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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 447167Generated: October 30, 2026

Cyclopentylamine → HCID 67236358, compound

https://huagongshe.com/reaction/447167

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopentylamineHCID 2906—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 86654770HCID 86654770—
SolventDichloromethaneHCID 6344—
ProductHCID 67236358HCID 67236358—

Reaction Steps

(S)-tert-Butyl 1-(4-(6-formylbenzo[d]thiazol-2-yl)piperazin-1-yl)-1-oxo-3-(thiophen-2-yl)propan-2-ylcarbamate (45 mg), cyclopentylamine (12 mg), and sodium triacetoxyborohydride (29 mg) were combined in DCM (1 mL), and the resulting mixture stirred at room temperature overnight, then heated to reflux for 24 hours. The resulting mixture was then cooled to room temperature, quenched with saturated aqueous sodium bicarbonate, extracted with DCM, and chromatographed (0 to 5% MeOH in DCM) to yield (S)-tert-butyl 1-(4-(6-((cyclopentylamino)methyl)benzo[d]thiazol-2-yl)piperazin-1-yl)-1-oxo-3-(thiophen-2-yl)propan-2-ylcarbamate as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481547B2
Source datasetuspto-grants-2013_07
ORD IDord-4e6e1c40898b467ca65dacf61356b8f2
Source noteuspto-grants-2013_07