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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 851005Generated: October 25, 2026

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

https://huagongshe.com/reaction/851005

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantMethyl chloroformateHCID 6586—
Reactant4-MethylmorpholineHCID 7972—
ReactantTriethylamineHCID 8471—
ReactantN-Acetyl-L-alanineHCID 88064—
Reactant7-Amino-4-hydroxyquinoline-3-carboxylic acidHCID 10262322—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
Product7-[[2-(Acetylamino)-1-oxopropyl]-amino]-1,4-dihydro-4-oxo-3-quinolinecarboxylic acidHCID 1313687662.7%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04382089
Source datasetuspto-grants-1983_05
ORD IDord-f223e7d94c4c4fdab919dac0959f113f
Source noteuspto-grants-1983_05