Patent Application
20230069174
The present invention relates to a nitrogen-containing heterocyclic compound, or a stereoisomer, a solvate, a deuterated form, a pharmaceutically acceptable salt, or a cocrystal thereof or a pharmaceutical composition containing same, and the use thereof in the preparation of a drug for treating/preventing diseases mediated by autotaxin.
Autotaxin (ATX) is an enzyme which is responsible for the increase in lysophosphatidic acid in ascites and plasma, and is a secretory enzyme important for converting lysophosphatidylcholine (LPC) into lysophosphatidic acid (LPA) as a biologically active signaling molecule. Autotaxin (ATX) is a secreted enzyme also referred to as an ectonucleotide pyrophosphatase/phosphodiesterase 2 or lysophospholipase D, and is important for converting lysophosphatidylcholine (LPC) into lysophosphatidic acid (LPA) as a biologically active signaling molecule. ATX plays a role in causing pathological conditions including fibrosis, arthritis, neurodegeneration, neuropathic pain, and cancer.
LPA is a physiologically active lipid having an influence on the migration, proliferation, and survival of various types of cells. Since the LPA level in plasma is highly related to the activity of ATX, it is believed that ATX is an important supply source of extracellular LPA. It has been shown that, in pathological conditions, inhibition of ATX reduces the LPA level. Early experiments with a prototype ATX inhibitor have shown that such a compound is able to inhibit the LPA synthesizing activity in mouse plasma. Early work conducted has demonstrated that LPA can elicit a wide range of cellular response including smooth muscle cell contraction, platelet activation, cell proliferation, chemotaxis, etc. LPA mediates its effects via signaling to several G protein coupled receptors (GPCRs); the first members were originally denoted Edg (endothelial cell differentiation gene) receptors or ventricular zone gene-1 but are now called LPA receptors. The prototypic group now consists of LPA1/Edg-2, VZG-1, LPA2/Edg-4 and LPA3/Edg-7. Recently, three additional LPA receptors LPA4/p2y9/GPR23, LPA5/GPR92 and LPA6/p2y5 have been described that are more closely related to nucleotide-selective purinergic receptors than to the prototypic LPA1-3 receptors. The ATX-LPA signaling axis is involved in a large range of physiological and pathophysiological functions, including, for example, nervous system function, vascular development, cardiovascular physiology, reproduction, immune system function, chronic inflammation, tumor metastasis and progression, organ fibrosis and obesity and/or other metabolic diseases such as diabetes.
Therefore, increased activity of ATX and/or increased levels of LPA, altered LPA receptor expression and altered responses to LPA may contribute to the initiation, progression and/or outcome of a number of different pathophysiological conditions related to the ATX/LPA axis.
As a first technical solution of the present invention, the present invention first provides a nitrogen-containing heterocyclic compound of formula (I) having an inhibitory activity against ATX, or a stereoisomer, a solvate, a deuterated form, a pharmaceutically acceptable salt or a cocrystal thereof,
wherein, M1 is
L1 is a bond, —(CR1R2)a—(NR7)b—W—(CR3R4)c—(NR8)d—(CR5R6)e—, or —C(O)—(CR3R4)c—C═CR7—; W is —C(═X)—, or a 3-6 membered heterocyclene containing 1-3 heteroatoms selected from N, O or S;
X is O, S or NRx, and Rx is H or cyano;
each of R1 to R6 is independently selected from H, halogen, C1-4 alkyl or C3-6 cycloalkyl;
R7 and R8 are each independently selected from H, C1-4 alkyl or C3-6 cycloalkyl; alternatively, R1 and R2 on the same carbon atom, R3 and R4 on the same carbon atom, or R5 and R6 on the same carbon atom together with the carbon atom to which they are attached form a 3-6-membered carbocyclic ring, wherein the carbocyclic ring is optionally substituted with 1-4 substituents selected from halogen or C1-4 alkyl;
a, c and e are independently selected from an integer of 0-5, and b and d are independently 0 or 1;
A is C3-6 cycloalkylene,
C2-4 alkynylene, —RaC(O)NRa′—, —RaNRa′C(O)—, —RaNRa′—, —RaC(O)—, —Ra(CRa′Ra″)n— or a bond;
Ra′ and Ra″ are independently H or C1-4 alkyl;
n is an integer of 1-2;
X1 and X2 are independently N or CRA1, and are not both CRA1 at the same time, and X3 is S, O or NRA1;
X4, X5 and X6 are independently N, NRA1, S, O or CRA1, and are not all CRA1 at the same time;
each RA1 is independently H, cyano, —RA, halogen, —C1-4 alkyl RA, —NHC(O)RA, —C(O)RA, —C1-4 alkyl-O—C1-4 alkyl, —NHRA, —C(O)NHRA or —ORA;
RA is C1-4 alkyl, C3-6 cycloalkyl, C3-6 cycloalkyloxy, C1-4 alkoxy, C1-4 haloalkyl, C1-4 haloalkoxy or a 3-6 membered heterocyclyl containing 1-3 heteroatoms selected from N, O or S, the alkyl, cycloalkyl, cycloalkyloxy, alkoxy, haloalkyl, haloalkoxy and heterocyclyl are optionally further substituted with 1-6 groups selected from C3-6 cycloalkyl, C1-4 alkyl, halogen, —S(O)2C1-4 alkyl, —OC1-4 alkyl or cyano;
Y1 is O, S or NRB3;
Cy has a structure:
wherein, represents a single bond or a double bond, Z1 is C or N, ring E is a 5-membered heterocycle containing 1-3 heteroatoms selected from N, O or S, and ring D is a 6-membered ring containing 0-3 heteroatoms selected from N, O or S; the 5-membered heterocycle and the 6-membered ring are independently and optionally substituted with 1-3 RB2;
RB1 and RB2 are each independently selected from H, oxo, OH, halogen, cyano, C1-4 alkyl, halo C1-4 alkyl, C1-4 alkyloxy or C3-6 cycloalkyl; R33 is selected from H, C1-4 alkyl or C3-6 cycloalkyl;
alternatively, group RA1 on A and group RB1 on B together with the atoms to which they are attached form a 6-10-membered heterocycle containing 1-3 heteroatoms selected from N, S, and O;
f is an integer of 0-3;
L2 is —O—, —NR9—, —C(O)NR9—, —NR9C(O)NR9—, —(CR10R11)g—, —NR9—(CR10R11)g— or a bond,
wherein g is an integer of 1-3;
R9 is H or C1-4 alkyl;
R10 and R11 are each independently H, halogen, C1-4 alkyl or C3-6 cycloalkyl; alternatively,
R10 and R11 on the same carbon atom together with the carbon atom to which they are attached form a 3-6 membered carbocyclic ring;
M2 is
Z2 and Z3 are CRM or N, and Z4 is O, S or NRM1;
each RM is independently H, C1-4 alkyl, C1-4 alkoxyalkyl, cyano, C3-6 cycloalkyl, C3-6 cycloalkyloxy, —SRm′, —S(O)2Rm′, —C(O)NRmRm′, —NRmC(O)Rm′, C2-6 alkenyl, C2-6 alkynyl, —NRM1, a 3-6 membered heterocyclyl containing 1-3 heteroatoms selected from N, O or S, or a halogen, the alkyl, alkenyl, alkynyl, and cycloalkyl are optionally substituted with 1-3 groups selected from halogen, cyano, C1-4 alkoxy, halo C1-4 alkyl or halo C1-4 alkoxy, the heterocyclyl is optionally substituted with 1-3 groups selected from halogen, oxo, and C1-4 alkyl;
alternatively, two RM on adjacent ring carbon atoms in M2 together with the carbon atom to which they are attached form a 3-6 membered carbocyclic ring or a 3-6 membered heterocyclyl containing 0-3 heteroatoms selected from N, O or S;
Rm is H, C1-4 alkyl, and halo C1-4 alkyl;
Rm′ is C1-4 alkyl, and halo C1-4 alkyl;
RM1 is H, C1-4 alkyl, C3-6 cycloalkyl, C1-4 haloalkyl or C1-4 alkoxyalkyl;
RM2 is halo C1-4 alkoxy;
each R12 is independently H, halogen, C1-4 alkyl, C3-6 cycloalkyl or halo C1-4 alkyl;
h is an integer of 0-3;
i is 0, 1 or 2; provided that: when M1 is
L1 is —C(O)—CH2—, A is
L2 is —NH—, and M2 is
RB1 and RB2 are not both H at the same time;
when M1 is
L1 is —C(O)—CH2—, A is
and L2 is NH—CH2—, M2 is not
when M1 is
L1 is —C(O)—CH2—, A is
L2 is —NH—, and M2 is
at least one substituent RA1 in A is selected from cyano, halogen, C3-4 cycloalkyloxy, cyclopropylmethyloxy, C1-4 haloalkoxy, cyclopropylmethyl, —C1-4 alkyl-O—C1-4 alkyl, —NHC(O) RA, —C(O)NHRA, —C(O)—C3-6 cycloalkyl,
and when M1 is
L1 is —C(O)—CH2—, A is
L2 is —NH—, and M2 is
RA1 is not methyl, ethyl or cyclopropyl.
In some embodiments, the nitrogen-containing heterocyclic compound of formula (I), or the stereoisomer, the solvate, the deuterated form, the pharmaceutically acceptable salt or the cocrystal thereof,
wherein, M1 is
L1 is —(CR1R2)a—(NR7)b—W—(CR3R4)c—(NR8)d—(CR5R6)e—, or —C(O)—(CR3R4)c—C═CR7—;
W is —C(═X)—, or a 3-6 membered heterocyclene containing 1-3 heteroatoms selected from N, O or S;
X is O, S or NRx, and Rx is H or cyano;
each of R1 to R6 is independently selected from H, halogen, C1-4 alkyl or C3-6 cycloalkyl;
R7 and R8 are each independently selected from H, C1-4 alkyl or C3-6 cycloalkyl;
alternatively, R1 and R2 on the same carbon atom, R3 and R4 on the same carbon atom, or R5 and R6 on the same carbon atom together with the carbon atom to which they are attached form a 3-6-membered carbocyclic ring, wherein the carbocyclic ring is optionally substituted with 1-4 substituents selected from halogen or C1-4 alkyl;
a, c and e are independently selected from an integer of 0-5, and b and d are independently 0 or 1;
A is C3-6 cycloalkylene,
C2-4 alkynylene or a bond;
n is an integer of 1-2;
X1 and X2 are independently N or CRA1, and are not both CRA1 at the same time, and X3 is S, O or NRA1;
each RA1 is independently H, cyano, —RA, halogen, —C1-4 alkyl RA, —NHC(O) RA, —C(O) RA, —C1-4 alkyl-O—C1-4 alkyl, —NHRA, —C(O)NHRA or —ORA;
RA is C1-4 alkyl, C3-6 cycloalkyl or a 3-6 membered heterocyclyl containing 1-3 heteroatoms selected from N, O or S, wherein the alkyl, cycloalkyl, and heterocyclyl are optionally further substituted with 1-6 groups selected from C3-6 cycloalkyl, C1-4 alkyl, halogen, —S(O)2C1-4 alkyl, —OC1-4 alkyl or cyano;
Y1 is O, S or NRB3;
Cy has a structure:
wherein, represents a single bond or a double bond, Z1 is C or N, ring E is a 5-membered heterocycle containing 1-3 heteroatoms selected from N, O or S, and ring D is a 6-membered ring containing 0-3 heteroatoms selected from N, O or S; the 5-membered heterocycle and the 6-membered ring are independently and optionally substituted with 1-3 RB2;
RB1 and RB2 are each independently selected from H, oxo, OH, halogen, cyano, C1-4 alkyl, halo C1-4 alkyl, C1-4 alkyloxy or C3-6 cycloalkyl; RB3 is selected from H, C1-4 alkyl or C3-6 cycloalkyl;
alternatively, group RA1 on A and group RB1 on B together with the atoms to which they are attached form a 6-10-membered heterocycle containing 1-3 heteroatoms selected from N, S, and O;
f is an integer of 0-3;
L2 is —O—, —NR9—, —(CR10R11)g— or a bond, wherein g is an integer of 1-3;
R9 is H or C1-4 alkyl;
R10 and R11 are each independently H, halogen, C1-4 alkyl or C3-6 cycloalkyl; alternatively,
R10 and R11 on the same carbon atom together with the carbon atom to which they are attached form a 3-6 membered carbocyclic ring;
Z2 and Z3 are CRM or N, and Z4 is O, S or NRM1;
each RM is independently H, C1-4 alkyl, cyano, C3-6 cycloalkyl or halogen, the alkyl and cycloalkyl are optionally substituted with 1-3 groups selected from halogen and cyano;
RM1 is H, C1-4 alkyl or C3-6 cycloalkyl;
h is an integer of 0-3;
provided that: when M1 is
L1 is —C(O)—CH2—, A is
L2 is —NH—, and M2 is
RB1 and RB2 are not both H at the same time;
when M1 is
L1 is —C(O)—CH2—, A is
L2 is —NH—, and M2 is
at least one of substituent RA1 in A is selected from cyano, halogen, C3-4 cycloalkyloxy, cyclopropylmethoxy, C1-4 haloalkoxy, cyclopropylmethyl, —C1-4 alkyl-O—C1-4 alkyl, —NHC(O) RA, —C(O)NHRA, —C(O)—C3-6 cycloalkyl,
and when M1 is
L1 is —C(O)—CH2—, A is
L2 is —NH—, and M2 is
RA1 is not methyl, ethyl or cyclopropyl.
As a second technical solution of the present invention, provided are a nitrogen-containing heterocyclic compound of formula (I), or a stereoisomer, a solvate, a deuterated form, a pharmaceutically acceptable salt or a cocrystal thereof, wherein,
a, c and e are independently selected from an integer of 0-3, and b and d are independently 0 or 1;
W is —C(═X)— or a 5-membered heterocyclene containing 1-2 heteroatoms selected from N and O, wherein X is O, S or NRx, and Rx is cyano;
each of R1 to R6 is independently selected from H, halogen, and C1-4 alkyl, and R7 and R8 are independently selected from H or C1-4 alkyl;
alternatively, R3 and R4 on the same carbon atom, or R5 and R6 on the same carbon atom together with the carbon atom to which they are attached form a 3-4-membered carbocyclic ring, wherein the carbocyclic ring is optionally substituted with 1-2 substituents selected from halogen and C1-2 alkyl;
A is C3-6 cycloalkylene,
alkynylene or a bond;
RA is C1-4 alkyl, C3-4 cycloalkyl, a 4-6-membered heterocyclyl containing 1-2 heteroatoms selected from N and O, wherein the alkyl and heterocyclyl are optionally further substituted with 1-5 groups selected from C3-4 cycloalkyl, C1-4 alkyl, halogen, —S(O)2C1-2 alkyl, —OC1-2 alkyl or cyano,
and the rest of the groups are as defined in the above-mentioned first technical solution.
As a third technical solution of the present invention, provided are a nitrogen-containing heterocyclic compound of formula (I), or a stereoisomer, a solvate, a deuterated form, a pharmaceutically acceptable salt or a cocrystal thereof, wherein,
L1 is —C(═O)—(NH)a—CR3R4—, d is 0 or 1, at least one of R3 and R4 is halogen, or R3 and R4 and the carbon atom to which they are attached form a 3-4-membered carbocyclic ring; or
L1 is —C(═S)—CR3R4—, wherein R3 and R4 are independently selected from H, halogen or C1-4 alkyl; or
L1 is —C(═N—CN)—CR3R4—, wherein R3 and R4 are independently selected from H, halogen or C1-4 alkyl; or
L1 is —C(O)—CR3R4—C═CR7—, wherein R3 and R4 are independently selected from H, halogen or C1-4 alkyl, and R7 is H or C1-4 alkyl; or
L1 is —W—(CR3R4)c—, wherein W is a 5-membered heterocyclene containing 1-2 heteroatoms selected from N or O, and c is an integer of 0-3,
and the rest of the groups are as defined in the above-mentioned first or second technical solution.
As a fourth technical solution of the present invention, provided are a nitrogen-containing heterocyclic compound of formula (I), or a stereoisomer, a solvate, a deuterated form, a pharmaceutically acceptable salt or a cocrystal thereof, wherein the compound has a more specific structure of formula (II):
and the rest of the groups are as defined in the above-mentioned third technical solution.
As a fifth technical solution of the present invention, provided are a nitrogen-containing heterocyclic compound of formula (I), or a stereoisomer, a solvate, a deuterated form, a pharmaceutically acceptable salt or a cocrystal thereof, when L1 is —W—(CR3R4)c—, W is a 5-membered heterocyclene containing 1-2 heteroatoms selected from N and O, and c is an integer of 0-3, the 5-membered heterocyclene is
and the rest of the groups are as defined in the above-mentioned third technical solution.
As a sixth technical solution of the present invention, provided are a nitrogen-containing heterocyclic compound as shown in formula (I), or a stereoisomer, a solvate, a deuterated form, a pharmaceutically acceptable salt or a cocrystal thereof, wherein,
and the rest of the groups are as defined in the above-mentioned first or second technical solution.
As a seventh technical solution of the present invention, provided are a nitrogen-containing heterocyclic compound as shown in formula (I), or a stereoisomer, a solvate, a deuterated form, a pharmaceutically acceptable salt or a cocrystal thereof, wherein M1 is
L2 is —NH—, and M2 is
L2 is —NH—, and M2 is
and the rest of the groups are as defined in the above-mentioned sixth technical solution.
As an eighth technical solution of the present invention, provided are a nitrogen-containing heterocyclic compound as shown in formula (I), or a stereoisomer, a solvate, a deuterated form, a pharmaceutically acceptable salt or a cocrystal thereof, wherein, L2 is —C(O)NR9—, —NR9C(O)NR9—, —O—, or —CR10R11—, at least one of R10 and R11 is halogen or C1-4 alkyl, or R10 and R11 together with the carbon atom to which they are attached form a 3-4-membered carbocyclic ring, and the rest of the groups are as defined in the above-mentioned first or second technical solution.
As a ninth technical solution of the present invention, provided are a nitrogen-containing heterocyclic compound as shown in formula (I), or a stereoisomer, a solvate, a deuterated form, a pharmaceutically acceptable salt or a cocrystal thereof, wherein the compound has a more specific structure of formula (III)
and the rest of the groups are as defined in the above-mentioned eighth technical solution.
As a tenth technical solution of the present invention, provided are a nitrogen-containing heterocyclic compound as shown in formula (I), or a stereoisomer, a solvate, a deuterated form, a pharmaceutically acceptable salt or a cocrystal thereof, wherein:
A is C3-6 cycloalkylene, C2-4 alkynylene,
X1 is N or CRA1, X3 is S, O or NRA1, each RA1 is independently H, cyano, —RA, halogen, —C1-4 alkyl RA, —NHC(O)RA, —C(O)RA, —C1-4 alkyl-O—C1-4 alkyl, —NHRA, —C(O)NHRA or —ORA, Ra is
Ra′ is H or C1-4 alkyl, and the rest of the groups are as defined in the above-mentioned first or second technical solution; or
n is not 0, at least one RA1 is selected from cyano, halogen, C3-4 cycloalkyloxy, cyclopropylmethoxy, halo C1-4 alkoxy, cyclopropylmethyl, —C1-4 alkyl-O—C1-4 alkyl, —NHC(O)RA, —C(O)NHRA, —C(O)—C3-6 cycloalkyl,
and the rest of the groups are as defined in the above-mentioned first or second technical solution.
As an eleventh technical solution of the present invention, provided are a nitrogen-containing heterocyclic compound as shown in formula (I), or a stereoisomer, a solvate, a deuterated form, a pharmaceutically acceptable salt or a cocrystal thereof, wherein the compound has a more specific structure of formula (IV)
L1 is —C(O)—(CR5R6)e—, and the definition of the rest of the groups are as defined in the above-mentioned tenth technical solution.
As a twelfth technical solution of the present invention, provided are a nitrogen-containing heterocyclic compound as shown in formula (I), or a stereoisomer, a solvate, a deuterated form, a pharmaceutically acceptable salt or a cocrystal thereof, wherein:
wherein at least one of RB1 and RB2 is selected from OH, halogen, cyano, halo C1-4 alkyl, C1-4 alkyloxy and C3-6 cycloalkyl, or group RA1 on A and group RB1 on B together with the atoms to which they are attached form a 6-8-membered heterocycle containing 1 O atom, and the rest of the groups are as defined in the above-mentioned first or second technical solution; or
wherein RB2 is halogen or cyano, f is 1, 2 or 3, and the rest of the groups are as defined in the above-mentioned first or second technical solution; or
wherein the rest of the groups are as defined in the above-mentioned first or second technical solution.
As a thirteenth technical solution of the present invention, provided are a nitrogen-containing heterocyclic compound as shown in formula (I), or a stereoisomer, a solvate, a deuterated form, a pharmaceutically acceptable salt or a cocrystal thereof, wherein the compound has a more specific structure of formula (V)
wherein B is
at least one of RB1 and RB2 is selected from OH, halogen, cyano, halo C1-4 alkyl, C1-4 alkyloxy or C3-6 cycloalkyl, and the rest of the groups are as defined in the above-mentioned twelfth technical solution; or
RB2 is halogen or cyano, f is 1, 2 or 3, and the rest of the groups are as defined in the above-mentioned twelfth technical solution; or
and the rest of the groups are as defined in the above-mentioned twelfth technical solution.
As a fourteenth technical solution of the present invention, provided are a nitrogen-containing heterocyclic compound as shown in formula (I), or a stereoisomer, a solvate, a deuterated form, a pharmaceutically acceptable salt or a cocrystal thereof, wherein the compound has a more specific structure of formula (VI)
wherein, L1 is —C(═O)—(CR3R4)c—(NR8)c—, c is an integer of 0-3, d is 0 or 1, R3, R4 and R8 are independently selected from H, C1-3 alkyl or halogen, and R3 and R4 together with the carbon atom to which they are attached form a 3-6 membered carbocyclic ring, wherein the carbocyclic ring is optionally substituted with 1-4 substituents selected from halogen or C1-4 alkyl; A is
or a bond;
Cy has a structure:
wherein, represents a single bond or a double bond, Z1 is C or N, ring E is a 5-membered heterocycle containing 1-3 heteroatoms selected from N, O or S, ring D is a saturated or unsaturated 6-membered ring containing 0-3 heteroatoms selected from N, O or S; the 5-membered heterocycle and the 6-membered ring are independently and optionally substituted with 1-3 RB2;
each RB2 is independently selected from H, halogen, cyano, C1-4 alkyl and halo C1-4 alkyl; L2 is —NH— or a bond,
and the rest of the groups are as defined in the above-mentioned first or second technical solution.
As a fifteenth technical solution of the present invention, provided are a nitrogen-containing heterocyclic compound as shown in formula (I), or a stereoisomer, a solvate, a deuterated form, a pharmaceutically acceptable salt or a cocrystal thereof, wherein,
is selected from one of the following structures, and the rest of the groups are as defined in the above-mentioned fourteenth technical solution:
As a sixteenth technical solution of the present invention, provided are a nitrogen-containing heterocyclic compound as shown in formula (I), or a stereoisomer, a solvate, a deuterated form, a pharmaceutically acceptable salt or a cocrystal thereof, wherein: when M2 is
h is not 0, and at least one RM is halo C1-4 alkyl, cyano, C3-6 cycloalkyl, C2-6 alkynyl or a 3-6 membered heterocyclyl containing 1-3 heteroatoms selected from N, O or S, the alkyl is optionally substituted with 1-3 groups selected from halogen or cyano, and the heterocyclyl is optionally substituted with 1-3 groups selected from halogen, oxo or C1-4 alkyl; or, alternatively, two RM on adjacent ring carbon atoms in M2 together with the carbon atoms to which they are attached form a 3-6 membered carbocyclic ring or a 3-6 membered heterocyclyl containing 0-3 heteroatoms selected from N, O or S; and the rest of the groups are as defined in the above-mentioned first or second technical solution; preferably, M2 is
wherein RM is trifluoromethyl, difluoromethyl, cyclopropyl, ethynyl, furan-3-yl, methylaminocarbonyl, azetidin-1-yl, oxetan-3-yl, 3,3-difluoro-azetidin-1-yl, acetamido, 1-methyl-1H-pyrazol-4-yl, tetrahydrofuran-3-yl, methylthio, 4-methyl-5-oxo-1,2,4-triazol-1-yl, 2-oxo-pyrrolidin-1-yl, methylsulfonyl, methoxymethyl, difluoromethoxymethylor trifluoromethyl ethynyl; more preferably, M2 is
preferably, M2 is
wherein RM is C1-4 alkyl, and the alkyl is substituted with 1-3 halogens (preferably F); preferably trifluoromethyl or difluoromethyl; when M2 is
each substituent is as defined in the above-mentioned first or second technical solution.
As a seventeenth technical solution of the present invention, provided are a nitrogen-containing heterocyclic compound as shown in formula (I), or a stereoisomer, a solvate, a deuterated form, a pharmaceutically acceptable salt or a cocrystal thereof, wherein the compound has a more specific structure of formula (VII)
and M2 is as defined in the above-mentioned sixteenth technical solution.
As a eighteenth technical solution of the present invention, provided are a nitrogen-containing heterocyclic compound as shown in formula (I), or a stereoisomer, a solvate, a deuterated form, a pharmaceutically acceptable salt or a cocrystal thereof,
wherein, M1 is
L1 is —(CR1R2)a—(NR7)b—W—(CR3R4)c—(NR8)d—(CR5R6)e—;
a and b are 0, c is 1 or 2, and d and e are 0;
R3 and R4 are each independently selected from H, halogen and C1-4 alkyl, and are not both
H at the same time;
wherein both RB1 and RB2 are H;
L2 is —NR9—, and R9 is H;
wherein Z2 and Z3 are CRM, and Z4 is O or S;
each R12 is independently H, halogen, C1-4 alkyl, C3-6 cycloalkyl or halo C1-4 alkyl;
h is 0, 1 or 2;
each RM is independently H or C1-4 alkyl, the alkyl is optionally substituted with 1-3 halogens;
and the rest of the groups are as defined in the above-mentioned first or second technical solution.
As a nineteenth technical solution of the present invention, provided are a nitrogen-containing heterocyclic compound as shown in formula (I), or a stereoisomer, a solvate, a deuterated form, a pharmaceutically acceptable salt or a cocrystal thereof,
wherein, M1 is
L1 is a bond or —(CR1R2)a—(NR7)b—W—(CR3R4)c—(NR8)d—(CR5R6)e—;
X is O, S or NRx, and Rx is H or cyano;
each of R1 to R6 is independently selected from H, halogen, C1-4 alkyl or C3-6 cycloalkyl;
R7 and R8 are each independently selected from H, C1-4 alkyl or C3-6 cycloalkyl; alternatively, R1 and R2 on the same carbon atom, R3 and R4 on the same carbon atom, or R5 and R6 on the same carbon atom together with the carbon atom to which they are attached form a 3-6-membered carbocyclic ring, wherein the carbocyclic ring is optionally substituted with 1-4 substituents selected from halogen or C1-4 alkyl;
a, c and e are independently selected from 0, 1, 2 and 3, and b and d are independently 0 or 1;
Ra′ and Ra″ are H or C1-4 alkyl;
n is 1 or 2;
X1 and X2 are independently N, NRA1 or CRA1, and are not both CRA1 at the same time;
X4, X5 and X6 are independently N, NRA1, S, O or CRA1, and are not all CRA1 at the same time;
each RA1 is independently substituted with substituents of H, cyano, —RA, halogen, —C1-4 alkyl RA, —NHC(O)RA, —C(O)RA, —C1-4 alkyl-O—C1-4 alkyl, —NHRA, —C(O)NHRA, and —ORA;
RA is C1-4 alkyl, C3-6 cycloalkyl or a 3-6 membered heterocyclyl containing 1-3 heteroatoms selected from N, O or S, the alkyl, cycloalkyl, and heterocyclyl are optionally further substituted with 1-6 groups selected from C3-6 cycloalkyl, C1-4 alkyl, halogen, —S(O)2C1-4 alkyl, —OC1-4 alkyl or cyano;
RB1 and RB2 are each independently selected from H, OH, halogen, cyano, C1-4 alkyl, halo C1-4 alkyl, C1-4 alkyloxy or C3-6 cycloalkyl;
L2 is —O—, —NR9—, —(CR10R11)g—, —NR9—(CR10R11)g— or a bond, wherein g is an integer of 1-3; R9 is H or C1-4 alkyl;
R10 and R11 are each independently H, halogen, C1-4 alkyl or C3-6 cycloalkyl; alternatively,
R10 and R11 on the same carbon atom together with the carbon atom to which they are attached form a 3-6 membered carbocyclic ring;
Z2 and Z3 are CRM or N, and Z4 is O, S or NRM1;
each RM is independently H, C1-4 alkyl, cyano, C3-6 cycloalkyl, —SRm′, —S(O)2Rm′, —C(O)NRmRm′, —NRmC(O)Rm′, C2-6 alkynyl, a 3-6 membered heterocyclyl containing 1-3 heteroatoms selected from N, O or S, or halogen, the alkyl, alkynyl, and cycloalkyl are optionally substituted with 1-3 groups selected from halogen, cyano, C1-4 alkoxy, halo C1-4 alkyl or halo C1-4 alkoxy, the heterocyclyl is optionally substituted with 1-3 groups selected from halogen, oxo, and C1-4 alkyl;
Rm is H, C1-4 alkyl, and halo C1-4 alkyl, Rm′ is C1-4 alkyl and halo C1-4 alkyl; alternatively, two RM on adjacent ring carbon atoms in M2 together with the carbon atom to which they are attached form a 3-6 membered carbocyclic ring or a 3-6 membered heterocyclyl containing 0-2 heteroatoms selected from N, O or S;
RM1 is H, C1-4 alkyl or C3-6 cycloalkyl;
RM2 is halo C1-4 alkoxy;
each R12 is independently H, halogen, C1-4 alkyl, C3-6 cycloalkyl or halo C1-4 alkyl;
h is an integer of 0-3;
i is 0, 1 or 2;
provided that, the compound is not:
As a twentieth technical solution of the present invention, provided are a nitrogen-containing heterocyclic compound as shown in formula (I), or a stereoisomer, a solvate, a deuterated form, a pharmaceutically acceptable salt or a cocrystal thereof, wherein, L1 is a bond or —W—(CR3R4)c—;
R3 and R4 are each independently selected from H, halogen or C1-4 alkyl;
alternatively, R3 and R4 on the same carbon atom together with the carbon atom to which they are attached form a 3-6 membered carbocyclic ring;
c is selected from 0, 1 and 2;
Ra′ and Ra″ are H or C1-4 alkyl;
n is 1 or 2;
X1 and X2 are independently N, NRA1 or CRA1, and are not both CRA1 at the same time;
X4, X5 and X6 are independently N, NRA1, S, O or CRA1, and are not all CRA1 at the same time;
each RA1 is independently H;
both RB1 and RB2 are H;
L2 is —NR9— or —NR9—(CR10R11)g—, wherein g is an integer of 1-3;
R10 and R11 are each independently H;
Z2 and Z3 are CRM, and Z4 is O or S;
each RM is independently H, C1-4 alkyl, C3-6 cycloalkyl, —SRm′, —S(O)2Rm′, —C(O)NRmRm′, —NRmC(O)Rm′, C2-6 alkynyl, a 3-6 membered heterocyclyl containing 1-3 heteroatoms selected from N, O or S, or halogen, the alkyl, alkynyl, and cycloalkyl are optionally substituted with 1-3 groups selected from halogen, C1-4 alkoxy, halo C1-4 alkyl or halo C1-4 alkoxy, the heterocyclyl is optionally substituted with 1-3 groups selected from halogen, oxo, and C1-4 alkyl;
Rm is H or C1-4 alkyl, and Rm′ is C1-4 alkyl;
alternatively, two RM on adjacent ring carbon atoms in M2 together with the carbon atom to which they are attached form a 3-6 membered carbocyclic ring or a 3-6 membered heterocyclyl containing 0-2 heteroatoms selected from N, O or S; RM2 is halo C1-4 alkoxy;
h is 0, 1 or 2;
i is 0, 1 or 2;
and the rest of the groups are as defined in the above-mentioned nineteenth technical solution.
As a twenty-first technical solution of the present invention, provided are a nitrogen-containing heterocyclic compound as shown in formula (I), or a stereoisomer, a solvate, a deuterated form, a pharmaceutically acceptable salt or a cocrystal thereof, wherein, M2 is
h is 1 or 2,
RM is C1-4 alkyl, C3-6 cycloalkyl, —SRm′, —S(O)2Rm′, —C(O)NRmRm′, —NRmC(O)Rm′, C2-6 alkynyl or a 3-6 membered heterocyclyl containing 1-3 heteroatoms selected from N, O or S, the alkyl is optionally substituted with 1-3 groups selected from halogen, C1-4 alkoxy or halo C1-4 alkoxy, and the heterocyclyl is optionally substituted with 1-3 groups selected from halogen, oxo, and C1-2 alkyl;
alternatively, two RM on adjacent ring carbon atoms in M2 together with the carbon atom to which they are attached form a 3-6 membered carbocyclic ring or a 3-6 membered heterocyclyl containing 0-2 heteroatoms selected from N, O or S;
and the rest of the groups are as defined in the above-mentioned twentieth technical solution.
As a twenty-second technical solution of the present invention, provided are a nitrogen-containing heterocyclic compound as shown in formula (I), or a stereoisomer, a solvate, a deuterated form, a pharmaceutically acceptable salt or a cocrystal thereof, wherein, M2 is
and the rest of the groups are as defined in the above-mentioned twentieth technical solution.
As a twenty-third technical solution of the present invention, provided are a nitrogen-containing heterocyclic compound as shown in formula (I), or a stereoisomer, a solvate, a deuterated form, a pharmaceutically acceptable salt or a cocrystal thereof, wherein, c is 1 or 2, and R3 and R4 on the same carbon atom together with the carbon atom to which they are attached form a 3-6 membered carbocyclic ring, and the rest of the groups are as defined in the above-mentioned twentieth technical solution.
As a twenty-fourth technical solution of the present invention, provided are a nitrogen-containing heterocyclic compound as shown in formula (I), or a stereoisomer, a solvate, a deuterated form, a pharmaceutically acceptable salt or a cocrystal thereof, wherein,
L1 is —W—(CR3R4)c— or —W—(NR8)d—(CR5R6)e—;
R3, R4, R5 and R6 are each independently selected from H, halogen or C1-4 alkyl; each R8 is independently selected from H, C1-4 alkyl or C3-6 cycloalkyl;
alternatively, R3 and R4 on the same carbon atom, or R5 and R6 on the same carbon atom together with the carbon atom to which they are attached form a 3-6 membered carbocyclic ring;
c and e are independently selected from 0 or 1, and d is 1;
X1 and X2 are independently N or CRA1, and are not both CRA1 at the same time;
RA1 is cyano, C1-4 alkyl, —RA or halogen;
RA is C3-6 cycloalkyl, C3-6 cycloalkyloxy, C1-4 alkoxy, C1-4 haloalkyl, and C1-4 haloalkoxy, wherein the cycloalkyl, cycloalkyloxy, alkoxy, haloalkyl, and haloalkoxy are optionally further substituted with 1-3 groups selected from C1-4 alkyl, halogen and cyano;
both RB1 and RB2 are H;
L2 is —NR9—;
R9 is H or C1-4 alkyl;
Z2 and Z3 are CRM or N, and Z4 is O or S;
each RM is independently H, C1-4 alkyl, C1-4 alkoxyalkyl, cyano, C3-6 cycloalkyl, C3-6 cycloalkyloxy, C2-6 alkenyl, C2-6 alkynyl, —NRM1, or a 3-6 membered heterocyclyl containing 1-3 heteroatoms selected from N, O or S, wherein the alkyl, alkenyl, alkynyl, and cycloalkyl are optionally substituted with 1-3 groups selected from halogen and cyano, and the heterocyclyl is optionally substituted with 1-3 groups selected from halogen or C1-4 alkyl; alternatively, two RM on adjacent ring carbon atoms in M2 together with the carbon atoms to which they are attached form a 3-6 membered carbocyclic ring or a 3-6 membered heterocyclyl containing 0-3 heteroatoms selected from N, O or S;
RM1 is H, C1-4 alkyl, C3-6 cycloalkyl, C1-4 haloalkyl or C1-4 alkoxyalkyl;
each R12 is independently H, halogen or C1-4 alkyl;
h is an integer of 0-3;
and i is 0, 1 or 2.
As a twenty-fifth technical solution of the present invention, provided are a nitrogen-containing heterocyclic compound as shown in formula (I), or a stereoisomer, a solvate, a deuterated form, a pharmaceutically acceptable salt or a cocrystal thereof, wherein,
Z2 is CRM;
each RM is independently H, C1-4 alkyl, C1-4 alkoxyalkyl, C3-6 cycloalkyloxy, C2-6 alkenyl, C2-4 alkynyl, —NRM1, or a 3-6 membered heterocyclyl containing 1-3 heteroatoms selected from N, O or S, the alkyl, alkenyl and alkynyl are optionally substituted with 1-3 halogens and cyano;
alternatively, two RM on adjacent ring carbon atoms in M2 together with the carbon atoms to which they are attached form a 3-6 membered carbocyclic ring or a 3-6 membered heterocyclyl containing 0-3 heteroatoms selected from N, O or S; RM1 is H, C1-4 alkyl or C3-6 cycloalkyl;
h is 1 or 2;
and the rest of the groups are as defined in the above-mentioned seventeenth or twenty-fourth technical solution.
As a twenty-sixth technical solution of the present invention, provided are a nitrogen-containing heterocyclic compound as shown in formula (I), or a stereoisomer, a solvate, a deuterated form, a pharmaceutically acceptable salt or a cocrystal thereof, wherein, L1 is —C(O)CR3R4—;
R3 and R4 are independently selected from H, halogen and C1-4 alkyl;
h is 1 or 2;
each RM is independently H, C1-4 alkyl or C2-4 alkynyl; the alkyl or alkynyl is optionally substituted with 1-3 groups selected from halogen and cyano;
and R3, R4 and RM are not all H at the same time.
As a twenty-seventh technical solution of the present invention, provided are a nitrogen-containing heterocyclic compound as shown in formula (I), or a stereoisomer, a solvate, a deuterated form, a pharmaceutically acceptable salt or a cocrystal thereof, wherein, the compound is selected from one of the following structures:
Secondly, the present invention also provides a pharmaceutical composition comprising a pharmaceutically effective amount of the nitrogen-containing heterocyclic compound of any one of the above-mentioned embodiments, or the stereoisomer, the solvate, the deuterated form, the pharmaceutically acceptable salt or the cocrystal thereof, and a pharmaceutically acceptable adjuvant and/or carrier.
Further, the present invention also provides the use of the nitrogen-containing heterocyclic compound of any one of the above-mentioned embodiments, or the stereoisomer, the solvate, the deuterated form, the pharmaceutically acceptable salt, or the cocrystal thereof or the composition containing same in the preparation of a drug for treating/preventing diseases mediated by autotaxin; and the use of the nitrogen-containing heterocyclic compound of any one of the above-mentioned embodiments, or the stereoisomer, the solvate, the deuterated form, the pharmaceutically acceptable salt or the cocrystal thereof, or the composition containing same for treating or preventing diseases mediated by autotaxin.
Use of the above-mentioned two items, wherein, the diseases mediated by autotaxin are selected from cardiovascular conditions, cancers, metabolism disorders, kidney conditions, hepatic conditions, inflammatory conditions, nervous system conditions, respiratory system conditions, fibrotic diseases, ophthalmic conditions, cholestasis and other forms of chronic itch and acute or chronic organ-graft rejection.
preferably, the inflammatory conditions include but are not limited to arthritis, atopic dermatitis, arthritis and asthma.
A nitrogen-containing heterocyclic compound as shown in formula (I) having an inhibitory activity against ATX, or a stereoisomer, a solvate, a deuterated form, a pharmaceutically acceptable salt or a cocrystal thereof,
in some embodiments, M1 is
and in some embodiments, M1 is
in some embodiments, M1 is
in some embodiments, L1 is a bond, —(CR1R2)a—(NR7)b—W—(CR3R4)c—(NR8)d—(CR5R6)e—, or —C(O)—(CR3R4)c—C═CR7—; in some embodiments, L1 is —C(═O)—(NH)a—CR3R4—; in some embodiments, L1 is —C(═S)—CR3R4—; in some embodiments, L1 is C(═N—CN)—CR3R4—; in some embodiments, L1 is —C(O)—CR3R4—C═CR7—; in some embodiments, L1 is —W—(CR3R4)c—; in some embodiments, L1 is —W—(CR3R4)c— or —W—(NR8)d—(CR5R6)e—; in some embodiments, L1 is —C(O)—CF2—; in some embodiments, L1 is —C(O)—CHF—; in some embodiments, L1 is —C(O)—C(CH3)(F)—; in some embodiments, L1 is —C(O)—(CR3R4)—, wherein R3 and R4 form a 3-4-membered carbocyclic ring together, such as cyclopropyl; in some embodiments, L1 is —C(O)—NH—(CR5R6)—, wherein R5 and R6 form a 3-4-membered carbocyclic ring together; in some embodiments, W is —C(═X)—, or a 3-6 membered heterocyclene containing 1-3 heteroatoms selected from N, O or S; in some embodiments, W is —C(═X)—, or a 5-membered heterocyclene containing 1-2 heteroatoms selected from N and O; in some embodiments, the 5-membered heterocyclene is N.
in some embodiments, X is O, S or NRx, wherein Rx is H or cyano; in some embodiments, X is O, S or NRx, wherein Rx is cyano; in some embodiments, X is O or S;
in some embodiments, each of R1 to R6 is independently selected from H, halogen, C1-4 alkyl or C3-6 cycloalkyl; in some embodiments, each of R1 to R6 is independently selected from H, halogen or C1-4 alkyl;
in some embodiments, R1 and R2 on the same carbon atom, R3 and R4 on the same carbon atom, or R5 and R6 on the same carbon atom together with the carbon atom to which they are attached form a 3-6 membered carbocyclic ring, wherein the carbocyclic ring is optionally substituted with 1-4 substituents selected from halogen or C1-4 alkyl; in some embodiments, R3 and R4 on the same carbon atom, or R5 and R6 on the same carbon atom together with the carbon atom to which they are attached form a 3-4-membered carbocyclic ring, the carbocyclic ring is optionally substituted with 1-2 substituents selected from halogen or C1-2 alkyl;
in some embodiments, R7 and R8 are each independently selected from H, C1-4 alkyl or C3-6 cycloalkyl;
in some embodiments, a, c and e are independently selected from an integer of 0-5; in some embodiments, a, c and e are independently selected from an integer of 0-3; in some embodiments, a, c and e are independently 0 or 1;
in some embodiments, b and d are independently 0 or 1;
in some embodiments, L1 is —C(O)—CF2—, —C(O)—CHF—, —C(O)—C(CH3)F—,
in some embodiments, A is C3-6 cycloalkylene,
C2-4 alkynylene, —RaC(O)NRa′—, —RaNRa′C(O)—, —RaNRa′—, —RaC(O)—, —Ra(CRa′Ra″)n— or a bond; in some embodiments, A is C3-6 cycloalkylene, C2-4 alkynylene,
in some embodiments, A is
in some embodiments, Ra is
i some embodiments, A is
in some embodiments, A is
Ra′ and Ra″ are independently H or C1-4 alkyl;
in some embodiments, n is an integer of 1-2;
in some embodiments, X1 and X2 are independently N or CRA1; in some embodiments, X1 and X2 are not both CRA1 at the same time; in some embodiments, X3 is S, O or NRA1;
in some embodiments, X4, X5 and X6 are independently N, NRA1, S, O or CRA1, and are not all CRA1 at the same time;
in some embodiments, each RA1 is independently H, cyano, —RA, halogen, —C1-4 alkyl RA, —NHC(O) RA, —C(O) RA, —C1-4 alkyl-O—C1-4 alkyl, —NHRA, —C(O)NHRA or —ORA;
in some embodiments, RA is C1-4 alkyl, C3-6 cycloalkyl, C3-6 cycloalkyloxy, C1-4 alkoxy, C1-4 haloalkyl, C1-4 haloalkoxy or a 3-6 membered heterocyclyl containing 1-3 heteroatoms selected from N, O or S, the alkyl, cycloalkyl, cycloalkyloxy, alkoxy, haloalkyl, haloalkoxy and heterocyclyl are optionally further substituted with 1-6 groups selected from C3-6 cycloalkyl, C1-4 alkyl, halogen, —S(O)2C1-4 alkyl, —OC1-4 alkyl or cyano; in some embodiments, RA is C1-4 alkyl, C3-6 cycloalkyl or a 3-6 membered heterocyclyl containing 1-3 heteroatoms selected from N, O or S, the alkyl, cycloalkyl, and heterocyclyl are optionally further substituted with 1-6 groups selected from C3-6 cycloalkyl, C1-4 alkyl, halogen, —S(O)2C1-4 alkyl, —OC1-4 alkyl or cyano; in some embodiments, RA is C1-4 alkyl, C3-4 cycloalkyl, a 4-6-membered heterocyclyl containing 1-2 heteroatoms selected from N and O, the alkyl and heterocyclyl are optionally further substituted with 1-5 groups selected from C3-4 cycloalkyl, C1-4 alkyl, halogen, —S(O)2C1-2 alkyl, —OC1-2 alkyl or cyano; in some embodiments, RA is C3-6 cycloalkyl, C3-6 cycloalkyloxy, C1-4 alkoxy, C1-4 haloalkyl, and C1-4 haloalkoxy, the cycloalkyl, cycloalkyloxy, alkoxy, haloalkyl, and haloalkoxy are optionally further substituted with 1-3 groups selected from C1-4 alkyl, halogen and cyano;
in some embodiments, A is
cyclopropylidene, ethynylene,
in a preferred embodiment, A is
in some embodiments, B
in some embodiments, B is
wherein at least one of RB1 and RB2 is selected from OH, halogen, cyano, halo C1-4 alkyl, C1-4 alkyloxy and C3-6 cycloalkyl, or group RA1 on A and group RB1 on B together with the atoms to which they are attached form a 6-8-membered heterocycle containing 1 O atom; in some embodiments, B is
wherein RB2 is halogen or cyano, and f is not 0; in some embodiments, B is
embodiments, B is
wherein both RB1 and RB2 are H;
in some embodiments, Y1 is O, S or NRB3;
In some embodiments, Cy has a structure:
wherein, represents a single bond or a double bond, Z1 is C or N, ring E is a 5-membered heterocycle containing 1-3 heteroatoms selected from N, O or S, and ring D is a 6-membered ring containing 0-3 heteroatoms selected from N, O or S; the 5-membered heterocycle and the 6-membered ring are independently and optionally substituted with 1-3 RB2; in some embodiments, Cy is selected from one of the following structures:
in some embodiments, RB1 and RB2 are each independently selected from H, oxo, OH, halogen, cyano, C1-4 alkyl, halo C1-4 alkyl, C1-4 alkyloxy, C3-6 cycloalkyl, and RB3 is selected from H, C1-4 alkyl, C3-6 cycloalkyl; in some embodiments, group RA1 on A and group RB1 on B together with the atoms to which they are attached form a 6-10-membered heterocycle containing 1-3 heteroatoms selected from N, S, and O;
in some embodiments, f is an integer of 0-3;
in some embodiments, B
in some embodiments, L2 is —O—, —C(O)NR9—, —NR9C(O)NR9—, —NR9—, —(CR10R11)g—, —NR9—(CR10R11)g— or a bond, wherein g is an integer of 1-3;
in some embodiments, L2 is —O— or —CR10R11—, wherein at least one of R10 and R11 is halogen or C1-4 alkyl, or R10 and R11 together with the carbon atom to which they are attached form a 3-4-membered carbocyclic ring, such as cyclopropyl;
in some embodiments, L2 is —NR9—, wherein R9 is H or C1-4 alkyl;
in some embodiments, R10 and R11 are each independently H, halogen, C1-4 alkyl or cycloalkyl; alternatively, R10 and R11 on the same carbon atom together with the carbon atom to which they are attached form a 3-6 membered carbocyclic ring;
in some embodiments, L2 is —NH—, —O—,
in some embodiments, M2 is
in some embodiments, M2 is
in some embodiments, M2 is
and in some embodiments,
In some embodiments, Z2 and Z3 are CRM or N, and Z4 is O, S or NRM1; in some embodiments, Z2 is CRM;
in some embodiments, each RM is independently H, C1-4 alkyl, C1-4 alkoxyalkyl, cyano, C3-6 cycloalkyl, C3-6 cycloalkyloxy, —SRm′, —S(O)2Rm′, —C(O)NRmRm′, —NRmC(O)Rm′, C2-6 alkenyl, C2-6 alkynyl, —NRM1, a 3-6 membered heterocyclyl containing 1-3 heteroatoms selected from N, O or S, or a halogen, the alkyl, alkenyl, alkynyl, and cycloalkyl are optionally substituted with 1-3 groups selected from halogen, cyano, C1-4 alkoxy, halo C1-4 alkyl or halo C1-4 alkoxy, the heterocyclyl is optionally substituted with 1-3 groups selected from halogen, oxo, and C1-4 alkyl; in some embodiments, each RM is independently H, C1-4 alkyl, C2-6 alkynyl or a 3-6 membered heterocyclyl containing 1-3 heteroatoms selected from N, O or S, wherein the alkyl is optionally substituted with 1-3 groups selected from halogen; in some embodiments, each RM is independently cyano, difluoroalkyl, trifluoroalkyl, C2-4 alkynyl, C3-4 cycloalkyl, a 5-6-membered heterocyclyl containing 1-3 heteroatoms selected from N, O or S, the heterocyclyl is optionally substituted with 1-3 groups selected from C1-4 alkyl;
alternatively, two RM on adjacent ring carbon atoms in M2 together with the carbon atom to which they are attached form a 3-6 membered carbocyclic ring or a 3-6 membered heterocyclyl containing 0-3 heteroatoms selected from N, O or S; further, two RM on adjacent ring carbon atoms in M2 together with the carbon atom to which they are attached form a 3-5 membered carbocyclic ring or a 3-5 membered heterocyclyl containing 0-3 heteroatoms selected from N, O or S; furthermore, two RM on adjacent ring carbon atoms in M2 together with the carbon atom to which they are attached form a 4-5 membered carbocyclic ring or a 4-5 membered heterocyclyl containing 0-3 heteroatoms selected from N, O or S; furthermore, two RM on adjacent ring carbon atoms in M2 together with the carbon atom to which they are attached form cyclobutane or a 5-membered heterocyclyl containing 1-2 heteroatoms selected from N, O or S;
Rm is H, C1-4 alkyl or halo C1-4 alkyl;
Rm′ is C1-4 alkyl or halo C1-4 alkyl; in some embodiments, M2 is
wherein RM is trifluoromethyl, difluoromethyl, cyclopropyl, ethynyl, furan-3-yl, methylaminocarbonyl, azetidin-1-yl, oxetan-3-yl, 3,3-difluoro-azetidin-1-yl, acetamido, 1-methyl-1H-pyrazol-4-yl, tetrahydrofuran-3-yl, methylthio, 4-methyl-5-oxo-1,2,4-triazol-1-yl, 2-oxo-pyrrolidin-1-yl, methylsulfonyl, methoxymethyl, difluoromethoxymethyl or trifluoromethyl ethynyl;
in some embodiments, M2 is
wherein RM is C1-4 alkyl, and the alkyl is substituted with 1-3 halogens (preferably F); preferably trifluoromethyl or difluoromethyl; in some embodiments, M2 is
in some embodiments, RM1 is H, C1-4 alkyl, C3-6cycloalkyl, C1-4haloalkyl or C1-4 alkoxyalkyl;
in some embodiments, RM1 is H, C1-4 alkyl or C3-6 cycloalkyl;
In some embodiments, each R12 is independently H, halogen, C1-4 alkyl, C3-6 cycloalkyl or halo C1-4 alkyl; In some embodiments, each R12 is independently H;
In some embodiments, h is an integer of 0-3; In some embodiments, h is 1 or 2;
is 0, 1 or 2;
provided that: when M1 is
L1 is —C(O)—CH2—, A is
L2 is —NH—, and M2 is
RB1 and RB2 are not both H at the same time;
when M1 is
L1 is —C(O)—CH2—, A is
and L2 is —NH—CH2—, M2 is not
when M1 is
L1 is —C(O)—CH2—, A is
L2 is —NH—, and M2 is
at least one of substituent RA1 in A is selected from cyano, halogen, C3-4 cycloalkyloxy, cyclopropylmethoxy, C1-4 haloalkoxy, cyclopropylmethyl, —C1-4 alkyl-O—C1-4 alkyl, —NHC(O) RA, —C(O)NHRA, —C(O)—C3-6 cycloalkyl,
and when M1 is
L1 is —C(O)—CH2—, A is
L2 is —NH—, and M2 is
RA1 is not methyl, ethyl or cyclopropyl.
Patent document CN 109476664 A introduces a method for preparing a class of ATX inhibitors. One skilled in the art may combine the document and known organic synthesis techniques to prepare the compound of the present invention. The starting materials for the compound are commercially available chemicals and (or) the compounds described in the chemical literature. “Commercially available chemicals” are obtained from formal commercial sources, and the suppliers include: Titan Technology Co., Ltd., Energy Chemical Co., Ltd., Shanghai Demo Co., Ltd., Chengdu Kelong Chemical Co., Ltd., Accela ChemBio Co., Ltd., Nanjing PharmaBlock Co., Ltd., WuXi Apptec Co., Ltd., and J & K Scientific Co., Ltd. and other companies.
Reference books and monographs in the field introduce in detail the synthesis of reactants useful for the preparation of the compound described herein, or provide articles describing the preparation method for reference. These reference books and monographs include: “Synthetic Organic Chemistry”, John Wiley & Sons, Inc., New York; S. R. Sandler et al., “Organic Functional Group Preparations,” 2nd Ed., Academic Press, New York, 1983; H. O. House, “Modern Synthetic Reactions”, 2nd Ed., W. A. Benjamin, Inc. Menlo Park, Calif. 1972; T. L. Gilchrist, “Heterocyclic Chemistry”, 2nd Ed., John Wiley & Sons, New York, 1992; J. March, “Advanced Organic Chemistry: Reactions, Mechanisms and Structure”, 4th Ed., Wiley-Interscience, New York, 1992; Fuhrhop, J. and Penzlin G. “Organic Synthesis: Concepts, Methods, Starting Materials”, Second, Revised and Enlarged Edition (1994) John Wiley & Sons ISBN: 3-527-29074-5; Hoffman, R. V. “Organic Chemistry, An Intermediate Text” (1996) Oxford University Press, ISBN 0-19-509618-5; Larock, R. C. “Comprehensive Organic Transformations: A Guide to Functional Group Preparations” 2nd Edition (1999) Wiley-VCH, ISBN: 0-471-19031-4; March, J. “Advanced Organic Chemistry: Reactions, Mechanisms, and Structure” 4th Edition (1992) John Wiley & Sons, ISBN: 0-471-60180-2; Otera, J. (editor) “Modern Carbonyl Chemistry” (2000) Wiley-VCH, ISBN: 3-527-29871-1; Patai, S. “Patai's 1992 Guide to the Chemistry of Functional Groups” (1992) Interscience ISBN: 0-471-93022-9; Solomons, T. W. G. “Organic Chemistry” 7th Edition (2000) John Wiley & Sons, ISBN: 0-471-19095-0; Stowell, J. C., “Intermediate Organic Chemistry” 2nd Edition (1993) Wiley-Interscience, ISBN: 0-471-57456-2; “Industrial Organic Chemicals: Starting Materials and Intermediates: An Ullmann's Encyclopedia” (1999) John Wiley & Sons, ISBN: 3-527-29645-X, in 8 volumes; “Organic Reactions” (1942-2000) John Wiley & Sons, in over 55 volumes; and “Chemistry of Functional Groups” John Wiley & Sons, in 73 volumes.
Specific and similar reactants can be selectively identified through indexes of known chemicals made by the Chemical Abstracts Service of the American Chemical Society, and these indexes are available in most public and university libraries and online. Chemicals that are known but not commercially available in the catalog are optionally prepared by custom chemical synthesis facilities, wherein many standard chemical supply facilities (e.g., those listed above) provide custom synthesis services. A reference document for the preparation and selection of pharmaceutically acceptable salts of the compound described herein is P. H. Stahl & C. G. Wermuth “Handbook of Pharmaceutical Salts”, Verlag Helvetica Chimica Acta, Zurich, 2002.
“Halogen” as used herein refers to F, Cl, Br, I, or their isotopes.
“Halo” or “substituted with halogen” refers to substitution with more than one halogens selected from F, Cl, Br, I, or their isotopes, and the upper limit of the number of halogen substituents is equal to the sum of the number of hydrogens that can be substituted with substituent groups. Without particular limitation, the number of halogen substituents is any integer between 1 and the upper limit. When the number of halogen substituents is greater than 1, identical or different halogens may be used for substitution.
The term “alkyl” refers to a monovalent straight or branched chain saturated aliphatic hydrocarbon group. Unless otherwise specified, the term “alkyl” refers to alkyl containing 1 to 20 carbon atoms, preferably alkyl containing 1 to 8 carbon atoms, more preferably alkyl containing 1 to 6 carbon atoms, and further preferably alkyl containing 1 to 4 carbon atoms. Non-limiting examples include methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, neobutyl, tert-butyl, n-pentyl, isoamyl, neopentyl, n-hexyl and various branched isomers thereof.
The term “alkylene” refers to a bivalent straight or branched chain saturated alkyl. Examples of alkylene include, but are not limited to, methylene, ethylene, etc.
The definition of “ring” includes a carbocyclic ring and heterocycle. Unless otherwise specified, it is usually a 3-12-membered monocyclic ring containing 0 to 3 heteroatoms selected from N, O or S, preferably a 4-7-membered ring, more preferably a five-membered ring or a six-membered ring.
The term “cycloalkyl” refers to a monovalent saturated, substituted or unsubstituted carbocyclic hydrocarbon group, unless otherwise specified, usually has 3 to 10 carbon atoms, preferably 3-6 carbon atoms, and further preferably 3-4 carbon atoms. Non-limiting examples include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or cycloheptyl, etc.
The term “cycloalkylene” refers to a divalent saturated, substituted or unsubstituted cycloalkyl. Non-limiting examples include,
The term “carbocyclic ring” or “carbocyclyl” refers to a substituted or unsubstituted, saturated or unsaturated carbocyclic group, and includes a monocyclic carbocyclic ring, a bicyclic bridged ring, a bicyclic fused ring, a bicyclic spiro ring, etc., usually having 3 to 12 carbon atoms, preferably 3-10 carbon atoms, and further preferably 3-6 carbon atoms. In non-limiting examples, a monocyclic carbocyclic ring includes cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl or phenyl, etc., a bicyclic bridged ring includes
etc., a bicyclic fused ring includes
etc., and a bicyclic spiro ring includes
etc.
The term “heterocycle” or “heterocyclyl” refers to a substituted or unsubstituted, saturated or unsaturated aromatic ring or non-aromatic ring, and when not particularly limited, contains 1 to 3 heteroatoms selected from N, O or S, including a monocyclic heterocycle, a bicyclic bridged heterocycle, a bicyclic fused heterocycle, a bicyclic spiro heterocycle, etc., preferably a 3- to 12-membered heterocycle, more preferably a 4-12-membered heterocycle, and more preferably a 4-10-membered heterocycle. The selectively substituted N and S in the heterocyclyl can be oxidized to various oxidation states. Heterocyclyl can be connected to a heteroatom or carbon atom. Non-limiting examples include oxiranyl, azacyclopropyl, oxetanyl, azetidinyl, 1,3-dioxolane, 1,4-dioxolane, 1,3-dioxane, piperazinyl, azacycloheptyl, pyridyl, furanyl, thienyl, pyranyl, N-alkylpyrrolyl, pyrimidinyl, pyrazinyl, pyrazolyl, pyridazinyl, imidazolyl, piperidyl, piperidinyl, morpholinyl, thiomorpholinyl, 1,3-dithianyl, dihydrofuranyl, dihydropyranyl, dithiolanyl, tetrahydrofuranyl, tetrahydropyrrolyl, tetrahydroimidazolyl, oxazolyl, dihydrooxazolyl, tetrahydrooxazolyl, tetrahydrothiazolyl, tetrahydropyranyl, benzimidazolyl, benzopyridyl, pyrrolopyridyl, benzodihydrofuranyl, azabicyclo[3.2.1]octyl, azabicyclo[5.2.0]nonyl, oxatricyclic[5.3.1.1]dodecyl, azaadamantyl and oxaspiro[3.3]heptyl,
etc.
The term “heterocyclene” refers to a substituted or unsubstituted, saturated or unsaturated, aromatic or non-aromatic, divalent heterocyclic group. Non-limiting examples include
etc.
The term “alkynyl” refers to a straight or branched chain monovalent unsaturated hydrocarbon group containing a carbon-carbon triple bond. Unless otherwise specified, alkynyl contains 2-6 carbon atoms, preferably 2-4 carbon atoms, and non-limiting example includes ethynyl. The term “alkynylene” refers to a straight or branched chain divalent unsaturated hydrocarbon group containing a carbon-carbon triple bond.
The term “alkoxy” or “alkyloxy” refers to —O-alkyl. Non-limiting examples include methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, sec-butoxy, tert-butoxy, n-pentoxy, n-hexyloxy, cyclopropoxy, cyclobutoxy, etc.
The expression “optional” or “optionally” refers to that events or circumstances subsequently described may but not necessarily occur, and the description includes the occasions where the events or circumstances occur or do not occur. For example, the expression “alkyl optionally substituted with F” means that the alkyl may but not necessarily be substituted with F, and the description includes the case where the alkyl is substituted with F and the case where the alkyl is not substituted with F.
“Pharmaceutically acceptable salt” refers to a salt of the compound of the present invention maintaining the biological effectiveness and characteristics of the free acid or free base, and obtained by reacting the free acid with a non-toxic inorganic base or organic base, reacting the free base with a non-toxic inorganic acid or organic acid.
The term “deuterated form” refers to a compound in which one or more hydrogen atoms are substituted with a corresponding number of deuterium atoms.
The term “pharmaceutical composition” refers to a mixture of one or more compounds described herein, or stereoisomers, solvates, deuterated forms, pharmaceutically acceptable salts or cocrystals thereof, and other components, wherein the other components comprise physiologically/pharmaceutically acceptable carriers and/or excipients.
The term “carrier” refers to: a system that does not cause significant irritation to the organism, does not eliminate the biological activity and characteristics of the administered compound, can change the way the drug enters the human body and the distribution of the drug in the body, controls the release rate of the drug, and delivers the drug to targeted organs, and non-limiting examples include microcapsules and microspheres, nanoparticles, liposomes, etc.
The term “excipient” refers to: an excipient which itself is not a therapeutic agent, but used as a diluent, adjuvant, binder, and/or vehicle for addition to a pharmaceutical composition to improve its handling or storage properties or to permit or facilitate formation of a compound or pharmaceutical composition into a unit dosage form for administration. As will be known to those in the art, pharmaceutically acceptable excipients can provide a variety of functions and can be described as wetting agents, buffering agents, suspending agents, lubricating agents, emulsifiers, disintegrants, absorbents, preservatives, surfactants, colorants, flavorants, and sweeteners. Examples of pharmaceutically acceptable excipients include, but are not limited to: (1) sugars, such as lactose, glucose and sucrose; (2) starches, such as corn starch and potato starch; (3) cellulose and its derivatives, such as sodium carboxymethyl cellulose, ethyl cellulose, cellulose acetate, hydroxypropylmethylcellulose, hydroxypropylcellulose, microcrystalline cellulose, and croscarmellose, such as croscarmellose sodium; (4) tragacanth powder; (5) malt; (6) gelatin; (7) talc; (8) excipients, such as cocoa butter and suppository waxes; (9) oils, such as peanut oil, cottonseed oil, safflower oil, sesame oil, olive oil, corn oil and soybean oil; (10) glycols, such as propylene glycol; (11) polyols, such as glycerin, sorbitol, mannitol and polyethylene glycol; (12) esters, such as ethyl oleate and ethyl laurate; (13) agar; (14) buffering agents, such as magnesium hydroxide and aluminum hydroxide; (15) alginic acid; (16) pyrogen-free water; (17) isotonic saline; (18) Ringer's solution; (19) ethanol; (20) pH buffer solutions; (21) polyesters, polycarbonates and/or polyanhydrides; and (22) other non-toxic compatible substances employed in pharmaceutical formulations.
The term “stereoisomer” refers to an isomer produced by different arrangements of atoms in a molecule in space, including cis-trans isomers, enantiomers and conformational isomers.
The compounds of the present invention also include tautomers thereof, for example, when the present invention describes the left side compound in which the pyrimidine ring is substituted with OH, the right side tautomer compound is also included.
The term “solvate” refers to substance formed by combining compounds of the present invention or salts thereof with stoichiometric or non-stoichiometric solvents bound by non-covalent intermolecular forces. When the solvent is water, the solvate is a hydrate.
“Co-crystal” refers to a crystal formed by the combination of active pharmaceutical ingredient (API) and co-crystal former (CCF) under the action of hydrogen bonds or other non-covalent bonds. The pure states of API and CCF are both solid at room temperature, and there is a fixed stoichiometric ratio between various components. The co-crystal is a multi-component crystal, which includes both a binary co-crystal formed between two neutral solids and a multi-element co-crystal formed between a neutral solid and a salt or solvate.
The contents of the present invention will be described below in detail by examples. In the examples, experimental methods without specifying specific conditions are performed under conventional conditions. The listed examples are intended to better illustrate the contents of the present invention, but this should not be understood as that the contents of the present invention are only limited to the listed examples. Non-essential improvements and adjustments made by one of ordinary skill in the art to the embodiments based on the above-mentioned contents of the present invention should still fall within the protection scope of the present invention.
The following abbreviations are used in the present invention:
The structures of the compounds are determined by nuclear magnetic resonance (NMR) and/or mass spectrometry (MS). The NMR shift (6) is given in the unit of 10−6 (ppm). NMR is measured with (Bruker Avance III 400 and Bruker Avance 300) NMR instrument, wherein the solvent for determination is deuterated form of dimethyl sulfoxide (DMSO-d6), deuterated form of chloroform (CDCl3), deuterated form of methanol (CD3OD), and the internal standard is tetramethylsilane (TMS); MS is measured with (Agilent 6120B(ESI) and Agilent 6120B(APCI)); HPLC is measured with Agilent 1260DAD high pressure liquid chromatography (Zorbax SB-C18 100×4.6 mm, 3.5 μM); Yantai Huanghai HSGF254 or Qingdao GF254 silica gel plate is used for thin layer chromatography silica plate, and the silica gel plate for the thin layer chromatography (TLC) is of the specification of 0.15 mm-0.20 mm, and the specification when separating and purifying a product by thin layer chromatography is 0.4 mm-0.5 mm. For the column chromatography, Yantai Huanghai silica gel of 200-300 mesh silica gel is generally used as a carrier.
2-chloro-5-nitro pyrimidin (1A) (4.8 g, 30 mmol), 2-aminoindan (1B) (4.01 g, 30 mmol) and N,N-diisopropylethylamine (5.2 g, 40 mmol) were dissolved in ethanol (50 mL), and stirred at 90° C. for 2 hours. After the reaction was completed, the mixture was cooled to room temperature, and the resulting solid was filtered, washed with ethanol (20 mL), and dried to obtain the title compound 1C as a beige solid (5.6 g, 73%). LC-MS (ESI): m/z=257.1 [M+H]+
1C (5.6 g, 22 mmol), iron powder (5.6 g, 100 mmol) and ammonium chloride (0.54 g, 10 mmol) were dissolved in ethanol (50 mL) and water (15 mL), and stirred at 80° C. for 2 hours. After the reaction was completed, the mixture was cooled to room temperature, and filtered. The filtrate was concentrated under reduced pressure, and then separated by silica gel column chromatography to obtain the title compound intermediate 1 as a yellow solid (3.6 g, 72%). LC-MS (ESI): m/z=227.2 [M+H]+.
Compound 2A (2.5 g, 15.8 mmol) was dissolved in DCM (40 ml), and DMF (0.1 ml) was added. The resulting solution was cooled to 0° C. with an ice bath, and oxalyl chloride (3.0 g, 23.7 mmol) was added dropwise. After the addition was completed, the reaction mixture was slowly returned to room temperature and stirred overnight. The reaction mixture was evaporated to dryness under reduced pressure to obtain compound 2B (2.8 g, 99%).
Ethyl 3-oxo-3-hydrazinyl propanoate (3.5 g, 23.7 mmol) and triethylamine (4.8 g, 47.4 mmol) were dissolved in DCM (60 ml), and cooled to 0° C. with an ice bath. A solution of compound 2B (2.8 g, 15.8 mmol) in DCM (15 ml) was slowly added dropwise. After the addition was completed, the mixture was slowly returned to room temperature and stirred overnight. The reaction mixture was evaporated to dryness under reduced pressure, and the residue was directly purified by silica gel column chromatography (PE/EA=2/1) to obtain 2C (2.7 g, 60.0%).
2C (2.7 g, 9.4 mmol) was placed into a 100 ml single-necked flask, anhydrous THF (50 ml) was added, and Burgess reagent (3.4 g, 14.1 mmol) was added at room temperature. After the addition was completed, the mixture was warmed to 70° C., and stirred for 2 hours. The reaction mixture was directly purified by silica gel column chromatography (PE/EA=2/1) to obtain intermediate 2 (1.6 g, 59.3%).
Compound 1a (5.04 g, 40 mmol) was dissolved in toluene (50 mL). At 0° C., cyclopropanol (2.9 g, 50 mmol) and triphenylphosphine (15.8 g, 60 mmol) were added successively, and stirred uniformly, then DBAD (13.8 g, 60 mmol) was added to the system in portions, and the mixture was reacted under nitrogen protection at 110° C. for 5 hours. After the reaction was completed, the system was concentrated under reduced pressure, and then directly separated by silica gel column chromatography to obtain target compound (1b) (1.2 g, 18%). LC-MS (ESI): m/z=167.2 [M+H]+. 1H NMR (400 MHz, CDCl3) δ 8.08 (d, 1H), 6.04 (d, 1H), 4.12-4.05 (m, 1H), 2.61 (s, 3H), 0.87-0.68 (m, 4H).
Sodium iodide (1.08 g, 7.2 mmol), iodine (2.79 g, 11 mmol) and potassium carbonate (3.86 g, 28 mmol) were added successively to a solution of compound 1b (1.2 g, 7.2 mmol) in a mixed solvent of water (10 mL) and ethanol (6 mL), and the mixture was stirred at room temperature for 1.5 hours. After the reaction was completed, the mixture was diluted with saturated sodium bicarbonate solution (30 mL), and extracted with ethyl acetate (50 mL). The organic phase was dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated under reduced pressure, and then directly used in the next step of reaction. LC-MS (ESI): m/z=251.1 [M+H]+
Cesium carbonate (2.28 g, 7 mmol) and tert-butyl bromoacetate (0.99 g, 5.1 mmol) were added successively to a solution of compound 1c (0.85 g, 3.4 mmol) in N,N-dimethylformamide (10 mL), and the mixture was stirred at room temperature for 1 hour. After the reaction was completed, the mixture was diluted with saturated brine (30 mL), and extracted with ethyl acetate (30 mL×2). The organic phase was dried over anhydrous sodium sulfate, filtered and concentrated. The residue was purified by silica gel column chromatography to obtain white solid 1e (1.1 g, 89%). LC-MS (ESI): m/z=365.1 [M+H]+. 1H NMR (400 MHz, DMSO-d6) δ 7.69 (s, 1H), 4.77 (s, 2H), 4.06-4.00 (m, 1H), 1.42 (s, 9H), 0.68-0.64 (m, 4H).
Tetrakis(triphenylphosphine)palladium(0) (0.35 g, 0.6 mmol) and sodium carbonate (0.64 g, 6 mmol) were added to a mixture of compound 1e (1.1 g, 3 mmol) and compound if (1.0 g, 3 mmol) in a mixed solvent of 1,4-dioxane (9 mL) and distilled water (3 mL), and the mixture was stirred at 80° C. under nitrogen protection for 90 minutes. After the reaction was completed, the mixture was cooled to room temperature, diluted with saturated brine (50 mL), and extracted with ethyl acetate (80 mL). The organic layer was dried over anhydrous sodium sulfate, and concentrated. The residue was separated and purified by silica gel column chromatography to obtain the title compound 1g as a yellow solid (0.84 g, 63%). LC-MS (ESI): m/z=448.3 [M+H]+
A solution (3 mL) of 4N hydrogen chloride in dioxane was added to a solution of compound 1g (0.45 g, 1 mmol) in dichloromethane (3 mL), and the mixture was stirred at room temperature overnight. After the reaction was completed, the solvent was removed by filtration to obtain a solid, which was slurried with diethyl ether, filtered and dried to obtain the title compound 1h as a light brown solid (0.22 g, 56%). LC-MS (ESI): m/z=392.3 [M+H]+
At 0° C., compound 1h (0.22 g, 0.58 mmol), N,N-diisopropylethylamine (1 mL) and benzotriazol-1-yl-oxy-tripyrrolidinophosphonium hexafluorophosphate (0.45 g, 0.87 mmol) were sequentially added slowly to a solution of compound 1i (0.11 g, 0.68 mmol) in N,N-dimethylformamide (10 mL), and the mixture was stirred at room temperature under nitrogen protection overnight. After the reaction was completed, the reaction mixture was diluted with distilled water (30 mL), and extracted with ethyl acetate (50 mL×2). The organic layer was washed with distilled water and saturated brine (50 mL), dried over anhydrous sodium sulfate and concentrated. The silica gel column chromatography was used for separation and purification to obtain the title compound 1 (12 mg). LC-MS (ESI): m/z=498.3 [M+H]+. 1H NMR (400 MHz, DMSO-d6) δ 8.45 (s, 2H), 7.87 (d, 1H), 7.37 (d, 1H), 7.24-7.19 (m, 2H), 7.16-7.11 (m, 2H), 5.18-5.09 (m, 2H), 4.82-4.54 (m, 4H), 4.12-4.06 (m, 2H), 3.86-3.78 (m, 3H), 2.93-2.85 (m, 4H), 0.73-0.65 (m, 4H).
Compound 2a (3.3 g, 19 mmol) was dissolved in acetonitrile (30 mL). 1d (4.1 g, 21 mmol) and potassium carbonate (8.1 g, 58 mmol) were added, and the mixture was reacted at room temperature for 5 hours. After the reaction was completed, water was added, and the resulting solution was extracted with ethyl acetate, washed with saturated brine, and dried over anhydrous sodium sulfate. The concentrate was separated and purified by silica gel column chromatography to obtain target compound (2b) (4.3 g, 78%). 1H NMR (400 MHz, CDCl3) δ 7.61 (s, 1H), 4.83 (s, 2H), 1.49 (s, 9H).
Compound 2b (0.31 g, 1.08 mmol) was dissolved in a mixed solvent of 1,4-dioxane/water (4:1), and if (0.4 g, 1.18 mmol), tetratriphenylphosphine palladium (0.12 g, 1.08 mmol) and potassium carbonate (0.35 g, 3.23 mmol) were added successively. The mixture was reacted under nitrogen protection at 80° C. for 5 h. After the reaction was completed, the concentrate was separated and purified by silica gel column chromatography to obtain target compound (2c) (0.15 g, 33%). LC-MS (ESI): m/z=417.3 [M+H]+
Compound 2c (0.13 g, 0.31 mmol) was dissolved in a mixed solvent of THF/H2O=4:1. After dissolution, LiOH (0.02 g, 0.62 mmol) was added and the mixture was reacted at room temperature for 2 h. Water was added, and the resulting solution was extracted with DCM. The aqueous phase was collected, diluted to pH=4, and extracted with DCM. The extraction solution was washed with saturated brine, dried over anhydrous sodium sulfate and concentrated. A white solid 2d (0.12 g, 90%) was obtained. LC-MS (ESI): m/z=361.2 [M+H]+
Compound 2d (67 mg, 0.19 mmol), compound 1i (46 mg, 0.37 mmol), DPEA (72 mg, 0.56 mmol) and HATU (106 mg, 0.28 mmol) were dissolved in DMF, and the mixture was reacted at room temperature overnight. After the reaction was completed, water was added, and the resulting solution was extracted with ethyl acetate. The extraction solution was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated. The concentrate was separated and purified by silica gel column chromatography to obtain compound 2 (7 mg, 8%). LC-MS (ESI): m/z=467.3 [M+H]+. 1H NMR (400 MHz, DMSO-d6) δ 8.57 (s, 2H), 8.26 (d, 1H), 7.80 (d, 1H), 7.23-7.13 (m, 4H), 5.52-5.48 (m, 2H), 4.77-4.63 (m, 3H), 3.84-3.82 (m, 2H), 3.26-3.24 (m, 2H), 2.95-2.89 (m, 4H), 2.77-2.74 (m, 1H).
Compound 3a (0.5 g, 1.88 mmol) was dissolved in 2-methyl tetrahydrofuran (10 mL) and distilled water (2 ml), and then KOH (0.2 g, 3.76 mmol) was added; Then the mixture was reacted at 60° C. for 2 hours. After the reaction was completed, the reaction solution was cooled, and 20 mL of water was added. The resulting solution was extracted with ethyl acetate (20 mL×3). The aqueous phase was adjusted to pH=3 with acid, and then extracted with ethyl acetate (50 mL×3). The organic phase was dried over anhydrous sodium sulfate, and filtered. The filtrate was concentrated under reduced pressure to obtain target compound (3b) (0.43 g, 95%). LC-MS (ESI): m/z=239.2 [M+H]+. 1H NMR (400 MHz, DMSO-d6) δ 13.66 (s, 2H), 7.88 (s, 1H).
N,N-diisopropylethylamine (0.65 g, 5.04 mmol), methanamine hydrochloride (0.08 g, 2.52 mmol) and 2-(7-azabenzotriazole)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (0.528 g, 1.39 mmol) were added successively to a solution of compound 3b (0.3 g, 1.26 mmol) in N,N-dimethylformamide (10 mL), and the mixture was stirred at room temperature overnight. After the reaction was completed, the reaction was quenched by adding water, and extracted with ethyl acetate (50 mL×3). The organic phase was dried over anhydrous sodium sulfate, and filtered. The filtrate was concentrated under reduced pressure, and separated and purified by silica gel column chromatography (eluent: petroleum ether:ethyl acetate=1: 0-0:1) to obtain 3c as an off-white solid (0.150 g, 47%). LC-MS (ESI): m/z=252.1 [M+H]+. 1H NMR (400 MHz, DMSO-d6) δ 13.60 (s, 1H), 8.07 (s, 1H), 7.97 (s, 1H), 2.71 (s, 3H).
Cesium carbonate (0.25 g, 1.79 mmol) and tert-butyl bromoacetate (0.13 g, 0.66 mmol) were added successively to a solution of compound 3c (0.15 g, 0.60 mmol) in acetonitrile (10 mL), and the mixture was stirred at room temperature for 2 hours. After the reaction was completed, the mixture was diluted with saturated brine (30 mL), and extracted with ethyl acetate (30 mL×2). The organic phase was dried over anhydrous sodium sulfate, filtered and concentrated. The residue was separated and purified by silica gel column chromatography (eluent:petroleum ether:ethyl acetate=1: 0-0:1) to obtain 3e as a white solid (0.170 g, 78%). LC-MS (ESI): m/z=366.1 [M+H]+. 1H NMR (400 MHz, DMSO-d6) δ 8.04 (s, 1H), 7.98 (s, 1H), 4.99 (s, 2H), 2.70 (s, 3H), 1.43 (s, 9H).
Tetrakis(triphenylphosphine)palladium(0) (0.057 g, 0.05 mmol) and sodium carbonate (0.16 g, 1.48 mmol) were added to a mixture of compound 3e (0.18 g, 0.49 mmol) and compound if (0.2 g, 0.59 mmol) in a mixed solvent of 1,4-dioxane (18 mL) and distilled water (4 mL), and the mixture was stirred at 80° C. under nitrogen protection for 2 hours. After the reaction was completed, the mixture was cooled to room temperature, diluted with saturated brine (50 mL), and extracted with ethyl acetate (80 mL). The organic phase was dried over anhydrous sodium sulfate, and concentrated. The silica gel column chromatography (eluent:petroleum ether:ethyl acetate=1:0-0:1) was used for separation and purification to obtain the title compound 3g as light yellow solid (0.115 g, 52%). LC-MS (ESI): m/z=449.3 [M+H]+. 1H NMR (400 MHz, DMSO-d6) δ 8.46 (s, 2H), (d, 1H), 8.01 (s, 1H), 7.48 (d, 1H), 7.23-7.21 (m, 2H), 7.16-7.13 (m, 2H), 5.01 (s, 2H), 4.67-4.61 (m, 1H), 3.25 (t, 2H), 2.91 (q, 2H), 2.71 (d, 3H), 1.45 (s, 9H).
A solution (6 mL) of 4N hydrogen chloride in dioxane was added to a solution of compound 3g (0.115 g, 0.26 mmol) in dichloromethane (4 mL), and the mixture was stirred at room temperature overnight. After the reaction was completed, the solvent was removed by filtration to obtain a solid, which was slurried with diethyl ether, filtered and dried to obtain the title compound 3h as a light brown solid (0.08 g, 80%). LC-MS (ESI): m/z=393.3 [M+H]+. 1H NMR (400 MHz, DMSO-d6) δ 8.46 (s, 2H), 8.05 (d, 1H), 8.01 (s, 1H), 7.48 (d, 1H), 7.23-7.21 (m, 2H), 7.16-7.13 (m, 2H), 5.01 (s, 2H), 4.67-4.61 (m, 1H), 3.25 (t, 2H), 2.91 (q, 2H), 2.71 (d, 3H).
At 0° C., compound 3h (0.080 g, 0.20 mmol), N,N-diisopropylethylamine (0.09 g, 0.71 mmol) and benzotriazol-1-yl-oxy-tripyrrolidinophosphonium hexafluorophosphate (0.16 g, 0.31 mmol) were sequentially added slowly to a solution of compound 1i (0.05 g, 0.41 mmol) in N,N-dimethylformamide (6 mL), and the mixture was stirred at room temperature under nitrogen protection overnight. After the reaction was completed, the reaction mixture was diluted with distilled water (20 mL), and extracted with ethyl acetate (30 mL×3). The organic phase was washed with distilled water and saturated brine (50 mL), dried over anhydrous sodium sulfate and concentrated. The silica gel column chromatography (eluent:dichloromethane:ethyl acetate:methanol=1:0:0-: 2:10:1) was used for separation and purification to obtain compound 3 (14 mg). LC-MS (ESI): m/z=499.3 [M+H]+. 1H NMR (400 MHz, DMSO-d6) δ 8.47 (s, 2H), 7.94 (d, 2H), 7.46 (d, 1H), 7.23-7.21 (m, 2H), 7.15-7.13 (m, 2H), 5.34 (d, 2H), 4.79 (s, 1H), 4.68-4.62 (m, 2H), 3.83 (d, 2H), 3.25 (t, 2H), 2.91 (q, 2H), 2.71 (d, 3H).
Compound 4a (500 mg, 1.96 mmol) was dissolved in DMF (10 mL), HATU (1.11 g, 2.94 mmol) and DIPEA (758 mg, 5.88 mmol) were added and stirred at room temperature, and then hydrazine hydrate (0.25 mL) was added. The mixture was reacted at room temperature overnight. The reaction was completed and then directly used in the next step.
HATU (1.11 g, 2.94 mmol) and DIEA (758 mg, 5.88 mmol) were added to the reaction solution of the first step, then 1,1-cyclopropanedicarboxylic acid monoethyl ester (620 mg, 3.92 mmol) was added and the mixture was stirred at room temperature for 3 hours. After the reaction was completed, water was added, and the resulting solution was extracted with ethyl acetate. The organic phase was combined and dried to obtain compound 4c (675 mg, 84%).
LC-MS (ESI): m/z=410.2 [M+H]+.
Compound 4c (500 mg, 1.22 mmol) was dissolved in anhydrous tetrahydrofuran, (methoxycarbonylsulfamoyl)triethylammonium hydroxide (582 mg, 2.44 mmol) was added, and the mixture was heated to 75° C. and stirred for 1 hour. After the reaction was completed, the reaction solution was extracted twice with ethyl acetate and water. The organic phase was dried and concentrated, and separated and purified by silica gel column chromatography (DCM:MeOH=40:1) to obtain compound 4d (465 mg, 97%). LC-MS (ESI): m/z=392.2 [M+H]+.
Compound 4d (465 mg, 1.19 mmol) was dissolved in anhydrous ethanol (10 mL), and lithium hydroxide (143 mg, 5.95 mmol) dissolved in 2 mL of water was added. The mixture was stirred at room temperature and reacted for 2 hours. After TLC detected that the reaction was completed, the reaction solution was concentrated, and diluted with water, and then 2N hydrochloric acid aqueous solution was added to adjust pH to 3. A large number of solids were precipitated and filtered by suction. The filter cake was dried to obtain compound 4e (205 mg, 48%). LC-MS (ESI): m/z=364.2 [M+H]+.
Compound 4e (205 mg, 0.56 mmol) was dissolved in 10 mL of N,N-dimethylformamide; HATU (322 mg, 0.85 mmol), N,N-diisopropylethylamine (0.3 mL, 1.68 mmol) and compound 1i (139 mg, 1.12 mmol) were added; and the mixture was reacted at room temperature for 2 hours. After TLC detected that the reaction was completed, the reaction solution was extracted with ethyl acetate and water, and washed twice with saturated brine. The organic phase was dried and concentrated to obtain a crude product, which was separated and purified by silica gel column chromatography (DCM:MeOH=20:1) to obtain compound 4 (25 mg, 9%).
LC-MS (ESI): m/z=470.2 [M+H]+.
1H NMR (400 MHz, DMSO-d6): 8.79-8.85 (m, 2H), 8.38-8.40 (d, 1H), 7.14-7.24 (m, 4H), 4.81-4.68 (m, 3H), 4.44 (d, 2H), 3.28 (m, 2H), 2.91-3.00 (m, 3H), 2.73-2.76 (m, 1H), 1.88-1.91 (m, 4H).
Step 1: methyl 6-((2,3-dihydro-1H-inden-2-yl)amino)pyridazine-3-carboxylate (5b)
A solution of compound 5a (6.95 g, 32 mmol) dissolved in DMF (100 mL) was added to a 250 mL single-necked flask, and 2,3-dihydro-1H-inden-2-amine hydrochloride (5.71 g, 33.6 mmol) and cesium carbonate (22.95 g, 70.4 mmol) were added. The mixture was reacted at 80° C. for 2 h, cooled to room temperature, filtered, poured into 300 ml of water, and extracted with ethyl acetate (100 mL×3). The organic phase was combined, washed with saturated sodium chloride (100 mL), dried over anhydrous sodium sulfate, concentrated under reduced pressure and separated and purified by silica gel column chromatography to obtain compound 5b (4.0 g, yield 46%). LC-MS (ESI): m/z=270.2 [M+H]+.
Compound 5b (4.0 g, 14.9 mmol) was dissolved in 30 ml of THF and 10 ml of water, and lithium hydroxide monohydrate (1.87 g, 44.6 mmol) was added. The mixture was stirred at room temperature and reacted for 1 hour. After TLC detected that the reaction was completed, potassium bisulfate aqueous solution was added to adjust pH to 4-5, and then dimethyl tetrahydrofuran was added. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to obtain compound 5c (3.2 g, 84%). LC-MS (ESI): m/z=256.2 [M+H]+.
Compound 5c (2.84 g, 11.1 mmol) was dissolved in DMF (50 mL), and then HATU (5.1 g, 13.4 mmol) and DIPEA (4.3 g, 33.5 mmol) were added. The mixture was stirred and reacted for 10 minutes, and then ethyl 3-oxo-3-hydrazinyl propanoate (2.0 g, 13.4 mmol) was added. The mixture was stirred at room temperature overnight. The reaction solution was poured into water (200 mL), extracted with ethyl acetate (50 mL×3), washed with saturated brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure to obtain compound 5d (3.0 g, 71%). LC-MS (ESI): m/z=384.2 [M+H]+.
Compound 5d (1.0 g, 2.6 mmol) was dissolved in anhydrous tetrahydrofuran (15 mL), and Burgess reagent (1.24 g, 5.2 mmol) was added. The mixture was heated to 90° C. and reacted under microwave and nitrogen protection for 30 minutes. After the reaction was completed, water was added and the resulting solution was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, concentrated, and separated and purified by silica gel column chromatography (PE/EA=1/1) to obtain compound 5e (480 mg, 51%). LC-MS (ESI): m/z=366.2 [M+H]+.
Compound 5e (480 mg, 1.32 mmol) was dissolved in 10 ml of THF and 5 ml of water, and lithium hydroxide monohydrate (166 mg, 3.95 mmol) was added. The mixture was stirred at room temperature and reacted for 1 hour. After TLC detected that the reaction was completed, the reaction solution was concentrated, and diluted with water, and then potassium bisulfate aqueous solution was added to adjust pH to 4-5. A large number of solids were precipitated and filtered by suction. The filter cake was dried to obtain compound 5f (420 mg, 94%). LC-MS (ESI): m/z=338.2 [M+H]+.
Compound 5f (100 mg, 0.3 mmol) was dissolved in 3 ml of DMF, and CDI (58 mg, 0.36 mmol) was added. The mixture was stirred at room temperature for 30 minutes. In addition, 4,5,6,7-tetrahydro-1H-[1,2,3]triazolo[4,5-c]pyridine hydrochloride (192 mg, 1.2 mmol) was dissolved in 2 ml of DMF and DIEA (155 mg, 1.2 mmol) was added, and then the resulting solution was added to the reaction solution of 5f, reacted for 1 h, concentrated, separated firstly with HPLC (acetonitrile and water), and then separated with a preparative silica gel plate (MeOH/DCM=1/8) to obtain compound 5 (6 mg, 5%).
LC-MS (ESI): m/z=444.2 [M+H]+.
1H NMR (400 MHz, DMSO-d6) δ 7.91-7.88 (m, 2H), 7.28-7.25 (m, 2H), 7.18-7.16 (m, 2H), 6.99 (d, 1H), 4.82-4.75 (m, 2H), 4.69 (s, 1H), 4.48 (d, 2H), 3.88-3.82 (m, 2H), 3.40-3.34 (m, 2H), 2.94-2.89 (m, 3H), 2.76-2.74 (m, 1H).
Compound 6a (8.0 g, 43.0 mmol) was dissolved in DMF (100 mL), and then compounds bromobenzene (13.5 g, 85.9 mmol), 1,1′-binaphthyl-2,2′-bisdiphenylphosphino (4.0 g, 6.44 mmol), cesium carbonate (22.5 g, 68.9 mmol) and palladium acetate (965 mg, 4.3 mmol) were successively added. Under nitrogen protection, the mixture was reacted at 100° C. for 4 hours. The reaction solution was cooled to room temperature and filtered. The resulting solution was poured into water (200 mL), and extracted with ethyl acetate (60 mL×3). The organic phase was washed with saturated brine, dried over anhydrous sodium sulfate, concentrated, and separated and purified by silica gel column chromatography (PE/EA=4/1) to obtain compound 6b (5.6 g, 50%). LC-MS (ESI): m/z=263.2 [M+H]+.
At room temperature, a solution (60 mL) of 4N hydrochloric acid in 1,4-dioxane was added to compound 6b (5.6 g, 21.4 mmol). The mixture was stirred and reacted for 1 hour. After the reaction was completed, the reaction solution was concentrated to obtain 6c (5.5 g, a crude product), which was directly used in the next step. LC-MS (ESI): m/z=163.2 [M+H]+.
Compound 6c (5.5 g, a crude product) was dissolved in NMP (80 mL), DIEA (8.27 g, 64.1 mmol) and 5-bromo-2-chloropyridine (4.13 g, 21.4 mmol) were added, and the mixture was stirred and reacted at 100° C. for 2 hours. The reaction solution was poured into water (300 mL). A large number of solids were precipitated and filtered. The filter cake was dried to obtain compound 6d (4.0 g, two-step yield: 58%). LC-MS (ESI): m/z=319.2 and 321.2 [M+H]+.
Compound 6d (1.0 g, 3.1 mmol) was dissolved in N,N-dimethylacetylamide (15 mL), and copper cyanide (563 mg, 6.29 mmol), triethylamine (951 mg, 9.42 mmol) and 1,1′-bis(diphenylphosphine)ferrocene palladium dichloride (234 mg, 0.32 mmol) were successively added. Under nitrogen protection, the mixture was heated to 130° C., and reacted under microwave for 1 hour. After the reaction was completed, a system of water and ethyl acetate was poured into the reaction solution. The resulting solution was filtered, and then extracted twice with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated to obtain compound 6e (600 mg, 73%). LC-MS (ESI): m/z=266.2 [M+H]+.
Compound 6e (1.2 g, 4.5 mmol) was dissolved in 20 ml of isopropanol and 5 ml of water, potassium hydroxide (1.26 g, 22.5 mmol) was added, and the reaction mixture was refluxed for 3 hours. After TLC detected that the reaction was completed, the reaction solution was concentrated, diluted with water and extracted with ethyl acetate. The organic phase was adjusted to pH=4-5 with potassium bisulfate aqueous solution, and then extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate and concentrated to obtain compound 6f (510 mg, 40%). LC-MS (ESI): m/z=285.2 [M+H]+.
Compound 6f (500 mg, 1.76 mmol) was dissolved in DMF (10 mL), and then HATU (802 mg, 2.11 mmol) and DIPEA (681 mg, 5.28 mmol) were added. The mixture was stirred and reacted for 10 minutes, and then ethyl 3-hydrazinyl-3-oxopropanoate (309 mg, 2.11 mmol) was added and stirred at room temperature overnight. The reaction solution was poured into water (200 mL), extracted with ethyl acetate (50 mL×3), washed with saturated brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure to obtain compound 6g (400 mg, 55%). LC-MS (ESI): m/z=413.2 [M+H]+.
Compound 6g (1.0 g, 2.4 mmol) was dissolved in anhydrous tetrahydrofuran (15 mL), and Burgess reagent (1.15 g, 4.9 mmol) was added. The mixture was stirred at room temperature and reacted under nitrogen protection for 1 hour. After TLC detected that the reaction was completed, water was added and the resulting solution was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, concentrated, and then subjected to column chromatography (PE/EA=1/1) to obtain compound 6h (300 mg, 32%). LC-MS (ESI): m/z=395.2 [M+H]+.
Compound 6h (250 mg, 0.63 mmol) was dissolved in 9 ml of THF and 3 ml of water, and lithium hydroxide monohydrate (133 mg, 3.17 mmol) was added. The mixture was stirred at room temperature and reacted for 1 hour. After TLC detected that the reaction was completed, the reaction solution was concentrated, diluted with water and extracted with ethyl acetate. Then the aqueous layer was adjusted to pH=4-5 with potassium bisulfate aqueous solution, and extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate and concentrated to obtain compound 6i (120 mg, 52%). LC-MS (ESI): m/z=367.2 [M+H]+.
Compound 6i (120 mg, 0.33 mmol) was dissolved in 3 ml of DMF, and CDI (64 mg, 0.39 mmol) was added. The mixture was stirred at room temperature for 30 minutes. In addition, 4,5,6,7-tetrahydro-1H-[1,2,3]triazolo[4,5-c]pyridine hydrochloride (212 mg, 1.32 mmol) was dissolved in 2 ml of DMF and DIEA (170 mg, 1.32 mmol) was added, and then the resulting solution was added to the reaction solution of 6i, reacted for 1 h, separated firstly with HPLC (acetonitrile and water), and then separated and purified by silica gel column chromatography (MeOH/DCM=1/8) to obtain compound 6 (11 mg, 7%).
LC-MS (ESI): m/z=473.2 [M+H]+.
1H NMR (400 MHz, DMSO-d6) δ 8.83-8.79 (m, 2H), 8.38 (d, 1H), 7.15 (t, 2H), 6.61-6.52 (m, 3H), 4.81 (s, 1H), 4.68-4.62 (m, 2H), 4.41 (d, 2H), 3.85-3.83 (m, 2H), 3.62-3.58 (m, 1H), 3.34-3.28 (m, 1H), 3.24-3.20 (m, 1H), 2.92-2.89 (m, 1H), 2.76-2.73 (m, 1H), 2.34-2.29 (m, 1H), 2.10-2.05 (m, 1H).
Starting material 7a (20 g, 68.2 mmol) was dissolved in 200 mL of methanol, and then di-tert-butyl dicarbonate (16.4 g, 75.1 mmol) and triethylamine (20.7 g, 204.6 mmol) were added. The mixture was stirred at room temperature overnight until the reaction was completed (monitored by TLC). Most of the solvent was removed by rotation. 300 mL of saturated sodium bicarbonate solution was added, and then the resulting solution was extracted three times with 300 mL of ethyl acetate. The organic phase was combined, dried over anhydrous sodium sulfate and spun to dryness to obtain white solid 7b (21 g, yield 71.2%). LC-MS (ESI): m/z=313.2 [M+H]+.
Compound 7b (6.0 g, 19.2 mmol) was added to a 250 mL single-necked flask, and dissolved with toluene (60 mL) and water (6 mL). Cyclopropyl boronic acid (2.2 g, 25.0 mmol), potassium phosphate (8.2 g, 38.4 mmol), Pd2(dba)3 (1.8 g, 1.9 mmol) and Xphos (1.8 g, 3.8 mmol) were added, and the mixture was subjected to nitrogen replacement 3 times, reacted at 100° C. for 5 h, quenched with aqueous solution (100 mL), and extracted with EA (50 mL×3). The organic phase was combined, washed with saturated sodium chloride (5 mL×1), dried over anhydrous sodium sulfate, concentrated under reduced pressure, and subjected to column chromatography (PE:EA=4:1) to obtain compound 7c (6.2 g, a crude product), which was directly used in the next reaction. LC-MS (ESI): m/z=218.2 [M−55]+.
Compound 7c (6.2 g, a crude product) was added to a 250 mL single-necked flask, and dissolved with DCM (50 mL). TFA (50 mL) was added. The mixture was stirred at room temperature for 18 h, adjusted to pH=9 with saturated sodium bicarbonate (10 mL), and extracted with DCM (50 mL×2). The organic phase was combined, washed with saturated sodium chloride (5 mL×1), dried over anhydrous sodium sulfate, concentrated under reduced pressure, and separated and purified by silica gel column chromatography (PE/EA=2/1) to obtain compound 7d (2.3 g, 68%). LC-MS (ESI): m/z=174.2 [M+H]+.
Compound 7d (2.3 g, 11.9 mmol) was added to a 100 mL single-necked flask, and dissolved with EtOH (15 mL). DIPEA (3.8 g, 29.7 mmol) and 5-bromo-2-chloropyrimidin (3.8 g, 29.7 mmol) were added. The mixture was stirred at 90° C. for 3 h, cooled to room temperature, filtered by suction, and dried to obtain compound 7e as a white solid (2.2 g, 56%). LC-MS (ESI): m/z=330.1 [M+H]+.
Compound 7e (2.2 g, 6.7 mmol) was added to a 250 mL autoclave, and dissolved with methanol (20 mL) and DMF (20 mL). Pd(dppf)Cl2 (2.0 g, 2.7 mmol) was added. The mixture was subjected to carbon monoxide replacement 3 times, reacted at 20 atm and 100° C. for 10 h, filtered with diatomite, concentrated, separated and purified by silica gel column chromatography (PE/EA=3/1) to obtain compound 7f as a white solid (0.45 g, 22%). LC-MS (ESI): m/z=310.3 [M+H]+.
Compound 7f (0.45 g, 1.5 mmol) was added to a 100 mL eggplant-shaped flask, and dissolved with THF (5 mL) and water (5 mL). The mixture was stirred and reacted at room temperature for 3 h, adjusted to pH=4-5 with HCl (1M), and filtered to obtain compound 7g as a white solid (0.36 g, 84%).
LC-MS (ESI): m/z=296.2 [M+H]+.
Compound 7g (0.36 g, 1.2 mmol) was added to a 100 mL eggplant-shaped flask, and dissolved with DMF (5 mL). DIPEA (0.39 g, 3.0 mmol) and HATU (0.6 g, 1.6 mmol) were added. The mixture was stirred at room temperature for 10 minutes, and ethyl 3-oxo-3-hydrazinyl propanoate (0.36 g, 1.2 mmol) was added. The mixture was continuously stirred and reacted at room temperature overnight, and water (10 mL) was added. The resulting solution was extracted with EA (2×20 mL), separated and purified by silica gel column chromatography (PE/EA=2/3) to obtain compound 7h as a white solid (0.6 g). LC-MS (ESI): m/z=424.3 [M+H]+.
Compound 7h (550 mg, 1.3 mmol) was dissolved in dichloromethane (10 mL) and DMF (2 mL), triethylamine (328 mg, 3.3 mmol) was added, and p-toluenesulfonyl chloride (297 mg, 1.56 mmol) was added under an ice bath. The mixture was warmed to room temperature, and reacted under nitrogen protection for 4 hours with stirring. After TLC detected that the reaction was completed, the reaction solution was extracted with sodium bicarbonate aqueous solution and dichloromethane. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, concentrated, and separated and purified by silica gel column chromatography (PE/EA=1/1) to obtain compound 7i (200 mg, 38%). LC-MS (ESI): m/z=406.2 [M+H]+.
Compound 7i (200 mg, 0.49 mmol) was dissolved in 9 ml of THF and 3 ml of water, and lithium hydroxide monohydrate (104 mg, 2.5 mmol) was added. The mixture was stirred at room temperature and reacted for 1 hour. After TLC detected that the reaction was completed, the reaction solution was concentrated, diluted with water and extracted with ethyl acetate. Then the aqueous layer was adjusted to pH=4-5 with potassium bisulfate aqueous solution, and extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate and concentrated to obtain compound 7j (140 mg, 76%). LC-MS (ESI): m/z=378.2 [M+H]+.
Compound 7j (120 mg, 0.32 mmol) was dissolved in 3 ml of DMF, and CDI (62 mg, 0.38 mmol) was added. The mixture was stirred at room temperature for 30 minutes. Then 4,5,6,7-tetrahydro-1H-[1,2,3]triazolo[4,5-c]pyridine hydrochloride (205 mg, 1.28 mmol) was dissolved in 2 ml of DMF and dissociated with DIEA (165 mg, 1.28 mmol), and then the resulting solution was added to the reaction solution of 6i, reacted for 1 h, separated firstly with preparative HPLC (acetonitrile and water), and then separated and purified with a preparative silica gel plate (MeOH/DCM (v/v)=1/8) to obtain compound 7 (5 mg, 3%).
LC-MS (ESI): m/z=484.3 [M+H]+.
1H NMR (400 MHz, DMSO-d6) δ 14.63 (s, 1H), 8.82-8.79 (m, 2H), 8.36 (d, 1H), 7.08 (d, 1H), 6.92-6.87 (m, 2H), 4.81-4.66 (m, 3H), 4.41 (d, 2H), 3.86-3.82 (m, 2H), 3.25-3.21 (m, 2H), 2.91-2.88 (m, 3H), 2.78-2.76 (m, 1H), 1.90-1.86 (m, 1H), 0.91-0.89 (m, 2H), 0.62-0.60 (m, 2H).
Compound 8a (28.9 g, 98.6 mmol) was dissolved in methanol (500 ml), and triethylamine (29.9 g, 296 mmol) was added. The mixture was stirred at room temperature for 10 minutes, and (Boc)2O (21.5 g, 98.6 mmol) was added in portions. After the addition was completed, the resulting solution was stirred at room temperature overnight. The reaction solution was evaporated to dryness under reduced pressure, 600 ml of water was added to the residue and the mixture was stirred for 1 hour, and then filtered. The filter cake was dried to obtain compound 8b (30.0g, 97.4%).
Compound 8b (6.8 g, 21.8 mmol) was dissolved in DMF (80 ml), and Zn(CN)2 (3.5 g, 29.9 mmol) was added. The mixture was subjected to nitrogen replacement 3 times, then Pd(PPh3)4 (3.9 g, 3.4 mmol) was added, the resulting mixture was subjected to nitrogen replacement 3 times, and then warmed to 100° C. and stirred overnight. The reaction solution was subjected to evaporation under increased pressure to remove DMF, and the residue was separated and purified by silica gel column chromatography (PE/EA=5/1) to obtain 8c (4.8 g, 85.2%). LC-MS (ESI): m/z=259.3 [M+H]+.
8c (4.8 g, 18.6 mmol) was placed into a 100 ml single-necked flask, and HCl-dioxane (60 ml) was added. After the addition was completed, the mixture was stirred at room temperature overnight. The reaction solution was evaporated to dryness under increased pressure to obtain compound 8d (3.6 g, 100%).
Compound 8d (3.6 g, 18.6 mmol) and 5-bromopyrimidin-2-amine (3.2 g, 18.6 mmol) were dissolved in anhydrous ethanol (100 ml), and DIPEA (12.0 g, 93.0 mmol) was added. After the addition was completed, the mixture was warmed to 90° C. and stirred overnight. The reaction solution was evaporated to dryness under reduced pressure, 100 ml of water was added to the residue and the mixture was stirred for 30 minutes, and then filtered. The filter cake was dried to obtain compound 8e (5.1 g, 87.0%). LC-MS (ESI): m/z=315.3 [M+H]+.
Compound 8b (4.0 g, 12.7 mmol) was placed into an autoclave, DMF (30 ml), MeOH (30 ml) and DIPEA (4.9 g, 38.1 mmol) were added, and finally Pd(dppf)Cl2.CH2Cl2 (490 mg, 0.6 mmol) was added. After the addition was completed, the mixture was subjected to carbon monoxide replacement 3 times, then carbon monoxide was introduced until a pressure of 3.0 MPa, and the resulting mixture was heated to 110° C. and reacted for 15 hours. The reaction solution was evaporated to dryness under reduced pressure, and the residue was separated and purified by silica gel column chromatography (PE/EA=4/1) to obtain 8f (2.8 g, 74.9%). LC-MS (ESI): m/z=295.3 [M+H]+.
8f (2.8 g, 9.5 mmol) was placed into a 100 ml single-necked flask, methanol/water=1/1 (40 ml) and LiOH.H2O (2.0 g, 47.5 mmol) were successively added. After the addition was completed, the mixture was stirred at room temperature for 5 hours, and then subjected to evaporation under reduced pressure to remove methanol. The aqueous phase was adjusted to pH=5 with 1N dilute hydrochloric acid, stirred for 10 minutes, and then filtered. The filter cake was dried to obtain compound 8g (2.5 g, 93.9%).
8g (2.5 g, 8.9 mmol) and ethyl 3-oxo-3-hydrazinyl propanoate (1.4 g, 9.3 mmol) were dissolved in DMF (50 ml), and DIPEA (2.3 g, 17.8 mmol) and HATU (4.1 g, 10.7 mmol) were successively added. After the addition was completed, the mixture was stirred at room temperature overnight. 80 ml of water was added to the reaction solution, and the resulting solution was extracted 4 times with ethyl acetate. The organic phase was washed 3 times with saturated NaCl aqueous solution, dried over anhydrous sodium sulfate, and filtered. The filtrate was evaporated to dryness under reduced pressure. The residue was separated and purified by silica gel column chromatography (PE/EA=2/1) to obtain compound 8h (1.9 g, 52.3%).
Compound 8h (1.9 g, 6.8 mmol) was dissolved in anhydrous THF (30 ml), and Burgess reagent (3.2 g, 13.6 mmol) was added. After the addition was completed, the mixture was stirred at room temperature overnight. The reaction solution was evaporated to dryness under reduced pressure. The residue was separated and purified by silica gel column chromatography (PE/EA=2/1) to obtain compound 8i (1.0 g, 37.7%). LC-MS (ESI): m/z=391.2 [M+H]+.
Compound 8i (1.0 g, 2.6 mmol) was dissolved in THF/H2O=2/1 (15 ml), and LiOH—H2O (328 mg, 7.8 mmol) was added. After the addition was completed, the mixture was stirred at room temperature overnight. The reaction solution was subjected to evaporation under reduced pressure to remove THF. The aqueous phase was adjusted to pH=5 with 1N dilute hydrochloric acid, stirred for 10 minutes and then filtered. The filter cake was dried to obtain 8j (0.8 g, 84.9%).
8j (0.8 g, 2.2 mmol) and 4,5,6,7-tetrahydro-1H-[1,2,3]triazolo[4,5-c]pyridine hydrochloride (707 mg, 4.4 mmol) were dissolved in DMF (20 ml), and DIPEA (1.4 g, 11 mmol) and HATU (988 mg, 2.6 mmol) were successively added. After the addition was completed, the mixture was stirred at room temperature overnight. The reaction solution was slowly added dropwise into ice water, stirred for 2 minutes and then filtered. The filter cake was separated and purified by silica gel column chromatography (DCM/MeOH=15/1) to obtain compound 8 (47 mg, 4.6%).
1H NMR (400 MHz, DMSO-d6) δ 8.81 (brs, 2H), 8.42 (d, 1H), 7.69 (s, 1H), 7.63 (d, 1H), 7.45 (s, 1H), 8.81 (s, 1H), 4.77-4.72 (m, 1H), 4.68 (s, 1H), 4.43 (s, 1H), 4.39 (S, 1H), 3.87-381 (m, 2H), 3.41-3.32 (m, 1H), 3.06-2.97 (m, 2H), 2.91 (t, 1H), 2.75 (t, 1H). LC-MS (ESI): m/z=469.1 [M+H]+.
Starting material 8b (10 g, 32.1 mmol) was dissolved in 400 mL of anhydrous tetrahydrofuran, and then n-butyl lithium (2.5M, 32 mL, 80.1 mmol) was added under the condition of −78° C. The reaction mixture was stirred for 30 minutes under the same temperature, and then DMF (12.5 mL, 160.5 mmol) was added under the condition of −78° C. The mixture was returned to room temperature slowly, and then stirred for 15 minutes. After the reaction was completed, saturated ammonium chloride solution was added. Then the mixture was extracted three times with ethyl acetate. The organic phase was combined, dried over anhydrous sodium sulfate, spun to dryness, and separated and purified by silica gel column chromatography (PE/EA=6/1) to obtain 9b as a white solid (5.8 g, yield 69%). LC-MS (ESI): m/z=262.2 [M+H]+.
Compound 9b (5.8 g, 22.2 mmol) and dichloromethane (100 mL) were added to a 250 mL single-necked flask, and DAST (7.2 g, 44.4 mmol) was added at −10° C. The mixture was warmed to room temperature, reacted for 48 h, quenched with aqueous solution (100 mL), and extracted with dichloromethane (50 mL×3). The organic phase was combined, washed with saturated sodium chloride (50 mL×1), dried over anhydrous sodium sulfate, concentrated under reduced pressure, and separated and purified by silica gel column chromatography (PE/EA=9/1) to obtain 9c as a white solid (4.2 g, 67%). LC-MS (ESI): m/z=284.2 [M−55]+.
At room temperature, a solution (60 mL) of 4N hydrochloric acid in 1,4-dioxane was added to compound 9c (4.2 g, 14.8 mmol). The mixture was stirred and reacted for 1 hour. After the reaction was completed, the reaction solution was concentrated to obtain 9d (3.3 g, a crude product), which was directly used in the next step. LC-MS (ESI): m/z=184.2 [M+H]+.
Compound 9d (3.3 g, 18.0 mmol) was added to a 100 mL single-necked flask, and dissolved with NMP (40 mL). DIPEA (7.0 g, 54.1 mmol) and methyl 2-chloropyrimidin-5-carboxylate (3.1 g, 18.0 mmol) were added. The mixture was stirred at 100° C. for 2 h, cooled to room temperature, and poured into water. Solids were precipitated, filtered by suction, and dried to obtain compound 9e as a light yellow solid (2.5 g, 44%). LC-MS (ESI): m/z=320.1 [M+H]+.
Compound 9e (2.5 g, 7.84 mmol) was added to a 100 mL eggplant-shaped flask, and dissolved with THF (30 mL) and water (20 mL). Sodium hydroxide (940 mg, 23.51 mmol) was added. The mixture was stirred and reacted for 3 h under reflux, concentrated to remove tetrahydrofuran, adjusted to pH=4-5 with HCl (1M), and filtered to obtain compound 9f as a white solid (2.0 g, 84%). LC-MS (ESI): m/z=306.2 [M+H]+.
Compound 9f (3.6 g, 11.76 mmol) was added to a 100 mL eggplant-shaped flask, and dissolved with DMF (50 mL). DIPEA (4.55 g, 35.29 mmol) and HATU (6.7 g, 17.64 mmol) were added. The mixture was stirred at room temperature for 10 minutes, and ethyl 3-oxo-3-hydrazinyl propanoate (2.06 g, 14.11 mmol) was added. The resulting mixture was continuously stirred and reacted at room temperature overnight, and poured into water. A yellow solid was precipitated and filtered. The filter cake was dried to obtain compound 9g as a yellow solid (4.0 g, 78%). LC-MS (ESI): m/z=434.3 [M+H]+.
Compound 9g (4.0 g, 9.24 mmol) was dissolved in anhydrous tetrahydrofuran (50 mL), and Burgess reagent (4.4 g, 18.48 mmol) was added. The mixture was reacted under nitrogen protection at 70° C. for 1 hour. After TLC detected that the reaction was completed, water was added and the resulting solution was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, concentrated, and separated and purified by silica gel column chromatography (PE/EA=1/1) to obtain compound 9h (2.8 g, 73%). LC-MS (ESI): m/z=416.2 [M+H]+.
Compound 9h (2.8 g, 6.75 mmol) was dissolved in 30 ml of THF and 10 ml of water, and lithium hydroxide monohydrate (850 mg, 20.24 mmol) was added. The mixture was stirred at room temperature and reacted for 1 hour. After TLC detected that the reaction was completed, the reaction solution was concentrated, diluted with water and extracted with ethyl acetate. Then the aqueous layer was adjusted to pH=4-5 with potassium bisulfate aqueous solution, and extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate and concentrated to obtain compound 9i (2.3 g, 88%). LC-MS (ESI): m/z=388.2 [M+H]+.
Compound 9i (387 mg, 1.0 mmol) was dissolved in 5 ml of DMF, and CDI (195 mg, 1.2 mmol) was added. The mixture was stirred at room temperature for 30 minutes. Then 4,5,6,7-tetrahydro-1H-[1,2,3]triazolo[4,5-c]pyridine hydrochloride (482 mg, 3.0 mmol) was dissolved in 2 ml of DMF, and dissociated with DIEA (516 mg, 4.0 mmol), and the resulting solution was added to the reaction solution of 9i, reacted for 1 h, poured into water, and extracted with a mixed solvent of DCM/MeOH/MeCN. The extraction solution was spun to dryness, firstly separated with HPLC (acetonitrile and water), and then separated and purified by silica gel column chromatography (THF/DCM=1/3) to obtain compound 9 (70 mg, 14%). LC-MS (ESI): m/z=494.2 [M+H]+. 1H NMR (400 MHz, DMSO-d6) δ 8.83-8.79 (m, 2H), 8.38-8.36 (m, 1H), 7.40 (d, 3H), 6.97 (t, 1H), 4.81-4.68 (m, 3H), 4.43-4.39 (m, 2H), 3.87-3.81 (m, 2H), 3.35-3.31 (m, 2H), 3.02-2.72 (m, 4H).
Tert-butyl 3-amino-4-hydroxybenzoate (10a) (3 g, 14.34 mmol) and ethyl 3-ethoxy-3-iminopropionate hydrochloride 10b (3.37 g, 17.20 mmol) were dissolved in ethanol (20 mL), and stirred at 80° C. overnight. After the reaction was completed, the reaction was cooled to room temperature and the ethanol was concentrated under reduced pressure. Then the residue was dissolved in dichloromethane. The organic phase was washed with distilled water. The layers were separated. The organic phase was concentrated under reduced pressure to obtain target compound (10c) as a white solid (4 g, 91.37%). LC-MS (ESI): m/z=306.1 [M+H]+
Trifluoroacetic acid (2 mL) was added to a solution of compound 10c (4.9 g, 4.5 mmol) in dichloromethane (10 mL), and stirred at room temperature for 3 hours. After the reaction was completed, saturated sodium bicarbonate aqueous solution was added thereto to adjust the pH value to neutral, and then the resulting solution was extracted with dichloromethane. The organic layer was successively washed with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated to obtain the title compound 10d as a light yellow solid (3.9 g, 97.51%). LC-MS (ESI): m/z=250.3 [M+H]+
Compound 10d (1.2 g, 4.81 mmol), DMF (20 mL), HATU (2.2 g, 5.78 mmol) and N,N-diisopropylethylamine (1.3 g, 10 mmol) were successively added into a single-necked flask. The mixture was stirred and reacted for 15 minutes, then compound 1B (0.77 g, 5.78 mmol) was added, and the resulting mixture was continuously stirred and reacted at room temperature for 1 hour. After the reaction was completed, the reaction solution was diluted with water (30 mL), and extracted with ethyl acetate. The organic layer was washed with water and saturated brine, dried over anhydrous sodium sulfate and concentrated. The silica gel column chromatography (DCM:MeOH=60:1) was used for separation to obtain target compound 10f as a white solid (1.2 g, 68.4%). LC-MS (ESI): m/z=365.3 [M+H]+
Lithium hydroxide (0.44 g, 11 mmol) was added to a mixed solvent of compound 10f (1.2 g, 3.29 mmol) in tetrahydrofuran (10 mL) and water (5 mL), and the mixture was stirred at room temperature for 1 hour. After the reaction was completed, the mixture was treated with 10% citric acid aqueous solution to adjust to pH=6, and then extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated. The residue was slurried with diethyl ether to obtain target compound 10g as a yellow solid (1.0 g, 90.2%). LC-MS (ESI): m/z=337.2 [M+H]+
At room temperature, intermediate 1i (0.11 g, 0.61 mmol) and N,N-diisopropylethylamine (0.13 g, 1 mmol) were sequentially added slowly to a solution of compound 10g (0.12 g, 0.35 mmol), chloridized tetramethyluronium hexafluorophosphate (0.12 g, 0.42 mmol) and N-methyl imidazole (0.04 g, 0.52 mmol) in N,N-dimethylformamide (10 mL), and the mixture was stirred at room temperature under nitrogen protection for 3 h. After the reaction was completed, the reaction mixture was diluted with water (30 mL), and extracted with ethyl acetate (50 mL×2). The organic layer was washed with saturated brine (50 mL), dried over anhydrous sodium sulfate and concentrated to obtain a crude product. The crude product was separated and purified by silica gel column chromatography (DCM:MeOH=25:1) to obtain compound 10 (15 mg, 9.5%).
LC-MS (ESI): m/z=443.2 [M+H]+.
1H NMR (400 MHz, DMSO-d6) δ 8.77-8.75 (m, 1H), 8.26-8.24 (m, 1H), 7.96-7.93 (m, 1H), 7.77-7.73 (m, 1H), 7.25-7.22 (m, 2H), 7.18-7.13 (m, 2H), 4.81-4.69 (m, 3H), 4.43-4.40 (m, 2H), 3.88-3.81 (m, 2H), 3.31-3.32 (m, 2H), 3.03-2.97 (m, 2H), 2.87-2.74 (m, 2H).
Compound 11a (2.00 g, 12.98 mmol) and compound 11b (2.03 g, 12.98 mmol) were dissolved in tetrahydrofuran (40 mL), and Cs2CO3 (8.46 g, 25.95 mmol) was slowly added under an ice bath. The mixture was subjected to nitrogen replacement, and then reacted at 45° C. for 5 hours. After the reaction was completed, the reaction solution was cooled to room temperature. Water was added, and the resulting solution was extracted three times with ethyl acetate, washed with saturated brine, dried over anhydrous sodium sulfate, spun to dryness, and separated and purified by silica gel column chromatography (PE:EA=40:1) to obtain (11c) (3.00 g, 92.4%). LC-MS (ESI): m/z=251.1 [M+H]+. 1H NMR (400 MHz, CDCl3) δ 8.45 (d, 1H), 8.32 (dd, 1H), 7.85-7.80 (m, 1H), 4.27 (q, 2H), 4.10-4.05 (m, 2H), 2.04 (s, 1H), 1.31 (dd, 3H).
Compound 11c (1.6 g, 6.4 mmol) was dissolved in methanol, and Pd/C (160 mg) was added. The mixture was subjected to hydrogen replacement, and reacted overnight. DCM:MeOH=10:1 showed that the reaction was completed. The reaction solution was filtered, and concentrated under reduced pressure to obtain (11d) (1.18 g, 84%).
Compound 11d (1.18 g, 5.36 mmol) and compound 1B (1.09 g, 6.43 mmol) were dissolved in anhydrous dichloromethane, triphosgene (557 mg, 1.88 mmol) was added, and DIPEA (2.71 g, 26.8 mmol) was slowly added dropwise. The mixture was reacted at room temperature for 10 min. After the reaction was completed, the reaction solution was quenched with saturated ammonium chloride, and extracted with ethyl acetate (30 mL×2). The organic phase was washed with saturated brine, dried over anhydrous sodium sulfate, filtered and concentrated. The silica gel column chromatography (DCM:MeOH=60:1) was used for separation and purification to obtain product 11f as a white solid (1.15 g, 56.6%).
Compound 11f (1.15 g, 3.03 mmol) was dissolved in methanol, and an aqueous solution of lithium hydroxide (318 mg, 7.58 mmol) was slowly added dropwise. The mixture was reacted at room temperature. After the reaction was completed, the mixture was concentrated, water was added and the resulting solution was filtered. The filtrate was adjusted to pH=3-4 with HCl, and extracted with ethyl acetate (30 mL×2). The organic phase was washed with saturated brine, dried over anhydrous sodium sulfate, filtered and concentrated. Product 11g as a white solid (1.0 g, 93.9%) was obtained.
Compound 11g (400 mg, 1.138 mmol) and 11h (212 mg, 1.707 mmol) were dissolved in DMF, HATU (866 mg, 2.277 mmol) was added, and DIPEA (0.79 ml, 5.692 mmol) was added dropwise. The mixture was reacted at room temperature. After the reaction was completed, the mixture was diluted with water, and extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated. The silica gel column chromatography (DCM:MeOH=15:1) was used for separation and purification to obtain compound 11 (386 mg, 74.1%).
LC-MS (ESI): m/z=458.2 [M+H]+.
1H NMR (400 MHz, DMSO-d6) δ 8.58 (d, 1H), 7.94 (dd, 1H), 7.54-7.48 (m, 1H), 7.25 (dt, 2H), 7.18-7.13 (m, 2H), 7.08 (m, 1H), 6.50 (d, 1H), 4.80 (s, 1H), 4.68 (s, 1H), 4.49-4.39 (m, 1H), 4.30 (d, 2H), 3.91-3.80 (m, 2H), 3.22 (d, 1H), 3.18 (d, 1H), 2.88-2.72 (m, 4H).
Ethyl 2-chloro-4-methoxypyrimidine-5-carboxylate (12a) (2.2 g, 10 mmol), 2-aminoindan (1B) (1.33 g, 10 mmol) and N,N-diisopropylethylamine (2.6 g, 20 mmol) were dissolved in ethanol (20 mL), and stirred at 90° C. for 2 hours. After the reaction was completed, the mixture was cooled to room temperature, and the resulting solid was filtered, washed with ethanol (20 mL), and dried to obtain the title compound (12c) as a beige solid (1.4 g, 45%). LC-MS (ESI): m/z=314.1 [M+H]+.
Lithium hydroxide (1.08 g, 27 mmol) was added to a solution of compound ethyl 2-((2,3-dihydro 1H-inden 2-yl)amino)-4-methoxypyrimidine-5-carboxylate (12c) (1.2 g, 4.5 mmol) in tetrahydrofuran (30 mL) and distilled water (10 mL), and the reaction mixture was stirred at room temperature for 15 hours. After the reaction was completed, 2N hydrochloric acid aqueous solution was added thereto to adjust the pH value to 3, and then the resulting solution was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated to obtain the title compound (12d) (1.05 g) as a light yellow solid. LC-MS (ESI): m/z=286.2 [M+H]+
At 0° C., compound (2e) (0.65 g, 4 mmol), N,N-diisopropylethylamine (1.3 g, 10 mmol) and HATU (1.52 g, 4 mmol) were sequentially added slowly to a solution of compound (12d) (1.05 g, 3.7 mmol) in N,N-dimethylformamide (30 mL), and the mixture was stirred at room temperature under nitrogen flow for 1 hour. After the reaction was completed, the reaction mixture was cooled to room temperature, diluted with distilled water (30 mL), and extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate and concentrated. The silica gel column chromatography was used for separation to obtain the title compound (12f) as a white solid (1.21 g, 79%). LC-MS (ESI): m/z=414.2 [M+H]+
At 0° C., methyl N-(triethylamidosulfonyl)carbamate (1.6 g, 5.5 mmol) was added to a solution of compound (12f) (1.21 g, 2.9 mmol) in anhydrous tetrahydrofuran (50 mL), and the mixture was stirred at 70° C. under nitrogen atmosphere for 2 hours. After the reaction was completed, the mixture was cooled to room temperature, diluted with distilled water (80 mL), and extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate and concentrated. The residue was separated and purified by silica gel column chromatography to obtain the title compound (12g) as a yellow solid (0.86 g, 75%).
LC-MS (ESI): m/z=396.2 [M+H]+
Lithium hydroxide (0.44 g, 11 mmol) was added to a solution of compound (12g) (0.86 g, 2.2 mmol) in a mixed solvent of tetrahydrofuran (10 mL) and distilled water (5 mL), and the mixture was stirred at room temperature for 2 hour. After the reaction was completed, the mixture was treated with 2N hydrochloric acid aqueous solution to adjust to pH 2 or less, and then extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated. The residue was slurried with diethyl ether to obtain target compound 12h as a yellow solid (0.59 g, 73%). LC-MS (ESI): m/z=368.2 [M+H]+
At 0° C., intermediate 1i (0.11 g, 0.66 mmol), N,N-diisopropylethylamine (0.5 mL) and HATU (0.14 g, 0.36 mmol) were sequentially added slowly to a solution of compound (12h) (0.12 g, 0.33 mmol) in N,N-dimethylformamide (10 mL), and the mixture was stirred at room temperature under nitrogen protection for 3 h. After the reaction was completed, the reaction mixture was diluted with distilled water (30 mL), and extracted with ethyl acetate (50 mL×2). The organic layer was washed with saturated brine (50 mL), dried over anhydrous sodium sulfate and concentrated. The silica gel column chromatography was used for separation and purification to obtain compound 12 (14 mg).
LC-MS (ESI): m/z=474.2 [M+H]+.
1H NMR (400 MHz, CDCl3) δ 8.61 (s, 1H), 8.24 (s, 1H), 7.79 (s, 1H), 7.33-7.12 (m, 4H), 4.87 (s, 2H), 4.19 (s, 3H), 4.06-3.85 (m, 3H), 3.49-3.40 (m, 4H), 3.10-2.85 (m, 4H).
N-iodosuccinimide (14.8 g, 65.8 mmol) was added to solution of compound 13a (10.0 g, 59.8 mmol) in N,N-dimethylformamide (100 mL), and the mixture was stirred at 70° C. for 16 hours. After the reaction was completed, the mixture was diluted with distilled water (30 mL), and extracted with ethyl acetate (100 mL×3). The organic phase was washed with saturated brine (50 mL), dried over anhydrous sodium sulfate and concentrated. The silica gel column chromatography (eluent: petroleum ether:ethyl acetate=1: 0-0:1) was used for separation and purification to obtain the title compound 13b as a white solid (10.0 g, 57%). LC-MS (ESI): m/z=294.0 [M+H]+. 1H NMR (400 MHz, DMSO-d6) δ 12.48 (s, 1H), 8.36 (s, 1H), 8.08 (s, 1H), 4.24 (q, 2H), 1.28 (t, 3H).
Zinc cyanide (4.0 g, 34.1 mmol) and tetrakis(triphenylphosphine)palladium (0.99 g, 0.86 mmol) were added to a solution of compound 13b (5.0 g, 17.1 mmol) in N,N-dimethylformamide (10 mL), and the mixture was stirred at 110° C. for 4 hours. After the reaction was completed, the mixture was diluted with water (100 mL), and extracted with ethyl acetate (100 mL×4). The organic phase was washed with saturated brine, dried over anhydrous sodium sulfate and concentrated. The silica gel column chromatography (eluent: petroleum ether:ethyl acetate=1: 0-0:1) was used for separation and purification to obtain the title compound 13c as a white solid (1.3 g, 40%).
LC-MS (ESI): m/z=193.1 [M+H]+.
1H NMR (400 MHz, DMSO-d6) δ 13.12 (s, 1H), 8.46 (s, 1H), 8.34 (s, 1H), 4.26 (q, 2H), 1.29 (t, 3H).
Phosphorus oxychloride (6 ml) was added to a solution of compound 13c (1.3 g, 6.8 mmol) in 1,4-dioxane (10 mL), and the mixture was stirred at 100° C. for 2 hours. After the reaction was completed, the reaction solution was concentrated. The silica gel column chromatography (eluent: petroleum ether:ethyl acetate=1: 0-1:1) was used for separation and purification to obtain the title compound 13d as a white solid (0.9 g, 64%). LC-M S (ESI): m/z=211.1 [M+H]+. 1H NMR (400 MHz, DMSO-d6) δ 9.12 (s, 1H), 8.91 (s, 1H), 4.38 (q, 2H), 1.35 (t, 3H).
1B (1.1 g, 6.4 mmol) and cesium carbonate (2.8 g, 8.5 mmol) were added to a solution of compound 13d (0.9 g, 4.2 mmol) in N,N-dimethylformamide (10 mL), and the mixture was stirred at 110° C. for 2 hours. After the reaction was completed, the mixture was diluted with distilled water (30 mL), and extracted with ethyl acetate (30 mL×3). The organic phase was washed with saturated brine, dried over anhydrous sodium sulfate and concentrated. The silica gel column chromatography (eluent:petroleum ether:ethyl acetate=1:0-0:1) was used for separation and purification to obtain the title compound 13f as an off-white solid (1.25 g, 96%).
LC-MS (ESI): m/z=308.2 [M+H]+.
1H NMR (400 MHz, DMSO-d6) δ 8.81 (s, 1H), 8.32 (s, 1H), 8.06 (s, 1H), 7.23-7.20 (m, 2H), 7.17-7.14 (m, 2H), 4.96-4.92 (m, 1H), 4.28 (q, 2H), 3.25 (dd, 2H), 3.06 (dd, 2H), 1.30 (t, 3H).
Hydrazine hydrate (4 ml) was added to a solution of compound 13f (0.7 g, 2.0 mmol) in ethanol (10 mL), and the mixture was reacted at 80° C. for 16 hours. After the reaction was completed, the reaction solution was filtered, washed with ethanol and spun to dryness to obtain the title compound 13g as a grey solid (350 mg, 63%). LC-MS (ESI): m/z=294.1 [M+H]+. 1H NMR (400 MHz, DMSO-d6) δ 8.81 (s, 1H), 8.32 (s, 1H), 8.06 (s, 1H), 7.23-7.20 (m, 2H), 7.17-7.14 (m, 2H), 4.96-4.92 (m, 1H), 4.28 (q, 2H), 3.25 (dd, 2H), 3.06 (dd, 2H), 1.30 (t, 3H).
13h (0.23 g, 1.4 mmol), 2-(7-azabenzotriazole)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (0.54 g, 1.4 mmol) and N,N-diisopropylethylamine (0.39 g, 3.0 mmol) were added to a solution of compound 13g (0.35 g, 1.2 mmol) in N,N-dimethylformamide (6 mL), and the mixture was reacted at room temperature for 2 hours. After the reaction was completed, the mixture was diluted with distilled water (30 mL), and extracted with dichloromethane (20 mL×3). The organic phase was washed with distilled water and saturated brine, dried over anhydrous sodium sulfate and concentrated. Title compound 13i as a brown solid (720 mg) was obtained. LC-MS (ESI): m/z=434.1 [M−H]+.
4-toluene sulfonyl chloride (0.63 g, 3.3 mmol) and N,N,N′,N′-tetramethyl-1,6-hexanediamine (0.57 g, 3.3 mmol) were added to a solution of compound 13i (0.72 g, 1.7 mmol) in dichloromethane (10 mL), and the mixture was reacted at room temperature for 2 hours. After the reaction was completed, the mixture was diluted with dichloromethane (30 mL). The organic phase was washed with saturated brine, dried over anhydrous sodium sulfate and concentrated. The title compound 13j as a grey solid (150 mg, two-step yield: 30%) was obtained. LC-MS (ESI): m/z=418.2 [M+H]+. 1H NMR (400 MHz, DMSO-d6) δ 8.87 (s, 1H), 8.42 (s, 1H), 8.03 (d, 1H), 7.24-7.22 (m, 2H), 7.17-7.15 (m, 2H), 4.98-4.92 (m, 1H), 8.12 (s, 2H), 3.27 (dd, 2H), 3.06 (dd, 2H), 1.43 (s, 9H).
TFA (4 ml) was added to a solution of compound 13j (0.15 g, 0.36 mmol) in dichloromethane (6 mL), and the mixture was reacted at room temperature for 16 hours. After the reaction was completed, the reaction solution was diluted with dichloromethane (20 mL). The organic phase was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated to obtain the title compound 13k as a grey solid (120 mg, 92%). LC-MS (ESI): m/z=362.1 [M+H]+
Compound 1i (0.11 g, 0.66 mmol), N,N-diisopropylethylamine (0.21 g, 1.7 mmol) and benzotriazol-1-yl-oxy-tripyrrolidinophosphonium hexafluorophosphate (0.26 g, 0.50 mmol) were sequentially added slowly to a solution of compound 13k (0.12 g, 0.33 mmol) in N,N-dimethylformamide (6 mL), and the mixture was stirred at room temperature for 2 hours. After the reaction was completed, dichloromethane (20 mL) was added to the reaction solution, and the resulting mixture was diluted with water (20 mL), and extracted with dichloromethane (20 mL×3). The organic phase was washed with saturated brine, dried over anhydrous sodium sulfate and concentrated. The silica gel column chromatography (eluent:dichloromethane:ethyl acetate:methanol=1:0:0-2:10:1) was used for separation and purification to obtain white compound 13 (20 mg, 13%). LC-MS (ESI): m/z=468.2 [M+H]+. 1H NMR (400 MHz, DMSO-d6) δ 8.84 (dd, 1H), 8.39 (dd, 1H), 8.02 (d, 1H), 7.24-7.20 (m, 2H), 7.17-7.14 (m, 2H), 4.98-4.92 (m, 1H), 4.81 (s, 1H), 4.68 (s, 1H), 4.41 (d, 1H), 3.27 (dd, 2H), 3.06 (dd, 2H), 2.91 (t, 1H), 2.75 (t, 1H).
Starting material 14a (8.63 g, 50 mmol) was dissolved in 200 mL of NMP, and then 2,3-dihydro-1H-inden-2-amine hydrochloride (8.48 g, 50 mmol) and DIEA (14.2 g, 110 mmol) were added. The mixture was stirred and reacted at 100° C. for 2 hours. The reaction solution was poured into water (600 mL). A large number of solids were precipitated and filtered. The filter cake was dried to obtain compound 14b (9.8 g, 73%). LC-MS (ESI): m/z=270.2 [M+H]+.
Compound 14b (8.5 g, 31.6 mmol) and ethanol (100 mL) were added into a 250 mL single-necked flask, and then hydrazine hydrate (39.5 g, 632 mmol) was added. The mixture was stirred at room temperature overnight. A large number of solids were precipitated and then filtered. The filter cake was dried to obtain compound 14c (6.8 g, 80%). LC-MS (ESI): m/z=270.2 [M+H]+.
Compound 14c (6.8 g, 25.28 mmol) was dissolved in DMF (80 mL), and then HATU (14.41 g, 37.92 mmol) and DIPEA (9.78 g, 75.84 mmol) were added. The mixture was stirred and reacted for 10 minutes, and then 1-((tertbutoxycarbonyl)amino)cyclopropane-1-carboxylic acid (5.09 g, 25.28 mmol) was added. The mixture was stirred at room temperature overnight. The reaction solution was poured into water (250 mL). A large number of solids were precipitated and filtered. The filter cake was dried to obtain compound 14d (8.0 g 70%). LC-MS (ESI): m/z=453.2 [M+H]+.
Compound 14d (4.0 g, 8.85 mmol) was dissolved in anhydrous tetrahydrofuran (50 mL), and Burgess reagent (4.22 g, 17.7 mmol) was added. The mixture was heated to 70° C. and reacted under nitrogen protection for 1 h. After the reaction was completed, water was added and the resulting solution was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, concentrated, and separated and purified by silica gel column chromatography (PE/EA=1/1) to obtain compound 14e (2.1 g, 55%). LC-MS (ESI): m/z=435.1 [M+H]+.
At room temperature, a solution (10 mL) of 4N hydrochloric acid in 1,4-dioxane was added to compound 14e (500 mg, 1.15 mmol). The mixture was stirred and reacted for 1 hour. After the reaction was completed, the reaction solution was concentrated to obtain 14f (400 mg, a crude product), which was directly used in the next step. LC-MS (ESI): m/z=335.2 [M+H]+.
Compound 14f (400 mg, 1.19 mmol) was dissolved in 5 ml of DMF, and triethylamine (721 mg, 7.14 mmol) and CDI (193 mg, 1.19 mmol) were added. The mixture was stirred at room temperature for 1 h, and then 4,5,6,7-tetrahydro-1H-[1,2,3]triazolo[4,5-c]pyridine hydrochloride (191 mg, 1.19 mmol) was added. The resulting mixture was reacted overnight, and poured into water. Solids were precipitated. The solids were directly separated and purified by silica gel column chromatography (MeOH/DCM=1/8) to obtain compound 14 (70 mg, 12%).
LC-MS (ESI): m/z=485.2 [M+H]+.
1H NMR (400 MHz, DMSO-d6) δ 8.75 (d, 2H), 8.35 (d, 1H), 7.87 (s, 1H), 7.23-6.95 (m, 4H), 4.73-4.67 (m, 1H), 4.55 (s, 2H), 3.70-3.67 (m, 2H), 3.29-3.25 (m, 2H), 2.96-2.91 (m, 2H), 2.75-2.74 (m, 2H), 1.55-1.52 (m, 2H), 1.31-1.28 (m, 2H).
4e (100 mg, 0.28 mmol) was dissolved in DMF (2 mL). The resulting solution was cooled to 0° C. in an ice bath. 4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridine dihydrochloride (70 mg, 0.36 mmol) was added with stirring. HATU (136 mg, 0.36 mmol) was added, triethylamine (0.4 mL, 2.75 mmol) was added dropwise, and the mixture was stirred at room temperature overnight. Water (50 mL) was add and the resulting mixture was extracted with ethyl acetate (50 mL×2). The organic phase was combined, and washed once with water (100 mL), dried over sodium sulfate, filtered and spun to dryness. The residue was separated and purified by silica gel column chromatography to obtain compound 15 (30 mg, 23%).
LC-MS (ESI): m/z=469.2 [M+H]+.
1H NMR (400 MHz, DMSO-d6) δ 11.82 (s, 1H), 8.77 (m, 2H), 8.47-8.27 (m, 1H), 7.48 (s, 1H), 7.33-7.18 (m, 2H), 7.18-7.03 (m, 2H), 4.79-4.61 (m, 1H), 4.48 (s, 2H), 3.81 (s, 2H), 3.29-3.23 (m, 2H), 2.93 (dd, 2H), 2.64-2.52 (m, 2H), 1.72-1.63 (m, 2H), 1.63-1.48 (m, 2H).
Compound 4e (130 mg, 0.3577 mmol) and 16h (72 mg, 0.5366 mmol) were dissolved in DMF, HATU (272 mg, 0.7155 mmol) was added, and DIPEA (0.25 ml, 13.789 mmol) was added dropwise. The mixture was reacted at room temperature. After the reaction was completed, the mixture was diluted with water, and extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated. The silica gel column chromatography was used for separation and purification to obtain compound 16 (65 mg, 37.89%).
LC-MS (ESI): m/z=480.2 [M+H]+.
1H NMR (400 MHz, DMSO-d6) δ 8.80 (d, 2H), 8.39 (t, 1H), 7.75 (d, 1H), 7.25-7.19 (m, 4H), 7.17-7.13 (m, 2H), 7.09 (s, 1H), 6.96 (s, 1H), 6.83 (dd, 1H), 4.69 (dd, 1H), 3.27 (dd, 2H), 2.93 (dd, 2H), 2.07 (dd, 2H), 1.97 (dd, 2H).
Diisopropylamine (0.038 g, 0.38 mmol) and tetrahydrofuran (4 ml) were added to a flask, and n-BuLi (0.15 ml, 0.38 mmol) was added dropwise at −78° C. The mixture was stirred for 0.5 h, and then a solution of compound 17a (0.036 g, 0.075 mmol) in tetrahydrofuran (2 ml) was added dropwise to the flask and stirred at −78° C. for 0.5 h. Then a solution of N-fluorodibenzenesulfonimide (0.12 g, 0.38 mmol) in tetrahydrofuran (2 ml) was added dropwise to the reaction solution and stirred at −78° C. for 0.5 h. Then the mixture was continuously stirred to room temperature. After the reaction was completed, the reaction mixture was quenched with saturated ammonium chloride (20 mL) solution, and extracted with dichloromethane (30 mL×3). The organic phase was washed with saturated brine, dried over anhydrous sodium sulfate and concentrated. The silica gel column chromatography (eluent:dichloromethane:ethyl acetate:methanol=1:0:0-2:10:1) was used for separation and purification to obtain compound 17 (7 mg, 18%).
LC-MS (ESI): m/z=480.1 [M+H]+.
1H NMR (400 MHz, DMSO-d6) δ 8.95 (s, 1H), 8.89 (s, 1H), 8.59 (d, 2H), 7.24-7.22 (m, 2H), 7.18-7.14 (m, 2H), 4.84 (s, 2H), 4.76-4.71 (m, 1H), 3.99 (s, 1H), 3.93 (s, 1H), 3.29 (dd, 2H), 2.95 (dd, 2H), 2.87-2.83 (m, 2H).
4e (100 mg, 0.28 mmol) was dissolved in DMF (2 mL). The resulting solution was cooled to 0° C. in an ice bath. 1-(methylsulfonyl)piperazine trifluoroacetic acid salt (100 mg, 0.36 mmol) was added with stirring. HATU (136 mg, 0.36 mmol) was added, triethylamine (0.4 mL, 2.75 mmol) was added dropwise, and the mixture was stirred at room temperature overnight. Water (50 mL) was added. The mixture was stirred uniformly. Solids was precipitated and filtered by suction. The solids were separated and purified by silica gel column chromatography to obtain compound 18 (20 mg, 14%).
LC-MS (ESI): m/z=510.3 [M+H]+.
1H NMR (400 MHz, DMSO-d6) δ 8.83 (d, 2H), 8.39 (d, 1H), 7.25-7.19 (m, 2H), 7.18-7.11 (m, 2H), 4.76-4.64 (m, 1H), 3.73-3.54 (m, 4H), 3.34-3.30 (m, 1H), 3.28-3.23 (m, 1H), 3.20-3.07 (m, 4H), 2.94 (dd, 2H), 2.89 (s, 3H), 1.73-1.62 (m, 2H), 1.62-1.49 (m, 2H).
Ethyl 2-chlorooxazole-4-carboxylate (350 mg, 2 mmol), compound 1i (320 mg, 2 mmol) and N,N-diisopropylethylamine (1.3 g, 10 mmol) were dissolved in DMF (10 mL), and the mixture was stirred at 90° C. for 2 hours. After the reaction was completed, the mixture was cooled to room temperature, quenched by adding water (10 ml×2), extracted with dichloromethane (20 ml×2), washed with saturated brine (20 ml), dried, spun to dryness and separated and purified by silica gel column chromatography to obtain the title compound (19a) (350 mg, 67%).
LC-MS (ESI): m/z=264.1 [M+H]+.
Compound 19a (350 mg, 1.33 mmol), tetrahydrofuran (2 mL), methanol (5 ml), distilled water (2 mL) and lithium hydroxide monohydrate (300 mg, 7 mmol) were successively added to a single-necked flask, and the mixture was stirred at room temperature for 3 h. The reaction was quenched by adding dilute hydrochloric acid and extracted with dichloromethane (50 mL×2). The combined organic phase was dried over anhydrous sodium sulfate and concentrated under reduced pressure to obtain a crude product of compound 19b (280 mg, 89%). The crude product can be directly used in the next reaction.
LC-MS (ESI): m/z=236.1 [M+H]+.
Under nitrogen protection, compound 19b (100 mg, 0.42 mmol), DMF (10 mL), HATU (190 mg, 0.5 mmol), DIPEA (91 mg, 0.7 mmol) and intermediate 1 (113 mg, 0.5 mmol) were successively added to a single-necked flask, and the mixture was stirred at room temperature for 3 h. The reaction was quenched by adding aqueous solution (30 mL), extracted and allowed to stand for phase separation. The aqueous phase was washed with dichloromethane (100 mL×2). The combined organic phase was dried over anhydrous sodium sulfate and concentrated under reduced pressure to obtain a crude product which was separated and purified by silica gel column chromatography to obtain compound 19 (20 mg, 11%).
LC-MS (ESI): m/z=444.2 [M+H]+.
1H NMR (400 MHz, DMSO-d6) δ 7.81 (s, 3H), 7.27 (s, 1H), 6.42-6.41 (m, 3H), 6.35-6.33 (m, 3H), 3.94-3.91 (m, 2H), 3.20-3.17 (m, 4H), 2.19-2.10 (m, 5H).
At room temperature, ethanol (44 mL) was added to known compound 20a (10.0 g, 50 mmol), and then potassium hydroxide (2.8 g, 50 mmol) was added. The mixture was stirred at room temperature for 16 h and adjusted to pH to 5-6 with 6N HCl, water was added and the resulting solution was extracted with EA The EA phase was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to obtain 20b (8.5 g, 99%). LC-MS (ESI): m/z=173.1 [M+H]+.
Dichloromethane (30 mL), tert-butoxycarbonyl hydrazine (2.5 g, 19.2 mmol), HATU (7.3 g, 19.2 mmol) and DIEA (6.7 g, 52.2 mmol) were added to compound 20b (3.0 g, 17.4 mmol) at room temperature. The mixture was stirred at room temperature for 2 hours. Water was added and the resulting solution was extracted with DCM. The DCM phase was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. Then the residue was separated and purified by silica gel column chromatography (PE:EA=5:1) to obtain 20c (4.0 g, 81%). LC-MS (ESI): m/z=231.1 [M+H−56]+.
HCl/dioxane solution (50 mL) was added to compound 20c (4.0 g, 14 mmol), and the mixture was stirred at room temperature for 2 hours, and concentrated under reduced pressure to obtain 20d (2.6 g, a crude product).
At room temperature, dichloromethane (20 mL), compound 20d (1.6 g, 8.4 mmol), HATU (2.95 g, 7.7 mmol) and DIEA (1.6 g, 21.0 mmol) were successively added to intermediate 4a (1.8 g, 7.0 mmol), and the mixture was stirred at room temperature for 2 hours. The reaction solution was diluted with water, and extracted with dichloromethane. The organic phase was washed with saturated brine (50 mL), dried over anhydrous sodium sulfate, and concentrated under reduced pressure. Then the residue was separated and purified by silica gel column chromatography (PE:EA=2:1) to obtain 20f (1.5 g, 50%). LC-MS (ESI): m/z=424.2 [M+H]+.
At room temperature, dichloromethane (10 mL), N1,N1,N6,N6-tetramethylhexane-1,6-diamine (0.49 g, 2.8 mmol) and p-toluenesulfonyl chloride (0.54 g, 2.8 mmol) were successively added to compound 20f (0.8 g, 1.9 mmol). The mixture was stirred at room temperature for 2 hours, diluted by adding water, and extracted with dichloromethane. The dichloromethane phase was washed with saturated brine (20 mL), dried over anhydrous sodium sulfate, and concentrated under reduced pressure. Then the residue was separated and purified with silica gel column chromatography (PE:EA=1:1) to obtain 20g (500 mg, 76.6%).
At room temperature, tetrahydrofuran (5 mL), water (1 mL), and LiOH (0.26 g, 6.15 mmol) were successively added to compound 20g (0.5 g, 1.23 mmol), and the mixture was stirred at room temperature for 2 hour and adjusted to pH to 5-6 with 1N dilute hydrochloric acid, and extracted with ethyl acetate. The ethyl acetate phase was washed with saturated brine (20 mL), dried over anhydrous sodium sulfate, concentrated under reduced pressure to obtain 20h (0.45 g, 96.7%). LC-MS (ESI): m/z=378.2 [M+H]+.
At room temperature, DMF (2 mL), HATU (0.55 g, 1.44 mmol), 1i (0.4 g, 2.5 mmol) and DIEA (0.67 g, 3.6 mmol) were successively added to compound 20h (0.45 g, 1.2 mmol). The mixture was stirred at room temperature for 2 hours, diluted by adding water, and extracted with ethyl acetate. The organic phase was washed with saturated brine (20 mL), dried over anhydrous sodium sulfate, and concentrated under reduced pressure. Then the residue was separated and purified by silica gel column chromatography (DCM:MeoH=100: 1-20:1) to obtain Compound 20 (0.012 g, 1.7%).
1H NMR (400 MHz, CDCl3) δ 12.36 (s, 1H), 8.86-8.47 (m, 2H), 7.18-7.16 (m, 2H), 7.19-7.10 (m, 2H), 6.18-5.94 (m, 1H), 4.82-4.78 (m, 2H), 4.44 (s, 1H), 3.91-3.89 (m, 1H), 3.59-3.57 (m, 1H), 3.37-3.31 (m, 2H), 2.97-2.77 (m, 7H), 2.57-2.55 (m, 1H), 2.21-2.13 (m, 1H), 1.95-1.93 (m, 1H). LC-MS (ESI): m/z=484.2 [M+H]+.
Compound (21a) (5.0 g, 26.5 mmol) was added to a 250 mL single-necked flask, and dissolved with ethanol (50 mL). DIEA (13.7 g, 106 mmol) and 2,3-dihydro-1H-inden-2-amine hydrochloride (6.75 g, 39.8 mmol) were added at room temperature. Upon completion of the addition, the mixture was warmed to 85° C. and reacted for 3 hours. After the reaction was completed, the reaction solution was concentrated under reduced pressure. The crude product was directly used in the next step without purification. LC-MS (ESI): m/z=273.1 [M+H]+.
Compound (21b) (7.0 g, 25.7 mmol) and LiOH (5.13 g, 129 mmol) were added to a 250 mL single-necked flask, and dissolved with methanol (50 mL), water (50 mL) and tetrahydrofuran (50 mL). The mixture was reacted at room temperature for 3 hours. After the reaction was completed, 100 mL of water was added. The resulting solution was concentrated under reduced pressure to remove the organic solvent, and then adjusted to pH=2-3 with 4N hydrochloric acid. A large number of solids were precipitated and filtered. The filter cake was washed with water (20 mL×3). The filter cake was azeotropically dried by distilling off toluene and water three times, and concentrated to dryness to obtain compound 21c (5.0 g, 79.6%). LC-MS (ESI): m/z=245.1 [M+H]+.
Compound 21c (2.0 g, 8.19 mmol) was added into a 100 mL single-necked flask, and dissolved with DCM (20 mL). HATU (4.05 g, 10.6 mmol), triethylamine (2.45 g, 24.6 mmol) and ethyl 3-hydrazinyl-3-oxopropanoate (1.56 g, 10.6 mmol) were added. The mixture was reacted at room temperature for 16 h, washed with aqueous solution (10 mL), stirred at room temperature for 10 min, and then extracted with DCM (5 mL×3). The organic phase was combined, washed with saturated sodium chloride (5 mL×1), dried over anhydrous sodium sulfate, and concentrated under reduced pressure to obtain compound 21d (3.5 g, a crude product), which was directly used in the next reaction. LC-MS (ESI): m/z=373.1 [M+H]+.
Compound 21d (3.5 g) was added into a 100 mL single-necked flask, and dissolved with DCM (40 mL). TsCl (3.6 g, 19 mmol) and N1,N1,N6,N6-tetramethylhexane-1,6-diamine (3.2 g, 19 mmol) were added at room temperature, and then the mixture was reacted at room temperature overnight. The reaction solution was washed with aqueous solution (40 mL), stirred at room temperature for 10 min, and then extracted with DCM (50 mL×3). The organic phase was combined, washed with saturated sodium chloride (5 mL×1), dried over anhydrous sodium sulfate, concentrated under reduced pressure, and separated and purified by silica gel column chromatography to obtain compound 21e (0.6 g, 1.7 mmol). LC-MS (ESI): m/z=355.2 [M+H]+.
Compound (21e) (0.3 g, 0.847 mmol) and LiOH (0.169 g, 4.23 mmol) were added to a 100 mL single-necked flask, and dissolved with methanol (10 mL), water (10 mL) and tetrahydrofuran (10 mL). The mixture was reacted at room temperature for 3 hours. After the reaction was completed, 20 mL of water was added. The resulting solution was concentrated under reduced pressure to remove the organic solvent, then adjusted to pH=2-3 with 4N hydrochloric acid, and extracted with ethyl acetate (20 mL×3). The organic phase was combined, and concentrated to obtain compound 21f (0.2 g, 0.61 mmol, 72%). LC-MS (ESI): m/z=327.0 [M+H]+.
Compound 21f (0.20 g, 0.61 mmol) was added into a 100 mL single-necked flask, and dissolved with DMF (5 mL). PyBop (0.431 g, 0.827 mmol), DIPEA (0.317 g, 2.45 mmol) and 4,5,6,7-tetrahydro-1H-[1,2,3]triazolo[4,5-c]pyridine hydrochloride (0.197 g, 1.23 mmol) were added. The mixture was reacted at room temperature for 16 h, washed with aqueous solution (20 mL), stirred at room temperature for 10 min, and then extracted with ethyl acetate (20 mL×3). The organic phase was combined, washed with saturated sodium chloride (5 mL×1), dried over anhydrous sodium sulfate, concentrated under reduced pressure, and separated and purified by silica gel column chromatography (DCM:MeOH=20:1) to obtain compound 21 (0.016 g, 0.038 mmol, 6%).
LC-MS (ESI): m/z=433.2 [M+H]+.
1H NMR (400 MHz, CD3OD) δ 8.03 (d, 1H), 7.21 (dd, 2H), 7.14 (dd, 2H), 4.86 (s, 1H), 4.53 (dd, 1H), 4.37 (d, 2H), 3.96 (dd, 2H), 3.37 (d, 2H), 3.34 (d, 2H), 2.97 (t, 2H), 2.92 (d, 1H), 2.85 (t, 1H).
Compound 22a (500 mg, 1.98 mmol), acetyl chloride (312 mg, 3.95 mmol) and NMP (5 mL) were added into a microwave tube, heated to 120° C. under microwave and reacted for 1.5 hours. After the reaction was completed, the reaction system was added into water, and extracted with ethyl acetate (50 mL×3). The organic layer was dried over anhydrous sodium sulfate, and concentrated. The silica gel column chromatography was used for separation and purification to obtain the title compound 22b as a light yellow solid (170 mg, 70%).
1H NMR (400 MHz, CDCl3) δ 4.79 (s, 2H), 2.33 (s, 3H).
Compound 22b (200 mg, 1.63 mmol) was added to a solution of acetonitrile (10 mL), and copper bromide (725 mg, 3.26 mmol) and tert-butyl nitrite (335 mg, 3.26 mmol) were added successively under an ice bath. The mixture was stirred under an ice bath for 1 hour. After the reaction was completed, the mixture was diluted with a solution of saturated sodium bicarbonate (30 mL), and extracted with ethyl acetate (50 mL). The organic phase was dried over anhydrous sodium sulfate, and filtered. The filtrate was concentrated under reduced pressure, and then purified and separated by silica gel column chromatography (petroleum ether:ethyl acetate=10:1) to obtain compound 22c (100 mg, 33%).
1H NMR (400 MHz, CDCl3) δ 2.52 (s, 3H).
Compound 22c (400 mg, 2.14 mmol) was added to a mixed solvent of dioxane (10 mL) and water (1 mL), and then N-(2,3-dihydro-1H-inden-2-yl)-5-(4,4,5-trimethyl-1,3,2-dioxa-ol-2-yl)pyrimidin-2-amine (691 mg, 2.14 mmol), potassium carbonate (591 mg, 4.28 mmol) and Pd(dppf)Cl2 (73 mg, 0.1 mmol) were added. Under nitrogen protection, the mixture was warmed to 100° C. and stirred for 3 h. The reaction was cooled to room temperature, and filtered. The filtrate was concentrated, and separated and purified by silica gel column chromatography (petroleum ether:ethyl acetate=2:1) to obtain 22d (400 mg, 59%).
LC-MS (ESI): m/z=318.1 [M+H]+.
Diisopropylamine (127 mg, 1.26 mmol) was added to anhydrous tetrahydrofuran (3 mL), n-butyl lithium (0.5 mL, 1.26 mmol, 2.5M) was added under nitrogen protection and an ice bath, and the mixture was stirred for half an hour. Then the temperature was cooled to −78° C., then 22d (200 mg, 0.63 mmol) dissolved with tetrahydrofuran was added, and the mixture was continuously stirred for half an hour. Then dimethyl carbonate (114 mg, 1.26 mmol) was added, and the resulting mixture was stirred for half an hour, then warmed to room temperature and stirred for half an hour. After the reaction was completed, the reaction was quenched with saturated aqueous ammonium chloride solution, and extracted with ethyl acetate (80 mL). The organic layer was dried over anhydrous sodium sulfate, and concentrated. The silica gel column chromatography (petroleum ether:ethyl acetate=1:2) was used for separation and purification to obtain the title compound 22e as a yellow solid (110 mg, 47%). LC-MS (ESI): m/z=376.1 [M+H]+. 1H NMR (400 MHz, DMSO-d6) δ 7.23-7.26 (m, 4H), 7.19-7.22 (m, 2H), 6.42-6.43 (m, 1H), 4.89-4.93 (m, 1H), 3.93 (s, 2H), 3.80 (m, 3H), 3.41-3.47 (m, 2H), 2.93-2.98 (m, 2H).
Compound 22e (110 mg, 0.29 mmol) was dissolved in a mixed solution of dioxane (2 mL) and water (1 mL), then lithium hydroxide monohydrate (24 mg, 0.58 mmol) was added. The mixture was stirred at room temperature. After TLC detected that the reaction was completed, the reaction was adjusted to pH to 5-6 with 1M dilute hydrochloric acid, directly concentrated to dryness to obtain a crude product of the title compound 22f. The crude product was directly used in the next reaction. LC-MS (ESI): m/z=362.1 [M+H]+
At 0° C., compound 1i (66 mg, 0.42 mmol), N,N-diisopropylethylamine (0.5 mL) and benzotriazol-1-yl-oxy-tripyrrolidinophosphonium hexafluorophosphate (160 mg, 0.42 mmol) were sequentially added slowly to a solution of compound 22f (100 mg, 0.28 mmol) in N,N-dimethylformamide (3 mL). The mixture was stirred and reacted at room temperature. After the reaction was completed, the reaction mixture was diluted with distilled water (30 mL), and extracted with ethyl acetate (50 mL×2). The organic layer was washed with saturated brine (50 mL), dried over anhydrous sodium sulfate and concentrated. The silica gel column chromatography (DCM:THF=1:1) was used for separation and purification to obtain compound 22 (12 mg, 9%).
LC-MS (ESI): m/z=468.2 [M+H]+.
1H NMR (400 MHz, DMSO-d6) δ 8.70-8.73 (m, 2H), 8.46 (d, 1H), 7.21-7.24 (m, 2H), 7.14-7.17 (m, 2H), 4.68-4.78 (m, 4H), 4.33 (d, 2H), 3.82-3.83 (m, 1H), 3.26-3.32 (m, 2H), 2.88-2.97 (m, 3H), 2.72-2.74 (m, 1H).
Compound 4b (6 g, 22.3 mmol) and 3-ethoxy-2-fluoro-3-oxopropanoic acid (3.34 g, 22.3 mmol) were added to a solution of N,N-dimethylformamide (100 mL), and then N,N-diisopropylethylamine (5.75 g, 44.6 mmol) and benzotriazol-1-yl-oxy-tripyrrolidinophosphonium hexafluorophosphate (11 g, 28.99 mmol) were sequentially added slowly. The mixture was stirred and reacted at room temperature, and LCMS detected that the reaction was completed. After the reaction was completed, the reaction mixture was diluted with distilled water (200 mL), and extracted with ethyl acetate (200 mL×2). The organic layer was washed with distilled water and saturated brine (100 mL), dried over anhydrous sodium sulfate and concentrated. The crude product was purified and separated by silica gel column chromatography (petroleum ether:ethyl acetate=1:2) to obtain compound 23b as a white solid (3.4 g, 38%). LC-MS (ESI): m/z=402.1 [M+H]+
Compound 23b (2.4 g, 5.99 mmol) was added to a solution of anhydrous tetrahydrofuran (80 mL), and then Burgess reagent (1.71 g, 7.18 mmol) was added. The mixture was warmed to 75° C. and stirred for 2 hours. After the reaction was completed, the reaction solution was cooled, and the residue was purified by silica gel column chromatography (petroleum ether:ethyl acetate=1:1) to obtain the title compound 23c as white solid (1.6 g, 70%). LC-MS (ESI): m/z=384.1 [M+H]+
Compound 23c (1.5 g, 3.92 mmol) was dissolved in a mixed solution of dioxane (15 mL) and water (4 mL), and then lithium hydroxide monohydrate (329 mg, 7.84 mmol) was added. The mixture was stirred at room temperature. After TLC detected that the reaction was completed, the reaction solution was adjusted to pH to 3-4 with 1M dilute hydrochloric acid, extracted with ethyl acetate, dried over anhydrous sodium sulfate, filtered and concentrated to obtain the title compound 23d as a light yellow solid (1.4 g, 100%). LC-MS (ESI): m/z=356.1 [M+H]+
At 0° C., 1i (90 mg, 0.56 mmol), N,N-diisopropylethylamine (108 mg, 0.84 mmol) and benzotriazol-1-yl-oxy-tripyrrolidinophosphonium hexafluorophosphate (160 mg, 0.42 mmol) were sequentially added slowly to a solution of compound 23d (100 mg, 0.28 mmol) in N,N-dimethylformamide (3 mL). The mixture was stirred and reacted at room temperature, and LCMS detected that the reaction was completed. After the reaction was completed, the reaction mixture was diluted with distilled water (30 mL), and extracted with ethyl acetate (50 mL*3). The organic layer was washed with distilled water and saturated brine (50 mL), dried over anhydrous sodium sulfate and concentrated. The silica gel column chromatography (DCM:THF=1:1) was used for purification to obtain compound 23 (16 mg, 12%).
LC-MS (ESI): m/z=462.2 [M+H]+.
1H NMR (400 MHz, DMSO-d6) δ 8.77-8.90 (m, 2H), 8.50-8.51 (m, 1H), 7.22-7.24 (m, 2H), 7.11-7.17 (m, 2H), 4.60-4.82 (m, 3H), 3.76-3.88 (m, 2H), 3.23-3.32 (m, 2H), 2.90-2.97 (m, 2H), 2.67-2.89 (m, 3H).
Compound 24a (18 g, 90 mmol) and n-butyl nitrite (10.8 g, 90 mmol) were added to a solution of anhydrous methanol (270 mL), and then concentrated hydrochloric acid (4.5 mL) was added. The mixture was warmed to 75° C. and stirred for 10 hours. After the reaction was completed, the reaction solution was cooled and concentrated to dryness. The solid was washed with a small amount of ethyl acetate, and dried to obtain compound 24b (13 g, 63%). LC-MS (ESI): m/z=230.1 [M+H]+
A mixed solvent of compound 24b (5 g, 21.8 mmol), glacial acetic acid (100 mL) and concentrated sulphuric acid (5 mL), and palladium-carbon (500 mg) were successively added to a 250 mL autoclave, and 4 MPa of hydrogen gas was filled. The mixture was warmed to 95° C. and stirred for 15 h. The reaction was cooled to room temperature, and filtered through celite. The filtrate was concentrated, and separated and purified by silica gel column chromatography (DCM:MeOH=10:1) to obtain 24c (1.2 g, 27%). LC-MS (ESI): m/z=202.1 [M+H]+
Compound 24c (400 mg, 1.99 mmol) and ethyl 2-(5-(2-chloropyrimidin-5-yl)-1,3,4-oxadiazol-2-yl) acetate (533 mg, 1.99 mmol) were added to solution of NMP (10 mL), and then DIPEA (770 mg, 5.97 mmol) was added. The mixture was warmed to 100° C. and stirred for 2 hours, and cooled. The reaction mixture was diluted with distilled water (30 mL), and extracted with ethyl acetate (50 mL×2). The organic layer was washed with distilled water and saturated brine (50 mL), dried over anhydrous sodium sulfate and concentrated. The residue was purified by silica gel column chromatography to obtain the title compound 24d as a brown oil (120 mg, 14%). LC-MS (ESI): m/z=434.1 [M+H]+
Compound 24d (120 mg, 0.28 mmol) was dissolved in a mixed solution of dioxane (2 mL) and water (1 mL), and then lithium hydroxide hydrate (35 mg, 0.84 mmol) was added. The mixture was stirred at room temperature. After TLC detected that the reaction was completed, the reaction solution was concentrated under reduced pressure to dryness, then adjusted to pH to 5-6 with 1M dilute hydrochloric acid, and filtered. The solid was dried to obtain the title compound 24e as a brown solid (75 mg, 66%). LC-MS (ESI): m/z=406.1 [M+H]+
At 0° C., compound 1i (61 mg, 0.38 mmol), N,N-diisopropylethylamine (0.5 mL) and benzotriazol-1-yl-oxy-tripyrrolidinophosphonium hexafluorophosphate (108 mg, 0.29 mmol) were sequentially added slowly to a solution of compound 24e (75 mg, 0.19 mmol) in N,N-dimethylformamide (3 mL), and the mixture was stirred and reacted at room temperature. LCMS detected that the reaction was completed. After the reaction was completed, the reaction mixture was diluted with distilled water (30 mL), and extracted with ethyl acetate (50 mL×4). The organic layer was washed with distilled water and saturated brine (50 mL), dried over anhydrous sodium sulfate and concentrated. The silica gel column chromatography (DCM:THF=1:1) was used for purification to obtain compound 24 (18 mg, 19%).
LC-MS (ESI): m/z=512.2 [M+H]+.
1H NMR (400 MHz, DMSO-d6) δ 8.81-8.83 (m, 2H), 8.42 (d, 1H), 7.59 (s, 1H), 0.44-7.52 (m, 2H), 4.81 (s, 1H), 4.74-4.79 (m, 1H), 4.69 (s, 1H), 4.41 (d, 2H), 3.83-3.86 (m, 2H), 3.35-3.41 (m, 2H), 2.99-3.05 (m, 2H), 2.90-2.91 (m, 1H), 2.74-2.75 (m, 1H).
Compound 25a (4.0 g, 28.9 mmol) was dissolved in methanol (60 ml), and warmed to 40° C. N-butyl nitrite (3.3 g, 32.0 mmol) and hydrochloric acid (1.6 ml) were added quickly. After the addition was completed, the mixture was kept at 40° C. with stirring for 2 hours, and then subjected to evaporation under reduced pressure to remove methanol. PE/EtOH=10/1 (30 ml) was added to the residue, stirred for 5 minutes, and filtered. The filter cake was dried to obtain compound 25b (2.5 g, 52.1%).
Compound 25b (2.5 g, 15.0 mmol) was dissolved in MeOH (50 ml), and Pd/C (0.5 g) and (Boc)2O (3.9 g, 18.0 mmol) were added. After the addition was completed, the mixture was subjected to nitrogen replacement 3 times, and then H2 was introduced. The resulting mixture was stirred at room temperature overnight. The reaction solution was filtered. The filtrate was evaporated to dryness under reduced pressure. The residue was purified by silica gel column chromatography (PE/EA=5/1) to obtain 25c (2.6 g, 68.4%).
NaBH4 (783 mg, 20.6 mmol) was placed into a 100 ml single-necked flask, THF (2.5 ml) was added, and a methanol solution (10 ml) of 25c (2.6 g, 10.3 mmol) was added dropwise at room temperature. After the addition was completed, the mixture was stirred at room temperature overnight. Water (30 ml) was added to the reaction solution, and the resulting solution was stirred for 10 minutes, and then extracted 3 times with EA. The organic phase was combined, washed once with saturated NaCl aqueous solution, dried over anhydrous sodium sulfate, and filtered. The filtrate was evaporated to dryness under reduced pressure to obtain compound 25d (2.2 g, 91.7%).
Compound 25d (2.2 g, 9.3 mmol) was dissolved in DCM (30 ml), and trifluoroacetic acid (1.0 g) was added. The resulting solution was cooled to 0° C. with an ice bath, and Et3SiH (1.1 g) was added dropwise. After the addition was completed, the mixture was slowly returned to room temperature and stirred for 2 hours. The reaction solution was evaporated to dryness under reduced pressure. Diethyl ether (30 ml) was added to the residue, and the resulting mixture was stirred for 10 minutes, and then filtered. The filter cake was dried to obtain compound 25e (1.2 g, 94.5%).
Compound 25e (1.2 g, 8.7 mmol) was dissolved in methanol (50 ml), and Pd/C (1.2 g) was added. After the addition was completed, the mixture was subjected to hydrogen gas replacement 3 times, and stirred at room temperature overnight. LC-MS detected that the reaction was completed. The reaction solution was filtered. The filtrate was evaporated to dryness under reduced pressure to obtain 25f (0.8 g, 66.7%). LC-MS (ESI): m/z=140.1 [M+H]+.
25f (200 mg, 1.4 mmol) and intermediate 2 (376 mg, 1.4 mmol) were placed into a 100 ml single-necked flask, and NMP (30 ml) and DIPEA (80 mg, 4.2 mmol) were added. After the addition was completed, the mixture was warmed to 100° C. and stirred and reacted for 2 hours. LC-MS detected that the reaction was completed. The reaction solution was purified by silica gel column chromatography (PE/EA=2/1) to obtain compound 25g (180 mg, 34.6%). LC-MS (ESI): m/z=372.2 [M+H]+.
25g (180 mg, 0.5 mmol) was dissolved in THF (5 ml) and H2O (2 ml), and LiOH—H2O (63 mg, 1.5 mmol) was added. After the addition was completed, the mixture was stirred at room temperature for 3 hours. The reaction solution was evaporated to dryness under reduced pressure. Water (5 ml) was added to the residue. The mixture was adjusted to pH=5 with 2N dilute hydrochloric acid, and extracted 4 times with ethyl acetate. The organic phase was combined, dried over anhydrous sodium sulfate, and filtered. The filtrate was evaporated to dryness under reduced pressure to obtain compound 25h (150 mg, 87.2%). LC-MS (ESI): m/z=344.1 [M+H]+.
Compound 25h (50 mg, 0.15 mmol) was dissolved in DMF (5 ml), and CDI (29 mg, 0.18 mmol) was added. The mixture was stirred at room temperature for 10 minutes, and then a solution (2 ml) of triethylamine (606 mg, 6 mmol) and 1i (61 mg, 0.38 mmol) in DMF was added. After the addition was completed, the resulting mixture was stirred at room temperature for 2 hours and filtered. The filtrate was purified by silica gel column chromatography (DCM/MeOH=15/1) to obtain compound 25 (40 mg, 59.7%).
LC-MS (ESI): m/z=450.2 [M+H]+.
1H NMR (400 MHz, DMSO-d6) δ 14.72 (m, 1H), 8.84-8.77 (m, 2H), 8.53 (d, 1H), 7.37 (d, 1H), 6.89 (d, 1H), 5.16-5.07 (m, 1H), 4.81 (s, 1H), 4.68 (s, 1H), 4.43 (s, 1H), 4.39 (s, 1H), 3.87-3.81 (m, 2H), 3.35-3.32 (m, 1H), 3.18-3.12 (m, 1H), 2.92-2.83 (m, 2H), 2.78-2.72 (m, 2H).
Compound 26a (10 g, 58.1 mmol) was added to a 500 mL single-necked flask, and dissolved in 40 mL of THF. A solution of borane in THF (145 mL, 145 mmol, 1.0M) was added at 0° C. The mixture was stirred at room temperature overnight. The reaction was quenched with 100 ml THF/H2O (1:1), and then 150 ml of saturated sodium bicarbonate solution was added. The resulting solution was extracted with EA (100 mL×3). The organic phase was combined, washed with saturated sodium chloride (100 mL), dried over anhydrous sodium sulfate, and concentrated under reduced pressure to obtain compound 26b (5.1 g, yield 61%). LC-MS (ESI): m/z=145.2 [M+H]+.
Compound 26b (5.1 g, 35.4 mmol) was dissolved in 60 ml of DCM, and thionyl chloride (6 mL) was added under an ice bath. Then the mixture was warmed to room temperature and reacted overnight. After TLC detected that the reaction was completed, the reaction was quenched with ice water, extracted with DCM, washed with saturated sodium bicarbonate and brine, dried over anhydrous sodium sulfate, spun to dryness, and separated and purified by silica gel column chromatography (PE/EA=10/1) to obtain compound 26c (2.6 g, 41%). LC-MS (ESI): m/z=181.1 [M+H]+.
Diethyl malonate (6.5 g, 40.9 mmol) was dissolved in anhydrous THF (100 mL), and 60% sodium hydride (4.1 g, 102.2 mmol) was added under the condition of ice bath, and then stirred for 30 minutes under an ice bath. Then compound 26c (7.4 g, 40.9 mmol) was added under reflux, and the reaction was continued for 3 h. The reaction was quenched with water, extracted with ethyl acetate (50 mL×3), washed with saturated brine, dried over anhydrous sodium sulfate, concentrated, and separated and purified by silica gel column chromatography (PE/EA=6/1) to obtain compound 26d (6.0 g, 55%). LC-MS (ESI): m/z=269.2 [M+H]+.
Compound 26d (5.2 g, 19.4 mmol) was dissolved in DMSO (40 mL), water (2 mL) was added, and then sodium chloride solid (5.2 g) was added. The mixture was heated to reflux and reacted for 5 hours. The reaction solution was cooled to room temperature, water was added and the resulting solution was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, concentrated, and separated and purified by silica gel column chromatography (PE/EA=10/1) to obtain compound 26e (2.0 g, 52%). LC-MS (ESI): m/z=197.2 [M+H]+.
Compound 26e (2.0 g, 10.2 mmol) was dissolved in 15 ml of ethanol and 5 ml of water, and potassium hydroxide (1.71 g, 30.6 mmol) was added. The mixture was stirred at room temperature and reacted for 1 hour. After TLC detected that the reaction was completed, the reaction solution was concentrated, diluted by adding water, and extracted with diethyl ether. The aqueous phase was then adjusted to a pH of less than 5 with 4N HCl, and extracted with DCM. The organic phase was washed with brine, dried over anhydrous sodium sulfate, filtered and spun to dryness to obtain compound 26f (1.3 g, 76%). LC-MS (ESI): m/z=169.2 [M+H]+.
Compound 26f (1.1 g, 6.5 mmol) was dissolved in 10 ml of tert-butanol, and then triethylamine (661 mg, 6.5 mmol) and DPPA (1.8 g, 6.5 mmol) were successively added. The mixture was refluxed and reacted overnight under nitrogen protection, cooled to room temperature and concentrated, and separated by silica gel column chromatography (PE/EA=2/1) to obtain compound 26g (1.2 g, 77%). LC-MS (ESI): m/z=184.2 [M−55]+.
Compound 26g (1.2 g, 5.0 mmol) was dissolved in a solution of 4N 1,4-dioxane (20 ml), stirred at room temperature, and reacted for 1 hour. After TLC detected that the reaction was completed, the reaction solution was concentrated to obtain compound 26h (755 mg, 86%). LC-MS (ESI): m/z=140.2 [M+H]+.
Compound 26h (177 mg, 1.0 mmol) was added to a 100 mL single-necked flask, and dissolved with NMP (4 mL). DIPEA (387 mg, 3.0 mmol) and intermediate 2 (268 mg, 1.0 mmol) were added. The mixture was stirred at 100° C. for 2 h, cooled to room temperature, and poured into water. Solids were precipitated, filtered by suction, and dried to obtain compound 26i as a light yellow solid (205 mg, 55%). LC-MS (ESI): m/z=372.2 [M+H]+.
Compound 26i (205 mg, 0.55 mmol) was dissolved in 5 ml of THF and 2 ml of water, and lithium hydroxide monohydrate (69 mg, 1.65 mmol) was added. The mixture was stirred at room temperature and reacted for 1 hour. After TLC detected that the reaction was completed, the reaction solution was concentrated, diluted by adding water, and extracted twice with diethyl ether. The aqueous phase was adjusted to pH to 4-5 by adding additional 4N hydrochloric acid aqueous solution, extracted with dichloromethane, dried over anhydrous sodium sulfate, filtered, and spun to dryness to obtain compound 26j (165 mg, 87%). LC-MS (ESI): m/z=344.2 [M+H]+.
Compound 26j (165 mg, 0.48 mmol) was dissolved in 3 ml of DMF, and CDI (94 mg, 0.58 mmol) was added. The mixture was stirred at room temperature for 30 minutes. Then 4,5,6,7-tetrahydro-1H-[1,2,3]triazolo[4,5-c]pyridine hydrochloride (231 mg, 1.44 mmol) was dissolved in 2 ml of DMF, and dissociated with DIPEA (248 mg, 1.92 mmol), and the resulting solution was added to the reaction solution of 26j for reacting for 1 h, and directly separated by silica gel column chromatography (MeOH/DCM=10/1) to obtain compound 26 (25 mg, 12%).
LC-MS (ESI): m/z=450.2 [M+H]+.
1H NMR (400 MHz, DMSO-d6) δ 8.84-8.78 (m, 2H), 8.46 (d, 1H), 7.06 (s, 2H), 4.95-4.90 (m, 1H), 4.81 (s, 1H), 4.68 (s, 1H), 4.41 (d, 2H), 3.87-3.81 (m, 2H), 3.14-3.08 (m, 2H), 2.69 (t, 1H), 2.74-2.67 (m, 3H).
Compound 27a (10.0 g, 52 mmol) was dissolved in anhydrous ethanol (100 mL), and then potassium hydroxide (2.92 g, 52 mmol) was added. The reaction mixture was heated to reflux and reacted for 4 hours. The reaction solution was cooled to room temperature and the ethanol was concentrated. Water and diethyl ether were added. The aqueous phase was adjusted to pH to 3-4 with additional 4N hydrochloric acid, and extracted with ethyl acetate (50 mL×3). The organic phase was washed with saturated brine, dried over anhydrous sodium sulfate, filtered and concentrated to obtain compound 27b (5.5 g, 64%). LC-MS (ESI): m/z=165.2 [M+H]+.
Compound 27b (1.8 g, 11 mmol) was dissolved in DMF (80 mL), and then HATU (5.7 g, 15 mmol) and DIPEA (3.87 g, 30 mmol) were added. The mixture was stirred and reacted for 10 minutes, and then compound 4b (2.69 g, 10 mmol) was added. The mixture was stirred at room temperature overnight. The reaction solution was poured into water (250 mL). A large number of solids were precipitated and filtered. The filter cake was dried to obtain compound 27c (2.4 g 58%). LC-MS (ESI): m/z=416.2 [M+H]+.
Compound 27c (2.48 g, 5.98 mmol) was dissolved in anhydrous tetrahydrofuran (25 mL), and Burgess reagent (4.27 g, 17.93 mmol) was added. The mixture was stirred at room temperature and refluxed and reacted under nitrogen protection for 1 hour. After TLC detected that the reaction was completed, water was added and the resulting solution was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, concentrated, and purified by silica gel column chromatography (PE/EA=1/1) to obtain compound 27d (1.2 g, 50%). LC-MS (ESI): m/z=398.2 [M+H]+.
Compound 27d (1.2 g, 3.02 mmol) was dissolved in 9 ml of THF and 3 ml of water, and lithium hydroxide monohydrate (381 mg, 9.07 mmol) was added. The mixture was stirred at room temperature and reacted for 1 hour. After TLC detected that the reaction was completed, the reaction solution was concentrated, diluted with water and extracted with diethyl ether. Then the aqueous layer was adjusted to pH to 4-5 with 4N hydrochloric acid aqueous solution, and extracted with dichloromethane. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate and concentrated to obtain compound 27e (850 mg, 76%). LC-MS (ESI): m/z=370.2 [M+H]+.
Compound 27e (123 mg, 0.33 mmol) was dissolved in 3 ml of anhydrous DCM, and oxalyl chloride (64 mg, 0.5 mmol) and a catalytic amount of DMF were added. The mixture was stirred at room temperature for 30 minutes. Then 4,5,6,7-tetrahydro-1H-[1,2,3]triazolo[4,5-c]pyridine hydrochloride (133 mg, 0.83 mmol) was dissolved in 3 ml of anhydrous DMSO, and triethylamine (134 mg, 1.32 mmol) was added. Then the solution was added to the above-mentioned reaction solution and reacted for 1 h. The resulting solution was concentrated to remove DCM, and then purified by silica gel column chromatography (THF/DCM=1/3) to obtain compound 27 (40 mg, 26%).
LC-MS (ESI): m/z=476.2 [M+H]+.
1H NMR (400 MHz, DMSO-d6) δ 8.92-8.81 (m, 2H), 8.50 (d, 1H), 7.24-7.14 (m, 4H), 4.76-4.69 (m, 3H), 4.00-3.90 (m, 2H), 3.32-3.26 (m, 2H), 2.99-2.95 (m, 2H), 2.83-2.81 (m, 2H), 2.16-2.07 (m, 3H).
28b (2.0 g, 10.71 mmol) and triethylamine (4.3 g, 42.87 mmol) were added to a solution of compound 28a (3.0 g, 10.71 mmol) in ethanol (30 mL), and the mixture was stirred at 80° C. for 4 hours. After the reaction was completed, the mixture was diluted with distilled water (30 mL), and extracted with ethyl acetate (30 mL×3). The organic phase was washed with distilled water and saturated brine, dried over anhydrous sodium sulfate and concentrated. The silica gel column chromatography (eluent: petroleum ether:ethyl acetate=1: 0-0:1) was used for separation and purification to obtain the title compound 28c as an off-white solid (3.7 g, 100%). LC-MS (ESI): m/z=348.1, 350.1 [M+H]+. 1H NMR (400 MHz, DMSO-d6) δ 8.79 (s, 1H), 8.73 (s, 1H), 8.44 (d, 1H), 7.42 (s, 1H), 7.33 (d, 1H), 7.18 (d, 1H), 4.73-4.66 (m, 1H), 3.80 (s, 3H), 3.27-3.20 (m, 2H), 2.96-2.86 (m, 2H).
Compound 28c (5.0 g, 14.36 mmol) was dissolved in tetrahydrofuran (50 mL)/methanol (5 ml) and distilled water (5 ml), and then LiOH (1.0 g, 43.08 mmol) was added. Then the mixture was reacted at room temperature for 16 hours. After the reaction was completed, the reaction solution was cooled, adjusted to pH=3 by adding acid, and then extracted with ethyl acetate (50 mL×3). The organic phase was dried over anhydrous sodium sulfate, and filtered. The filtrate was concentrated under reduced pressure to obtain target compound 28d as an off-white solid (4.5 g, 94%). LC-MS (ESI): m/z=334.1, 336.1 [M+H]+. 1H NMR (400 MHz, DMSO-d6) δ 12.67 (s, 1H), 8.77 (s, 1H), 8.71 (s, 1H), 8.31 (d, 1H), 7.42 (s, 1H), 7.33 (m, 1H), 7.18 (d, 1H), 4.73-4.67 (m, 1H), 3.31-3.17 (m, 2H), 2.96-2.85 (m, 2H).
2e (0.23 g, 1.4 mmol), 2-(7-azabenzotriazole)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (0.54 g, 1.4 mmol) and N,N-diisopropylethylamine (0.39 g, 3.0 mmol) were added to a solution of compound 28d (0.35 g, 1.2 mmol) in N,N-dimethylformamide (6 mL), and the mixture was reacted at room temperature for 2 hours. After the reaction was completed, the mixture was diluted with distilled water (30 mL), and extracted with dichloromethane (20 mL×3). The organic phase was washed with distilled water and saturated brine, dried over anhydrous sodium sulfate and concentrated. Title compound 28e as a brown solid (720 mg) was obtained. LC-MS (ESI): m/z=460.1, 462.1 [M−H]+.
4-toluene sulfonyl chloride (0.83 g, 4.33 mmol) and N,N,N′,N′-tetramethyl-1,6-hexanediamine (1.12 g, 6.49 mmol) were added to a solution of compound 28e (1.0 g, 2.16 mmol) in dichloromethane (20 mL), and the mixture was reacted at room temperature for 2 hours. After the reaction was completed, the mixture was diluted with dichloromethane (30 mL). The organic phase was washed with distilled water and saturated brine, dried over anhydrous sodium sulfate and concentrated. The silica gel column chromatography (eluent: petroleum ether:ethyl acetate=1:0-0:1) was used for separation and purification to obtain the title compound 28f as a grey solid (550 mg, two-step yield: 42%). LC-MS (ESI): m/z=444.1, 446.1, [M+H]+. 1H NMR (400 MHz, DMSO-d6) δ 8.86 (s, 1H), 8.81 (s, 1H), 8.43 (d, 1H), 7.43 (s, 1H), 7.33 (d, 1H), 7.19 (d, 1H), 4.74-4.69 (m, 1H), 4.23 (s, 2H), 4.17 (q, 2H), 3.33-3.22 (m, 2H), 2.98-2.87 (m, 2H), 1.22 (t, 3H).
Compound 28i (0.15 g, 1.33 mmol), tri-potassium phosphate monohydrate (1.23 g, 3.65 mmol) and bis(triphenylphosphine)palladium dichloride (0.04 g, 0.06 mmol) were added to a solution of compound 28f (0.54 g, 1.22 mmol) in dioxane/water (10 ml/1 ml), and the mixture was stirred at 90° C. for 4 hours. After the reaction was completed, the mixture was diluted with distilled water (30 mL), and extracted with ethyl acetate (20 mL×4). The organic phase was washed with distilled water and saturated brine, dried over anhydrous sodium sulfate, concentrated and subjected to silica gel column chromatography (eluent: petroleum ether:ethyl acetate=1:0-0:1) to obtain the title compound 28g as a light yellow solid (0.3 g, 56%). LC-MS (ESI): m/z=432.2 [M+H]+. 1H NMR (400 MHz, DMSO-d6) δ 8.87 (s, 1H), 8.81 (s, 1H), 8.43 (d, 1H), 8.12 (s, 1H), 7.71 (t, 1H), 7.48 (s, 1H), 7.41 (d, 1H), 7.24 (d, 1H), 6.92 (s, 1H), 4.77-4.72 (m, 1H), 4.23 (s, 2H), 4.17 (q, 2H), 3.34-3.26 (m, 2H), 3.00-2.95 (m, 2H), 1.22 (t, 3H).
Compound 28g (0.3 g, 0.70 mmol) was dissolved in tetrahydrofuran (6 mL)/methanol (2 ml) and distilled water (2 ml), and then LiOH (0.05 g, 2.09 mmol) was added. Then the mixture was reacted at room temperature for 3 hours. After the reaction was completed, 20 mL of water was added, and the mixture was adjusted to pH=3 by adding acid, and then extracted with DCM (30 mL×3). The organic phase was dried over anhydrous sodium sulfate, and filtered. The filtrate was concentrated under reduced pressure to obtain target compound 28h (0.25 g, 96%). LC-MS (ESI): m/z=404.2 [M+H]+
Compound 1i (0.40 g, 2.48 mmol), N,N-diisopropylethylamine (0.40 g, 3.1 mmol) and benzotriazol-1-yl-oxy-tripyrrolidinophosphonium hexafluorophosphate (0.48 g, 0.93 mmol) were sequentially added slowly to a solution of compound 28h (0.25 g, 0.62 mmol) in N,N-dimethylformamide (8 mL), and the mixture was stirred at room temperature for 2 hours. After the reaction was completed, dichloromethane (20 mL) was added to the reaction solution, and the resulting mixture was diluted with distilled water (20 mL), and extracted with dichloromethane (20 mL×3). The organic phase was washed with distilled water and saturated brine, dried over anhydrous sodium sulfate and concentrated. The silica gel column chromatography (eluent:dichloromethane:ethyl acetate:methanol=1:0:0-2:10:1) was used to obtain compound 28 (52 mg, 18%). LC-MS (ESI): m/z=510.1 [M+H]+. 1H NMR (400 MHz, DMSO-d6) δ 8.85 (s, 1H), 8.79 (s, 1H), 8.40 (d, 1H), 8.12 (s, 1H), 7.71 (t, 1H), 7.48 (s, 1H), 7.41 (d, 1H), 7.23 (d, 1H), 6.92 (s, 1H), 4.81 (s, 1H), 4.77-4.71 (m, 1H), 4.68 (s, 1H), 4.41 (d, 2H), 3.87-3.81 (m, 2H), 3.30 (m, 2H), 2.97 (m, 2H), 2.91 (t, 1H), 2.74 (t, 1H).
29a (180 mg, 1.02 mmol) was dissolved in ethanol (3 mL), intermediate 2 (546 mg, 2.03 mmol) was added, and then DIPEA (0.51 ml, 3.05 mmol) was added. The mixture was warmed to 50° C. and stirred for 4 hours. 1 mol/L of dilute hydrochloric acid (50 mL) was added. The mixture was extracted with dichloromethane (50 mL×2). The organic phase was combined, washed once with water (100 mL), dried over sodium sulfate, filtered and spun to dryness to obtain crude product 29b (200 mg) as a brown-black solid. LC-MS (ESI): m/z=410.2 [M+H]+.
Crude product 29b (200 mg) was dissolved in methanol (1.5 mL), THF (1.5 mL) was added, and then a solution of KOH (275 mg, 4.91 mmol) in water (1.5 mL) was added. The mixture was heated to reflux and stirred overnight. The reaction solution was cooled. Water (50 mL) was added. The mixture was adjusted to a pH of about 6 with dilute hydrochloric acid (1 moL/L), and extracted with ethyl acetate (50 mL×2). The organic phase was combined, washed once with water (100 mL), dried over sodium sulfate, filtered and spun to dryness to obtain crude product 29c (205 mg) as an ash black solid. LC-MS (ESI): m/z=382.1 [M+H]+.
Crude product 29c (205 mg) was dissolved in DMF (1.5 mL). 4,5,6,7-tetrahydro-3H-[1,2,3]triazolo[4,5-c]pyridine hydrochloride (169 mg, 1.05 mmol) was added, then triethylamine (0.73 mL, 5.25 mmol) was added dropwise, and BOP (348 mg, 0.79 mmol) was added. The mixture was stirred at room temperature overnight. Water (50 mL) was added. The mixture was adjusted to a pH of about 6 with dilute hydrochloric acid (2 moL/L), and extracted with ethyl acetate (50 mL×2). The organic phase was combined, washed once with water (100 mL), dried over sodium sulfate, filtered and spun to dryness to obtain a brown oil, which was separated and purified by silica gel column chromatography to obtain compound 29 (20 mg).
LC-MS (ESI): m/z=488.3 [M+H]+.
1H NMR (400 MHz, DMSO-d6) δ 9.00-8.62 (m, 2H), 8.37 (d, 1H), 6.79 (s, 2H), 5.94 (d, 2H), 4.81 (s, 1H), 4.74-4.66 (m, 2H), 4.41 (d, 2H), 3.89-3.79 (m, 2H), 3.18 (dd, 2H), 2.90 (t, 1H), 2.82 (dd, 2H), 2.77-2.71 (m, 1H).
Intermediate 30a (300 mg, 1.90 mmol) was dissolved in methanol (5 mL), concentrated hydrochloric acid (0.3 mL) was added, and then tert-pentyl nitrite (244 mg, 2.09 mmol) was added dropwise. The mixture was stirred at room temperature for 3 hours. A large number of white solids were precipitated and filtered. The filter cake was rinsed with a small amount of methanol, and spun to dryness under reduced pressure to obtain 30b as a white solid (300 mg, 84.5%). LC-MS (ESI): m/z=188.1 [M+H]+.
30b (300 mg, 1.6 mmol) was dissolved in acetic acid (10 mL), 4N hydrochloric acid in dioxane (1 ml) was added, and then wet palladium carbon (100 mg) was added. The mixture was subjected to hydrogen gas replacement three times with a hydrogen balloon. The resulting mixture was reacted at room temperature overnight under a hydrogen atmosphere. After the reaction was completed, the reaction solution was filtered, and spun to dryness to obtain crude product 30c as an off-white solid (250 mg). LC-MS (ESI): m/z=174.1 [M+H]+.
Crude product 30c (250 mg) was dissolved in DCM (10 mL), triethylhydrosilane (5 mL) was added, and then boron trifluoride diethyl etherate (5 mL) was added dropwise. The mixture was reacted at 45° C. for 16 hours. After the reaction was completed, the reaction solution was concentrated, then basified by adding sodium bicarbonate aqueous solution, and extracted with ethyl acetate (30 mL×2). The organic phase was combined, dried over sodium sulfate, filtered and spun to dryness to obtain 30d as a reddish-brown solid (200 mg). LC-MS (ESI): m/z=160.2 [M+H]+.
With reference to the synthetic method of the first to third steps for compound 29, compound 30 was prepared.
LC-MS (ESI): m/z=470.2 [M+H]+.
1H NMR (400 MHz, DMSO-d6) δ 8.89-8.73 (m, 2H), 8.34 (d, 1H), 6.93 (s, 2H), 4.75 (d, 2H), 4.65 (dd, 2H), 4.41 (d, 2H), 3.91-3.79 (m, 2H), 3.26-3.20 (m, 2H), 3.04 (s, 4H), 2.92-2.84 (m, 3H), 2.74 (t, 1H).
Compound 8b (1.0 g, 3.203 mmol), bistriphenylphosphine palladium dichloride (450 mg, 0.6406 mmol) and cuprous iodide (61 mg, 0.3203 mmol) were dissolved in DMF (32 ml), and triethylamine (1.12 ml, 8.008 mmol) and trimethylsilylacetylene (378 mg, 3.844 mmol) were added. The mixture was reacted at 90° C. for about 6 h under nitrogen protection. After the reaction was completed, the reaction solution was cooled to room temperature, filtered and washed with ethyl acetate. Water was added and the mixture was extracted with ethyl acetate. The organic phase was washed with saturated brine, dried over anhydrous sodium sulfate, filtered and concentrated. The silica gel column chromatography (PE:EA=5:1) was used for purification to obtain product 31a as a white solid (640 mg, 61%).
Compound 31a (640 mg, 1.94 mmol) was dissolved in hydrochloric acid-1,4-dioxane (20 ml), and reacted at room temperature. After the reaction was completed, the reaction solution was concentrated. Product 31b as a white solid (420 mg, 95%) was obtained.
Compound 31b (420 mg, 1.83 mmol), and intermediate 2 (541 mg, 2.01 mmol) were dissolved in NMP (20 ml), and DIPEA (591 mg, 4.575 mmol) was added. The mixture was reacted at 80° C. under nitrogen protection for 4 h. After the reaction was completed, water (100 ml) was added and the mixture was extracted with ethyl acetate. The organic phase was washed with saturated brine, dried over anhydrous sodium sulfate, filtered and concentrated. The silica gel column chromatography (DCM:MeOH=60:1) was used for purification to obtain product 31c as a white solid (640 mg, 79%).
Compound 31c (640 mg, 1.77 mmol) was dissolved in methanol, and an aqueous solution of lithium hydroxide (149 mg, 3.54 mmol) was slowly added dropwise. The mixture was reacted at room temperature. After the reaction was completed, the mixture was concentrated, water was added and the resulting solution was filtered. The filtrate was adjusted to pH=3-4 with HCl, and extracted with ethyl acetate (30 mL×2). The organic phase was washed with saturated brine, dried over anhydrous sodium sulfate, filtered and concentrated to obtain product 31d as a white solid (480 mg, 95%).
Compound 31d (480 mg, 1.328 mmol) and 1i (427 mg, 2.657 mmol) were dissolved in DMF, HATU (616 mg, 1.594 mmol) was added, and DIPEA (1.12 ml, 6.64 mmol) was added dropwise. The mixture was reacted at room temperature. After the reaction was completed, the mixture was diluted with water, and extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated. The silica gel column chromatography (DCM:MeOH=40:1) was used for purification to obtain compound 31 (9 mg). LC-MS (ESI): m/z=468.3 [M+H]+. 1H NMR (400 MHz, DMSO-d6) δ 8.80 (s, 2H), 8.39 (d, 1H), 7.34 (s, 1H), 7.26 (q, 2H), 4.81 (s, 1H), 4.71 (dd, 2H), 4.41 (d, 2H), 4.06 (s, 1H), 3.89-3.80 (m, 2H), 3.29 (m, 2H), 2.93 (m, 3H), 2.75 (t, 1H).
Hydrazine hydrate (16 ml) was added to a solution of compound 32a (3.6 g, 2.0 mmol) in ethanol (40 mL), and the mixture was reacted at 80° C. for 16 hours. After the reaction was completed, the reaction solution was filtered, washed with ethanol and spun to dryness to obtain the title compound 32b as a grey solid (3.5 g, 100%). LC-MS (ESI): m/z=348.1, 350.1 [M+H]+. 1H NMR (400 MHz, DMSO-d6) δ 9.57 (s, 1H), 8.69 (s, 2H), 8.05 (d, 1H), 7.42 (s, 1H), 7.32 (d, 1H), 7.18 (d, 1H), 4.69-4.64 (m, 1H), 4.40 (s, 2H), 3.28-3.16 (m, 2H), 2.94-2.83 (m, 2H).
32c (0.55 g, 3.45 mmol), 2-(7-azabenzotriazole)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (1.30 g, 3.45 mmol) and N,N-diisopropylethylamine (0.93 g, 7.18 mmol) were added to a solution of compound 32b (1.0 g, 2.87 mmol) in N,N-dimethylformamide (10 mL), and the mixture was reacted at room temperature for 2 hours. After the reaction was completed, the mixture was diluted with distilled water (30 mL), and extracted with dichloromethane (20 mL×3). The organic phase was washed with distilled water and saturated brine, dried over anhydrous sodium sulfate and concentrated to obtain the title compound 32d as brown solid (1.8 g, a crude product). LC-MS (ESI): m/z=490.1, 492.1 [M−H]+.
4-toluene sulfonyl chloride (1.95 g, 10.20 mmol) and N,N,N′,N′-tetramethyl-1,6-hexanediamine (2.11 g, 12.23 mmol) were added to a solution of compound 32d (1.8 g, 3.67 mmol) in dichloromethane (20 mL), and the mixture was reacted at room temperature for 2 hours. After the reaction was completed, the mixture was diluted with dichloromethane (30 mL). The organic phase was washed with distilled water and saturated brine, dried over anhydrous sodium sulfate and concentrated. The silica gel column chromatography (eluent: petroleum ether:ethyl acetate=1:0-0:1) was used for purification to obtain the title compound 32e as a grey solid (450 mg, two-step yield: 33%). LC-MS (ESI): m/z=472.1, 474.1 [M+H]+. 1H NMR (400 MHz, DMSO-d6) δ 8.86 (s, 1H), 8.80 (s, 1H), 8.42 (d, 1H), 7.43 (s, 1H), 7.33 (d, 1H), 7.19 (d, 1H), 4.76-4.67 (m, 1H), 4.12 (s, 2H), 3.23-3.23 (m, 2H), 2.98-2.87 (m, 2H), 1.43 (s, 9H).
Compound 32f (0.2 g, 0.9 mmol), tri-potassium phosphate monohydrate (1.23 g, 3.65 mmol) and bis(triphenylphosphine)palladium dichloride (0.04 g, 0.06 mmol) were added to a solution of compound 32e (0.4 g, 0.8 mmol) in dioxane/water (10 ml/1 ml), and the mixture was stirred at 90° C. for 4 hours. After the reaction was completed, the mixture was diluted with distilled water (100 mL), and extracted with ethyl acetate (100 mL×4). The organic phase was washed with distilled water and saturated brine, dried over anhydrous sodium sulfate and concentrated. The silica gel column chromatography (eluent: petroleum ether:ethyl acetate=1:0-0:1) was used for separation and purification to obtain the title compound 32g as a white solid (0.2 g, 53%). LC-MS (ESI): m/z=473.2 [M+H]+. 1H NMR (400 MHz, DMSO-d6) δ 8.86 (s, 1H), 8.81 (s, 1H), 8.42 (d, 1H), 8.06 (s, 1H), 7.78 (s, 1H), 7.42 (s, 1H), 7.35 (d, 1H), 7.19 (d, 1H), 4.76-4.70 (m, 1H), 4.11 (s, 2H), 3.85 (s, 3H), 3.23-3.24 (m, 2H), 2.98-2.89 (m, 2H), 1.43 (s, 9H).
Trifluoroacetic acid (4 ml) was added to a solution of compound 32g (0.2 g, 0.42 mmol) in dichloromethane (6 mL), and the mixture was reacted at room temperature for 16 hours. After the reaction was completed, the reaction solution was diluted with dichloromethane (20 mL). The organic phase was washed with distilled water and saturated brine, dried over anhydrous sodium sulfate, and concentrated to obtain the title compound 32h as a grey solid (165 mg, 94%). LC-MS (ESI): m/z=418.1 [M+H]+.
Compound 1i (0.29 g, 1.8 mmol), N,N-diisopropylethylamine (0.40 g, 3.1 mmol) and benzotriazol-1-yl-oxy-tripyrrolidinophosphonium hexafluorophosphate (0.48 g, 0.93 mmol) were sequentially added slowly to a solution of compound 32h (0.25 g, 0.60 mmol) in N,N-dimethylformamide (6 mL), and the mixture was stirred at room temperature for 2 hours. After the reaction was completed, dichloromethane (20 mL) was added to the reaction solution, and the resulting mixture was diluted with distilled water (20 mL), and extracted with dichloromethane (20 mL×3). The organic phase was washed with distilled water and saturated brine, dried over anhydrous sodium sulfate and concentrated. The silica gel column chromatography (eluent:dichloromethane:ethyl acetate:methanol=1:0:0-2:10:1) was used for purification to obtain compound 32 (19 mg, 6%).
LC-MS (ESI): m/z=524.2 [M+H]+.
1H NMR (400 MHz, DMSO-d6) δ 8.85 (s, 1H), 8.80 (s, 1H), 8.39 (d, 1H), 8.06 (s, 1H), 7.80 (s, 1H), 7.42 (s, 1H), 7.34 (d, 1H), 7.19 (d, 1H), 4.81 (s, 1H), 4.75-4.70 (m, 1H), 4.68 (s, 1H), 4.43 (s, 1H), 4.39 (s, 1H), 3.87-3.83 (m, 5H), 3.32-3.23 (m, 2H), 2.98-2.89 (m, 3H), 2.74 (t, 1H).
1B (1.6 g, 9.43 mmol) and triethylamine (3.18 g, 31.42 mmol) were added to a solution of compound 33a (2.0 g, 7.86 mmol) in ethanol (40 mL), and the mixture was stirred at 80° C. for 4 hours. After the reaction was completed, the mixture was diluted with distilled water (30 mL), and extracted with ethyl acetate (30 mL×3). The organic phase was washed with distilled water and saturated brine, dried over anhydrous sodium sulfate and concentrated. The silica gel column chromatography (eluent: petroleum ether:ethyl acetate=1: 0-0:1) was used for separation and purification to obtain the title compound 33c as an off-white solid (3.0 g, 100%). LC-MS (ESI): m/z=352.1 [M+H]+. 1H NMR (400 MHz, DMSO-d6) δ 8.96-8.86 (m, 2H), 7.22 (s, 2H), 7.17-7.14 (m, 2H), 4.74-4.65 (m, 1H), 4.28 (q, 2H), 3.25 (dd, 2H), 3.06 (m, 2H), 1.29 (t, 3H).
Hydrazine hydrate (6 ml) was added to a solution of compound 33c (1.0 g, 2.85 mmol) in ethanol (10 mL), and the mixture was reacted at 80° C. for 16 hours. After the reaction was completed, the reaction solution was filtered, washed with ethanol and spun to dryness to obtain the title compound 33d as a grey solid (400 mg, 42%). LC-MS (ESI): m/z=338.1 [M+H]+. 1H NMR (400 MHz, DMSO-d6) δ 8.52 (s, 1H), 7.22 (t, 1H), 7.17-7.14 (m, 2H), 7.11-7.08 (m, 2H), 4.68-4.53 (m, 1H), 3.68 (s, 1H), 3.26 (dd, 1H), 3.01 (dd, 2H), 2.91 (dd, 1H), 2.56 (dd, 2H).
33e (0.20 g, 1.2 mmol), 2-(7-azabenzotriazole)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (0.50 g, 1.2 mmol) and N,N-diisopropylethylamine (0.4 g, 3.0 mmol) were added to a solution of compound 33d (0.40 g, 1.0 mmol) in N,N-dimethylformamide (6 mL), and the mixture was reacted at room temperature for 2 hours. After the reaction was completed, the mixture was diluted with distilled water (30 mL), and extracted with dichloromethane (20 mL×3). The organic phase was washed with distilled water and saturated brine, dried over anhydrous sodium sulfate and concentrated to obtain the title compound 33f as brown solid (800 mg, a crude product). LC-MS (ESI): m/z=480.1 [M−H]+
4-toluene sulfonyl chloride (0.80 g, 4.0 mmol) and N,N,N′,N′-tetramethyl-1,6-hexanediamine (0.90 g, 5.0 mmol) were added to a solution of compound 33f (0.8 g, 2.0 mmol) in dichloromethane (10 mL), and the mixture was reacted at room temperature for 2 hours. After the reaction was completed, the mixture was diluted with dichloromethane (30 mL). The organic phase was washed with distilled water and saturated brine, dried over anhydrous sodium sulfate and concentrated. The silica gel column chromatography (eluent: petroleum ether:ethyl acetate=1:0-0:1) was used for separation and purification to obtain the title compound 33g as a grey solid (200 mg, two-step yield: 37%). LC-MS (ESI): m/z=462.1 [M+H]+. 1H NMR (400 MHz, DMSO-d6) δ 8.96 (s, 1H), 8.28 (s, 1H), 7.24-7.21 (m, 2H), 7.17-7.13 (m, 2H), 4.76-4.67 (m, 1H), 4.14 (s, 2H), 3.30 (dd, 1H), 3.17 (dd, 1H), 2.97 (dd, 1H), 2.75 (dd, 1H), 1.39 (s, 9H).
TFA (4 ml) was added to a solution of compound 33g (0.20 g, 0.43 mmol) in dichloromethane (6 mL), and the mixture was reacted at room temperature for 16 hours. After the reaction was completed, the reaction solution was diluted with dichloromethane (20 mL). The organic phase was washed with distilled water and saturated brine, dried over anhydrous sodium sulfate, and concentrated to obtain the title compound 33h as a grey solid (150 mg, 86%). LC-MS (ESI): m/z=406.1 [M+H]+.
Compound 1i (0.40 g, 2.48 mmol), N,N-diisopropylethylamine (0.40 g, 3.10 mmol) and benzotriazol-1-yl-oxy-tripyrrolidinophosphonium hexafluorophosphate (0.48 g, 0.93 mmol) were sequentially added slowly to a solution of compound 33h (0.25 g, 0.62 mmol) in N,N-dimethylformamide (6 mL), and the mixture was stirred at room temperature for 2 hours. After the reaction was completed, dichloromethane (20 mL) was added to the reaction solution, and the resulting mixture was diluted with distilled water (20 mL), and extracted with dichloromethane (20 mL×3). The organic phase was washed with distilled water and saturated brine, dried over anhydrous sodium sulfate and concentrated. The silica gel column chromatography (eluent:dichloromethane:ethyl acetate:methanol=1:0:0-2:10:1) was used for separation and purification to obtain compound 33 (50 mg, 13%).
LC-MS (ESI): m/z=512.1 [M+H]+.
1H NMR (400 MHz, DMSO-d6) δ 9.01-8.87 (m, 2H), 7.24-7.22 (m, 2H), 7.17-7.15 (m, 2H), 4.80 (s, 1H), 4.74-4.71 (m, 1H), 4.68 (s, 1H), 4.44 (d, 2H), 3.86-3.81 (m, 2H), 3.30 (dd, 2H), 2.97 (dd, 2H), 2.89 (t, 1H), 2.74 (t, 1H).
Compound 24 was resolved by chiral HPLC to obtain compound 34 and compound 35 (chiral HPLC resolution method: instrument name: MG II preparative SFC(SFC-14); chromatographic column: ChiralPak AD, 250×30 mm I.D., 10 μm; mobile phase: A (for CO2) and B (for isopropanol) (0.1% NH3H2O); gradient: B 40%; flow rate: 80 mL/min; column pressure: 100 bar; column temperature: 38° C.; absorption wavelength: 220 nm cycle time: about 8 min).
Retention time for compound 34: 3.635 min
LC-MS (ESI): m/z=512.2 [M+H]+, 1H NMR (400 MHz, DMSO-d6) δ 8.81-8.83 (m, 2H), 8.42 (d, 1H), 7.59 (s, 1H), 0.44-7.52 (m, 2H), 4.81 (s, 1H), 4.74-4.79 (m, 1H), 4.69 (s, 1H), 4.41 (d, 2H), 3.83-3.86 (m, 2H), 3.35-3.41 (m, 2H), 2.99-3.05 (m, 2H), 2.90-2.91 (m, 1H), 2.74-2.75 (m, 1H).
Retention time for compound 35: 5.492 min
LC-MS (ESI): m/z=512.2 [M+H]+, 1H NMR (400 MHz, DMSO-d6) δ 8.81-8.83 (m, 2H), 8.42 (d, 1H), 7.59 (s, 1H), 0.44-7.52 (m, 2H), 4.81 (s, 1H), 4.74-4.79 (m, 1H), 4.69 (s, 1H), 4.41 (d, 2H), 3.83-3.86 (m, 2H), 3.35-3.41 (m, 2H), 2.99-3.05 (m, 2H), 2.90-2.91 (m, 1H), 2.74-2.75 (m, 1H).
Compound 9 was resolved by chiral HPLC to obtain compound 36 and compound 37 (chiral HPLC resolution method: instrument name: MG II preparative SFC(SFC-1); chromatographic column: ChiralPakAD, 250×30 mm I.D., 10 μm; mobile phase: A (for CO2) and B (for isopropanol); gradient: B 50%; flow rate: 80 mL/min; column pressure: 100 bar; column temperature: 38° C.; absorption wavelength: 220 nm cycle time: about 7 min).
Retention time for compound 36: 3.832 min
LC-MS (ESI): m/z=494.3 [M+H]+, 1H NMR (400 MHz, DMSO-d6) δ 8.83-8.79 (m, 2H), 8.38-8.36 (m, 1H), 7.40 (d, J=28 Hz, 3H), 6.97 (t, J=56 Hz, 1H), 4.81-4.68 (m, 3H), 4.43-4.39 (m, 2H), 3.87-3.81 (m, 2H), 3.35-3.31 (m, 2H), 3.02-2.72 (m, 4H).
Retention time for compound 37: 5.717 min
LC-MS (ESI): m/z=494.3 [M+H]+, 1H NMR (400 MHz, DMSO-d6) δ 8.83-8.79 (m, 2H), 8.38-8.36 (m, 1H), 7.40 (d, J=28 Hz, 3H), 6.97 (t, J=56 Hz, 1H), 4.81-4.68 (m, 3H), 4.43-4.39 (m, 2H), 3.87-3.81 (m, 2H), 3.35-3.31 (m, 2H), 3.02-2.72 (m, 4H).
Compound 27 was resolved by chiral HPLC to obtain compound 38 (peak 1) and compound 39 (peak 2) (chiral HPLC resolution method: instrument name: MG II preparative SFC(SFC-14); chromatographic column: cellulose-2, 250×30 mm I.D., 5 μm; mobile phase: A (for CO2) and B (for ethanol) (0.1% NH3H2O); gradient: B 45%; flow rate: 60 mL/min; column pressure: 100 bar; column temperature: 38° C.; absorption wavelength: 220 nm cycle time: about 9 min).
Retention time for peak 1: 4.300 min, LC-MS (ESI): m/z=476.2 [M+H]+, 1H NMR (400 MHz, DMSO-d6) δ 8.92-8.81 (m, 2H), 8.50 (d, J=8 Hz, 1H), 7.24-7.14 (m, 4H), 4.76-4.69 (m, 3H), 4.00-3.90 (m, 2H), 3.32-3.26 (m, 2H), 2.99-2.95 (m, 2H), 2.83-2.81 (m, 2H), 2.16-2.07 (m, 3H).
Retention time for peak 2: 5.784 min, LC-MS (ESI): m/z=476.2 [M+H]+, 1H NMR (400 MHz, DMSO-d6) δ 8.92-8.81 (m, 2H), 8.50 (d, J=8 Hz, 1H), 7.24-7.14 (m, 4H), 4.76-4.69 (m, 3H), 4.00-3.90 (m, 2H), 3.32-3.26 (m, 2H), 2.99-2.95 (m, 2H), 2.83-2.81 (m, 2H), 2.16-2.07 (m, 3H).
Compound 31 was resolved by chiral HPLC to obtain compound 40 (peak 1) and compound 41 (peak 2) (chiral HPLC resolution method: instrument name: MG II preparative SFC(SFC-14); chromatographic column: cellulose-2, 250×30 mm I.D., 5 μm; mobile phase: A (for CO2) and B (for ethanol) (0.1% NH3H2O); gradient: B 45%; flow rate: 60 mL/min; column pressure: 100 bar; column temperature: 38° C.; absorption wavelength: 220 nm cycle time: about 9 min).
Retention time for peak 1: 7.004 min, LC-MS (ESI): m/z=468.2 [M+H]+, 1H NMR (400 MHz, DMSO-d6) δ 14.63 (s, 1H), 8.80 (s, 2H), 8.39 (d, 1H), 7.34 (s, 1H), 7.26 (q, 2H), 4.81 (s, 1H), 4.71 (dd, 2H), 4.41 (d, 2H), 4.07-4.04 (m, 1H), 3.89-3.79 (m, 2H), 3.27 (d, 2H), 2.99-2.88 (m, 3H), 2.75 (s, 1H).
Retention time for peak 2: 8.086 min, LC-MS (ESI): m/z=468.2 [M+H]+, 1H NMR (400 MHz, DMSO-d6) δ 14.65 (s, 1H), 8.80 (s, 2H), 8.39 (d, 1H), 7.34 (s, 1H), 7.30-7.21 (m, 2H), 4.81 (s, 1H), 4.77-4.63 (m, 2H), 4.41 (d, 2H), 4.06 (s, 1H), 3.89-3.78 (m, 2H), 3.27 (d, 2H), 2.93 (dt, 3H), 2.75 (t, 1H).
Compound 28 was resolved by chiral HPLC to obtain compound 42 (peak 1) and compound 43 (peak 2) (chiral HPLC resolution method: instrument name: MG II preparative SFC(SFC-14); chromatographic column: cellulose-2, 250×30 mm I.D., 5 μm; mobile phase: A (for CO2) and B (for Ethanol) (0.1% NH3H2O); gradient: B 45%; flow rate: 60 mL/min; column pressure: 100 bar; column temperature: 38° C.; absorption wavelength: 220 nm cycle time: about 9 min).
Retention time for peak 1: 4.886 min, LC-MS (ESI): m/z=510.1 [M+H]+.
Retention time for peak 2: 5.716 min, LC-MS (ESI): m/z=510.1 [M+H]+.
Experimental subject: compounds to be tested.
ATX activity was detected by detecting LPA production in pooled human plasma. Whole blood anticoagulated with heparin was collected and centrifuged, and then plasma was collected. 5-μL gradient dilution of the compound to be tested or DMSO was added to 95-μL plasma, incubated at 37° C. for 2 h, then a stop solution (40 mM disodium hydrogen phosphate buffer, containing a buffer solution (containing 30 mM citric acid, pH=4)) was added. LPA in plasma was detected by LC-MS-MS before and after incubation.
LPA (18:2) and (20:4) LC-MS-MS analytical method
Using a 1.5 mL EP tube, 3.0 μL of each of the working solutions for standard curve and quality control was taken and added to 27.0 μL of water. After homogeneously mixing by vortex, 400 μL of internal standard solution was added. After homogeneously mixing by vortex, the mixture was centrifuged at 4° C. for 10 min. 180 μL of supernatant was taken and added into a 96-well plate, waiting for sample injection.
10 μL of the compound to be tested (10 mg/ml) was precisely pipetted into an EP tube, 990 μL of DMSO solution was added, and the mixture was vortexed to completely dissolve to obtain a solution (100 μg/mL).
Solvent: n-Butanol
Series of working solution concentration for standard curve: 5 μg/mL, 2 μg/mL, 1 μg/mL, 500 ng/mL, 200 ng/mL, 100 ng/mL, 50 ng/mL, 20 ng/mL, and 10 ng/mL
Working solution concentration for quality control: 4 μg/mL, 800 ng/mL, and 30 ng/mL
1.4.3 Internal Standard Solution (Solvent: n-Butanol)
LPA17: 025.0 ng mL−1
Inhibition rate of ATX receptor activity was calculated in the following way: inhibition rate %=((LPAc−LPA0)−(LPAi−LPA0))/(LPAc−LPA0)*100%, wherein LPAc was the LPA content in plasma after DMSO was added and incubated for 2 h, LPA0 was the LPA content in plasma before DMSO was added for incubation, and LPAi was the LPA content in plasma after test compound was added and incubated for 2 h.
Test results: The compounds of the present invention showed inhibitory activity against ATX receptor, and the IC50 values of the example compounds against LPA 18:2/20:4 cells were in the range of 0.01-20 nM. The test results of some examples were shown in Table 1:
Conclusion: The compounds of the present invention showed relatively high inhibitory activity against ATX receptor.
Experimental objective: In this experiment, a single dose of each test compound was administered to C57 mice intravenously and intragastrically, the concentrations of the compounds 35, 37 and 38 in plasma of the mice were measured, and the pharmacokinetic characteristics and bioavailability of each test compound in mice were evaluated.
Experimental animals: Male C57 mice, 20-25 g, 6-8 weeks old, 18 mice/compound. The experimental animals were purchased from CHENGDU DOSSY EXPERIMENTAL ANIMALS CO., LTD.
Experimental method: On the day of the experiment, 18 C57 mice were randomly grouped according to their body weight. The animals were fasted with water available for 12 to 14 hours one day before the administration of a test compound, and were fed 4 hours after the administration.
Before and after the administration, 0.08 ml of blood was taken from the orbit of the rats under isoflurane anesthesia, and placed in an EDTAK2 centrifuge tube. Centrifugation was carried out at 5000 rpm at 4° C. for 10 min and the plasma was collected.
Time points for plasma collection in G1 group: 0, 5, 15, 30 min, 1, 2, 4, 6, 8, and 24 h.
Time points for plasma collection in G2 group: 0, 15, 30 min, 1, 2, 4, 6, 8, and 24 h.
Before analysis and detection, all samples were stored at −80° C.
30 μL of each of plasma sample, standard curve and quality control sample was taken, and 200 μL of acetonitrile solution containing internal standard was added, and the mixture was homogeneously mixed by vortex, and then centrifuged at 12000 rpm for 10 min at 4° C. The supernatant was taken and added into a 96-well plate and analyzed by LC-MS/MS.
The main pharmacokinetic parameters were analyzed by non-compartmental model using WinNonlin 8.0 software. The experimental results were as shown in the following table.
Conclusion: The compounds of the present invention have relatively high bioavailability and good pharmacokinetic characteristics.
| Number | Date | Country | Kind |
|---|---|---|---|
| 201911248204.6 | Dec 2019 | CN | national |
| 202010292562.3 | Apr 2020 | CN | national |
| 202010541043.6 | Jun 2020 | CN | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/CN2020/135220 | 12/10/2020 | WO |
