Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412642Generated: October 29, 2026

Acrylamide → (2S)-N2-[(3S)-1-(aminocarbonylethyl)pyrrolidin-3-yl]-1-(1,3-benzoxazol-2-yl)-2-piperidinecarboxamide

https://huagongshe.com/reaction/412642

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcrylamideHCID 6579—
Reactant(2S)-1-(1,3-benzoxazol-2-yl)-N2-[(3S)-pyrrolidin-3-yl]-2-piperidinecarboxamideHCID 57068119—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductAmmoniaHCID 222—
Product(2S)-N2-[(3S)-1-(aminocarbonylethyl)pyrrolidin-3-yl]-1-(1,3-benzoxazol-2-yl)-2-piperidinecarboxamideHCID 5717084583.9%

Reaction Steps

Acrylamide (11.6 mg) was added to a solution of (2S)-1-(1,3-benzoxazol-2-yl)-N2-[(3S)-pyrrolidin-3-yl]-2-piperidinecarboxamide (51.6 mg) [see Example 4] in diethyl ether (3 ml). The reaction mixture was refluxed for 18 hours, after which time the ethereal layer was diluted with water. The aqueous layer was separated and then extracted with ethyl acetate. The combined organic layers were dried over magnesium sulphate and the solvent removed under reduced pressure. The crude product was purified by column chromatography on silica gel eluting with a solvent gradient of 93:7:1, changing to 90:10:1, dichloromethane:methanol:0.88 aqueous ammonia solution to afford (2S)-N2-[(3S)-1-(aminocarbonylethyl)pyrrolidin-3-yl]-1-(1,3-benzoxazol-2-yl)-2-piperidinecarboxamide (26.4 mg) as an off-white foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06562964B1
Source datasetuspto-grants-2003_05
ORD IDord-de57429a710849f19f7ee529482f6266
Source noteuspto-grants-2003_05