HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(Bromoacetyl)-5-chlorothiophene → 1-[(E)-(4-chlorophenyl)methylideneamino]-4-(5-chlorothiophen-2-yl)imidazol-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(Bromoacetyl)-5-chlorothiophene | HCID 2063634 | — |
| Reactant | DE(2-chloro)-4-chloro-icerguastat | HCID 178513142 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-[(E)-(4-chlorophenyl)methylideneamino]-4-(5-chlorothiophen-2-yl)imidazol-2-amine | HCID 21949754 | 72% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07462723B2 |
| Source dataset | uspto-grants-2008_12 |
| ORD ID | ord-aa5aa84886cf41e1bd70a001bb3e6e44 |
| Source note | uspto-grants-2008_12 |