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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172434Generated: November 2, 2026

Sodium hydride → HCID 68679539, compound

https://huagongshe.com/reaction/1172434

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantHCID 68677297HCID 68677297—
ReactantHCID 178465666HCID 178465666—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 68679539HCID 68679539—

Reaction Conditions

Temperature65 °C

Reaction Steps

To a mixture of 9.4 mg of N-hydroxyacetamidine, molecular sieves 4A and 1 ml of tetrahydrofuran was added sodium hydride followed by stirring at 65° C. for 1 hour. To the reaction solution was added a solution of 22.6 mg of methyl 2-((4-(3-chloro-2-fluorobenzoyl)piperazin-1-yl)methyl)6-((3-(methoxymethyl)-thiazol-2(3H)-ylidene)amino)isonicotinate in 1 ml of tetrahydrofuran, followed by heating under reflux for 6 hours. The reaction solution was cooled to room temperature, diluted with ethyl acetate, and washed with saturated sodium bicarbonate and brine. The resulting organic layer was dried over magnesium sulfate and filtered, and the filtrate was concentrated. The resulting residue was purified by a thin-layer chromatography for fractionation (eluent: chloroform/methanol=10/1) to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834018B2
Source datasetuspto-grants-2010_11
ORD IDord-acaf3e3ce59f4071a7c91cbe04daef6a
Source noteuspto-grants-2010_11