(2R,3S)-1-(t-butoxycarbonyl)-3-(3-chlorophenyl)-N-phenylaziridine-2-carboxamide

Base Information

Chemical Name:(2R,3S)-1-(t-butoxycarbonyl)-3-(3-chlorophenyl)-N-phenylaziridine-2-carboxamide
CAS No.:1073903-20-4
Molecular Formula:C₂₀H₂₁ClN₂O₃
Molecular Weight:372.851
Hs Code.:

Synonyms:(2R,3S)-1-(t-butoxycarbonyl)-3-(3-chlorophenyl)-N-phenylaziridine-2-carboxamide

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Chemical Property of (2R,3S)-1-(t-butoxycarbonyl)-3-(3-chlorophenyl)-N-phenylaziridine-2-carboxamide

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Technology Process of (2R,3S)-1-(t-butoxycarbonyl)-3-(3-chlorophenyl)-N-phenylaziridine-2-carboxamide

There total 2 articles about (2R,3S)-1-(t-butoxycarbonyl)-3-(3-chlorophenyl)-N-phenylaziridine-2-carboxamide 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: 54.0%

: 848194-74-1
3-chlorobenzaldehyde N-(tert-butoxycarbonyl)imine

: 98554-96-2
N-phenyl-α-diazoacetamide

: 1073903-20-4
(2R,3S)-1-(t-butoxycarbonyl)-3-(3-chlorophenyl)-N-phenylaziridine-2-carboxamide

Guidance literature:: With (S)-1,1-bis(2-biphenyl)-2-phenylethanediol; 2-carboxyphenylboronic acid; In dichloromethane; at -20 ℃; for 4h; enantioselective reaction; Molecular sieve;
DOI:10.1021/ja407764u

Reference yield: 50.0%

: 848194-74-1
3-chlorobenzaldehyde N-(tert-butoxycarbonyl)imine

: 98554-96-2
N-phenyl-α-diazoacetamide

: (Z)-3-(t-butoxycarbonylamino)-2-(3-chlorophenyl)-N-phenylacrylamide

: 1073903-20-4
(2R,3S)-1-(t-butoxycarbonyl)-3-(3-chlorophenyl)-N-phenylaziridine-2-carboxamide

Guidance literature:: With (R)-3,3'-dimesityl-1,1'-binaphthyl-2,2'-dicarboxylic acid; In toluene; at 0 ℃; for 5h; optical yield given as %ee; enantioselective reaction; Molecular sieve;
DOI:10.1021/ja805635c