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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1062449Generated: October 30, 2026

Acetone → HCID 86591637, compound

https://huagongshe.com/reaction/1062449

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 69747343HCID 69747343—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86591637HCID 8659163726.4%

Reaction Steps

To a solution of 2-{[trans-2-({[2-(2-chlorophenyl)-1-(4-chlorophenyl)-1H-imidazol-4-yl]carbonyl}amino)cyclohexyl]oxy}-ethyl acetate (Table entry 286) (31 mg, 0.06 mmol) in THF (7 mL) and water (0.7 mL) was added NaBH4 (5 mg, 0.13 mmol) portionwise over 1 h with the temperature kept below 20° C. The mixture was stirred at rt overnight, cooled to 5° C., treated with acetone (1 mL), and then concentrated. The residue was dissolved in CH2Cl2 and washed with brine. The organic layer was dried over MgSO4, filtered, and concentrated. The residue was purified by flash chromatography (2.5% methanol in EtOAc) to give the product 2-(2-chlorophenyl)-1-(4-chlorophenyl)-N-[(1R, 2S)-2-(2-hydroxyethoxy)cyclohexyl]-1H-imidazole-4-carboxamide (7.5 mg, 26% yield): LC-MS m/z (474.8 MH+), retention time 2.91 min (method 1); Rf=0.17 (EtOAc).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06960601B2
Source datasetuspto-grants-2005_11
ORD IDord-ba80d72d81b04a47b4004e41c26c02cb
Source noteuspto-grants-2005_11