Patent Application
20240383908
The present invention belongs to the chemistry-medicinal field, and specifically relates to the synthesis and application of a phosphatase degrader.
SHP2 (the Src homology-2 domain) is a non-receptor tyrosine phosphatase encoded by the PTPN11 gene, and contains a conserved tyrosine phosphatase domain, two N-terminal SH2 domains, and a C-terminal tail. The two SH2 domains determine the subcellular localization and functional regulation of SHP2. In the inactive state, the N-terminal SH2 domain will bind to the PTP domain and cause it to lose activity. When the SH2 domain binds to receptors or specific tyrosine residues in adapter proteins, the PTP domain is released. For example, the exposure of catalytic sites by the stimulation of cytokines and growth factors leads to the activation of SHP2. SHP2 is widely expressed and participates in various cell signaling pathways, such as Ras-Erk, PI3K-Akt, Jak-Stat, Met, FGFR, EGFR, as well as insulin receptor and NF-kB pathways, thereby playing important roles in cell proliferation, differentiation, migration, and cell cycles. Superactivation of SHP2 caused by germline or somatic mutations has been found in Noonan syndrome, Leopard syndrome, juvenile myelomonocytic leukemia, myelodysplastic syndrome, B-cell acute lymphoblastic leukemia, and acute myeloid leukemia. In addition, activation and mutations of PTPN11 have also been found in solid tumors such as lung cancer, colon cancer, melanoma, neuroblastoma, and liver cancer. Therefore, activated SHP2 or upregulated SHP2 protein in human tumors or other diseases has become new therapeutic targets.
SHP2 represents a promising target for many cancers, such as triple negative and HER2+ breast cancers, as well as cancers caused by abnormal activation of receptor protein tyrosine kinase (PTK). Therefore, discovering and searching for SHP2 protein degraders with good druggability have gradually become a hot research field in the industrial and academic circles.
The present invention is to provide the synthesis and application of a phosphatase degrader.
The present invention provides a compound represented by formula I, or a salt thereof, or a deuterated compound thereof, or a stereoisomer thereof, or a solvate thereof, or a hydrate thereof, or a prodrug thereof:
Further,
substituted with 0-2 R5,
substituted with 0-2 R5,
substituted with 0-2 R5,
substituted with 0-2 R5, and
substituted with 0-2 R5;
substituted with 0-3 R13,
substituted with 0-3 R13,
substituted with 0-3 R13,
substituted with 0-3 R13,
substituted with 0-3 R13,
substituted with 0-3 R13,
substituted with 0-3 R13,
substituted with 0-3 R13,
substituted with 0-3 R13, phenyl substituted with 0-3 R13,
substituted with 0-3 R13,
substituted with 0-3 R13,
substituted with 0-3 R13,
substituted with 0-3 R13,
substituted with 0-3 R13,
substituted with 0-3 R13,
substituted with 0-3 R13,
substituted with 0-3 R13, and
substituted with 0-3 R13;
substituted with 0-3 R13,
substituted with 0-3 R13,
substituted with 0-3 R13,
substituted with 0-3 R13,
substituted with 0-3 R13, and
substituted with 0-3 R13;
substituted with 0-3 R13,
substituted with 0-3 R13, and
substituted with 0-3 R13;
Further, the compound is as represented by formula II:
Further, the compound is as represented by formula III:
Further, the compound is as represented by formula IV:
Further, the compound is as represented by formula V:
Further,
Further, the compound is as represented by formula VI:
Further, the compound is as represented by formula VII:
Further, the compound is as represented by formula VIII:
Further, the compound is as represented by formula IX:
Further, the compound is selected from the group consisting of:
The present invention further provides the use of the compound mentioned above, or a salt thereof, or a deuterated compound thereof, or a stereoisomer thereof, or a solvate thereof, or a hydrate thereof, or a prodrug thereof in the manufacturer of phosphatase degraders.
The present invention further provides the use of the compound mentioned above, or a salt thereof, or a deuterated compound thereof, or a stereoisomer thereof, or a solvate thereof, or a hydrate thereof, or a prodrug thereof in the manufacturer of medicaments for treatment of cancer, Noonan syndrome, Leopard syndrome, juvenile myelomonocytic leukemia, and myelodysplastic syndrome.
Further, the medicament is used to treat lung cancer, colon cancer, rectal cancer, melanoma, neuroblastoma, pancreatic cancer, liver cancer, esophageal cancer, prostate cancer, breast cancer, bile duct cancer, hematoma, and acute leukemia.
The present invention further provides a medicament, which is a preparation formed by the compound mentioned above, or a salt thereof, or a deuterated compound thereof, or a stereoisomer thereof, or a solvate thereof, or a hydrate thereof, or a prodrug thereof as active ingredient, in combination with pharmaceutically acceptable excipients or adjuvant ingredients. The present invention further provides a drug combination, which comprises the compound mentioned above, or a salt thereof, or a deuterated compound thereof, or a stereoisomer thereof, or a solvate thereof, or a hydrate thereof, or a prodrug thereof and other anti-tumor drugs at the same or different specifications, which are administered simultaneously or separately, in combination with pharmaceutically acceptable carriers.
The compounds and derivatives provided in the present invention can be named according to IUPAC (International Union of Pure and Applied Chemistry) or CAS (Chemical Abstracting Service, Columbus, OH) naming system.
For the definition of terms used in the present invention: unless defined otherwise, the initial definition provided for the group or term herein applies to the group or term of the whole specification; for the terms that are not specifically defined herein, they should have the same meaning as commonly understood by one of ordinary skill in the art to which the disclosure belongs.
“Substitution” means that the hydrogen in a molecule is substituted with other different atoms or molecules.
“Alkyl” refers to an aliphatic hydrocarbon group, that is, a saturated hydrocarbon group. The alkyl moiety can be either a straight alkyl or a branched alkyl. Typical alkyls include but are not limited to methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tert-butyl, pentanyl, hexanyl, and so on.
The C1-Cn used in the present invention includes C1-C2, C1-C3 . . . C1-Cn, where n is an integer of >1; as a prefix for a substituent, n represents the minimum and maximum number of carbons in the substituent. For example, “C1-C8 alkyl” refers to a straight or branched alkyl containing 1-8 carbons.
The “ring” in the present invention can be a single ring or a multi-ring, and can also be a fused ring, a spiral ring, or a bridged ring.
“Cycloalkyl” refers to a saturated or unsaturated cyclic hydrocarbon substituent, for example, “3-10 membered cycloalkyl” denotes a cyclic alkyl comprising 3-6 carbons; “cycloalkyl” includes but is not limited to
and the same.
“Heterocyclic group” refers to a cycloalkyl containing at least one heteroatom in the ring skeleton. Heteroatoms include but are not limited to O, S, N, P, Si, etc. “Heterocyclic groups” include but are not limited to
and the same.
“Aryl” refers to a planar ring which has a delocalized π-electron system and contains 4n+2π electrons, where n is an integer. Aryl ring can be composed of five, six, seven, eight, nine or more atoms. Aryl includes but is not limited to phenyl, naphthyl, phenanthryl, anthracyl, fluorenyl, and indenyl. The aryl of the present invention also includes but is not limited to
and the same.
“Heteroaryl” refers to an aryl in which a carbon is substituted with an atom other than carbon, such as N, O, S, etc. “Heteroaryl” includes but is not limited to pyrimidinyl, pyridazinyl, pyrazolyl, pyridyl, pyrazinyl, pyrazolyl, thienyl, furyl,
and the same.
“Halogen” or “halo” refers to fluorine, chlorine, bromine, or iodine.
In the present invention, cis refers to the compound being a cis isomer, while trans refers to the compound being a trans isomer.
The compound of the present invention has a good inhibitory effect on both hematomas and solid tumor cell lines. It has strong inhibitory effects on the proliferation of acute leukemia, esophageal cancer, KRAS mutant non-small cell lung cancer and pancreatic cancer cell lines. Moreover, when it is combined with other anti-tumor medicaments, a significant synergistic effect is found. In addition, the compound of the present invention has a rather different mechanism of action compared to traditional small-molecule targeting drugs or macromolecular drugs such as antibodies, and has good application prospects. The compound of the present invention can be used as a phosphatase degrader, especially as a SHP2 protein degrader, so that it can be used in the manufacturer of medicaments for treating diseases such as cancer, and has good application prospects.
The compound of the present invention can be used as a phosphatase degrader, especially as a SHP2 protein degrader, so that it can be used in the manufacturer of medicaments for treating cancer, Noonan syndrome, Leopard syndrome, juvenile myelomonocytic leukemia, and myelodysplastic syndrome, and has good application prospects.
Obviously, based on the above content of the present invention, according to the common technical knowledge and the conventional means in the field, other various modifications, alternations, or changes can further be made, without department from the above basic technical spirits.
With reference to the following specific examples, the above content of the present invention is further illustrated. But it should not be construed that the scope of the above subject matter of the present invention is limited to the following examples. The techniques realized based on the above content of the present invention are all within the scope of the present invention.
The starting materials and equipment used in the specific examples of the present invention are all known products obtained by purchasing those commercially available.
Under nitrogen protection, to a solution of HWH-1-1 (10.0 g, 52.11 mmol, 1.0 eq) and HWH-1-2 (6.5 g, 52.11 mmol, 1.0 eq) in dioxane (100 mL), were added diisopropylethylamine (13.3 g, 104.22 mmol, 2.0 eq), Xantphos (3.0 g, 5.21 mmol, 0.1 eq.), and Pd2(dba)3 (2.4 g, 2.60 mmol, 0.05 eq.), and then the resultant mixture was allowed to react at 100° C. After completion of the reaction, the solvent was removed by evaporation, and the residue was purified by silica gel column chromatography, to provide the intermediate HWH-1-3 (10.7 g, 45.15 mmol). MS (M+1): m/z 237.9.
To a solution of HWH-1-3 (10.7 g, 45.15 mmol, 1.0 eq.) and HWH-1-4 (12.6 g, 58.88 mmol, 1.3 eq.) in NMP (15 mL), was added diisopropylethylamine (60 mL, 344.65 mmol, 7.6 eq). The mixture was allowed to react at about 120° C. for about 10 h. After completion of the reaction, the mixture was poured into water (400 mL) and then extracted with EA (2*100 mL). The organic layer was washed with saturated brine (2*400 mL) and then dried with anhydrous Na2SO4. After rotatory evaporation, the residue was purified by silica gel column chromatography to obtain HWH-1 (17.7 g, yield 94.5%). MS (M+1): m/z 416.1.
Using a similar method to the synthesis of HWH-1, the intermediate HWH-2 can be prepared by replacing HWH-1-4 used in the synthesis of HWH-1 with tert-butyl ((3S,4S)-3-methyl-2-oxa-8-azaspiro[4.5]decan-4-yl)carbamate.
Under nitrogen protection, to a solution of compound TC-1 (1.0 g, 5.13 mmol, 1.0 eq) and KOAc (1.5 g, 15.39 mmol, 3.0 eq) in ethanol (10 mL), was added Pd(dppf)Cl2 (373 mg, 0.51 mmol, 0.1 eq.), and the reaction mixture was allowed to react at about 70° C. under CO atmosphere. After completion of the reaction, the reaction solution was diluted by adding EA (20 mL), and then filtered to remove insoluble solids. The filtrate was concentrated, and the residue was purified by silica gel column chromatography, to obtain the target product TC-2 (0.9 g, 4.76 mmol, yield 92.3%).
To a solution of TC-2 (8.5 g, 50.5 mmoL, 1.0 eq) and NBS (17.8 g, 100.0 mmoL, 2.0 eq) in acetonitrile (100 mL), was added AIBN (820 mg, 5.0 mmol, 0.1 eq), and then the mixture was allowed to react at about 80° C. under nitrogen protection. After completion of the reaction, the solvent was removed. The residue was diluted with EA (100 mL), and the ethyl acetate layer was washed with saturated NaHSO3 solution (100 mL) and brine (100 mL), then dried with anhydrous Na2SO4. After rotatory evaporation of the solvent, the residue was purified by silica gel column chromatography to obtain TC-3 (9.0 g, 33.71 mmol, yield 75.8%).
To a solution of TC-3 (35.7 g, 133.15 mmol, 1.0 eq.) and TC-4 (43.8 g, 266.30 mmol, 2.0 eq.) in DMF (400 mL), was added NaHCO3 (22.4 g, 266.30 mmol, 2.0 eq.), and then the mixture reacted at about 80° C. for 3 h, followed by reaction at room temperature. After the reaction was completed, water (2 L) was added. After precipitation and filtration, TC-5 (25.1 g, 93.24 mmol, yield 70.0%) was obtained by beating with ethanol. MS (M+H+): m/z 270.1.
To a solution of compound TC-5 (19.0 g, 70.63 mmol, 1.0 eq.) and (Boc)2O (22.8 g, 218.25 mmol, 1.5 eq.) in DMF (2 L), was added wet Pd/C (4.0 g, 10%, c.a.55% water), and then the mixture reacted at 40° C. under hydrogen atmosphere. After completion of the reaction, the catalyst was removed by filtering, and the filtrate was concentrated. The residue was triturated with methanol to obtain the target product TC-6 (15.1 g, 40.48 mmol, yield 57.3%). MS (M+H+): m/z 374.1.
A solution of compound TC-6 (3.7 g, 10.0 mmol, 1.0 eq) in HCl/EA (3 M, 35 mL, 10.5 eq.) was stirred at room temperature. After completion of the reaction, the solvent was removed to obtain the target product TC (3.1 g, 10.0 mmol, yiled 100% for crude product). MS (M+H+): m/z 274.2.
To a solution of TV-2 (10.0 g, 33.31 mmol, 1.0 eq.) in DMF (150 mL), were added TV-1 (6.61 g, 66.62 mmol, 2.0 eq.), KOAc (6.53 g, 66.62 mmol, 2.0 eq.), and Pd(OAc)2 (305.05 mg, 0.33 mmol, 0.01 eq.), and then the reaction was allowed to react at about 120° C. under nitrogen protection. After completion of the reaction, the reaction solution was concentrated, and the residue was purified by silica gel column chromatography, to obtain the target product TV-3 (10 g, 31.40 mmol, yield 94.3%). LCMS [M+H]: m/z 319.1.
Compound TV-3 (10.0 g, 31.40 mmol, 1.0 eq.) and TFA (20.0 mL, 261.36 mmol, 8.3 eq.) were stirred in DCM (20 mL), until the reaction was completed. After concentration, trifluoroacetate of TV-4 (10.7 g, 31.40 mmol, crude product, ca.100%) was obtained, which was directly used in the next step. LCMS [M+H]+: m/z 219.1.
At room temperature, to a solution of TV-4 (10.0 g, 30.09 mmol, 1.0 eq.) and TV-5 (6.96 g, 30.09 mmol, 1.0 eq.) in DCM (500 mL), were added triethylamine (16.02 mL, 90.27 mmol, 3.0 eq.) and HATU (17.15 g, 45.13 mmol, 1.5 eq.). The mixture was stirred at room temperature, until the reaction was completed. After concentration, the residue was purified by silica gel column chromatography, to obtain the target compound TV-6 (11.0 g, 25.49 mmol, yield 84.7%). LCMS [M+H]: m/z 432.4.
Compound TV-6 (1.0 g, 2.32 mmol, 1.0 eq.) and TFA (5.0 mL, 65.34 mmol, 28.1 eq.) were stirred in DCM (10 mL) at room temperature, until the reaction was completed. After the reaction solution was concentrated to remove the solvent, TV-7 (1.03 g, 2.32 mmol, crude product, ca.100%) was obtained, which was directly used in the next step. LCMS [M+H]: m/z 332.2.
To a solution of compounds TV-7 (2.0 g, 4.04 mmol, 1.0 eq.) and TV-8 (934.6 mg, 4.04 mmol, 1.0 eq.) in DCM (40 mL), were added TEA (3.59 mL, 20.2 mmol, 5.0 eq.), HOBt (659.6 mg, 4.85 mmol, 1.2 eq.), and EDC (931.2 mg, 4.85 mmol, 1.2 eq.). The mixture was reacted until completion of the reaction. The mixture was washed with brine (2*20 mL), and then the mixed solution was separated. The organic layer was dried over Na2SO4, followed by rotatory evaporation. The residue was chromatographed over silica gel column, to obtain TV-9 (1.7 g, 3.12 mmol, yield 77.2%). LCMS [M+H]: m/z 545.5.
Compound TV-9 (1.7 g, 3.12 mmol, 1.0 eq.) and TFA (5.0 mL, 65.34 mmol, 20.9 eq.) were stirred in DCM (10 mL) at room temperature, until the reaction was completed. After the reaction solution was concentrated to remove the solvent, TV (1.74 g, 3.12 mmol, crude product, ca.100%) was obtained, which was directly used in the next step. LCMS [M+H]: m/z 445.2.
Intermediate tert-butyl (1-(5-((3-aminophenyl)thio)pyrazin-2-yl)4-methylpyridin-4-yl)carbamate (200 mg, 0.48 mmol), 8-bromooctanoic acid (108 mg, 0.48 mmol), 2-(7-azobenzotriazole)-N,N,N′,N′-tetramethylurea hexafluorophosphate (274 mg, 0.72 mmol) and N,N-diisopropylethylamine (124 mg, 0.96 mmol) were dissolved in dichloromethane (5 mL); and then the mixture was reacted under stirring at room temperature for 2 h. The reaction solution was washed once with water, saturated NaHCO3 aqueous solution, and saturated brine, respectively, and then the reaction solution was separated. The organic layer was dried over anhydrous Na2SO4, and then concentrated, to obtain 215 mg of product (68-1), with a yield of 71.4%. MS: m/z 620 (M+H+); 622 (M+2+H+).
68-2 (2.9 g, 17.5 mmol) and imidazole (2.4 g, 35 mmol) were added to dichloromethane (40 mL), to which was then added tert-butyldimethylsilyl chloride (3.1 g, 20 mmol) dropwise in an ice bath. After addition, the mixture was stirred at room temperature for 1 h. After the reaction was completed, the reaction solution was directly poured into water. The organic phase was washed with water, dried with anhydrous Na2SO4, and rotatory evaporated to obtain the intermediate 68-3 (5.2 g, yield: 100%). MS: m/z 281 [M+H]+.
Compound 68-3 (5.2 g, 17.5 mmol) was dissolved in tetrachloromethane, to which was added N-bromosuccinimide (3.3 g, 18.4 mmol), and then the mixture was reacted at 80° C. for 2 h. After completion of the reaction, the intermediate 68-4 (5.62 g, yield 89.5%) was obtained by purification via column chromatography. MS: m/z 359 [M+H]+, 361 [M+2+H]+.
68-4 (3.6 g, 10 mmol), 3-aminopiperidin-2,6-dionehydrochloride (1.65 g, 10 mmol), and NaHCO3 (1.68 g, 20 mmol) were added into NMP (20 mL), and then the mixture was stirred at 80° C. for 2 h. After that, the reaction solution was stirred overnight at room temperature. Once completion of the reaction, the reaction solution was concentrated, and the residue was purified by column chromatography, to obtain the intermediate 68-5 (1.7 g, yield 65.3%). MS: m/z 261 [M+H]+.
68-5 (1.7 g, 6.5 mmol), 1,4-bis(bromomethyl)benzene (1.72 g, 6.5 mmol), and K2CO3 (1.79 g, 13 mmol) were added into acetonitrile (50 mL), and then the mixture was stirred at 60° C. for 2 h. After completion of the reaction, the reaction solution was concentrated, and the residue was purified by column chromatography, to obtain the intermediate 68-6 (1.1 g, yiled 38.3%). MS: m/z 443 [M+H]+, 445 [M+2+H]+.
Intermediate 68-6 (200 mg, 0.45 mmol), tert-butyl 2,6-diazaspiro[3.4]octan-2-carboxylate (96 mg, 0.45 mmol), diisopropylethylamine (116 mg, 0.9 mmol) and acetonitrile (5 mL) were mixed, and then heated to 40° C., and allowed to react for 1 h. After completion of the reaction, the reaction was directly purified by column chromatography, to obtain the intermediate 68-7 (210 mg, yield 81.4%). MS: m/z 575 [M+H]+.
68-7 (210 mg, 0.36 mmol) and trifluoroacetic acid (1 ml) were added in dichloromethane (2 ml), and then allowed to react for 0.5 h. After completion of the reaction, the solvent was removed by rotatory evaporation, and compound (68-8) (220 mg, yield 100%) was obtained. MS: m/z 475 [M+H]+.
Intermediate 68-1 (100 mg, 0.17 mmol), intermediate 68-8 (109 mg, 0.17 mmol), K2CO3 (49 mg, 0.35 mmol) and acetonitrile (5 mL) were mixed, and then heated to 60° C., and allowed to react for 2 h. After completion of the reaction, the reaction solution was directly subjected to suction filtration, and washed with ethyl acetate (5 mL×3). The organic layers were combined, dried, concentrated, and purified by column chromatography, to obtain the intermediate 68-9 (110 mg, yield 62.1%). MS: m/z 1014 [M+H]+.
68-9 (110 mg, 0.11 mmol) and trifluoroacetic acid (0.5 mL) were added into dichloromethane (1 mL), and allowed to react for 0.5 h. After completion of the reaction, the solvent was removed by rotatory evaporation, and then methanol (3 mL) was added. The resultant solution was adjusted to be pH ˜7 with NaHCO3 solid, filtered, concentrated, and then dissolved by adding dichloromethane (3 mL) and methanol (0.3 mL), followed by filtration and concentration, to obtain compound (68) (81 mg, yield 82%). MS: m/z 914 [M+H]+.
1H NMR (400 MHz, DMSO-d6) δ 9.91 (s, 2H), 9.80 (m, 2H), 8.52-8.01 (m, 3H), 7.52-7.30 (m, 10H), 5.14 (s, 2H), 4.42-4.20 (m, 3H), 3.66 (s, 2H), 3.50-3.11 (m, 10H), 2.50-2.11 (m, 10H), 1.78-1.50 (m, 6H), 1.50-1.27 (m, 10H), 1.23 (s, 3H).
The starting material N-Boc-4-hydroxypiperidine (80-1) (2 g, 10 mmol) and trimethylamine (2 g, 20 mmol) were dissolved in 20 mL of acetonitrile, to which was added methanesulfonic anhydride (1.74 g, 10 mmol) dropwise in an ice water bath, and then the mixture was reacted at room temperature for 5 h. The reaction solution was poured into 20 mL of water, and extracted with 50 mL of ethyl acetate. The organic layer was washed once with 20 mL of saturated NaHCO3 aqueous solution and 20 mL of saturated brine, respectively, dried with anhydrous sodium sulfate, and concentrated to obtain 2.79 g of crude product (80-2), with a yield of 99%. MS: m/z 280 [M+H]+.
Intermediate 80-2 (2.79 g, 10 mmol) and the starting material ethyl 3-methyl-1H-pyrazol-5-carboxylate (80-3) (1.54 g, 10 mmol) were dissolved in 20 mL of N,N-dimethylacetamide, to which was added cesium carbonate (9.9 g, 30 mmol), and then the reaction system was heated to 90° C. and reacted for 15 h. The reaction solution was poured into 20 mL of water, extracted with 50 mL of ethyl acetate, dried over anhydrous sodium sulfate, concentrated, and subjected to column chromatography, to obtain 1.35 g of product (80-4) with a yield of 40%. MS: m/z 338 [M+H]+.
To a reaction flask, was added intermediate 80-4 (1.35 g, 4 mmol), followed by addition of 20 mL of HCl in dioxane (4 mol/L), and then the mixture was allowed to react at room temperature for 2 h. The reaction solution was concentrated to obtain 1.1 g of crude product (80-5), with a yield of 98%. MS: 238 [M+H]+.
The starting material 9-hydroxylnonanoic acid (80-6) (1.74 g, 10 mmol) was dissolved in 35 mL of dichloromethane, to which was added Dess-Martin periodinane (4.7 g, 11 mmol), and the mixture was allowed to react for 1 h. The reaction solution was filtered over diatomaceous earth, and the filter cake was washed with 50 mL of dichloromethane. The filtrate was combined and concentrated, to obtain the crude product (80-7), which was directly used in the next step.
Intermediate 80-5 (474 mg, 2 mmol) and intermediate 80-7 (344 mg, 4 mmol) were dissolved in 10 mL of tetrahydrofuran, to which were added two drops of acetic acid and 1 g of MgSO4, and then the mixture was stirred at room temperature for 1 h. Then, sodium triacetoxyborohydride (2.1 g, 10 mmol) was added, and then the mixture was allowed to react for 3 h. The reaction solution was filtered over diatomaceous earth. The filter cake was washed with 30 mL mixed solvent of dichloromethane/methanol (v/v=10:1). The filtrate was combined, concentrated, and purified over reversed-phase column, to obtain 300 mg of product (80-8), with a yield of 40%. MS: m/z 394 [M+H]+.
Intermediate 80-8 (393 mg, 1 mmol), tert-butyl (1-(5-((3-aminophenyl)thio)pyrazin-2-yl)-4-methylpyridin-4-yl)carbamate (HWH-1) (415 mg, 1 mmol), HATU (380 mg, 1 mmol), and DIEA (390 mg, 3 mmol) were dissolved in 5 mL of N,N-dimethylacetamide, and the mixture was allowed to react at room temperature for 2 h. The reaction solution was poured into 10 mL of water, and extracted with 30 mL of ethyl acetate. The organic layer was dried with anhydrous sodium sulfate, concentrated, and purified by column chromatography to obtain 395 mg of product (80-9), with a yield of 50%. MS: m/z 791 [M+H]+.
Intermediate 80-9 (395 mg, 0.5 mmol) was dissolved in a mixed solvent of 10 mL methanol and 2 mL water, to which was added lithium hydroxide monohydrate (210 mg, 5 mmol), and the mixture was reacted at room temperature for 2 h. The pH of the reaction solution was adjusted to 6 with 0.5 N of dilute hydrochloric acid, and then the solution was extracted with 30 mL of dichloromethane. The organic phase was dried with anhydrous sodium sulfate, and concentrated to obtain 350 mg of product (80-10), with a yield of 90%. MS: m/z 763 [M+H]+.
Intermediate 80-10 (762 mg, 1 mmol), intermediate 3-(5-(aminomethyl)-1-oxoisoindol-2-yl)piperidin-2,6-dione hydrochloride (TC) (273 mg, 1 mmol), HATU (380 mg, 1 mmol), and DIPEA (390 mg, 3 mmol) were dissolved in 6 mL of N,N-dimethylacetamide, and the mixture was reacted at room temperature for 2 h. The reaction was purified by column chromatography, to obtain 509 mg of product (80-11), with a yield of 50%. MS: m/z 459 (M−100+H+)/2.
Intermediate 80-11 (509 mg, 0.5 mmol) was dissolved in 10 mL of dichloromethane, to which was added 1 mL of trifluoroacetic acid, and then the mixture was reacted at room temperature for 2 h. Dichloromethane was removed by rotatory evaporation, and then 10 mL of dichloromethane was added, followed by rotatory evaporation to dry again, that was repeated twice. The residue was dissolved in 5 mL of methanol, and NaHCO3 solid was added to adjust the pH to be 7-8. The resultant solution was filtered, and the filtrate was rotatory evaporated to dry. The residue was dissolved in a mixed solvent of dichloromethane/methanol (V/V=10:1), and then the resultant solution was filtered. The filtrate was rotatory evaporated to dry, and the residue was dissolve in a mixed solvent of dichloromethane/methanol (V/V=10:1), followed by filtration. The filtrate was rotatory evaporated to dry, to obtain 430 mg of compound 80 with a yield of 95%. MS: m/z 459 [M+H]+/2.
Intermediate tert-butyl (1-(5-((3-aminophenyl)thio)pyrazin-2-yl)4-methylpyridin-4-yl)carbamate (200 mg, 0.48 mmol), 9-bromononanoic acid (114 mg, 0.48 mmol), 2-(7-azobenzotriazole)-N,N,N′,N′-tetramethylurea hexafluorophosphate (274 mg, 0.72 mmol), and N,N-diisopropylethylamine (124 mg, 0.96 mmol) were dissolved in dichloromethane (5 ml); and then the mixture was reacted under stirring at room temperature for 2 h. The reaction solution was successively washed once with water, saturated NaHCO3 aqueous solution, and saturated brine, and then the reaction solution was separated. The organic layer was dried over anhydrous Na2SO4, and then concentrated, to obtain 230 mg of product (188-1), with a yield of 76% o. MS: m/z 634 [M+H]+; 636 [M+2+H]+.
188-2 (216 mg, 1 mmol), tert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborinan-2-yl)-3,6-dihydropyridin-1(2H)-carboxylate (371 mg, 1.2 mmol), tetrakis(triphenylphosphine)palladium (57 mg, 0.05 mmol), and K2CO3 (276 mg, 2 mmol) were dissolved in 9 mL of acetonitrile and 1 mL of water, and then the reaction system was purged with nitrogen thrice. The reaction solution was stirred at 80° C. for 10 h, cooled, and then extracted three times with ethyl acetate. The organic layer was dried with anhydrous sodium sulfate and concentrated. The residue was purified by column chromatography to obtain 240 mg of solid (188-3), with a yield of 78.7%.
Compound 188-3 (100 mg, 0.32 mmol), 3-(5-(aminomethyl)-1-oxoisoindol-2-yl)piperidin-2,6-dione hydrochloride (102 mg, 0.32 mmol), 2-(7-azobenzotriazole)-N,N,N′,N′-tetramethylurea hexafluorophosphate (183 mg, 0.48 mmol), N,N-diisopropylethylamine (83 mg, 0.64 mmol) and N,N-dimethylacetamide (2 ml) were allowed to react overnight. After completion of the reaction, the intermediate 88-4 (81 mg, yield 55.1%) was obtained by purification via column chromatography. MS: m/z 461 [M−100+H]+.
188-4 (81 mg, 0.17 mmol), trifluoroacetic acid (0.5 ml) and dichloromethane (1 mL) were allowed to react for 0.5 h. After completion of the reaction, the reaction solution was concentrated to obtain 188-5 (80 mg, yield 100%). MS: m/z 461 [M+H]+.
Intermediate 188-1 (91 mg, 0.14 mmol), intermediate 188-5 (80 mg, 0.14 mmol), NaHCO3 (36 mg, 0.42 mmol), and acetonitrile (3 mL) were mixed, and then heated to 50° C., and allowed to react overnight. After completion of the reaction, the reaction solution was directly subjected to suction filtration, and washed with ethyl acetate (5 mL×3). The organic layers were combined, dried, concentrated, and purified by column chromatography, to obtain the intermediate 188-6 (61 mg, yield 42%). MS: m/z 1014 [M+H]+.
188-6 (61 mg, 0.06 mmol) and trifluoroacetic acid (0.5 mL) were added into dichloromethane (1 mL), and allowed to react for 0.5 h. After completion of the reaction, the solvent was removed by rotatory evaporation, and then methanol (3 mL) was added. The resultant solution was adjusted to be pH ˜7 with NaHCO3 solid, filtered, concentrated, and then dissolved by adding dichloromethane (3 mL) and methanol (0.3 mL), followed by filtration and concentration, to obtain compound (188) (31 mg, yield 52.5%). MS: m/z 914 [M+H]+.
1H NMR (400 MHz, DMSO) δ 11.01 (s, 1H), 9.98-9.90 (m, 2H), 8.45-8.11 (m, 5H), 7.86-7.82 (m, 1H), 7.60-7.62 (m, 2H), 7.55-7.40 (m, 2H), 7.25-7.20 (m, 1H), 5.20-5.10 (m, 1H), 4.60 (s, 2H), 4.41-4.20 (m, 3H), 3.30-2.50 (m, 10H), 2.40-1.91 (m, 6H), 1.80-1.70 (m, 2H), 1.60-1.49 (m, 2H), 1.40-1.20 (m, 10H), 1.23 (s, 3H).
Intermediate tert-butyl (1-(5-((3-aminophenyl)thio)pyrazin-2-yl)4-methylpyridin-4-yl)carbamate (200 mg, 0.48 mmol), 7-bromohexanoic acid (100 mg, 0.48 mmol), 2-(7-azobenzotriazole)-N,N,N′,N′-tetramethylurea hexafluorophosphate (274 mg, 0.72 mmol) and N,N-diisopropylethylamine (124 mg, 0.96 mmol) were dissolved in dichloromethane (5 ml); and then the mixture was reacted under stirring at room temperature for 2 h. The reaction solution was successively washed once with water, saturated NaHCO3 aqueous solution, and saturated brine, and then the reaction solution was separated. The organic layer was dried over anhydrous Na2SO4, and then concentrated, to obtain 210 mg of product (193-1), with a yield of 72.4%. MS: m/z 606 [M+H]+; 608 [M+2+H]+.
193-2 (344 mg, 2 mmol), tert-butyl 2,6-diazaspiro[3.4]octan-2-carboxylate (425 mg, 2 mmol), and K2CO3 (552 mg, 4 mmol) were added to acetonitrile (10 ml), and then the mixture was stirred at 80° C. for 5 h. After completion of the reaction, the intermediate 193-3 (520 mg, yield 75.1%) was obtained by purification via column chromatography. MS: m/z 349 [M+H]+.
Compound 193-3 (520 mg, 1.49 mmol) was dissolved in dichloromethane, and then cooled to ˜50° C. Then, DIBAL-H (1.64 mL, 1.64 mmol) was added dropwise, and the reaction was detected by LCMS. After completion of the reaction, the intermediate 193-4 (402 mg, yield 84.8%) was obtained by purification via column chromatography. MS: 319 [M+H]+.
193-4 (242 mg, 0.76 mmol) and K2CO3 (210 mg, 1.52 mmol) were added into DMF (3 ml), and then cooled to 0° C., to which was then added trifluoromethyltrimethylsilane (119 mg, 0.84 mmol) dropwise. After addition, the mixture was allowed to react for 0.5 h. After completion of the reaction, the reaction solution was concentrated, and the residue was purified by column chromatography, to obtain intermediate 193-5 (223 mg, yield 75.6%). MS: m/z 389 [M+H]+.
193-6 (116 mg, 0.3 mmol) and triethylamine (61 mg, 0.6 mmol) were dissolved in dichloromethane, to which was then added methanesulfonic anhydride (58 mg, 0.33 mmol), and the mixture was stirred at room temperature for 10 min. LCMS indicated completion of the reaction. Then, the reaction solution was poured into water, and extracted with dichloromethane. The organic phase was washed with 1N hydrochloric acid, dried, and rotatory evaporated, to obtain 193-6 (128 mg, yield 92%). MS: m/z 467 [M+H]+.
Intermediate 193-6 (128 mg, 0.27 mmol), 3-(5-(aminomethyl)-1-oxoisoindol-2-yl)piperidin-2,6-dionehydrochloride (93 mg, 0.3 mmol), NaHCO3 (46 mg, 0.54 mmol), and acetonitrile (5 mL) were mixed, and then heated to 40° C., and allowed to react overnight. After completion of the reaction, the reaction solution was directly subjected to suction filtration, and washed with ethyl acetate (5 mL×3). The organic layers were combined, dried, concentrated, and purified by column chromatography, to obtain the intermediate 193-7 (65 mg, yield 37.6%). MS: m/z 644 [M+H]+.
193-7 (65 mg, 0.1 mmol) and trifluoroacetic acid (0.5 ml) were added into dichloromethane (1 m1), and allowed to react for 0.5 h. After completion of the reaction, the solvent was removed by rotatory evaporation, to obtain compound (193-8) (60 mg, yield 100%). MS: m/z 544 [M+H]+.
Intermediate 193-8 (60 mg, 0.09 mmol), intermediate 193-1 (57 mg, 0.09 mmol), NaHCO3 (16 mg, 0.18 mmol) and acetonitrile (3 mL) were mixed, and then heated to 60° C., and allowed to react overnight. After completion of the reaction, the reaction solution was directly subjected to suction filtration, and washed with ethyl acetate (5 mL×3). The organic layers were combined, dried, concentrated, and purified by column chromatography, to obtain the intermediate 193-9 (27 mg, yield 27%). MS: m/z 1069 [M+H]+.
193-9 (27 mg, 0.025 mmol) and trifluoroacetic acid (0.5 ml) were added into dichloromethane (1 mL), and allowed to react for 0.5 h. After completion of the reaction, the solvent was removed by rotatory evaporation, and then methanol (3 mL) was added. The resultant solution was adjusted to be pH ˜7 with NaHCO3 solid, filtered, concentrated, and then dissolved by adding dichloromethane (3 mL) and methanol (0.3 mL), followed by filtration and concentration, to obtain compound (193) (21 mg, yield 86%). MS: m/z 969 [M+H]+.
1H NMR (400 MHz, DMSO-d6) δ 11.01 (s, 1H), 10.03 (s, 1H), 8.36 (s, 2H), 8.23-6.82 (m, 12H), 5.05-5.02 (m, 1H), 4.42-3.20 (m, 19H), 2.60-1.10 (m, 20H), 1.21 (s, 3H).
To a 25 mL single-necked flask, were added compound tert-butyl (1-(5-(((3-aminophenyl)thio)pyrazin-2-yl)-4-methylpyridin-4-yl)carbamate (HWH-1, 100 mg, 0.24 mmol), 14-oxo-3,6,9,12,15-pentaoxaheptadecanoic acid (85 mg, 0.29 mmol), 2-(7-azobenzotriazole)-N,N,N,N-tetramethylurea hexafluorophosphate (137 mg, 0.36 mmol), N,N-diisopropylethylamine (62 mg, 0.48 mmol) and dichloromethane (5 mL), and then the mixture was stirred overnight at room temperature. After completion of the reaction, water (5 mL) was added to the reaction solution, which was separated. The organic layer was dried, concentrated, and then purified by column chromatography, to obtain intermediate (3-1, 135 mg, yield 81%). MS: m/z 692 [M+H]+.
To a 25 mL single-necked flask, were added compound 3-1 (135 mg, 0.2 mmol), lithium hydroxide monohydrate (25 mg, 0.6 mmol), methanol (3 mL) and water (1 mL), and then the mixture was stirred at room temperature for 3-4 h. After completion of the reaction, the pH of the reaction solution was adjusted to 4-5 with 1 N of hydrochloric acid, and then the solution was extracted with dichloromethane (3 mL×3). The organic phase was combined, dried, and concentrated to obtain intermediate 3-2 (100 mg, yield 77%). MS: m/z 664 [M+H]+.
To a 25 mL single-necked flask, were added compound 3-2 (50 mg, 0.075 mmol), 3-(5-(aminomethyl)-1-oxoisoindol-2-yl)piperidin-2,6-dionehydrochloride (23 mg, 0.075 mmol), 2-(7-azobenzotriazole)-N,N,N′,N′-tetramethylurea hexafluorophosphate (38 mg, 0.1 mmol), N,N-diisopropylethylamine (29 mg, 0.23 mmol), and N,N-dimethylacetamide (1 mL), and the mixture was allowed to react overnight. After completion of the reaction, the reaction was purified by pre-TLC, to obtain intermediate 3-3 (35 mg, yield 51%). MS: m/z 919 [M+H]+.
To a 25 mL single-necked flask, were added 3-3 (35 mg, 0.036 mmol), trifluoroacetic acid (1 mL), and dichloromethane (1 mL), and the mixture was allowed to react for 1-2 h. After completion of the reaction, the solvent was removed by rotatory evaporation, and then methanol (3 mL) was added. The resultant solution was adjusted to be pH ˜7 with NaHCO3 solid, filtered, concentrated, and then dissolved by adding dichloromethane (3 mL) and methanol (0.3 mL), followed by filtration and concentration, to obtain compound 3 (14 mg, yield 44%). MS: m/z 819 [M+H]+.
1H NMR (400 MHz, DMSO-d6) δ 1.00 (s, 1H), 9.93 (s, 1H), 8.34 (d, J=1.5 Hz, 1H), 8.23 (s, 1H), 8.15 (d, J=1.4 Hz, 1H), 7.82-7.17 (m, 8H), 6.91-6.83 (m, 1H), 4.36-4.06 (m, 9H), 3.61-3.52 (m, 12H), 3.03-2.85 (m, 4H), 2.24-2.12 (m, 4H), 1.56-1.40 (m, 4H), 1.25-1.15 (m, 3H).
To a 100 mL single-necked flask, were added tert-butyl 4-hydroxylpiperidin-1-carboxylate (79-1, 1 g, 5 mmol) and tetrahydrofuran (15 mL), and then sodium hydride (300 mg, 7.5 mmol) was added in batches in an ice bath. After addition, the ice bath was removed, and the reaction mixture was stirred at room temperature for 0.5 h. Ethyl 8-bromooctanoate (1.9 g, 7.5 mmol) was added, and the reaction was further stirred at room temperature for 4 h, followed by addition of ammonium chloride aqueous solution (20 mL). The resultant solution was extracted with ethyl acetate (20 mL×3). After extraction, the organic layers were combined, dried, concentrated, and purified by column chromatography, to obtain intermediate 79-2 (1 g, yiled 54%). MS: m/z 372 [M+H]+.
To a 50 mL single-necked flask, were added intermediate 79-2 (1 g, 2.7 mmol) and concentrated hydrochloric acid (10 mL), and then allowed to react for 48 h. After completion of the reaction, the reaction solution was rotatory evaporated to remove water and obtain intermediate 79-3 (250 mg, yield 33%). MS: m/z 244 [M+H]+.
To a 50 mL single-necked flask, were added 79-3 (250 mg, 0.9 mmol), ethyl 2-chloropyrimidine-5-carboxylate (168 mg, 0.9 mmol), K2CO3 (500 mg, 3.6 mmol), and acetonitrile (3 mL), and then the mixture was heated to 60° C., and allowed to react overnight. After completion of the reaction, the reaction solution was diluted with water, and extracted with ethyl acetate (5 mL×3). The organic layers were combined, dried, concentrated, and purified by column chromatography, to obtain the intermediate 79-4 (136 mg, yield 39%). MS: m/z 394 [M+H]+.
To a 50 mL single-necked flask, were added intermediate 79-4 (136 mg, 0.35 mmol), HWH-1 (145 mg, 0.35 mmol), 2-(7-azobenzotriazole)-N,N,N′,N′-tetramethylurea hexafluorophosphate (173 mg, 0.46 mmol), N,N-diisopropylethylamine (136 mg, 1.1 mmol), and dichloromethane (2 mL), and the mixture was allowed to react overnight. After completion of the reaction, purification by pTLC provided intermediate 79-5 (230 mg, yield 83%). MS: m/z 791 [M+H]+.
To a 25 mL single-necked flask, were added intermediate 79-5 (230 mg, 0.29 mmol), lithium hydroxide monohydrate (122 mg, 2.9 mmol), methanol (3 mL) and water (1 mL), and then the mixture was stirred at room temperature for 3-4 h. After completion of the reaction, the pH of the reaction solution was adjusted to 4-5 with 1 N of hydrochloric acid, and then the solution was extracted with dichloromethane (3 mL×3). The organic phase was combined, dried, and concentrated to obtain intermediate 79-6 (210 mg, yield 95%). MS: m/z 763 [M+H]+.
To a 25 mL single-necked flask, were added intermediate 79-6 (50 mg, 0.07 mmol), 3-(5-(aminomethyl)-1-oxoisoindol-2-yl)piperidin-2,6-dionehydrochloride (23 mg, 0.075 mmol), 2-(7-azobenzotriazole)-N,N,N′,N′-tetramethylurea hexafluorophosphate (38 mg, 0.1 mmol), N,N-diisopropylethylamine (29 mg, 0.23 mmol), and N,N-dimethylacetamide (1 mL), and the mixture was allowed to react overnight. After completion of the reaction, the reaction mixture was directly purified by pTLC, to obtain intermediate 79-7 (28 mg, yield 42%). MS: m/z 1018 [M+H]+.
To a 25 mL single-necked flask, were added 79-7 (28 mg, 0.028 mmol), trifluoroacetic acid (1 mL), and dichloromethane (3 mL), and the mixture was allowed to react for 1-2 h. After completion of the reaction, the solvent was removed by rotatory evaporation, and then methanol (3 mL) was added. The resultant solution was adjusted to be pH ˜7 with NaHCO3 solid, filtered, concentrated, and then dissolved by adding dichloromethane (3 mL) and methanol (0.3 mL), followed by filtration and concentration, to obtain compound 79 (15 mg, yield 60%). MS: m/z 918 [M+H]+.
1H NMR (400 MHz, DMSO-d6) δ 11.00 (s, 1H), 9.94 (s, 1H), 9.02 (t, J=6.0 Hz, 1H), 8.81 (s, 2H), 8.38 (d, J=1.5 Hz, 1H), 8.18 (d, J=1.4 Hz, 1H), 8.02 (d, J=43.3 Hz, 2H), 7.69 (d, J=7.8 Hz, 1H), 7.64-7.50 (m, 2H), 7.45 (d, J=8.1 Hz, 2H), 7.23 (t, J=8.0 Hz, 1H), 6.90 (dd, J=7.8, 1.7 Hz, 1H), 5.11 (dd, J=13.3, 5.1 Hz, 1H), 4.57 (d, J=5.9 Hz, 2H), 4.48-3.96 (m, 6H), 3.43-3.37 (m, 7H), 2.98-2.83 (m, 1H), 2.62-2.57 (m, 1H), 2.38-2.22 (m, 2H), 2.06-1.63 (m, 7H), 1.58-1.25 (m, 16H).
To a 100 mL single-necked flask, were added 3-(5-bromo-1-oxoisoindol-2-yl)piperidin-2,6-dione (157-1, 5 g, 15.5 mmol), ethynyltrimethylsilane (7.6 g, 77.6 mmol), [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium (2.3 g, 3.1 mmol), CuI (589 mg, 3.1 mmol), trimethylamine (10 mL), and N,N-dimethylformamide (15 mL), and then the mixture was heated to 70° C. and reacted overnight under nitrogen protection. After completion of the reaction, the reaction solution was diluted with water (20 mL), and extracted with dichloromethane (20 mL×3). The organic layers were combined, dried, and purified by column chromatography, to obtain intermediate 157-2 (2.5 g, yield 47%). MS: m/z 341 [M+H]+.
To a 100 mL single-necked flask, were added 157-2 (4.4 mmol, 1.5 g), tetrabutylammonium fluoride (4.6 g, 17.6 mmol), and tetrahydrofuran (200 mL), and then the reaction solution was heated to 70° C. for about 2 h. After completion of the reaction, the solvent was removed by rotatory evaporation, and then the residue was triturated with tetrahydrofuran (3 mL), followed by filtration, to obtain intermediate 157-3 (700 mg, yield 59%). MS: m/z 269 [M+H]+.
To a 100 mL single-necked flask, were added HWH-1 (200 mg, 0.48 mmol), 7-bromohexanoic acid (120 mmol, 0.58 mmol), 2-(7-azobenzotriazole)-N,N,N′,N′-tetramethylurea hexafluorophosphate (237 mg, 0.62 mmol), N,N-diisopropylethylamine (124 mg, 0.96 mmol), and dichloromethane (5 mL), and then the mixture was allowed to react overnight. After completion of the reaction, the reaction solution was diluted with water (5 mL), and extracted with dichloromethane (5 mL×3). The organic layers were combined, dried, and purified by column chromatography, to obtain intermediate 157-4 (250 mg, yield 86%). MS: m/z 606, 608 [M+H]+.
To a 100 mL single-necked flask, were added 3,6-diiodopyridazine (157-5, 3 g, 9 mmol), tert-butyl 2,6-diazaspiro[3.4]octan-2-carboxylate (1.9 g, 9 mmol), K2CO3 (3.7 g, 27 mmol) and acetonitrile (30 mL), and the mixed solution was heated to 80° C. and reacted overnight, followed by addition of water (10 mL). The resultant solution was extracted with ethyl acetate (20 mL×3) thrice. The organic layers were combined, dried, and purified by column chromatography, to obtain intermediate 157-6 (3 g, yield 80%). MS: m/z 417 [M+H]+.
To a 25 mL single-necked flask, were added 157-6 (300 mg, 0.72 mmol), 157-3 (193 mg, 0.72 mmol), [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium (110 mg, 0.15 mmol), CuI (29 mg, 0.15 mmol), trimethylamine (2 mL), and N,N-dimethylformamide (2 mL), and then the mixture was heated to 70° C. and reacted overnight under nitrogen protection. After completion of the reaction, the solution was cooled to room temperature and filtered. The filter cake was washed with acetonitrile (3 mL) and dried, to obtain intermediate 157-7 (270 mg, yield 68%). MS: m/z 557 [M+H]+.
To a 25 mL single-necked flask, were added 157-7 (100 mg, 0.18 mmol) and concentrated hydrochloric acid (3 mL), and the mixture was reacted for about 1 h. After completion of the reaction, the solution was concentrated to obtain intermediate 157-8 (88 mg, yield 99%). MS: m/z 457 [M+H]+.
To a 25 mL single-necked flask, were added 157-8 (88 mg, 0.18 mmol), 157-4 (109 mg, 0.18 mmol), K2CO3 (100 mg, 0.72 mmol), KI (30 mg, 0.18 mmol), and dimethylsulfoxide (2 mL), and then the reaction solution was heated to 70° C. for about 3 h. After completion of the reaction, the reaction solution was diluted with water (3 mL), and extracted with dichloromethane (5 mL×3). The organic layers were combined, dried, and purified by pTLC, to obtain intermediate 157-9 (14 mg, yield 8%). MS: m/z 982 [M+H]+.
To a 25 mL single-necked flask, were added 157-9 (14 mg, 0.014 mmol), trifluoroacetic acid (1 mL), and dichloromethane (3 mL), and the mixture was allowed to react for 1-2 h. After completion of the reaction, the solvent was removed by rotatory evaporation, and then methanol (3 mL) was added. The resultant solution was adjusted to be pH ˜7 with NaHCO3 solid, filtered, concentrated, and then dissolved by adding dichloromethane (3 mL) and methanol (0.3 mL), followed by filtration and concentration, to obtain compound 157 (12 mg, yield 95%). MS: m/z 882 [M+H]+.
1H NMR (400 MHz, DMSO-d6) δ 11.00 (s, 1H), 9.95 (s, 1H), 8.38 (d, J=1.5 Hz, 1H), 8.18 (d, J=1.4 Hz, 1H), 7.84-7.60 (m, 7H), 7.24 (t, J=8.0 Hz, 2H), 6.90 (dd, J=8.3, 2.8 Hz, 2H), 5.32 (t, J=4.9 Hz, 1H), 4.76 (dd, J=10.3, 5.0 Hz, 1H), 4.71-4.45 (m, 3H), 4.05 (d, J=14.0 Hz, 3H), 3.69-3.39 (m, 9H), 2.34-2.24 (m, 6H), 1.72-1.62 (m, 4H), 1.44-1.26 (m, 13H).
To a 100 mL single-necked flask, were added HWH-1 (400 mg, 0.96 mmol), 8-bromooctanoic acid (258 mmol, 1.16 mmol), 2-(7-azobenzotriazole)-N,N,N′,N′-tetramethylurea hexafluorophosphate (471 mg, 1.24 mmol), N,N-diisopropylethylamine (248 mg, 1.92 mmol), and dichloromethane (10 mL), and the mixture was allowed to react overnight. After completion of the reaction, the reaction solution was diluted with water (10 mL), and extracted with dichloromethane (10 mL×3). The organic layers were combined, dried, and purified by column chromatography, to obtain intermediate 172-1 (520 mg, yield 87%). MS: m/z 620, 622 [M+H]+.
To a 100 mL single-necked flask, were added tert-butyl 6-hydroxyl-2-azaspiro[3.3]heptan-2-carboxylate (172-2, 1 g, 4.7 mmol), methanesulfonic anhydride (900 mg, 5.2 mmol), trimethylamine (950 mg, 9.4 mmol) and dichloromethane (20 mL), and the mixture was allowed to react overnight. After completion of the reaction, the reaction solution was diluted with 1 N of dilute HCl aqueous solution (10 mL), and then separated. The organic layer was dried and concentrated, to obtain intermediate 172-3 (1.36 g, 100%). MS: m/z 292 [M+H]+.
To a 100 mL single-necked flask, were added 172-3 (1.36 g, 4.7 mmol), 4-iodo-1H-pyrazole (1.8 g, 9.4 mmol), K2CO3 (1.3 g, 9.4 mmol) and acetonitrile (20 mL), and then the reaction solution was heated to 60° C. overnight. After completion of the reaction, the reaction solution was diluted with water (10 mL) and then extracted with ethyl acetate (20 mL×3). The organic layers were combined, dried, and purified by column chromatography, to obtain intermediate HC-172-4 (1.5 g, 82%). MS: m/z 390 [M+H]+.
To a 100 mL single-necked flask, were added 172-4 (389 mg, 1 mmol), 157-3 (322 mg, 1.2 mmol), [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium (146 mg, 0.2 mmol), CuI (38 mg, 0.2 mmol), trimethylamine (2 mL), and N,N-dimethylformamide (2 mL), and then the mixture was heated to 70° C. and reacted overnight under nitrogen protection. After completion of the reaction, the reaction solution was cooled to room temperature, diluted with water (4 mL), and then extracted with dichloromethane (5 mL×3). The organic layers were combined, dried, and purified by column chromatography, to obtain intermediate 172-5 (300 mg, yield 82%). MS: m/z 530 [M+H]+.
To a 25 mL single-necked flask, were added 172-5 (300 mg, 0.57 mmol) and concentrated hydrochloric acid (5 mL), and the mixture was reacted for about 1 h. After completion of the reaction, the solution was concentrated to obtain intermediate 172-6 (264 mg, yield 1001). MS: m/z 430 [M+H]+.
To a 25 mL single-necked flask, were added 172-6 (264 mg, 0.57 mmol), 172-1 (353 mg, 0.57 mmol), K2CO3 (315 mg, 2.28 mmol), KI (95 mg, 0.57 mmol), and dimethylsulfoxide (4 mL), and then the reaction solution was heated to 70° C. for about 3 h. After completion of the reaction, the reaction solution was diluted with water (3 mL), and extracted with dichloromethane (5 mL×3). The organic layers were combined, dried, and purified by pTLC, to obtain intermediate 172-7 (60 mg, yield 110%). MS: m/z 969[M+H]+.
To a 25 mL single-necked flask, were added 172-7 (20 mg, 0.02 mmol), trifluoroacetic acid (1 mL), and dichloromethane (3 mL), and the mixture was allowed to react for 1-2 h. After completion of the reaction, the solvent was removed by rotatory evaporation, and then methanol (3 mL) was added. The resultant solution was adjusted to be pH 7 with NaHCO3 solid, filtered, concentrated, and then dissolved by adding dichloromethane (3 mL) and methanol (0.3 mL), followed by filtration and concentration, to obtain compound 172 (15 mg, yield 83%). MS: m/z 869 [M+H]+.
1H NMR (400 MHz, DMSO-d6) δ 11.00 (s, 1H), 9.93 (s, 1H), 8.34 (d, J=1.5 Hz, 1H), 8.23 (s, 1H), 8.15 (d, J=1.4 Hz, 1H), 7.82-7.17 (m, 9H), 6.92-6.82 (m, 1H), 5.36-5.05 (m, 1H), 4.83-4.16 (m, 4H), 3.76-3.58 (m, 4H), 3.16-3.01 (m, 5H), 2.54 (d, J=8.0 Hz, 3H), 2.26 (q, J=7.8 Hz, 5H), 2.07-1.92 (m, 2H), 1.56-1.40 (m, 7H), 1.20-1.05 (m, 10H).
(E)-ethyl p-hydroxycinnamate (1.92 g, 10.00 mmol) and (bromomethyl)benzene (1.88 g, 11.00 mmol) were dissolved in 60 mL of N,N-dimethylformamide, to which was added K2CO3 (3.73 g, 27.00 mmol), and then the mixture was allowed to react for 2 h at 30° C. The reaction solution was diluted with 50 mL of water, stirred, and extracted with 50 mL of ethyl acetate. The organic layer was dried with anhydrous Na2SO4, filtered, concentrated, and purified by column chromatography, to obtain 2.68 g of solids (189-3), with a yield of 95%. MS: m/z 283 [M+H]+.
Trimethylsulfoxonium iodide (440 mg, 2.00 mmol) was dissolved in 5 mL dimethylsulfoxide, and then the reaction system was purged with argon thrice, to which was added NaH (60 mg, 0.50 mmol) in portions. The mixture was allowed to react at 22° C. for 0.5 h, followed by addition of 189-3 (282 mg, 1.00 mmol), and then the reaction was further stirred for 1 h. 10 mL of water was added for quenching reaction, and then the resultant solution was extracted with 10 mL of ethyl acetate. The organic layer was dried with anhydrous sodium sulfate, filtered, concentrated, and purified with column chromatography to obtain 137 mg of solid (189-4), with a yield of 46%. MS: m/z 297 [M+H]+.
189-4 (96 mg, 0.32 mmol) and Pd/C (24 mg, 0.03 mmol) were dissolved in 3 mL mixed solvent of methanol/ethyl acetate (1:1), and then the system was purged with hydrogen for three times. The mixture was allowed to react at 35° C. for 3 h. The reaction solution was filtered, concentrated, and purified by column chromatography, to obtain 64 mg of solid (189-5), with a yield of 91%. MS: m/z 207 [M+H]+.
HWH-1 (830 mg, 2.00 mmol), 6-bromohexanoic acid (390 mg, 2.00 mmol), HATU (837 mg, 2.20 mmol) and DIPEA (517 mg, 4.00 mmol) were dissolved in 15 mL of dichloromethane, and then the mixture was allowed to react overnight at room temperature. The reaction solution was successively washed with 10 mL of water, 10 mL of HCl solution (0.5 mol/L), 10 mL of saturated NaHCO3 solution, and 10 mL of saturated brine, and then separated. The water layer was re-extracted with 10 mL of dichloromethane. The organic layers were combined, dried with anhydrous sodium sulfate, filtered, concentrated, and purified by column chromatography to obtain 1.03 g of solid (189-7), with a yield of 87%. MS: m/z 592 [M+H]+.
189-7 (120 mg, 0.20 mmol) and 189-5 (64 mg, 0.2 mmol) were dissolved in 1 mL of N,N-dimethylformamide, to which was added K2CO3 (56 mg, 0.40 mmol), and then the mixture was allowed to react overnight at 80° C. The reaction solution was cooled to room temperature and concentrated. The residue was purified by column chromatography to obtain 90 mg of solids (189-8), with a yield of 62%. MS: m/z 618 [M−100+H]+
189-8 (90 mg, 0.13 mmol) was dissolved in a mixed solvent of tetrahydrofuran/methanol/water (1:1:1, 3 mL), to which was added lithium hydroxide monohydrate (82 mg, 1.95 mmol), and the mixture was reacted at room temperature for 0.5 h. The pH of the reaction solution was adjusted to 6-7 with 0.5 mol/L of dilute hydrochloric acid, and then the solution was extracted with 10 mL of dichloromethane. The organic phase was dried with anhydrous sodium sulfate, filtered, and concentrated to obtain 70 mg of crude product (189-9), with a yield of 81%. MS: m/z 329 ((M−100)/2+H+).
189-9 (70 mg, 0.10 mmol), TC (29 mg, 0.11 mmol), HATU (46 mg, 0.12 mmol), and DIPEA (33 mg, 0.25 mmol) were dissolved in 0.5 mL of N,N-dimethylformamide, and then the mixture was allowed to react at room temperature overnight. Purification by column chromatography provided 40 mg of solids (189-10), with a yield of 42%. MS: m/z 945 [M+H]+.
189-10 (40 mg, 0.42 mmol) was dissolved in 3 mL of dichloromethane, to which was added 1 mL of trifluoroacetic acid, and then the mixture was reacted at room temperature for 0.5 h. The reaction solution was concentrated to dry, and the residue was dissolved in 10 mL of dichloromethane, followed by concentration to remove trifluoroacetic acid, that was repeated twice. To the residue, was added 5 mL of methanol, and then the pH value was adjusted to be 7-8 with NaHCO3, followed by filtration and concentration. The residue was dissolved in 5 mL of dichloromethane/methanol (10:1), and the resultant solution was filtered and concentrated, to obtain 29 mg of product (189), with a yield of 81%. MS: m/z 845 [M+H]+.
1H NMR (400 MHz, DMSO-d6) δ 9.95 (s, 1H), 8.36 (d, J=1.5 Hz, 1H), 8.16 (d, J=1.4 Hz, 1H), 7.66 (ddd, J=15.3, 8.0, 5.0 Hz, 1H), 7.55 (t, J=1.9 Hz, 1H), 7.48-7.43 (m, 2H), 7.37 (q, J=8.3, 7.1 Hz, 1H), 7.25-7.18 (m, 2H), 7.05 (dd, J=14.0, 8.4 Hz, 2H), 6.89 (d, J=7.8 Hz, 1H), 6.84-6.79 (m, 2H), 4.49-4.33 (m, 3H), 3.95-3.79 (m, 4H), 3.58-3.46 (m, 4H), 2.33-2.22 (m, 3H), 2.15 (t, J=7.4 Hz, 1H), 2.08-1.96 (m, 3H), 1.78 (t, J=7.5 Hz, 1H), 1.73-1.68 (m, 2H), 1.64-1.58 (m, 4H), 1.48-1.38 (m, 4H), 1.30-1.20 (m, 7H).
Tert-butyl (1-(5-((3-amino-2-chlorophenyl)thio)pyrazin-2-yl)-4-methylpyridin-4-yl)carbamate (92.8 mg, 0.2 mmol) and 4-(4-(9-methoxy-9-oxocarbonyl)piperazin-1-yl)-4-oxobutyric acid (71.3 mg, 0.2 mmol) were dissolved in 5 mL of DCM, to which were added T3P (318.2 mg, 1 mmol) and DIPEA (154.8 mg, 1.2 mmol), respectively. The mixture was stirred at room temperature for 12 h. After the reaction was completed, to the reaction solution, was added saturated brine (5 mL), and the resultant solution was rested to separate the organic layer. The water layer was extracted with dichloromethane. The organic layers were combined, dried with anhydrous sodium sulfate, and concentrated. The residue was purified by TLC to obtain 121 mg of intermediate 15-1, with a yield of 75%. MS: m/z 802 [M+H]+.
Methyl 9-(4-(4-((3-((5-(4-((tert-butoxycarbonyl)amino)methyl)-4-methylpyridin-1-yl)pyrazin-2-yl)thio)-2-chlorophenyl)amino)-4-oxobutyryl)piperazin-1-yl)nonanoate (intermediate 15-1) (96.3 mg, 0.12 mmol) was dissolved in methanol (3 mL), to which was added lithium hydroxide monohydrate (100.7 mg, 2.4 mmol), and the mixture was stirred at room temperature for 3 h. After completion of the reaction, the pH of the reaction solution was adjusted to about 6 with 0.5 N of hydrochloric acid, and then the solution was diluted with dichloromethane. After standing, the organic layer was separated, and the water layer was extracted with dichloromethane. The organic layers were combined, dried with anhydrous sodium sulfate, and concentrated. The residue was purified by TLC to obtain 80 mg of intermediate 15-2, with a yield of 85%. MS: m/z 788 [M+H]+.
9-(4-(4-((3-((5-(4-((tert-butoxycarbonyl)amino)methyl)-4-methylpyridin-1-yl)pyrazin-2-yl)thio)-2-chlorophenyl)amino)-4-oxobutyryl)piperazin-1-yl)nonanoic acid (intermediate 15-2) (39.4 mg, 0.05 mmol) and 3-(5-(aminomethyl)-1-oxoisoindol-2-yl)piperidin-2,6-dione (13.7 mg, 0.05 mmol) were dissolved in 0.5 mL of DMA, to which were added HATU (28.5 mg, 0.075 mmol) and DIPEA (12.9 mg, 0.1 mmol), respectively. The mixture was stirred at room temperature for 12 h. After completion of the reaction, purification by TLC provided 35 mg of intermediate 15-3, with a yield of 67%. MS: m/z 1043 [M+H]+.
Tert-butyl (1-(5-((2-chloro-3-(4-(4-((2-(2,6-dioxopiperidin-3-yl)-1-oxoisoquinolin-5-yl)methyl)amino)-9-oxononyl)piperazin-1-yl)-4-oxobutylamido)phenyl)thio)pyrazin-2-yl)-4-methylpyridin-4-yl)carbamate (intermediate 15-3) (31.3 mg, 0.03 mmol) was dissolved in a mixed solvent of 3 mL DCM and 1 mL TFA, and then the mixture was reacted at room temperature under stirring for 3 h. After the reaction was completed, the solvent was removed by evaporation under reduced pressure. 3 mL of methanol was added, and the pH of the resultant solution was adjusted to about 8 with NaHCO3. The insoluble substances were filtered out. After methanol was removed by evaporation under reduced pressure, the obtained solid was dissolved in a solution of dichloromethane/methanol (10:1, 5 mL). The insoluble substances were removed by filtration, and the solvent was removed by evaporation under reduced pressure, to obtain 25 mg of compound 15, with a yield of 88%. MS: m/z 943 [M+H]+.
Ethyl 2-chloropyrimidine-5-carboxylate (1.87 g, 10 mmol) and tert-butyl piperazin-1-carboxylate (1.86 g, 10 mmol) were dissolved in 20 mL of acetonitrile, to which was added K2CO3 (2.76 g, 20 mmol). The mixture was stirred at 80° C. for 12 h. The reaction solution was cooled, diluted with 30 mL of water, and extracted three times with ethyl acetate. The organic layer was dried with anhydrous sodium sulfate and concentrated. The crude product was recrystallized in ethyl acetate to obtain 3.1 g of intermediate 48-1, with a yield of 92%. MS: m/z 337 [M+H]+.
Ethyl 2-(4-(tert-butoxycarbonyl)piperazin-1-yl)pyrimidine-5-carboxylate (intermediate 48-1) (1.68 g, 5 mmol) was dissolved in a mixed solvent of 10 mL DCM and 5 mL TFA, and then the solution was stirred at room temperature for 3 h. After completion of the reaction, the solvent was removed by evaporation under reduced pressure, and to residue, was added saturated NaHCO3 solution. The resultant solution was extracted three times with dichloromethane. The organic layer was dried with anhydrous sodium sulfate, and concentrated, to obtain 1.1 g of intermediate 48-2, with a yield of 92%. MS: m/z 337 [M+H]+.
Ethyl 2-(piperazin-1-yl)pyrimidine-5-carboxylate (intermediate 48-2) (236 mg, 1 mmol) and 9-bromononanoic acid (237 mg, 1 mmol) were dissolved in 10 mL of acetonitrile, to which were added K2CO3 (0.69 g, 5 mmol) and NaI (15 mg, 0.1 mmol). The mixture was stirred at 80° C. for 12 h, and then cooled. The pH of the resultant solution was adjusted to around 6 with 0.5 N hydrochloric acid. The solution was extracted three times with ethyl acetate. The organic layer was dried with anhydrous sodium sulfate and concentrated. Purification by column chromatography provided 300 mg of intermediate 48-3, with a yield of 76.4%. MS: m/z 393 [M+H]+.
9-(4-(5-(ethoxycarbonyl)pyrimidine-2-yl)piperazin-1-yl)nonanoic acid (intermediate 48-3) (118 mg, 0.3 mmol) and tert-butyl (1-(5-((3-aminophenyl)thio)pyrazin-2-yl)-4-methylpyridin-4-yl)carbamate (125 mg, 0.3 mmol) were dissolved in 5 mL of dichloromethane, to which were added HATU (171 mg, 0.45 mmol) and DIPEA (77 mg, 0.6 mmol). The mixture was stirred at room temperature for 12 h. After completion of the reaction, purification by TLC provided 160 mg of intermediate 48-4, with a yield of 67.6%. MS: m/z 790 [M+H]+.
Ethyl 2-(4-(9-((3-((5-(4-((tert-butoxycarbonyl)amino)-4-methylpyridin-1-yl)pyrazin-2-yl)thio)phenyl)amino)-9-oxononyl)piperazin-1-yl)pyrimidine-5-carboxylate (intermediate 48-4) (158 mg, 0.2 mmol) was dissolved in methanol (3 mL), to which was added lithium hydroxide monohydrate (168 mg, 4 mmol), and the mixture was stirred at room temperature for 3 h. After completion of the reaction, the pH of the reaction solution was adjusted to about 6 with 0.5 N of hydrochloric acid, and then the solution was diluted with dichloromethane. After standing, the organic layer was separated, and the water layer was extracted with dichloromethane. The organic layers were combined, dried with anhydrous sodium sulfate, and concentrated. The residue was purified by TLC to obtain 145 mg of intermediate 48-5, with a yield of 95%. MS: m/z 762 [M+H]+.
2-(4-(9-((3-((5-(4-((tert-butoxycarbonyl)amino)-4-methylpyridin-1-yl)pyrazin-2-yl)thio)phenyl)amino)-9-oxononyl)piperazin-1-yl)pyrimidine-5-carboxylic acid (intermediate 48-5) (38 mg, 0.05 mmol) and 3-(5-(aminomethyl)-1-oxoisoindol-2-yl)piperidin-2,6-dione (13.7 mg, 0.05 mmol) were dissolved in 0.5 mL of DMA, to which were added HATU (28.5 mg, 0.075 mmol) and DIPEA (12.9 mg, 0.1 mmol). The mixture was stirred at room temperature for 12 h. After completion of the reaction, purification by TLC provided 40 mg of intermediate 48-6, with a yield of 78.6%. MS: m/z 1017 [M+H]+.
Tert-butyl (1-(5-((3-(9-(4-(5-((2-(2,6-dioxopiperidin-3-yl)-1-oxoisoindol-5-yl)methyl)carbamoyl)pyrimidine-2-yl)piperazin-1-yl)oxononylamino)phenyl)thio)pyrazin-2-yl)-4-methylpyridin-4-yl)carbamate (48-6) (30.3 mg, 0.03 mmol) was dissolved in 3 mL DCM and 1 mL TFA, and then the solution was stirred and reacted at room temperature for 3 h. After completion of the reaction, the solvent was removed by evaporation under reduced pressure, and to the residue, was added 3 mL of methanol. The pH of the resultant solution was adjusted to about 8 with NaHCO3 solution. The insoluble substances were filtered out. After methanol was removed by evaporation under reduced pressure, the obtained solid was dissolved in a solution of dichloromethane/methanol (10:1, 5 mL). The insoluble substances were removed by filtration, and the solvent was evaporated under reduced pressure, to obtain 21 mg of compound 48, with a yield of 76.3%. MS: m/z 917 [M+H]+.
Tert-butyl 2,6-diazaspiro[3.3]heptan-2-carboxylate (198.3 mg, 1 mmol) and (E)-4-methoxy-4-oxobutyl-2-en-1-carboxylic acid (130.1 mg, 1 mmol) were dissolved in 5 mL of dichloromethane, to which were added HATU (570 mg, 1.5 mmol) and DIPEA (258 mg, 2 mmol). The mixture was stirred at room temperature for 12 h. After completion of the reaction, purification by TLC provided 250 mg of intermediate 114-1, with a yield of 80.6%. MS: m/z 311 [M+H]+.
Tert-butyl (E)-6-(4-methoxy-4-oxobutan-2-ene)-2,6-diazaspiro[3.3]heptan-2-carboxylate (intermediate 114-1) (248 mg, 0.8 mmol) were dissolved in 10 mL DCM and 5 mL TFA, and then the mixture was stirred and reacted at room temperature for 3 h. After completion, to the reaction solution, was added saturated NaHCO3 aqueous solution, and the resultant solution was extracted with dichloromethane. The organic phase was dried with anhydrous sodium sulfate, and evaporated under reduced pressure to remove the solvent, and obtain 145 mg of intermediate 114-2, with a yield of 86.2%. MS: m/z 211 [M+H]+.
8-bromooctanoic acid (111.5 mg, 0.5 mmol) and tert-butyl (1-(5-((3-aminophenyl)thio)pyrazin-2-yl)-4-methylpyridin-4-yl)carbamate (207.8 mg, 0.5 mmol) were dissolved in 5 mL of dichloromethane, to which were added HATU (285 mg, 0.75 mmol) and DIPEA (129 mg, 1 mmol). The mixture was stirred at room temperature for 12 h. After completion of the reaction, purification by TLC provided 210 mg of intermediate 114-3, with a yield of 67.7%. MS: m/z 620 [M+H]+.
Tert-butyl (1-(5-((3-(8-bromooctamide)phenyl)thio)pyrazin-2-yl)-4-methylpyridin-4-yl)carbamate (intermediate 114-3) (124 mg, 0.2 mmol) and methyl (E)-4-oxo-4-(2,6-diazaspiro[3.3]heptan-2-yl)butan-2-en-1-carboxylate (intermediate 114-2) (42 mg, 0.2 mmol) were dissolved in 10 mL of acetonitrile, to which were added K2CO3 (138 mg, 1 mmol) and NaI (3 mg, 0.02 mmol). The mixture was stirred at 80° C. for 12 h, and then cooled. The pH of the resultant solution was adjusted to around 6 with 0.5 N hydrochloric acid. The solution was extracted three times with ethyl acetate. The organic layer was dried with anhydrous sodium sulfate and concentrated. Purification by column chromatography provided 115 mg of intermediate 114-4, with a yield of 76.7%. MS: m/z 750 [M+H]+.
Methyl (E)-4-(6-(8-((3-((5-(4-((tert-butoxycarbonyl)amino)-4-methylpyridin-1-yl)pyrazin-2-yl)thio)phenyl)amino)-8-oxyoctyl)-2,6-diazaspiro[3.3]heptan-2-yl)-4-oxobutan-2-en-1-carboxylate (intermediate 114-4) (112 mg, 0.15 mmol) was dissolved in methanol (3 mL), to which was added lithium hydroxide monohydrate (126 mg, 3 mmol), and the mixture was stirred at room temperature for 3 h. After completion of the reaction, the pH of the reaction solution was adjusted to about 6 with 0.5 N of hydrochloric acid, and then the solution was diluted with dichloromethane. After standing, the organic layer was separated, and the water layer was extracted with dichloromethane. The organic layers were combined, dried with anhydrous sodium sulfate, and concentrated. The residue was purified by TLC to obtain 95 mg of intermediate 114-5, with a yield of 86%. MS: m/z 736 [M+H]+.
(E)-4-(6-(8-((3-((5-(4-((tert-butoxycarbonyl)amino)-4-methylpyridin-1-yl)pyrazin-2-yl)thio)phenyl)amino)-8-oxyoctyl)-2,6-diazaspiro[3.3]heptan-2-yl)-4-oxo-2-en-1-carboxylic acid (intermediate 114-5) (38 mg, 0.05 mmol) and 3-(5-(aminomethyl)-1-oxoisoindol-2-yl)piperidin-2,6-dione (13.7 mg, 0.05 mmol) were dissolved in 0.5 mL of DMA, to which were added HATU (28.5 mg, 0.075 mmol) and DIPEA (12.9 mg, 0.1 mmol). The mixture was stirred at room temperature for 12 h. After completion of the reaction, purification by TLC provided 37 mg of intermediate 114-6, with a yield of 74.7%. MS: m/z 991 [M+H]+.
Tert-butyl ((E)-(1-(5-((3-(8-(6-(4-((2-(2,6-dioxopiperidin-3-yl)-1-oxoisoquinolin-5-yl)methyl)amino)-4-oxobutan-2-en-1-carbonyl)-2,6-diazaspiro[3.3]heptan-2-yl)octamido)phenyl)thio)pyrazin-2-yl)-4-methylpyridin-4-yl)carbamate (intermediate 114-6) (29.7 mg, 0.03 mmol) was dissolved in 3 mL DCM and 1 mL TFA, and then the solution was stirred and reacted at room temperature for 3 h. After completion of the reaction, the solvent was removed by evaporation under reduced pressure, and to the residue, was added 3 mL of methanol. The pH of the resultant solution was adjusted to about 8 with NaHCO3 solution. The insoluble substances were filtered out. After methanol was removed by evaporation under reduced pressure, the obtained solid was dissolved in a solution of dichloromethane/methanol (10:1, 5 mL). The insoluble substances were removed by filtration, and the solvent was evaporated under reduced pressure, to obtain 22 mg of compound 114, with a yield of 82.3%. MS: m/z 891 [M+H]+.
Ethyl 4-oxocyclohexane-1-formate (200 mg, 1.176 mmol) and tert-butyl 2,6-diazaspiro[3.4]octan-6-formate (274 mg, 1.294 mmol) were dissolved in DCM/MeOH (10:1, 5 ml), to which was added one drop of acetic acid, and then the mixture was stirred and reacted at room temperature for 1 h. Then, sodium triacetoxyborohydride (498 mg, 2.353 mmol) was added, and then the mixture was stirred for 3 h. The reaction solution was sequentially washed with hydrochloric acid (0.5 N, 10 ml) and saturated brine. Then, the organic phase was separated, dried with anhydrous sodium sulfate, and concentrated to obtain 400 mg of crude product (158-3), with a yield of 92.8%. MS: m/z 367 [M+H]+.
158-3 (400 mg, 1.092 mmol) was dissolved in a solution of HCl in 1,4-dioxane (4 M, 10 ml), and then the mixture was allowed to react at room temperature for 1 h. The reaction solution was concentrated to obtain 315 mg of product (158-4), with a yield of 95.45%. MS: m/z 267 [M+H]+.
Intermediate tert-butyl (1-(5-((3-aminophenyl)thio)pyrazin-2-yl)-4-methylpyridin-4-yl)carbamate (2 g, 4.81 mmol), 7-bromohexanoic acid (838 mg, 4.01 mmol), HATU (1.83 g, 4.816 mmol) and N,N-diisopropylethylamine (1.04 g, 8.06 mmol) were dissolved in dichloromethane (20 m1); and then the mixture was reacted under stirring at room temperature for 2 h. The reaction solution was successively washed once with water, saturated NaHCO3 aqueous solution, and saturated brine, and then the reaction solution was separated. The organic layer was dried over anhydrous Na2SO4, and then concentrated, to obtain 2.3 g of product (158-5), with a yield of 79.3%. MS: m/z 606 [M+H]+; 608 [M+2+H]+.
158-4 (120 mg, 0.397 mmol), 158-5 (264 mg, 0.436 mmol), and K2CO3 (164 mg, 1.192 mmol) were added into acetonitrile (5 ml), and then the mixture was stirred overnight at 60° C. After cooling to room temperature, the reaction solution was poured into water, extracted with ethyl acetate. The organic phase was separated, successively washed with hydrochloric acid (1N) and saturated brine, dried with anhydrous sodium sulfate, and concentrated. The residue was purified by column chromatography to obtain 77 mg of product (intermediate for 158-6 and isomer 159), with a yield of 24.5%. MS: m/z 792 [M+H]+.
158-6 (77 mg, 0.101 mmol) and lithium hydroxide monohydrate (17 mg, 0.404 mmol) were added into a mixed solvent of tetrahydrofuran (4 ml), methanol (1 ml) and water (2 ml), and then the mixture was allowed to react overnight at room temperature. The pH of the reaction solution was adjusted to 3-4 with hydrochloric acid (0.5 N). The resultant solution was extracted with ethyl acetate, washed with saturated brine, dried with anhydrous sodium sulfate, and concentrated, to obtain 70 mg of crude product (158-7), with a yield of 94.2%. MS: m/z 764 [M+H]+.
Intermediate 158-7 (70 mg, 0.0917 mmol), 3-(5-(aminomethyl)-1-oxoisoindol-2-yl)piperidin-2,6-dionehydrochloride (28 mg, 0.0917 mmol), HATU (42 mg, 0.11 mmol), and N,N-diisopropylethylamine (23 mg, 0.185 mmol) were dissolved in N,N-dimethylacetamide (1 ml), and then the mixture was stirred overnight at room temperature. Purification by pre-TLC afforded 30 mg of product (158-8), with a yield of 32.13%. MS: m/z 460.7 ((M−100)/2+H+).
158-8 (30 mg, 0.029 mmol) was dissolved in dichloromethane (3 mL), to which was added trifluoroacetic acid (1 ml), and then the mixture was stirred 1 h at room temperature. The reaction solution was rotatory evaporated, and then the residue was dissolved in dichloromethane, followed by evaporation, that was repeated twice. To the residue, was added anhydrous methanol (4 ml), and the pH was adjusted to 7-8 with NaHCO3. The resultant solution was filtered and concentrated, to obtain 25 mg of product (158), with a yield of 92.6%. MS: m/z 460.7 (M/2+H+). 1H NMR (400 MHz, DMSO-d6) δ 11.00 (s, 1H), 10.05 (s, 1H), 8.62-8.02 (m, 5H), 7.65 (s, 1H), 7.57 (s, 1H), 7.44 (d, J=13.6 Hz, 2H), 7.34 (d, J=8.2 Hz, 1H), 7.25-7.17 (m, 1H), 6.88 (d, J=7.8 Hz, 1H), 5.35-5.05 (m, 1H), 4.89-4.69 (m, 1H), 4.57 (d, J=17.7 Hz, 1H), 4.46-4.39 (m, 1H), 4.35 (d, J=5.8 Hz, 2H), 4.19 (d, J=6.8 Hz, 2H), 4.09-3.81 (m, 6H), 3.08-2.95 (m, 3H), 2.88 (s, 1H), 2.31-2.22 (m, 4H), 2.21-2.14 (m, 1H), 2.04-1.95 (m, 2H), 1.87 (d, J=9.2 Hz, 2H), 1.75 (dd, J=10.4, 5.0 Hz, 7H), 1.52 (d, J=6.9 Hz, 4H), 1.37 (s, 8H), 1.25 (d, J=5.9 Hz, 6H).
4-(4-oxopiperidin-1-yl)benzoic acid (intermediate 264-1) (658 mg, 3 mmol) and tert-butyl (1-(5-((3-aminophenyl)thio)pyrazin-2-yl)-4-methylpyridin-4-yl)carbamate (1.25 g, 3 mmol) were dissolved in 30 mL of acetonitrile, to which were added N-methylimidazole (739 mg, 9 mmol) and TCFH (1.09 g, 3.9 mmol), and then the mixture was stirred 3 h at room temperature. After the reaction was completed, the solvent was removed by evaporation under reduced pressure, and then 300 mL of dichloromethane was added, followed by washing twice with saturated brine. The organic phase was evaporated under reduced pressure to remove the solvent, and the residue was purified by column chromatography (mobile phase: PE:EA=1:1) to obtain 1.57 g of intermediate 264-2, with a yield of 85%. MS: m/z 617 [M+H]+.
Tert-butyl (4-methyl-1-(5-((3-(4-(4-oxopiperidin-1-yl)benzamido)phenyl)thio)pyrazin-2-yl)piperidin-4-yl)carbamate (264-2) (1.54 g, 2.5 mmol) and ethyl 6-(1,2,3,6-tetrahydropyridin-4-yl)pyridazin-3-carboxylate (0.54 g, 2.5 mmol) were dissolved in a mixed solvent of isopropanol and dichloromethane (v:v=1:1). The pH value of the solution was adjusted to about 5 with acetic acid, to which was added sodium cyanoborohydride (0.39 g, 6.25 mmol), and then the solution was stirred at room temperature for 12 h. Once completion of the reaction, dichloromethane was added, and after standing, the organic layer was separated. The water layer was extracted with dichloromethane. The organic layers were combined, dried with anhydrous sodium sulfate, and concentrated. The residue was subjected to column chromatography (mobile phase DCM:MeOH=20:1), to obtain 1.5 g of intermediate 264-3, with a yield of 72%. MS: m/z 834 [M+H]+.
Ethyl (6-(1-(1-(4-((3-((5-(4-((tert-butoxycarbonyl)amino)-4-methylpyridin-1-yl)pyrazin-2-yl)thio)phenyl)carbamoyl)phenyl)piperidin-4-yl)-1,2,3,6-tetrahydropyridin-4-yl)pyridazin-3-carboxylate (intermediate 264-3) (1.5 g, 1.8 mmol) was dissolved in a mixed solvent of tetrahydrofuran, methanol and water (v:v:v=4:1:1), to which was added lithium hydroxide monohydrate (1.5 g, 36 mmol), and the mixture was stirred at room temperature for 3 h. After completion of the reaction, the pH of the reaction solution was adjusted to about 4 with 0.5 N of hydrochloric acid, and white solid precipitated, which was filtered to remove solvent. Then, the solid was dried, to obtain 1.25 g of intermediate 264-4, with a yield of 86%. MS: m/z 806 [M+H]+.
6-(1-(1-(4-((3-((5-(4-((tert-butoxycarbonyl)amino)-4-methylpyridin-1-yl)pyrazin-2-yl)thio)phenyl)carbamoyl)phenyl)piperidin-4-yl)-1,2,3,6-tetrahydropyridin-4-yl)pyridazin-3-carboxylic acid (intermediate 264-4) (1.21 g, 1.5 mmol) and 3-(5-(aminomethyl)-1-oxoisoindol-2-yl)piperidin-2,6-dione (0.41 g, 1.5 mmol) were dissolved in 10 mL of DMA, to which were added HATU (0.86 g, 2.25 mmol) and DIPEA (0.39 g, 3 mmol), and then the mixture was stirred at room temperature for 12 h. After completion of the reaction, purification by column chromatography (mobile phase DCM:MeOH=20:1) afforded 1.15 g of intermediate 264-5, with a yield of 72%. MS: m/z 1061 [M+H]+.
Tert-butyl (1-(5-((3-(4-(4-(4-(6-((2-(2,6-dioxopiperidin-3-yl)-1-oxoisoindol-5-yl)methyl)carbamoyl)pyridazin-3-yl)-3,6-dihydropyridin-1(2H)-yl)piperidin-1-yl)benzamido)phenyl)thio)pyrazin-2-yl)-4-methylpyridin-4-yl)carbamate (intermediate 264-5) (600 mg, 0.57 mmol) was dissolved in 800 mL of DCM, and under stirring, dry HCl gas was introduced, and then the mixture was stirred for 1 h. After the reaction was completed, the solvent was removed by evaporation under reduced pressure, to obtain 520 mg of compound 264 with a yield of 95.8%. MS: m/z 962 [M+H]+.
1H NMR (400 MHz, DMSO-d6) δ 11.45 (s, 1H), 10.98 (s, 1H), 10.11-9.90 (m, 2H), 8.49-8.15 (m, 5H), 7.98-7.47 (m, 7H), 7.42-6.87 (m, 5H), 5.10 (dd, J=13.4, 5.1 Hz, 1H), 4.62 (d, J=6.3 Hz, 2H), 4.48-4.26 (m, 3H), 3.80 (s, 2H), 3.68 (d, J=11.3 Hz, 2H), 3.39 (s, 1H), 3.24 (s, 1H), 2.99 (s, 1H), 2.94-2.74 (m, 4H), 2.59 (d, J=17.0 Hz, 2H), 2.41-2.31 (m, 2H), 2.23 (s, 1H), 1.98 (s, 3H), 1.77 (d, J=19.0 Hz, 4H), 1.37 (s, 3H), 1.20 (d, J=22.9 Hz, 3H).
Tert-butyl (4-methyl-1-(5-((3-(4-(4-oxopiperidin-1-yl)benzamido)phenyl)thio)pyrazin-2-yl)piperidin-4-yl)carbamate (264-2) (1.54 g, 2.5 mmol) and methyl 1′,2′,3′,6′-tetrahydro-[3,4′-bipyridine]-6-carboxylate (0.55 g, 2.5 mmol) were dissolved in a mixed solvent of isopropanol and dichloromethane (v:v=1:1). The pH value of the solution was adjusted to about 5 with acetic acid, to which was added sodium cyanoborohydride (0.39 g, 6.25 mmol), and then the solution was stirred at room temperature for 12 h. Once completion of the reaction, dichloromethane was added, and after standing, the organic layer was separated. The water layer was extracted with dichloromethane. The organic layers were combined, dried with anhydrous sodium sulfate, and concentrated. The residue was subjected to column chromatography (mobile phase DCM:MeOH=20:1), to obtain 1.38 g of intermediate 312-1, with a yield of 67%. MS: m/z 819 [M+H]+.
Methyl 1′-(1-(4-((3-((5-(4-((tert-butoxycarbonyl)amino)-4-methylpyridin-1-yl)pyrazin-2-yl)thio)phenyl)carbamoyl)phenyl)piperidin-4-yl)-1′,2′,3′,6′-tetrahydro-[3,4′-bipyridine]-6-carboxylate (312-1) (1.3 g, 1.6 mmol) was dissolved in a mixed solvent of tetrahydrofuran, methanol and water (v:v:v=4:1:1), to which was added lithium hydroxide monohydrate (1.3 g, 32 mmol), and the mixture was stirred at room temperature for 3 h. After completion of the reaction, the pH of the reaction solution was adjusted to about 4 with 0.5 N of hydrochloric acid, and then the solution was extracted with a mixed solvent of dichloromethane and methanol (v:v=10:1). The organic phase was dried with anhydrous Na2SO4, and then, concentrated under reduced pressure, to obtain 1.1 g of intermediate 312-2, with a yield of 85%. MS: m/z 805 [M+H]+.
1′-(1-(4-((3-((5-(4-((tert-butoxycarbonyl)amino)-4-methylpyridin-1-yl)pyrazin-2-yl)thio)phenyl)carbamoyl)phenyl)piperidin-4-yl)-1′,2′,3′,6′-tetrahydro-[3,4′-bipyridine]-6-carboxylic acid (intermediate 312-2) (1.05 g, 1.3 mmol) and 3-(5-(aminomethyl)-1-oxoisoindol-2-yl)piperidin-2,6-dione (0.36 g, 1.3 mmol) were dissolved in 10 mL of DMA, to which were added N-methylimidazole (320 mg, 3.9 mmol) and TCFH (477 mg, 1.7 mmol), and the mixture was stirred at room temperature for 3 h. After the reaction was completed, the reaction solution was dropped into water, and solid was precipitated, which was filtered. The obtained solid was purified by column chromatography (mobile phase DCM:MeOH=10:1) to obtain 1.45 g of intermediate 312-3, with a yield of 81%. MS: m/z 1060 [M+H]+.
Tert-butyl (1-(5-((3-(4-(4-(6-((2-(2,6-dioxopiperidin-3-yl)-1-oxoisoindol-5-yl)methyl) carbamoyl)-3′,6′-dihydro-[3,4′-bipyridine]-1′(2′H)-yl)piperidin-1-yl)benzamido)phenyl)thio) pyrazin-2-yl)-4-methylpyridin-4-yl)carbamate (intermediate 312-3) (600 mg, 0.57 mmol) was dissolved in 800 mL of DCM, and under stirring, dry HCl gas was introduced, and then the mixture was stirred for 1 h. After the reaction was completed, the solvent was removed by evaporation under reduced pressure, to obtain 510 mg of compound 312, with a yield of 94%. MS: m/z 960 [M+H]+.
1H NMR (400 MHz, DMSO-d6) δ 11.35 (s, 1H), 10.96 (s, 1H), 10.15-9.95 (m, 2H), 8.46-8.14 (m, 6H), 7.96-7.45 (m, 7H), 7.41-6.89 (m, 5H), 5.10 (dd, J=13.4, 5.1 Hz, 1H), 4.62 (d, J=6.3 Hz, 2H), 4.48-4.26 (m, 3H), 3.80 (s, 2H), 3.68 (d, J=11.3 Hz, 2H), 3.39 (s, 1H), 3.24 (s, 1H), 2.99 (s, 1H), 2.94-2.74 (m, 4H), 2.59 (d, J=17.0 Hz, 2H), 2.41-2.31 (m, 2H), 2.23 (s, 1H), 1.98 (s, 3H), 1.77 (d, J=19.0 Hz, 4H), 1.37 (s, 3H), 1.20 (d, J=22.9 Hz, 3H).
Intermediates 295-1 (930 mg, 5 mmol), 295-2 (787 mg, 5.5 mmol), and DIPEA (1290 mg, 10 mmol) were successively added to a single-necked flask containing DMSO (10 mL), and then the mixture was stirred at 80° C. for 12 h. After completion of the reaction, the solution was cooled and then added into water dropwise. The resultant solution was extracted with ethyl acetate (10 mL×3). The organic phase was washed with saturated brine, dried with anhydrous sodium sulfate, and rotatory evaporated, to obtain 1 g of intermediate compound 295-3.
The intermediate compound obtained in the previous step was dissolved in THF/MeOH/H2O (12 mL/3 mL/3 mL), to which was added LiOH (840 mg, 20 mmol), and then the mixture was stirred at room temperature for 1 h. The reaction was detected by TLC. After completion of the reaction, the pH value of the solution was adjusted to 2 with HCl (1N). The resultant solution was extracted with ethyl acetate. The organic phase was dried with anhydrous sodium sulfate, and then rotatory evaporated, to obtain 920 mg of intermediate compound 295-4.
The intermediate obtained in the previous step was dissolved in THF (10 mL), to which was added HCl (3N, 10 mL), and then the mixture was stirred at 60° C. for 12 h. The reaction solution was extracted with ethyl acetate. Separation by column chromatography provided 820 mg of intermediate compound 295-5, with a three-step yield of 69.2%. MS: m/z 238 [M+H]+.
HWH-1 (1 g, 2.4 mmol), 295-5 (569 mg, 2.4 mmol), and 1-methylimidazole (590 mg, 7.2 mmol) were added into acetonitrile (10 mL), to which was added TCFH (875 mg, 3.12 mmol), and then the mixture was stirred at room temperature for 2 h. The reaction solution was rotatory evaporated to remove the solvent. The residue was separated by column chromatography, to obtain 1.4 g of intermediate 295-6, with a yield of 92%. MS: m/z 635 [M+H]+.
Intermediate 295-6 (1.4 g, 2.2 mmol) and methyl 1′,2′,3′,6′-tetrahydro-[3,4′-bipyridine]-6-carboxylate hydrochloride (456 mg, 1.8 mmol) were added into a mixed solvent of isopropanol (10 mL) and dichloromethane (10 mL), and then the pH value of the reaction solution was adjusted to 7-8 with DIPEA, and then adjusted to 5-6 with AcOH. Finally, sodium cyanoborohydride (227 mg, 3.6 mmol) was added to the reaction solution, and then the solution was stirred at room temperature. TLC was used to detect the progress of the reaction. After completion of the reaction, to the solution, was added 20 mL of saturated NaHCO3 aqueous solution, and then extracted with dichloromethane. Separation by column chromatography afforded 840 mg of intermediate compound 295-7, with a yield of 56%; MS: m/z 837 [M+H]+.
Intermediate 295-7 (840 mg, 1 mmol) was dissolved in THF/MeOH/H2O (8 mL/2 mL/2 mL), to which was added lithium hydroxide monohydrate (168 mg, 4 mmol), and then the mixture was stirred at room temperature for 1 h. The pH value of the solution was adjusted to 2 with HCl (1N). The reaction solution was extracted with DCM/MeOH (10/1). The organic phase was dried with anhydrous sodium sulfate, and rotatory evaporated to obtain 863 mg of intermediate 295-8 as crude product, with a yield of 100%. MS: m/z 823 [M+H]+.
Intermediate 295-8 (863 mg, 1 mmol), TC (310 mg, 1 mmol), and 1-methylimidazole (246 mg, 3 mmol) were dissolved in DMAc (10 mL), to which was added TCFH (364 mg, 1.3 mmol), and then the mixture was stirred for 1 h. The reaction solution was added to water dropwise, and then extracted with dichloromethane. Purification by TLC afforded 600 mg of intermediate 295-9, with a yield of 56%. MS: m/z 539 [1/2M+H]+.
295-9 (600 mg) was dissolved in dichloromethane (20 mL), to which was continuously introduced HCl gas. The reaction was monitored by TLC. After completion of the reaction, the reaction solution was rotatory evaporated, and the residue was beaten in methyl tert-butyl ether, followed by filtration, to obtain 600 mg of compound 295, with a yield of 100%, MS: m/z 489 [1/2M+H]+. 1H NMR (400 MHz, DMSO-d6) δ 10.98 (s, 1H), 10.19 (s, 1H), 9.49 (s, 1H), 8.81 (d, J=2.0 Hz, 1H), 8.39 (s, 1H), 8.24 (s, 2H), 8.20 (s, 1H), 8.16-8.10 (m, 1H), 8.07 (d, J=8.1 Hz, 1H), 7.78 (d, J=12.8 Hz, 3H), 7.68 (d, J=7.8 Hz, 2H), 7.54 (s, 1H), 7.47 (d, J=8.0 Hz, 1H), 7.30 (t, J=8.0 Hz, 1H), 7.17 (t, J=8.8 Hz, 1H), 6.99 (d, J=7.9 Hz, 1H), 6.52 (s, 1H), 5.10 (dd, J=13.4, 5.1 Hz, 1H), 4.62 (d, J=6.3 Hz, 2H), 4.48-4.26 (m, 3H), 3.80 (s, 2H), 3.68 (d, J=11.3 Hz, 2H), 3.39 (s, 1H), 3.24 (s, 1H), 2.99 (s, 1H), 2.94-2.74 (m, 4H), 2.59 (d, J=17.0 Hz, 2H), 2.41-2.31 (m, 2H), 2.23 (s, 1H), 1.98 (s, 3H), 1.77 (d, J=19.0 Hz, 4H), 1.37 (s, 3H), 1.20 (d, J=22.9 Hz, 3H).
To a solution of compounds 344-1 (400 mg, 1.89 mmol, 1.0 eq) and 344-2 (706 mg, 3.79 mmol, 2.0 eq) in methanol, were added HOAC (two drops) and NaBH3CN (238 mg, 3.79 mmol, 2.0 eq). The mixture was stirred at room temperature until the reaction was completed. After completion of the reaction, the reaction solution was quenched with 1N HCl, adjusted to pH 7-8 with sodium carbonate, and then extracted with EA (2*100 ml). The organic layer was dried and rotatory evaporated. The residue was purified by silica gel column chromatography to obtain 344-3 (600 mg, yield 83.03%). MS: m/z 383.2 [M+H]+.
To a solution of compound 344-3 (600 mg, 1.57 mmol, 1.0 eq) in EtOH (8 mL), were added KOAC (462 mg, 4.72 mmol, 3.0 eq) and Pd(dppf)Cl2 (58 mg, 0.079 mmol, 0.05 eq). After mixed and degassed, the mixture was allowed to react at about 80° C. under CO atmosphere. After the reaction was completed, the solid was filtered out, and the solvent was removed by rotatory evaporation. The residue was purified by silica gel column chromatography to obtain 344-4 (530 mg, yield 89.9%). MS: m/z 375.2 [M+H]+.
Compound 344-4 (530 mg, 1.41 mmol, 1.0 eq) was added to a solution of dioxane/HCl (4 M, 6 mL), and the resulting mixture was stirred at room temperature until the reaction was completed. The solvent was evaporated to obtain the target product 344-5 (437 mg, crude, yield 100%), which was directly used in the next step. MS: m/z 275.3 [M+H]+.
To a solution of compounds 344-5 (437 mg, 1.41 mmol, 1.0 eq) and 344-6 (230 mg, 1.55 mmol, 1.1 eq) in DMA (10 mL), were added K2CO3 (584 mg, 4.23 mmol, 3.0 eq) and KI (468 mg, 2.82 mmol, 2.0 eq). The mixture was stirred at about 120° C. until the reaction was completed. The mixture was poured into saturated brine (50 mL) and extracted with EA (2*50 mL). The organic layer was dried and rotatory evaporated. The residue was purified by silica gel column chromatography to obtain 344-7 (350 mg, yield 64.4%). MS: m/z 387.3 [M+H]+.
To a solution of compound 344-7 (350 mg, 0.91 mmol, 1.0 eq) in MeOH (3 mL), THF (3 mL), and H2O (3 mL), was added LiOH (109 mg, 4.55 mmol, 5.0 eq). The obtained mixture was stirred at room temperature until the reaction was completed, and then the solvent was concentrated. The residue was diluted with water, and the pH value was adjusted to 5-6 with 1 N hydrochloric acid. The precipitated solid was filtered and dried, to obtain 344-8 (300 mg, yield 92.4%). MS: m/z 359.1 [M+H]+.
To a solution of compounds 344-8 (280 mg, 0.78 mmol, 1.0 eq) and HWH-1 (324 mg, 0.78 mmol, 1.0 eq) in ACN (10 mL), were added N-methylimidazole (192 mg, 2.34 mmol, 3.0 eq) and TCFH (262 mg, 0.94 mmol, 1.2 eq). The mixture was stirred at room temperature until the reaction was completed, and then the solvent was evaporated. The residue was purified by silica gel column chromatography to obtain 344-10 (85 mg, yield 14.4%). MS: m/z 756.5 [M+H]+.
To a solution of compound 344-10 (85 mg, 0.11 mmol, 1.0 eq) in EtOH (5 mL), were added KOAC (33 mg, 0.33 mmol, 3.0 eq) and Pd(dppf)Cl2 (24 mg, 0.033 mmol, 0.3 eq). After degassed, the mixture was stirred and reacted at 70° C. under CO atmosphere. After completion of the reaction, the reaction solution was concentrated. The residue was purified by silica gel column chromatography to obtain 344-11 (70 mg, yield 78.5%). MS: m/z 794.6 [M+H]+.
To a solution of compound 344-11 (70 mg, 0.088 mmol, 1.0 eq) in a mixed solvent of MeOH (2 mL)/THF (2 mL)/H2O (2 mL), was added LiOH (21 mg, 0.88 mmol, 10.0 eq). The mixture was stirred at room temperature. After completion of the reaction, the solvent was evaporated, and the residue was diluted with water. The pH value of the obtained mixture was adjusted to 5-6 using 1N HCl. The precipitated solid was filtered and dried to obtain 344-12 (70 mg, crude, yield ca. 100%). MS: m/z 766.5 [M+H]+.
To a solution of compounds 344-12 (70 mg, 0.091 mmol, 1.0 eq), 344-13 (30 mg, 0.11 mmol, 1.2 eq) and HATU (52 mg, 0.14 mmol, 1.5 eq) in DMA (3 mL), was added DMAP (17 mg, 0.14 mmol, 1.5 eq). The obtained mixture was stirred at room temperature until the reaction was completed. The crude product obtained after conventional treatment was purified by reversed-phase column (acetonitrile/water), to obtain 344-14 (75 mg, yield 80.6%). MS: m/z 1021.3 [M+H]+.
Compound 344-14 (75 mg, 0.073 mmol, 1.0 eq) was added into HCl/EA (3 M, 5 mL), and the resultant mixture was stirred at room temperature until the reaction was completed. The crude product was purified by reversed-phase column (acetonitrile/0.1% HCl), to obtain compound 344 (62.5 mg, yield 92.4%). MS: m/z 921.3 [M+H]+.
1H NMR (400 MHz, DMSO-d6): δ 11.93 (s, 1H), 10.97 (s, 1H), 10.27 (s, 1H), 9.59 (t, J=6.2 Hz, 1H), 8.39 (d, J=1.2 Hz, 1H), 8.20-8.17 (m, 4H), 7.97-7.95 (m, 1H), 7.84-7.77 (m, 3H), 7.69 (d, J=8.0 Hz, 2H), 7.54-7.41 (m, 4H), 7.30 (t, J=8.0 Hz, 1H), 6.98 (d, J=8.0 Hz, 1H), 5.10-5.07 (m, 1H), 4.69-4.61 (m, 4H), 4.45-4.41 (m, 1H), 4.32-4.27 (m, 1H), 4.17-4.08 (m, 2H), 3.63-3.56 (m, 11H), 3.24-3.21 (m, 2H), 2.95-2.86 (m, 1H), 2.67-2.61 (m, 2H), 2.39-2.32 (m, 1H), 2.00-1.97 (m, 1H), 1.78-1.74 (m, 4H), 1.37 (s, 3H).
To a solution of compounds 343-1 (1.00 g, 6.06 mmol, 1.0 eq) and 343-2 (1.71 g, 6.06 mmol, 1.0 eq) in dioxane (20 mL) and water (5 mL), were added K2CO3 (2.51 g, 18.18 mmol, 3.0 eq) and Pd(dppf)Cl2 (222 mg, 0.30 mmol, 0.05 eq). The mixture was allowed to react at about 100° C. After completion of the reaction, the mixture was diluted with saturated brine (100 mL), and then extracted with ethyl acetate (2*100 mL). The organic layer was dried and rotary evaporated, to obtain crude product 343-3 (700 mg, yield 41.9%). MS (M−2): m/z 275.0.
Compound 343-3 (600 mg, 2.16 mmol, 1.0 eq) was dissolved in THE (10 mL), to which was added oxalyl chloride (1.37 g, 10.83 mmol, 5.0 eq) dropwise, together with catalytic amount of DMF. The mixture was reacted at 40° C. until the reaction was completed. The reaction solution was concentrated, to obtain the crude product 343-4 (640 mg, yield 100%), which was directly used in the next step.
To a solution of compounds 343-4 (640 mg, 2.16 mmol, 1.0 eq) and 343-5 (720 mg, 1.73 mmol, 0.8 eq) in dichloromethane (10 mL), was added TEA (873 mg, 8.64 mmol, 4.0 eq), and the mixture was stirred at room temperature until the reaction was completed. The mixture was poured into saturated brine (50 mL) and extracted with EA (2*50 mL). The organic layer was dried and rotatory evaporated, and then the residue was purified by silica gel column chromatography (EA/PE=3/1), to obtain 343-6 (960 mg, yield 82.1%). MS: m/z 674.5 [M+H]+.
To a solution of compounds 343-6 (150 mg, 0.22 mmol, 1.0 eq) and 343-7 (98 mg, 0.44 mmol, 2.0 eq) in dioxane (5 mL), were added Cs2CO3 (215 mg, 0.66 mmol, 3.0 eq) and XPhos Pd G2 (22 mg, 0.022 mmol, 0.1 eq). The mixture was stirred at 100° C. until the reaction was completed. The mixture was diluted with ethyl acetate, and insoluble substances were filtered out. After the solvent was evaporated, the residue was purified by reversed-phase column chromatography (acetonitrile/water), to obtain 343-8 (50 mg, yield 27.5%). MS: m/z 815.4 [M+H]+.
To a solution of compound 343-8 (50 mg, 0.061 mmol, 1.0 eq) in a mixed solvent of MeOH (2 mL)/THF (2 mL)/H2O (2 mL), was added LiOH (15 mg, 0.61 mmol, 10.0 eq). The mixture was stirred at room temperature. After completion of the reaction, the solvent was evaporated, and the residue was diluted with water. The pH value of the obtained mixture was adjusted to 5-6 using 1N HCl. The precipitated solid was filtered and dried to obtain the target compound 343-9 (50 mg, crude, yield ca. 100%).
To a solution of compounds 343-9 (50 mg, 0.062 mmol, 1.0 eq), 343-10 (20 mg, 0.074 mmol, 1.2 eq), and HATU (36 mg, 0.094 mmol, 1.5 eq) in DMA (2 mL), was added DMAP (12 mg, 0.094 mmol, 1.5 eq). The mixture was stirred at room temperature until the reaction was completed. Purification by reversed-phase column (acetonitrile/water) provided the target compound 343-11 (20 mg, yield 30.3%). MS: m/z 1056.3 [M+H]+.
Compound 343-11 (20 mg, 0.019 mmol, 1.0 eq) was added into HCl/EA (3M/L, 3 mL), and the resultant mixture was stirred at room temperature until the reaction was completed. The crude product was purified by reversed-phase column (acetonitrile/0.1% HCl), to obtain compound 343 (7.25 mg, yield 40.3%). MS: m/z 956.3 [M+H]+.
1H NMR (400 MHz, DMSO-d6): δ 10.97 (s, 1H), 10.29-10.20 (m, 1H), 9.19 (t, J=6.2 Hz, 1H), 8.41-8.37 (m, 2H), 8.20-8.15 (m, 4H), 8.09-7.92 (m, 3H), 7.83-7.69 (m, 6H), 7.59-7.53 (m, 2H), 7.51-7.47 (m, 1H), 7.39-7.32 (m, 2H), 7.30-7.22 (m, 1H), 7.19-6.99 (m, 1H), 5.12-5.07 (m, 1H), 4.59-4.58 (d, J=6.0 Hz, 2H), 4.45-4.41 (m, 1H), 4.37-4.21 (m, 1H), 4.08-4.03 (m, 2H), 3.43-3.35 (m, 10H), 2.94-2.86 (m, 2H), 2.67-2.56 (m, 2H), 2.39-2.32 (m, 1H), 2.02-1.95 (m, 3H), 1.82-1.74 (m, 4H), 1.38 (d, J=4.4 Hz, 3H), 1.29-1.98 (m, 4H).
Step 1: Synthesis of Intermediate ethyl 2-(4-(tert-butoxycarbonyl)piperazin-1-yl)pyrimidine-5-carboxylate (294-12)
To a solution of compound 294-10 (1.9 g, 10.0 mmol, 1.0 eq) and compound 294-11 (1.9 g, 10.0 mmol, 1.0 eq) in DMA (20 mL), was added diisopropylethylamine (2.6 g, 20.0 mmol, 2.0 eq). The obtained mixture was allowed to react at about 70° C. After completion of the reaction, the reaction solution was poured into water (100 mL). The precipitated solid was filtered, collected, and dried, to obtain the target product 294-12 (3.4 g, crude product, 10.0 mmol, yield ca. 100%). MS: m/z 337.1 [M+H]+.
Compound 294-12 (3.4 g, 10.0 mmol, 1.0 eq) was added into HCl/EA (35 mL, 10.5 eq., 3M), and the mixture was stirred at room temperature. After completion of the reaction, the solvent was evaporated, to obtain 294-13-hydrochloride (2.4 g, 8.82 mmol, yield 88.2%), which was directly used in the next step.
To a solution of compounds 294-13 (200 mg, 1.75 mmol, 1.0 eq) and 294-14 (414 mg, 1.75 mmol, 1.0 eq) in DCM (10 mL), was added NaBH(OAc)3 (740 mg, 3.51 mmol, 2.0 eq). The obtained mixture was stirred at about 40° C. until the reaction was completed. The reaction was quenched with 1N HCl (50 mL). After routine working-up, 294-15 (2.6 g, crude product) was obtained. MS: m/z 335.1 [M+H]+.
To a solution of compound 294-15 (30 mg, 0.09 mmol, 1.0 eq) and HWH-2 (42 mg, 0.09 mmol, 1.0 eq) in DMA (5 mL), were added HATU (41 mg, 0.11 mmol, 1.2 eq) and diisopropylethylamine (29 mg, 0.22 mmol, 2.5 eq), and the resultant mixture was allowed to react at room temperature. After completion of the reaction, the mixture was diluted with water (30 mL), and then extracted with EA (30 mL*2). The organic layer was washed with saturated brine (50 mL*3), dried with Na2SO4, and rotatory evaporated. The residue was purified by reversed-phase column, to obtain 294-16 (40 mg, yield 56.5%). MS: m/z 788.2 [M+H]+.
To a solution of compound 294-16 (40 mg, 0.05 mmol, 1.0 eq) in MeOH/THF/H2O (1 mL/1 mL/1 mL), was added LiOH (4.9 mg, 0.20 mmol, 4.0 eq), and the resultant mixture was stirred at room temperature. After completion of the reaction, the solvent was evaporated, and the residue was diluted with water. The pH value of the reaction solution was adjusted to 5 using 0.5 N HCl, and then extracted with EA (5 mL*2). The solvent was evaporated, to obtain the crude product 294-17 (20 mg, yield 51.8%), which was directly used in the next step. MS: m/z 760.3 [M+H]+.
To a solution of compound 294-17 (20 mg, 0.026 mmol, 1.0 eq) and TV (12 mg, 0.026 mmol, 1.0 eq) in DMA (2 mL), were added HATU (12 mg, 0.031 mmol, 1.2 eq) and diisopropylethylamine (8 mg, 0.066 mmol, 2.5 eq), and the obtained mixture was stirred at room temperature until the reaction was completed. The reaction was diluted with water (5 mL) and then extracted with EA (5 mL*2). The organic layer was subjected to the routine processing, and then the residue was purified by reversed-phase column (water), to obtain 294-18 (15 mg, yield 48.1%). MS: m/z 1186.5 [M+H]+.
Compound 294-18 (15 mg, 0.013 mmol, 1.0 eq) was added into HCl/EA (2 mL), and then the resultant mixture was stirred at room temperature until the reaction was completed. The solvent was evaporated. The crude product was purified by Prep-HPLC (0.1% HCl), to obtain compound 294 (9.88 mg, yield 69.6%). MS: m/z 1086.5 [M+H]+.
1H NMR (400 MHz, MeOD): δ 9.73 (d, J=2.4 Hz, 1H), 8.85-8.84 (m, 2H), 8.22-8.16 (m, 2H), 7.67-7.64 (m, 1H), 7.55-7.49 (m, 4H), 7.45 (d, J=8.0 Hz, 1H), 7.24 (t, J=8.0 Hz, 1H), 6.98 (d, J=7.2 Hz, 1H), 5.10-5.00 (m, 4H), 4.60 (t, J=8.4 Hz 1H), 4.46 (s, 1H), 4.33-4.18 (m, 3H), 4.00-3.80 (m, 5H), 3.64-3.61 (m, 2H), 3.48-3.38 (m, 4H), 3.24-2.93 (m, 5H), 2.77-2.61 (m, 4H), 2.58 (s, 4H), 2.25-2.20 (m, 1H), 2.03-1.78 (m, 6H), 1.52 (d, J=7.2 Hz, 3H), 1.31 (d, J=6.8 Hz, 6H), 1.11 (s, 9H).
Methyl 5-bromo-6-methylpyridine-2-formate (500 mg, 2.17 mmol), 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolane-2-yl)-1,2,3,6-tetrahydropyridin-1-formic acid-2-methylpropyl-2-yl ester (739 mg, 2.39 mmol), and K2CO3 (601 mg, 4.35 mmol) were successively added into a mixed solvent of 1,4-dioxane (9 mL) and water (0.6 mL), and then the system was purged with argon for three times. Under argon protection, [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium (159 mg, 0.22 mmol) was added to the reaction solution, and then the reaction system was heated to 80° C. and reacted for 16 h. The reaction solution was cooled to room temperature, and filtered over diatomaceous earth. The filtrate was concentrated under reduced pressure, and the residue was purified by column chromatography, to obtain 661 mg of product (intermediate 461-3), with a yield of 91.6%. MS: m/z 333.1 [M+H]+.
Intermediate 461-3 (660 mg, 1.98 mmol) was dissolved in 15 mL of dichloromethane, to which was added 15 mL of HCl-dioxane solution (4 mol/L), and then the mixture was allowed to react for 2 h at room temperature. The reaction solution was concentrated, and the residue was triturated with 10 mL of dichloromethane, followed by filtration. The filter cake was successively washed with 5 mL of dichloromethane and 5 mL of methyl tert-butyl ether, and then dried, to obtain 520 mg of product (intermediate 461-4), with a yield of 97.4%. MS: m/z 233.1 [M+H]+.
Methyl 3,4-difluorobenzoate (1.72 g, 10 mmol), 8-aza-1,4-dioxaspiro[4.5]decane (1.43 g, 10 mmol), and K2CO3 (1.81 g, 13 mmol) were successively added into 35 mL of dimethylsulfoxide, and then the reaction solution was heated to 65° C. and reacted for 16 h. The reaction solution was slowly poured into 100 mL of ice water after cooling to room temperature. The resultant solution was stirred for 1 h, and filtered. The solid was triturated with 40 mL mixed solvent of petroleum ether/ethyl acetate (10:1), and then filtered. The filter cake was dried, to obtain 2.73 g of product (intermediate 461-7), with a yield of 92.4%. MS: m/z 296.1 [M+H]+.
Intermediate 461-7 (2.73 g, 9.24 mmol) and lithium hydroxide monohydrate (1.94 g, 46.22 mmol) were successively added into a mixed solvent of tetrahydrofuran (50 mL), methanol (25 mL), and water (25 mL), and then the reaction system was heated to 40° C. and reacted for 4 h. The pH value of the reaction system was adjusted to 7 with 1N HCl aqueous solution. The organic solvent in the system was concentrated under reduced pressure, and then the pH vale of the reaction system was adjusted to 2-3 with 1N HCl aqueous solution, to which was added 25 mL of water. The reaction solution was stirred for 0.5 h, and filtered. The solid was dried to obtain 2.4 g of product (intermediate 461-8), with a yield of 92.3%. MS: m/z 282.1 [M+H]+.
Intermediate 461-8 (2.4 g, 8.53 mmol) was dispersed in 50 mL of tetrahydrofuran, to which was added 50 mL of HCl aqueous solution (1.5 N), and then the system was heated to 70° C. and reacted for 16 h. The reaction solution was cooled to room temperature, and the pH value of the system was adjusted to 4 with saturated NaHCO3 aqueous solution. The reaction solution was concentrated under reduced pressure to remove organic solvents, followed by adding 50 mL of water. The resultant solution was stirred for 0.5 h, and filtered. The filter cake was washed with 10 mL of water, and dried, to obtain 1.87 g of product (intermediate 461-9), with a yield of 92.4%. MS: m/z 238.1 [M+H]+.
Intermediate 461-9 (1.87 g, 7.88 mmol), {[(3S,4S)-8-{5-[(3-aminophenyl)thio]pyrazin-2-yl}-3-methyl-8-aza-2-oxaspiro[4.5]decan-4-yl]amino}formic acid-2-methylpropyl-2-yl ester (3.53 g, 7.49 mmol), HATU (3.13 g, 8.24 mmol), and N,N-diisopropylethylamine (1.94 g, 14.98 mmol) were successively added into 40 mL of dichloromethane, and then the mixture was allowed to react at room temperature for 16 h. The reaction solution was diluted with 60 mL of dichloromethane, and then washed sequentially with 50 mL of water, 50 mL of 1N HCl aqueous solution, 50 mL of saturated NaHCO3 aqueous solution, and 50 mL of saturated brine. The organic layer was dried with anhydrous sodium sulfate, filtered, and then concentrated under reduced pressure. The residue was purified by column chromatography to obtain 3.61 g of product (intermediate 461-11), with a yield of 69.8%. MS: m/z 691.1 [M+H]+.
Intermediate 461-11 (500 mg, 0.72 mmol) and intermediate 461-4 (233 mg, 0.87 mmol) were successively added into a mixed solvent of dichloromethane (10 mL) and isopropanol (10 mL), and then the pH value of the system was adjusted to 7-8 with N,N-diisopropylethylamine. Subsequently, the pH was adjusted to 6 with acetic acid, followed by addition of sodium cyanodorohydride (91 mg, 1.45 mmol). The mixture was allowed to react at room temperature for 16 h. The reaction solution was quenched with 20 mL of saturated NaHCO3 aqueous solution, and extracted with 50 mL of dichloromethane. The organic layer was dried with anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by column chromatography to obtain 360 mg of product (intermediate 461-12), with a yield of 54.8%. MS: m/z 907.3 [M+H]+.
Intermediate 461-12 (360 mg, 0.40 mmol) and lithium hydroxide monohydrate (166 mg, 3.97 mmol) were successively added into a mixed solvent of tetrahydrofuran (4 mL), methanol (2 mL), and water (2 mL), and then the mixture was reacted at room temperature for 1 h. The pH value of the reaction system was adjusted to 4 with 1N HCl aqueous solution, and extracted with 30 mL of dichloromethane. The organic layer was dried with anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to obtain 342 mg of product (intermediate 461-13), with a yield of 96.5%. MS: m/z 893.2 [M+H]+.
Intermediate 461-13 (342 mg, 0.38 mmol), 3-[5-(aminomethyl)-1-oxo-2,3-dihydro-1H-isoindol-2-yl]hexahydropyridine-2,6-dione (105 mg, 0.38 mmol), HATU (175 mg, 0.46 mmol), and N,N-diisopropylethylamine (124 mg, 0.96 mmol) were successively added into 4 mL of N,N-dimethylacetamide, and then the mixture was allowed to react at room temperature for 16 h. The reaction solution was slowly added into 40 mL of water dropwise, and filtered. The solid was purified by column chromatography to obtain 230 mg of product (intermediate 461-14) with a yield of 52.3%. MS: m/z 574.8 [M/2+H]+.
Intermediate 461-14 (230 mg, 0.20 mmol) was dissolved in 25 mL of dichloromethane, to which was continuously introduced dry HCl gas at room temperature, and TLC indicated completion of the reaction. The reaction solution was concentrated under reduced pressure. The residue was triturated with 25 mL of dichloromethane, and filtered. The filter cake was sequentially washed with 5 mL of dichloromethane and 5 mL of methyl tert-butyl ether. The solid was dried to obtain 220 mg of product (compound 461), with a yield of 98.0%. MS: m/z 524.7 [M/2+H]+.
1H NMR (400 MHz, DMSO-d6) δ 11.81 (s, 1H), 10.99 (s, 1H), 10.27 (s, 1H), 9.49-9.42 (m, 1H), 8.41-8.29 (m, 4H), 8.18 (d, J=1.4 Hz, 1H), 7.94 (d, J=7.9 Hz, 1H), 7.83-7.66 (m, 6H), 7.54 (s, 1H), 7.47 (d, J=7.6 Hz, 1H), 7.29 (t, J=8.0 Hz, 1H), 7.17 (t, J=8.7 Hz, 1H), 7.00-6.95 (m, 1H), 5.79 (s, 1H), 5.10 (dd, J=13.3, 5.1 Hz, 1H), 4.62 (d, J=6.4 Hz, 2H), 4.47-4.26 (m, 2H), 4.26-4.11 (m, 3H), 3.96-3.85 (m, 3H), 3.77-3.61 (m, 4H), 3.49 (s, 1H), 3.34 (t, J=5.6 Hz, 1H), 3.28-3.17 (m, 1H), 3.12-2.98 (m, 4H), 2.96-2.78 (m, 3H), 2.66-2.54 (m, 4H), 2.44-2.23 (m, 3H), 2.06-1.91 (m, 3H), 1.86-1.75 (m, 2H), 1.70-1.56 (m, 2H), 1.24 (d, J=6.5 Hz, 3H).
Step 1: Synthesis of Compound intermediate 4-[6-(ethoxycarbonyl)-1,2-diazacyclohexane-3-yl]-1,2,3,6-tetrahydropyridin-l-formic acid-2-methylpropyl-2-yl ester (519-3)
Ethyl 6-bromo-1,2-diazacyclohexane-3-formate (20.0 g, 0.11 mol), 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolane-2-yl)-1,2,3,6-tetrahydropyridin-1-formic acid-2-methylpropyl-2-yl ester (36.4 g, 0.12 mol), and Na2CO3 (22.8 g, 0.21 mol) were added into a mixed solvent of 1,4-dioxane (200 mL) and water (13 mL), and then the system was purged with argon three times, followed by addition of [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium (7.8 g, 0.01 mmol) under argon protection. The reaction system was heated to 100° C. and reacted for 12 h, and then the reaction solution was cooled to room temperature, and filtered over diatomaceous earth. The filtrate was concentrated under reduced pressure. The residue was purified by column chromatography to provide 18.4 g of the product (intermediate 519-3), with a yield of 63.7%. MS: m/z 334.2 [M+H]+.
Intermediate 519-3 (18.4 g, 0.05 mol) was dissolved in 60 mL of dichloromethane, and then added into 100 mL of HCl-dioxane solution (4 mol/L). The mixture was allowed to react at room temperature for 3 h. The reaction solution was concentrated, and the residue was triturated with 50 mL of dichloromethane and filtered. The filter cake was sequentially rinsed once with 20 mL of dichloromethane and 20 mL of methyl tert-butyl ether, and then dried, to obtain 14.5 g of product (intermediate 519-4), with a yield of 97.4%. MS: m/z 234.1 [M+H]+.
The procedures are the same as that of intermediate 461-11.
Intermediate 519-4 (222 mg, 0.87 mmol) and intermediate 519-5 (500 mg, 0.72 mmol) were successively added into a mixed solvent of dichloromethane (10 mL) and isopropanol (10 mL), and then the pH value of the system was adjusted to 7-8 with N,N-diisopropylethylamine. Subsequently, the pH was adjusted to 6 with acetic acid, followed by addition of sodium cyanodorohydride (91 mg, 1.45 mmol). The mixture was allowed to react at room temperature for 16 h. The reaction solution was quenched with 20 mL of saturated NaHCO3 aqueous solution, and extracted with 50 mL of dichloromethane. The organic layer was dried with anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by column chromatography to obtain 370 mg of product (intermediate 519-6), with a yield of 56.3%. MS: m/z 454.8 [M/2+H]+.
Intermediate 519-6 (370 mg, 0.41 mmol) and lithium hydroxide monohydrate (174 mg, 4.14 mmol) were successively added into a mixed solvent of tetrahydrofuran (4 mL), methanol (2 mL), and water (2 mL), and then the mixture was reacted at room temperature for 1 h. The pH value of the reaction system was adjusted to 5 with 1N HCl aqueous solution, and extracted with 30 mL of dichloromethane. The organic layer was dried with anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to obtain 347 mg of product (intermediate 519-7), with a yield of 96.8%. MS: m/z 440.8 [M/2+H]+.
Intermediate 519-7 (347 mg, 0.39 mmol), 3-[5-(aminomethyl)-1-oxo-2,3-dihydro-1H-isoindol-2-yl]hexahydropyridine-2,6-dione (134 mg, 0.43 mmol), HATU (180 mg, 0.47 mmol), and N,N-diisopropylethylamine (127 mg, 0.98 mmol) were successively added into 4 mL of N,N-dimethylacetamide, and then the mixture was allowed to react at room temperature for 16 h. The reaction solution was slowly added into 40 mL of water dropwise, and filtered. The solid was purified by column chromatography to obtain 200 mg of product (intermediate 519-8) with a yield of 44.7%. MS: m/z 568.4 [M/2+H]+.
Intermediate 519-8 (200 mg, 0.18 mmol) was dissolved in a mixed solvent of dichloromethane (20 mL) and methanol (1 mL), to which was continuously introduced dry HCl gas at room temperature, and TLC indicated completion of the reaction. The reaction solution was concentrated under reduced pressure. The residue was triturated with 20 mL of dichloromethane, and filtered. The filter cake was sequentially rinsed with 5 mL of dichloromethane and 5 mL of methyl tert-butyl ether. The solid was dried to obtain 180 mg of product (compound 519), with a yield of 92.2%. MS: m/z 518.3 [M/2+H]+.
1H NMR (400 MHz, DMSO-d6) δ 11.73 (s, 1H), 10.99 (s, 1H), 10.28 (s, 1H), 9.98 (t, J=6.3 Hz, 1H), 8.43-8.30 (m, 4H), 8.27-8.17 (m, 3H), 7.84-7.66 (m, 5H), 7.57 (s, 1H), 7.53-7.48 (m, 1H), 7.29 (t, J=7.9 Hz, 1H), 7.16 (t, J=8.7 Hz, 1H), 7.01-6.95 (m, 2H), 5.10 (dd, J=13.3, 5.1 Hz, 1H), 4.66 (d, J=6.3 Hz, 2H), 4.47-4.26 (m, 2H), 4.26-4.02 (m, 5H), 3.93 (d, J=9.0 Hz, 1H), 3.88-3.79 (m, 1H), 3.71-3.61 (m, 3H), 3.55-3.45 (m, 1H), 3.34 (t, J=5.6 Hz, 1H), 3.29-3.18 (m, 1H), 3.17-3.02 (m, 4H), 2.96-2.77 (m, 3H), 2.63-2.54 (m, 1H), 2.44-2.22 (m, 3H), 2.07-1.91 (m, 3H), 1.87-1.74 (m, 2H), 1.70-1.56 (m, 2H), 1.24 (d, J=6.5 Hz, 3H).
Methyl 5-bromopicolinate (2.15 g, 10 mmol) was added into a 100 m1 single-necked flask, to which was added acetonitrile (22 ml), and then AgF2 (5.83 g, 40 mmol) was added under stirring at room temperature. After addition, the reaction solution was stirred for additional 16 h, and filtered over diatomaceous earth. The filter cake was rinsed with acetonitrile (22 mL), and then subjected to column chromatography, to obtain the target intermediate 483-1 (2.3 g). MS: m/z 234/236 [M+H]+.
483-1 (2 g, 8.5 mmol), 461-2 (2.9 g, 9.4 mmol), Pd(dppf)Cl2 (0.31 g, 0.43 mmol), and TEA (1.72 g, 17 mmol) were added into dioxane/H2O (10/1, 30 mL), and then under nitrogen protection, the mixture was stirred at 80° C. The progress of the reaction was detected with TLC. After completion of the reaction, the reaction solution was diluted with water (30 mL), and then extracted with EA (30 mL×3). Purification by column chromatography provided the target compound 483-2 (2.4 g). MS: m/z 337 [M+H]+.
483-2 (2.4 g, 7.1 mmol) was dissolved in dichloromethane (24 mL), to which was added the solution of HCl in dioxane (24 mL), and then the mixture was stirred for 2 h at room temperature. The reaction solution was rotatory evaporated, to obtain the target compound 483-3 (2.2 g). MS: m/z 237 [M+H]+.
461-11 (2 g, 2.9 mmol) and 483-3 (0.95 g, 3.5 mmol) were added into a mixed solvent of isopropanol (20 mL) and dichloromethane (20 mL), to which were successively added DIEA (0.57 g, 4.4 mmol), HOAc (1.04 g, 17.4 mmol), and sodium cyanoborohydride (0.73 g, 11.6 mmol) at room temperature. After addition, the mixture was continually stirred, and the reaction was detected with TLC. After completion of the reaction, saturated NaHCO3 aqueous solution (40 mL) was added, and the resultant solution was extracted with dichloromethane (40 mL×2). Purification by column chromatography afforded the target compound 483-4 (1.6 g). MS: m/z 911 [M+H]+.
483-4 (1.6 g, 1.76 mmol) was placed in a 50 mL single-necked flask, to which were added tetrahydrofuran (10 mL), methanol (2.5 mL), water (2.5 mL), and lithium hydroxide monohydrate (0.59 g, 14.07 mmol), and then the mixture was stirred at room temperature for 2 h. The pH of the reaction solution was adjusted to neutral with HCl (1N). The organic solvent was removed by rotatory evaporation. To the residue, was added 10 mL of water, and then the pH was adjusted to 2 with HCl (1N), followed by filtration. The filter cake was washed with water, and air dried, to obtain the target compound 483-5 (1.28 g). MS: m/z 897 [M+H]+.
483-5 (1.28 g, 1.4 mmol), compound TC (0.5 g, 1.6 mmol), HATU (0.64 g, 1.7 mmol) and DIEA (0.45 g, 3.5 mmol) were added into DMAc (15 mL), and then the mixture was stirred at room temperature. The reaction was detected with TLC. After completion of the reaction, the reaction solution was added to water (60 mL) dropwise, and filtered. The filter cake was rinsed with water (10 mL), and subjected to column chromatography, to obtain the target compound 486-6 (1 g). MS: m/z 1152 [M+H]+.
Compound 483-6 (1 g, 0.86 mmol) was dissolved in DCM (20 mL), to which was continuously introduced HCl gas at room temperature under stirring. The reaction was monitored by TLC. After completion of the reaction, the reaction solution was rotatory evaporated, and then the residue was dissolved in DCM, followed by rotatory evaporation, that was repeated once, to obtain compound 483 (1 g). MS: m/z 1052 [M+H]+.
1H NMR: (400 MHz, DMSO-d6) δ 11.61 (s, 1H), 10.99 (s, 1H), 10.27 (s, 1H), 9.45 (t, J=6.3 Hz, 1H), 8.39 (d, J=1.4 Hz, 1H), 8.37-8.22 (m, 3H), 8.21-8.11 (m, 2H), 8.01 (dd, J=7.7, 1.8 Hz, 1H), 7.84-7.77 (m, 2H), 7.77-7.70 (m, 2H), 7.68 (d, J=7.9 Hz, 1H), 7.53 (s, 1H), 7.50-7.41 (m, 1H), 7.29 (t, J=8.0 Hz, 1H), 7.16 (t, J=8.7 Hz, 1H), 7.01-6.92 (m, 1H), 6.33 (s, 1H), 5.10 (dd, J=13.3, 5.1 Hz, 1H), 4.58 (d, J=6.3 Hz, 2H), 4.43 (d, J=17.4 Hz, 1H), 4.29 (d, J=17.5 Hz, 1H), 4.25-4.04 (m, 3H), 3.93 (d, J=9.0 Hz, 2H), 3.75 (s, 1H), 3.65 (t, J=11.1 Hz, 3H), 3.48 (s, 1H), 3.35 (t, J=5.6 Hz, 1H), 3.19 (d, J=23.2 Hz, 1H), 3.06 (s, 4H), 2.86 (dt, J=32.3, 12.6 Hz, 3H), 2.69 (d, J=15.9 Hz, 1H), 2.59 (d, J=16.9 Hz, 1H), 2.44-2.19 (m, 3H), 1.99 (d, J=12.3 Hz, 3H), 1.80 (t, J=12.2 Hz, 2H), 1.72-1.52 (m, 2H), 1.24 (d, J=6.6 Hz, 3H).
Methyl 2,4-difluorobenzoate (1.72 g, 10 mmol), 1-Boc-piperazine (1.86 g, 10 mmol), and Na2CO3 (2.12 g, 20 mmol) were successively added into 15 mL of dimethylsulfoxide, and then the reaction system was heated to 80° C. and reacted for 16 h. The reaction solution was cooled to room temperature, and poured into 100 mL of water, followed by extraction with ethyl acetate. The obtained organic phase was dried with anhydrous sodium sulfate. After the solvent was evaporated under reduced pressure, the crude product was recrystallized in ethyl acetate, and filtered to remove the filtrate. The filter cake was dried to obtain 1.62 g of product (intermediate 501-2), with a yield of 48%. MS: m/z 339.1 [M+H]+.
Intermediate 501-2 (1.02 g, 3 mmol) was dissolved in 30 mL of dichloromethane, to which was added 30 mL of HCl-dioxane solution (4 mol/L), and the mixture was allowed to react at room temperature for 2 h. The reaction solution was concentrated, and the residue was triturated with 10 mL of dichloromethane and filtered. The filter cake was sequentially rinsed with 10 mL of dichloromethane and 10 mL of methyl tert-butyl ether, and then dried, to obtain 783 mg of product (intermediate 501-3), with a yield of 95%. MS: m/z 239.1 [M+H]+.
Intermediate 461-11 (500 mg, 0.72 mmol) and intermediate 501-3 (239 mg, 0.87 mmol) were successively added into a mixed solvent of dichloromethane (10 mL) and isopropanol (10 mL), and then the pH value of the system was adjusted to 7-8 with N,N-diisopropylethylamine. Subsequently, the pH was adjusted to 6 with acetic acid, followed by addition of sodium cyanodorohydride (91 mg, 1.45 mmol). The mixture was allowed to react at room temperature for 16 h. The reaction solution was quenched with 20 mL of saturated NaHCO3 aqueous solution, and extracted with 50 mL of dichloromethane. The organic layer was dried with anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by column chromatography to obtain 437 mg of product (intermediate 501-4), with a yield of 55%. MS: m/z 913.4 [M+H]+.
Intermediate 501-4 (365 mg, 0.40 mmol) and lithium hydroxide monohydrate (166 mg, 3.97 mmol) were successively added into a mixed solvent of tetrahydrofuran (4 mL), methanol (2 mL), and water (2 mL), and then the mixture was reacted at room temperature for 1 h. The pH value of the reaction system was adjusted to 4 with 1N HCl aqueous solution, and extracted with 30 mL of dichloromethane. The organic layer was dried with anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to obtain 360 mg of product (intermediate 501-5, with a yield of 95%. MS: m/z 899.4 [M+H]+.
Intermediate 501-5 (342 mg, 0.38 mmol), 3-[5-(aminomethyl)-1-oxo-2,3-dihydro-1H-isoindol-2-yl]hexahydropyridine-2,6-dione (105 mg, 0.38 mmol), HATU (175 mg, 0.46 mmol), and N,N-diisopropylethylamine (124 mg, 0.96 mmol) were successively added into 4 mL of N, N-dimethylacetamide, and then the mixture was allowed to react at room temperature for 16 h. The reaction solution was slowly added into 40 mL of water dropwise, and filtered. The solid was purified by column chromatography to obtain 232 mg of product (intermediate 501-6), with a yield of 53%. MS: m/z 574.8 [M/2+H]+.
Intermediate 501-6 (231 mg, 0.20 mmol) was dissolved in 25 mL of dichloromethane, to which was continuously introduced dry HCl gas at room temperature, and TLC indicated completion of the reaction. The reaction solution was concentrated under reduced pressure. The residue was triturated with 25 mL of dichloromethane, and filtered. The filter cake was sequentially rinsed with 5 mL of dichloromethane and 5 mL of methyl tert-butyl ether. The solid was dried to obtain 220 mg of product (compound 501), with a yield of 98.0%. MS: m/z 1054.5 [M+H]+.
1H NMR (400 MHz, DMSO-d6) δ 11.78 (s, 1H), 11.00 (s, 1H), 10.24 (s, 1H), 8.63 (q, J=5.8 Hz, 1H), 8.45-8.14 (m, 5H), 7.87-7.64 (m, 6H), 7.59-7.41 (m, 2H), 7.23 (dt, J=53.8, 8.4 Hz, 2H), 7.02-6.85 (m, 3H), 5.11 (dd, J=13.3, 5.1 Hz, 1H), 4.56 (d, J=5.9 Hz, 2H), 4.44 (d, J=17.4 Hz, 1H), 4.36-4.11 (m, 4H), 4.03 (d, J=12.8 Hz, 2H), 3.92 (d, J=9.1 Hz, 1H), 3.72-3.57 (m, 5H), 3.48-3.31 (m, 4H), 3.23-3.02 (m, 4H), 2.98-2.73 (m, 3H), 2.64-2.54 (m, 1H), 2.46-2.23 (m, 3H), 1.97 (dt, J=16.9, 6.8 Hz, 3H), 1.87-1.74 (m, 2H), 1.71-1.56 (m, 2H), 1.24 (d, J=6.6 Hz, 3H).
By using a synthesis method similar to the above examples, the compounds listed in Table 1 could be synthesized by selecting appropriate reactants, reagents, and reaction conditions.
1H NMR
1H NMR (400 MHz, DMSO-d6) δ 10.99 (s, 1H), 10.14 (d, J = 2.7 Hz, 1H), 10.06 (s, 1H), 8.38 (d, J = 1.5 Hz, 1H), 8.16 (d, J = 1.4 Hz, 1H), 8.11 (d, J = 1.9 Hz, 1H), 7.88 (s, 2H), 7.70 (dd, J = 8.3, 2.0 Hz, 1H), 7.60 (t, J = 1.9 Hz, 1H), 7.54-7.46 (m, 2H), 7.24 (t, J = 8.0 Hz, 1H), 6.92 (m, 1H), 5.10 (dd, J = 13.3, 5.1 Hz, 1H), 4.44-4.21 (m, 2H), 4.03 (m, 2H), 3.49-3.25 (m, 5H), 3.13 (q, J = 8.4 Hz, 1H), 2.91 (m, 1H), 2.60 (m, 1H), 2.45-2.16 (m, 9H), 2.08-1.92 (m, 3H), 1.66 (m, 10H), 1.41-1.21 (m, 15H).
1H NMR (400 MHz, DMSO-d6) δ 10.05 (s, 1H), 8.42 (t, J = 6.0 Hz, 1H), 8.38 (d, J = 1.4 Hz, 1H), 8.16 (d, J = 1.4 Hz, 1H), 7.67 (d, J = 7.8 Hz, 1H), 7.59 (t, J = 2.0 Hz, 1H), 7.48 (dd, J = 7.7, 2.0 Hz, 1H), 7.45 (s, 1H), 7.38 (dd, J = 7.9, 1.4 Hz, 1H), 7.23 (t, J = 8.0 Hz, 1H), 6.91 (dt, J = 8.0, 1.3 Hz, 1H), 5.11 (dd, J = 13.3, 5.1 Hz, 1H), 4.47-4.25 (m, 4H), 3.97 (m, 2H), 3.52-3.25 (m, 5H), 3.13 (q, J = 8.5 Hz, 1H), 2.92 (m, 1H), 2.60 (m, 1H), 2.45-2.31 (m, 1H), 2.31-2.09 (m, 8H), 2.06-1.92 (m, 3H), 1.77-1.44 (m, 10H), 1.41-1.18 (m, 15H).
1H NMR (400 MHz, DMSO-d6) δ 10.03 (s, 1H), 8.98 (s, 1H), 8.39 (d, J = 7.8 Hz, 1H), 8.33 (d, J = 1.5 Hz, 1H), 8.13 (d, J = 1.4 Hz, 1H), 7.80 (d, J = 9.3 Hz, 1H), 7.52 (t, J = 2.0 Hz, 1H), 7.50- 7.31 (m, 5H), 7.21 (t, J = 8.0 Hz, 1H), 6.89 (dt, J = 7.8, 1.3 Hz, 1H), 5.11 (s, 1H), 4.91 (p, J = 7.1 Hz, 1H), 4.51 (d, J = 9.3 Hz, 1H), 4.41 (t, J = 8.0 Hz, 1H), 4.27 (d, J = 4.0 Hz, 1H), 3.78-3.66 (m, 2H), 3.65-3.52 (m, 4H), 3.48-3.39 (m, 4H), 3.11 (q, J = 8.4 Hz, 2H), 2.45 (s, 3H), 2.28-1.95 (m, 12H), 1.83- 1.69 (m, 2H), 1.66-1.54 (m, 3H), 1.48- 1.41 (m, 5H), 1.39-1.30 (d, J = 7.0 Hz, 5H), 1.27-1.18 (m, 10H), 1.11 (s, 3H), 0.93 (s, 9H).
1H NMR (400 MHz, DMSO-d6) δ 10.03 (s, 1H), 8.98 (s, 1H), 8.39 (d, J = 7.8 Hz, 1H), 8.33 (d, J = 1.5 Hz, 1H), 8.13 (d, J = 1.4 Hz, 1H), 7.80 (d, J = 9.3 Hz, 1H), 7.52 (t, J = 2.0 Hz, 1H), 7.50- 7.31 (m, 5H), 7.21 (t, J = 8.0 Hz, 1H), 6.89 (dt, J = 7.8, 1.3 Hz, 1H), 5.11 (s, 1H), 4.91 (p, J = 7.1 Hz, 1H), 4.51 (d, J = 9.3 Hz, 1H), 4.41 (t, J = 8.0 Hz, 1H), 4.27 (d, J = 4.0 Hz, 1H), 3.78-3.66 (m, 2H), 3.65-3.52 (m, 2H), 3.48-3.39 (m, 2H), 3.11 (q, J = 8.4 Hz, 2H), 2.45 (s, 3H), 2.28-1.95 (m, 8H), 1.83-1.69 (m, 2H), 1.66-1.54 (m, 3H), 1.48- 1.41 (m, 4H), 1.39-1.30 (d, J = 7.0 Hz, 5H), 1.27-1.18 (m, 16H), 1.11 (s, 3H), 0.93 (s, 9H).
1H NMR (400 MHz, DMSO-d6) δ 11.01 (s, 1H), 10.04 (s, 1H), 8.44 (t, J = 6.1 Hz, 1H), 8.38 (s, 1H), 8.18 (s, 1H), 7.67 (d, J = 7.8 Hz, 1H), 7.59 (d, J = 2.0 Hz, 1H), 7.48 (d, J = 8.1 Hz, 1H), 7.45 (s, 1H), 7.38 (d, J = 7.9 Hz, 1H), 7.24 (t, J = 8.0 Hz, 1H), 6.91 (d, J = 7.9 Hz, 1H), 5.11 (dd, J = 13.3, 5.1 Hz, 1H), 4.48-4.26 (m, 4H), 4.12-4.00 (m, 2H), 3.51-3.35 (m, 2H), 3.12 (s, 2H), 2.98-2.85 (m, 1H), 2.65-2.54 (m, 2H), 2.42-2.35 (m, 2H), 2.14 (t, J =
1H NMR (400 MHz, DMSO-d6) δ 9.97 (s, 1H), 8.98 (s, 1H), 8.49 (d, J = 7.7 Hz, 1H), 8.38 (s, 1H), 8.34 (d, J = 9.7 Hz, 1H), 8.17 (s, 1H), 8.14 (s, 2H), 7.85 (d, J = 9.5 Hz, 1H), 7.58 (s, 1H), 7.48- 7.32 (m, 6H), 7.23 (t, J = 8.0 Hz, 1H), 6.90 (d, J = 7.8 Hz, 1H), 5.18 (s, 1H), 4.91 (t, J = 7.3 Hz, 1H), 4.71 (d, J = 9.8 Hz, 1H), 4.46 (t, J = 8.2 Hz, 1H), 4.30 (s, 1H), 4.07-4.01 (m, 2H), 3.76-3.61 (m, 6H), 2.45 (s, 3H), 2.35-2.23 (m, 4H), 2.10-2.05 (m, 1H), 1.82-1.68 (m, 5H), 1.59-1.42 (m, 5H), 1.40- 1.31 (m, 7H), 1.28-1.23 (m, 12H), 1.00 (s, 9H).
1H NMR (400 MHz, DMSO-d6) δ 10.98 (s, 1H), 9.96 (s, 1H), 9.55 (t, J = 6.4 Hz, 1H), 8.38 (d, J = 1.5 Hz, 1H), 8.17 (d, J = 1.3 Hz, 1H), 8.14 (s, 2H), 7.85 (d, J = 9.5 Hz, 1H), 7.68 (d, J = 7.8 Hz, 1H), 7.57 (d, J = 2.0 Hz, 1H), 7.53 (s, 1H), 7.47 (dd, J = 8.3, 2.3 Hz, 2H), 7.36 (d, J = 9.6 Hz, 1H), 7.23 (t, J = 8.0 Hz, 1H), 6.90 (dd, J = 7.8, 1.9 Hz, 1H), 5.10 (dd, J = 13.3, 5.1 Hz, 1H), 4.60 (d, J = 6.3 Hz, 2H), 4.47-4.25 (m, 2H), 4.09-4.01 (m, 2H), 3.71 (s, 4H), 2.96- 2.85 (m, 1H), 2.65-2.53 (m, 3H), 2.44-2.31 (m, 1H), 2.27 (t, J = 7.4 Hz,
1H NMR (400 MHz, DMSO-d6) δ 10.99 (s, 1H), 9.93 (s, 1H), 9.47 (s, 1H), 8.37 (d, J = 1.5 Hz, 1H), 8.17 (d, J = 1.4 Hz, 1H), 7.84 (d, J = 9.2 Hz, 1H), 7.67 (d, J = 7.9 Hz, 1H), 7.59 (t, J = 1.9 Hz, 1H), 7.52 (s, 1H), 7.45 (d, J = 9.1 Hz, 2H), 7.23 (t, J = 8.0 Hz, 1H), 6.89 (d, J = 8.6 Hz, 1H), 6.85 (d, J = 9.3 Hz, 1H), 5.10 (dd, J = 13.3, 5.1 Hz, 1H), 4.59 (t, J = 5.1 Hz, 2H), 4.47-4.25 (m, 2H),
1H NMR (400 MHz, DMSO-d6) δ 10.98 (s, 1H), 9.99 (s, 1H), 8.37 (d, J = 1.5 Hz, 1H), 8.16 (d, J = 1.4 Hz, 1H), 7.58 (t, J = 2.0 Hz, 1H), 7.49-7.41 (m, 4H), 7.33 (p, J = 5.9 Hz, 4H), 7.22 (t, J = 8.0 Hz, 1H), 6.91-6.87 (m, 1H), 5.22 (d, J = 2.7 Hz, 2H), 5.11 (dd, J = 13.3, 5.1 Hz, 1H), 4.44-4.22 (m, 2H), 4.09-3.98 (m, 2H), 3.63-3.29 (m,4H), 2.96-2.85 (m, 1H), 2.78- 2.63 (m, 4H), 2.61-2.52 (m, 2H), 2.47- 2.40 (m, 4H), 2.30-2.23 (m, 3H), 2.03-1.94 (m, 2H), 1.77-1.68 (m,
1H NMR (400 MHz, DMSO-d6) δ 9.88 (s, 1H), 8.33 (d, J = 1.5 Hz, 1H), 8.14 (d, J = 1.3 Hz, 1H), 7.52-7.39 (m, 5H), 7.31 (dd, J = 8.1, 5.6 Hz, 4H), 7.21 (t, J = 8.0 Hz, 1H), 6.88 (d, J = 7.8 Hz, 1H), 5.21 (s, 2H), 5.11 (dd, J = 13.3, 5.1 Hz, 1H), 4.45-4.20 (m, 2H), 3.98-3.86 (m, 1H), 3.80-3.69 (m, 2H), 3.60- 3.46 (m, 4H), 3.30-3.20 (m, 3H), 2.97- 2.84 (m, 1H), 2.71-2.61 (m, 1H), 2.58 (d, J = 3.4 Hz, 1H), 2.44-2.33 (m, 3H), 2.29-2.20 (m, 3H), 2.03-1.91 (m, 2H), 1.64-1.49 (m, 3H), 1.47- 1.37 (m, 6H), 1.30-1.17 (m, 7H), 1.08 (s, 3H).
1H NMR (400 MHz, DMSO-d6) δ 10.99 (s, 1H), 10.10 (s, 1H), 9.49 (t, J = 6.3 Hz, 1H), 8.38 (d, J = 1.4 Hz, 1H), 8.18 (d, J = 1.3 Hz, 1H), 7.82 (d, J = 9.4 Hz, 1H), 7.67 (d, J = 7.8 Hz, 1H), 7.57 (d, J = 2.0 Hz, 1H), 7.53 (s, 1H), 7.49- 7.41 (m, 2H), 7.24 (t, J = 8.0 Hz, 1H), 6.93 (dd, J = 15.0, 8.6 Hz, 2H), 5.10 (dd, J = 13.3, 5.1 Hz, 1H), 4.59 (d, J = 6.3 Hz, 2H), 4.48-4.24 (m, 2H), 4.14 (s, 1H), 4.06-3.92 (m, 2H), 3.69-3.47
1H NMR (400 MHz, DMSO-d6) δ 10.11 (s, 1H), 8.98 (d, J = 3.3 Hz, 1H), 8.50 (d, J = 7.6 Hz, 1H), 8.37 (d, J = 1.5 Hz, 1H), 8.33 (d, J = 9.7 Hz, 1H), 8.17 (d, J = 1.4 Hz, 1H), 7.83 (d, J = 9.4 Hz, 1H), 7.56 (t, J = 1.9 Hz, 1H), 7.49- 7.33 (m, 5H), 7.24 (t, J = 7.9 Hz, 1H), 6.97 (d, J = 9.5 Hz, 1H), 6.94-6.89 (m, 1H), 5.20 (s, 1H), 4.98-4.87 (m, 1H), 4.71 (d, J = 9.8 Hz, 1H), 4.46 (t, J = 8.2 Hz, 1H), 4.30 (s, 1H), 4.00-3.87 (m, 2H), 3.69-3.27 (m, 11H), 3.21-3.09 (m, 5H), 2.68 (t, J = 6.9 Hz, 2H), 2.45 (s, 3H), 2.30 (t, J = 6.9 Hz, 2H), 2.19- 2.04 (m, 3H), 1.82-1.73 (m, 1H), 1.70- 1.63 (m, 3H), 1.38 (d, J = 7.0 Hz, 2H), 1.30 (s, 3H), 0.99 (s, 9H).
1H NMR (400 MHz, DMSO-d6) δ 10.99 (s, 1H), 10.14 (s, 1H), 9.50 (t, J = 6.4 Hz, 1H), 8.38 (d, J = 1.6 Hz, 1H), 8.20-8.14 (m, 1H), 7.83 (d, J = 9.4 Hz, 1H), 7.67 (d, J = 7.8 Hz, 1H), 7.58- 7.51 (m, 2H), 7.50-7.42 (m, 2H), 7.24 (t, J = 8.0 Hz, 1H), 6.94 (d, J = 9.4 Hz, 1H), 6.90 (dd, J = 7.6, 1.9 Hz, 1H), 5.10 (dd, J = 13.3, 5.1 Hz, 1H), 4.59 (d, J = 6.3 Hz, 2H), 4.45-4.26 (m, 2H), 4.21- 4.01 (m, 3H), 3.83 (d, J = 9.0 Hz, 1H), 3.72-3.61 (m, 3H), 3.54 (s, 3H), 3.33-
1H NMR (400 MHz, DMSO-d6) δ 10.99 (s, 1H), 10.14 (s, 1H), 9.50 (t, J = 6.4 Hz, 1H), 8.38 (d, J = 1.6 Hz, 1H), 8.20-8.14 (m, 1H), 7.83 (d, J = 9.4 Hz, 1H), 7.67 (d, J = 7.8 Hz, 1H), 7.58- 7.51 (m, 2H), 7.50-7.42 (m, 2H), 7.24 (t, J = 8.0 Hz, 1H), 6.94 (d, J = 9.4 Hz, 1H), 6.90 (dd, J = 7.6, 1.9 Hz, 1H), 5.10 (dd, J = 13.3, 5.1 Hz, 1H), 4.59 (d, J = 6.3 Hz, 2H), 4.45-4.26 (m, 2H), 4.21- 4.01 (m, 3H), 3.83 (d, J = 9.0 Hz, 1H), 3.72-3.61 (m, 3H), 3.54 (s, 3H), 3.33- 3.26 (m, 4H), 3.22-2.97 (m, 4H), 2.95-2.76 (m, 3H), 2.61 (s, 1H), 2.41- 2.30 (m, 3H), 2.17 (t, J = 6.9 Hz, 2H), 2.04-1.93 (m, 1H), 1.79-1.50 (m, 4H), 1.38-1.28 (m, 2H), 1.29-1.20 (m, 2H), 1.16 (d, J = 6.5 Hz, 3H).
1H NMR (400 MHz, DMSO-d6) δ 10.99 (s, 1H), 9.99 (s, 1H), 9.50 (t, J = 6.4 Hz, 1H), 8.38 (d, J = 1.5 Hz, 1H), 8.17 (d, J = 1.4 Hz, 1H), 7.86 (d, J = 9.4 Hz, 1H), 7.68 (d, J = 7.8 Hz, 1H), 7.59 (t, J = 2.0 Hz, 1H), 7.53 (s, 1H), 7.47 (d, J = 7.9 Hz, 2H), 7.23 (t, J = 8.0 Hz, 1H), 6.94 (d, J = 9.4 Hz, 1H), 6.89 (d, J = 8.1 Hz, 1H), 5.10 (dd, J = 13.3, 5.1 Hz, 1H), 4.59 (d, J = 6.4 Hz, 2H), 4.47- 4.25 (m, 2H), 4.13 (q, J = 5.3 Hz, 1H), 4.10-3.99 (m, 2H), 3.78 (s, 2H), 3.54 (s, 3H), 3.42-3.35 (m, 1H), 3.10-2.84 (m, 3H), 2.64-2.53 (m, 1H), 2.44- 2.21 (m, 5H), 2.05-1.93 (m, 2H), 1.80- 1.66 (m, 4H), 1.54 (s, 2H), 1.47-1.34 (m, 5H), 1.32-1.18 (m, 8H).
1H NMR (400 MHz, DMSO-d6) δ 11.00 (s, 1H), 9.91 (d, J = 4.9 Hz, 1H), 8.34 (s, 1H), 8.15 (s, 1H), 7.56-7.39 (m, 5H), 7.31 (dd, J = 10.1, 7.0 Hz, 4H), 7.21 (t, J = 8.0 Hz, 1H), 6.88 (d, J = 7.8 Hz, 1H), 5.22 (s, 2H), 5.11 (dd, J = 13.3, 5.1 Hz, 1H), 4.45-4.21 (m, 2H), 4.10-4.01 (m, 1H), 3.89-3.81 (m, 1H), 3.66 (d, J = 8.4 Hz, 1H), 3.52 (s, 2H), 3.47 (d, J = 8.5 Hz, 1H), 3.39- 3.35 (m, 5H), 3.01 (d, J = 6.5 Hz, 2H), 2.98-2.84 (m, 4H), 2.61-2.52 (m, 3H), 2.42 (t, J = 7.0 Hz, 2H), 2.29- 2.21 (m, 4H), 2.02-1.93 (m, 1H), 1.86 (t, J = 6.9 Hz, 2H), 1.80-1.69 (m, 1H),
1H NMR (400 MHz, DMSO-d6) δ 11.00 (s, 1H), 9.98 (s, 1H), 9.03 (t, J = 6.0 Hz, 1H), 8.82 (s, 2H), 8.42 (d, J = 1.4 Hz, 1H), 8.18 (d, J = 1.4 Hz, 1H), 7.69 (d, J = 7.8 Hz, 1H), 7.60-7.51 (m, 2H), 7.46 (d, J = 7.9 Hz, 2H), 7.24 (t, J = 7.9 Hz, 1H), 6.91 (d, J = 7.9 Hz, 1H), 5.11 (dd, J = 13.3, 5.1 Hz, 1H), 4.57 (d, J = 5.7 Hz, 2H), 4.44 (d, J = 17.4 Hz, 1H), 4.30 (d, J = 17.3 Hz, 1H), 4.25 (s, 1H), 4.22 (s, 1H), 4.12 (s, 3H), 3.71 (s, 2H), 3.62-3.50 (m, 5H), 3.23 (t, J = 11.7 Hz, 2H), 3.08 (d, J = 20.7 Hz, 2H), 2.97-2.86 (m, 1H), 2.62 (dd, J = 21.6, 17.9 Hz, 1H), 2.40 (d, J = 4.3 Hz, 1H), 2.35 (dd, J = 12.7, 3.3 Hz, 1H), 2.29 (t, J = 7.3 Hz, 2H), 2.18 (t, J = 7.0 Hz, 2H), 2.00 (d, J = 7.0 Hz, 2H), 1.91 (d, J =
1H NMR (400 MHz, DMSO-d6) δ 10.99 (s, 1H), 10.11 (s, 1H), 8.40-8.34 (m, 1H), 8.17 (s, 1H), 7.56-7.42 (m, 4H), 7.39 (d, J = 8.1 Hz, 1H), 7.33 (d, J = 7.4 Hz, 1H), 7.24 (t, J = 8.0 Hz, 1H), 6.89 (t, J = 9.0 Hz, 2H), 5.32 (s, 2H), 5.10 (dd, J = 13.3, 5.1 Hz, 1H), 4.44- 4.20 (m, 2H), 4.19-4.09 (m, 1H), 4.07- 3.91 (m, 2H), 3.77 (d, J = 9.0 Hz, 1H), 3.60-3.54 (m, 3H), 3.50-3.43 (m, 3H), 3.27-3.13 (m, 6H), 3.08-2.98 (m, 1H), 2.96-2.86 (m, 1H), 2.72 (t, J = 6.6 Hz, 2H), 2.61-2.54 (m, 1H), 2.45-2.39 (m, 1H), 2.32 (t, J = 6.9 Hz, 2H), 2.12 (t, J = 6.8 Hz, 2H), 2.03- 1.94 (m, 1H), 1.78-1.58 (m, 3H), 1.55- 1.44 (m, 2H), 1.14 (d, J = 6.5 Hz, 3H).
1H NMR (400 MHz, DMSO-d6) δ 10.07 (s, 1H), 8.33 (d, J = 1.5 Hz, 1H), 8.15 (d, J = 1.4 Hz, 1H), 7.53-7.42 (m, 4H), 7.38 (d, J = 8.1 Hz, 1H), 7.32 (d, J = 7.4 Hz, 1H), 7.22 (t, J = 8.0 Hz, 1H), 6.92-6.85 (m, 2H), 5.31 (s, 2H), 5.10 (dd, J = 13.4, 5.1 Hz, 1H), 4.42-4.19 (m, 2H), 3.80-3.70 (m, 2H), 3.60- 3.52 (m, 4H), 3.48-3.43 (m, 2H), 3.13 (q, J = 7.2 Hz, 4H), 2.67 (t, J = 6.9 Hz, 2H), 2.61-2.53 (m, 1H), 2.46-2.39 (m, 1H), 2.29 (t, J = 6.9 Hz, 2H), 2.11 (t, J = 6.8 Hz, 2H), 2.03-1.93 (m, 2H), 1.47-1.39 (m, 4H), 1.28-1.22 (m, 2H), 1.08 (s, 3H).
1H NMR (400 MHz, DMSO-d6) δ 9.92 (s, 1H), 9.49 (t, J = 6.4 Hz, 1H), 8.41 (d, J = 1.5 Hz, 1H), 8.17 (d, J = 1.4 Hz, 1H), 7.83 (d, J = 9.4 Hz, 1H), 7.68 (d, J = 7.8 Hz, 1H), 7.57-7.51 (m, 2H), 7.46 (t, J = 7.8 Hz, 2H), 7.23 (t, J = 8.0 Hz, 1H), 6.97 (d, J = 9.4 Hz, 1H), 6.93- 6.87 (m, 1H), 5.10 (dd, J = 13.3, 5.1 Hz, 1H), 4.60 (d, J = 6.3 Hz, 2H), 4.43 (d, J = 17.4 Hz, 1H), 4.29 (d, J = 17.4 Hz, 1H), 4.20 (d, J = 3.7 Hz, 2H), 4.12 (d, J = 5.5 Hz, 2H), 3.61 (s, 2H), 3.43 (q, J = 6.8 Hz, 2H), 3.22 (t, J = 11.6 Hz, 2H), 3.17 (s, 2H), 2.96-2.88 (m, 1H), 2.87 (s, 1H), 2.63-2.55 (m, 1H), 2.40 (dd, J = 13.1, 4.5 Hz, 1H), 2.34 (dd, J = 9.8, 3.4 Hz, 1H), 2.24 (t, J = 7.3 Hz, 2H), 2.09 (d, J = 5.1 Hz, 2H), 2.02- 1.93 (m, 2H), 1.87 (t, J = 12.3 Hz, 2H),
1H NMR (400 MHz, DMSO-d6) δ 10.03 (d, J = 5.4 Hz, 1H), 8.75 (d, J = 9.9 Hz, 2H), 8.56 (d, J = 7.3 Hz, 1H), 8.48 (d, J = 7.5 Hz, 1H), 8.44-8.39 (m, 1H), 8.20-8.13 (m, 1H), 7.57 (d, J = 17.5 Hz, 1H), 7.47 (d, J = 8.2 Hz, 1H), 7.35 (d, J = 7.8 Hz, 1H), 7.24 (t, J = 8.0 Hz, 1H), 7.16 (t, J = 8.1 Hz, 2H), 6.91 (d, J = 7.8 Hz, 1H), 4.70-4.44 (m, 3H), 4.24 (d, J = 16.1 Hz, 2H), 3.76 (d, J = 13.6 Hz, 5H), 3.56 (s, 2H), 3.23 (t, J = 12.2 Hz, 3H), 3.12 (d, J = 20.7 Hz, 1H), 2.93 (s, 1H), 2.44 (s, 2H), 2.34 (s, 1H), 2.30 (d, J = 7.0 Hz, 2H), 2.21 (t, J = 6.7 Hz, 2H), 2.08 (s, 10H), 1.95 (dd, J = 24.2, 9.5 Hz, 2H), 1.82 (d, J = 11.4 Hz, 1H), 1.73 (d, J = 16.6 Hz, 1H), 1.57 (d,
1H NMR (400 MHz, DMSO-d6) δ 10.07 (s, 1H), 9.51 (t, J = 6.3 Hz, 1H), 8.42 (d, J = 1.5 Hz, 1H), 8.17 (d, J = 1.4 Hz, 1H), 7.84 (d, J = 9.4 Hz, 1H), 7.69 (d, J = 7.9 Hz, 1H), 7.61-7.52 (m, 2H), 7.51-7.44 (m, 2H), 7.24 (t, J = 8.0 Hz, 1H), 6.98-6.88 (m, 2H), 5.11 (dd, J = 13.3, 5.1 Hz, 1H), 4.61 (d, J = 6.4 Hz, 2H), 4.44 (d, J = 17.5 Hz, 1H), 4.31 (d, J = 17.3 Hz, 1H), 4.24 (d, J = 13.6 Hz, 1H), 3.68 (s, 2H), 3.52 (d, J = 15.1 Hz, 5H), 3.38 (s, 2H), 3.23 (t, J = 11.6
1H NMR (400 MHz, DMSO-d6) δ (s, 1H), 9.93 (s, 1H), 9.54 (s, 2H), 8.38 (s, 1H), 8.17 (s, 1H), 8.00 (s, 3H), 7.72- 7.38 (m, 6H), 7.23 (t, J = 7.9 Hz, 1H), 6.89 (d, J = 7.8 Hz, 1H), 5.32 (s, 1H), 5.10 (dd, J = 13.3, 5.1 Hz, 1H), 4.61 (d, J = 6.4 Hz, 2H), 4.43 (d, J = 17.3 Hz, 2H), 4.29 (d, J = 17.5 Hz, 2H), 4.05 (d, J = 14.0 Hz, 2H), 2.61 (s, 2H), 2.26 (t, J = 7.2 Hz, 4H), 1.99 (d, J = 8.8 Hz, 2H), 1.72 (s, 3H), 1.55 (s, 3H), 1.41- 1.13 (m, 21H).
1H NMR (400 MHz, DMSO-d6) δ 10.01-9.89 (m, 2H), 9.16 (dd, J = 15.7, 8.5 Hz, 1H), 8.38 (d, J = 1.5 Hz, 1H), 8.17 (d, J = 1.3 Hz, 1H), 7.81 (d, J = 9.5 Hz, 1H), 7.59 (d, J = 2.0 Hz, 1H), 7.44 (d, J = 7.8 Hz, 1H), 7.38-7.28 (m, 2H), 7.23 (t, J = 8.0 Hz, 1H), 7.14 (t, J = 8.3 Hz, 2H), 6.90 (d, J = 7.6 Hz, 1H), 6.67 (s, 1H), 5.32 (t, J = 4.8 Hz, 1H), 4.62 (dd, J = 15.0, 7.5 Hz, 3H), 4.47 (d, J = 8.7 Hz, 1H), 4.29 (d, J = 11.9 Hz, 2H), 4.16-3.99 (m, 3H), 3.70-3.57 (m, 2H), 2.75-2.55 (m, 6H), 2.37- 2.23 (m, 5H), 2.04-1.93 (m, 3H), 1.71 (d, J = 5.8 Hz, 3H), 1.50 (d, J = 37.6 Hz, 4H), 1.36 (s, 2H), 1.25 (d, J = 12.0 Hz, 18H), 1.06 (d, J = 5.9 Hz, 5H), 0.96 (d, J = 10.3 Hz, 7H).
1H NMR (400 MHz, DMSO-d6) δ 10.99 (s, 1H), 10.02 (s, 1H), 9.50 (t, J = 6.4 Hz, 1H), 8.41 (s, 1H), 8.16 (d, J = 1.4 Hz, 1H), 7.85 (d, J = 9.3 Hz, 1H), 7.68 (d, J = 7.8 Hz, 1H), 7.58 (d, J = 2.0 Hz, 1H), 7.53 (s, 1H), 7.50-7.44 (m, 2H), 7.24 (t, J = 8.0 Hz, 1H), 6.92 (dd, J = 19.0, 8.6 Hz, 2H), 5.32 (t, J = 4.9 Hz, 1H), 5.14-5.06 (m, 2H), 4.97 (s, 1H), 4.59 (d, J = 6.3 Hz, 2H), 4.45 (dd, J = 16.0, 11.9 Hz, 3H), 4.29 (d, J = 17.4 Hz, 2H), 3.04-2.86 (m, 4H), 2.61 (s, 4H), 2.33-2.22 (m, 5H), 1.99 (p, J = 6.9, 6.3 Hz, 5H), 1.58 (t, J = 7.5 Hz, 3H), 1.44 (s, 5H).
1H NMR (400 MHz, DMSO-d6) δ 10.99 (s, 1H), 9.94 (s, 1H), 9.56 (t, J = 6.4 Hz, 1H), 8.38 (d, J = 1.5 Hz, 1H), 8.17 (d, J = 1.4 Hz, 1H), 8.08 (s, 2H), 7.84 (d, J = 9.5 Hz, 1H), 7.67 (d, J = 7.8 Hz, 1H), 7.58 (t, J = 2.0 Hz, 1H), 7.53 (s, 1H), 7.50-7.40 (m, 3H), 7.23 (t, J = 7.9 Hz, 1H), 6.93-6.87 (m, 1H), 5.32 (t, J = 4.9 Hz, 1H), 5.10 (dd, J = 13.3, 5.1 Hz, 1H), 4.60 (d, J = 6.3 Hz, 3H), 4.43 (d, J = 17.4 Hz, 1H), 4.29 (d, J = 17.3 Hz, 1H), 4.04 (d, J = 13.9 Hz, 2H), 3.74 (dt, J = 14.0, 7.5 Hz, 1H), 3.59-3.51 (m, 2H), 3.18-3.09 (m, 2H), 2.90 (ddd, J = 17.8, 13.4, 5.5 Hz, 1H), 2.63-2.55 (m, 1H), 2.43-2.31 (m, 2H), 2.26 (t, J = 7.4 Hz, 2H), 1.99 (q, J = 7.3, 6.5 Hz, 3H), 1.78-1.68 (m,
1H NMR (400 MHz, DMSO-d6) δ 9.91 (s, 1H), 9.58 (t, J = 6.4 Hz, 1H), 8.32 (d, J = 1.5 Hz, 1H), 8.14 (d, J = 1.4 Hz, 1H), 7.87 (d, J = 9.5 Hz, 1H), 7.67 (d, J = 7.9 Hz, 1H), 7.55-7.43 (m, 5H), 7.21 (t, J = 8.0 Hz, 1H), 6.87 (d, J = 8.0 Hz, 1H), 5.09 (dd, J = 13.3, 5.1 Hz, 1H), 4.60 (d, J = 6.2 Hz, 2H), 4.46- 4.20 (m, 2H), 4.13-3.99 (m, 2H), 3.97- 3.82 (m, 2H), 3.81-3.73 (m, 2H), 3.68 (s, 1H), 3.62-3.57 (m, 2H), 3.56- 3.47 (m, 3H), 3.18-3.14 (m, 1H), 2.96-2.84 (m, 1H), 2.62-2.55 (m, 1H), 2.42-2.31 (m, 1H), 2.26 (t, J =
1H NMR (400 MHz, DMSO-d6) δ 11.01 (d, J = 6.9 Hz, 1H), 9.97 (s, 1H), 8.46 (s, 1H), 8.38 (d, J = 1.5 Hz, 1H), 8.18 (d, J = 1.4 Hz, 3H), 7.67 (d, J = 8.1 Hz, 1H), 7.59 (d, J = 1.9 Hz, 1H), 7.48- 7.41 (m, 2H), 7.36 (d, J = 8.1 Hz, 1H), 7.23 (t, J = 7.9 Hz, 1H), 6.89 (d, J = 7.9 Hz, 1H), 5.35-5.06 (m, 2H), 4.47- 4.39 (m, 1H), 4.35 (d, J = 6.2 Hz, 2H), 4.29 (d, J = 17.4 Hz, 1H), 4.17 (d, J = 4.6 Hz, 1H), 4.05 (d, J = 13.6 Hz, 1H), 3.90 (s, 2H), 3.09 (q, J = 7.3 Hz, 3H), 3.04-2.94 (m, 2H), 2.90 (d, J = 10.3 Hz, 2H), 2.45-2.32 (m, 2H), 2.26 (q, J = 7.2 Hz, 3H), 2.16 (s, 3H), 2.09-1.94 (m, 5H), 1.85 (d, J = 10.8 Hz, 2H), 1.74 (q, J = 6.8, 5.8 Hz, 4H), 1.55 (s, 2H), 1.39 (d, J = 19.7 Hz, 8H), 1.27 (s, 6H).
1H NMR (400 MHz, DMSO-d6) δ 11.00 (s, 1H), 9.96 (s, 1H), 8.38 (d, J = 1.5 Hz, 1H), 8.18 (d, J = 1.4 Hz, 1H), 8.04 (s, 2H), 7.69-7.58 (m, 2H), 7.49- 7.41 (m, 2H), 7.35 (t, J = 9.0 Hz, 1H), 7.27-7.16 (m, 2H), 6.92-6.86 (m, 1H), 5.32 (t, J = 4.8 Hz, 1H), 5.11 (dd, J = 13.2, 5.0 Hz, 1H), 4.73 (dd, J = 10.4, 4.6 Hz, 1H), 4.58 (d, J = 17.6 Hz, 1H), 4.45 (s, 1H), 4.42-4.30 (m, 3H), 4.05 (d, J = 14.0 Hz, 3H), 3.64 (s, 1H), 3.50 (s, 2H), 3.16 (d, J = 4.6 Hz, 2H), 2.27 (q, J = 8.1, 7.7 Hz, 5H), 2.09-1.90 (m, 5H), 1.78-1.67 (m, 4H), 1.55 (s, 2H), 1.37 (s, 4H), 1.30-1.13 (m, 12H)
1H NMR (400 MHz, DMSO-d6) δ 11.00 (s, 1H), 10.02 (s, 1H), 9.50 (s, 1H), 8.37 (d, J = 1.5 Hz, 1H), 8.17 (d, J = 1.4 Hz, 1H), 8.02 (s, 2H), 7.86 (d, J = 9.4 Hz, 1H), 7.66 (dd, J = 14.6, 7.8 Hz, 1H), 7.59 (t, J = 1.9 Hz, 1H), 7.53 (s, 1H), 7.47 (d, J = 8.2 Hz, 2H), 7.23 (t, J = 8.0 Hz, 1H), 6.91 (dd, J = 20.2, 8.3 Hz, 2H), 5.65 (s, 1H), 5.32 (t, J = 4.9 Hz, 1H), 5.10 (dd, J = 13.3, 5.1 Hz, 1H), 4.47-4.39 (m, 2H), 4.29 (d, J = 17.4 Hz, 1H), 4.12 (dd, J = 18.9, 7.0 Hz, 4H), 3.91 (dd, J = 13.5, 7.5 Hz, 4H), 3.77 (s, 2H), 2.90 (ddd, J = 17.8, 12.6, 5.4 Hz, 1H), 2.28 (t, J = 7.2 Hz, 4H), 1.98 (t, J = 7.9 Hz, 2H), 1.82 (d, J = 14.1 Hz, 2H), 1.71-1.65 (m, 2H), 1.50 (d, J = 38.4 Hz, 6H), 1.26 (d, J = 24.6 Hz, 9H).
1H NMR (400 MHz, DMSO-d6) δ 11.01 (s, 1H), 9.97 (s, 1H), 8.37 (d, J = 1.5 Hz, 1H), 8.17 (d, J = 1.3 Hz, 1H), 7.84-7.63 (m, 3H), 7.63-7.55 (m, 2H), 7.54-7.40 (m, 3H), 7.23 (t, J = 7.9 Hz, 1H), 6.91 (dd, J = 22.5, 8.1 Hz, 2H), 5.61 (s, 1H), 5.32 (t, J = 4.8 Hz, 1H), 5.12 (d, J = 13.1 Hz, 1H), 4.46 (dd, J = 17.5, 11.4 Hz, 1H), 4.32 (dd, J = 17.4, 10.9 Hz, 1H), 4.12 (d, J = 5.4 Hz, 1H), 3.94 (s, 3H), 3.76 (s, 2H), 3.60 (s, 2H), 2.91 (d, J = 19.8 Hz, 5H), 2.75- 2.55 (m, 2H), 2.28 (d, J = 11.1 Hz, 3H), 2.06-1.91 (m, 3H), 1.81 (d, J = 14.0 Hz, 2H), 1.68 (d, J = 9.1 Hz, 2H), 1.49 (d, J = 49.9 Hz, 5H), 1.27-1.18 (m, 10H).
1H NMR (400 MHz, DMSO-d6) δ 9.91 (s, 1H), 8.32 (d, J = 1.5 Hz, 1H), 8.14 (d, J = 1.4 Hz, 1H), 7.87 (d, J = 9.5 Hz, 1H), 7.67 (d, J = 7.9 Hz, 1H), 7.55- 7.43 (m, 5H), 7.21 (t, J = 8.0 Hz, 1H), 6.87 (d, J = 8.0 Hz, 1H), 5.09 (dd, J = 13.3, 5.1 Hz, 1H), 4.60 (d, J = 6.2 Hz, 2H), 4.46-4.20 (m, 2H), 4.13-3.99 (m, 2H), 3.97-3.82 (m, 2H), 3.81- 3.73 (m, 2H), 3.68 (s, 1H), 3.62-3.57 (m, 2H), 3.56-3.47 (m, 3H), 3.18- 3.14 (m, 1H), 2.96-2.84 (m, 4H), 2.62- 2.55 (m, 1H), 2.42-2.31 (m, 1H), 2.26 (t, J = 7.4 Hz, 2H), 2.01-1.93 (m,
1H NMR (400 MHz, DMSO-d6) δ 10.99 (s, 1H), 9.96 (s, 1H), 9.07 (t, J = 6.0 Hz, 1H), 8.38 (d, J = 1.5 Hz, 1H), 8.18-8.09 (m, 3H), 7.70-7.65 (m, 3H), 7.64-7.57 (m, 1H), 7.51 (s, 1H), 7.45 (t, J = 8.6 Hz, 2H), 7.23 (t, J = 8.0 Hz, 1H), 7.06 (t, J = 8.7 Hz, 1H), 6.90 (dt, J = 7.8, 1.4 Hz, 1H), 5.10 (dd, J = 13.3, 5.1 Hz, 1H), 4.56 (d, J = 5.8 Hz, 2H), 4.43 (d, J = 17.4 Hz, 1H), 4.29 (d, J = 17.3 Hz, 1H), 4.13 (s, 1H), 4.04 (d, J = 14.1 Hz, 2H), 3.93 (p, J = 7.1 Hz, 1H), 3.62 (td, J = 6.6, 3.9 Hz, 1H), 3.25 (t, J = 6.4 Hz, 2H), 3.05-2.85 (m, 5H), 2.59 (d, J = 17.0 Hz, 1H), 2.39 (td, J =
1H NMR (400 MHz, DMSO-d6) δ 9.89 (s, 1H), 9.47 (t, J = 6.2 Hz, 1H), 8.32 (d, J = 1.5 Hz, 1H), 8.14 (d, J = 1.4 Hz, 1H), 7.81 (d, J = 9.4 Hz, 1H), 7.67 (d, J = 7.8 Hz, 1H), 7.53-7.48 (m, 2H), 7.48-7.43 (m, 2H), 7.20 (t, J = 8.0 Hz, 1H), 6.93 (d, J = 9.4 Hz, 1H), 6.87 (dt, J = 7.9, 1.4 Hz, 1H), 5.09 (dd, J = 13.3, 5.1 Hz, 1H), 4.59 (d, J = 6.3 Hz, 2H), 4.45-4.24 (m, 2H), 3.95-3.87 (m,
1H NMR (400 MHz, DMSO-d6) δ 9.89 (s, 1H), 8.31 (d, J = 1.5 Hz, 1H), 8.14 (d, J = 1.5 Hz, 1H), 7.72 (dd, J = 11.2, 7.9 Hz, 1H), 7.61 (dd, J = 9.4, 6.2 Hz, 1H), 7.55-7.39 (m, 4H), 7.21 (t, J = 8.0 Hz, 1H), 6.97-6.90 (m, 1H), 6.89- 6.84 (m, 1H), 5.16-5.05 (m, 1H), 4.95-4.78 (m, 2H), 4.50-4.25 (m, 2H), 3.96-3.83 (m, 1H), 3.82-3.61 (m, 4H), 3.57-3.40 (m, 4H), 3.31-
1H NMR (400 MHz, DMSO-d6) δ 10.99 (s, 1H), 9.93 (s, 1H), 9.50 (t, J = 6.4 Hz, 1H), 8.34 (d, J = 1.5 Hz, 1H), 8.15 (d, J = 1.4 Hz, 1H), 7.82 (dd, J = 9.3, 3.4 Hz, 1H), 7.68 (d, J = 7.8 Hz, 1H), 7.55-7.43 (m, 4H), 7.21 (t, J = 8.0 Hz, 1H), 7.02-6.85 (m, 3H), 5.10 (dd, J = 13.3, 5.1 Hz, 1H), 4.59 (d, J = 6.2 Hz, 2H), 4.43 (d, J = 17.4 Hz, 1H), 4.29 (d, J = 17.4 Hz, 1H), 3.90 (dd, J = 9.6, 5.2 Hz, 4H), 3.59 (d, J = 53.4 Hz, 5H), 3.25 (t, J = 11.7 Hz, 4H), 3.16 (d, J = 4.6 Hz, 1H), 2.91 (ddd, J = 18.5, 13.8, 5.3 Hz, 1H), 2.59 (d, J = 16.9 Hz,
1H NMR (400 MHz, DMSO-d6) δ 11.00 (s, 1H), 9.97 (s, 1H), 8.42-8.34 (m, 2H), 8.18 (d, J = 1.3 Hz, 1H), 8.12 (s, 2H), 7.68 (d, J = 7.8 Hz, 1H), 7.58 (t, J = 1.9 Hz, 1H), 7.46 (q, J = 2.8, 2.0 Hz, 2H), 7.43-7.38 (m, 1H), 7.23 (t, J = 8.0 Hz, 1H), 7.08-7.01 (m, 2H), 6.91 (dt, J = 7.9, 1.4 Hz, 1H), 6.84- 6.77 (m, 2H), 5.11 (dd, J = 13.3, 5.1 Hz, 1H), 4.43 (d, J = 17.5 Hz, 1H), 4.39 (d, J = 5.8 Hz, 2H), 4.29 (d, J = 17.3 Hz, 1H), 4.04 (dd, J = 11.5, 6.9 Hz, 2H),
1H NMR (400 MHz, DMSO-d6) δ 9.91 (s, 1H), 9.49 (t, J = 6.2 Hz, 1H), 8.20 (d, J = 1.4 Hz, 1H), 8.00 (d, J = 1.5 Hz, 1H), 7.83 (d, J = 9.4 Hz, 1H), 7.68 (d, J = 7.9 Hz, 1H), 7.53 (s, 2H), 7.49- 7.42 (m, 2H), 7.21 (t, J = 8.0 Hz, 1H), 6.95 (d, J = 9.5 Hz, 1H), 6.86-6.82 (m, 1H), 5.10 (dd, J = 13.2, 5.1 Hz, 1H), 4.60 (d, J = 6.6 Hz, 2H), 4.43 (d, J =
1H NMR (400 MHz, DMSO-d6): δ 11.74 (s, 1H), 10.97 (s,1H), 10.22 (s, 1H), 9.32 (s, 1H), 8.38 (s, 5H), 8.19 (s, 1H), 8.03-7.99 (m, 1H), 7.80-7.60 (m, 6H), 7.53-7.45 (m, 2H), 7.32-7.28 (m, 1H), 7.18-7.14 (m, 1H), 7.00-6.98 (m, 1H), 5.11-5.08 (m, 1H), 4.60-4.59 (m, 2H), 4.45-4.41 (m, 1H), 4.32-4.27 (m, 1H), 3.68-3.66 (m, 5H), 3.51-3.39 (m, 5H), 3.23-3.20 (m, 2H), 2.94-2.78 (m, 3H), 2.61-2.57 (m, 1H), 2.39-2.27 (m, 3H), 1.96-1.72 (m, 8H), 1.38 (s, 3H), 1.23 (s, 1H).
1H NMR (400 MHz, DMSO-d6): δ 11.77-11.76 (m, 1H), 10.97(s,1H), 10.21(s,1H), 9.61-9.58 (m, 1H), 8.39- 8.33 (m, 4H), 8.20 (s, 1H), 7.97-7.95 (m, 1H), 7.80-7.67 (m, 5H), 7.54-7.46 (m, 3H), 7.18-7.14 (m, 1H), 7.01-6.99 (m, 1H), 6.98-6.96 (m, 1H), 5.12-5.07 (m, 1H), 4.66-4.61 (m, 4H), 4.46- 4.41(m, 1H), 4.32-4.27 (m, 1H), 3.68- 3.62 (m, 8H), 3.43-3.39 (m, 4H),3.21- 3.19 (m, 2H), 2.91-2.84 (m, 4H), 2.61- 2.51 (m, 1H), 2.40-2.36 (m,3H), 2.02- 1.75 (m,3H), 1.38 (s, 3H), 1.23-1.19 (m,2H).
1H NMR (400 MHz, DMSO-d6): δ 10.97 (s, 1H), 9.99 (s, 1H), 9.17 (s, 1H), 8.38 (s, 2H), 8.19-8.18 (m, 1H), 8.04 (s, 3H), 7.91-7.81 (m, 4H), 7.68- 7.66 (m, 2H), 7.51-7.44 (m, 3H), 7.30- 7.26 (m, 1H), 7.06-7.04 (m, 2H), 6.96- 6.94 (m, 1H), 5.11-5.07 (m, 1H), 4.59- 4.57 (m, 2H), 4.45-4.27 (m, 3H), 4.06- 4.02 (m, 5H), 3.70-3.59 (m, 3H), 2.95- 2.81 (m, 4H), 2.67-2.56 (m, 2H), 2.40- 2.32 (m, 1H), 2.22-2.17 (m, 1H), 2.00- 1.95 (m, 2H), 1.74-1.72 (m, 6H), 1.37 (s, 3H), 1.23-1.22, (m, 1H).
1H NMR (400 MHz, DMSO-d6) δ 11.56 (s, 1H), 11.00 (s, 1H), 10.05 (d, J = 1.9 Hz, 1H), 9.25 (t, J = 6.4 Hz, 1H), 8.39 (d, J = 1.4 Hz, 2H), 8.31 (s, 3H), 8.20 (d, J = 1.3 Hz, 1H), 7.94 (d, J = 8.8 Hz, 1H), 7.68 (d, J = 7.4 Hz, 2H), 7.64- 7.49 (m, 4H), 7.46 (d, J = 7.9 Hz, 1H), 7.28 (t, J = 7.9 Hz, 1H), 6.96 (d, J = 7.8 Hz, 1H), 6.93-6.86 (m, 2H), 5.10 (dd, J = 13.3, 5.1 Hz, 1H), 4.59 (d, J = 6.3 Hz, 2H), 4.48-4.24 (m, 2H), 3.62 (d, J = 11.4 Hz, 2H), 3.42 (tt, J = 9.7, 5.4 Hz, 6H), 3.19 (d, J = 10.9 Hz, 3H), 2.98- 2.79 (m, 4H), 2.64-2.55 (m, 1H), 2.44- 2.30 (m, 1H), 2.23 (d, J = 11.5 Hz, 2H), 2.05-1.94 (m, 2H), 1.76 (ddd, J = 23.7, 11.5, 6.8 Hz, 6H), 1.37 (s, 3H).
1H NMR (400 MHz, DMSO-d6) δ 11.88 (s, 1H), 10.99 (s, 1H), 10.06 (d, J = 1.8 Hz, 1H), 9.62 (t, J = 6.4 Hz, 1H), 8.47-8.36 (m, 4H), 8.19 (d, J = 1.3 Hz, 1H), 7.97 (d, J = 9.5 Hz, 1H), 7.71- 7.64 (m, 2H), 7.62-7.49 (m, 4H), 7.47 (d, J = 7.8 Hz, 1H), 7.27 (t, J = 8.0 Hz, 1H), 6.96 (dd, J = 8.2, 1.8 Hz, 1H), 6.92 6.84 (m, 2H), 5.10 (dd, J = 13.3, 5.1- Hz, 1H), 4.61 (d, J = 5.8 Hz, 3H), 4.48- 4.23 (m, 2H), 4.13-3.98 (m, 4H), 3.66-3.57 (m, 5H), 3.43-3.36 (m, 2H), 3.17 (d, J = 11.6 Hz, 3H), 2.86 (q, J = 12.4 Hz, 3H), 2.63-2.54 (m, 1H), 2.37 (qd, J = 13.4, 4.6 Hz, 1H), 2.22 (d, J = 11.6 Hz, 2H), 1.98 (ddd, J = 9.0, 6.7, 4.4 Hz, 1H), 1.80 (dq, J = 9.5, 5.4, 4.7
1H NMR (400 MHz, DMSO-d6δ 11.75 (s, 1H),δ 10.99 (s, 1H), 10.00 (s, 1H), 9.18 (s, 1H), 8.39-8.28 (m, 3H), 8.20 (d, J = 1.4 Hz, 1H), 8.05 (s, 3H), 7.93- 7.78 (m, 4H), 7.67 (dd, J = 7.9, 2.8 Hz, 2H), 7.51 (s, 1H), 7.45 (d, J = 7.9 Hz, 1H), 7.28 (t, J = 8.0 Hz, 1H), 7.05 (s, 2H), 6.95 (dd, J = 7.7, 1.6 Hz, 1H), 5.10 (dd, J = 13.2, 5.1 Hz, 1H), 4.58 (d, J = 6.4 Hz, 2H), 4.45-4.25 (m, 2H), 4.05 (d, J = 15.1 Hz, 5H), 3.64-3.35 (m, 8H), 2.87 (dt, J = 28.0, 12.5 Hz, 4H), 2.59 (d, J = 17.2 Hz, 3H), 2.44-2.29 (m, 1H), 2.21 (s, 1H), 2.06-1.89 (m, 2H), 1.73 (s, 5H), 1.37 (s, 3H).
1H NMR (400 MHz, DMSO-d6): δ 11.74 (s, 1H), 10.97 (s, 1H), 10.22 (s, 1H), 9.32 (s, 1H), 8.38 (s, 5H), 8.19 (s, 1H), 8.03-7.99 (m, 1H), 7.80-7.60 (m, 6H), 7.53-7.45 (m, 2H), 7.32-7.28 (m, 1H), 7.18-7.14 (m, 1H), 7.00-6.98 (m, 1H), 5.11-5.08 (m, 1H), 4.60-4.59 (m, 2H), 4.45-4.41 (m, 1H), 4.32-4.27 (m, 1H), 3.68-3.66 (m, 5H), 3.51-3.39 (m, 5H), 3.23-3.20 (m, 2H), 2.94-2.78 (m, 3H), 2.61-2.57 (m, 1H), 2.39-2.27 (m, 3H), 1.96-1.72 (m, 8H), 1.38 (s, 3H), 1.23 (s, 1H).
1H NMR (400 MHz, DMSO-d6) δ 11.19 (s, 1H), 10.99 (s, 1H), 10.05 (s, 1H), 9.42 (t, J = 6.4 Hz, 1H), 8.47-8.19 (m, 5H), 8.07 (d, J = 7.7 Hz, 1H), 7.98- 7.67 (m, 6H), 7.59-7.41 (m, 2H), 7.28 (t, J = 8.0 Hz, 1H), 7.16-6.92 (m, 3H), 5.95 (d, J = 2.8 Hz, 1H), 5.10 (dd, J = 13.3, 5.1 Hz, 1H), 4.71-4.25 (m, 4H), 4.19-3.87 (m, 6H), 3.48-3.35 (m, 3H), 3.21 (d, J = 10.8 Hz, 1H), 3.11-2.80 (m, 4H), 2.61 (s, 2H), 2.43-2.19 (m, 3H), 2.07-1.69 (m, 6H), 1.37 (s, 3H).
1H NMR (400 MHz, DMSO-d6) δ 11.19 (s, 1H), 10.99 (s, 1H), 10.05 (s, 1H), 9.42 (t, J = 6.4 Hz, 1H), 8.46-8.17 (m, 5H), 8.07 (d, J = 7.7 Hz, 1H), 8.00- 7.64 (m, 6H), 7.62-7.38 (m, 2H), 7.28 (t, J = 8.0 Hz, 1H), 7.16-6.92 (m, 3H), 5.95 (d, J = 2.8 Hz, 1H), 5.10 (dd, J = 13.3, 5.1 Hz, 1H), 4.60 (d, J = 6.4 Hz, 2H), 4.52-4.23 (m, 2H), 4.20-3.88 (m, 6H), 3.77 (s, 1H), 3.45-3.35 (m, 3H), 3.21 (d, J = 10.8 Hz, 1H), 3.08-2.81 (m, 4H), 2.59 (d, J = 17.7 Hz, 2H), 2.44- 2.17 (m, 3H), 1.99 (ddd, J = 11.3, 6.6, 4.1 Hz, 1H), 1.78 (dtd, J = 24.5, 13.7, 11.9, 6.6 Hz, 6H), 1.37 (s, 3H).
1H NMR (400 MHz, DMSO-d6) δ 11.05 (s, 1H), 10.99 (s, 1H), 10.03 (s, 1H), 9.38 (t, J = 6.3 Hz, 1H), 8.67 (s, 1H), 8.39 (d, J = 1.5 Hz, 1H), 8.27 (s, 2H), 8.19 (d, J = 1.4 Hz, 1H), 8.04 (dd, J = 12.1, 1.9 Hz, 1H), 7.87 (d, J = 8.6 Hz, 2H), 7.78 (t, J = 2.0 Hz, 1H), 7.72- 7.64 (m, 2H), 7.55 (s, 1H), 7.48 (d, J = 8.1 Hz, 1H), 7.28 (t, J = 8.0 Hz, 1H), 7.07 (d, J = 8.9 Hz, 2H), 6.99-6.92 (m, 1H), 6.61 (s, 1H), 5.11 (dd, J = 13.3, 5.0 Hz, 1H), 4.58 (d, J = 6.3 Hz, 2H), 4.45 (d, J = 17.4 Hz, 2H), 4.30 (d, J = 17.3 Hz, 1H), 3.86 (s, 3H), 3.76 (s, 1H), 3.57-3.48 (m, 1H), 3.45-3.35 (m, 2H), 3.19 (d, J = 23.7 Hz, 2H), 3.00-2.80 (m, 5H), 2.75 (d, J = 21.3 Hz, 1H), 2.59 (d, J = 16.6 Hz, 1H), 2.42-2.13 (m, 4H), 2.05-1.93 (m, 2H), 1.78 (dd, J = 22.2, 13.5 Hz, 5H), 1.37 (s, 3H).
1H NMR (400 MHz, DMSO-d6) δ 11.44 (s, 1H), 10.99 (s, 1H), 10.31 (s, 1H), 9.50 (t, J = 6.4 Hz, 1H), 8.76 (dd, J = 33.2, 2.3 Hz, 2H), 8.51-8.04 (m, 9H), 7.81-7.41 (m, 6H), 7.37-7.17 (m, 2H), 6.98 (d, J = 7.8 Hz, 1H), 6.51 (s, 1H), 5.65 (dd, J = 48.9, 17.1 Hz, 1H), 5.17-4.95 (m, 2H), 4.68 (dd, J = 58.6, 9.8 Hz, 4H), 4.43 (d, J = 17.4 Hz, 2H), 3.79 (s, 1H), 3.40 (dt, J = 13.3, 4.8 Hz,
1H NMR (400 MHz, DMSO-d6) δ 12.37 (s, 1H), 10.99 (s, 1H), 10.22 (s, 1H), 9.53 (t, J = 6.4 Hz, 1H), 8.86 (d, J = 2.1 Hz, 1H), 8.39 (d, J = 1.5 Hz, 1H), 8.32 (s, 3H), 8.24-8.15 (m, 2H), 8.09 (d, J = 8.2 Hz, 1H), 7.83-7.74 (m, 3H), 7.69 (t, J = 7.9 Hz, 2H), 7.55 (s, 1H), 7.48 (d, J = 7.9 Hz, 1H), 7.30 (t, J = 8.0
1H NMR (400 MHz, DMSO-d6) δ 11.28 (s, 1H), 10.99 (s, 1H), 10.06 (s, 1H), 9.50 (t, J = 6.4 Hz, 1H), 8.80 (d, J = 2.2 Hz, 1H), 8.39 (d, J = 1.5 Hz, 1H), 8.28-8.20 (m, 3H), 8.19 (d, J = 1.4 Hz, 1H), 8.11 (dd, J = 8.3, 2.2 Hz, 1H), 8.06 (d, J = 8.2 Hz, 1H), 7.88 (d, J = 8.6 Hz, 2H), 7.77 (d, J = 2.0 Hz, 1H), 7.69 (dd, J = 10.2, 7.8 Hz, 2H), 7.54 (s, 1H), 7.47 (d, J = 7.9 Hz, 1H), 7.28 (t, J = 8.0 Hz, 1H), 7.09 (d, J = 8.7 Hz, 2H), 6.95 (d,
1H NMR (400 MHz, DMSO-d6) δ 11.14 (s, 1H), 10.99 (s, 1H), 10.21 (s, 1H), 9.50 (t, J = 6.4 Hz, 1H), 8.81 (d, J = 2.1 Hz, 1H), 8.40 (d, J = 1.4 Hz, 1H), 8.28-8.00 (m, 6H), 7.87-7.62 (m, 5H), 7.59-7.42 (m, 2H), 7.30 (t, J = 8.0 Hz, 1H), 7.17 (t, J = 8.7 Hz, 1H), 6.98 (d, J = 7.8 Hz, 1H), 6.52 (s, 1H), 5.10 (dd, J = 13.2, 5.0 Hz, 1H), 4.61 (d, J = 6.3 Hz, 2H), 4.48-4.26 (m, 2H), 4.19 (d, J = 107.0 Hz, 2H), 4.00 (s, 2H),
1H NMR (400 MHz, DMSO-d6) δ 11.02 (s, 1H), 10.21 (s, 1H), 9.43 ((t, J = 6.4 Hz, 1H), 8.73 (s, 1H), 8.4 (s, 1H),8.49-8.35 (m, 3H), 8.19-8.08 (m, 2H), 7.85-7.64 (m, 5H), 7.53 (s, 1H), 7.29 (t, J = 8.0 Hz, 1H), 7.13 (d, J = 8.3 Hz, 1H), 7.00-6.93 (m, 1H), 6.6 (s, 1H), 5.12 (dd, J = 13.3, 5.1 Hz, 1H), 4.61 (d, J = 6.4 Hz, 2H), 4.46-4.26 (m, 2H), 4.09-3.94 (m, 4H), 3.54-3.19 (m, 6H), 3.10 (t, J = 12.9 Hz, 1H), 2.76 (t, J = 11.6 Hz, 2H), , 2.44-2.21 (m, 6H), 2.10-1.94 (m, 4H), 1.89-1.68 (m, 4H), 1.38 (s, 3H).
1H NMR (400 MHz, DMSO-d6) δ 11.19 (s, 1H), 11.00 (s, 1H), 10.21 (s, 1H), 9.38 (d, J = 6.6 Hz, 1H), 8.68 (s, 1H), 8.39 (d, J = 1.4 Hz, 1H), 8.30 (s, 3H), 8.20 (d, J = 1.3 Hz, 1H), 8.10- 8.02 (m, 1H), 7.83-7.64 (m, 5H), 7.55 (s, 1H), 7.48 (d, J = 8.3 Hz, 1H), 7.38- 7.22 (m, 2H), 7.16 (dd, J = 18.9, 10.0 Hz, 1H), 7.03-6.93 (m, 1H), 6.63 (s, 1H), 5.11 (dd, J = 13.3, 5.0 Hz, 1H), 4.66-4.25 (m, 4H), 4.13-3.75 (m, 2H), 3.73-3.60 (m, 2H), 3.55-3.34 (m, 2H), 3.23 (d, J = 10.5 Hz, 1H), 3.06-2.76 (m, 5H), 2.59 (d, J = 17.0 Hz, 1H), 2.42-2.11 (m, 2H), 1.97 (d, J = 10.5 Hz, 3H), 1.85-1.65 (m, 4H), 1.37 (s, 3H), 1.24 (d, J = 9.3 Hz, 1H).
1H NMR (400 MHz, DMSO-d6) δ 11.85 (s, 1H), 10.99 (s, 1H), 10.44 (s, 1H), 10.13 (d, J = 37.0 Hz, 1H), 9.50 (t, J = 6.4 Hz, 1H), 8.81 (d, J = 2.4 Hz, 1H), 8.49-8.30 (m, 4H), 8.19-8.15 (m, 1H), 8.15-8.04 (m, 2H), 7.68 (d, J = 7.8 Hz, 1H), 7.62-7.51 (m, 3H), 7.47 (d, J = 7.8 Hz, 1H), 7.24 (td, J = 8.1, 2.5 Hz, 1H), 6.95-6.86 (m, 1H), 6.50 (s, 1H), 5.93-5.62 (m, 2H), 5.10
1H NMR (400 MHz, DMSO-d6) δ 11.32 (s, 1H), 10.99 (s, 1H), 10.18 (s, 1H), 9.50 (t, J = 6.4 Hz, 1H), 8.80 (d, J = 2.2 Hz, 1H), 8.41-8.31 (m, 4H), 8.19 (d, J = 1.4 Hz, 1H), 8.12 (dd, J = 8.3, 2.2 Hz, 1H), 8.06 (d, J = 8.2 Hz, 1H), 7.70-7.66 (m, 2H), 7.66-7.61 (m, 1H), 7.54 (s, 1H), 7.47 (d, J = 7.9 Hz, 1H), 7.41 (d, J = 8.3 Hz, 1H), 7.27 (t, J = 8.0 Hz, 1H), 7.04-6.91 (m, 3H),
1H NMR (400 MHz, DMSO-d6) δ 11.17 (s, 1H), 10.99 (s, 1H), 10.16 (s, 1H), 9.54-9.47 (m, 1H), 8.82 (d, J = 2.1 Hz, 1H), 8.39 (d, J = 1.5 Hz, 1H), 8.30 (s, 3H), 8.20 (d, J = 1.4 Hz, 1H), 8.13 (dd, J = 8.2, 2.3 Hz, 1H), 8.07 (d, J = 8.2 Hz, 1H), 7.82-7.74 (m, 3H), 7.69 (dd, J = 8.4, 5.0 Hz, 2H), 7.54 (s, 1H), 7.47 (d, J = 7.9 Hz, 1H), 7.29 (t, J = 8.0 Hz, 1H), 7.12 (d, J = 8.3 Hz, 1H),
1H NMR (400 MHz, DMSO-d6) δ 11.00 (s, 1H), 10.41 (s, 1H), 8.51 (t, J = 6.2 Hz, 1H), 8.42-8.29 (m, 4H), 8.21 (d, J = 1.3 Hz, 1H), 8.10-8.01 (m, 2H), 7.96-7.89 (m, 3H), 7.87 (d, J = 8.2 Hz, 2H), 7.78 (d, J = 2.0 Hz, 1H), 7.74 (dd, J = 7.8, 2.1 Hz, 1H), 7.68 (d, J = 7.8 Hz, 1H), 7.46 (s, 1H), 7.39 (dd, J = 8.7, 4.4 Hz, 2H), 7.35-7.28 (m, 1H), 7.03- 6.97 (m, 1H), 5.11 (dd, J = 13.3, 5.1 Hz, 1H), 4.49-4.26 (m, 5H), 4.05 (dt, J = 13.9, 4.9 Hz, 2H), 3.61 (s, 5H), 3.41 (ddd, J = 13.6, 9.4, 3.6 Hz, 2H), 2.91 (ddd, J = 17.8, 13.7, 5.3 Hz, 1H), 2.71- 2.53 (m, 1H), 2.41 (td, J = 12.1, 4.0 Hz, 2H), 2.26 (d, J = 9.3 Hz, 1H), 2.17
1H NMR (400 MHz, DMSO-d6) δ 11.16 (s, 1H), 11.00 (s, 1H), 10.27 (s, 1H), 9.38 (t, J = 6.3 Hz, 1H), 8.67 (s, 1H), 8.39 (d, J = 1.5 Hz, 1H), 8.28 (s, 2H), 8.20 (d, J = 1.4 Hz, 1H), 8.07- 8.00 (m, 1H), 7.75 (t, J = 2.0 Hz, 1H), 7.70 (d, J = 7.9 Hz, 2H), 7.55 (s, 1H), 7.48 (d, J = 7.9 Hz, 1H), 7.30 (t, J = 8.0 Hz, 1H), 7.18 (d, J = 8.9 Hz, 1H), 7.01- 6.94 (m, 1H), 6.61 (s, 1H), 5.11 (dd, J = 13.4, 5.1 Hz, 1H), 4.67 (d, J = 13.1
1H NMR (400 MHz, DMSO-d6) δ 11.16 (s, 1H), 10.99 (s, 1H), 10.31 (s, 1H), 9.49 (t, J = 6.4 Hz, 1H), 8.80 (d, J = 2.1 Hz, 1H), 8.73 (d, J = 1.1 Hz, 1H), 8.45-8.35 (m, 2H), 8.27 (s, 3H), 8.20 (d, J = 1.3 Hz, 1H), 8.14-8.09 (m, 1H), 8.06 (d, J = 8.2 Hz, 1H), 7.91 (t, J = 1.9 Hz, 1H), 7.80-7.64 (m, 2H), 7.58- 7.43 (m, 2H), 7.29 (t, J = 8.0 Hz, 1H), 7.00-6.93 (m, 1H), 6.51 (s, 1H), 5.10
1H NMR (400 MHz, DMSO-d6) δ 10.99 (s, 1H), 10.87 (s, 1H), 10.50 (s, 1H), 9.50 (t, J = 6.4 Hz, 1H), 9.06 (d, J = 2.3 Hz, 1H), 8.83 (s, 1H), 8.47-8.03 (m, 10H), 7.83-7.68 (m, 4H), 7.61- 7.30 (m, 3H), 7.08-6.83 (m, 2H), 6.54 (s, 1H), 5.32 (t, J = 4.8 Hz, 1H), 5.10 (dd, J = 13.2, 5.1 Hz, 1H), 4.73-4.56 (m, 3H), 4.51-4.25 (m, 3H), 4.05 (d, J = 14.5 Hz, 6H), 3.38 (s, 4H), 3.11- 2.56 (m, 3H), 2.15-1.68 (m, 7H), 1.23 (s, 3H).
1H NMR (400 MHz, DMSO-d6) δ 11.80 (s, 1H), 11.00 (s, 1H), 10.10- 10.01 (m, 2H), 8.51 (m, 1H), 8.20-7.75 (m, 6H), 7.70-7.55 (m, 4H), 7.47-7.12 (m, 4H), 6.99-6.95 (m, 1H), 5.11 (dd, J = 13.3, 5.1 Hz, 1H), 4.59 (d, J = 5.8 Hz, 2H), 4.49-4.27 (m, 2H), 4.08- 3.94 (m, 4H), 3.77 (s, 1H),3.40 (s,3H), 3.46-3.21 (m, 6H), 3.07-2.97 (m, 1H), 2.91-2.69 (m, 4H), 2.64-2.55 (m, 1H), 2.44-2.20 (m, 6H), 2.06- 1.93 (m, 3H), 1.87-1.69 (m, 4H)
1H NMR (400 MHz, DMSO-d6) δ 11.83 (s, 1H), 10.99 (s, 1H), 10.51 (s, 1H), 9.33 (s, 1H), 8.72 (d, J = 2.4 Hz, 1H), 8.46-8.25 (m, 6H), 8.20 (d, J = 1.3 Hz, 1H), 8.00 (d, J = 8.4 Hz, 1H), 7.77-7.55 (m, 4H), 7.52 (s, 1H), 7.49- 7.40 (m, 1H), 7.33 (dt, J = 16.3, 8.9 Hz, 2H), 6.99 (dt, J = 7.7, 1.5 Hz, 1H), 5.10 (dd, J = 13.3, 5.1 Hz, 1H), 4.68 (d, J = 13.1 Hz, 2H), 4.59 (d, J = 6.2 Hz,
1H NMR (400 MHz, DMSO-d6) δ 11.77 (s, 1H), 10.99 (s, 1H), 10.38 (s, 1H), 9.61 (t, J = 6.5 Hz, 1H), 8.72 (d, J = 2.4 Hz, 1H), 8.43-8.24 (m, 5H), 8.20 (d, J = 1.3 Hz, 1H), 7.95 (d, J = 9.5 Hz, 1H), 7.79-7.62 (m, 3H), 7.58- 7.43 (m, 3H), 7.30 (t, J = 8.0 Hz, 2H), 6.99 (d, J = 7.7 Hz, 1H), 5.10 (dd, J = 13.3, 5.0 Hz, 1H), 4.71-4.57 (m, 2H), 4.45-4.27 (m, 2H), 4.12-3.98 (m,
1H NMR (400 MHz, DMSO-d6) δ 11.00 (s, 1H), 10.90 (s, 1H), 10.13 (s, 1H), 9.39 (d, J = 6.4 Hz, 1H), 8.68 (s, 1H), 8.39 (d, J = 1.5 Hz, 1H), 8.19 (d, J = 1.3 Hz, 2H), 8.05 (d, J = 12.1 Hz, 1H), 7.72 (dd, J = 4.7, 2.7 Hz, 1H), 7.67 (d, J = 15.5 Hz, 1H), 7.62 (d, J = 8.5 Hz, 1H), 7.55 (s, 1H), 7.48 (d, J = 8.3 Hz, 1H), 7.38 (d, J = 8.3 Hz, 1H), 7.27 (t, J = 8.0 Hz, 1H), 6.91 (q, J = 10.6, 9.3 Hz, 3H), 6.61 (s, 1H), 5.11 (dd, J = 13.2, 5.0 Hz, 1H), 4.58 (d, J = 6.3 Hz, 2H), 4.45
1H NMR (400 MHz, DMSO-d6) δ 11.33 (s, 1H), 11.00 (s, 1H), 10.18 (s, 1H), 9.45-9.35 (m, 1H), 8.68 (s, 1H), 8.48-8.28 (m, 4H), 8.20 (d, J = 1.3 Hz, 1H), 8.05 (dd, J = 12.2, 1.7 Hz, 1H), 7.85-7.74 (m, 3H), 7.70 (dd, J = 7.9, 2.5 Hz, 2H), 7.62-7.45 (m, 2H), 7.29 (t, J = 8.0 Hz, 1H), 7.11 (d, J = 8.4 Hz, 1H), 7.03-6.94 (m, 1H), 6.64 (s, 1H), 5.11 (dd, J = 13.3, 5.1 Hz, 1H), 4.59 (d,
1H NMR (400 MHz, DMSO-d6) δ 11.30 (s, 1H), 11.00 (s, 1H), 10.17 (s, 1H), 9.33 (t, J = 7.3, 6.8 Hz, 1H), 8.75 (d, J = 1.9 Hz, 1H), 8.46-8.29 (m, 4H), 8.23-8.15 (m, 2H), 7.86-7.74 (m, 3H), 7.75-7.67 (m, 2H), 7.61-7.45 (m, 2H), 7.29 (t, J = 8.0 Hz, 1H), 7.12 (d, J = 8.4 Hz, 1H), 7.01-6.93 (m, 1H), 6.59 (s, 1H), 5.11 (dd, J = 13.3, 5.1 Hz, 1H), 4.59 (d, J = 6.2 Hz, 2H), 4.50-
1H NMR (400 MHz, DMSO-d6) δ 11.48 (s, 1H), 10.99 (s, 1H), 10.19 (s, 1H), 9.43 (t, J = 6.3 Hz, 1H), 8.51-8.31 (m, 4H), 8.26-7.90 (m, 3H), 7.85-7.67 (m, 5H), 7.59-7.41 (m, 2H), 7.29 (t, J = 8.0 Hz, 1H), 7.20-6.91 (m, 2H), 5.96 (s, 1H), 5.10 (dd, J = 13.3, 5.1 Hz, 1H), 4.61 (d, J = 6.3 Hz, 2H), 4.48-4.26 (m, 2H), 4.09-3.91 (m, 5H), 3.75 (s, 1H), 3.58-3.17 (m, 5H), 3.13-2.82 (m, 2H),
1H NMR (400 MHz, DMSO-d6) δ 11.48 (s, 1H), 10.99 (s, 1H), 10.24 (s, 1H), 9.42 (t, J = 6.3 Hz, 1H), 8.54-8.29 (m, 4H), 8.27-7.85 (m, 3H), 7.84-7.64 (m, 5H), 7.61-7.40 (m, 2H), 7.23 (dt, J = 52.9, 8.3 Hz, 2H), 7.04-6.95 (m, 1H), 5.96 (s, 1H), 5.10 (dd, J = 13.3, 5.1 Hz, 1H), 4.61 (d, J = 6.3 Hz, 2H), 4.52-4.23 (m, 2H), 4.03-3.92 (m, 4H), 3.87-3.63 (m, 3H), 3.59-3.36 (m, 3H), 3.29-2.76
1H NMR (400 MHz, DMSO-d6) δ 11.41 (s, 1H), 11.00 (s, 1H), 10.20 (s, 1H), 9.34 (s, 1H), 8.74 (d, J = 1.9 Hz, 1H), 8.51-8.31 (m, 4H), 8.17 (dd, J = 11.1, 1.6 Hz, 2H), 7.74-7.61 (m, 3H), 7.57 (s, 1H), 7.50 (d, J = 7.9 Hz, 1H), 7.42 (d, J = 8.4 Hz, 1H), 7.27 (t, J = 8.0 Hz, 1H), 7.05 (s, 2H), 6.95 (s, 0H), 6.57 (s, 1H), 5.11 (dd, J = 13.3, 5.1 Hz, 1H), 4.59 (d, J = 6.2 Hz, 2H), 4.46 (d, J =
1H NMR (400 MHz, DMSO-d6) δ 11.41 (s, 1H), 10.99 (s, 1H), 10.18 (s, 1H), 9.42 (t, J = 6.4 Hz, 1H), 8.41- 8.31 (m, 4H), 8.19 (d, J = 1.4 Hz, 1H), 8.07 (d, J = 7.8 Hz, 1H), 7.92 (d, J = 7.7 Hz, 1H), 7.73-7.66 (m, 2H), 7.63 (dd, J = 7.7, 2.1 Hz, 1H), 7.54 (s, 1H), 7.43 (dd, J = 22.5, 8.1 Hz, 2H), 7.27 (t, J = 7.9 Hz, 1H), 6.99 (d, J = 12.1 Hz, 2H), 6.95-6.91 (m, 1H), 5.95 (s, 1H), 5.10
1H NMR (400 MHz, DMSO-d6) δ 11.81 (brs, 1H), 10.99 (s, 1H), 10.50 (s, 1H), 9.70-9.68 (m, 1H), 8.41-8.29 (m, 4H), 8.18 (s, 1H), 8.10-7.90 (m, 3H), 7.80-7.70 (m, 2H), 7.60-7.47 (m, 4H), 7.29-7.27 (m, 1H), 7.00-6.95 (m, 1H), 5.12 (dd, J = 13.3, 5.1 Hz, 1H), 4.62 (d, J = 6.4 Hz, 2H), 4.26-4.11 (m, 3H), 3.96-3.85 (m, 3H), 3.77-3.61 (m, 4H),3.28-3.17 (m, 1H), 3.12-
1H NMR (400 MHz, DMSO-d6) δ 11.80 (brs, 1H), 11.00 (s, 1H), 10.50 (s, 1H), 9.40-9.38 (m, 1H), 8.50-8.40 (m, 5H), 8.23 (s, 1H), 8.15-8.01 (m, 2H), 7.91 (s, 1H), 7.85-7.61 (m, 4H), 7.51 (s, 1H), 7.48-7.46 (m, 1H), 7.31-7.27 (m, 1H), 7.02-6.93 (m, 1H), 6.49 (s, 1H), 5.12 (dd, J = 13.3, 5.1 Hz, 1H), 4.58 (d, J = 6.3 Hz, 2H), 4.49-4.10 (m, 5H), 4.03-3.90 (m, 3H), 3.82-3.73
1H NMR (400 MHz, DMSO-d6): δ 11.71-11.70 (m, 1H), 10.97 (s, 1H), 10.52 (s, 1H), 9.59 (t, J = 6.2 Hz, 1H), 8.65(s, 2H), 8.40 (s,1H), 8.29 (s,3H), 8.21 (d, J = 0.8 Hz, 1H), 7.95 (d, J = 9.6 Hz, 1H), 7.87 (s, 1H), 7.72-7.67 (m, 2H), 7.54-7.46 (m, 3H), 7.30 (t, J = 8 Hz, 1H), 6.99 (d, J = 7.6 Hz, 1H), 5.12-5.07 (m, 1H), 4.65-4.60 (m, 4H), 4.45-4.23 (m, 5H), 3.63-3.50 (m, 6H),
1H NMR (400 MHz, DMSO-d6): δ 11.70-11.67 (m, 1H), 10.97 (s, 1H), 10.77 (s, 1H), 9.27 (t, J = 6.2 Hz, 1H), 8.39-8.32(m, 5H), 8.21 (d, J = 1.2 Hz, 1H), 7.98-7.95 (m, 2H), 7.91-7.89 (m, 1H), 7.80 (d, J = 8 Hz, 1H), 7.67 (d, J = 7.6 Hz, 1H), 7.60-7.51(m, 3H), 7.45 (d, J = 8 Hz, 1H), 7.30 (t, J = 8.2 Hz, 1H), 6.99 (d, J = 8 Hz, 1H), 5.12-5.07 (m, 2H), 4.72 (d, J = 13.2 Hz, 2H), 4.59
1H NMR (400 MHz, DMSO-d6): δ 11.29-11.27 (m, 1H), 10.97 (s, 1H), 10.52 (s, 1H), 9.19 (t, J = 6.6 Hz, 1H), 8.65(s, 2H), 8.40-8.38 (m,2H), 8.22- 8.17 (m,3H), 7.94-7.89 (m, 2H), 7.71- 7.66 (m, 2H), 7.55-7.52 (m, 2H), 7.45 (d, J = 8.4 Hz, 1H), 7.30 (t, J = 7.8 Hz, 1H), 7.17 (s, 1H), 7.04-6.98(m, 1H), 5.12-5.07 (m, 1H), 4.58 (d, J = 6 Hz, 2H), 4.45-4.23 (m, 4H), 4.12-4.03 (m,
1H NMR (400 MHz, DMSO-d6) δ 11.56 (s, 1H), 11.00 (s, 1H), 10.21 (s, 1H), 9.63 (t, J = 6.4 Hz, 1H), 8.53 (s, 1H), 8.49-8.35 (m, 4H), 8.19 (d, J = 1.3 Hz, 1H), 8.08 (s, 1H), 7.85-7.64 (m, 5H), 7.53 (s, 1H), 7.46 (d, J = 7.9 Hz, 1H), 7.29 (t, J = 8.0 Hz, 1H), 7.13 (d, J = 8.3 Hz, 1H), 7.00-6.93 (m, 1H), 6.02 (s, 1H), 5.10 (dd, J = 13.3, 5.1 Hz, 1H), 4.61 (d, J = 6.4 Hz, 2H), 4.46- 4.26 (m, 2H), 4.09-3.94 (m, 4H), 3.75
1H NMR (400 MHz, DMSO-d6) δ 11.19 (s, 1H), 11.00 (s, 1H), 10.19 (s, 1H), 9.29 (t, J = 5.9 Hz, 1H), 8.41- 8.34 (m, 4H), 8.20 (d, J = 1.3 Hz, 1H), 7.96 (d, J = 8.1 Hz, 2H), 7.81-7.75 (m, 3H), 7.70 (dd, J = 8.6, 5.7 Hz, 2H), 7.63 (d, J = 8.2 Hz, 2H), 7.55 (s, 1H), 7.47 (d, J = 7.9 Hz, 1H), 7.29 (t, J = 8.0 Hz, 1H), 7.12 (d, J = 8.3 Hz, 1H), 6.99- 6.95 (m, 1H), 6.38 (s, 1H), 5.11 (dd, J =
1H NMR (400 MHz, DMSO-d6) δ 11.02 (s, 1H), 10.21 (s, 1H), 9.43 ((t, J = 6.4 Hz, 1H), 8.73 (s, 1H), 8.4 (s, 1H), 8.49-8.35 (m, 3H), 8.19-8.08 (m, 2H), 7.85-7.64 (m, 5H), 7.53 (s, 1H), 7.29 (t, J = 8.0 Hz, 1H), 7.13 (d, J = 8.3 Hz, 1H), 7.00-6.93 (m, 1H), 6.6 (s, 1H), 5.12 (dd, J = 13.3, 5.1 Hz, 1H), 4.62 (d, J = 6.4 Hz, 2H), 4.26-4.11 (m, 3H), 3.96-3.85 (m, 3H), 3.77-3.61
1H NMR (400 MHz, DMSO-d6) δ 11.02 (s, 1H), 10.21 (s, 1H), 9.43 ((t, J = 6.4 Hz, 1H), 8.73 (s, 1H), 8.4 (s, 1H), 8.49-8.35 (m, 3H), 8.19-8.08 (m, 2H), 7.85-7.64 (m, 5H), 7.53 (s, 1H), 7.29 (t, J = 8.0 Hz, 1H), 7.13 (d, J = 8.3 Hz, 1H), 7.00-6.93 (m, 1H), 6.6 (s, 1H), 5.12 (dd, J = 13.3, 5.1 Hz, 1H), 4.61 (d, J = 6.4 Hz, 2H), 4.46-4.26 (m, 2H), 4.09-3.94 (m, 4H), 3.54-3.19
1H NMR (400 MHz, DMSO-d6) δ 11.27 (s, 1H), 11.00 (s, 1H), 10.21 (s, 1H), 9.49 (d, J = 5.6 Hz, 1H), 8.94 (d, J = 2.0 Hz, 1H), 8.40 (d, J = 1.5 Hz, 1H), 8.28 (s, 1H), 8.23-8.11 (m, 3H), 7.76 (dd, J = 4.2, 2.3 Hz, 2H), 7.70 (dd, J = 8.1, 3.6 Hz, 2H), 7.56 (s, 1H), 7.48 (d, J = 8.0 Hz, 1H), 7.30 (t, J = 8.0 Hz, 1H), 7.18 (t, J = 8.6 Hz, 1H), 7.01-6.95 (m, 1H), 6.04 (s, 1H), 5.11 (dd, J = 13.3, 5.1
1H NMR (400 MHz, DMSO-d6) δ 11.48 (s, 1H), 10.99 (s, 1H), 10.25 (s, 1H), 9.44 (t, J = 5.9 Hz, 1H), 8.39 (d, J = 1.4 Hz, 1H), 8.30 (s, 2H), 8.19 (d, J = 1.3 Hz, 1H), 8.04 (d, J = 1.6 Hz, 1H), 7.92 (dd, J = 8.0, 1.7 Hz, 1H), 7.86- 7.64 (m, 5H), 7.54 (s, 1H), 7.44 (dd, J = 24.7, 7.9 Hz, 2H), 7.29 (t, J = 7.9 Hz, 1H), 7.17 (t, J = 8.7 Hz, 1H), 7.03- 6.93 (m, 1H), 5.84 (s, 1H), 5.14-5.04
1H NMR (400 MHz, DMSO-d6) δ 11.43 (s, 1H), 10.99 (s, 1H), 10.23 (s, 1H), 9.63 (t, J = 6.3 Hz, 1H), 8.53 (s, 1H), 8.40 (d, J = 1.5 Hz, 1H), 8.24 (s, 3H), 8.19 (d, J = 1.3 Hz, 1H), 8.08 (s, 1H), 7.83-7.74 (m, 3H), 7.69 (dd, J = 10.3, 7.8 Hz, 2H), 7.56-7.43 (m, 2H), 7.30 (t, J = 8.0 Hz, 1H), 7.18 (t, J = 8.7 Hz, 1H), 7.02-6.94 (m, 1H), 6.03 (s, 1H), 5.10 (dd, J = 13.3, 5.1 Hz, 1H), 4.61 (d, J = 6.3 Hz, 2H), 4.33-4.10 (m, 4H), 3.97 (s, 2H), 3.92 (d, J = 9.0 Hz, 1H), 3.74 (d, J = 8.6 Hz, 1H), 3.67 (t,
1H NMR (400 MHz, DMSO-d6) δ 11.81 (s, 1H), 10.99 (s, 1H), 10.27 (s, 1H), 9.49-9.42 (m, 1H), 8.41-8.29 (m, 4H), 8.18 (d, J = 1.4 Hz, 1H), 7.94 (d, J = 7.9 Hz, 1H), 7.83-7.66 (m, 6H), 7.54 (s, 1H), 7.47 (d, J = 7.6 Hz, 1H), 7.29 (t, J = 8.0 Hz, 1H), 7.17 (t, J = 8.7 Hz, 1H), 7.00-6.95 (m, 1H), 5.79 (s, 1H), 5.10 (dd, J = 13.3, 5.1 Hz, 1H), 4.62 (d, J = 6.4 Hz, 2H), 4.47-4.26 (m,
1H NMR (400 MHz, DMSO-d6) δ 11.50 (s, 1H), 11.00 (s, 1H), 10.26 (s, 1H), 9.36 (t, J = 6.3 Hz, 1H), 8.63 (d, J = 2.0 Hz, 1H), 8.43-8.25 (m, 4H), 8.19 (d, J = 1.3 Hz, 1H), 7.91 (d, J = 2.2 Hz, 1H), 7.85-7.66 (m, 5H), 7.55 (s, 1H), 7.48 (d, J = 7.8 Hz, 1H), 7.29 (t, J = 8.0 Hz, 1H), 7.16 (t, J = 8.6 Hz, 1H), 7.02-6.93 (m, 1H), 6.49 (s, 1H), 5.10 (dd, J = 13.3, 5.1 Hz, 1H), 4.58 (d, J =
1H NMR (400 MHz, DMSO-d6) δ 11.63 (s, 1H), 10.99 (s, 1H), 10.26 (s, 1H), 9.42 (d, J = 6.3 Hz, 1H), 8.35 (d, J = 31.8 Hz, 3H), 8.19 (d, J = 1.2 Hz, 1H), 8.07 (d, J = 7.7 Hz, 1H), 7.92 (d, J = 7.7 Hz, 1H), 7.83-7.76 (m, 2H), 7.70 (t, J = 1.7 Hz, 3H), 7.54 (s, 1H), 7.46 (d, J = 8.2 Hz, 1H), 7.29 (t, J = 8.0 Hz, 1H), 7.17 (t, J = 8.6 Hz, 1H), 6.97 (d, J = 7.7 Hz, 1H), 5.95 (s, 1H), 5.10
1H NMR (400 MHz, DMSO-d6) δ 11.39 (s, 1H), 10.99 (s, 1H), 10.23 (s, 1H), 9.42-9.35 (m, 1H), 8.68 (s, 1H), 8.40 (d, J = 1.5 Hz, 1H), 8.28-8.18 (m, 3H), 8.04 (dd, J = 12.2, 1.8 Hz, 1H), 7.83-7.65 (m, 5H), 7.55 (s, 1H), 7.48 (d, J = 8.0 Hz, 1H), 7.33-7.26 (m, 1H), 7.21-7.13 (m, 1H), 7.00-6.95 (m, 1H), 6.63 (s, 1H), 5.11 (dd, J = 13.3, 5.1 Hz, 1H), 4.45 (d, J = 17.3 Hz, 2H), 4.33 (s, 1H), 4.26-4.14 (m, 3H), 4.00 (s,
1H NMR (400 MHz, DMSO-d6) δ 11.12 (s, 1H), 11.00 (s, 1H), 10.20 (s, 1H), 9.46 (t, J = 6.4 Hz, 1H), 8.39 (d, J = 1.5 Hz, 1H), 8.27 (s, 3H), 8.22-8.15 (m, 2H), 8.02 (dd, J = 7.7, 1.8 Hz, 1H), 7.82-7.78 (m, 1H), 7.76 (d, J = 2.5 Hz, 2H), 7.69 (dd, J = 8.2, 4.0 Hz, 2H), 7.54 (s, 1H), 7.46 (d, J = 7.9 Hz, 1H), 7.30 (t, J = 8.0 Hz, 1H), 7.17 (t, J = 8.7 Hz, 1H), 7.02-6.96 (m, 1H), 6.34 (s, 1H),
1H NMR (400 MHz, DMSO-d6) δ 10.99 (s, 1H), 10.93 (s, 1H), 10.13 (s, 1H), 9.45 (t, J = 6.3 Hz, 1H), 8.39 (d, J = 1.5 Hz, 1H), 8.26-8.14 (m, 4H), 8.02 (dd, J = 7.7, 1.9 Hz, 1H), 7.74- 7.66 (m, 2H), 7.62 (d, J = 8.6 Hz, 1H), 7.53 (s, 1H), 7.46 (d, J = 7.9 Hz, 1H), 7.38 (d, J = 8.4 Hz, 1H), 7.27 (t, J = 8.0 Hz, 1H), 6.97-6.86 (m, 3H), 6.33 (s, 1H), 5.10 (dd, J = 13.2, 5.1 Hz, 1H),
1H NMR (400 MHz, DMSO-d6) δ 11.33 (s, 1H), 10.99 (s, 1H), 10.17 (s, 1H), 9.46 (t, J = 6.4 Hz, 1H), 8.45- 8.30 (m, 4H), 8.23-7.97 (m, 3H), 7.87- 7.64 (m, 5H), 7.58-7.43 (m, 2H), 7.29 (t, J = 8.0 Hz, 1H), 7.12 (d, J = 8.4 Hz, 1H), 7.01-6.94 (m, 1H), 6.35 (s, 1H), 5.10 (dd, J = 13.3, 5.0 Hz, 1H), 4.59 (d, J = 6.4 Hz, 2H), 4.46 (s, 1H), 4.41 (s, 1H), 4.29 (d, J = 17.4 Hz, 1H),
1H NMR (400 MHz, DMSO-d6) δ 11.36 (s, 1H), 11.00 (s, 1H), 10.22 (s, 1H), 9.25-9.15 (m, 1H), 8.40 (d, J = 1.5 Hz, 1H), 8.32-8.16 (m, 5H), 7.84- 7.67 (m, 6H), 7.57 (s, 1H), 7.50 (d, J = 7.9 Hz, 1H), 7.30 (t, J = 8.0 Hz, 1H), 7.17 (t, J = 8.7 Hz, 1H), 7.02-6.96 (m, 1H), 6.88 (s, 1H), 5.11 (dd, J = 13.3, 5.1 Hz, 1H), 4.60 (d, J = 5.9 Hz, 2H), 4.51- 4.28 (m, 2H), 4.28-4.11 (m, 4H), 4.07-3.85 (m, 2H), 3.79 (d, J = 10.8
1H NMR (400 MHz, DMSO-d6) δ 11.41 (s, 1H), 10.99 (s, 1H), 9.99 (s, 1H), 9.50 (t, J = 6.3 Hz, 1H), 8.78 (s, 1H), 8.39 (d, J = 1.4 Hz, 1H), 8.24 (s, 3H), 8.17 (d, J = 1.3 Hz, 1H), 8.12- 8.03 (m, 2H), 7.68 (d, J = 7.8 Hz, 1H), 7.53 (t, J = 7.3 Hz, 3H), 7.47 (d, J = 7.8 Hz, 1H), 7.23 (t, J = 7.9 Hz, 1H), 6.90 (d, J = 7.7 Hz, 1H), 6.45 (s, 1H), 5.10 (dd, J = 13.3, 5.1 Hz, 1H),4.69-4.55 (m, 2H), 4.43 (d, J = 17.4 Hz, 2H), 4.29
1H NMR (400 MHz, DMSO-d6) δ 11.01 (s, 1H), 10.2-10.1(m, 1H), 9.49 (m, 1H), 8.80 (m, 1H), 8.41-8.21 (m, 5H), 8.15 (s, 1H),8.10-7.94 (m, 2H), 7.70 (m, 1H), 7.64-7.42 (m, 3H), 7.29- 7.17 (m, 1H), 7.00-6.95 (m, 1H), 6.57 (s, 1H), 5.12 (dd, J = 13.3, 5.1 Hz, 1H), 4.62 (d, J = 6.4 Hz, 2H), 4.47-4.26 (m, 2H), 4.26-4.11 (m, 3H), 3.96-3.85 (m,2H), 3.77-3.61 (m, 4H), 3.49 (s, 1H), 3.34(m, 3H), 3.12-2.98 (m, 4H),
1H NMR (400 MHz, DMSO-d6) δ 11.00 (s, 1H), 10.94 (s, 1H), 10.26 (s, 1H), 9.50 (t, J = 6.4 Hz, 1H), 8.79 (d, J = 2.2 Hz, 1H), 8.40 (d, J = 1.5 Hz, 1H), 8.28-8.17 (m, 3H), 8.15-8.03 (m, 2H), 7.68 (d, J = 7.8 Hz, 1H), 7.61- 7.52 (m, 3H), 7.47 (d, J = 7.9 Hz, 1H), 7.25 (t, J = 8.0 Hz, 1H), 6.92 (d, J = 7.6 Hz, 1H), 6.46 (s, 1H), 5.10 (dd, J = 13.3, 5.1 Hz, 1H), 4.62 (s, 2H), 4.45 (s, 1H), 4.41 (s, 1H), 4.31 (s, 1H), 4.26 (d,
1H NMR (400 MHz, DMSO-d6) δ 11.58 (s, 1H), 11.00 (s, 1H), 10.19 (s, 1H), 9.41 (s, 1H), 8.61 (s, 1H), 8.39 (d, J = 1.5 Hz, 1H), 8.30 (s, 1H), 8.22- 8.17 (m, 2H), 7.69 (t, J = 7.6 Hz, 1H), 7.55 (t, J = 10.2 Hz, 3H), 7.47 (d, J = 7.9 Hz, 1H), 7.25 (t, J = 8.0 Hz, 1H), 6.92 (d, J = 8.1 Hz, 1H), 5.11 (dd, J = 13.3, 5.1 Hz, 1H), 4.57 (s, 2H), 4.44 (d, J = 17.4 Hz, 2H), 4.32 (s, 1H), 4.28 (s, 1H), 4.21 (d, J = 5.8 Hz, 2H), 4.15 (d, J = 5.0 Hz, 3H), 4.08 (s, 1H), 4.00 (d, J =
1H NMR (400 MHz, DMSO-d6) δ 11.33 (s, 1H), 10.99 (s, 1H), 10.06 (s, 1H), 9.45 (t, J = 6.4 Hz, 1H), 8.44- 8.30 (m, 4H), 8.24-8.10 (m, 2H), 8.01 (dd, J = 7.7, 1.8 Hz, 1H), 7.88 (d, J = 8.6 Hz, 2H), 7.77 (t, J = 2.0 Hz, 1H), 7.69 (dd, J = 11.3, 8.0 Hz, 2H), 7.53 (s, 1H), 7.46 (d, J = 7.9 Hz, 1H), 7.28 (t, J = 8.0 Hz, 1H), 7.09 (d, J = 8.7 Hz, 2H), 6.95 (dd, J = 8.2, 1.8 Hz, 1H), 6.32 (s,
1H NMR (400 MHz, DMSO-d6) δ 11.41 (s, 1H), 11.01 (s, 1H), 10.24 (s, 1H), 9.30 (t, J = 5.9 Hz, 1H), 8.64 (s, 1H), 8.39 (s, 1H), 8.23 (d, J = 32.7 Hz, 3H), 7.75 (ddd, J = 23.1, 13.2, 7.3 Hz, 6H), 7.59 (s, 1H), 7.51 (d, J = 7.8 Hz, 1H), 7.29 (t, J = 8.0 Hz, 1H), 7.17 (t, J = 8.6 Hz, 1H), 6.98 (d, J = 7.6 Hz, 1H), 6.87 (s, 1H), 5.11 (dd, J = 13.3, 5.0 Hz, 1H), 4.59 (d, J = 5.8 Hz, 2H), 4.51- 4.29 (m, 6H), 4.02 (s, 2H), 3.92 (d, J =
1H NMR (400 MHz, DMSO-d6) δ 11.92 (s, 1H), 10.99 (s, 1H), 10.29 (s, 1H), 9.51 (t, J = 6.4 Hz, 1H), 8.80 (d, J = 2.1 Hz, 1H), 8.40 (s, 1H), 8.22 (d, J = 19.0 Hz, 3H), 8.14-8.05 (m, 2H), 7.93 (d, J = 8.1 Hz, 2H), 7.78-7.60 (m, 6H), 7.54 (s, 1H), 7.47 (d, J = 8.1 Hz, 1H), 7.30 (t, J = 8.0 Hz, 1H), 6.98 (d, J = 7.7 Hz, 1H), 6.50 (s, 1H), 5.10 (dd, J = 13.3, 5.1 Hz, 1H), 4.61 (d, J = 6.4 Hz, 2H), 4.46 (s, 1H), 4.41 (s, 1H), 4.31 (s, 1H), 4.21-4.16 (m, 3H), 3.98-3.90
1H NMR (400 MHz, DMSO-d6) δ 11.73 (s, 1H), 10.99 (s, 1H), 10.39 (s, 1H), 9.45 (t, J = 6.4 Hz, 1H), 8.72 (d, J = 2.3 Hz, 1H), 8.48-8.25 (m, 6H), 8.20 (d, J = 1.3 Hz, 1H), 8.02 (s, 1H), 7.78-7.60 (m, 3H), 7.51 (s, 1H), 7.47- 7.40 (m, 1H), 7.29 (q, J = 8.3 Hz, 2H), 7.03-6.94 (m, 1H), 5.09 (dd, J = 13.3, 5.1 Hz, 1H), 4.66 (d, J = 13.1 Hz, 2H), 4.58 (d, J = 6.2 Hz, 2H), 4.47-4.20 (m, 2H), 4.19-3.95 (m, 4H), 3.60 (d, J =
1H NMR (400 MHz, DMSO-d6) δ 11.32 (s, 1H), 10.99 (s, 1H), 9.51 (t, J = 6.4 Hz, 1H), 8.81 (d, J = 2.2 Hz, 1H), 8.36 (d, J = 1.5 Hz, 1H), 8.27 (s, 3H), 8.16-8.04 (m, 3H), 7.68 (d, J = 7.8 Hz, 1H), 7.54 (s, 1H), 7.47 (d, J = 7.9 Hz, 1H), 7.21-6.98 (m, 4H), 6.73-6.45 (m, 4H), 5.10 (dd, J = 13.3, 5.1 Hz, 1H), 4.81-4.49 (m, 2H), 4.47-4.26 (m, 2H), 4.26-4.11 (m, 5H), 4.02-3.90
1H NMR (400 MHz, DMSO-d6) δ 11.41 (s, 1H), 11.00 (s, 1H), 10.24 (s, 1H), 9.30 (t, J = 5.9 Hz, 1H), 8.64 (s, 1H), 8.39 (s, 1H), 8.28 (s, 2H), 8.19 (s, 1H), 7.82-7.74 (m, 3H), 7.74-7.67 (m, 3H), 7.59 (s, 1H), 7.51 (d, J = 7.8 Hz, 1H), 7.29 (t, J = 8.0 Hz, 1H), 7.18 (d, J = 8.6 Hz, 1H), 6.98 (d, J = 7.7 Hz, 1H), 6.87 (s, 1H), 5.11 (dd, J = 13.3, 5.0 Hz, 1H), 4.59 (d, J = 5.8 Hz, 2H), 4.47
1H NMR (400 MHz, DMSO-d6) δ 11.01 (s, 1H), 10.2-10.1(m, 1H), 9.49 (m, 1H), 8.80 (m, 1H), 8.41-8.21 (m, 5H), 8.15 (s, 1H),8.10-7.94 (m, 2H), 7.70 (m, 1H), 7.64-7.42 (m, 3H), 7.29- 7.17 (m, 1H), 7.00-6.95 (m, 1H), 6.57 (s, 1H), 5.12 (dd, J = 13.3, 5.1 Hz, 1H), 4.62 (d, J = 6.4 Hz, 2H), 4.47-4.26 (m, 2H), 4.26-4.11 (m, 3H), 3.96-3.85 (m, 3H), 3.77-3.61 (m, 4H), 3.49 (s, 1H), 3.28-3.17 (m, 1H), 3.12-2.98 (m, 4H), 2.96-2.78 (m, 3H), 2.66- 2.54 (m, 4H), 2.44-2.23 (m, 3H), 1.86- 1.75 (m, 2H), 1.70-1.56 (m, 2H), 1.24 (d, J = 6.5 Hz, 3H).
1H NMR (400 MHz, DMSO-d6) δ 11.81 (s, 1H), 10.99 (s, 1H), 10.07 (d, J = 4.0 Hz, 1H), 9.90-9.70 (m, 1H), 8.47-8.26 (m, 4H), 8.17 (d, J = 11.6 Hz, 1H), 7.87 (dd, J = 8.9, 4.5 Hz, 2H), 7.76 (q, J = 1.8 Hz, 1H), 7.69 (tq, J = 8.7, 4.4, 3.8 Hz, 2H), 7.54 (s, 1H), 7.49-7.43 (m, 1H), 7.32-7.25 (m, 1H), 7.10 (d, J = 8.4 Hz, 2H), 6.95 (d, J = 8.1 Hz, 1H), 5.10 (dd, J = 13.3, 5.0 Hz, 1H), 4.46-4.25 (m, 2H), 4.18 (d, J =
1H NMR (400 MHz, DMSO-d6) δ 11.94 (s, 1H), 10.99 (s, 1H), 10.50 (s, 1H), 9.84 (t, J = 6.5 Hz, 1H), 8.72 (d, J = 2.4 Hz, 1H), 8.43-8.31 (m, 5H), 8.22-8.13 (m, 2H), 7.77-7.64 (m, 3H), 7.54 (s, 1H), 7.50-7.42 (m, 1H), 7.33 (dt, J = 15.8, 8.7 Hz, 2H), 6.99 (dt, J = 7.7, 1.4 Hz, 1H), 5.10 (dd, J = 13.3, 5.0 Hz, 1H), 4.29 (d, J = 17.4 Hz,2H), 4.18 (d, J = 13.3 Hz, 2H), 4.09-3.98 (m, 2H), 3.76-3.56 (m, 6H), 3.41 (q,
1H NMR (400 MHz, DMSO-d6) δ 11.92 (s, 1H), 10.99 (s, 1H), 10.23 (s, 1H), 9.85 (t, J = 6.2 Hz, 1H), 8.39 (s, 4H), 8.18 (d, J = 13.4 Hz, 2H), 7.80- 7.64 (m, 5H), 7.54 (s, 1H), 7.47 (d, J = 7.8 Hz, 1H), 7.29 (t, J = 8.0 Hz, 1H), 7.16 (t, J = 9.1 Hz, 1H), 6.98 (d, J = 7.8 Hz, 1H), 5.10 (dd, J = 13.2, 5.0 Hz, 1H), 4.65-4.57 (m, 2H), 4.46-4.28 (m, 2H), 4.22-4.00 (m, 4H), 3.75- 3.61 (m, 6H), 3.44-3.39 (m, 2H), 3.26
1H NMR (400 MHz, DMSO-d6) δ 11.08 (s, 1H), 11.00 (s, 1H), 10.04 (s, 1H), 9.83 (t, J = 6.2 Hz, 1H), 8.39 (d, J = 1.5 Hz, 1H), 8.23-8.15 (m, 2H), 8.10 (s, 3H), 7.77-7.64 (m, 2H), 7.55 (q, J = 10.4, 9.5 Hz, 3H), 7.47 (d, J = 8.1 Hz, 1H), 7.28 (t, J = 8.0 Hz, 1H), 7.03-6.93 (m, 1H), 6.93-6.84 (m, 2H), 5.10 (dd, J = 13.2, 5.0 Hz, 1H), 17.4 Hz, 1H), 4.29 (d, J = 17.4 Hz, 1H), 4.63 (d, J = 6.1 Hz, 2H), 4.43 (d, J =
1H NMR (400 MHz, DMSO-d6) δ 11.78 (s, 1H), 10.99 (s, 1H), 10.19 (s, 1H), 9.46 (t, J = 6.4 Hz, 1H), 8.45 (s, 1H), 8.42-8.34 (m, 4H), 8.19 (d, J = 1.3 Hz, 1H), 8.03 (s, 1H), 7.80 (d, J = 2.1 Hz, 1H), 7.76 (q, J = 2.1 Hz, 2H), 7.72-7.65 (m, 2H), 7.52 (s, 1H), 7.45 (d, J = 7.7 Hz, 1H), 7.29 (t, J = 8.0 Hz, 1H), 7.12 (d, J = 8.4 Hz, 1H), 6.99- 6.93 (m, 1H), 5.10 (dd, J = 13.3, 5.1 Hz, 1H), 4.59 (d, J = 6.2 Hz, 2H), 4.47- 4.24 (m, 2H), 4.04 (dt, J = 14.0, 4.8 Hz, 2H), 3.76-3.62 (m, 4H), 3.54 (t, J = 11.7 Hz, 2H), 3.47-3.39 (m, 3H), 3.29 (dd, J = 25.9, 10.3 Hz, 4H), 2.90 (ddd, J = 17.9, 13.5, 5.3 Hz, 1H), 2.72 (t, J = 11.6 Hz, 3H), 2.63-2.54 (m, 1H), 2.33
1H NMR (400 MHz, DMSO-d6) δ 11.73 (s, 1H), 10.99 (s, 1H), 10.21 (s, 1H), 9.46 (t, J = 6.4 Hz, 1H), 8.44 (s, 1H), 8.42-8.31 (m, 4H), 8.19 (d, J = 1.3 Hz, 1H), 8.02 (s, 1H), 7.82-7.73 (m, 3H), 7.72-7.65 (m, 2H), 7.51 (s, 1H), 7.44 (d, J = 7.9 Hz, 1H), 7.29 (t, J = 8.0 Hz, 1H), 7.16 (t, J = 8.7 Hz, 1H), 7.04-6.92 (m, 1H), 5.09 (dd, J = 13.3, 5.1 Hz, 1H), 4.42 (d, J = 17.4 Hz, 1H),
1H NMR (400 MHz, DMSO-d6) δ 11.70 (s, 1H), 10.99 (s, 1H), 10.05 (d, J = 1.9 Hz, 1H), 9.45 (t, J = 6.3 Hz, 1H), 8.44 (s, 1H), 8.40-8.34 (m, 4H), 8.19 (d, J = 1.4 Hz, 1H), 8.02 (s, 1H), 7.68 (d, J = 2.2 Hz, 1H), 7.59 (dd, J = 7.9, 2.1 Hz, 1H), 7.51 (s, 1H), 7.46-7.40 (m, 2H), 7.31-7.23 (m, 2H), 6.96 (d, J = 7.9 Hz, 1H), 6.91 (d, J = 4.5 Hz, 1H), 6.87 (s, 1H), 5.09 (dd, J = 13.2, 5.2 Hz,
1H NMR (400 MHz, DMSO-d6) δ 11.90 (s, 1H), 10.99 (s, 1H), 10.79 (s, 1H), 9.61 (t, J = 6.4 Hz, 1H), 8.49- 8.31 (m, 4H), 8.20 (d, J = 1.3 Hz, 1H), 7.96 (dd, J = 9.5, 4.2 Hz, 2H), 7.87 (t, J = 2.0 Hz, 1H), 7.80 (dd, J = 7.9, 2.1 Hz, 1H), 7.68 (d, J = 7.8 Hz, 1H), 7.59- 7.51 (m, 3H), 7.47 (d, J = 7.9 Hz, 1H), 7.30 (t, J = 7.9 Hz, 1H), 7.02-6.94 (m, 1H), 5.10 (dd, J = 13.3, 5.1 Hz, 1H),
1H NMR (400 MHz, DMSO-d6) δ 11.53 (brs, 1H), 10.99 (s, 1H), 10.22 (s, 1H), 9.20 (m, 1H), 8.43 (s, 1H), 8.30 (s, 2H), 8.20 (s, 1H), 7.84-7.66 (m, 6H), 7.52(s, 1H), 7.48-7.45 (m, 1H), 7.21- 7.05 (m, 3H), 7.01-6.95 (m, 1H), 5.12 (dd, J = 13.3, 5.1 Hz, 1H), 4.61 (d, J = 6.4 Hz, 2H), 4.46-4.26 (m, 2H), 4.09-3.94 (m, 4H), 3.54-3.19 (m, 5H), 3.10 (t, J = 12.9 Hz, 1H), 2.76 (t, J = 11.6 Hz, 2H), 2.50 (s,3H), 2.44- 2.21 (m, 6H), 2.10-1.94 (m, 4H), 1.89-
1H NMR (400 MHz, DMSO-d6) δ 11.52 (s, 1H), 11.00 (s, 1H), 10.06 (s, 1H), 8.63 (q, J = 5.7 Hz, 1H), 8.39 (d, J = 1.5 Hz, 1H), 8.21 (d, J = 16.5 Hz, 4H), 7.87 (d, J = 8.5 Hz, 2H), 7.76 (d, J = 2.0 Hz, 1H), 7.73-7.61 (m, 3H), 7.53 (s, 1H), 7.46 (d, J = 7.9 Hz, 1H), 7.28 (t, J = 8.0 Hz, 1H), 7.08 (d, J = 8.6 Hz, 2H), 6.99-6.84 (m, 3H), 5.11 (dd, J = 13.3, 5.1 Hz, 1H), 4.55 (d, J = 5.9
1H NMR (400 MHz, DMSO-d6) δ 11.53 (s, 1H), 11.00 (s, 1H), 10.07 (s, 1H), 8.63 (q, J = 5.7 Hz, 1H), 8.48-8.29 (m, 4H), 8.19 (d, J = 1.3 Hz, 1H), 8.00- 7.61 (m, 6H), 7.56-7.44 (m, 2H), 7.28 (t, J = 8.0 Hz, 1H), 7.19-6.81 (m, 5H), 5.20-5.09 (m, 1H), 4.56 (d, J = 5.9 Hz, 3H), 4.13-3.98 (m, 6H), 3.66-3.30 (m, 8H), 3.25-3.05 (m, 2H), 2.90 (ddd, J = 25.9, 13.4, 6.9 Hz, 3H), 2.70-2.56 (m,
1H NMR (400 MHz, DMSO-d6) δ 11.66 (s, 1H), 11.00 (s, 1H), 10.22 (s, 1H), 8.63 (q, J = 5.7 Hz, 1H), 8.47-8.28 (m, 4H), 8.20 (d, J = 1.4 Hz, 1H), 7.86- 7.61 (m, 6H), 7.60-7.43 (m, 2H), 7.23 (dt, J = 56.6, 8.3 Hz, 2H), 7.04-6.85 (m, 3H), 5.11 (dd, J = 13.3, 5.1 Hz, 1H), 4.65-4.43 (m, 3H), 4.04 (dt, J = 13.6, 4.6 Hz, 5H), 3.64 (dd, J = 19.3, 11.7 Hz, 4H), 3.48-3.34 (m, 5H), 3.16 (d, J =
1H NMR (400 MHz, DMSO-d6) δ 11.91 (s, 1H), 10.99 (s, 1H), 9.98 (s, 1H), 9.50 (t, J = 6.4 Hz, 1H), 8.82 (d, J = 2.2 Hz, 1H), 8.39 (d, J = 1.5 Hz, 1H), 8.27-8.04 (m, 6H), 7.90 (d, J = 8.4 Hz, 2H), 7.77 (d, J = 2.0 Hz, 1H), 7.69 (dd, J = 8.5, 5.6 Hz, 2H), 7.54 (s, 1H), 7.47 (d, J = 7.9 Hz, 1H), 7.28 (t, J = 8.0 Hz, 1H), 6.94 (d, J = 7.7 Hz, 1H), 6.74-
1H NMR (400 MHz, DMSO-d6) δ 12.03 (s, 1H), 10.99 (s, 1H), 10.22 (s, 1H), 9.32-9.04 (m, 1H), 8.42-8.29 (m, 3H), 8.20 (d, J = 1.3 Hz, 1H), 7.94 (d, J = 8.0 Hz, 2H), 7.83-7.64 (m, 4H), 7.54 (s, 1H), 7.44 (dd, J = 22.7, 8.0 Hz, 3H), 7.30 (t, J = 8.0 Hz, 1H), 7.17 (t, J = 8.7 Hz, 1H), 6.98 (d, J = 7.8 Hz, 1H), 5.41 (d, J = 48.4 Hz, 1H), 5.10 (dd, J = 13.2, 5.1 Hz, 1H), 4.60 (d, J = 5.7 Hz,
1H NMR (400 MHz, DMSO-d6): δ 11.52-11.46 (m, 1H), 10.97 (s, 1H), 10.13 (s,1H), 9.84 (t, J = 1.2 Hz, 1H), 9.39 (d, J = 1.2 Hz, 1H), 8.27-8.17 (m, 5H), 7.78-7.77 (m, 3H), 7.70-7.69 (m, 2H), 7.55-7.47 (m,2H), 7.31-7.27 (m, 1H), 7.12-7.10 (m, 1H), 6.98-6.96 (m, 1H), 5.11-5.09 (m, 1H), 4.4.64- 4.63(m, 2H), 4.44-4.41 (m, 1H), 4.32- 4.23 (m, 4H), 3.72-3.64 (m,5H), 3.42- 3.39 (m, 3H), 3.37-3.30 (m,4H), 2.94-
1H NMR (400 MHz, DMSO-d6): δ 11.61-11.58 (m, 1H), 10.97 (s, 1H), 10.04 (s, 1H), 9.43 (t, J = 6.4 Hz, 1H), 8.44 (s, 1H), 8.38 (d, J = 1.2 Hz, 1H), 8.31(s, 3H), 8.19 (d, J = 1.2 Hz, 1H), 8.02 (s, 1H), 7.87 (d, J = 8.8 Hz, 2H), 7.78-7.76 (m, 1H), 7.71-7.66(m,2H), 7.52 (s, 1H), 7.45(d, J = 8.4 Hz, 1H), 7.28 (t, J = 8 Hz, 1H), 7.08 (d, J = 8.8 Hz, 1H), 6.96 (d, J = 7.2 Hz, 1H), 5.12-5.07 (m, 1H), 4.59 (d, J = 6 Hz,
1H NMR (400 MHz, DMSO-d6) δ 11.96 (s, 1H), 10.99 (s, 1H), 10.31 (s, 1H), 9.62 (t, J = 6.4 Hz, 1H), 8.72 (d, J = 1.2 Hz, 1H), 8.45-8.37 (m, 4H), 8.19 (d, J = 1.3 Hz, 1H), 7.96 (d, J = 9.5 Hz, 1H), 7.88 (t, J = 2.0 Hz, 1H), 7.78- 7.71 (m, 1H), 7.68 (d, J = 7.8 Hz, 1H), 7.55 (d, J = 10.3 Hz, 2H), 7.50-7.43 (m, 1H), 7.28 (t, J = 8.0 Hz, 1H), 6.96 (dd, J = 7.8, 1.6 Hz, 1H), 5.10 (dd, J =
1H NMR (400 MHz, DMSO-d6) δ 12.01 (s, 1H), 11.00 (s, 1H), 10.22 (s, 1H), 9.23 (t, J = 5.9 Hz, 1H), 8.40 (d, J = 1.4 Hz, 1H), 8.28-8.15 (m, 4H), 7.94 (d, J = 8.0 Hz, 2H), 7.82-7.73 (m, 3H), 7.69 (dd, J = 8.5, 5.2 Hz, 2H), 7.54 (s, 1H), 7.47 (d, J = 8.1 Hz, 1H), 7.41 (d, J = 8.1 Hz, 2H), 7.30 (t, J = 8.1 Hz, 1H), 7.17 (t, J = 8.9 Hz, 1H), 6.98 (d, J = 7.8 Hz, 1H), 5.10 (dd, J = 13.3, 5.0 Hz, 1H), 4.60 (d, J = 5.8 Hz, 2H), 4.49-
1H NMR (400 MHz, DMSO-d6) δ 11.00 (s, 1H), 10.29 (s, 1H), 10.18 (s, 1H), 8.45-8.37 (m, 2H), 8.28-8.17 (m, 4H), 7.80-7.74 (m, 3H), 7.68 (dd, J = 7.9, 3.0 Hz, 2H), 7.45 (s, 1H), 7.38 (d, J = 7.8 Hz, 1H), 7.30 (t, J = 8.0 Hz, 1H), 7.15 (t, J = 8.7 Hz, 1H), 6.98 (d, J = 7.7 Hz, 1H), 5.40 (s, 1H), 5.11 (dd, J = 13.3, 5.1 Hz, 1H), 4.44 (d, J = 17.3 Hz, 2H), 4.37 (d, J = 5.8 Hz, 2H), 4.29
1H NMR (400 MHz, DMSO-d6) δ 11.53 (brs, 1H), 10.99 (s, 1H), 10.22 (s, 1H), 9.20 (m, 1H), 8.43 (s, 1H), 8.30 (s, 2H), 8.20 (s, 1H), 7.84-7.66 (m, 6H), 7.52(s, 1H), 7.48-7.45 (m, 1H), 7.21- 7.05 (m, 4H), 7.01-6.95 (m, 1H), 5.12 (dd, J = 13.3, 5.1 Hz, 1H), 4.61 (d, J = 6.4 Hz, 2H), 4.46-4.26 (m, 2H), 4.09-3.94 (m, 4H), 3.54-3.19 (m, 5H), 3.10 (t, J = 12.9 Hz, 1H), 2.76 (t,
1H NMR (400 MHz, DMSO-d6) δ 11.49 (s, 1H), 11.00 (s, 1H), 10.20 (s, 1H), 9.19 (t, J = 6.0 Hz, 1H), 8.40 (d, J = 1.5 Hz, 1H), 8.24-8.11 (m, 4H), 7.81-7.72 (m, 5H), 7.69 (dd, J = 7.9, 2.4 Hz, 2H), 7.53 (s, 1H), 7.45 (d, J = 8.0 Hz, 1H), 7.30 (t, J = 8.0 Hz, 1H), 7.18 (q, J = 9.4 Hz, 2H), 7.00-6.95 (m, 1H), 5.10 (dd, J = 13.3, 5.1 Hz, 1H), 4.57 (d, J = 5.7 Hz, 2H), 4.44 (d, J = 17.4 Hz,
1H NMR (400 MHz, DMSO-d6) δ 11.31 (s, 1H), 10.99 (s, 1H), 9.51 (t, J = 6.4 Hz, 1H), 8.81 (d, J = 2.2 Hz, 1H), 8.48-8.32 (m, 3H), 8.17-8.03 (m, 3H), 7.68 (d, J = 7.8 Hz, 1H), 7.54 (s, 1H), 7.47 (d, J = 7.9 Hz, 1H), 7.22- 6.99 (m, 4H), 6.76-6.59 (m, 3H), 6.51 (s, 1H), 5.09 (dd, J = 13.3, 5.0 Hz, 1H), 4.61 (d, J = 6.4 Hz, 2H), 4.47-4.26 (m, 2H), 4.26-4.18 (m, 2H), 4.11-3.94
1H NMR (400 MHz, DMSO-d6) δ 11.37 (s, 1H), 10.99 (s, 1H), 9.42 (t, J = 6.3 Hz, 1H), 8.36 (d, J = 1.5 Hz, 1H), 8.24 (d, J = 5.4 Hz, 3H), 8.12-8.04 (m, 2H), 7.92 (d, J = 7.8 Hz, 1H), 7.69 (d, J = 7.9 Hz, 1H), 7.54 (s, 1H), 7.46 (d, J = 7.9 Hz, 1H), 7.19-6.98 (m, 4H), 6.65-6.47 (m, 3H), 5.95 (s, 1H), 5.10 (dd, J = 13.3, 5.1 Hz, 1H), 4.60 (d, J = 6.3 Hz, 2H), 4.47-4.06 (m, 6H), 3.93
1H NMR (400 MHz, DMSO-d6) δ 11.73 (s, 1H), 10.99 (s, 1H), 10.28 (s, 1H), 9.98 (t, J = 6.3 Hz, 1H), 8.43- 8.30 (m, 4H), 8.27-8.17 (m, 3H), 7.84- 7.66 (m, 5H), 7.57 (s, 1H), 7.53-7.48 (m, 1H), 7.29 (t, J = 7.9 Hz, 1H), 7.16 (t, J = 8.7 Hz, 1H), 7.01-6.95 (m, 2H), 5.10 (dd, J = 13.3, 5.1 Hz, 1H), 4.66 (d, J = 6.3 Hz, 2H), 4.47-4.26 (m, 2H), 4.26-4.02 (m, 5H), 3.93 (d, J = 9.0 Hz,
1H NMR (400 MHz, DMSO-d6) δ 11.93 (s, 1H), 10.99 (s, 1H), 9.98 (d, J = 4.9 Hz, 2H), 8.32-8.06 (m, 6H), 7.91 (d, J = 8.5 Hz, 2H), 7.78 (s, 1H), 7.69 (d, J = 7.9 Hz, 2H), 7.58 (s, 1H), 7.51 (d, J = 7.9 Hz, 1H), 7.28 (t, J = 8.0 Hz, 1H), 7.02-6.92 (m, 2H), 6.70 (d, J = 8.5 Hz, 2H), 5.10 (dd, J = 13.3, 5.1 Hz, 1H), 4.66 (d, J = 6.2 Hz, 2H), 4.44 (d, J = 17.3 Hz, 2H), 4.34-4.11 (m,
The beneficial effects of the present invention were demonstrated by specific Experimental Examples.
(1) MV-411 cells were cultured in the cell culture medium, and then well-growing cells were selected and inoculated in a 12-well plate, with 1 mL/well and 1×106 cells/well. The plate was incubated overnight in a 5% CO2 cell incubator at 37° C.
(2) 10 mM storage solution of each drug was prepared using dimethylsulfoxide (DMSO). The stock solution was diluted gradually with DMSO before use, and then 1 μL of the compound solution was added to the cell culture well (to ensure that the DMSO concentration in the culture system was 0.1), so that the final drug concentration is 100 nM, 10 nM, 3 nM, 1 nM, 0.3 nM, and 0.1 nM. Two wells were set for each concentration. The plate was gently shaken and mixed. Additionally, negative control wells (containing an equal amount of DMSO) and positive control wells were included.
(3) After 24 hours of cultivation, the cells were lysed using RIPA cell lysate, and the proteins were extracted. The protein concentration was measured using a BCA assay kit. 5× concentrated protein buffer was loaded, heated at 100° C. for 5 min, and then the sample was stored at −20° C.
(4) For each well, 30 μg of protein was loaded to polyacrylamide gel for electrophoresis.
(5) The protein was transferred from polyacrylamide gel to PVDF membrane, and sealed at room temperature with 5% skimmed milk for 1 h, which was then incubated with the primary antibodies (Anti-SHP2 rabbit mAb and Anti-GAPDH rabbit mAb) at 4° C. overnight. The membrane was washed three times with TBST solution, 10 minutes for each time. After that, the membrane was incubated with the secondary antibodies (horseradish peroxidase labeled goat anti-rabbit IgG) at room temperature for 2 h, and then washed three times with TBST solution, 10 minutes for each time, followed by exposure.
(6) The images were analyzed with Image J grayscale, and the degradation ratio of protein bands in the test group was calculated, based on the negative control group (DMSO) (100%).
(7) Using the Dose-response-inhibition equation in the data processing software GraphPad Prism 8, the DC50 value was obtained (which represents the drug concentration corresponding to 50% degradation of the target protein).
Finally, ECL detection solution was added for color development, and photos were taken with an automatic chemiluminescence instrument, so as to collect images and analyze them.
Using similar methods and different cell lines, the degradation activity of the compound according to the present invention on SHP2 protein of different cell lines was tested under suitable culture conditions.
The results are shown in Table 2: (++++: DC50>1 μM; +++: 0.1 μM<DC50<1 μM; ++: DC50<0.1 μM)
The results in Table 2 above indicated that the compound of the present invention had a good degradation effect on SHP2 protein in different cells.
(1) MV-411 cells were cultured in the cell culture medium, and then well-growing cells were selected and inoculated in a 96-well plate at 80 μL/well, with 2×104 cells/well. The plate was incubated overnight in a 5% CO2 cell incubator at 37° C.
(2) 10 mM storage solution of each drug was prepared using dimethylsulfoxide (DMSO). The stock solution was diluted in a ratio of 1:3 with DMSO before use, and then the solution was serially diluted in a ratio of 1:3, to obtain 9 gradient concentrations. Each concentration was further diluted with the medium in a ratio of 1:200 (to ensure that the DMSO concentration in the culture system was 0.1%). Two wells were set for each concentration. 20 μL of each compound solution was added to the cell culture well (with a final concentration of 10 μM, 3.3 μM, 1.1 μM . . . ). The plate was gently shaken and mixed. Additionally, 3 negative control wells (only containing cells) and 3 blank control wells (only containing the medium) were included (6 wells were each added with 20 μL of DMSO diluted with the medium in a ratio of 1:200).
(1) After 5 days of cultivation, 10 μL of CCK-8 was added to each well, and then the plate was further cultured for 3 h at 37° C. in a 5% CO2 cell incubator.
(2) The absorbance (OD value) was measured at 450 nm with a multifunctional microplate reader. (3) The data were analyzed using the Dose-response-inhibition equation in GraphPad Prism8 software to obtain the IC50 value.
Using a similar method, the IC50 value (nM) for the inhibitory activity of the compound according to the present invention against different cell lines was obtained, and the results are shown in Table 3 (++++: IC50>5 μM; +++: 1 μM<IC50<5 μM; ++: IC50<1 μM).
The results in Table 3 above indicated that compounds of the present invention, such as 63, 96, etc., exhibited excellent anti-proliferative activity against different cell lines.
In summary, the compound of the present invention had a good inhibitory effect on both hematomas and solid tumor cell lines. It had strong inhibitory effects on the proliferation of acute leukemia, esophageal cancer, KRAS mutant non-small cell lung cancer and pancreatic cancer cell lines. Moreover, when it was combined with other anti-tumor medicaments, a significant synergistic effect was demonstrated. In addition, the compound of the present invention had a rather different mechanism of action compared to traditional small-molecule targeting drugs or macromolecular drugs such as antibodies, and had good application prospects. The compound of the present invention could be used as a phosphatase degrader, especially as a SHP2 protein degrader, so that it could be used in the manufacturer of medicaments for treating diseases such as cancer, and had good application prospects.
| Number | Date | Country | Kind |
|---|---|---|---|
| 202110769589.1 | Jul 2021 | CN | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/CN2022/104221 | 7/6/2022 | WO |
