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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1995333Generated: October 26, 2026

Dimethylformamide → 1,4-Dihydro-4-oxo-7-[[(5-oxo-2-pyrrolidinyl)carbonyl]amino]-3-quinolinecarboxylic acid

https://huagongshe.com/reaction/1995333

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantL-Pyroglutamic AcidHCID 7405—
ReactantTriethylamineHCID 8471—
ReactantThionyl ChlorideHCID 24386—
Reactant7-Amino-4-hydroxyquinoline-3-carboxylic acidHCID 10262322—
SolventDichloromethaneHCID 6344—
Product1,4-Dihydro-4-oxo-7-[[(5-oxo-2-pyrrolidinyl)carbonyl]amino]-3-quinolinecarboxylic acidHCID 1313687074.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 3.87 g (30 mmol) of 5-oxo-L-proline, 2.32 ml (30 mmol) of dimethylformamide, 2.19 ml (30 mmol) of thionyl chloride, and 75 ml of dichloromethane is stirred with cooling for 50 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 200 ml of dichloromethane is stirred at room temperature for 50 minutes and then cooled to 0° C. The cold acid chloride solution is added to the cold silylated quinoline and is stirred with cooling for 3 hours and at room temperature overnight. The reaction mixture is evaporated to dryness and the residue is treated with water and ethanol. The solid is filtered to give 4.72 g of 1,4-dihydro-4-oxo-7-[[(5-oxo-2-pyrrolidinyl)carbonyl]amino]-3-quinolinecarboxylic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04404201
Source datasetuspto-grants-1983_09
ORD IDord-792583580aa74d08b6f51429eaf53be9
Source noteuspto-grants-1983_09