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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

반응식

참여 물질

역할이름HCID투입량
반응물ChlorotrimethylsilaneHCID 6397—
반응물4-MethylmorpholineHCID 7972—
반응물TriethylamineHCID 8471—
반응물Isobutyl chloroformateHCID 62365—
반응물N-Acetyl-L-prolineHCID 66141—
반응물L-ProlineHCID 145742—
반응물6-Amino-2-oxo-1,2-dihydroquinoline-3-carboxylic acidHCID 13106330—
용매DichloromethaneHCID 6344—
생성물6-[[(1-Acetyl-2-pyrrolidinyl)carbonyl]-amino]-1,2-dihydro-2-oxo-3-quinolinecarboxylic acidHCID 1313686464.4%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04382089
출처 데이터셋uspto-grants-1983_05
ORD IDord-f517b170a6ef4c969b8511f3ac9afc36
출처 메모uspto-grants-1983_05