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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 251344Generated: October 31, 2026

Hydrochloric Acid → 3-[5-Amino-1-(5-cyclopropylcarbamoyl-2-methyl-phenyl)-1H-imidazole-4-carbonyl]-benzoic acid

https://huagongshe.com/reaction/251344

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl 3-iodobenzoateHCID 18386959—
ReactantHCID 58088961HCID 58088961—
ReactantHCID 178478990HCID 178478990—
SolventTetrahydrofuranHCID 8028—
Product3-[5-Amino-1-(5-cyclopropylcarbamoyl-2-methyl-phenyl)-1H-imidazole-4-carbonyl]-benzoic acidHCID 58089033—

Reaction Conditions

Temperature42.5 °C

Reaction Steps

To a solution of 3-iodobenzoic acid tert-butyl ester (4.6g) in THF (20 mL) at −40° C. under N2 was added cyclohexylmagnesium chloride (2M in THF, 8.5 mL). The solution was kept at −40° C. to 0° C. for 20 min., when 3-(5-amino-4-cyano-imidazol-1-yl)-N-cyclopropyl-4-methyl-benzamide was added and the reaction was kept at rt for 1 h. Then HCl (4 M, 10 mL) was added and the mixuture was heated at 40 to 45° C. overnight. The mixture was neutralized with K2CO3 solution and extracted with EtOAc (2×100 mL) and the combined organics dried over Na2SO4, and concentrated. Purification of the crude product by column chromatography (EtOAc: MeOH=6:1) gave the desired product (0.46 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07863314B2
Source datasetuspto-grants-2011_01
ORD IDord-e8895aa343314f75a84b0cc7426139e9
Source noteuspto-grants-2011_01