Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212051Generated: November 4, 2026

(S)-1-(pyrrolidin-2-ylmethyl)piperidine → (S)-(2-(piperidin-1-ylmethyl)pyrrolidin-1-yl)(6-(trifluoromethyl)benzofuran-2-yl)methanone

https://huagongshe.com/reaction/2212051

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-1-(pyrrolidin-2-ylmethyl)piperidineHCID 7022796—
Reactant6-(Trifluoromethyl)benzofuran-2-carboxylic acidHCID 21964142—
Product(S)-(2-(piperidin-1-ylmethyl)pyrrolidin-1-yl)(6-(trifluoromethyl)benzofuran-2-yl)methanoneHCID 44411624—

Reaction Steps

71 mg of the title compound were synthesized as described for (E)-3-(4-bromophenyl)-1-((S)-2-((pyrrolidin-1-yl)methyl)pyrrolidin-1-yl)propenone, using 6-(trifluoromethyl)benzofuran-2-carboxylic acid instead of (E)-4-bromocinnamic acid and 1-(((S)-pyrrolidin-2-yl)methyl)piperidine instead of (S)-2-((pyrrolidin-1-yl)methyl)pyrrolidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07101898B2
Source datasetuspto-grants-2006_09
ORD IDord-0c764bd5f91645b9bacdee365f8c44f6
Source noteuspto-grants-2006_09