Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 604870생성일: 2026년 10월 26일
Phosgene → [5-(3-Chloro-benzyl)-4-methyl-thiazol-2-yl]-(4-[1,2,4]triazol-1-yl-phenyl)-amine
https://huagongshe.com/reaction/604870
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Phosgene | HCID 6371 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | 3-Chloro-4-(3-chlorophenyl)-2-butanone | HCID 4250985 | — |
| 반응물 | 4-(1,2,4-Triazol-1-yl)phenylthiourea | HCID 5260678 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | [5-(3-Chloro-benzyl)-4-methyl-thiazol-2-yl]-(4-[1,2,4]triazol-1-yl-phenyl)-amine | HCID 25106457 | — |
반응 단계
A suspension of 55 mg (0.25 mmol) 4-(1,2,4-triazol-1-yl)phenylthiourea, of 60 mg (0.28 mmol) 3-chloro-4-(3-chlorophenyl)-2-butanone and of 65 mg (0.5 mmol) N,N-diisopropyl ethyl amine in ethanol (2.5 ml) was refluxed over night. The same amount of chloro ketone was added and the reaction was heated to reflux over night. Again 1.1 equivalent of chloro ketone was added and the reaction was heated for 10 minutes in a microwave oven to 170° C. The solvent was evaporated and the residue was purified on silica gel with methylene chloride/methanol 19/1 yielding 27 mg (28%) [5-(3-chloro-benzyl)-4-methyl-thiazol-2-yl]-(4-[1,2,4]triazol-1-yl-phenyl)-amine as a yellow solid. MS ISP (m/e): 382.1 (100) (M+H)+. 1H NMR (CDCl3, 250 MHz): δ (ppm)=8.48 (s, 1H), 8.09 (s, 1H), 7.60 (d, 2H), 7.46 (d, 2H), 7.25-7.18 (m, 3H), 7.09 (d, 1H), 3.96 (s, 2H), 2.29 (s, 3H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07910740B2 |
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| 출처 데이터셋 | uspto-grants-2011_03 |
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| ORD ID | ord-a3be7135f3944c2087df2195ee7e0bd6 |
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| 출처 메모 | uspto-grants-2011_03 |
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