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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 47448생성일: 2026년 10월 25일

Acetone → 2-Chloroquinoline-4-carbonyl azide

https://huagongshe.com/reaction/47448

반응식

참여 물질

역할이름HCID투입량
반응물AcetoneHCID 180—
반응물Sodium AzideHCID 33557—
반응물2-Chloroquinoline-4-carbonyl chlorideHCID 75438—
반응물2-Chloroquinoline-4-carboxylic acidHCID 230582—
용매WaterHCID 962—
용매1,4-DioxaneHCID 31275—
생성물2-Chloroquinoline-4-carbonyl azideHCID 22745141—

반응 단계

2-Chloro-4-chlorocarbonylquinoline (0.5 g), prepared by standard methods from 2-chloroquinoline-4-carboxylic acid, was added to sodium azide in aqueous dioxan (2.1 ml 1:3) at 0° C. Acetone was then added and the mixture stirred for 16 h. Water (10 ml) was added, the precipitated solid collected by filtration and air dried to give 2-chloroquinoline-4-carbonyl azide (0.455 g). The azide (0.232 g) in toluene (10 ml) was warmed from room temperature to 75° C. and then heating continued for 1 h. After cooling to room temperature 6-amino-2-methylbenzoxazole (0.148 g) in dichloromethane (15 ml) containing 4-N,N-dimethylaminopyridine (20 mg) was added and the mixture stirred for 16 h. The precipitated solid was separated by filtration to give a solid (0.25 g). Column chromatography (silica gel, dichloromethane/methanol/ammonia mixtures) gave the title compound (0.072 g). 1H NMR δ: 5 2.60 (3H, s), 7.25 (1H, d, J=8.5 Hz), 7.61 (1H, d, J=8.5 Hz), 7.73 (1H, t, J=7.0 Hz), 7.84 (1H, t, J=6.7 Hz), 7.91 (1H, d, J=8.0 Hz), 8.05 (1H, s), 8.20 (1H, d, J=8.25 Hz), 8.28 (1H, s), 9.49 (1H, s), 9.61 (1H, s). m/z (API+): 353, 355(MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06699879B1
출처 데이터셋uspto-grants-2004_03
ORD IDord-fed1940bbfb744c0a7d8ffbbe771e0bf
출처 메모uspto-grants-2004_03