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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Water | HCID 962 | — |
| 반응물 | 5-Chloro-2-methylphenyl isocyanate | HCID 2769632 | — |
| 반응물 | 2-{3-[2-(Piperidin-4-yl)-1,3-thiazol-4-yl]-4,5-dihydro-1,2-oxazol-5-yl}benzaldehyde hydrochloride | HCID 86665225 | — |
| 촉매 | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | Diisopropylethylamine | HCID 81531 | — |
| 생성물 | 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 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09006266B2 |
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| 출처 데이터셋 | uspto-grants-2015_04 |
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| ORD ID | ord-9942e7d385704c3cb69d1bdecb6f6b4b |
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| 출처 메모 | uspto-grants-2015_04 |
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