(S)-N-((S)-5-((2-chloro-1-(2-cyanophenyl)-1H-indol-3-yl)methyl)-4-oxo-2,3,4,5-tetrahydrobenzo[b][1,4]oxazepin-3-yl)-2-(methylamino)propanamide

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Chemical Name:(S)-N-((S)-5-((2-chloro-1-(2-cyanophenyl)-1H-indol-3-yl)methyl)-4-oxo-2,3,4,5-tetrahydrobenzo[b][1,4]oxazepin-3-yl)-2-(methylamino)propanamide
CAS No.:1562198-63-3
Molecular Formula:C₂₉H₂₆ClN₅O₃
Molecular Weight:528.01
Hs Code.:

Synonyms:(S)-N-((S)-5-((2-chloro-1-(2-cyanophenyl)-1H-indol-3-yl)methyl)-4-oxo-2,3,4,5-tetrahydrobenzo[b][1,4]oxazepin-3-yl)-2-(methylamino)propanamide

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Chemical Property of (S)-N-((S)-5-((2-chloro-1-(2-cyanophenyl)-1H-indol-3-yl)methyl)-4-oxo-2,3,4,5-tetrahydrobenzo[b][1,4]oxazepin-3-yl)-2-(methylamino)propanamide

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Technology Process of (S)-N-((S)-5-((2-chloro-1-(2-cyanophenyl)-1H-indol-3-yl)methyl)-4-oxo-2,3,4,5-tetrahydrobenzo[b][1,4]oxazepin-3-yl)-2-(methylamino)propanamide

There total 9 articles about (S)-N-((S)-5-((2-chloro-1-(2-cyanophenyl)-1H-indol-3-yl)methyl)-4-oxo-2,3,4,5-tetrahydrobenzo[b][1,4]oxazepin-3-yl)-2-(methylamino)propanamide 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: 43.0%

: 1562198-66-6
tert-butyl (S)-1-((S)-5-((2-chloro-1-(2-cyanophenyl)-1H-indol-3-yl)methyl)-4-oxo-2,3,4,5-tetrahydrobenzo[b][1,4]oxazepin-3-ylamino)-1-oxopropan-2-yl(methyl)carbamate

: 1562198-63-3
(S)-N-((S)-5-((2-chloro-1-(2-cyanophenyl)-1H-indol-3-yl)methyl)-4-oxo-2,3,4,5-tetrahydrobenzo[b][1,4]oxazepin-3-yl)-2-(methylamino)propanamide

Guidance literature:: With trifluoroacetic acid; In dichloromethane; at 20 ℃; for 16h;

Reference yield:

: 5059-30-3
2-chloroindole-3-carboxaldehyde

: 1562198-63-3
(S)-N-((S)-5-((2-chloro-1-(2-cyanophenyl)-1H-indol-3-yl)methyl)-4-oxo-2,3,4,5-tetrahydrobenzo[b][1,4]oxazepin-3-yl)-2-(methylamino)propanamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium hydride / mineral oil; 1-methyl-pyrrolidin-2-one / 0.17 h

1.2: 16 h / 150 °C / Microwave irradiation; Sealed tube

2.1: sodium tetrahydroborate; methanol / dichloromethane / 2.25 h / 0 - 20 °C

3.1: diethylazodicarboxylate; triphenylphosphine / tetrahydrofuran; toluene / 60 h / 20 °C

4.1: trifluoroacetic acid / dichloromethane / 16 h / 20 °C

With methanol; sodium tetrahydroborate; sodium hydride; triphenylphosphine; trifluoroacetic acid; diethylazodicarboxylate; In tetrahydrofuran; 1-methyl-pyrrolidin-2-one; dichloromethane; toluene; mineral oil;

Reference yield:

: 394-47-8
2-fluorobenzonitrile

: 1562198-63-3
(S)-N-((S)-5-((2-chloro-1-(2-cyanophenyl)-1H-indol-3-yl)methyl)-4-oxo-2,3,4,5-tetrahydrobenzo[b][1,4]oxazepin-3-yl)-2-(methylamino)propanamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium hydride / mineral oil; 1-methyl-pyrrolidin-2-one / 0.17 h

1.2: 16 h / 150 °C / Microwave irradiation; Sealed tube

2.1: sodium tetrahydroborate; methanol / dichloromethane / 2.25 h / 0 - 20 °C

3.1: diethylazodicarboxylate; triphenylphosphine / tetrahydrofuran; toluene / 60 h / 20 °C

4.1: trifluoroacetic acid / dichloromethane / 16 h / 20 °C

With methanol; sodium tetrahydroborate; sodium hydride; triphenylphosphine; trifluoroacetic acid; diethylazodicarboxylate; In tetrahydrofuran; 1-methyl-pyrrolidin-2-one; dichloromethane; toluene; mineral oil;