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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 536298Generated: October 30, 2026

(S)-3-(Toluene-4-sulfonyloxy)-pyrrolidine-1-carboxylic acid tert-butyl ester → (2R,3'R)-2-Methyl-[1,3]bipyrrolidinyl-1'-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/536298

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-3-(Toluene-4-sulfonyloxy)-pyrrolidine-1-carboxylic acid tert-butyl esterHCID 57957824—
Reactant(2R,3'S)-2-Methyl-[1,3]bipyrrolidinyl-1'-carboxylic acid tert-butyl esterHCID 59401895—
Product(2R,3'R)-2-Methyl-[1,3]bipyrrolidinyl-1'-carboxylic acid tert-butyl esterHCID 59401893—

Reaction Steps

The title compound was prepared in a manner substantially the same as intermediate (2R,3′S)-2-Methyl-[1,3′]bipyrrolidinyl-1′-carboxylic acid tert-butyl ester by condensing 3-(3S)-(toluene-4-sulfonyloxy)-pyrrolidine-1-carboxylic acid tert-butyl ester and R-(−)-2-methylpiperindine (obtained from Advanced Asymmetrics). LCMS:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859588B2
Source datasetuspto-grants-2014_10
ORD IDord-57ea2f8c8fb24190940c7b8325ceac3a
Source noteuspto-grants-2014_10