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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1374307Generated: October 31, 2026

Triethylamine → HCID 16064151, compound

https://huagongshe.com/reaction/1374307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Chloro-6-(trifluoromethyl)quinazolineHCID 21075095—
ReactantHCID 131726203HCID 131726203—
SolventEthanolHCID 702—
ProductHCID 16064151HCID 16064151—
ProductHCID 68768701HCID 68768701—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of (S)-3-amino-1-((1S,2S,4R/S)-2-isopropyl-4-(isopropyl(methyl)amino)cyclohexyl)pyrrolidin-2-one (85 mg) in EtOH (2.5 mL) was added triethylamine (0.2 mL) and 4-chloro-6-(trifluoromethyl)quinazoline (100.1 mg). The mixture was heated at 80° C. for 14 h before it was filtered and concentrated in vacuo. The residue was purified by chiral chromatography (AD column, EtOH as mobile phase) to afford (S)-1-((1S,2S,4R)-2-isopropyl-4-(isopropyl(methyl)amino)cyclohexyl)-3-(6-(trifluoromethyl)quinazolin-4-ylamino)pyrrolidin-2-one [52 mg; MS found: (M+H)+=492.4] and (S)-1-((1S,2S,4S)-2-isopropyl-4-(isopropyl(methyl)amino)cyclohexyl)-3-(6-(trifluoromethyl)quinazolin-4-ylamino)pyrrolidin-2-one [8 mg; MS found: (M+H)+=492.4].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07163937B2
Source datasetuspto-grants-2007_01
ORD IDord-e6162b2692414b3b909ef1dbe2b716a7
Source noteuspto-grants-2007_01