6-[1-cyclobutyl-4-(4-morpholinylcarbonyl)-1H-pyrazol-5-yl]-13-cyclohexyl-3-methoxy-N-[(2-methylpropyl)sulfonyl]-7H-indolo[2,1-a][2]benzazepine-10-carboxamide

Base Information

Chemical Name:6-[1-cyclobutyl-4-(4-morpholinylcarbonyl)-1H-pyrazol-5-yl]-13-cyclohexyl-3-methoxy-N-[(2-methylpropyl)sulfonyl]-7H-indolo[2,1-a][2]benzazepine-10-carboxamide
CAS No.:1195778-94-9
Molecular Formula:C₄₁H₄₉N₅O₆S
Molecular Weight:739.936
Hs Code.:

6-[1-cyclobutyl-4-(4-morpholinylcarbonyl)-1H-pyrazol-5-yl]-13-cyclohexyl-3-methoxy-N-[(2-methylpropyl)sulfonyl]-7H-indolo[2,1-a][2]benzazepine-10-carboxamide

Synonyms:6-[1-cyclobutyl-4-(4-morpholinylcarbonyl)-1H-pyrazol-5-yl]-13-cyclohexyl-3-methoxy-N-[(2-methylpropyl)sulfonyl]-7H-indolo[2,1-a][2]benzazepine-10-carboxamide

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Chemical Property of 6-[1-cyclobutyl-4-(4-morpholinylcarbonyl)-1H-pyrazol-5-yl]-13-cyclohexyl-3-methoxy-N-[(2-methylpropyl)sulfonyl]-7H-indolo[2,1-a][2]benzazepine-10-carboxamide

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Technology Process of 6-[1-cyclobutyl-4-(4-morpholinylcarbonyl)-1H-pyrazol-5-yl]-13-cyclohexyl-3-methoxy-N-[(2-methylpropyl)sulfonyl]-7H-indolo[2,1-a][2]benzazepine-10-carboxamide

There total 6 articles about 6-[1-cyclobutyl-4-(4-morpholinylcarbonyl)-1H-pyrazol-5-yl]-13-cyclohexyl-3-methoxy-N-[(2-methylpropyl)sulfonyl]-7H-indolo[2,1-a][2]benzazepine-10-carboxamide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 81.0%

: 110-91-8,99108-56-2
morpholine

: 1195778-74-5
1-cyclobutyl-5-[13-cyclohexyl-3-methoxy-10-[[[(2-methylpropyl)sulfonyl]amino]carbonyl]-7H-indolo[2,1-a][2]benzazepin-6-yl]-1H-pyrazole-4-carboxylic acid

: 1195778-94-9
6-[1-cyclobutyl-4-(4-morpholinylcarbonyl)-1H-pyrazol-5-yl]-13-cyclohexyl-3-methoxy-N-[(2-methylpropyl)sulfonyl]-7H-indolo[2,1-a][2]benzazepine-10-carboxamide

Guidance literature:: 1-cyclobutyl-5-[13-cyclohexyl-3-methoxy-10-[[[(2-methylpropyl)sulfonyl]amino]carbonyl]-7H-indolo[2,1-a][2]benzazepin-6-yl]-1H-pyrazole-4-carboxylic acid; With O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine; In dimethyl sulfoxide; at 20 ℃; for 0.25h;

morpholine; In dimethyl sulfoxide; at 20 ℃;

Reference yield:

: 1127234-87-0
13-cyclohexyl-10-[(1,1-dimethylethoxy)carbonyl]-3-methoxy-beta-oxo-7H-indolo[2,1-a][2]benzazepine-6-propanoic acid ethyl ester

: 1195778-94-9
6-[1-cyclobutyl-4-(4-morpholinylcarbonyl)-1H-pyrazol-5-yl]-13-cyclohexyl-3-methoxy-N-[(2-methylpropyl)sulfonyl]-7H-indolo[2,1-a][2]benzazepine-10-carboxamide

Guidance literature:: Multi-step reaction with 6 steps

1.1: 2.75 h / 110 °C / Inert atmosphere

2.1: triethylamine / ethanol / 2 h / 160 °C / microwave condition

3.1: trifluoroacetic acid / 1,2-dichloro-ethane / 20 °C

4.1: 1,1'-carbonyldiimidazole / tetrahydrofuran / 1 h / 60 °C

4.2: 4 h / 60 °C

5.1: sodium hydroxide / tetrahydrofuran; ethanol / 96 h / 20 °C

6.1: O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine / dimethyl sulfoxide / 0.25 h / 20 °C

6.2: 20 °C

With O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; triethylamine; N-ethyl-N,N-diisopropylamine; 1,1'-carbonyldiimidazole; trifluoroacetic acid; sodium hydroxide; In tetrahydrofuran; ethanol; dimethyl sulfoxide; 1,2-dichloro-ethane;

Reference yield:

: 1127234-89-2
tert-butyl 13-cyclohexyl-6-((2E,Z)-3-(dimethylamino)-2-(ethoxycarbonyl)-2-propenoyl)-3-methoxy-7H-indolo[2,1-a][2]benzazepine-10-carboxylate

: 1195778-94-9
6-[1-cyclobutyl-4-(4-morpholinylcarbonyl)-1H-pyrazol-5-yl]-13-cyclohexyl-3-methoxy-N-[(2-methylpropyl)sulfonyl]-7H-indolo[2,1-a][2]benzazepine-10-carboxamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: triethylamine / ethanol / 2 h / 160 °C / microwave condition

2.1: trifluoroacetic acid / 1,2-dichloro-ethane / 20 °C

3.1: 1,1'-carbonyldiimidazole / tetrahydrofuran / 1 h / 60 °C

3.2: 4 h / 60 °C

4.1: sodium hydroxide / tetrahydrofuran; ethanol / 96 h / 20 °C

5.1: O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine / dimethyl sulfoxide / 0.25 h / 20 °C

5.2: 20 °C

With O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; triethylamine; N-ethyl-N,N-diisopropylamine; 1,1'-carbonyldiimidazole; trifluoroacetic acid; sodium hydroxide; In tetrahydrofuran; ethanol; dimethyl sulfoxide; 1,2-dichloro-ethane;