12-(phenylsulfonyl)-7-oxo-5,6,7,12-tetrahydroindolo[3,2-d][2]benzazepine-6-carboxylic acid tert-butyl ester

Base Information

Chemical Name:12-(phenylsulfonyl)-7-oxo-5,6,7,12-tetrahydroindolo[3,2-d][2]benzazepine-6-carboxylic acid tert-butyl ester
CAS No.:869985-78-4
Molecular Formula:C₂₇H₂₄N₂O₅S
Molecular Weight:488.564
Hs Code.:

Synonyms:12-(phenylsulfonyl)-7-oxo-5,6,7,12-tetrahydroindolo[3,2-d][2]benzazepine-6-carboxylic acid tert-butyl ester

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Chemical Property of 12-(phenylsulfonyl)-7-oxo-5,6,7,12-tetrahydroindolo[3,2-d][2]benzazepine-6-carboxylic acid tert-butyl ester

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Technology Process of 12-(phenylsulfonyl)-7-oxo-5,6,7,12-tetrahydroindolo[3,2-d][2]benzazepine-6-carboxylic acid tert-butyl ester

There total 3 articles about 12-(phenylsulfonyl)-7-oxo-5,6,7,12-tetrahydroindolo[3,2-d][2]benzazepine-6-carboxylic acid tert-butyl ester 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:

: 923603-92-3
N-(2-iodobenzyl)-1-(phenylsulfonyl)-1H-indole-3-carboxamide

: 869985-78-4
12-(phenylsulfonyl)-7-oxo-5,6,7,12-tetrahydroindolo[3,2-d][2]benzazepine-6-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 99 percent / DMAP / acetonitrile / 20 °C

2: 92 percent / PPh₃; silver carbonate / Pd(OAc)2 / dimethylformamide / 2 h / 100 °C

With dmap; triphenylphosphine; silver carbonate; palladium diacetate; In N,N-dimethyl-formamide; acetonitrile; 2: Heck coupling;
DOI:10.1016/j.tet.2006.11.042

Reference yield:

: 39959-51-8
2-iodobenzylamine

: 869985-78-4
12-(phenylsulfonyl)-7-oxo-5,6,7,12-tetrahydroindolo[3,2-d][2]benzazepine-6-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 82 percent / DMAP; EDCI / CH₂Cl₂ / 24 h / 0 - 20 °C

2: 99 percent / DMAP / acetonitrile / 20 °C

3: 92 percent / PPh₃; silver carbonate / Pd(OAc)2 / dimethylformamide / 2 h / 100 °C

With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triphenylphosphine; silver carbonate; palladium diacetate; In dichloromethane; N,N-dimethyl-formamide; acetonitrile; 3: Heck coupling;
DOI:10.1016/j.tet.2006.11.042

Reference yield:

: 278593-17-2
1-(phenylsulfonyl)-1H-indole-3-carboxylic acid

: 869985-78-4
12-(phenylsulfonyl)-7-oxo-5,6,7,12-tetrahydroindolo[3,2-d][2]benzazepine-6-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 82 percent / DMAP; EDCI / CH₂Cl₂ / 24 h / 0 - 20 °C

2: 99 percent / DMAP / acetonitrile / 20 °C

3: 92 percent / PPh₃; silver carbonate / Pd(OAc)2 / dimethylformamide / 2 h / 100 °C

With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triphenylphosphine; silver carbonate; palladium diacetate; In dichloromethane; N,N-dimethyl-formamide; acetonitrile; 3: Heck coupling;
DOI:10.1016/j.tet.2006.11.042