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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1399033Generated: November 1, 2026

HCID 57786099, compound → HCID 57785945, compound

https://huagongshe.com/reaction/1399033

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57786099HCID 57786099—
ReactantHCID 178418630HCID 178418630—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57785945HCID 5778594576%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 1-(2,4-dichlorophenyl)-1,2,3,4-tetrahydropyrimido[1,2-a]benzimidazole-6-carbaldehyde (3.00 g, 8.67 mmol) in tetrahydrofuran (25 mL) was added dropwise cyclopropylmagnesium bromide (1.0 M solution in tetrahydrofuran, 11.6 mL, 11.6 mmol) at 0° C., and the mixture was stirred at 0° C. for 1 h. The reaction was quenched by methanol, and the mixture was neutralized with aqueous saturated ammonium chloride, and 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 20-60% ethyl acetate/n-hexane gradient mixture. The filtrate was concentrated in vacuo to give the solid, which was recrystallized from ethanol to give the title compound as a colorless crystal (1.71 g, 4.40 mmol, 76%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901141B2
Source datasetuspto-grants-2014_12
ORD IDord-107c1020e6034a41b37ddaeac3a6a15c
Source noteuspto-grants-2014_12