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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1190082Generated: October 31, 2026

Ethanol → HCID 178510376, compound

https://huagongshe.com/reaction/1190082

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant1-PropanolHCID 1031—
ReactantTrifluoroacetic acidHCID 6422—
Reactant4-Cyano-1-(2-trimethylsilanyl-ethoxymethyl)-1H-imidazole-2-carboxylic acid (4-bromo-2-cyclohex-1-enyl-phenyl)-amideHCID 59457532—
SolventDichloromethaneHCID 6344—
ProductHCID 178510376HCID 17851037696%

Reaction Steps

To a solution of 4-cyano-1-(2-trimethylsilanyl-ethoxymethyl)-1H-imidazole-2-carboxylic acid (4-bromo-2-cyclohex-1-enyl-phenyl)-amide (as prepared in the previous step, 1.20 g, 2.39 mmol) in 10 mL of DCM (CH2Cl2) was added 0.30 mL of EtOH followed by 5.0 mL of TFA. After stirring at RT for 3 h, the mixture was treated with 20 mL of n-propanol and concentrated in vacuo. The residue was triturated with DCM to afford 853 mg (96%) of the title compound as a white solid. 1H-NMR (dimethylsulfoxide (DMSO)-d6; 400 MHz): δ 9.80 (s, 1H), 8.30 (s, 1H), 7.94 (d, 1H, J=8.6 Hz), 7.50 (dd, 1H, J=8.6, 2.3 Hz), 7.39 (d, 1H, J=2.3 Hz), 5.80 (m, 1H), 2.12-2.25 (m, 4H), 1.61-1.77 (m, 4H). Mass spectrum (ESI, m/z): Calcd. for C17H15BrN4O, 371.0 (M+H). found 371.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08674100B2
Source datasetuspto-grants-2014_03
ORD IDord-a8f1d6d8fe424f62a83171633f92d8e9
Source noteuspto-grants-2014_03