Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 389670생성일: 2026년 10월 26일
Hydrochloric Acid → (S)-methyl 2-((tert-butoxycarbonyl)amino)-3-(5-chlorothiophene-2-carboxamido)propanoate
https://huagongshe.com/reaction/389670
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Diisopropylcarbodiimide | HCID 12734 | — |
| 반응물 | N-Hydroxysuccinimide | HCID 80170 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | 5-Chloro-2-thiophenecarboxylic acid | HCID 95048 | — |
| 반응물 | Trimethylsilyldiazomethane | HCID 167693 | — |
| 반응물 | Boc-Dap-OH | HCID 2755946 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | (S)-methyl 2-((tert-butoxycarbonyl)amino)-3-(5-chlorothiophene-2-carboxamido)propanoate | HCID 67155290 | 91.1% |
반응 단계
Commercially available (S)-3-amino-2-tert-butoxycarbonylamino-propionic acid (BOC-Dap-OH) (18.09 g, 88.56 mmol) was suspended in 100 ml DCM with N-hydroxy-succinimide (16.99 g, 147.61 mmol) and N,N′-diisopropylcarbodiimide (11.43 ml, 73.8 mmol), then 5-Chloro-thiophene-2-carboxylic acid (12 g, 73.8 mmol) and DIPEA (25.51 ml, 147.61 mmol) in 60 ml DCM were slowly added. The mixture was stirred at RT for 2 h, then cooled to 0° C. and TMS-diazomethane was slowly added. The reaction was stirred for 2 h at RT, HCl solution (0.5 M) was added and the organic layer was separated, washed with H2O, dried with Na2SO4, filtered and evaporated to dryness. The resulting solid was triturated 16 h with diisopropyl ether, filtered and washed with diisopropyl ether and dried under vacuum at 60° C. 24.4 g of crude product were obtained and used without further purification.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08378092B2 |
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| 출처 데이터셋 | uspto-grants-2013_02 |
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| ORD ID | ord-c93bffd3f83441cabd5fc5ba89627ea6 |
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| 출처 메모 | uspto-grants-2013_02 |
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