HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N'-(4,5-Dimethyl-2-thiazolyl)-N,N-dimethyl-methanimidamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| Reactant | 4,5-Dimethyl-1,3-thiazol-2-amine--hydrogen chloride (1/1) | HCID 16211387 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N'-(4,5-Dimethyl-2-thiazolyl)-N,N-dimethyl-methanimidamide | HCID 54260345 | 78.4% |
Reaction Steps
A suspension of 2-amino-4,5-dimethylthiazole hydrochloride (4.92 g, 30 mmol) (Formula A-1) in toluene (60 mL) was treated with triethylamine (4.5 mL, 35 mmol) and vigorously stirred for 30 minutes. The mixture was treated with dimethylformamide dimethyl acetal (7.3 mL, 60 mmol) and heated at reflux temperature for 2 hours. The solution was cooled, diluted with ethyl acetate, washed with saline, dried and evaporated. The residue was crystallized from hexane to provide pure N′-(4,5-Dimethyl-2-thiazolyl)-N,N-dimethyl-methanimidamide (Formula A-2) (4.31 g, 77%), m.p. 47-58°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06191124B1 |
| Source dataset | uspto-grants-2001_02 |
| ORD ID | ord-69ae5c2f0e624d4aab625b260fb1bdc1 |
| Source note | uspto-grants-2001_02 |