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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1399073Generated: October 31, 2026

HCID 57786105, compound → HCID 57786226, compound

https://huagongshe.com/reaction/1399073

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57786105HCID 57786105—
ReactantHCID 178455851HCID 178455851—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57786226HCID 57786226—

Reaction Steps

n-Propylmagnesium bromide (2.0 M solution in tetrahydrofuran, 0.25 mL, 0.50 mmol) was added to a stirred solution of 9-chloro-1-(2,4-dichloro-6-methylphenyl)-1,2,3,4-tetrahydropyrimido[1,2-a]benzimidazole-6-carbaldehyde (179 mg, 0.453 mmol) in tetrahydrofuran (2.0 mL) at 0° C., and the mixture was stirred at room temperature for 12 hr. The reaction was quenched by aqueous saturated ammonium chloride, and the mixture was extracted with ethyl acetate. The combined organic layer was washed with brine, dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel eluting with a 2-50% ethyl acetate/n-hexane gradient mixture. The filtrate was concentrated in vacuo to give the title compound as a colorless amorphous (rotamer 1; 72.3 mg, 0.165 mmol, 36%, rotamer 2; 68.7 mg, 0.157 mmol, 35%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901141B2
Source datasetuspto-grants-2014_12
ORD IDord-983b2035227a4918896f1e1489d57063
Source noteuspto-grants-2014_12