Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1075185생성일: 2026년 10월 27일
Chlorotrimethylsilane → alpha-(4-Ethyl-2,3-dioxo-1-piperazinecarboxamido)-2-furylacetic acid
https://huagongshe.com/reaction/1075185
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Chlorotrimethylsilane | HCID 6397 | — |
| 반응물 | Triethylamine hydrochloride | HCID 11130 | — |
| 반응물 | 4-Ethyl-2,3-dioxopiperazinecarbonyl chloride | HCID 108813 | — |
| 반응물 | 2-Amino-2-(furan-2-yl)acetic acid | HCID 298385 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | Triethylamine | HCID 8471 | — |
| 생성물 | alpha-(4-Ethyl-2,3-dioxo-1-piperazinecarboxamido)-2-furylacetic acid | HCID 15573352 | 85.6% |
반응 단계
To an ice-cooled suspension of 2.55 g of DL-α-amino-2-furylacetic acid in 35 ml of methylene chloride was added 4.81 ml of trimethylchlorosilane. To the resulting mixture was added dropwise 5.04 ml of triethylamine over a period of 10 minutes at 5° to 10° C. The reaction was allowed to proceed at 15° to 20° C. for one hour. To the reaction mixture was added over a period of 15 minutes at 5° to 10° C. 7.01 g of a mixture of 4-ethyl-2,3-dioxo-1-piperazinecarbonyl chloride and triethylamine hydrochloride, said mixture containing 58.02% of the former. The reaction was allowed to proceed at 10° to 15° C. for one hour. After addition of 20 ml of water, the reaction mixture was stirred at room temperature for one hour, then at 5° to 7° C. for 30 minutes. The precipitated crystals were collected by filtration, washed with 5 ml of methylene chloride and 5 ml of water in this order, and then dried to obtain 4.75 g of DL-α-(4-ethyl-2,3-dioxo-1-piperazinecarboxamido)-2-furylacetic acid, m.p. 179°-181° C. (decomp.), yield 85.6%.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04395412 |
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| 출처 데이터셋 | uspto-grants-1983_07 |
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| ORD ID | ord-817204799dfb4e57a572672069df7a31 |
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| 출처 메모 | uspto-grants-1983_07 |
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