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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1190086Generated: October 31, 2026

Acetyl chloride → HCID 178474717, compound

https://huagongshe.com/reaction/1190086

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
Reactant2-DimethylaminopyridineHCID 21885—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 178476304HCID 178476304—
SolventChloroformHCID 6212—
SolventEthyl AcetateHCID 8857—
ProductHCID 178474717HCID 17847471716%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 4-cyano-1H-imidazole-2-carboxylic acid [4-(1-amino-1-methyl-ethyl)-2-cyclohex-1-enyl-phenyl]-amide acetic acid salt (as prepared in the previous step, 50.0 mg, 0.122 mmol) and DIEA (85.0 μL, 0.488 mmol) in 2 mL of CHCl3 was stirred at RT for 5 min before dimethylaminopyridine (DMAP) (4.1 mg, 0.037 mmol) was added. The mixture was cooled to 0° C. and a solution of acetyl chloride (10 μL, 0.15 mmol) in 2 mL of CHCl3 was added dropwise. The reaction was warmed to RT and stirred for 18 h under Ar. The mixture was treated with EtOAc (40 mL), washed with saturated aqueous NaHCO3 (5 mL), brine (10 mL) and dried over Na2SO4. Removal of the solvent under reduced pressure followed by flash chromatography of the residue on silica gel (1-2% MeOH/DCM) gave 7.6 mg (16%) of the title compound as a white solid. 1H-NMR (CD3OD; 400 MHz): δ 8.17 (s, 1H), 8.10 (d, 1H, J=8.6 Hz), 7.99 (s, 1H), 7.27 (dd, 1H, J=8.6, 2.3 Hz), 7.16 (d, 1H, J=2.3 Hz), 5.80 (m, 1H), 2.20-2.32 (m, 4H), 1.94 (s, 3H), 1.74-1.88 (m, 4H), 1.62 (s, 6H). Mass spectrum (ESI, m/z): Calcd. for C22H25N5O2, 392.2 (M+H). found 391.8.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08674100B2
Source datasetuspto-grants-2014_03
ORD IDord-a9b5f463741645428c339182add45854
Source noteuspto-grants-2014_03