Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 352664생성일: 2026년 10월 25일
Diisopropylethylamine → tert-butyl (2S)-2-benzyloxycarbonylamino-3-(4-(2-methoxycarbonylethyl)benzoylamino)propionate
https://huagongshe.com/reaction/352664
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | O-[(Ethoxycarbonyl)cyanomethylenamino]-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733286 | — |
| 반응물 | (S)-tert-Butyl 3-amino-2-(((benzyloxy)carbonyl)amino)propanoate | HCID 10803731 | — |
| 반응물 | 4-(3-Methoxy-3-oxopropyl)benzoic acid | HCID 11310294 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | tert-butyl (2S)-2-benzyloxycarbonylamino-3-(4-(2-methoxycarbonylethyl)benzoylamino)propionate | HCID 15512203 | — |
반응 단계
354 mg (1.7 mmol) of 4-(2-methoxycarbonyl-ethyl)benzoic acid and 500 mg (1.7 mmol) of tert-butyl (2S)-3-amino-2-benzyloxycarbonylaminopropionate were dissolved in 3 ml of dimethylformamide and treated with 557 mg (1.7 mmol) of O-((cyano-(ethoxycarbonyl)-methylidene)amino)-1,1,3,3-tetramethyluronium tetrafluoroborate (TOTU) and 204 mg (1.7 mmol) of diisopropylethylamine, and the mixture was stirred at room temperature for 7 hours at pH 7-8. The solvent was removed in vacuo, the residue was dissolved in ethyl acetate and the solution was washed three times each with KHSO4 solution and NaHCO3 solution until neutral. The organic phase was separated off and dried and the solvent was removed by distillation in vacuo. Yield 770 mg. MS (ES+): m/e=485.2 (M+H+).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06747148B2 |
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| 출처 데이터셋 | uspto-grants-2004_06 |
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| ORD ID | ord-17e93918d6ef4da9a9adfbebc89eb617 |
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| 출처 메모 | uspto-grants-2004_06 |
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