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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428991Generated: November 2, 2026

Diisopropylethylamine → N-(3 hydroxyadamant-1-yl)-2,5-dimethyl-1-phenyl-1H-imidazole-4-carboxamide

https://huagongshe.com/reaction/1428991

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant3-Amino-1-adamantanolHCID 658645—
Reactant2-Chloro-1,3-dimethylimidazolidin-1-ium;hexafluorophosphateHCID 21868419—
Reactant2,5-dimethyl-1-phenyl-1H-imidazole-4-carboxylic acidHCID 54579222—
SolventDichloromethaneHCID 6344—
ProductN-(3 hydroxyadamant-1-yl)-2,5-dimethyl-1-phenyl-1H-imidazole-4-carboxamideHCID 5869577667.1%

Reaction Steps

To a magnetically stirred solution of 2,5-dimethyl-1-phenyl-1H-imidazole-4-carboxylic acid (0.66 gram, 0.00306 mol) in dichloromethane (35 ml) was successively added diisopropylethylamine (DIPEA) (3.1 ml), CIP (2-chloro-1,3-dimethylimidazolinium hexafluorophosphate). (2.55 gram) and 3-hydroxyadamantane amine (0.612 gram, 0.00366 mol). The resulting mixture was reacted at 20° C. for 16 hours and subsequently concentrated in vacuo. The resulting residue was taken up in dichloromethane and washed with 5% aqueous NaHCO3 solution. The organic layer was dried over MgSO4, filtered and concentrated in vacuo. The resulting residue was purified by flash chromatography (dichoromethane/methanol=98/2 (v/v)) to give N-(3 hydroxyadamant-1-yl)-2,5-dimethyl-1-phenyl-1H-imidazole-4-carboxamide (0.75 gram, 67% yield). Rf (silica gel/dichoromethane/methanol=98/2 (v/v))˜0.6. Melting point: 215-220° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08937184B2
Source datasetuspto-grants-2015_01
ORD IDord-1393384b68b146fdafa96a648774b271
Source noteuspto-grants-2015_01