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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2351319Generated: November 2, 2026

Piperidine → 3-(5-Cyclopropyl-1,2,4-oxadiazol-3-yl)-4-methyl-5-oxo-6-(1-piperidyl)-4,5-dihydro-imidazo(1,5-a)quinazoline

https://huagongshe.com/reaction/2351319

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantHCID 14460518HCID 14460518—
SolventDimethylformamideHCID 6228—
Product3-(5-Cyclopropyl-1,2,4-oxadiazol-3-yl)-4-methyl-5-oxo-6-(1-piperidyl)-4,5-dihydro-imidazo(1,5-a)quinazolineHCID 1446053281%

Reaction Steps

3-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)-4-methyl-5-oxo-6-chloro-4,5-dihydro-imidazo(1,5-a)quinazoline (0.28 g, 0.8 mmol) was heated to 110° C. for 2 1/4 h in a mixture of 20 ml of dimethylformamide and 1 ml of piperidine. The reaction mixture was then evaporated in vacuo and the residue triturated with 5 ml of water, filtered off and dried to give 0.26 g (81%) 3- (5-cyclopropyl-1,2,4-oxadiazol-3-yl)-4-methyl -5-oxo- 6-(1-piperidyl)-4,5-dihydro-imidazo(1,5-a)quinazoline, M.p. 185°-192° C..

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04873244
Source datasetuspto-grants-1989_10
ORD IDord-0d3e16847c6c4f3d8359b52f744a2844
Source noteuspto-grants-1989_10