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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 536301Generated: October 30, 2026

(S)-(+)-2-Methylpiperidine → (S)-3-((S)-2-Methyl-piperidin-1-yl)-pyrrolidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/536301

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-(+)-2-MethylpiperidineHCID 6427443—
Reactant(R)-tert-Butyl 3-(tosyloxy)pyrrolidine-1-carboxylateHCID 23560883—
Reactant(2R,3'S)-2-Methyl-[1,3]bipyrrolidinyl-1'-carboxylic acid tert-butyl esterHCID 59401895—
Product(S)-3-((S)-2-Methyl-piperidin-1-yl)-pyrrolidine-1-carboxylic acid tert-butyl esterHCID 58468060—

Reaction Steps

The title compound was prepared in a manner substantially the same as intermediate (iv), (2R,3′S)-2-methyl-[1,3′]bipyrrolidinyl-1′-carboxylic acid tert-butyl ester, by condensing 3-(3R)-(toluene-4-sulfonyloxy)-pyrrolidine-1-carboxylic acid tert-butyl ester (5 g) with (S)-2-Methyl-piperidine to get 1.5 g (38% yield) of the product as a beige oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859588B2
Source datasetuspto-grants-2014_10
ORD IDord-58da061e9bde46039ec9abe481065f2c
Source noteuspto-grants-2014_10