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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271497Generated: November 1, 2026

Trifluoroacetic acid → (R)-N-(1-(cyclopropylmethyl)-2-oxoazepan-3-yl)-4-(2-oxo-1,2-dihydroquinazolin-3(4H)-yl)piperidine-1-carboxamide

https://huagongshe.com/reaction/1271497

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-(2-oxo-1,4-dihydroquinazolin-3(2H)-yl)piperidine-1-carbonyl chlorideHCID 18321108—
Reactanttert-Butyl (3R)-1-(cyclopropylmethyl)-2-oxoazepan-3-ylcarbamateHCID 58695830—
Solvent1,2-DichloroethaneHCID 11—
SolventDichloromethaneHCID 6344—
Product(R)-N-(1-(cyclopropylmethyl)-2-oxoazepan-3-yl)-4-(2-oxo-1,2-dihydroquinazolin-3(4H)-yl)piperidine-1-carboxamideHCID 1122444156%

Reaction Steps

Trifluoroacetic acid (5 mL) was added to a solution of tert-butyl (3R)-1-(cyclopropylmethyl)-2-oxoazepan-3-ylcarbamate (257 mg, 0.91 mmol) in dichloromethane (10 mL). After 1 h, the mixture was concentrated and azeotroped with dichloromethane (3×) to give the crude amine. Diisopropylethylamine (0.070 mL, 0.40 mmol) was added to a solution of the crude amine (39 mg, 0.13 mmol) and 4-(2-oxo-1,4-dihydroquinazolin-3(2H)-yl)piperidine-1-carbonyl chloride (39 mg, 0.13 mmol) in 1,2-dichloroethane (2 mL) and the mixture was heated to reflux. After 1 h, the reaction was allowed to cool to ambient temperature. Purification by silica gel chromatography (1% methanol/dichloromethane→5% methanol/dichloromethane) gave the title compound (32 mg). MS 440 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07205292B2
Source datasetuspto-grants-2007_04
ORD IDord-0618bcc0c6284b3abe73c7cb36a6c385
Source noteuspto-grants-2007_04