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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 987008Generated: October 30, 2026

1,1'-Carbonyldiimidazole → Cyclopentyl 4-(2-chloro-6-fluorophenyl)-1,4-dihydro-5-(1-imidazolylcarbonyl)-2,6-dimethylpyridine-3-carboxylate

https://huagongshe.com/reaction/987008

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant4-(2-Chloro-6-fluorophenyl)-3-cyclopentyloxycarbonyl-1,4-dihydro-2,6-dimethylpyridine-5-carboxylic acidHCID 15285434—
ReactantToluene ethylacetateHCID 21584019—
SolventTetrahydrofuranHCID 8028—
ProductCyclopentyl 4-(2-chloro-6-fluorophenyl)-1,4-dihydro-5-(1-imidazolylcarbonyl)-2,6-dimethylpyridine-3-carboxylateHCID 15285435—

Reaction Steps

13.6 g (83 mmol) of carbonyldiimidazole are added to 33.0 g (83 mmol) of 4-(2-chloro-6-fluorophenyl)-3-cyclopentyloxycarbonyl-1.4-dihydro-2,6-dimethylpyridine-5-carboxylic acid in 350 ml of tetrahydrofuran and the mixture is heated to reflux for 3 h. Thin-layer chromatographic checking (silica gel, toluene/ethyl acetate 1:1) shows complete reaction, after which the reaction mixture is concentrated, the residue is taken up in ethyl acetate, and the solution is washed twice with water, dried over sodium sulphate and concentrated again. The target compound precipitates from ether in the form of white crystals of m.p. 150° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06630494B2
Source datasetuspto-grants-2003_10
ORD IDord-b3d851f4dd9344baa677055af27932aa
Source noteuspto-grants-2003_10