(S)-tert-butyl (1-amino-3-(4'-cyano-[1,1'-biphenyl]-4-yl)-1-oxopropan-2-yl)carbamate

Base Information

Chemical Name:(S)-tert-butyl (1-amino-3-(4'-cyano-[1,1'-biphenyl]-4-yl)-1-oxopropan-2-yl)carbamate
CAS No.:1254318-96-1
Molecular Formula:C₂₁H₂₃N₃O₃
Molecular Weight:365.432
Hs Code.:

Synonyms:(S)-tert-butyl (1-amino-3-(4'-cyano-[1,1'-biphenyl]-4-yl)-1-oxopropan-2-yl)carbamate

Suppliers and Price of (S)-tert-butyl (1-amino-3-(4'-cyano-[1,1'-biphenyl]-4-yl)-1-oxopropan-2-yl)carbamate

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of (S)-tert-butyl (1-amino-3-(4'-cyano-[1,1'-biphenyl]-4-yl)-1-oxopropan-2-yl)carbamate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (S)-tert-butyl (1-amino-3-(4'-cyano-[1,1'-biphenyl]-4-yl)-1-oxopropan-2-yl)carbamate

There total 1 articles about (S)-tert-butyl (1-amino-3-(4'-cyano-[1,1'-biphenyl]-4-yl)-1-oxopropan-2-yl)carbamate 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

: 1254318-96-1
(S)-tert-butyl (1-amino-3-(4'-cyano-[1,1'-biphenyl]-4-yl)-1-oxopropan-2-yl)carbamate

Guidance literature:: Multi-step reaction with 2 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: potassium carbonate / dichloro[1,1'-bis(di-t-butylphosphino)ferrocene]palladium(II) / 1,4-dioxane; water / 18 h / 75 °C / Inert atmosphere

With N-ethylmorpholine;; potassium carbonate; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; dichloro[1,1'-bis(di-t-butylphosphino)ferrocene]palladium(II); In 1,4-dioxane; water; N,N-dimethyl-formamide;

Reference yield:

: 1254318-96-1
(S)-tert-butyl (1-amino-3-(4'-cyano-[1,1'-biphenyl]-4-yl)-1-oxopropan-2-yl)carbamate

: 1352151-71-3
(S)-tert-butyl 1-(1-cyano-2-(4'-cyanobiphenyl-4-yl)ethylcarbamoyl)cyclohexylcarbamate

Guidance literature:: Multi-step reaction with 3 steps

1: trifluoroacetic acid / dichloromethane

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

3: Burgess Reagent / dichloromethane

With Burgess Reagent; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; triethylamine; trifluoroacetic acid; In dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 1254318-96-1
(S)-tert-butyl (1-amino-3-(4'-cyano-[1,1'-biphenyl]-4-yl)-1-oxopropan-2-yl)carbamate

: 1352151-70-2
(S)-tert-butyl-1-(1-amino-3-(4'-cyanobiphenyl-4yl)-1-oxopropan-2-yl carbamoyl)cyclohexylcarbamate

Guidance literature:: Multi-step reaction with 2 steps

1: trifluoroacetic acid / dichloromethane

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

With O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; triethylamine; trifluoroacetic acid; In dichloromethane; N,N-dimethyl-formamide;