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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1628716Generated: November 2, 2026

Lithium borohydride → HCID 57785980, compound

https://huagongshe.com/reaction/1628716

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium borohydrideHCID 4148881—
ReactantHCID 57786000HCID 57786000—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57785980HCID 5778598083%

Reaction Conditions

Temperature50 °C

Reaction Steps

Lithium borohydride (205 mg, 9.42 mmol) was added to a stirred solution of methyl 9-chloro-1-(2,4-dichloro-6-methylphenyl)-1,2,3,4-tetrahydropyrimido[1,2-a]benzimidazole-6-carboxylate (800 mg, 1.88 mmol) in tetrahydrofuran (4.0 mL) at room temperature, and the mixture was stirred at 50° C. for 13 hr. The reaction was quenched by aqueous saturated ammonium chloride at 0° C. 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 washed with ethyl acetate/diisopropyl ether to give the title compound as a colorless powder (620 mg, 1.56 mmol, 83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785460B2
Source datasetuspto-grants-2014_07
ORD IDord-4145e2bb57c549888419dec12e826ab5
Source noteuspto-grants-2014_07