Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1399178Generated: October 28, 2026

HCID 57785981, compound → HCID 57786231, compound

https://huagongshe.com/reaction/1399178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57785981HCID 57785981—
ReactantHCID 178418630HCID 178418630—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57786231HCID 5778623197%

Reaction Steps

To a solution of 9-chloro-1-(6-methoxy-2-methylpyridin-3-yl)-1,2,3,4-tetrahydropyrimido[1,2-a]benzimidazole-6-carbaldehyde (213.6 mg, 0.599 mmol) in tetrahydrofuran (3.0 mL) was added cyclopropylmagnesium bromide (1.0 M solution in tetrahydrofuran, 898 μL, 0.898 mmol) at 0° C. The reaction mixture was stirred at room temperature for 1 hr. The starting material wasn't consumed completely. To the mixture was added cyclopropylmagnesium bromide (1.0 M solution in tetrahydrofuran, 449 μL, 0.449 mmol) at 0° C. The reaction mixture was stirred at room temperature for 1 hr. The mixture was quenched with aqueous saturated ammonium chloride and extracted with ethyl acetate (×3). The combined organic layer was washed with brine, dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. The resulting solid was washed with diisopropyl ether to give the title compound as a colorless solid (231.2 mg, 0.580 mmol, 97%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901141B2
Source datasetuspto-grants-2014_12
ORD IDord-de349c0d8b294b03b689bd464ba37dbf
Source noteuspto-grants-2014_12