12 (dd, J=5.0, 13.1 Hz, 1H), 4.47 (d, J=17.4 Hz, 1H), 4.27 (d, J=17.5 Hz, 1H), 4.19-4.10 (m, 2H), 3.80 (s, 7H), 3.25 (br s, 3H), 3.15-3.04 (m, 3H), 2.99-2.86 (m, 4H), 2.81-2.66 (m, 3H), 2.59 (br d, J=18.1 Hz, 1H), 2.24-2.11 (m, 3H), 2.05-1.98 (m, 1H), 1.98-1.87 (m, 4H), 1.85-1.76 (m, 2H), 1.68 (br d, J=13.3 Hz, 6H), 1.31-1.21 (m, 1H), 0.99-0.73 (m, 3H); MS m/z (ESI): 921.4 [M+H]+
Title compound E133 (4.7 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (400 MHz, DMSO-d6) δ 12.60-11.37 (m, 3H), 10.98 (s, 1H), 9.25 (s, 1H), 9.12-8.84 (m, 1H), 8.77-8.57 (m, 1H), 7.84-7.76 (m, 1H), 7.67 (d, J=3.0 Hz, 1H), 7.58-7.47 (m, 2H), 7.43 (t, J=7.4 Hz, 1H), 7.35-7.29 (m, 2H), 7.26 (d, J=8.1 Hz, 1H), 5.16-5.07 (m, 1H), 4.47 (d, J=17.5 Hz, 1H), 4.27 (d, J=17.5 Hz, 1H), 4.17 (d, J=3.5 Hz, 2H), 3.79 (s, 6H), 3.31-3.18 (m, 6H), 3.14-3.02 (m, 3H), 2.99-2.86 (m, 2H), 2.78 (d, J=4.4 Hz, 3H), 2.75-2.69 (m, 2H), 2.61 (s, 1H), 2.60-2.53 (m, 1H), 2.39-2.31 (m, 2H), 2.24-2.12 (m, 2H), 2.06-1.98 (m, 1H), 1.95-1.87 (m, 3H), 1.84 (d, J=6.0 Hz, 3H), 1.69 (d, J=13.4 Hz, 6H), 1.04-0.75 (m, 3H). MS m/z (ESI): 935.4 [M+H]+.
Title compound E134 (white solid, 28.5 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (400 MHz, CD3OD) δ 8.13-7.99 (m, 1H), 7.74 (dd, J=7.9, 13.3 Hz, 1H), 7.66-7.33 (m, 5H), 7.24 (d, J=8.0 Hz, 1H), 7.04 (s, 1H), 5.17 (dd, J=5.1, 13.3 Hz, 1H), 4.58-4.42 (m, 2H), 4.23 (t, J=5.6 Hz, 2H), 3.97-3.66 (m, 12H), 3.45-3.37 (m, 4H), 3.15 (s, 6H), 2.85-2.74 (m, 1H), 3.00-2.73 (m, 1H), 2.66-2.51 (m, 3H), 2.41 (d, J=8.9 Hz, 2H), 2.29-2.15 (m, 3H), 2.12-2.05 (m, 2H), 2.01-1.91 (m, 2H), 1.84 (d, J=13.6 Hz, 6H), 1.40-1.33 (m, 3H), 1.09 (s, 3H). MS m/z (ESI): 949.8 [M+H]+.
Compound E135 (white solid, 35.22 mg, hydrochloride) was prepared with reference to the method for reference compound C-1.
1H NMR (400 MHz, CD3OD) δ 8.51 (br s, 1H), 7.87 (dd, J=7.8, 13.1 Hz, 1H), 7.66 (d, J=4.0 Hz, 2H), 7.57-7.46 (m, 2H), 7.34-7.22 (m, 3H), 6.89 (s, 1H), 5.19-5.14 (m, 1H), 4.59-4.42 (m, 2H), 4.29-4.17 (m, 3H), 4.09-3.51 (m, 12H), 3.44-3.35 (m, 2H), 3.25 (d, J=9.9 Hz, 2H), 3.00-2.86 (m, 3H), 2.85-2.74 (m, 1H), 2.66-2.41 (m, 2H), 2.33 (d, J=11.4 Hz, 3H), 2.25-2.15 (m, 1H), 2.08 (d, J=9.3 Hz, 4H), 2.01-1.90 (m, 2H), 1.84 (d, J=13.4 Hz, 6H), 1.27 (s, 3H), 1.25 (s, 3H), 1.00 (br s, 3H). MS m/z (ESI): 964.0 [M+H]+.
Compound E136 (white solid, 26 mg, hydrochloride) was prepared with reference to the method for compound E4.
1H NMR (500 MHz, DMSO-d6) δ 11.42-11.01 (m, 2H), 8.61 (s, 1H), 8.39 (s, 1H), 8.18 (s, 1H), 7.77 (d, J=7.6 Hz, 1H), 7.70 (d, J=7.1 Hz, 1H), 7.58 (dt, J=15.1, 7.7 Hz, 2H), 7.47 (s, 1H), 7.35 (s, 1H), 7.16 (t, J=7.1 Hz, 1H), 6.76 (s, 1H), 5.18 (dd, J=13.3, 5.1 Hz, 1H), 4.52 (d, J=17.7 Hz, 1H), 4.35 (d, J=17.7 Hz, 1H), 3.82-3.72 (m, 5H), 3.65-3.47 (m, 4H), 3.29-3.00 (m, 11H), 2.98-2.91 (m, 1H), 2.59-2.55 (m, 3H), 2.48-2.41 m, 3H), 2.22 (d, J=11.6 Hz, 2H), 2.10-1.99 (m, 1H), 1.79 (s, 3H), 1.76 (s, 3H), 1.07 (t, J=7.5 Hz, 3H). MS m/z (ESI): 447 [M/2+H]+.
Compound E137 (white solid, 35 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.17 (s, 2H), 7.72 (dd, J=13.9, 7.7 Hz, 1H), 7.61-7.50 (m, 2H), 7.49-7.41 (m, 3H), 7.30 (d, J=8.1 Hz, 1H), 7.18 (s, 1H), 5.19-5.15 (m, 1H), 4.99-4.93 (m, 2H), 4.75-4.36 (m, 6H), 4.28 (t, J=10.0 Hz, 1H), 4.13-3.85 (m, 7H), 3.63-3.36 (m, 4H), 2.98-2.86 (m, 1H), 2.81-2.56 (m, 6H), 2.50-2.30 (m, 4H), 2.23-2.14 (m, 1H), 1.89 (s, 3H), 1.86 (s, 3H), 1.10 (br s, 3H). MS m/z (ESI): 897.1 [M+H]+.
Compound E138 (white solid, 5 mg, hydrochloride) was prepared with reference to the method for reference compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.29 (br s, 1H), 8.19 (br s, 1H), 7.76 (d, J=8.5 Hz, 1H), 7.73-7.66 (m, 1H), 7.53 (s, 1H), 7.40 (t, J=7.1 Hz, 1H), 7.29 (t, J=6.4 Hz, 2H), 7.21 (dd, J=8.5, 2.2 Hz, 1H), 6.94 (s, 1H), 5.12 (dd, J=13.4, 5.2 Hz, 1H), 4.62-4.54 (m, 2H), 4.46 (t, J=14.1 Hz, 2H), 4.09-3.66 (m, 13H), 3.59 (s, 1H), 3.34-3.31 (m, 2H), 3.03-2.87 (m, 3H), 2.80-2.75 (m, 1H), 2.65-2.57 (m, 2H), 2.53-2.44 (m, 1H), 2.35 (d, J=11.3 Hz, 2H), 2.21-2.03 (m, 3H), 1.89 (s, 3H), 1.86 (s, 3H), 1.12 (br s, 3H). MS m/z (ESI): 884.8 [M+H]+.
Compound 139d (30 mg, 0.03 mmol), NH4Cl (5.20 mg, 0.09 mmol), HATU (18.47 mg, 0.05 mmol), and DIPEA (12.56 mg, 0.10 mmol) were added to DMF (1 mL). The reaction system was stirred at 25° C. for 1 h. The reaction mixture was filtered and concentrated at reduced pressure to give a crude product. The crude product was isolated by reverse-phase pre-HPLC (formic acid system) to give title compound E139. 1H NMR (400 MHz, DMSO-d6) δ 11.17 (s, 1H), 11.05-10.91 (m, 1H), 9.40-9.29 (m, 1H), 8.67-8.55 (m, 1H), 8.31 (s, 2H), 8.22-8.16 (m, 1H), 7.79-7.66 (m, 1H), 7.64-7.51 (m, 2H), 7.51-7.37 (m, 3H), 7.34-7.22 (m, 3H), 7.17 (t, J=7.1 Hz, 1H), 5.16-5.06 (m, 1H), 4.43-4.33 (m, 1H), 4.27-4.20 (m, 1H), 4.14 (t, J=6.2 Hz, 2H), 3.14-3.02 (m, 3H), 2.95-2.82 (m, 3H), 2.64-2.55 (m, 4H), 2.40 (td, J=4.2, 6.7 Hz, 3H), 2.35-2.27 (m, 4H), 2.15 (s, 1H), 2.04-1.96 (m, 1H), 1.84-1.71 (m, 12H), 1.63-1.56 (m, 2H), 1.52-1.40 (m, 2H), 1.14-1.07 (m, 3H). MS m/z (ESI): 925.5 [M+H]+.
Title compound E140 (white solid, 100 mg, hydrochloride) was prepared with reference to the synthesis method for compound C—1.
1H NMR (400 MHz, DMSO-d6) δ 12.86-12.02 (m, 2H), 10.99 (s, 1H), 9.95-9.70 (m, 1H), 8.37 (s, 1H), 7.65 (dd, J=13.51, 7.52 Hz, 1H), 7.54-7.44 (m, 1H), 7.32 (d, J=4.89 Hz, 2H), 7.29-7.15 (m, 3H), 7.07 (d, J=14.43 Hz, 2H), 6.46 (s, 1H), 5.12 (dd, J=13.02, 4.95 Hz, 1H), 4.47 (d, J=17.48 Hz, 1H), 4.27 (d, J=17.36 Hz, 2H), 4.16 (d, J=3.55 Hz, 3H), 3.82 (d, J=11.00 Hz, 2H), 3.48-3.14 (m, 8H), 2.99-2.73 (m, 4H), 2.72-2.54 (m, 4H), 2.21 (s, 5H) 2.06-1.89 (m, 5H), 1.83 (d, J=13.69 Hz, 8H), 1.15 (t, J=7.40 Hz, 3H). MS m/z (ESI): 901.4 [M+H]+.
Title compound E141 (white solid, 95 mg, hydrochloride) was prepared with reference to the synthesis method for compound C-1.
1H NMR (400 MHz, DMSO-d6) δ 12.28 (s, 1H), 11.82 (s, 1H), 11.01 (s, 1H), 8.50 (s, 1H), 7.73-7.49 (m, 2H), 7.40 (s, 1H), 7.25-7.18 (m, 2H), 7.13-7.03 (m, 2H), 6.86 (s, 1H), 6.47 (s, 1H), 5.12 (dd, J=13.33, 4.77 Hz, 1H), 4.48-4.40 (m, 1H), 4.31-4.21 (m, 1H), 4.18 (s, 2H), 4.28-4.13 (m, 1H), 3.81 (s, 7H), 3.51 (s, 1H), 3.19 (d, J=11.37 Hz, 7H), 2.96-2.75 (m, 4H), 2.69-2.58 (m, 4H), 2.33 (s, 1H), 2.21 (s, 1H), 2.05-1.88 (m, 5H), 1.83 (d, J=13.57 Hz, 8H), 1.13 (t, J=7.34 Hz, 3H). MS m/z (ESI): 935.7 [M+H]+.
Title compound E142 (white solid, 21 mg, formate) was prepared with reference to the synthesis method for compound C-1.
1H NMR (400 MHz, DMSO-d6) δ 11.56 (s, 1H), 11.18 (s, 1H), 11.01 (s, 1H), 9.39 (s, 1H), 8.90 (dd, J=8.3, 4.5 Hz, 1H), 8.23 (s, 1H), 8.08 (s, 1H), 7.60-7.46 (m, 1H), 7.49 (t, J=7.8 Hz, 1H), 7.41 (t, J=7.8 Hz, 1H), 7.31 (d, J=7.5 Hz, 1H), 7.25 (d, J=8.1 Hz, 1H), 7.06 (t, J=7.3 Hz, 1H), 6.97 (s, 1H), 6.95-6.90 (m, 1H), 6.35 (s, 1H), 5.79 (s, 1H), 5.11 (dd, J=13.6, 5.2 Hz, 1H), 4.42-4.35 (m, 1H), 4.22 (d, J=17.9 Hz, 1H), 4.14 (t, J=5.9 Hz, 2H), 3.06-2.83 (m, 4H), 2.62 (d, J=7.9 Hz, 2H), 2.66 (d, J=8.7 Hz, 2H), 2.57-2.54 (m, 1H), 2.44-2.16 (m, 9H), 2.18 (d, J=15.4 Hz, 2H), 2.03-1.97 (m, 1H), 1.86-1.72 (m, 10H), 1.62-1.51 (m, 9H), 1.52-1.49 (m, 1H), 1.36 (d, J=13.7 Hz, 1H), 1.14 (t, J=7.5 Hz, 3H). MS m/z (ESI): 945.7 [M+H]+.
Title compound E143 (21.3 mg, formate) was prepared with reference to the synthesis method for compound C-1.
1H NMR (400 MHz, DMSO-d6) δ 11.15 (s, 1H), 11.02 (s, 1H), 8.51-8.36 (m, 1H), 8.24 (s, 1H), 8.14 (s, 1H), 8.10 (s, 1H), 7.60-7.51 (m, 1H), 7.42 (s, 1H), 7.35-7.28 (m, 1H), 7.25-7.18 (m, 1H), 7.11 (s, 2H), 6.77 (s, 1H), 5.18-5.06 (m, 1H), 4.34 (s, 1H), 4.26-4.11 (m, 3H), 3.75 (s, 3H), 3.06-2.86 (m, 4H), 2.76-2.64 (m, 3H), 2.45-2.21 (m, 12H), 2.05-1.93 (m, 1H), 1.90-1.82 (m, 2H), 1.77 (d, J=13.6 Hz, 9H), 1.63-1.49 (m, 5H), 1.06 (s, 3H). MS m/z (ESI): 930.6 [M+H]+.
Title compound E144 (white solid, 10 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.02 (s, 2H), 7.62 (dd, J=13.9, 7.7 Hz, 1H), 7.44 (t, J=7.8 Hz, 2H), 7.37-7.30 (m, 2H), 7.26 (s, 1H), 7.18 (d, J=8.0 Hz, 1H), 6.93 (s, 1H), 5.08 (dd, J=13.3, 5.2 Hz, 1H), 4.40 (dd, J=28.5, 19.3 Hz, 4H), 3.87-3.70 (m, 9H), 3.59 (d, J=23.2 Hz, 2H), 3.28 (s, 2H), 3.12-2.98 (m, 2H), 2.87-2.75 (m, 2H), 2.72-2.63 (m, 1H), 2.59-2.45 (m, 3H), 2.32 (d, J=9.4 Hz, 2H), 2.16-2.02 (m, 3H), 1.79 (d, J=13.6 Hz, 6H), 1.31 (s, 2H), 1.11 (s, 2H), 1.02 (s, 3H). MS m/z (ESI): 910.8 [M+H]+.
Title compound E145 (white solid, 6 mg, hydrochloride) was prepared with reference to the method for compound E4.
1H NMR (500 MHz, CD3OD) δ 8.32-8.14 (m, 2H), 7.91 (s, 1H), 7.72 (dd, J=10.0, 5.0 Hz, 1H), 7.58 (s, 1H), 7.52 (t, J=5.0 Hz, 1H), 7.44 (t, J=5.0 Hz, 1H), 7.36 (s, 1H), 7.02 (s, 1H), 4.08 (t, J=7.5 Hz, 2H), 4.04 (s, 3H), 3.98-3.81 (m, 11H), 3.69-3.64 (m, 3H), 3.40-3.37 (m, 2H), 3.14-3.08 (m, 4H), 2.90 (t, J=7.5 Hz, 2H), 2.67-2.63 (m, 2H), 2.42-2.40 (m, 2H), 2.23-2.16 (m, 2H), 1.92 (s, 3H), 1.90 (s, 3H), 1.14-1.11 (m, 3H). MS m/z (ESI): 893.0 [M+H]+.
Compound E146 (pale yellow solid, 1.2 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.39-8.00 (m, 3H), 7.85 (s, 1H), 7.70-7.59 (m, 1H), 7.56-7.46 (m, 2H), 7.39 (dd, J=7.4, 4.0 Hz, 1H), 7.35-7.13 (m, 3H), 6.91 (s, 1H), 5.17 (dd, J=13.2, 5.1 Hz, 1H), 4.56-4.44 (m, 2H), 4.23 (t, J=5.9 Hz, 2H), 4.09-3.82 (m, 10H), 3.79-3.61 (m, 4H), 3.52 (s, 1H), 3.42-3.37 (m, 2H), 3.34 (s, 2H), 2.95-2.87 (m, 1H), 2.85-2.73 (m, 3H), 2.64-2.57 (m, 1H), 2.28 (d, J=12.8 Hz, 2H), 2.22-2.15 (m, 1H), 2.12-2.02 (m, 4H), 1.96 (d, J=6.5 Hz, 2H), 1.89 (s, 3H), 1.86 (s, 3H). MS m/z (ESI): 964.8 [M+H]+.
Title compound E147 (white solid, 10 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.46 (s, 1H), 7.95 (dd, J=13.0, 7.6 Hz, 1H), 7.78-7.70 (m, 3H), 7.65-7.53 (m, 2H), 7.50 (d, J=7.3 Hz, 2H), 7.33 (d, J=7.9 Hz, 1H), 7.06 (s, 1H), 6.81 (d, J=2.4 Hz, 1H), 5.20 (dd, J=13.3, 5.1 Hz, 1H), 4.75-4.52 (m, 4H), 3.96 (dd, J=42.1, 20.6 Hz, 16H), 3.69 (dd, J=16.5, 10.5 Hz, 2H), 3.42 (s, 2H), 3.26 (s, 1H), 2.99-2.90 (m, 1H), 2.86-2.79 (m, 1H), 2.60 (dt, J=13.3, 8.6 Hz, 1H), 2.44 (dd, J=29.9, 18.0 Hz, 4H), 2.23 (ddd, J=16.9, 14.3, 10.9 Hz, 3H), 1.86 (d, J=13.4 Hz, 6H), 0.99 (s, 3H). MS m/z (ESI): 931.0 [M+H]+.
Compound E148 (pale yellow solid, 30 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.28-7.92 (m, 2H), 7.74 (dd, J=13.5, 8.8 Hz, 1H), 7.65-7.51 (m, 2H), 7.49-7.40 (m, 2H), 7.35-7.29 (m, 2H), 6.89 (s, 1H), 5.17 (dd, J=13.3, 5.1 Hz, 1H), 4.69-4.47 (m, 4H), 4.00-3.71 (m, 12H), 3.66-3.60 (m, 4H), 3.57-3.49 (m 1H), 3.25 (s, 2H), 2.96-2.89 (m, 3H), 2.82-2.77 (m, 1H), 2.59-2.49 (m, 3H), 2.32 (d, J=11.1 Hz, 2H), 2.24-2.14 (m, 1H), 2.12-1.93 (m, 7H), 1.84 (s, 3H), 1.82 (s, 3H), 1.05 (br s, 3H). MS m/z (ESI): 947.9 [M+H]+.
Compound E149 (pale yellow solid, 42 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, DMSO-d6) δ 12.19 (s, 1H), 11.01 (s, 1H), 10.76 (s, 1H), 8.88 (s, 1H), 7.85-7.68 (m, 2H), 7.52 (dt, J=8.4, 4.4 Hz, 2H), 7.44 (s, 1H), 7.38 (dt, J=7.6, 3.9 Hz, 2H), 7.30 (d, J=8.1 Hz, 1H), 6.79 (s, 1H), 5.12 (dd, J=13.3, 5.1 Hz, 1H), 4.62-4.55 (m, 3H), 4.34 (d, J=17.6 Hz, 1H), 3.98-3.64 (m, 16H), 3.11 (s, 2H), 2.98-2.89 (m, 1H), 2.79 (s, 2H), 2.66-2.57 (m, 1H), 2.45-2.33 (m, 4H), 2.21 (d, J=10.0 Hz, 2H), 2.06-1.99 (m, 1H), 1.93 (d, J=9.0 Hz, 2H), 1.70 (s, 3H), 1.67 (s, 3H), 0.89 (s, 3H). MS m/z (ESI): 932.8 [M+H]+.
Compound E150 (yellow solid, 34 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, DMSO-d6) δ 12.38 (br s, 1H), 12.11 (s, 1H), 8.41-8.21 (m, 2H), 7.66 (dd, J=13.7, 8.7 Hz, 1H), 7.53 (t, J=7.8 Hz, 1H), 7.39-7.26 (m, 5H), 6.86 (s, 1H), 5.19 (dd, J=13.4, 5.1 Hz, 1H), 4.64-4.55 (m, 3H), 4.34 (d, J=17.6 Hz, 1H), 3.94-3.75 (m, 13H), 3.19 (d, J=10.3 Hz, 2H), 3.06-2.95 (m, 5H), 2.86-2.74 (m, 3H), 2.58-2.53 (m, 2H), 2.46-2.37 (m, 1H), 2.24 (d, J=10.5 Hz, 2H), 2.08-1.89 (m, 3H), 1.81 (s, 3H), 1.78 (s, 3H), 1.06 (t, J=7.4 Hz, 3H). MS m/z (ESI): 898.8 [M+H]+.
Title compound E151 (white solid, 41.92 mg, hydrochloride) was prepared with reference to the synthesis method for compound C-1.
1H NMR (400 MHz, DMSO-d6) δ 12.43 (s, 1H), 11.92 (s, 1H), 11.03 (s, 1H), 9.62 (s, 1H), 8.38-8.15 (m, 2H), 7.62 (dd, J=13.63, 7.52 Hz, 1H), 7.57-7.48 (m, 1H), 7.45-7.35 (m, 2H), 7.34-7.18 (m, 3H), 7.15-6.85 (m, 2H), 5.13 (dd, J=13.27, 4.83 Hz, 1H), 4.69-4.50 (m, 3H), 4.33 (d, J=17.73 Hz, 1H), 3.75 (s, 8H), 3.44 (s, 3H), 3.17 (d, J=10.15 Hz, 2H), 3.01-2.86 (m, 1H), 2.80-2.66 (m, 2H), 2.65-2.55 (m, 3H), 2.45-2.21 (m, 3H), 2.09-1.86 (m, 3H), 1.84-1.73 (m, 6H), 1.10 (t, J=7.40 Hz, 3H). MS m/z (ESI): MS m/z (ESI): 920.5 [M+Na]+.
Compound E152 (white solid, 51.1 mg, formate) was prepared with reference to the method for reference compound C-1.
1H NMR (400 MHz, DMSO-d6) δ 11.27 (s, 1H), 11.01 (s, 1H), 8.89 (s, 1H), 8.40 (br s, 2H), 8.11 (s, 1H), 7.59-7.38 (m, 2H), 7.33-7.27 (m, 4H), 7.10-7.05 (m, 1H), 7.02 (s, 1H), 5.12 (dd, J=13.20, 4.40 Hz, 1H), 4.40-4.36 (m, 1H), 4.26-4.21 (m, 3H), 3.30-3.20 (m, 2H), 3.05-3.02 (m, 2H), 2.74-2.30 (m, 15H), 2.00-1.95 (m, 1H), 1.88-1.79 (m, 2H), 1.75 (m, 3H), 1.59 (m, 3H), 1.50-1.40 (m, 2H), 1.12 (t, J=7.20 Hz, 3H). MS m/z (ESI): 960.5 [M+Na]+.
Title compound E153 (white solid, 8 mg, formate) was prepared with reference to the method for compound C-1.
1H NMR (400 MHz, DMSO-d6) δ ppm 11.54 (s, 1H), 11.10 (s, 1H), 11.01 (s, 1H), 8.85 (dd, J=8.3, 3.4 Hz, 1H), 8.19 (s, 1H), 7.95 (s, 1H), 7.55-7.46 (m, 2H), 7.31 (d, J=7.3 Hz, 1H), 7.28-7.20 (m, 2H), 7.16 (s, 1H), 7.05-6.93 (m, 1H), 6.94-6.93 (m, 1H), 6.87-6.81 (m, 1H), 6.31-6.28 (m, 1H), 5.11 (dd, J=13.4, 5.2 Hz, 1H), 4.42-4.34 (m, 1H), 4.26-4.11 (m, 4H), 3.04 (d, J=10.9 Hz, 2H), 2.99-2.85 (m, 1H), 2.72-2.55 (m, 10H), 2.47-2.28 (m, 8H), 2.03-1.97 (m, 1H), 1.90-1.72 (m, 10H), 1.59 (dd, J=12.6, 8.2 Hz, 4H), 1.14 (t, J=7.5 Hz, 3H), 1.08 (t, J=7.6 Hz, 3H). MS m/z (ESI): 915.6 [M+H]+.
Compound E154 (white solid, 31.3 mg, formate) was prepared with reference to the method for reference compound C-1.
1H NMR (400 MHz, DMSO-d6) δ 11.83 (s, 1H), 11.24 (s, 1H), 11.00 (s, 1H), 8.77 (br s, 1H), 7.91 (s, 1H), 7.57 (s, 1H), 7.51-7.49 (m, 3H), 7.32-7.24 (m, 4H), 6.91-6.90 (m, 1H), 6.89 (s, 1H), 6.33 (s, 1H), 5.15-5.11 (m, 1H), 4.40-4.21 (m, 4H), 4.15 (s, 2H), 3.10-3.07 (m, 1H), 2.95-2.90 (m, 5H), 2.34-2.31 (m, 10H), 2.00-1.95 (m, 1H), 1.90-1.80 (m, 11H), 1.61-1.58 (m, 4H), 1.17 (t, J=7.6, 3H). MS m/z (ESI): 955.6 [M+H]+.
Title compound E155 (white solid, 5 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.27-8.16 (m, 2H), 7.73 (dd, J=10.0, 5.0 Hz, 1H), 7.59-7.41 (m, 5H), 7.36 (d, J=10.0 Hz, 1H), 7.09 (s, 1H), 4.05 (t, J=7.5 Hz, 2H), 4.04 (s, 3H), 3.92-3.68 (m, 12H), 3.47-3.45 (m, 2H), 3.29-3.26 (m, 4H), 2.92 (t, J=7.5 Hz, 2H), 2.81 (t, J=7.5 Hz, 2H), 2.69-2.65 (m, 2H), 2.45-2.40 (m, 2H), 2.29-2.26 (m, 2H), 1.92 (s, 3H), 1.89 (s, 3H), 1.88-1.87 (m, 2H), 1.83-1.77 (m, 2H), 1.50-1.43 (m, 2H), 1.16-1.09 (m, 3H). MS m/z (ESI): 910.5 [M+H]+.
Title compound E156 (white solid, 6 mg, hydrochloride) was prepared with reference to the method for compound 21.
1H NMR (500 MHz, CD3OD) δ 8.30-8.12 (m, 2H), 7.88-7.85 (m, 2H), 7.72 (dd, J=20.0, 10.0 Hz, 1H), 7.62-7.55 (m, 2H), 7.43 (t, J=5.0 Hz, 1H), 7.32 (s, 1H), 6.95 (s, 1H), 5.23 (dd, J=10.0, 5.0 Hz, 1H), 4.83-4.64 (m, 2H), 4.02-3.88 (m, 8H), 3.73-3.49 (m, 4H), 3.31-3.29 (m, 3H), 3.02-2.91 (m, 3H), 2.85-2.79 (m, 1H), 2.73-2.62 (m, 3H), 2.37 (d, J=15.0 Hz, 2H), 2.25-2.21 (m, 1H), 2.16-2.09 (m, 1H), 1.92 (s, 3H), 1.89 (s, 3H), 1.88 (s, 6H), 1.17-1.14 (m, 3H). MS m/z (ESI): 906.8 [M+H]+.
Compound 157d (30 mg, 0.09 mmol) and compound 4c (54 mg, 0.09 mmol) were added to a single-necked flask at room temperature before DCE (5 mL) was added. Then AcOH (11 mg, 0.18 mmol) and TEA (27 mg, 0.27 mmol) were sequentially added. The reaction system was stirred at room temperature in a nitrogen atmosphere for 1 h. NaBH(OAc)3 (57 mg, 0.27 mmol) was then added. The system was then stirred at room temperature for 16 h. The solvent was removed at reduced pressure, and the crude product was separated and purified by prep-HPLC to give target product E157 (pale yellow solid, 30 mg, hydrochloride). 1H NMR (500 MHz, CD3OD) δ 8.40-8.10 (m, 2H), 7.74 (dd, J=13.9, 7.7 Hz, 1H), 7.63-7.51 (m, 4H), 7.49-7.41 (m, 2H), 7.14 (s, 1H), 5.20 (dd, J=13.3, 5.1 Hz, 1H), 4.69 (d, J=17.4 Hz, 1H), 4.56 (d, J=16.5 Hz, 1H), 4.20-3.98 (m, 8H), 3.93 (s, 3H), 3.81 (s, 3H), 3.55-3.47 (m, 2H), 3.35 (d, J=16.1 Hz, 2H), 3.00-2.91 (m, 1H), 2.86-2.79 (m, 1H), 2.72-2.62 (m, 3H), 2.48 (d, J=11.2 Hz, 2H), 2.40-2.28 (m, 2H), 2.26-2.19 (m, 1H), 1.92 (s, 3H), 1.89 (s, 3H), 1.67 (d, J=7.1 Hz, 6H), 1.13 (t, J=7.2 Hz, 3H). MS m/z (ESI): 912.5 [M+H]+.
Title compound E158 (pale yellow solid, 5.2 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.18-8.02 (m, 2H), 7.93 (d, J=31.0 Hz, 2H), 7.75-7.53 (m, 4H), 7.48 (d, J=6.2 Hz, 2H), 7.33 (s, 2H), 5.28-5.16 (m, 1H), 4.78-4.58 (m, 4H), 4.13-3.88 (m, 17H), 3.81-3.61 (m, 4H), 3.02-2.78 (m, 2H), 2.76-2.48 (m, 7H), 2.30-2.12 (m, 1H), 1.82 (d, J=9.2 Hz, 6H), 1.07 (t, J=7.2 Hz, 3H). MS m/z (ESI): 930.6 [M+H]+.
Compounds E159 (white solid, 6 mg, hydrochloride) and E160 (white solid, 10 mg, hydrochloride) were prepared with reference to the method for compound E67.
E159: 1H NMR (500 MHz, CD3OD) δ 8.26 (s, 1H), 8.10 (s, 1H), 7.72-7.67 (m, 1H), 7.60-7.49 (m, 2H), 7.45-7.38 (m, 2H), 7.33 (s, 1H), 7.12 (d, J=8.0 Hz, 1H), 6.99 (s, 1H), 5.14 (dd, J=13.3, 5.2 Hz, 1H), 4.55-4.42 (m, 2H), 4.14-3.47 (m, 14H), 3.39-3.32 (m, 2H), 3.14-2.96 (m, 4H), 2.91 (ddd, J=18.7, 13.5, 5.3 Hz, 1H), 2.82-2.75 (m, 1H), 2.63 (s, 4H), 2.52 (qd, J=13.2, 4.5 Hz, 1H), 2.36 (s, 2H), 2.23-2.07 (m, 3H), 1.89 (s, 3H), 1.86 (s, 3H), 1.11 (br s, 3H). MS m/z (ESI): 910.8 [M+H]+.
E160: 1H NMR (500 MHz, CD3OD) δ 8.26 (s, 1H), 8.11 (s, 1H), 7.75 (dd, J=13.5, 7.6 Hz, 1H), 7.65-7.57 (m, 2H), 7.51-7.36 (m, 4H), 7.03 (d, J=8.0 Hz, 1H), 5.18-5.15 (m, 2H), 4.47 (dd, J=38.1, 17.3 Hz, 2H), 4.26 (s, 1H), 4.15-3.71 (m, 16H), 3.12-3.01 (m, 2H), 3.00-2.88 (m, 1H), 2.81-2.58 (m, 9H), 2.53-2.49 (m, 1H), 2.25-2.10 (m, 1H), 1.89 (s, 3H), 1.86 (s, 3H), 1.07 (br s, 3H). MS m/z (ESI): 910.8 [M+H]+.
Compound E161 (yellow solid, 8.11 mg, formate) was prepared with reference to the method for reference compound C-1.
1H NMR (400 MHz, DMSO-d6) δ 13.18-12.83 (m, 1H), 12.68-12.42 (m, 1H), 12.35-12.14 (m, 1H), 11.03-10.90 (m, 1H), 10.02-9.66 (m, 1H), 8.41-8.28 (m, 1H), 7.81-7.71 (m, 1H), 7.51-7.45 (m, 1H), 7.39 (br s, 1H), 7.36-7.29 (m, 2H), 7.26 (d, J=8.1 Hz, 1H), 6.90 (br s, 1H), 5.17-5.07 (m, 1H), 4.47 (br d, J=17.4 Hz, 3H), 4.25 (br s, 3H), 4.20-4.13 (m, 4H), 3.84 (br s, 3H), 3.74-3.67 (m, 3H), 3.65-3.55 (m, 3H), 3.53-3.42 (m, 2H), 3.26-3.19 (m, 3H), 2.90 (br dd, J=12.6, 4.2 Hz, 3H), 2.69 (s, 3H), 2.31-2.21 (m, 2H), 2.21-2.14 (m, 2H), 1.94-1.87 (m, 3H), 1.84 (s, 3H), 1.81 (s, 3H), 1.09 (br s, 3H). MS m/z (ESI): 918.5 [M+H]+.
Title compound E162 (yellow solid, 8 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (400 MHz, DMSO-d6) δ 11.23 (s, 1H), 11.01 (s, 1H), 8.46-8.33 (m, 1H), 8.25-8.16 (m, 1H), 7.66-7.46 (m, 3H), 7.37-7.28 (m, 3H), 7.22-7.17 (m, 2H), 7.06 (dd, J=13.8, 7.3 Hz, 2H), 5.17-5.10 (m, 1H), 4.89-4.72 (m, 1H), 4.67-4.49 (m, 2H), 4.43-4.00 (m, 8H), 3.87-3.80 (m, 3H), 3.09-2.88 (m, 4H), 2.71-2.65 (m, 2H), 2.42-2.39 (m, 1H), 2.44-2.38 (m, 2H), 2.43-2.37 (m, 1H), 2.37-2.36 (m, 1H), 2.06-1.93 (m, 3H), 1.84-1.73 (m, 8H), 1.67-1.56 (m, 2H), 1.54-1.43 (m, 2H), 1.40-1.34 (m, 2H), 1.16-1.07 (m, 3H) MS m/z (ESI): 912.6 [M+H]+.
Title compound E163 (white solid, 5 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.13 (dd, J=10.0, 5.0 Hz, 1H), 7.96 (s, 1H), 7.57-7.52 (m, 2H), 7.41 (t, J=5.0 Hz, 1H), 7.34 (t, J=5.0 Hz, 1H), 7.24 (d, J=5.0 Hz, 1H), 7.19 (t, J=10.0 Hz, 1H), 7.07 (d, J=5.0 Hz, 1H), 6.67 (s, 1H), 5.05 (dd, J=10.0, 5.0 Hz, 1H), 3.74 (s, 3H), 3.33-3.20 (m, 2H), 3.07-3.05 (m, 1H), 2.98-2.95 (m, 2H), 2.84 (s, 3H), 2.81-2.72 (m, 1H), 2.71-2.40 (m, 15H), 2.27-2.21 (m, 1H), 2.13-2.06 (m, 2H), 1.91-1.88 (m, 2H), 1.76 (s, 3H), 1.73 (s, 3H), 1.60-1.49 (m, 3H), 0.90-0.88 (m, 3H). MS m/z (ESI): 897.5 [M+H]+.
Title compound E164 (white solid, 8 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.48 (s, 1H), 8.02-7.93 (m, 1H), 7.89-7.85 (m, 1H), 7.78-7.68 (m, 2H), 7.65-7.59 (m, 1H), 7.57 (t, J=7.8 Hz, 1H), 7.50 (d, J=7.4 Hz, 1H), 7.46 (s, 1H), 7.33 (d, J=8.0 Hz, 1H), 6.99 (s, 1H), 6.87 (d, J=2.6 Hz, 1H), 5.20 (dd, J=13.4, 5.2 Hz, 1H), 4.75-4.52 (m, 4H), 4.03-3.83 (m, 12H), 3.69-3.58 (m, 1H), 3.40-3.33 (m, 3H), 3.20-3.04 (m, 2H), 3.02-2.91 (m, 1H), 2.86-2.79 (m, 1H), 2.65-2.55 (m, 1H), 2.54-2.32 (m, 4H), 2.29-2.13 (m, 3H), 1.85 (d, J=13.4 Hz, 6H), 1.00 (s, 3H). MS m/z (ESI): 916.8 [M+H]+.
Title compound E165 (yellow solid, 12 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.18 (s, 1H), 8.07 (d, J=2.5 Hz, 1H), 7.97 (s, 1H), 7.87 (d, J=2.0 Hz, 1H), 7.76-7.72 (m, 1H), 7.59 (s, 1H), 7.56-7.53 (m, 1H), 7.48-7.44 (m, 2H), 7.36-7.26 (m, 2H), 6.91 (s, 1H), 6.64-6.58 (m, 1H), 5.17 (dd, J=13.5, 5.5 Hz, 1H), 4.68 (d, J=17.5 Hz, 1H), 4.63-4.58 (m, 2H), 4.53 (d, J=17.5 Hz, 1H), 3.84 (m, 13H), 3.56 (t, J=10.5 Hz, 1H), 3.26 (m, 2H), 3.03-2.86 (m, 3H), 2.86-2.75 (m, 1H), 2.57 (m, 3H), 2.34 (d, J=11.5 Hz, 2H), 2.20 (m, 1H), 2.14-2.02 (m, 2H), 1.80 (s, 3H), 1.77 (s, 3H), 1.07 (s, 3H). MS m/z (ESI): 916.9 [M+H]+.
Title compound E166 (yellow solid, 20 mg, hydrochloride) was to compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.73 (s, 1H), 8.11 (s, 1H), 7.95-7.87 (m, 1H), 7.74 (t, J=7.5 Hz, 2H), 7.61 (t, J=7.5 Hz, 2H), 7.57 (t, J=7.5 Hz, 2H), 7.50 (d, J=7.0 Hz, 2H), 7.46 (s, 1H), 7.33-7.32 (m, 1H), 6.90 (s, 1H), 5.20 (dd, J=13.0, 5.0 Hz, 1H), 4.69 (d, J=17.5 Hz, 1H), 4.62 (t, J=5.0 Hz, 2H), 4.55 (d, J=17.5 Hz, 1H), 4.00-3.64 (m, 13H), 3.58-3.54 (m, 1H), 3.26 (d, J=12.5 Hz, 2H), 2.99-2.92 (m, 3H), 2.87-2.80 (m, 1H), 2.63-2.33 (m, 1H), 2.25-2.20 (m, 1H), 2.12-2.04 (m, 2H), 1.86 (s, 3H), 1.84 (s, 3H), 0.99 (s, 3H). MS m/z (ESI): 917.7 [M+H]+.
Title compound E167 (pale yellow solid, 5.0 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.11 (s, 3H), 7.87 (s, 1H), 7.67 (dd, J=13.8, 7.7 Hz, 1H), 7.57 (t, J=7.8 Hz, 2H), 7.50 (d, J=7.5 Hz, 1H), 7.42 (t, J=6.9 Hz, 2H), 7.33 (d, J=8.1 Hz, 1H), 7.02 (s, 1H), 5.22-5.18 (m, 1H), 4.88-4.50 (m, 4H), 4.06-3.83 (m, 12H), 3.71-3.61 (m, 1H), 3.43-3.34 (m, 3H), 3.18-3.02 (m, 2H), 3.01-2.91 (m, 1H), 2.87-2.78 (m, 1H), 2.68-2.54 (m, 3H), 2.41 (d, J=11.4 Hz, 2H), 2.26-2.12 (m, 3H), 1.80 (d, J=13.5 Hz, 6H), 1.11 (t, J=7.2 Hz, 3H). MS m/z (ESI): 916.4 [M+H]+.
Title compound E168 (white solid, 6 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ7.98 (dd, J=8.2, 4.2 Hz, 1H), 7.91 (s, 1H), 7.78 (s, 1H), 7.72 (s, 1H), 7.62 (t, J=7.2 Hz, 1H), 7.56 (s, 1H), 7.53-7.40 (m, 2H), 7.16 (t, J=7.6 Hz, 1H), 7.05 (d, J=10.1 Hz, 1H), 7.02-6.97 (m, 1H), 6.66 (s, 1H), 5.05-4.97 (m, 1H), 4.48 (s, 2H), 4.41-4.27 (m, 2H), 4.16 (t, J=5.3 Hz, 2H), 3.86 (s, 3H), 3.76 (s, 3H), 2.95 (d, J=11.6 Hz, 2H), 2.85-2.75 (m, 4H), 2.71-2.58 (m, 8H), 2.40-2.30 (m, 4H), 2.07 (dd, J=11.5, 6.2 Hz, 1H), 1.92 (d, J=10.5 Hz, 2H), 1.69 (t, J=17.8 Hz, 6H), 1.64-1.56 (m, 2H), 0.83 (t, J=7.5 Hz, 3H). MS m/z (ESI): 930.7 [M+H]+.
Title compound E170 (white solid, 8 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ8.05 (s, 1H), 7.93 (s, 1H), 7.79 (s, 1H), 7.64 (s, 1H), 7.50 (dd, J=13.1, 7.1 Hz, 1H), 7.42 (t, J=7.8 Hz, 2H), 7.33 (d, J=7.5 Hz, 1H), 7.19 (t, J=16.3 Hz, 3H), 7.12 (s, 1H), 6.69 (s, 1H), 5.10-5.06 (m, 1H), 4.64 (s, 1H), 4.49 (s, 8H), 4.35 (dt, J=47.8, 23.9 Hz, 2H), 4.26 (s, 1H), 3.76 (s, 3H), 3.05 (dd, J=14.5, 5.8 Hz, 4H), 2.91 (s, 3H), 2.73-2.64 (m, 3H), 2.44-2.32 (m, 3H), 2.10 (d, J=5.4 Hz, 2H), 1.74 (d, J=13.6 Hz, 2H), 1.64 (d, J=13.5 Hz, 6H), 0.89 (t, J=7.4 Hz, 3H). MS m/z (ESI): 916.6 [M+H]+.
Title compound E171 (white solid, 6 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ9.03 (s, 1H), 8.39 (d, J=29.2 Hz, 2H), 7.72 (dd, J=13.6, 7.7 Hz, 1H), 7.57 (t, J=7.8 Hz, 3H), 7.52-7.36 (m, 3H), 7.33 (d, J=7.9 Hz, 1H), 7.05 (s, 1H), 5.20 (dd, J=13.3, 5.1 Hz, 1H), 4.79-4.42 (m, 2H), 4.22-3.82 (m, 10H), 3.80-3.50 (m, 4H), 3.41 (s, 2H), 3.32 (s, 2H), 3.26-3.04 (m, 2H), 3.02-2.88 (m, 1H), 2.82 (d, J=17.7 Hz, 1H), 2.71-2.53 (m, 3H), 2.43 (d, J=11.1 Hz, 2H), 2.23 (d, J=5.4 Hz, 3H), 1.81 (d, J=13.5 Hz, 6H), 1.15 (s, 3H). MS m/z (ESI): 917.5 [M+H]+.
Title compound E172 (white solid, 10 mg, hydrochloride) was prepared with reference to the method for compound E67.
1H NMR (500 MHz, CD3OD) δ 8.16-8.01 (m, 2H), 7.90 (s, 1H), 7.80 (s, 1H), 7.72-7.53 (m, 5H), 7.51-7.47 (m, 1H), 7.45 (t, J=7.0 Hz, 1H), 7.22 (d, J=7.5 Hz, 2H), 7.17 (d, J=5.7 Hz, 2H), 5.17 (dd, J=13.3, 5.1 Hz, 1H), 4.98 (dd, J=23.5, 11.3 Hz, 2H), 4.78 (d, J=9.2 Hz, 2H), 4.45 (q, J=17.3 Hz, 2H), 4.03 (d, J=12.0 Hz, 3H), 3.98 (s, 3H), 3.73-3.33 (m, 5H), 2.95-2.84 (m, 1H), 2.79 (ddd, J=17.5, 4.4, 2.3 Hz, 1H), 2.68 (dd, J=14.6, 7.2 Hz, 2H), 2.61-2.24 (m, 5H), 2.22-2.11 (m, 1H), 1.82 (d, J=13.5 Hz, 6H), 1.09 (d, J=7.2 Hz, 3H). MS m/z (ESI): 935.6 [M+H]+.
Title compound E173 (white solid, 3 mg, hydrochloride) was prepared with reference to the method for compound E67.
1H NMR (500 MHz, CD3OD) δ 8.27-8.19 (m, 2H), 7.84 (d, J=10.0 Hz, 1H), 7.77-7.58 (m, 5H), 7.48-7.37 (m, 5H), 7.18 (s, 1H), 5.16 (dd, J=10.0, 5.0 Hz, 1H), 4.81-4.75 (m, 2H), 3.94-3.87 (m, 4H), 3.53-3.37 (m, 4H), 2.95-2.67 (m, 4H), 2.54-2.16 (m, 6H), 1.92 (s, 3H), 1.89 (s, 3H), 1.15-1.13 (m, 3H). MS m/z (ESI): 905.6 [M+H]+.
Title compound E174 (white solid, 6 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 9.01 (s, 1H), 8.08-8.06 (m, 2H), 7.82 (s, 1H), 7.56 (dd, J=10.0, 5.0 Hz, 1H), 7.48-7.32 (m, 5H), 7.21 (d, J=5.0 Hz, 1H), 7.10 (s, 1H), 5.09 (dd, J=10.0, 5.0 Hz, 1H), 4.64-4.44 (m, 5H), 3.98-3.70 (m, 15H), 3.50-3.29 (m, 4H), 2.87-2.75 (m, 2H), 2.67-2.25 (m, 8H), 2.25-2.07 (m, 1H), 1.72 (s, 3H), 1.70 (s, 3H), 1.10-0.95 (m, 3H). MS m/z (ESI): 916.6 [M+H]+.
Title compound E175 (white solid, 5 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 9.12 (s, 1H), 8.24-8.23 (m, 2H), 7.95 (s, 1H), 7.68 (dd, J=10.0, 5.0 Hz, 1H), 7.61-7.44 (m, 5H), 7.32 (d, J=5.0 Hz, 2H), 5.20 (dd, J=10.0, 5.0 Hz, 1H), 4.74-4.56 (m, 5H), 4.05-3.91 (m, 16H), 3.72-3.60 (m, 4H), 2.99-2.91 (m, 1H), 2.84-2.71 (m, 3H), 2.66-2.48 (m, 5H), 2.24-2.19 (m, 1H), 1.86 (s, 3H), 1.83 (s, 3H), 1.19-1.05 (m, 3H). MS m/z (ESI): 930.7 [M+H]+.
Title compound E176 (yellow solid, 14 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.10 (d, J=8.5 Hz, 2H), 7.82 (d, J=2.0 Hz, 1H), 7.70-7.65 (m, 1H), 7.57 (t, J=8.0 Hz, 2H), 7.50 (d, J=7.5 Hz, 2H), 7.44-7.42 (m, 1H), 7.33 (d, J=8.0 Hz, 1H), 7.16 (s, 1H), 6.70 (d, J=2.0 Hz, 1H), 5.20 (dd, J=13.5, 5.0 Hz, 1H), 4.73 (d, J=17.5 Hz, 1H), 4.66 (t, J=5.0 Hz, 2H), 4.57 (d, J=18.0 Hz, 1H), 4.14-3.85 (m, 16H), 3.82-3.74 (m, 1H), 3.60-3.35 (m, 4H), 2.99-2.92 (m, 1H), 2.88-2.80 (m, 1H), 2.67-2.56 (m, 3H), 2.49 (d, J=12.0 Hz, 2H), 2.37 (s, 2H), 2.25-2.20 (m 1H), 1.79 (s, 3H), 1.77 (s, 3H), 1.12 (s, 3H). MS m/z (ESI): 930.5 [M+H]+.
Title compound E177 (yellow solid, 5 mg) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.68 (s, 1H), 7.96 (dd, J=12.5, 7.5 Hz, 1H), 7.73-7.65 (m, 2H), 7.62 (s, 1H), 7.56-7.50 (m, 2H), 7.43 (d, J=7.5 Hz, 1H), 7.27 (dd, J=8.0, 0.5 Hz, 1H), 6.75 (s, 1H), 5.17 (dd, J=13.5, 5.0 Hz, 1H), 4.46 (q, J=17.5 Hz, 2H), 4.40-4.32 (m, 2H), 3.85 (s, 3H), 3.26-2.87 (m, 9H), 2.85-2.69 (m, 4H), 2.63 (s, 3H), 2.56-2.47 (m, 1H), 2.32 (s, 2H), 2.12-2.16 (m, 3H), 1.88 (t, J=12.0 Hz, 2H), 1.82 (s, 3H), 1.79 (s, 3H), 1.35-1.25 (m, 3H), 0.94-0.82 (m, 3H). MS m/z (ESI): 932.7 [M+H]+.
Title compound E178 (yellow solid, 6 mg) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.16 (s, 1H), 8.02 (dd, J=8.0, 4.0 Hz, 1H), 7.99 (d, J=2.0 Hz, 1H), 7.83 (d, J=2.0 Hz, 1H), 7.75-7.71 (m, 3H), 7.58 (t, J=7.5 Hz, 1H), 7.36 (t, J=7.5 Hz, 1H), 7.18 (d, J=2.0 Hz, 1H), 7.13 (dd, J=8.5, 2.0 Hz, 1H), 6.78 (s, 1H), 6.57 (t, J=2.0 Hz, 1H), 5.14 (dd, J=13.5, 5.5 Hz, 1H), 4.52-4.43 (m, 2H), 4.28 (t, J=5.5 Hz, 2H), 3.87 (s, 3H), 3.07 (d, J=11.5 Hz, 2H), 2.95-2.89 (m, 3H), 2.84-2.72 (m, 9H), 2.52-2.41 (m, 4H), 2.22-2.16 (m, 1H), 2.04 (d, J=10.5 Hz, 2H), 1.80 (s, 3H), 1.78 (s, 3H), 1.75-1.67 (m, 2H), 1.36-1.31 (m, 2H), 0.97 (t, J=7.5 Hz, 3H). MS m/z (ESI): 916.7 [M+H]+.
Title compound E179 (yellow solid, 4.5 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (400 MHz, DMSO-d6) δ 12.60-12.40 (m, 1H), 12.55-12.21 (m, 1H), 12.12-11.92 (m, 1H), 10.99 (s, 1H), 9.84-9.62 (m, 1H), 8.40-8.31 (m, 1H), 8.21 (brs, 1H), 7.65 (dd, J=13.4, 7.7 Hz, 1H), 7.53-7.46 (m, 1H), 7.44-7.36 (m, 1H), 7.33 (d, J=7.5 Hz, 1H), 7.28-7.22 (m, 1H), 7.00 (s, 1H), 5.13 (dd, J=13.2, 5.1 Hz, 1H), 4.47 (d, J=17.5 Hz, 2H), 4.40-4.34 (m, 1H), 4.33-4.23 (m, 2H), 4.17 (d, J=4.3 Hz, 2H), 3.88 (s, 2H), 3.82 (s, 4H), 3.80-3.67 (m, 4H), 3.66-3.54 (m, 2H), 3.51-3.37 (m, 1H), 3.29 (d, J=7.1 Hz, 1H), 3.25 (brs, 1H), 3.14 (d, J=10.6 Hz, 2H), 2.99-2.80 (m, 3H), 2.64-2.60 (m, 1H), 2.27-2.14 (m, 2H), 2.05-1.89 (m, 5H), 1.85 (br s, 1H), 1.82 (s, 3H), 1.78 (s, 3H). MS m/z (ESI): 923.5 [M+H]+.
Title compound E180 (yellow solid, 6.6 mg, hydrochloride) was prepared with reference to the method for compound E4.
1H NMR (400 MHz, DMSO-d6) δ 11.18 (s, 1H), 11.06-11.01 (m, 1H), 8.46-8.35 (m, 1H), 8.26 (s, 1H), 8.12 (s, 1H), 7.75-7.68 (m, 1H), 7.66-7.58 (m, 2H), 7.49-7.49 (m, 1H), 7.58-7.49 (m, 2H), 7.42-7.33 (m, 1H), 7.12 (t, J=7.4 Hz, 1H), 6.92 (s, 1H), 5.22-5.14 (m, 1H), 4.51-4.41 (m, 1H), 4.35-4.24 (m, 1H), 3.81 (brs, 2H), 3.79 (s, 3H), 3.66-3.58 (m, 1H), 3.04-2.87 (m, 5H), 2.81-2.68 (m, 4H), 2.68-2.63 (m, 4H), 2.60 (brs, 3H), 2.33-2.24 (m, 4H), 2.09-1.96 (m, 2H), 1.78 (s, 3H), 1.75 (s, 3H), 1.66-1.58 (m, 2H). MS m/z (ESI): 903.4 [M+H]+.
Compound E83 was subjected to 3 SFC separations (mobile phase: 80% EtOH+ACN (0.1% NH3H2O) at supercritical CO2, flow rate: 120 g/min, gradient time: 12 min, total time: 120 min, volume per injection: 2.0 mL) & (mobile phase: 80% EtOH+ACN (0.1% NH3H2O) at supercritical CO2, flow rate: 120 g/min, gradient time: 20 min, total time: 40 min, volume per injection: 10.0 mL) & (mobile phase: 30% EtOH+ACN (0.1% TEA) at supercritical CO2, flow rate: 100 g/min, gradient time: 20 min, total time: 40 min, volume per injection: 10.0 mL) and reverse-phase preparative chromatography (hydrochloric acid system) to give compound E181 (yellow solid, 36.31 mg, hydrochloride, retention time: 5.406 min), compound E182 (yellow solid, 53.5 mg, hydrochloride, retention time: 6.466 min), compound E183 (yellow solid, 65.57 mg, hydrochloride, retention time: 3.052 min), and compound E184 (yellow solid, 44.13 mg, hydrochloride, retention time: 4.406 min).
E181: 1H NMR (400 MHz, DMSO-d6) δ 12.22 (br s, 1H), 11.70 (br s, 1H), 10.99 (s, 1H), 8.42 s, 1H), 8.27 (br s, 1H), 7.75-7.61 (m, 1H), 7.48 (t, J=8.0 Hz, 1H), 7.44-7.25 (m, 4H), 7.08 (d, J=8.0 Hz, 1H), 6.93 (s, 1H), 5.16-5.08 (m, 1H), 4.93-4.88 (m, 2H), 4.39-4.23 (m, 1H), 3.81 (s, 3H), 3.74-3.65 (m, 1H), 3.47 (d, J=5.4 Hz, 1H), 3.26-3.19 (m, 4H), 2.98-2.79 (m, 4H), 2.77-2.67 (m, 1H), 2.65-2.54 (m, 3H), 2.48-2.38 (m, 1H), 2.29-2.16 (m, 3H), 2.15-2.04 (m, 6H), 2.03-1.93 (m, 1H), 1.82 (s, 3H), 1.78 (s, 3H), 1.06 (t, J=7.1 Hz, 3H). MS m/z (ESI): 881.6 [M+H]+.
E182: 1H NMR (400 MHz, DMSO-d6) δ 12.20 (br s, 1H), 11.74 (br s, 1H), 10.99 (br s, 1H), 8.54-8.13 (m, 2H), 7.77-7.60 (m, 1H), 7.53-7.44 (m, 1H), 7.42-7.23 (m, 4H), 7.12 (br d, J=8.0 Hz, 1H), 6.93 (s, 1H), 5.16-5.08 (m, 1H), 4.99-4.86 (m, 2H), 4.39-4.23 (m, 1H), 3.90 (br d, J=10.5 Hz, 1H), 3.80 (s, 3H), 3.53 (br s, 2H), 3.28-3.22 (m, 4H), 2.98-2.77 (m, 3H), 2.70-2.53 (m, 5H), 2.47-2.38 (m, 1H), 2.34-2.26 (m, 1H), 2.26-2.09 (m, 5H), 2.09-1.95 (m, 3H), 1.81 (s, 3H), 1.78 (s, 3H), 1.05 (t, J=7.0 Hz, 3H). MS m/z (ESI): 881.3 [M+H]+.
E183: 1H NMR (400 MHz, DMSO-d6) δ 12.23 (br s, 1H), 11.73 (s, 1H), 10.99 (s, 1H), 8.44 (br s, 1H), 8.22 (br s, 1H), 7.68 (dd, J=13.6, 7.8 Hz, 1H), 7.54-7.43 (m, 1H), 7.43-7.24 (m, 4H), 7.12-6.91 (m, 2H), 5.15-5.08 (m, 1H), 4.95-4.88 (m, 2H), 4.39-4.19 (m, 2H), 3.81 (s, 3H), 3.74-3.66 (m, 1H), 3.47 (br d, J=5.4 Hz, 1H), 3.28-3.16 (m, 4H), 3.02-2.85 (m, 4H), 2.72 (br s, 1H), 2.65-2.55 (m, 3H), 2.48-2.37 (m, 1H), 2.30-2.19 (m, 3H), 2.19-2.05 (m, 5H), 2.04-1.94 (m, 1H), 1.82 (s, 3H), 1.78 (s, 3H), 1.12-1.00 (m, 3H). MS m/z (ESI): 881.3 [M+H]+.
E184: 1H NMR (400 MHz, DMSO-d6) δ 12.21 (br s, 1H), 11.73 (br s, 1H), 11.00 (s, 1H), 8.51 (br s, 1H), 8.34-8.13 (m, 1H), 7.68 (br dd, J=13.6, 7.7 Hz, 1H), 7.52-7.45 (m, 1H), 7.43-7.24 (m, 4H), 7.13 (d, J=8.0 Hz, 1H), 6.94 (br s, 1H), 5.16-5.09 (m, 1H), 4.95-4.89 (m, 2H), 4.42-4.24 (m, 2H), 3.80 (s, 3H), 3.54 (br s, 2H), 3.28-3.20 (m, 4H), 2.99-2.80 (m, 3H), 2.66 (br s, 1H), 2.63-2.55 (m, 4H), 2.49-2.39 (m, 1H), 2.34-2.27 (m, 1H), 2.26-2.11 (m, 5H), 2.10-1.95 (m, 3H), 1.82 (s, 3H), 1.78 (s, 3H), 1.05 (t, J=7.0 Hz, 3H). MS m/z (ESI): 881.6 [M+H]+.
Compound E185 (white solid, 25 mg) was prepared with reference to the method for reference compound C-1.
1H NMR (400 MHz, DMSO-d6) δ 11.23 (s, 1H), 10.99 (s, 1H), 8.41 (brs, 1H), 8.30 (s, 1H), 8.10 (s, 1H), 7.62 (s, 1H), 7.50-7.47 (m, 2H), 7.32-7.27 (m, 3H), 7.10-7.07 (m, 1H), 6.77 (s, 1H), 5.13 (d, J=4.80, 1H), 4.39-4.35 (m, 1H), 4.25-4.21 (m, 3H), 3.84 (s, 3H), 3.18-3.21 (m, 6H), 2.82-2.79 (m, 2H), 2.74-2.71 (m, 4H), 2.60-2.55 (m, 8H), 2.25-2.20 (m, 3H), 1.90-1.88 (m, 1H), 1.88 (s, 3H), 1.75 (s, 3H), 1.61-1.59 (m, 2H). MS m/z (ESI): 898.4 [M+H]+.
Title compound E186 (pale yellow solid, 45 mg) was prepared with reference to the method for compound E67.
1H NMR (400 MHz, DMSO-d6) δ 11.15 (s, 1H), 11.00 (s, 1H), 8.43 (br s, 1H), 8.13-8.11 (m, 2H), 7.58-7.54 (m, 3H), 7.50 (s, 1H), 7.48-7.43 (m, 1H), 7.19-7.17 (m, 2H), 6.90-6.87 (m, 2H), 6.80 (s, 1H), 5.15-5.12 (m, 1H), 4.46-4.27 (m, 2H), 3.98-3.95 (m, 4H), 3.76 (s, 3H), 3.05-2.60 (m, 5H), 2.59-2.53 (m, 4H), 2.48-2.33 (m, 1H), 2.03-1.98 (m, 3H), 1.79 (s, 3H), 1.75 (s, 3H), 1.69-1.60 (m, 2H), 1.07 (t, J=7.2, 3H). MS m/z (ESI): 907.3 [M+H]+.
Title compound E187 (white solid, 62.46 mg) was prepared with reference to the method for compound E67.
1H NMR (400 MHz, DMSO-d6) δ 11.14 (s, 1H), 10.98 (s, 1H), 8.43 (br s, 1H), 8.26-8.20 (m, 1H), 8.15-8.00 (m, 2H), 7.61-7.31 (m, 3H), 7.20-7.07 (m, 3H), 6.72 (s, 1H), 5.10-5.05 (m, 1H), 4.80-4.75 (m, 1H), 4.40-4.20 (m, 2H), 3.75 (s, 3H), 3.00-2.90 (m, 6H), 2.75-2.65 (m, 7H), 2.19-2.09 (m, 3H), 2.00-1.93 (m, 7H), 1.71-1.75 (m, 6H), 1.65-1.57 (m, 2H), 1.06 (br s, 3H). MS m/z (ESI): 881.4 [M+H]+.
Compound E188 (white solid, 35 mg) was prepared with reference to the method for compound E67.
1H NMR (400 MHz, DMSO-d6) δ 11.16 (s, 1H), 11.01 (s, 1H), 8.44 (br s, 1H), 8.15-8.10 (m, 1H), 7.56-7.45 (m, 5H), 7.39-7.36 (m, 2H), 7.25-7.23 (m, 1H), 7.20-7.15 (m, 1H), 7.11-6.98 (m, 1H), 6.80 (s, 1H), 5.16-5.12 (m, 1H), 4.55-4.35 (m, 2H), 3.95-3.90 (m, 4H), 3.78 (s, 3H), 3.05-3.02 (m, 2H), 2.95-2.85 (m, 1H), 2.56 (t, J==6.8, 2H), 2.55-2.53 (m, 5H), 2.03-1.99 (m, 3H), 1.79 (s, 3H), 1.75 (s, 3H), 1.67-1.60 (m, 2H), 1.07 (t, J=7.6, 3H). MS m/z (ESI): 907.4 [M+H]+.
Compound E189 (pale yellow solid, 200 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, DMSO-d6) δ 12.44 (s, 1H), 11.22 (s, 1H), 10.99 (s, 1H), 8.20-7.92 (m, 3H), 7.68 (s, 1H), 7.64-7.57 (m, 2H), 7.53 (d, J=7.2 Hz, 1H), 7.37 (s, 2H), 7.28 (t, J=7.3 Hz, 1H), 6.85 (s, 1H), 5.11-5.07 (m, 1H), 4.66 (s, 2H), 4.42 (d, J=17.4 Hz, 1H), 4.30 (d, J=17.3 Hz, 1H), 3.96-3.59 (m, 16H), 3.42 (d, J=6.4 Hz, 1H), 3.17 (d, J=8.7 Hz, 2H), 2.94-2.87 (m, 1H), 2.81 (s, 2H), 2.60 (d, J=17.1 Hz, 1H), 2.53 (s, 2H), 2.40 (ddd, J=26.4, 13.2, 4.3 Hz, 1H), 2.24 (d, J=8.6 Hz, 2H), 2.04-1.89 (m, 3H), 1.73 (s, 3H), 1.70 (s, 3H), 1.02 (s, 3H). MS m/z (ESI): 949.1 [M+H]+.
Title compound E190 (white solid, 8 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 1H NMR (500 MHz, MeOD) δ 8.17 (dd, J=8.2, 4.2 Hz, 1H), 7.97 (s, 1H), 7.65-7.58 (m, 2H), 7.55 (ddd, J=13.9, 7.7, 1.3 Hz, 1H), 7.42 (t, J=7.9 Hz, 1H), 7.18 (dd, J=11.3, 3.8 Hz, 1H), 6.92-6.84 (m, 2H), 6.68 (s, 1H), 5.09-4.91 (m, 1H), 4.76 (s, 3H), 4.48-4.29 (m, 2H), 3.75 (s, 3H), 3.09-2.90 (m, 4H), 2.87-2.59 (m, 7H), 2.49-2.33 (m, 7H), 2.24 (dd, J=12.9, 8.5 Hz, 3H), 2.13-2.00 (m, 1H), 1.93 (t, J=18.5 Hz, 2H), 1.75 (d, J=13.5 Hz, 6H), 1.69-1.60 (m, 2H), 0.91 (t, J=7.5 Hz, 3H). MS m/z (ESI): 917.1 [M+H]+.
Title compound E191 (white solid, 10 mg, hydrochloride) was prepared with reference to the method for compound C-6.
1H NMR (500 MHz, CD3OD) δ 8.17 (dd, J=8.2, 4.2 Hz, 1H), 7.97 (s, 1H), 7.64-7.58 (m, 2H), 7.55 (ddd, J=13.9, 7.7, 1.3 Hz, 1H), 7.42 (t, J=7.9 Hz, 1H), 7.18 (dd, J=11.3, 3.8 Hz, 1H), 6.92-6.85 (m, 2H), 6.68 (s, 1H), 5.10-4.96 (m, 1H), 4.84-4.77 (m, 2H), 4.40-4.28 (m, 2H), 3.75 (s, 3H), 3.10-2.93 (m, 4H), 2.87-2.51 (m, 8H), 2.47-2.32 (m, 7H), 2.24 (dd, J=12.9, 8.5 Hz, 3H), 2.15-2.01 (m, 1H), 1.95 (d, J=12.9 Hz, 2H), 1.75 (d, J=13.5 Hz, 6H), 1.68-1.55 (m, 2H), 0.91 (t, J=7.5 Hz, 3H). MS m/z (ESI): 911.0 [M+H]+.
Title compound E192 (off-white solid, 7.6 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.34 (s, 1H), 7.92 (dd, J=10.0, 5.0 Hz, 1H), 7.65 (s, 1H), 7.64-7.55 (m, 3H), 7.40 (t, J=10.0 Hz, 1H), 7.07 (s, 1H), 7.01 (d, J=10.0 Hz, 1H), 6.62 (s, 1H), 6.40 (s, 1H), 5.02 (dd, J=10.0, 5.0 Hz, 1H), 4.48 (s, 2H), 4.40-4.31 (m, 2H), 4.16 (t, J=5.0 Hz, 2H), 3.76 (s, 3H), 2.93-2.52 (m, 16H), 2.43-2.34 (m, 2H), 2.26 (s, 3H), 2.22-2.18 (m, 2H), 2.09-2.04 (m, 1H), 1.96-1.94 (m, 2H), 1.74 (s, 3H), 1.71 (s, 3H), 1.65-1.58 (m, 2H), 0.76-0.74 (m, 3H). MS m/z (ESI): 931.0 [M+H]+.
Title compound E193 (yellow solid, 15 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.50 (s, 1H), 8.42 (s, 1H), 7.92-7.88 (m, 1H), 7.84 (d, J=7.5 Hz, 1H), 7.79 (dd, J=8.5, 2.0 Hz, 1H), 7.76-7.69 (m, 1H), 7.64-7.51 (m, 2H), 7.32 (d, J=2.5 Hz, 1H), 7.29-7.17 (m, 2H), 5.15 (dd, J=13.0, 5.0 Hz, 1H), 4.62 (t, J=5.0 Hz, 2H), 4.58-4.44 (m, 2H), 4.24 (s, 3H), 4.04-3.89 (m, 12H), 3.59-3.46 (m, 4H), 2.99-2.78 (m, 2H), 2.64-2.35 (m, 7H), 2.22-2.17 (m, 1H), 1.87 (s, 3H), 1.84 (s, 3H), 1.03 (s, 3H). MS m/z (ESI): 932.2 [M+H]+.
Title compound E194 (pale yellow solid, 10 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.21 (s, 1H), 8.10-7.95 (m, 3H), 7.73-7.65 (m, 2H), 7.62 (t, J=7.8 Hz, 1H), 7.49-7.39 (m, 2H), 7.19-7.13 (m, 2H), 5.17 (dd, J=13.3, 5.1 Hz, 1H), 4.69 (d, J=17.5 Hz, 1H), 4.64 (t, J=4.5 Hz, 2H), 4.53 (d, J=17.5 Hz, 1H), 4.08-3.96 (m, 14H), 3.92-3.75 (m, 6H), 2.98-2.88 (m, 1H), 2.82-2.54 (m, 8H), 2.24-2.16 (m, 1H), 1.82 (s, 3H), 1.79 (s, 3H), 1.05 (t, J=7.1 Hz, 3H). MS m/z (ESI): 949.1 [M+H]+.
Compound E195 (pale yellow solid, 72 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, DMSO-d6) δ 12.51-12.43 (m, 1H), 12.14 (s, 1H), 11.04 (s, 1H), 8.35 (br s, 2H), 7.68-7.62 (m, 3H), 7.35 (br s, 2H), 7.27 (t, J=7.2 Hz, 1H), 6.86 (s, 1H), 5.16 (dd, J=13.3, 5.1 Hz, 1H), 4.84-4.65 (m, 3H), 4.46 (d, J=18.4 Hz, 1H), 3.97-3.66 (m, 13H), 3.50-3.38 (m, 1H), 3.19 (d, J=6.5 Hz, 2H), 3.00-2.90 (m, 1H), 2.81 (d, J=18.8 Hz, 2H), 2.66-2.53 (m, 3H), 2.41 (ddd, J=27.0, 13.6, 4.8 Hz, 1H), 2.25 (d, J=8.9 Hz, 2H), 2.09-1.90 (m, 3H), 1.81 (s, 3H), 1.79 (s, 3H), 1.07 (t, J=7.2 Hz, 3H). MS m/z (ESI): 953.3 [M+H]+.
Title compound E196 (white solid, 7.2 mg, hydrochloride) was prepared with reference to the method for compound C-6.
1H NMR (400 MHz, DMSO-d6) δ 2.24-11.92 (m, 1H), 10.99 (s, 1H), 9.97-9.70 (m, 1H), 8.50-8.13 (m, 2H), 7.72-7.60 (m, 1H), 7.57-7.36 (m, 4H), 7.31-7.17 (m, 2H), 7.05 (br dd, J=7.8, 11.3 Hz, 2H), 6.41 (br s, 1H), 6.29 (br d, J=7.8 Hz, 1H), 5.12 (br dd, J=4.8, 13.3 Hz, 1H), 3.82 (s, 1H), 3.94-3.73 (m, 1H), 3.98-3.65 (m, 1H), 3.52 (br t, J=7.9 Hz, 2H), 3.39-3.30 (m, 1H), 3.42-3.26 (m, 3H), 3.00-2.84 (m, 3H), 2.72 (br s, 2H), 2.53-2.52 (m, 1H), 2.58 (br d, J=17.1 Hz, 1H), 2.47-2.38 (m, 2H), 2.48-2.30 (m, 2H), 2.04-1.95 (m, 1H), 1.86 (br d, J=10.8 Hz, 2H), 1.81 (s, 3H), 1.78 (s, 3H), 1.46-1.45 (m, 1H), 1.05 (t, J=6.9 Hz, 3H); MS m/z (ESI): 889.3 [M+H]+.
Title compound E197 (white solid, 4 mg, hydrochloride) was prepared with reference to the method for compound E67.
1H NMR (500 MHz, CD3OD) δ 8.25-8.19 (m, 2H), 7.81-7.69 (m, 2H), 7.58 (s, 1H), 7.44 (t, J=7.1 Hz, 1H), 7.35 (s, 1H), 7.12 (s, 1H), 7.07 (dd, J=8.4, 2.0 Hz, 1H), 6.99 (s, 1H), 5.15 (dd, J=13.3, 5.2 Hz, 1H), 4.75 (dd, J=13.7, 6.9 Hz, 1H), 4.54-4.41 (m, 2H), 4.08-3.50 (m, 15H), 3.13 (ddd, J=57.2, 38.5, 9.1 Hz, 4H), 2.93 (ddd, J=16.6, 11.1, 4.3 Hz, 1H), 2.85-2.76 (m, 1H), 2.65 (d, J=6.7 Hz, 4H), 2.47-2.26 (m, 3H), 2.11 (dd, J=28.7, 23.6 Hz, 3H), 1.79 (d, J=13.5 Hz, 6H), 1.02 (s, 3H). MS m/z (ESI): 910.6 [M+H]+.
Title compound E198 (white solid, 10 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 7.88 (d, J=3.3 Hz, 1H), 7.81 (dd, J=13.2, 7.8 Hz, 1H), 7.69-7.58 (m, 4H), 7.49 (s, 1H), 7.17 (s, 1H), 7.11 (dd, J=8.4, 2.2 Hz, 1H), 6.78 (s, 1H), 5.04 (dd, J=13.3, 5.2 Hz, 1H), 4.44 (d, J=10.7 Hz, 2H), 4.36 (dd, J=17.7, 9.9 Hz, 2H), 3.97-3.48 (m, 14H), 3.13 (s, 2H), 2.87-2.71 (m, 3H), 2.35 (ddd, J=84.9, 44.7, 9.9 Hz, 6H), 2.07 (dd, J=6.6, 3.7 Hz, 1H), 1.94 (d, J=10.0 Hz, 2H), 1.73 (d, J=13.4 Hz, 6H), 0.88 (s, 3H). MS m/z (ESI): 933.6 [M+H]+.
Title compound E199 (white solid, 4 mg, hydrochloride) was prepared with reference to the method for compound C-6.
1H NMR (500 MHz, CD3OD) δ 8.13 (s, 1H), 8.03 (s, 1H), 7.84 (s, 1H), 7.77 (s, 1H), 7.68 (dd, J=14.3, 7.4 Hz, 1H), 7.56 (t, J=14.3 Hz, 2H), 7.44 (dd, J=18.6, 11.1 Hz, 2H), 7.28 (d, J=7.0 Hz, 1H), 7.08 (s, 1H), 5.14 (dd, J=13.3, 5.2 Hz, 1H), 4.84-4.77 (m, 1H), 4.47 (q, J=16.8 Hz, 2H), 4.01 (s, 3H), 3.86 (d, J=76.6 Hz, 12H), 3.51-3.42 (m, 3H), 3.28-3.12 (m, 4H), 2.93 (ddd, J=18.9, 13.7, 5.5 Hz, 1H), 2.84-2.76 (m, 1H), 2.75-2.58 (m, 4H), 2.56-2.48 (m, 1H), 2.43 (d, J=10.1 Hz, 2H), 2.27 (s, 2H), 2.19 (dd, J=9.0, 3.7 Hz, 1H), 1.81 (d, J=13.5 Hz, 6H), 1.10 (s, 3H). MS m/z (ESI): 975.1 [M+H]+.
Title compound E200 (white solid, 8 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.35 (s, 1H), 7.85 (dd, J=13.0, 7.7 Hz, 1H), 7.75 (d, J=2.6 Hz, 1H), 7.65-7.57 (m, 2H), 7.56-7.42 (m, 2H), 7.39-7.27 (m, 2H), 6.85 (s, 1H), 6.75 (d, J=2.5 Hz, 1H), 5.03 (dd, J=13.3, 5.2 Hz, 1H), 4.67-4.50 (m, 2H), 4.46-4.24 (m, 2H), 4.00-3.62 (m, 12H), 3.54-3.45 (m, 1H), 3.23-3.21 (m, 3H), 3.04-2.88 (m, 2H), 2.87-2.63 (m, 2H), 2.5-2.30 (m, 3H), 2.26 (d, J=11.8 Hz, 2H), 2.13-1.96 (m, 3H), 1.73 (d, J=13.4 Hz, 6H), 0.89 (s, 3H). MS m/z (ESI): 935.1 [M+H]+.
Title compound E201 (white solid, 5 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.29 (dd, J=10.0, 5.0 Hz, 1H), 8.15 (s, 1H), 8.02 (s, 1H), 7.94 (s, 1H), 7.88 (d, J=5.0 Hz, 1H), 7.81 (s, 1H), 7.78-7.69 (m, 2H), 7.42 (t, J=10.0 Hz, 1H), 7.32 (s, 1H), 7.26 (dd, J=20.0, 5.0 Hz, 1H), 6.87 (s, 1H), 5.29 (dd, J=10.0, 5.0 Hz, 1H), 4.65-4.56 (m, 2H), 4.41 (t, J=5.0 Hz, 2H), 4.11 (s, 3H), 4.02 (s, 3H), 3.28 (d, J=10.0 Hz, 2H), 3.07-2.80 (m, 14H), 2.68-2.59 (m, 2H), 2.34-2.29 (m, 1H), 2.20-2.18 (m, 5H), 1.94 (s, 3H), 1.92 (s, 3H), 1.91-1.83 (m, 2H). MS m/z (ESI): 917.0 [M+H]+.
Title compound E202 (yellow solid, 30 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.20 (s, 1H), 8.07 (d, J=2.5 Hz, 1H), 7.90 (s, 1H), 7.88 (d, J=2.0 Hz, 1H), 7.78-7.73 (m, 1H), 7.57-7.48 (m, 2H), 7.47-7.46 (m, 2H), 7.44 (s, 1H), 6.92 (s, 1H), 6.62 (t, J=2.0 Hz, 1H), 5.13 (dd, J=8.5, 5.5 Hz, 1H), 4.63 (t, J=4.5 Hz, 2H), 4.48 (dd, J=27.5, 17.0 Hz, 2H), 4.04-3.45 (m, 14H), 3.33-3.27 (m, 2H), 2.95-2.87 (m, 3H), 2.81-2.77 (m, 1H), 2.56-2.47 (m, 3H), 2.33 (d, J=11.5 Hz, 2H), 2.19-2.16 (m, 1H), 2.07-2.03 (m, 2H), 1.81 (s, 3H), 1.78 (s, 3H), 1.09 (s, 3H). MS m/z (ESI): 935.2 [M+H]+.
Compound E203 (white solid, 25 mg, hydrochloride) was prepared with reference to the method for reference compound C-1.
1H NMR (500 MHz, DMSO-d6) δ 13.04-11.92 (m, 2H), 10.98 (s, 1H), 8.53-8.21 (m, 1H), 8.17-7.97 (m, 1H), 7.75-7.66 (m, 3H), 7.43 (br s, 2H), 7.27 (s, 2H), 7.17 (dd, J=8.4, 2.0 Hz, 1H), 6.84 (s, 1H), 5.09 (dd, J=13.3, 5.0 Hz, 1H), 4.53 (s, 2H), 4.42 (d, J=17.3 Hz, 1H), 4.30 (d, J=17.3 Hz, 1H), 3.80 (s, 5H), 3.70-3.56 (m, 7H), 3.42 (d, J=6.5 Hz, 1H), 3.18 (s, 2H), 2.97-2.86 (m, 1H), 2.81 (s, 2H), 2.62 (dd, J=17.4, 7.3 Hz, 4H), 2.44-2.34 (m, 1H), 2.24 (s, 2H), 2.03-1.89 (m, 3H), 1.84 (d, J=13.7 Hz, 6H), 1.12 (s, 3H). MS m/z (ESI): 891.0 [M+H]+.
Title compound E204 (pale yellow solid, 8.2 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.31 (s, 2H), 7.62 (s, 1H), 7.38 (d, J=60.6 Hz, 3H), 7.12-7.04 (m, 2H), 6.94 (s, 1H), 5.07 (dd, J=13.3, 5.1 Hz, 1H), 4.59 (d, J=17.5 Hz, 1H), 4.53 (t, J=4.3 Hz, 2H), 4.43 (d, J=17.5 Hz, 1H), 4.01-3.72 (m, 13H), 3.64-3.54 (m, 1H), 3.38-3.28 (m, 2H), 3.15-2.96 (m, 2H), 2.92-2.78 (m, 1H), 2.76-2.66 (m, 1H), 2.63-2.53 (m, 2H), 2.52-2.42 (m, 1H), 2.32 (d, J=10.1 Hz, 2H), 2.19-2.05 (m, 3H), 1.81 (d, J=13.5 Hz, 6H), 1.07 (t, J=7.2 Hz, 3H). MS m/z (ESI): 909.0 [M+H]+.
Title product E205 (pale yellow solid, 3.6 mg, hydrochloride) was prepared with reference to the synthesis method for compound E67.
1H NMR (500 MHz, CD3OD) δ 8.50-8.02 (m, 2H), 7.73 (dd, J=13.8, 7.6 Hz, 1H), 7.64-7.52 (m, 2H), 7.45 (t, J=7.3 Hz, 1H), 7.41-7.31 (m, 1H), 7.20 (d, J=7.0 Hz, 1H), 7.04 (s, 1H), 5.24-5.17 (m, 1H), 5.14 (dd, J=13.3, 5.1 Hz, 1H), 4.47 (q, J=17.1 Hz, 2H), 4.32-4.21 (m, 1H), 4.04-3.62 (m, 12H), 3.47-3.37 (m, 2H), 3.21-3.07 (m, 4H), 2.98-2.87 (m, 1H), 2.84-2.72 (m, 3H), 2.66 (d, J=7.3 Hz, 2H), 2.55-2.38 (m, 3H), 2.28-2.16 (m, 3H), 1.91 (d, J=13.5 Hz, 6H), 1.15 (t, J=7.3 Hz, 3H). MS m/z (ESI): 929.1 [M+H]+.
Title product E206 (pale yellow solid, 6.2 mg, hydrochloride) was prepared with reference to the synthesis method for compound E67.
1H NMR (500 MHz, CD3OD) δ 8.16 (s, 1H), 8.08 (s, 1H), 7.96 (d, J=10.3 Hz, 1H), 7.95 (s, 1H), 7.74-7.60 (m, 3H), 7.53 (d, J=9.6 Hz, 1H), 7.47 (t, J=7.0 Hz, 1H), 7.38 (s, 1H), 7.21 (d, J=7.0 Hz, 1H), 5.19 (t, J=6.9 Hz, 1H), 5.14 (dd, J=13.3, 5.1 Hz, 1H), 4.53-4.42 (m, 2H), 4.32-4.23 (m, 1H), 4.06 (s, 3H), 4.04-3.70 (m, 15H), 3.19-3.09 (m, 2H), 2.98-2.88 (m, 1H), 2.83-2.55 (m, 9H), 2.55-2.45 (m, 1H), 2.23-2.15 (m, 1H), 1.82 (d, J=13.5 Hz, 6H), 1.07 (t, J=7.1 Hz, 3H). MS m/z (ESI): 974.5 [M+H]+.
Title compound E207 (white solid, 4.0 mg) was prepared with reference to the synthesis method for compound E111.
1H NMR (500 MHz, CD3OD) δ 8.39-8.19 (m, 1H), 8.16 (s, 1H), 7.77-7.70 (m, 1H), 7.62 (dd, J=7.1, 1.2 Hz, 1H), 7.60-7.52 (m, 3H), 7.45 (t, J=7.1 Hz, 1H), 7.40 (s, 1H), 7.08 (s, 1H), 5.20 (dd, J=13.3, 5.1 Hz, 1H), 4.69 (d, J=17.4 Hz, 1H), 4.57 (d, J=17.4 Hz, 1H), 4.15-3.97 (m, 8H), 3.92 (s, 3H), 3.80-3.70 (m, 3H), 3.46 (dd, J=9.8, 6.0 Hz, 2H), 3.29-3.16 (m, 2H), 2.99-2.91 (m, 1H), 2.86-2.80 (m, 1H), 2.70-2.63 (m, 3H), 2.45 (d, J=10.7 Hz, 2H), 2.31-2.19 (m, 3H), 1.92 (s, 3H), 1.89 (s, 3H), 1.68 (s, 3H), 1.66 (s, 3H), 1.14 (t, J=7.2 Hz, 3H). MS m/z (ESI): 912.6 [M+H]+.
Title compound E208 (pale yellow solid, 10 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.43 (s, 2H), 7.79-7.69 (m, 1H), 7.61-7.41 (m, 5H), 7.17 (s, 1H), 5.16 (dd, J=13.3, 5.1 Hz, 1H), 4.74-4.70 (m, 2H), 4.50 (q, J=17.1 Hz, 2H), 4.14-3.75 (m, 16H), 3.60-3.50 (m, 2H), 2.96-2.88 (m, 1H), 2.83-2.78 (m, 1H), 2.78-2.68 (m, 2H), 2.54-2.46 (m, 3H), 2.40-2.30 (m, 2H), 2.24-2.17 (m, 1H), 1.94 (s, 3H), 1.91 (s, 3H), 1.19 (t, J=7.2 Hz, 3H). MS m/z (ESI): 909.0 [M+H]+.
Target product E209 (pale yellow solid, 15 mg, hydrochloride) was prepared with reference to the synthesis method for compound E67.
1H NMR (500 MHz, CD3OD) δ 8.22 (s, 2H), 7.79-7.70 (m, 2H), 7.62 (t, J=7.7 Hz, 1H), 7.56-7.45 (m, 4H), 7.41 (d, J=7.9 Hz, 1H), 7.38-7.27 (m, 3H), 5.16 (dd, J=13.3, 5.2 Hz, 1H), 5.01-4.92 (m, 2H), 4.76 (d, J=12.8 Hz, 2H), 4.42-4.38 (m, 2H), 4.20 (s, 2H), 4.07-3.93 (m, 4H), 3.97 (s, 3H), 3.78-3.46 (m, 4H), 2.96-2.86 (m, 1H), 2.83-2.74 (m, 1H), 2.72 (q, J=7.3 Hz, 2H), 2.58-2.38 (m, 5H), 2.21-2.13 (m, 1H), 1.90 (d, J=13.6 Hz, 6H), 1.12 (t, J=6.8 Hz, 3H). MS m/z (ESI): 887.4 [M+H]+.
Title compound E210 (yellow solid, 1.5 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.47 (s, 1H), 8.37 (s, 1H), 7.87 (dd, J=13.0, 8.0 Hz, 2H), 7.78 (d, J=8.5 Hz, 1H), 7.71-7.69 (m, 1H), 7.57 (t, J=7.5 Hz, 1H), 7.43 (s, 1H), 7.30 (d, J=2.0 Hz, 1H), 7.24 (dd, J=8.5, 2.5 Hz, 1H), 7.01 (s, 1H), 5.14 (dd, J=13.5, 5.0 Hz, 1H), 4.59 (t, J=4.5 Hz, 2H), 4.48 (dd, J=27.5, 17.0 Hz, 2H), 3.97-3.85 (m, 14H), 3.38-3.32 (m, 2H), 3.18-3.14 (m, 2H), 2.84-2.80 (m, 2H), 2.52-2.40 (m, 5H), 2.21-2.18 (m, 3H), 1.85 (s, 3H), 1.82 (s, 3H), 1.02 (s, 3H). MS m/z (ESI): 917.9 [M+H]+.
Compound 2 (10.14 mg, 32.07 μmol) and p-toluenesulfonic acid (5.52 mg, 32.07 μmol) were added to a solution of compound 211d (20 mg, 32.07 μmol) in ethylene glycol (0.5 mL). The reaction system was then reacted at 80° C. for 10 h. The reaction system was directly separated by preparative chromatography (formic acid system) to give title compound E211 (yellow solid, 2.6 mg). 1H NMR (400 M, DMSO-d6) δ 11.16 (s, 1H), 10.99 (s, 1H), 8.46-8.43 (m, 1H), 8.15-8.11 (m, 2H), 7.67 (d, J=8.0 Hz, 1H), 7.61-7.52 (m, 3H), 7.49-7.46 (m, 1H), 7.40-7.32 (m, 2H), 7.28-7.25 (m, 1H), 7.20-7.01 (m, 2H), 6.88 (s, 1H), 5.12 (dd, J=13.2, 5.2 Hz, 1H), 4.58-4.11 (m, 5H), 3.78 (s, 4H), 3.11-3.08 (m, 2H), 3.00-2.87 (m, 3H), 2.04-1.95 (m, 3H), 1.87-1.80 (m, 3H), 1.77 (d, J=13.2 Hz, 6H), 1.68-1.65 (m, 2H), 1.09 (t, J=7.6 Hz, 3H). MS m/z (ESI): 903.7 [M+H]+.
Compound 212c (135 mg, 188.58 μmol) was dissolved in THE (2 mL) before PPh3 (80.00 mg, 3.05 μmol) and DEAD (45.00 mg, 258 μmol) were added. The system was stirred for 1 min before compound 189d-7 (50.00 mg, 179.7 μmol) was added, and then stirred overnight at 45° C. in a N2 atmosphere, and concentrated at reduced pressure. The crude product was separated by column chromatography and then subjected to prep-HPLC to give compound E212 (white solid, 4.4 mg). 1H NMR (400 MHz, DMSO-d6) δ 11.01 (s, 1H), 10.16 (s, 1H), 8.22-8.15 (m, 1H), 8.07 (s, 1H), 8.01 (s, 1H), 7.74-7.66 (m, 3H), 7.56-7.48 (m, 3H), 7.40 (t, J=7.3 Hz, 1H), 7.10 (t, J=7.0 Hz, 1H), 6.75 (s, 1H), 5.10 (dd, J=12.8, 4.3 Hz, 1H), 4.43-4.26 (m, 2H), 3.84 (s, 3H), 3.80 (s, 3H), 3.04-2.84 (m, 5H), 2.66-2.57 (m, 8H), 2.55-2.33 (m, 6H), 2.04-1.97 (m, 2H), 1.90-1.81 (m, 2H), 1.71 (s, 3H), 1.69 (s, 3H), 1.61-1.48 (m, 2H), 1.32 (s, 6H), 0.88-1.07 (m, 3H). MS m/z (ESI): 976.5 [M+H]+.
Compound E213 (white solid, 1.0 mg) was prepared with reference to the method of Example 212.
1H NMR (400 MHz, DMSO-d6) δ 10.99 (brs, 1H), 10.16 (s, 1H), 8.21-8.16 (m, 1H), 8.07 (s, 1H), 8.01 (s, 1H), 7.74 (s, 1H), 7.69 (s, 1H), 7.66 (s, 1H), 7.53-7.48 (m, 3H), 7.41-7.37 (m, 1H), 7.12-7.09 (m, 1H), 6.75 (s, 1H), 5.06-5.12 (m, 1H), 4.42-4.24 (m, 2H), 4.03 (br s, 2H), 3.84 (s, 3H), 3.79 (s, 3H), 2.93-3.00 (m, 5H), 2.67-2.62 (m, 8H), 2.44-2.24 (m, 5H), 2.01-1.98 (m, 1H), 1.86-1.82 (m, 2H), 1.72 (s, 3H), 1.69 (s, 3H), 1.24 (s, 2H), 1.15 (s, 6H), 0.88-1.07 (m, 3H). MS m/z (ESI): 976.5 [M+H]+.
Title compound E214 (white solid, 10 mg, hydrochloride) was prepared with reference to the method for reference compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.01 (s, 1H), 7.90 (s, 1H), 7.64-7.62 (m, 2H), 7.51 (dd, J=14.3, 8.2 Hz, 1H), 7.42 (t, J=7.8 Hz, 1H), 7.18 (t, J=7.2 Hz, 1H), 7.07 (s, 1H), 7.01 (dd, J=8.5, 2.2 Hz, 1H), 6.91 (s, 1H), 6.68 (s, 1H), 5.10-4.99 (m, 2H), 4.36 (q, J=17.2 Hz, 2H), 4.18 (s, 2H), 3.76 (d, J=4.4 Hz, 3H), 3.35 (t, J=7.1 Hz, 1H), 3.02 (d, J=11.6 Hz, 4H), 2.93-2.75 (m, 6H), 2.74-2.64 (m, 5H), 2.38 (dd, J=13.0, 5.1 Hz, 3H), 2.17 (s, 3H), 2.11-2.02 (m, 3H), 1.72 (s, 2H), 1.64 (d, J=13.5 Hz, 6H), 0.89 (t, J=7.5 Hz, 3H). MS m/z (ESI): 931.0 [M+H]+.
Title compound E215 (white solid, 4.4 mg, hydrochloride) was prepared with reference to the method for reference compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.24-8.16 (m, 2H), 7.81 (s, 1H), 7.79 (d, J=10.0 Hz, 1H), 7.69 (dd, J=15.0, 5.0 Hz, 1H), 7.61-7.56 (m, 2H), 7.45 (t, J=7.5 Hz, 1H), 7.33 (s, 1H), 7.24 (dd, J=20.0, 5.0 Hz, 1H), 5.15 (dd, J=10.0, 5.0 Hz, 1H), 4.63-4.46 (m, 4H), 4.04-3.90 (m, 16H), 3.68-3.62 (m, 4H), 2.97-2.66 (m, 8H), 2.58-2.47 (m, 5H), 2.21-2.18 (m, 1H), 1.87 (s, 3H), 1.84 (s, 3H), 1.22-1.10 (m, 3H). MS m/z (ESI): 944.5 [M+H]+.
Title compound E216 (white solid, 4 mg, hydrochloride) was prepared with reference to the method for compound E67.
1H NMR (500 MHz, CD3OD) δ 8.01 (s, 1H), 7.95 (d, J=7.7 Hz, 3H), 7.83 (d, J=8.2 Hz, 2H), 7.74 (s, 1H), 7.50 (d, J=12.9 Hz, 1H), 7.41 (d, J=7.5 Hz, 2H), 7.00 (s, 1H), 5.20 (dd, J=13.3, 5.1 Hz, 1H), 4.61 (dd, J=30.7, 18.1 Hz, 4H), 4.09-3.58 (m, 17H), 3.10 (s, 2H), 2.96 (d, J=15.4 Hz, 1H), 2.83 (d, J=2.4 Hz, 1H), 2.56 (dd, J=13.0, 8.5 Hz, 3H), 2.43 (s, 3H), 2.38 (d, J=11.9 Hz, 2H), 2.24-2.09 (m, 3H), 1.80 (s, 3H), 1.78 (s, 3H), 1.06 (s, 3H). MS m/z (ESI): 915.0 [M+H]+.
Title compound E217 (white solid, 4 mg, hydrochloride) was prepared with reference to the method for compound E67.
1H NMR (500 MHz, CD3OD) δ 8.01 (s, 1H), 7.89 (s, 1H), 7.87-7.81 (m, 2H), 7.70 (s, 2H), 7.63 (s, 1H), 7.55 (dd, J=12.9, 7.8 Hz, 1H), 7.46 (s, 1H), 7.35-7.23 (m, 2H), 6.91 (s, 1H), 5.09 (dd, J=13.4, 5.2 Hz, 1H), 4.63-4.19 (m, 4H), 3.90 (d, J=16.2 Hz, 3H), 3.84-3.44 (m, 12H), 3.26 (s, 2H), 3.06 (dd, J=14.1, 12.4 Hz, 2H), 2.89-2.64 (m, 2H), 2.52-2.38 (m, 3H), 2.27 (d, J=11.6 Hz, 2H), 2.10 (dd, J=9.1, 3.8 Hz, 3H), 1.69 (d, J=13.5 Hz, 6H), 0.97 (s, 3H). MS m/z (ESI): 901.0 [M+H]+.
Title compound E218 (white solid, 10 mg, hydrochloride) was prepared with reference to the method for reference compound C-1.
1H NMR (500 MHz, DMSO-d6) δ 12.47 (s, 1H), 11.40 (s, 1H), 10.98 (s, 1H), 9.92 (s, 1H), 8.76 (s, 1H), 8.50-7.92 (m, 2H), 7.69 (d, J=8.5 Hz, 1H), 7.61 (dd, J=13.6, 7.9 Hz, 1H), 7.51-7.21 (m, 4H), 7.18 (dd, J=8.4, 2.2 Hz, 1H), 6.88 (s, 1H), 5.12-5.08 (m, 1H), 4.58-4.53 (m, 2H), 4.43 (d, J=17.3 Hz, 1H), 4.31 (d, J=17.3 Hz, 1H), 3.99-3.65 (m, 13H), 3.51-3.34 (m, 1H), 3.27-3.11 (3, 2H), 3.01-2.73 (m, 3H), 2.65-2.53 (m, 3H), 2.45-2.36 (m, 1H), 2.34 (s, 3H), 2.29-2.21 (m, 2H), 2.09-1.90 (m, 3H), 1.70 (d, J=13.6 Hz, 6H), 1.08 (d, J=8.7 Hz, 3H). MS m/z (ESI): 932.1 [M+H]+.
Compound E219 (white solid, 3.71 mg) was prepared with reference to the method for reference compound C-1.
1H NMR (400 MHz, DMSO-d6) δ 10.99 (s, 1H), 10.46 (s, 1H), 8.29-8.50 (m, 2H), 8.08 (s, 1H), 8.05 (s, 1H), 7.64 (d, J=7.8 Hz, 1H), 7.47-7.28 (m, 3H), 7.20 (s, 1H), 7.12-7.04 (m, 2H), 6.79 (s, 1H), 5.09 (dd, J=13.5, 5.2 Hz, 1H), 4.36-4.16 (m, 4H), 3.78 (s, 3H), 3.33-3.11 (m, 5H), 2.92-2.76 (m, 10H), 2.42-2.32 (m, 5H), 2.29 (s, 3H), 2.02-1.81 (m, 5H), 1.66 (s, 3H), 1.62 (s, 3H), 1.07 (t, J=7.3 Hz, 3H). MS m/z (ESI): 931.4 [M+H]+.
Compound E220 (white solid, 2.31 mg) was prepared with reference to the method for reference compound C-1.
1H NMR (400 MHz, DMSO-d6) δ 10.99 (s, 1H), 10.58 (s, 1H), 8.52-8.33 (m, 3H), 8.05 (s, 1H), 7.89 (s, 1H), 7.63 (d, J=8.7 Hz, 1H), 7.55-7.33 (m, 2H), 7.32-7.23 (m, 1H), 7.21-7.15 (m, 1H), 7.07 (d, J=6.8 Hz, 2H), 6.80 (s, 1H), 5.08 (dd, J=13.2, 4.4 Hz, 1H), 4.42-4.10 (m, 4H), 3.77 (s, 3H), 3.08-2.98 (m, 3H), 2.96-2.85 (m, 2H), 2.71-2.60 (m, 11H), 2.42-2.23 (m, 4H), 2.01-1.94 (m, 1H), 1.92-1.83 (m, 2H), 1.70-1.50 (m, 8H), 1.11-1.02 (m, 3H). MS m/z (ESI): 917.4 [M+H]+.
Compound E221 (white solid, 4.55 mg) was prepared with reference to the method for reference compound C-1.
1H NMR (400 MHz, DMSO-d6) δ 11.16 (s, 1H), 10.99 (s, 1H), 8.49-8.39 (m, 1H), 8.34-8.23 (m, 1H), 8.12 (d, J=11.7 Hz, 1H), 7.65-7.60 (m, 1H), 7.58-7.51 (m, 1H), 7.45-7.40 (m, 1H), 7.36-7.28 (m, 1H), 7.20 (s, 1H), 7.13-7.04 (m, 2H), 6.77 (s, 1H), 5.13-5.04 (m, 1H), 4.43-4.37 (m, 1H), 4.31-4.25 (m, 1H), 4.22-4.15 (m, 2H), 3.75 (s, 3H), 3.07-2.97 (m, 4H), 2.75-2.65 (m, 6H), 2.45-2.35 (m, 5H), 2.04-1.94 (m, 2H), 1.91-1.83 (m, 3H), 1.78 (s, 3H), 1.75 (s, 3H), 1.66-1.50 (m, 3H). MS m/z (ESI): 889.5 [M+H]+.
Compound E222 (white solid, 9.56 mg, formate) was prepared with reference to the method for compound E67.
1H NMR (400 MHz, DMSO-d6) δ 11.02 (s, 1H), 10.16 (s, 1H), 8.32 (s, 1H), 8.19-8.18 (m, 1H), 8.07 (s, 1H), 8.00 (s, 1H), 7.73-7.72 (m, 2H), 7.66-7.51 (m, 1H), 7.47-7.39 (m, 1H), 7.11-7.09 (m, 2H), 6.96-6.94 (m, 1H), 6.75 (s, 1H), 5.14-5.13 (m, 1H), 4.95-4.90 (m, 1H), 4.40-4.19 (m, 2H), 3.84 (s, 3H), 3.79 (s, 3H), 3.70-3.60 (m, 3H), 2.99-2.96 (m, 3H), 2.90-2.29 (m, 12H), 2.20-1.83 (m, 8H), 1.71 (s, 3H), 1.68 (s, 3H), 1.56-1.50 (m, 2H), 0.96 (t, J=7.3 Hz, 3H). MS m/z (ESI): 974.5 [M+H]+.
Title compound E223 (white solid, 5 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.19-8.00 (m, 2H), 7.59 (d, J=10.0 Hz, 2H), 7.45-7.21 (m, 3H), 7.00 (s, 1H), 6.95 (d, J=10.0 Hz, 1H), 6.85 (s, 1H), 5.02 (dd, J=10.0, 5.0 Hz, 1H), 4.39-4.30 (m, 2H), 3.91-3.63 (m, 14H), 3.50-3.34 (m, 4H), 3.06 (s, 3H), 2.92-2.66 (m, 4H), 2.56-2.51 (m, 2H), 2.42-2.34 (m, 1H), 2.27-2.25 (m, 2H), 2.07-1.95 (m, 3H), 1.80 (s, 3H), 1.77 (s, 3H), 1.07-0.98 (m, 3H). MS m/z (ESI): 897.8 [M+H]+.
Title compound E224 (white solid, 5.5 mg, hydrochloride) was prepared with reference to the method for reference compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.03 (s, 1H), 7.84 (s, 1H), 7.73 (s, 1H), 7.58 (s, 1H), 7.56-7.51 (m, 2H), 7.44-7.34 (m, 2H), 7.25 (t, J=7.5 Hz, 1H), 6.81 (d, J=10.0 Hz, 2H), 6.75 (s, 1H), 5.00 (dd, J=10.0, 5.0 Hz, 1H), 4.35-4.26 (m, 2H), 3.87 (s, 3H), 3.77 (s, 3H), 3.62-3.45 (m, 4H), 3.13-3.06 (m, 4H), 3.02-2.93 (m, 5H), 2.83-2.32 (m, 12H), 2.17-1.78 (m, 6H), 1.70 (s, 3H), 1.67 (s, 3H), 0.95-0.94 (m, 3H). MS m/z (ESI): 944.1 [M+H]+.
Title compound E225 (white solid, 8 mg, hydrochloride) was prepared with reference to the method for compound C-1.
1H NMR (500 MHz, CD3OD) δ 8.21 (s, 1H), 7.80 (dd, J=10.0, 5.0 Hz, 1H), 7.70-7.68 (m, 2H), 7.62 (d, J=5.0 Hz, 1H), 7.54 (t, J=7.5 Hz, 1H), 7.25 (s, 1H), 7.06 (s, 1H), 6.98 (dd, J=10.0, 5.0 Hz, 1H), 6.62 (s, 1H), 5.01 (dd, J=10.0, 5.0 Hz, 1H), 4.40-4.31 (m, 2H), 4.16 (t, J=7.5 Hz, 2H), 3.76 (s, 3H), 2.94-2.53 (m, 15H), 2.44-2.34 (m, 2H), 2.30 (s, 3H), 2.26-2.21 (m, 2H), 2.09-1.94 (m, 4H), 1.75 (s, 3H), 1.72 (s, 3H), 1.66-1.59 (m, 2H), 0.78-0.75 (m, 3H). MS m/z (ESI): 930.6 [M+H]+.
The present invention is further described with reference to the following test examples, which, however, are not intended to limit the scope of the present invention.
The cell lines used in the present invention (supplied by WUXI APPTEC) are shown in the following table
Half maximal inhibitory concentration (IC50) assay of compounds:
IC50 of compounds in the present invention was determined by Cell Titer GLO reagent from Promega. The procedures are as follows:
Tumor cells were cultured in specified medium in an incubator at 37° C. and 5% CO2. The cells were passaged periodically. Cells at the logarithmic growth phase were collected for plating at a density of 2000-4000 cells/well. The next day, the compounds of the present invention were serially diluted and added to the cells, with DMSO being the negative control and the culture media without cells being the blank control. The plate was incubated in the incubator for 72 h. The cell viability assay was performed by adding the detection reagents to the cell culture media according to Cell Titer GLO reagent instructions and detecting luminescent signals on an EnVision microplate reader (PerkinElmer).
Inhibition of cell growth by the compounds of the present invention was plotted by Prism Graphpad software for statistically calculating the IC50 of the compound of the present invention. The specific data are shown in Tables 5 and 6 below:
The data in Tables 5, 6, and 7 show that the compounds of the examples of the present invention have good inhibitory effects and selectivity in the proliferation activity test of BaF3 cells with various EGFR mutants.
Mouse Ba/F3 cells stably expressing human EGFR-DTC, EGFR-LTC, or EGFR-DC were transferred to Petri dishes with RPMI-1640 medium (Gibco, Product No. 11875093) containing 10% fetal bovine serum (FBS, Biological Industries, Product No. 04-001-1A) and 0.1% penicillin/streptomycin (P/S) and incubated in an aseptic incubator at 37° C., 95% relative humidity, and 5% CO2. Cells at the logarithmic growth phase were taken and seeded at a density of 50000 cells/well in 12-well plates (Corning, Product No. 3513) containing 1 mL of medium per well. After 24 h, the compounds disclosed herein with different concentrations were added to the wells at a final DMSO concentration of 0.1%. After 24 h, cells were lysed in SDS lysis buffer (1.45 g of SDS, 0.2 g of Tris base, 6 mL of glycerol, 20 mg of bromophenol blue, 310 mg DTT; brought to 40 mL with d2H2O), and the EGFR levels were detected and analyzed by Western Blotting (immunoblotting) using standard molecular biological techniques. Cell lysates were boiled at 95° C. for 8 min, mixed and centrifuged. The total cell proteins in the lysates were subjected to SDS-PAGE (GenScript, Product No. M00654), transferred to NC membranes (GE, Product No. 1060002) by blotting, incubated in a blocking buffer (TAKARA, Product No. T7131A) at room temperature for 60 min, and co-incubated overnight at 4° C. with the following primary antibodies: anti-EGFR (#4267S, 1:1000), anti-phoso-EGFR (#3777S, 1:1000), anti-GAPDH (#5174S, 1:10000), anti-Actin (#5125 S, 1:10000) (all purchased from Cell Signaling Technology). The samples were washed three times with TBST at room temperature, each for 10 min, and then incubated for 60 minutes in a blocking buffer containing a secondary antibody (#7074S, 1:10000, purchased from Cell Signaling Technology) at room temperature. The samples were washed three times with TBST at room temperature, each for 10 min. Chemiluminescent substrates were added, and an Azure c300 system was used for imaging.
The DC50 of the compound of the present invention for degrading EGFR-DTC, EGFR-LTC and EGFR-DC is <50 nM, preferably <20 nM, more preferably <10 nM, and even more preferably <5 nM. See Table 8 for the specific results:
The above is a detailed description of the present invention with reference to specific preferred embodiments, and should not be construed as limitations to the present invention. For those skilled in the art of the present invention, various simple deductions or substitutions may be made without departing from the spirit of the present invention, and should be construed as falling within the scope of the present invention.
| Number | Date | Country | Kind |
|---|---|---|---|
| 202110716210.0 | Jun 2021 | CN | national |
| 202110979581.8 | Aug 2021 | CN | national |
| 202210234529.4 | Mar 2022 | CN | national |
| 202210556400.5 | May 2022 | CN | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/CN2022/101684 | 6/27/2022 | WO |
