(3R,4S)-tert-butyl 4-(((benzyloxy)carbonyl)amino)-3-fluoropiperidine-1-carboxylate

Base Information

Chemical Name:(3R,4S)-tert-butyl 4-(((benzyloxy)carbonyl)amino)-3-fluoropiperidine-1-carboxylate
CAS No.:1351866-21-1
Molecular Formula:C₁₈H₂₅FN₂O₄
Molecular Weight:352.406
Hs Code.:

Synonyms:(3R,4S)-tert-butyl 4-(((benzyloxy)carbonyl)amino)-3-fluoropiperidine-1-carboxylate

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Chemical Property of (3R,4S)-tert-butyl 4-(((benzyloxy)carbonyl)amino)-3-fluoropiperidine-1-carboxylate

Chemical Property:

Purity/Quality:

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Technology Process of (3R,4S)-tert-butyl 4-(((benzyloxy)carbonyl)amino)-3-fluoropiperidine-1-carboxylate

There total 1 articles about (3R,4S)-tert-butyl 4-(((benzyloxy)carbonyl)amino)-3-fluoropiperidine-1-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:

: 934536-10-4,577691-56-6
(trans)-tert-butyl 4-amino-3-fluoropiperidine-1-carboxylate

: 501-53-1,94274-21-2
benzyl chloroformate

: 1033748-75-2
(3S,4R)-tert-butyl 4-(((benzyloxy)carbonyl)amino)-3-fluoropiperidine-1-carboxylate

: 1351866-21-1
(3R,4S)-tert-butyl 4-(((benzyloxy)carbonyl)amino)-3-fluoropiperidine-1-carboxylate

Guidance literature:: (trans)-tert-butyl 4-amino-3-fluoropiperidine-1-carboxylate; benzyl chloroformate; With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 0 - 23 ℃; for 18h;

With carbon dioxide; diethylamine; In isopropyl alcohol; Supercritical conditions; Resolution of racemate;

Reference yield:

: 1351866-21-1
(3R,4S)-tert-butyl 4-(((benzyloxy)carbonyl)amino)-3-fluoropiperidine-1-carboxylate

: benzyl ((3R,4S)-3-fluoropiperidin-4-yl)carbamate hydrochloride

Guidance literature:: With hydrogenchloride; In water; ethyl acetate; at 0 ℃; for 2h;

Reference yield:

: 1351866-21-1
(3R,4S)-tert-butyl 4-(((benzyloxy)carbonyl)amino)-3-fluoropiperidine-1-carboxylate

: C₂₀H₂₇FN₆O₃

Guidance literature:: Multi-step reaction with 3 steps

1: sodium hydride / N,N-dimethyl-formamide

2: palladium on activated charcoal; hydrogen / ethanol

3: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide

With palladium on activated charcoal; hydrogen; sodium hydride; N-ethyl-N,N-diisopropylamine; HATU; In ethanol; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2011.10.033