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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 582143Generated: November 1, 2026

Aniline → HCID 178488982, compound

https://huagongshe.com/reaction/582143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
Reactant2,6-DimethylanilineHCID 6896—
ReactantThionyl ChlorideHCID 24386—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178488985HCID 178488985—
CatalystDimethylformamideHCID 6228—
SolventHydrochloric AcidHCID 313—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178488982HCID 17848898215%

Reaction Steps

A mixture of 2-(3-cyclopentyloxy-4-methoxyphenyl)-imidazole-4-carboxylic acid (400 mg, 1.32 mmol) and SOCl2 (10 ml) containing DMF (1 drop) was heated to reflux for 2 hours. The volatiles were removed in vacuo and to the residue was added toluene (25 ml) and the solvent evaporated. This procedure was repeated to remove dissolved gaseous by-products. The residue was dissolved in THF (10 ml) and added dropwise at 0° C. over 10 minutes, to a solution of the salt of 2,6-dimethylaniline (510 μl, 4.14 mmol) in THF (30 ml) (formed by adding a solution of the aniline in THF (15 ml) to a suspension of NaH (167 mg, 4.14 mmol) is THF (15 ml) at room temperature). The resultant solution was stirred at room temperature for 48 hours, diluted with 1N HCl (20 ml) and the mixture extracted with methylene chloride (2×50 ml) The combined organics were dried over Na2SO4 and the volatiles removed in vacuo. Flash chromatography (SiO2 ; CH2Cl2 :EtOH (97:3)) afforded 2-(3-cyclopentyloxy-4-methoxyphenyl)-imidazole-4-carboxylic acid-2,6-dimethylphenyl amide (80 mg, 15%) as a pale yellow solid, mp 118-122° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05922751
Source datasetuspto-grants-1999_07
ORD IDord-68fc3a344c794634b79be972ab8e41ec
Source noteuspto-grants-1999_07