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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1469110Generated: October 31, 2026

Triethylamine → HCID 86692087, compound

https://huagongshe.com/reaction/1469110

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantQuinazolineHCID 9210—
Reactant4-Chloro-6-iodoquinazolineHCID 11173809—
ReactantHCID 57088589HCID 57088589—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86692087HCID 8669208740%

Reaction Steps

0.75 g of 4-chloro-6-iodoquinazoline, 0.51 g of 2,3,4a,8a-tetrahydro-1H-quinolin-4-one and 0.96 ml of triethylamine in 5 ml of dioxane are heated at 80° C. in a flask until the quinazoline has reacted completely (HPLC check, about 24 hours). The cooled reaction solution is diluted with EA and washed 3 times with water. The organic phase is dried over sodium sulfate and purified by means of column chromatography (gradient heptane: EA 5-100% in 16 min.), giving 0.40 g of 1-(6-iodoquinazolin-4-yl)-2,3,4a,8a-tetrahydro-1H-quinolin-4-one as yellowish solid (yield 40%, content 91%); MS-FAB (M+H+)=402.0; Rf (polar method): 2.20 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006255B2
Source datasetuspto-grants-2015_04
ORD IDord-3293087f03c74bfb8cc8fc4a8b45d050
Source noteuspto-grants-2015_04