HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N'-[5-(2-chloro-benzoyl)-thiazol-2-yl]-N,N-dimethyl-formamidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | 2-Bromo-2'-chloroacetophenone | HCID 2735785 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N'-[5-(2-chloro-benzoyl)-thiazol-2-yl]-N,N-dimethyl-formamidine | HCID 66628633 | — |
Reaction Steps
A mixture of thiourea (4.95 g, 65.0 mmol) and dimethoxymethyl-dimethyl-amine (23.2 g, 195 mmol) in methanol (80 mL) was heated at reflux for 30 minutes. After allowing the mixture to cool, triethylamine (19.8 g, 195 mmol) and a solution of 2-bromo-1-(chloro-phenyl)-ethanone (crude from last step) in methanol (50 mL) were added. The mixture was heated at reflux for 4 hours. The solvent was removed and the residue was used directly in the next procedure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07977322B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-4e13dbc8740d49a09bb05a10efdbc2ac |
| Source note | uspto-grants-2011_07 |