tert-butyl 13-cyclohexyl-3-methoxy-6-(2-(morpholin-4-ylcarbonyl)-3-thienyl)-7H-indolo[2,1-a][2]benzazepine-10-carboxylate

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Chemical Name:tert-butyl 13-cyclohexyl-3-methoxy-6-(2-(morpholin-4-ylcarbonyl)-3-thienyl)-7H-indolo[2,1-a][2]benzazepine-10-carboxylate
CAS No.:1127234-64-3
Molecular Formula:C₃₈H₄₂N₂O₅S
Molecular Weight:638.828
Hs Code.:

Synonyms:tert-butyl 13-cyclohexyl-3-methoxy-6-(2-(morpholin-4-ylcarbonyl)-3-thienyl)-7H-indolo[2,1-a][2]benzazepine-10-carboxylate

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Chemical Property of tert-butyl 13-cyclohexyl-3-methoxy-6-(2-(morpholin-4-ylcarbonyl)-3-thienyl)-7H-indolo[2,1-a][2]benzazepine-10-carboxylate

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Technology Process of tert-butyl 13-cyclohexyl-3-methoxy-6-(2-(morpholin-4-ylcarbonyl)-3-thienyl)-7H-indolo[2,1-a][2]benzazepine-10-carboxylate

There total 1 articles about tert-butyl 13-cyclohexyl-3-methoxy-6-(2-(morpholin-4-ylcarbonyl)-3-thienyl)-7H-indolo[2,1-a][2]benzazepine-10-carboxylate 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:

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

: 1127234-58-5
6-(2-carboxy-3-thienyl)-13-cyclohexyl-3-methoxy-7H-indolo[2,1-a][2]benzazepine-10-carboxylic acid 10-(1,1-dimethylethyl)ester

: 1127234-64-3
tert-butyl 13-cyclohexyl-3-methoxy-6-(2-(morpholin-4-ylcarbonyl)-3-thienyl)-7H-indolo[2,1-a][2]benzazepine-10-carboxylate

Guidance literature:: 6-(2-carboxy-3-thienyl)-13-cyclohexyl-3-methoxy-7H-indolo[2,1-a][2]benzazepine-10-carboxylic acid 10-(1,1-dimethylethyl)ester; With O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; In N,N-dimethyl-formamide; at 20 ℃; for 1.33333h;

morpholine; With dmap; In N,N-dimethyl-formamide; at 20 ℃; for 48h;