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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1022397Generated: November 1, 2026

Acetonitrile → HCID 86639521, compound

https://huagongshe.com/reaction/1022397

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantTriethylamineHCID 8471—
ReactantO-Methylhydroxylamine hydrochlorideHCID 521874—
Reactant2,6-dichloro-4-phenylquinazolineHCID 1628221—
SolventWaterHCID 962—
ProductHCID 86639521HCID 8663952119.3%

Reaction Steps

To a mixture of 275 mg of 2,6-dichloro-4-phenylquinazoline (compound No. Ia1-3), 10 ml of acetonitrile and 334 mg of methoxyamine hydrochloride was added dropwise 506 mg of triethylamine at room temperature to obtain a mixture. The mixture was charged in a pressure-resistant reaction vessel made of stainless steel and the reaction was carried out at 105° C. for 3.5 hours. After cooling, the reaction solution was poured into 100 ml of water. The mixture was extracted with ethyl acetate and the resultant extract was washed with water and then concentrated. The resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=3:1) to obtain 156 mg of crude crystals. The crude crystals were recrystallized from ethyl acetate to obtain 55 mg of the titled compound. Mp.173.9° C. 1H NMR (CDCl3): 3.98 (3H, s), 7.47-7.72 (6H, m), 7.87 (1H, d, J=9.0 Hz), 7.89 (1H, d, J=2.2 Hz), 8.03 (1H, br. s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722580B2
Source datasetuspto-grants-2014_05
ORD IDord-b4cda63bc41d4228991113abf29b0927
Source noteuspto-grants-2014_05