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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 130382Generated: October 30, 2026

Triethylamine → N-(2-isopropyl-4-methoxymethyloctahydrocyclopenta[c]pyrrol-5-yl)-2-(6-trifluoromethylquinazolin-4-ylamino)acetamide

https://huagongshe.com/reaction/130382

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Chloro-6-(trifluoromethyl)quinazolineHCID 21075095—
Reactant2-amino-N-(2-isopropyl-4-methoxymethyloctahydrocyclopenta[c]pyrrol-5-yl)acetamideHCID 69221543—
SolventEthanolHCID 702—
ProductN-(2-isopropyl-4-methoxymethyloctahydrocyclopenta[c]pyrrol-5-yl)-2-(6-trifluoromethylquinazolin-4-ylamino)acetamideHCID 69224927—

Reaction Steps

A mixture of 2-amino-N-(2-isopropyl-4-methoxymethyloctahydrocyclopenta[c]pyrrol-5-yl)acetamide, 4-chloro-6-trifluoromethylquinazoline (see Armarego et al., J. Chem. Soc. B, 1967, 449) and triethylamine in ethanol is heated at reflux until the reaction is complete. The solution is concentrated under vacuum yielding a residue. The residue is purified by reverse phase HPLC and lyophilization providing the title product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07381738B2
Source datasetuspto-grants-2008_06
ORD IDord-9e161f22675b48dda1bbf83ba3010999
Source noteuspto-grants-2008_06