(S)-tert-butyl 1-(1-amino-1-oxo-3-(4-(2-oxoindolin-6-yl)phenyl)propan-2-ylcarbamoyl)cyclohexylcarbamate

Base Information

Chemical Name:(S)-tert-butyl 1-(1-amino-1-oxo-3-(4-(2-oxoindolin-6-yl)phenyl)propan-2-ylcarbamoyl)cyclohexylcarbamate
CAS No.:1352152-04-5
Molecular Formula:C₂₉H₃₆N₄O₅
Molecular Weight:520.629
Hs Code.:

Synonyms:(S)-tert-butyl 1-(1-amino-1-oxo-3-(4-(2-oxoindolin-6-yl)phenyl)propan-2-ylcarbamoyl)cyclohexylcarbamate

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (S)-tert-butyl 1-(1-amino-1-oxo-3-(4-(2-oxoindolin-6-yl)phenyl)propan-2-ylcarbamoyl)cyclohexylcarbamate

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of (S)-tert-butyl 1-(1-amino-1-oxo-3-(4-(2-oxoindolin-6-yl)phenyl)propan-2-ylcarbamoyl)cyclohexylcarbamate

There total 4 articles about (S)-tert-butyl 1-(1-amino-1-oxo-3-(4-(2-oxoindolin-6-yl)phenyl)propan-2-ylcarbamoyl)cyclohexylcarbamate 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:

: 103882-09-3,62129-44-6
N-Boc-4-I-Phe-OH

: 1352152-04-5
(S)-tert-butyl 1-(1-amino-1-oxo-3-(4-(2-oxoindolin-6-yl)phenyl)propan-2-ylcarbamoyl)cyclohexylcarbamate

Guidance literature:: Multi-step reaction with 4 steps

1.1: O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethylmorpholine; / N,N-dimethyl-formamide / 0.5 h / 20 °C

1.2: 16 h / 0 - 28 °C

2.1: trifluoroacetic acid / dichloromethane / 50 h

3.1: N-ethyl-N,N-diisopropylamine; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate / N,N-dimethyl-formamide / 2 h / 17 - 28 °C

4.1: potassium carbonate / dichloro[1,1'-bis(di-t-butylphosphino)ferrocene]palladium(II) / acetonitrile; water / 2 h / 80 °C / Inert atmosphere

With N-ethylmorpholine;; potassium carbonate; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; dichloro[1,1'-bis(di-t-butylphosphino)ferrocene]palladium(II); In dichloromethane; water; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 893441-85-5
6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)indoline-2-one

: 1352151-91-7
(S)-tert-butyl 1-(1-amino-3-(4-iodophenyl)-1-oxopropan-2-ylcarbamoyl)cyclohexylcarbamate

: 1352152-04-5
(S)-tert-butyl 1-(1-amino-1-oxo-3-(4-(2-oxoindolin-6-yl)phenyl)propan-2-ylcarbamoyl)cyclohexylcarbamate

Guidance literature:: With potassium carbonate; dichloro[1,1'-bis(di-t-butylphosphino)ferrocene]palladium(II); In water; acetonitrile; at 80 ℃; for 2h; Inert atmosphere;

Reference yield:

: 97964-72-2
(S)-2-amino-3-(4-iodophenyl)propionamamide

: 1352152-04-5
(S)-tert-butyl 1-(1-amino-1-oxo-3-(4-(2-oxoindolin-6-yl)phenyl)propan-2-ylcarbamoyl)cyclohexylcarbamate

Guidance literature:: Multi-step reaction with 2 steps

1: N-ethyl-N,N-diisopropylamine; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate / N,N-dimethyl-formamide / 2 h / 17 - 28 °C

2: potassium carbonate / dichloro[1,1'-bis(di-t-butylphosphino)ferrocene]palladium(II) / acetonitrile; water / 2 h / 80 °C / Inert atmosphere

With potassium carbonate; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine; dichloro[1,1'-bis(di-t-butylphosphino)ferrocene]palladium(II); In water; N,N-dimethyl-formamide; acetonitrile;