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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 851003Generated: October 25, 2026

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

https://huagongshe.com/reaction/851003

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
Reactant4-MethylmorpholineHCID 7972—
ReactantTriethylamineHCID 8471—
ReactantIsobutyl chloroformateHCID 62365—
ReactantN-Acetyl-L-prolineHCID 66141—
Reactant6-Amino-4-hydroxyquinoline-3-carboxylic acidHCID 3281201—
SolventDichloromethaneHCID 6344—
Product6-[[(1-Acetyl-2-pyrrolidinyl)-carbonyl]amino]-1,4-dihydro-4-oxo-quinolinecarboxylic acidHCID 7052424762.4%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04382089
Source datasetuspto-grants-1983_05
ORD IDord-23759aa6377740ca9a078275182f5948
Source noteuspto-grants-1983_05