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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 851008생성일: 2026년 10월 25일

Chlorotrimethylsilane → 8-[[2-(Acetylamino)-1-oxopropyl]amino]-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid

https://huagongshe.com/reaction/851008

반응식

참여 물질

역할이름HCID투입량
반응물ChlorotrimethylsilaneHCID 6397—
반응물Methyl chloroformateHCID 6586—
반응물4-MethylmorpholineHCID 7972—
반응물TriethylamineHCID 8471—
반응물N-Acetyl-L-alanineHCID 88064—
반응물8-Amino-4-hydroxyquinoline-3-carboxylic acidHCID 12866349—
용매AcetonitrileHCID 6342—
용매DichloromethaneHCID 6344—
생성물8-[[2-(Acetylamino)-1-oxopropyl]amino]-1,4-dihydro-4-oxo-3-quinolinecarboxylic acidHCID 1313687847.7%

반응 단계

A mixture of 3.93 g (30 mmol) of N-acetyl-L-alanine, 3.3 ml (30 mmol) of N-methyl morpholine, 2.33 ml (30 mmol) of methyl chloroformate, and 80 ml of acetonitrile is stirred at -10° to -20° for 30 minutes. A mixture of 4.08 g (20 mmol) of 8-amino-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid, 8.4 ml (60 mmol) of triethylamine, 7.6 ml (60 mmol) of chlorotrimethylsilane, and 100 ml of dichloromethane was stirred at room temperature for 40 minutes and then cooled to -20°. The cold mixed anhydride is added to the cold silylated quinoline and stirred for 4 hours with cooling and overnight at room temperature. The reaction mixture is evaporated to dryness and the residue is treated with acetonitrile and 1N hydrochloric acid. The solid is filtered to give 3.03 g of 8-[[2-(acetylamino)-1-oxopropyl]amino]-1,4-dihydro-4 -oxo-3-quinolinecarboxylic acid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04382089
출처 데이터셋uspto-grants-1983_05
ORD IDord-aefc5b7aaa064d9894f82adf7b1a2ce8
출처 메모uspto-grants-1983_05