(S)-tert-butyl 4-[(1S,2S)-2-(benzhydrylamino)-1-hydroxy-3-methoxy-3-oxopropyl]-2,2-dimethyloxazolidine-3-carboxylate

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Chemical Name:(S)-tert-butyl 4-[(1S,2S)-2-(benzhydrylamino)-1-hydroxy-3-methoxy-3-oxopropyl]-2,2-dimethyloxazolidine-3-carboxylate
CAS No.:1552271-54-1
Molecular Formula:C₂₇H₃₆N₂O₆
Molecular Weight:484.593
Hs Code.:

Synonyms:(S)-tert-butyl 4-[(1S,2S)-2-(benzhydrylamino)-1-hydroxy-3-methoxy-3-oxopropyl]-2,2-dimethyloxazolidine-3-carboxylate

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Chemical Property of (S)-tert-butyl 4-[(1S,2S)-2-(benzhydrylamino)-1-hydroxy-3-methoxy-3-oxopropyl]-2,2-dimethyloxazolidine-3-carboxylate

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Technology Process of (S)-tert-butyl 4-[(1S,2S)-2-(benzhydrylamino)-1-hydroxy-3-methoxy-3-oxopropyl]-2,2-dimethyloxazolidine-3-carboxylate

There total 1 articles about (S)-tert-butyl 4-[(1S,2S)-2-(benzhydrylamino)-1-hydroxy-3-methoxy-3-oxopropyl]-2,2-dimethyloxazolidine-3-carboxylate 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:

: 102308-32-7
(4S)-4-formyl-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester

: 81167-39-7
methyl N-(diphenylmethylene)glycinate

: 1552271-54-1
(S)-tert-butyl 4-[(1S,2S)-2-(benzhydrylamino)-1-hydroxy-3-methoxy-3-oxopropyl]-2,2-dimethyloxazolidine-3-carboxylate

: tert-butyl 4-[-2-(benzhydrylamino)-1-hydroxy-3-methoxy-3-oxopropyl]-2,2-dimethyloxazolidine-3-carboxylate

Guidance literature:: (4S)-4-formyl-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester; methyl N-(diphenylmethylene)glycinate; With ((2S,2'S,5S,5’S)-1,1'-((2-hydroxy-5-methyl-1,3-phenylene)-bis-(methylene))-bis-(5-phenylpyrrolidine-2,1-diyl))-bis-(diphenylmethanol); diethylzinc; In toluene; at 20 ℃; for 24h; Molecular sieve; Inert atmosphere;

With sodium cyanoborohydride; acetic acid; In methanol; at 20 ℃; for 16h; Overall yield = 73 %; Overall yield = 101 mg; diastereoselective reaction; Inert atmosphere; Molecular sieve;
DOI:10.1021/ja4129394