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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1507054Generated: October 25, 2026

Imidazole → HCID 178481629, compound

https://huagongshe.com/reaction/1507054

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantBenzylamineHCID 7504—
ReactantTriethylamineHCID 8471—
Reactant1-Methylimidazolidine-2,4,5-trioneHCID 123196—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
ProductHCID 178481629HCID 17848162962%

Reaction Steps

To a solution of 1-methyl-imidazolidine-2,4,5-trione (Example 1.3, Part A) (800 mg, 6.25 mmol), imidazole (467 mg, 6.87 mmol), N,N-dimethylaminopyridine (cat.) and triethylamine (1.82 mL, 13.1 mmol) in chloroform (13 mL) was added chlorotrimethylsilane (1.67 mL, 13.1 mmol) dropwise at room temperature under a nitrogen atmosphere, and the reaction mixture was stirred for 2 h. Benzylamine (0.75 mL, 6.87 mmol) was added and the reaction mixture was stirred for a further 22.5 h. The reaction mixture was diluted with chloroform and water and the chloroform extracts were dried and evaporated. The crude product was purified by column chromatography (PS with gradient elution to DCM:EtOAc 3:1) to give the product as a colourless solid (838 mg, 62%), mp 152-154° C. δH (300 MHz, CD3CN) 7.95 (v br s, 1H, NH), 7.41-7.27 (m, 5H, PhH), 4.64 (s, 2H, CH2), 2.95 (s, 3M, CH3). Mass spectrum (ESI) m/z 218 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221799B2
Source datasetuspto-grants-2015_12
ORD IDord-82fa9de6dd494da5901287e5a16c3745
Source noteuspto-grants-2015_12