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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2194489Generated: October 30, 2026

Dimethylformamide → HCID 87235675, compound

https://huagongshe.com/reaction/2194489

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 67009554HCID 67009554—
SolventDichloromethaneHCID 6344—
ProductHCID 87235675HCID 87235675—

Reaction Steps

2.20 g (8.3 mmol) of 1-(ethylthiomethyl)-2-oxo-1,2-dihydro-1,8-naphthyridine-3-carboxylic acid was dissolved in dichloromethane (80 mL), and 5.0 mL (60 mmol) of oxalyl chloride was added thereto. One droplet of N,N-dimethylformamide was added to the above mixture, and the resulting mixture was stirred for one hour at room temperature. The reaction solution was concentrated under reduced pressure, and thus 1-(ethylthiomethyl)-2-oxo-1,2-dihydro-1,8-naphthyridine-3-carboxylic acid chloride was obtained. The acid chloride thus obtained was dissolved in dichloromethane (80 mL), and 1.02 g (9.1 mmol) of 1,3-cyclohexanedione and 1.40 mL (10.0 mmol) of triethylamine were added to the above solution under ice cooling. The resulting mixture was stirred for 2 hours at room temperature. The reaction mixture was poured into an aqueous solution of sodium hydrogen carbonate, and the mixture was extracted with dichloromethane. The organic phase was dried and concentrated. The residue was washed with diisopropyl ether, and 2.99 g of the title compound was obtained as a light yellow solid (yield: quantitative).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08334236B2
Source datasetuspto-grants-2012_12
ORD IDord-04c5363b98b04c30bfdaba4b2ba4ebb2
Source noteuspto-grants-2012_12