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HRID 851008作成日:2026年10月26日

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

https://huagongshe.com/reaction/851008

反応式

関与物質

役割名称HCID仕込み量
反応物ChlorotrimethylsilaneHCID 6397—
反応物Methyl chloroformateHCID 6586—
反応物4-MethylmorpholineHCID 7972—
反応物TriethylamineHCID 8471—
反応物N-Acetyl-L-alanineHCID 88064—
反応物8-Amino-4-hydroxyquinoline-3-carboxylic acidHCID 12866349—
溶媒AcetonitrileHCID 6342—
溶媒DichloromethaneHCID 6344—
生成物8-[[2-(Acetylamino)-1-oxopropyl]amino]-1,4-dihydro-4-oxo-3-quinolinecarboxylic acidHCID 1313687847.7%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04382089
出典データセットuspto-grants-1983_05
ORD IDord-aefc5b7aaa064d9894f82adf7b1a2ce8
出典メモuspto-grants-1983_05