HuagongsheHuagongshe Chemistry Print Report · For research reference only
Guanidine, 1,1-dimethyl-, sulfate → 4-Amino-2(-N,N-dimethylamino)-5-(2,3,5-trichlorophenyl)-6-trifluoromethyl pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Guanidine, 1,1-dimethyl-, sulfate | HCID 220673 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | 2-(2,3,5-Trichlorophenyl)-4,4,4-trifluoro-3-methoxybut-2-enonitrile | HCID 54422853 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Amino-2(-N,N-dimethylamino)-5-(2,3,5-trichlorophenyl)-6-trifluoromethyl pyrimidine | HCID 11523878 | — |
Reaction Steps
To a solution of NaOEt (from 0.144 g of Na) in EtOH (12.5 ml) was added 1,1-dimethylguanidine sulphate (1.4 g), (Aldrich). The resulting white suspension was stirred at room temperature for 10 minutes. A solution of 2-(2,3,5-trichlorophenyl)-4,4,4-trifluoro-3-methoxybut-2-enonitrile (see Example 1.6) (0.85 g) in EtOH (2.5 ml) was added and the resulting mixture was stirred at reflux for 4.5 hours. After cooling, the suspension was filtered, and the filtrate was evaporated to dryness in vacuo. Chromatography on silica gel, eluting with CHCl3, gave the desired product, 0.61 g, mp. 124°-126° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05597827 |
| Source dataset | uspto-grants-1997_01 |
| ORD ID | ord-9ebc8bb0460d4ba8ba9626ee94e009e2 |
| Source note | uspto-grants-1997_01 |