(2S,4R)-N-tert-butyloxycarbonyl-2-[[N-[hydroxymethyl-((R)-isopropyl)methyl]amino]carbonyl]-4-hydroxyl-pyrrolidine

Base Information

Chemical Name:(2S,4R)-N-tert-butyloxycarbonyl-2-[[N-[hydroxymethyl-((R)-isopropyl)methyl]amino]carbonyl]-4-hydroxyl-pyrrolidine
CAS No.:369366-60-9
Molecular Formula:C₁₅H₂₈N₂O₅
Molecular Weight:316.398
Hs Code.:

Synonyms:(2S,4R)-N-tert-butyloxycarbonyl-2-[[N-[hydroxymethyl-((R)-isopropyl)methyl]amino]carbonyl]-4-hydroxyl-pyrrolidine

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Chemical Property of (2S,4R)-N-tert-butyloxycarbonyl-2-[[N-[hydroxymethyl-((R)-isopropyl)methyl]amino]carbonyl]-4-hydroxyl-pyrrolidine

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Technology Process of (2S,4R)-N-tert-butyloxycarbonyl-2-[[N-[hydroxymethyl-((R)-isopropyl)methyl]amino]carbonyl]-4-hydroxyl-pyrrolidine

There total 1 articles about (2S,4R)-N-tert-butyloxycarbonyl-2-[[N-[hydroxymethyl-((R)-isopropyl)methyl]amino]carbonyl]-4-hydroxyl-pyrrolidine 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: 36.0%

: 4276-09-9,473-75-6
(R)-2-amino-3-methylbutanol

: 13726-69-7,946610-68-0
(2S,4R)-4-hydroxy-1-[(2-methylpropan-2-yl)oxycarbonyl]pyrrolidine-2-carboxylic acid

: 369366-60-9
(2S,4R)-N-tert-butyloxycarbonyl-2-[[N-[hydroxymethyl-((R)-isopropyl)methyl]amino]carbonyl]-4-hydroxyl-pyrrolidine

Guidance literature:: With benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; In dichloromethane; at 20 ℃; for 24h;
DOI:10.1021/jo0158231

Reference yield:

: 369366-60-9
(2S,4R)-N-tert-butyloxycarbonyl-2-[[N-[hydroxymethyl-((R)-isopropyl)methyl]amino]carbonyl]-4-hydroxyl-pyrrolidine

: (2S,4S)-4-Diphenylphosphanyl-2-((R)-4-isopropyl-4,5-dihydro-oxazol-2-yl)-pyrrolidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: 54 percent / Et₃N / CH₂Cl₂ / 20 °C

2.1: NaNH₂ / tetrahydrofuran / 12 h / 20 °C

2.2: 39 percent / S₈ / tetrahydrofuran / 2 h / 20 °C

3.1: Raney nickel / acetonitrile / 20 °C

With sodium amide; triethylamine; nickel; In tetrahydrofuran; dichloromethane; acetonitrile;
DOI:10.1021/jo0158231

Reference yield:

: 369366-60-9
(2S,4R)-N-tert-butyloxycarbonyl-2-[[N-[hydroxymethyl-((R)-isopropyl)methyl]amino]carbonyl]-4-hydroxyl-pyrrolidine

: 369366-57-4
(2S,4'R,4S)-N-tert-butyloxycarbonyl-2-(4,5-dihydro-4-isopropyl-1,3-oxazole-2-yl)-4-diphenylphosphinothioyl-pyrrolidine

Guidance literature:: Multi-step reaction with 2 steps

1.1: 54 percent / Et₃N / CH₂Cl₂ / 20 °C

2.1: NaNH₂ / tetrahydrofuran / 12 h / 20 °C

2.2: 39 percent / S₈ / tetrahydrofuran / 2 h / 20 °C

With sodium amide; triethylamine; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jo0158231