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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1469224생성일: 2026년 10월 25일

Water → N-(5-Chloro-2-methylphenyl)-4-{4-[5-(2-formylphenyl)-4,5-dihydro-1,2-oxazol-3-yl]-1,3-thiazol-2-yl}piperidine-1-carboxamide

https://huagongshe.com/reaction/1469224

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물5-Chloro-2-methylphenyl isocyanateHCID 2769632—
반응물2-{3-[2-(Piperidin-4-yl)-1,3-thiazol-4-yl]-4,5-dihydro-1,2-oxazol-5-yl}benzaldehyde hydrochlorideHCID 86665225—
촉매1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
용매DichloromethaneHCID 6344—
용매DiisopropylethylamineHCID 81531—
생성물N-(5-Chloro-2-methylphenyl)-4-{4-[5-(2-formylphenyl)-4,5-dihydro-1,2-oxazol-3-yl]-1,3-thiazol-2-yl}piperidine-1-carboxamideHCID 86665224—

반응 단계

To a suspension of 2-{3-[2-(piperidin-4-yl)-1,3-thiazol-4-yl]-4,5-dihydro-1,2-oxazol-5-yl}benzaldehyde hydrochloride (1.43 g) in dichloromethane (30 ml) and diisopropylethylamine (0.73 ml) were added, at room temperature, 4-chloro-2-isocyanato-1-methylbenzene (700 mg) and one drop of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU). The mixture was stirred at room temperature overnight, and water was then added. The aqueous phase was removed and extracted with ethyl acetate. The combined organic phases were dried over sodium sulphate and concentrated under reduced pressure. The residue was purified by chromatography. This gave N-(5-chloro-2-methylphenyl)-4-{4-[5-(2-formylphenyl)-4,5-dihydro-1,2-oxazol-3-yl]-1,3-thiazol-2-yl}piperidine-1-carboxamide (1.23 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09006266B2
출처 데이터셋uspto-grants-2015_04
ORD IDord-9942e7d385704c3cb69d1bdecb6f6b4b
출처 메모uspto-grants-2015_04