N-((1R,2S,5R)-2-((S)-3-amino-2-oxopyrrolidin-1-yl)-5-(tert-butylamino)cyclohexyl)acetamide

Base Information

Chemical Name:N-((1R,2S,5R)-2-((S)-3-amino-2-oxopyrrolidin-1-yl)-5-(tert-butylamino)cyclohexyl)acetamide
CAS No.:1004536-75-7
Molecular Formula:C₁₆H₃₀N₄O₂
Molecular Weight:310.44
Hs Code.:

Synonyms:N-((1R,2S,5R)-2-((S)-3-amino-2-oxopyrrolidin-1-yl)-5-(tert-butylamino)cyclohexyl)acetamide

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Chemical Property of N-((1R,2S,5R)-2-((S)-3-amino-2-oxopyrrolidin-1-yl)-5-(tert-butylamino)cyclohexyl)acetamide

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Technology Process of N-((1R,2S,5R)-2-((S)-3-amino-2-oxopyrrolidin-1-yl)-5-(tert-butylamino)cyclohexyl)acetamide

There total 4 articles about N-((1R,2S,5R)-2-((S)-3-amino-2-oxopyrrolidin-1-yl)-5-(tert-butylamino)cyclohexyl)acetamide 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: 98.0%

: 1004536-73-5
benzyl ((S)-1-((1S,2R,4R)-2-acetamido-4-(tert-butylamino)cyclohexyl)-2-oxopyrrolidin-3-yI)carbamate

: 1004536-75-7
N-((1R,2S,5R)-2-((S)-3-amino-2-oxopyrrolidin-1-yl)-5-(tert-butylamino)cyclohexyl)acetamide

Guidance literature:: With hydrogen; palladium 10% on activated carbon; In methanol; at 20 ℃; for 5h;

Reference yield: 95.0%

: C₂₄H₃₄N₄O₄

: 1004536-75-7
N-((1R,2S,5R)-2-((S)-3-amino-2-oxopyrrolidin-1-yl)-5-(tert-butylamino)cyclohexyl)acetamide

Guidance literature:: With hydrogen; palladium(II) hydroxide; In ethyl acetate; under 775.743 Torr;
DOI:10.1021/acsmedchemlett.1c00082

Reference yield:

: 1004536-65-5
tert-butyl ((1R,3R,4S)-3-acetamido-4-((S)-3-(((benzyloxy)carbonyl)amino)-2-oxopyrrolidin-1-yl)cyclohexyl)carbamate

: 1004536-75-7
N-((1R,2S,5R)-2-((S)-3-amino-2-oxopyrrolidin-1-yl)-5-(tert-butylamino)cyclohexyl)acetamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: trifluoroacetic acid / dichloromethane / 1 h / 20 °C

1.2: 1 h / 20 °C

2.1: N-chloro-succinimide / acetonitrile / 20 °C

2.2: 20 °C

3.1: hydrogen; palladium(II) hydroxide / ethyl acetate / 775.74 Torr

With N-chloro-succinimide; hydrogen; palladium(II) hydroxide; trifluoroacetic acid; In dichloromethane; ethyl acetate; acetonitrile;
DOI:10.1021/acsmedchemlett.1c00082