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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 850998Generated: October 25, 2026

Chlorotrimethylsilane → 6-[[(1-Acetyl-2-pyrrolidinyl)carbonyl]-amino]-1,2-dihydro-2-oxo-3-quinolinecarboxylic acid

https://huagongshe.com/reaction/850998

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
Reactant4-MethylmorpholineHCID 7972—
ReactantTriethylamineHCID 8471—
ReactantIsobutyl chloroformateHCID 62365—
ReactantN-Acetyl-L-prolineHCID 66141—
ReactantL-ProlineHCID 145742—
Reactant6-Amino-2-oxo-1,2-dihydroquinoline-3-carboxylic acidHCID 13106330—
SolventDichloromethaneHCID 6344—
Product6-[[(1-Acetyl-2-pyrrolidinyl)carbonyl]-amino]-1,2-dihydro-2-oxo-3-quinolinecarboxylic acidHCID 1313686464.4%

Reaction Steps

A solution of 4.71 g (30 mmol) of N-acetyl-L-proline and 60 ml of dichloromethane is cooled to -18° and 3.3 ml (30 mmol) of N-methyl morpholine and 3.9 ml (30 mmol) of isobutyl chloroformate is added, and the reaction mixture is stirred for 30 minutes at -10° to -20°. A mixture of 4.08 g (20 mmol) of 6-amino-1,2-dihydro-2-oxo-3-quinolinecarboxylic acid, 150 ml of dichloromethane, 8.4 ml (60 mmol) of triethylamine, and 7.6 ml (60 mmol) of chlorotrimethylsilane is stirred at room temperature for 35 minutes. The silylation mixture is cooled to -20° and the mixed anhydride of proline is added and stirred with cooling overnight. The reaction mixture is evaporated to dryness, and the residue is treated with ethanol to yield 4.42 g of 6-[[(1-acetyl-2-pyrrolidinyl)carbonyl]-amino]-1,2-dihydro-2-oxo-3-quinolinecarboxylic acid, mp 303° dec.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04382089
Source datasetuspto-grants-1983_05
ORD IDord-f517b170a6ef4c969b8511f3ac9afc36
Source noteuspto-grants-1983_05