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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 851005생성일: 2026년 10월 25일

Chlorotrimethylsilane → 7-[[2-(Acetylamino)-1-oxopropyl]-amino]-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid

https://huagongshe.com/reaction/851005

반응식

참여 물질

역할이름HCID투입량
반응물ChlorotrimethylsilaneHCID 6397—
반응물Methyl chloroformateHCID 6586—
반응물4-MethylmorpholineHCID 7972—
반응물TriethylamineHCID 8471—
반응물N-Acetyl-L-alanineHCID 88064—
반응물7-Amino-4-hydroxyquinoline-3-carboxylic acidHCID 10262322—
용매AcetonitrileHCID 6342—
용매DichloromethaneHCID 6344—
생성물7-[[2-(Acetylamino)-1-oxopropyl]-amino]-1,4-dihydro-4-oxo-3-quinolinecarboxylic acidHCID 1313687662.7%

반응 단계

A mixture of 3.93 g (30 mmol) of N-acetyl-L-alanine, 3.30 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 7-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 is stirred at room temperature for 30 minutes and then cooled to -20°. The cold mixed anhydride is added to the cold silylated quinoline and stirred with cooling for 3 hours and overnight at room temperature. The reaction mixture is evaporated to dryness and the residue is treated with water. The solid is filtered to give 3.98 g of 7-[[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-f223e7d94c4c4fdab919dac0959f113f
출처 메모uspto-grants-1983_05