Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2245826Generated: November 2, 2026

Sodium hydride → HCID 10196736, compound

https://huagongshe.com/reaction/2245826

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantOxalyl chlorideHCID 65578—
Reactant3-Bromo-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carboxylic acidHCID 11587535—
ReactantHCID 68545554HCID 68545554—
CatalystDimethylformamideHCID 6228—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 10196736HCID 10196736—

Reaction Steps

To a solution of the quinazolinedione of Step G (245 mg, 0.825 mmol) in dimethylformamide (5 mL) was added sodium hydride (60% oil dispersion, 36 mg, 0.90 mmol) and the reaction was allowed to stir at room temperature. In a separate reaction flask containing a solution of the pyrazole acid of Step D (500 mg, 1.65 mmol) in dichloromethane (10 mL) was added oxalyl chloride (0.17 mL, 1.95 mmol) and one drop of DMF. This mixture was stirred for 2 hours, then concentrated and placed under vacuum. The acid chloride was divided into two equal portions. One of these portions was taken up in 5 mL of DMF and added to the quinazolinedione/NaH reaction mixture and the resulting mixture was stirred at room temperature for 3 hours. The reaction was partitioned between ethyl acetate and water, washed twice with water, then with brine and dried over sodium sulfate. The crude product was purified by chromatography on silica gel with 99:1 chloroform/acetone as eluent to afford the title compound, a compound of the present invention.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07683201B2
Source datasetuspto-grants-2010_03
ORD IDord-ced5035526ee43a8ac950ee79a167ecc
Source noteuspto-grants-2010_03