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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 851003생성일: 2026년 10월 24일

Chlorotrimethylsilane → 6-[[(1-Acetyl-2-pyrrolidinyl)-carbonyl]amino]-1,4-dihydro-4-oxo-quinolinecarboxylic acid

https://huagongshe.com/ko/reaction/851003

반응식

참여 물질

역할이름HCID투입량
반응물ChlorotrimethylsilaneHCID 6397—
반응물4-MethylmorpholineHCID 7972—
반응물TriethylamineHCID 8471—
반응물Isobutyl chloroformateHCID 62365—
반응물N-Acetyl-L-prolineHCID 66141—
반응물6-Amino-4-hydroxyquinoline-3-carboxylic acidHCID 3281201—
용매DichloromethaneHCID 6344—
생성물6-[[(1-Acetyl-2-pyrrolidinyl)-carbonyl]amino]-1,4-dihydro-4-oxo-quinolinecarboxylic acidHCID 7052424762.4%

반응 단계

A mixture of 7.07 g (45 mmol) of N-acetyl-L-proline, 5.85 ml (45 mmol) isobutyl chloroformate, 4.95 ml 45 mmol) N-methyl morpholine, and 90 ml of dichloromethane is stirred at -10° to -20° for 30 minutes. A mixture of 6.13 g (30 mmol) of 6-amino-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid, 12.6 ml (90 mmol) triethylamine, 11.4 ml (90 mmol) chlorotrimethylsilane, and 150 ml of dichloromethane is stirred at room temperature for 30 minutes and then is cooled to -20°. The cold mixed anhydride solution is added to the cold silylated quinoline and is stirred with cooling for 4 hours and at room temperature ovenight. The reaction mixture is evaporated to dryness and the residue is treated with 1 N hydrochloric acid and the solid is filtered. The solid is digested with ethanol and filtered to give 6.43 g of 6-[[(1-acetyl- 2-pyrrolidinyl)-carbonyl]amino]-1,4-dihydro-4-oxo-quinolinecarboxylic acid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04382089
출처 데이터셋uspto-grants-1983_05
ORD IDord-23759aa6377740ca9a078275182f5948
출처 메모uspto-grants-1983_05