5-tert-butoxycarbonylmethyl-13-cyclohexyl-6,7-dihydro-5H-benzo[5,6][1,4]diazepino[7,1-a]indole-10-carboxylic acid methyl ester

Base Information

Chemical Name:5-tert-butoxycarbonylmethyl-13-cyclohexyl-6,7-dihydro-5H-benzo[5,6][1,4]diazepino[7,1-a]indole-10-carboxylic acid methyl ester
CAS No.:863567-00-4
Molecular Formula:C₃₀H₃₆N₂O₄
Molecular Weight:488.627
Hs Code.:

Synonyms:5-tert-butoxycarbonylmethyl-13-cyclohexyl-6,7-dihydro-5H-benzo[5,6][1,4]diazepino[7,1-a]indole-10-carboxylic acid methyl ester

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Chemical Property of 5-tert-butoxycarbonylmethyl-13-cyclohexyl-6,7-dihydro-5H-benzo[5,6][1,4]diazepino[7,1-a]indole-10-carboxylic acid methyl ester

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Technology Process of 5-tert-butoxycarbonylmethyl-13-cyclohexyl-6,7-dihydro-5H-benzo[5,6][1,4]diazepino[7,1-a]indole-10-carboxylic acid methyl ester

There total 6 articles about 5-tert-butoxycarbonylmethyl-13-cyclohexyl-6,7-dihydro-5H-benzo[5,6][1,4]diazepino[7,1-a]indole-10-carboxylic acid methyl 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: 95.0%

: 863566-98-7
13-cyclohexyl-6,7-dihydro-5H-benzo[5,6][1,4]diazepino[7,1-a]indole-10-carboxylic acid methyl ester

: 5292-43-3
bromoacetic acid tert-butyl ester

: 863567-00-4
5-tert-butoxycarbonylmethyl-13-cyclohexyl-6,7-dihydro-5H-benzo[5,6][1,4]diazepino[7,1-a]indole-10-carboxylic acid methyl ester

Guidance literature:: With potassium carbonate; sodium iodide; In N,N-dimethyl-formamide; at 90 ℃; for 12h;
DOI:10.1021/jm0610245

Reference yield:

: 615-36-1
2-bromoaniline

: 863567-00-4
5-tert-butoxycarbonylmethyl-13-cyclohexyl-6,7-dihydro-5H-benzo[5,6][1,4]diazepino[7,1-a]indole-10-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 6 steps

1.1: 64 percent / Et₃N / PdCl₂(dppf)*CH₂Cl₂ / dioxane / 3 h / 100 °C

2.1: 96 percent / NaHCO₃ / Pd(PPh₃)4 / 1,2-dimethoxy-ethane; H₂O / 7 h / Heating

3.1: 100 percent / AcONa; AcOH / tetrahydrofuran / 2 h / 20 °C

4.1: 93 percent / NaH / dimethylformamide / 2 h / 20 °C

5.1: BH₃*THF / tetrahydrofuran / 4 h / 20 °C

5.2: 94 percent / aq. HCl / tetrahydrofuran / 1 h / 70 °C

6.1: 95 percent / K₂CO₃; NaI / dimethylformamide / 12 h / 90 °C

With borane-THF; sodium acetate; sodium hydride; sodium hydrogencarbonate; potassium carbonate; acetic acid; triethylamine; sodium iodide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In tetrahydrofuran; 1,4-dioxane; 1,2-dimethoxyethane; water; N,N-dimethyl-formamide; 2.1: Suzuki coupling;
DOI:10.1021/jm0610245

Reference yield:

: 191171-55-8
2-anilineboronic acid pinacol ester

: 863567-00-4
5-tert-butoxycarbonylmethyl-13-cyclohexyl-6,7-dihydro-5H-benzo[5,6][1,4]diazepino[7,1-a]indole-10-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: 96 percent / NaHCO₃ / Pd(PPh₃)4 / 1,2-dimethoxy-ethane; H₂O / 7 h / Heating

2.1: 100 percent / AcONa; AcOH / tetrahydrofuran / 2 h / 20 °C

3.1: 93 percent / NaH / dimethylformamide / 2 h / 20 °C

4.1: BH₃*THF / tetrahydrofuran / 4 h / 20 °C

4.2: 94 percent / aq. HCl / tetrahydrofuran / 1 h / 70 °C

5.1: 95 percent / K₂CO₃; NaI / dimethylformamide / 12 h / 90 °C

With borane-THF; sodium acetate; sodium hydride; sodium hydrogencarbonate; potassium carbonate; acetic acid; sodium iodide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; 1,2-dimethoxyethane; water; N,N-dimethyl-formamide; 1.1: Suzuki coupling;
DOI:10.1021/jm0610245