Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 483024생성일: 2026년 10월 26일
Dicyclohexylcarbodiimide → benzotriazol-1-yl (2Z)-2-methoxyimino-2-[2-(tritylamino)-1,3-thiazol-4-yl]acetate
https://huagongshe.com/reaction/483024
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dicyclohexylcarbodiimide | HCID 10868 | — |
| 반응물 | 1-Hydroxybenzotriazole | HCID 75771 | — |
| 반응물 | (Z)-2-methoxymino-2-(2-(tritylamino)thiazol-4-yl)acetic acid | HCID 5928144 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | benzotriazol-1-yl (2Z)-2-methoxyimino-2-[2-(tritylamino)-1,3-thiazol-4-yl]acetate | HCID 88675991 | 93% |
반응 단계
To a solution of 2-(2-tritylaminothiazol-4-yl)-(Z)-2-methoxyiminoacetic acid (2.22 g, 5 mmol) and 1-hydroxybenzotriazole (0.74 g, 5.5 mmol) in tetrahydrofuran (22 ml) was added N,N'-dicyclohexylcarbodiimide (1.14 g, 5.5 mmol) at 5°-10° C. and the mixture was stirred at the same temperature for 3 hours. Precipitated N,N'-dicyclohexylurea was removed by filtration and the filtrate was concentrated under reduced pressure. The residue was dissolved in chloroform (20 ml) and insoluble material was removed by filtration. The chloroform was evaporated and the residue was treated with a small quantity of ether to give colorless needles of 1-benzotriazolyl 2-(2-tritylaminothiazol-4-yl)-(Z)-2-methoxyiminoacetate (2.60 g, 93%), mp 178°-179° C. (decomposition).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04576938 |
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| 출처 데이터셋 | uspto-grants-1986_03 |
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| ORD ID | ord-de584faa82294b62aa037648a02c0640 |
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| 출처 메모 | uspto-grants-1986_03 |
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