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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1399211Generated: October 30, 2026

Acetic Acid → HCID 57786311, compound

https://huagongshe.com/reaction/1399211

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant(1-Ethoxycyclopropoxy)trimethylsilaneHCID 2734686—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant9-Chloro-1-(2,4-dichlorophenyl)-1,2,3,4-tetrahydropyrimido[1,2-a]benzimidazol-6-amineHCID 57786328—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductHCID 57786311HCID 5778631119%

Reaction Steps

A solution of 9-chloro-1-(2,4-dichlorophenyl)-1,2,3,4-tetrahydropyrimido[1,2-a]benzimidazol-6-amine (367 mg, 1.00 mmol), (1-ethoxycyclopropoxy)trimethylsilane (1.01 mL, 5.00 mmol), sodium cyanoborohydride (314 mg, 5.00 mmol), and acetic acid (572 μL, 10.0 mmol) in methanol (3.0 mL) was stirred at reflux for 40 h. The reaction mixture was diluted with ethyl acetate, quenched with aqueous sodium hydrogen carbonate, and filtrated. The organic layer was washed with brine, dried over sodium sulfate, filtered, and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel eluting with a 20% ethyl acetate/hexane mixture to give the title compound as a colorless solid (83.5 mg, 0.186 mmol, 19%). Analytically pure material was obtained by recrystallization from ethyl acetate/hexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901141B2
Source datasetuspto-grants-2014_12
ORD IDord-8346dc4976b6453ea567739f593eb275
Source noteuspto-grants-2014_12