(2S,4S)-4-[(tert-butyloxycarbonyl)(4-methylbenzenesulfonyl)amino]-2-hydroxymethyl-1-phenylpyrrolidine

Base Information

Chemical Name:(2S,4S)-4-[(tert-butyloxycarbonyl)(4-methylbenzenesulfonyl)amino]-2-hydroxymethyl-1-phenylpyrrolidine
CAS No.:1304774-26-2
Molecular Formula:C₂₃H₃₀N₂O₅S
Molecular Weight:446.568
Hs Code.:

Synonyms:(2S,4S)-4-[(tert-butyloxycarbonyl)(4-methylbenzenesulfonyl)amino]-2-hydroxymethyl-1-phenylpyrrolidine

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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 (2S,4S)-4-[(tert-butyloxycarbonyl)(4-methylbenzenesulfonyl)amino]-2-hydroxymethyl-1-phenylpyrrolidine

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Technology Process of (2S,4S)-4-[(tert-butyloxycarbonyl)(4-methylbenzenesulfonyl)amino]-2-hydroxymethyl-1-phenylpyrrolidine

There total 4 articles about (2S,4S)-4-[(tert-butyloxycarbonyl)(4-methylbenzenesulfonyl)amino]-2-hydroxymethyl-1-phenylpyrrolidine 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:

: 1304774-13-7
tert-butyl (2S,4S)-4-[(tert-butyloxycarbonyl)(4-methylbenzenesulfonyl)amino]-5-oxo-1-phenylprolinate

: 1304774-17-1
(2S,4S)-2-hydroxymethyl-4-(4-methylbenzenesulfonyl)amino-1-phenylpyrrolidine

: 1304774-26-2
(2S,4S)-4-[(tert-butyloxycarbonyl)(4-methylbenzenesulfonyl)amino]-2-hydroxymethyl-1-phenylpyrrolidine

: 1304774-27-3
(2S,4S)-4-[(tert-butyloxycarbonyl)(4-methylbenzenesulfonyl)amino]-2-tert-butyloxymethyl-1-phenylpyrrolidine

Guidance literature:: With dimethylsulfide borane complex; In tetrahydrofuran; at 0 - 40 ℃; for 576.5h; chemoselective reaction; Inert atmosphere;
DOI:10.1002/ejoc.201100049

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

: 1304774-26-2
(2S,4S)-4-[(tert-butyloxycarbonyl)(4-methylbenzenesulfonyl)amino]-2-hydroxymethyl-1-phenylpyrrolidine

: 1304774-27-3
(2S,4S)-4-[(tert-butyloxycarbonyl)(4-methylbenzenesulfonyl)amino]-2-tert-butyloxymethyl-1-phenylpyrrolidine

Guidance literature:: Multi-step reaction with 2 steps

1: pyridine; dmap / tert-butyl alcohol / 18 h / 20 °C

2: dimethylsulfide borane complex / tetrahydrofuran / 576.5 h / 0 - 40 °C / Inert atmosphere

With pyridine; dmap; dimethylsulfide borane complex; In tetrahydrofuran; tert-butyl alcohol;
DOI:10.1002/ejoc.201100049

Reference yield:

: 1032764-52-5
(2S,4S)-4-[(4-methylbenzenesulfonyl)amino]-5-oxo-1-phenylproline

: 1304774-17-1
(2S,4S)-2-hydroxymethyl-4-(4-methylbenzenesulfonyl)amino-1-phenylpyrrolidine

: 1304774-26-2
(2S,4S)-4-[(tert-butyloxycarbonyl)(4-methylbenzenesulfonyl)amino]-2-hydroxymethyl-1-phenylpyrrolidine

: 1304774-27-3
(2S,4S)-4-[(tert-butyloxycarbonyl)(4-methylbenzenesulfonyl)amino]-2-tert-butyloxymethyl-1-phenylpyrrolidine

Guidance literature:: Multi-step reaction with 2 steps

1: pyridine; dmap

2: dimethylsulfide borane complex / tetrahydrofuran / 576.5 h / 0 - 40 °C / Inert atmosphere

With pyridine; dmap; dimethylsulfide borane complex; In tetrahydrofuran;
DOI:10.1002/ejoc.201100049