Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 51864생성일: 2026년 10월 26일
2,2,2-Trichloroethyl chloroformate → (2-Benzoylamino-4-methoxy-benzothiazol-7-yl)-(4-methyl-benzyl)-carbamic acid 2,2,2-trichloro-ethyl ester
https://huagongshe.com/reaction/51864
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 2,2,2-Trichloroethyl chloroformate | HCID 87063 | — |
| 반응물 | N-{7-[bis-(4-methyl-benzyl)-amino]-4-methoxy-benzothiazol-2-yl}-benzamide | HCID 22015745 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | (2-Benzoylamino-4-methoxy-benzothiazol-7-yl)-(4-methyl-benzyl)-carbamic acid 2,2,2-trichloro-ethyl ester | HCID 86589019 | 40.4% |
반응 단계
To a stirred solution of 300 mg (0.59 mmol) N-{7-[bis-(4-methyl-benzyl)-amino]-4-methoxy-benzothiazol-2-yl}-benzamide in 10 ml acetonitrile was added dropwise 0.60 ml (4.46 mmol) 2,2,2-trichloroethyl chloroformate and the reaction mixture heated at 80° C. for 72 h. The mixture was then concentrated in vacuo. Flash chromatography (ethyl acetate/hexane) afforded 138 mg (40%) (2-benzoylamino-4-methoxy-benzothiazol-7-yl)-(4-methyl-benzyl)-carbamic acid 2,2,2-trichloro-ethyl ester as a yellow solid. ES-MS m/e (%):584 (M{37Cl, 37Cl, 37Cl}+H+, 5), 582 (M{37Cl, 37Cl, 35Cl}+H+, 32), 580 (M{37Cl, 35Cl, 35Cl}+H+, 100), 578 (M{35Cl, 35Cl, 35Cl}+H+, 92).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06713499B2 |
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| 출처 데이터셋 | uspto-grants-2004_03 |
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| ORD ID | ord-72ea1724071f4980b0661692dda3e538 |
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| 출처 메모 | uspto-grants-2004_03 |
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