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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1595407Generated: November 3, 2026

HCID 178440777, compound → HCID 178440776, compound

https://huagongshe.com/reaction/1595407

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178440777HCID 178440777—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178440776HCID 17844077646.9%

Reaction Steps

2-(4-tert-Butylphenyl)-5-(4-nitrophenyl)-N-(2-thiazolyl)-imidazole-4-carboxamide (16.3 g) was dissolved in a mixed solvent of dioxane and methanol and hydrogenated with Raney nickel. The catalyst was filtered off and the residue was concentrated and crystallized from ethyl acetate and isopropyl ether to give 5-(4-aminophenyl)-2-(4-tert-butylphenyl)-N-(2-thiazolyl)imidazole-4-carboxamide (7.13 g). 1.0 g therefrom was converted to hydrochloride to give 5-(4-aminophenyl)-2-(4-tert-butylphenyl)-N-(2-thiazolyl)imidazole-4-carboxamide hydrochloride (0.48 g), melting point 270-272° C. (decomposition).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06288061B1
Source datasetuspto-grants-2001_09
ORD IDord-f37e2e48015f4e8cb47b64c904c93bd6
Source noteuspto-grants-2001_09