(R)-tert-butyl (4-(2-phenylacetamido)-1-(2,4,5-trifluorophenyl)butan-2-yl)carbamate

Base Information

Chemical Name:(R)-tert-butyl (4-(2-phenylacetamido)-1-(2,4,5-trifluorophenyl)butan-2-yl)carbamate
CAS No.:1500076-38-9
Molecular Formula:C₂₃H₂₇F₃N₂O₃
Molecular Weight:436.474
Hs Code.:

Synonyms:(R)-tert-butyl (4-(2-phenylacetamido)-1-(2,4,5-trifluorophenyl)butan-2-yl)carbamate

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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 (R)-tert-butyl (4-(2-phenylacetamido)-1-(2,4,5-trifluorophenyl)butan-2-yl)carbamate

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Technology Process of (R)-tert-butyl (4-(2-phenylacetamido)-1-(2,4,5-trifluorophenyl)butan-2-yl)carbamate

There total 5 articles about (R)-tert-butyl (4-(2-phenylacetamido)-1-(2,4,5-trifluorophenyl)butan-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: 87.0%

: 1500076-35-6
(R)-tert-butyl (4-amino-1-(2,4,5-trifluorophenyl)butan-2-yl)carbamate

: 103-80-0
phenylacetyl chloride

: 1500076-38-9
(R)-tert-butyl (4-(2-phenylacetamido)-1-(2,4,5-trifluorophenyl)butan-2-yl)carbamate

Guidance literature:: With triethylamine; In dichloromethane; at 0 - 20 ℃; for 1h;
DOI:10.1002/cmdc.201300104

Reference yield:

: 1048703-14-5
(R)-tert-butyl (4-hydroxy-1-(2,4,5-trifluorophenyl)butan-2-yl)carbamate

: 1500076-38-9
(R)-tert-butyl (4-(2-phenylacetamido)-1-(2,4,5-trifluorophenyl)butan-2-yl)carbamate

Guidance literature:: Multi-step reaction with 4 steps

1: triethylamine / dichloromethane / 0.5 h / 20 °C

2: sodium azide / N,N-dimethyl-formamide / 18 h / 67 °C

3: palladium 10% on activated carbon; hydrogen / methanol / 5 h / 20 °C / Inert atmosphere

4: triethylamine / dichloromethane / 1 h / 0 - 20 °C

With sodium azide; palladium 10% on activated carbon; hydrogen; triethylamine; In methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1002/cmdc.201300104

Reference yield:

: 881995-73-9
3-(R)-tert-butoxycarbonylamino-4-(2,4,5-trifluorophenyl)butyric acid methyl ester

: 1500076-38-9
(R)-tert-butyl (4-(2-phenylacetamido)-1-(2,4,5-trifluorophenyl)butan-2-yl)carbamate

Guidance literature:: Multi-step reaction with 5 steps

1: lithium borohydride / tetrahydrofuran / 2 h / 0 - 20 °C

2: triethylamine / dichloromethane / 0.5 h / 20 °C

3: sodium azide / N,N-dimethyl-formamide / 18 h / 67 °C

4: palladium 10% on activated carbon; hydrogen / methanol / 5 h / 20 °C / Inert atmosphere

5: triethylamine / dichloromethane / 1 h / 0 - 20 °C

With lithium borohydride; sodium azide; palladium 10% on activated carbon; hydrogen; triethylamine; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1002/cmdc.201300104