Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 32828생성일: 2026년 10월 24일
Trifluoroacetic acid → (2S,3S)-2-(2-amino-3-phenyl-butyrylamino)-thiazole-4-carboxylic acid methyl ester
https://huagongshe.com/ko/reaction/32828
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Trifluoroacetic acid | HCID 6422 | — |
| 반응물 | 2-((2S,3S)-2-tert-butoxycarbonylamino-3-phenyl-butyrylamino)-thiazole-4-carboxylic acid methyl ester | HCID 86603389 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | (2S,3S)-2-(2-amino-3-phenyl-butyrylamino)-thiazole-4-carboxylic acid methyl ester | HCID 86603390 | 71.2% |
반응 단계
2-((2S,3S)-2-tert-butoxycarbonylamino-3-phenyl-butyrylamino)-thiazole-4-carboxylic acid methyl ester (0.65 g, 1.54 mmol) was mixed in dichloromethane (5 mL) in an ice-bath. Trifluoroacetic acid (5 mL) was added and the solution was stirred for 2 hours. The reaction mixture was evaporated and the residue was precipitated with ether. The mixture was stirred vigorously for 10 minutes and then filtered. The solid was partitioned between aqueous sodium bicarbonate and dichloromethane. The organic layer was separated and the aqueous layer was extracted with dichloromethane. The combined organic extracts were washed with brine and dried (sodium sulfate). Evaporation of the solvents gave 2-((2S,3S)-2-amino-3-phenyl-butyrylamino)-thiazole-4-carboxylic acid methyl ester (0.35 g, 71%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07427635B2 |
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| 출처 데이터셋 | uspto-grants-2008_09 |
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| ORD ID | ord-0d892e3e44a74ef9849795f2cc5c39e5 |
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| 출처 메모 | uspto-grants-2008_09 |
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