Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2374664Generated: October 25, 2026

2-(Bromoacetyl)-5-chlorothiophene → 1-[(E)-(4-chlorophenyl)methylideneamino]-4-(5-chlorothiophen-2-yl)imidazol-2-amine

https://huagongshe.com/reaction/2374664

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Bromoacetyl)-5-chlorothiopheneHCID 2063634—
ReactantDE(2-chloro)-4-chloro-icerguastatHCID 178513142—
SolventEthanolHCID 702—
Product1-[(E)-(4-chlorophenyl)methylideneamino]-4-(5-chlorothiophen-2-yl)imidazol-2-amineHCID 2194975472%

Reaction Steps

A solution of 2-bromo-1-(5-chloro-2-thienyl)-1-ethanone (1.07 g, 4.49 mmol), 2-[(E)-1- (4-chlorophenyl)methylidene]-1-hydrazinecarboximidamide (1.77 g, 8.98 mmol) was heated in ethanol (10 mL) for 2 h, then the mixture was left at room temperature for additional 10 h. The precipitate filtered, washed with hot water, and recrystallized from ethanol to give N1-[(E)-1-(4-chlorophenyl)methylidene]-4-(5-chloro-2-thienyl)-1H-1,2-imidazolediamine 2 (1.09 g, 72%) as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07462723B2
Source datasetuspto-grants-2008_12
ORD IDord-aa5aa84886cf41e1bd70a001bb3e6e44
Source noteuspto-grants-2008_12