Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 850998생성일: 2026년 10월 27일
Chlorotrimethylsilane → 6-[[(1-Acetyl-2-pyrrolidinyl)carbonyl]-amino]-1,2-dihydro-2-oxo-3-quinolinecarboxylic acid
https://huagongshe.com/reaction/850998
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Chlorotrimethylsilane | HCID 6397 | — |
| 반응물 | 4-Methylmorpholine | HCID 7972 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Isobutyl chloroformate | HCID 62365 | — |
| 반응물 | N-Acetyl-L-proline | HCID 66141 | — |
| 반응물 | L-Proline | HCID 145742 | — |
| 반응물 | 6-Amino-2-oxo-1,2-dihydroquinoline-3-carboxylic acid | HCID 13106330 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 6-[[(1-Acetyl-2-pyrrolidinyl)carbonyl]-amino]-1,2-dihydro-2-oxo-3-quinolinecarboxylic acid | HCID 13136864 | 64.4% |
반응 단계
A solution of 4.71 g (30 mmol) of N-acetyl-L-proline and 60 ml of dichloromethane is cooled to -18° and 3.3 ml (30 mmol) of N-methyl morpholine and 3.9 ml (30 mmol) of isobutyl chloroformate is added, and the reaction mixture is stirred for 30 minutes at -10° to -20°. A mixture of 4.08 g (20 mmol) of 6-amino-1,2-dihydro-2-oxo-3-quinolinecarboxylic acid, 150 ml of dichloromethane, 8.4 ml (60 mmol) of triethylamine, and 7.6 ml (60 mmol) of chlorotrimethylsilane is stirred at room temperature for 35 minutes. The silylation mixture is cooled to -20° and the mixed anhydride of proline is added and stirred with cooling overnight. The reaction mixture is evaporated to dryness, and the residue is treated with ethanol to yield 4.42 g of 6-[[(1-acetyl-2-pyrrolidinyl)carbonyl]-amino]-1,2-dihydro-2-oxo-3-quinolinecarboxylic acid, mp 303° dec.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04382089 |
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| 출처 데이터셋 | uspto-grants-1983_05 |
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| ORD ID | ord-f517b170a6ef4c969b8511f3ac9afc36 |
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| 출처 메모 | uspto-grants-1983_05 |
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