HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 2-(Benzimidazol-1-yl)-4-(cis-2,6-dimethyl-morpholino)-6-morpholino-1,3,5-triazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,6-Dimethylmorpholine, cis- | HCID 641500 | — |
| Reactant | 2-(Benzimidazol-1-yl)-4-chloro-6-morpholino-1,3,5-triazine | HCID 10734228 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(Benzimidazol-1-yl)-4-(cis-2,6-dimethyl-morpholino)-6-morpholino-1,3,5-triazine | HCID 10692084 | 91% |
Reaction Steps
The obtained 2-(benzimidazol-1-yl)-4-chloro-6-morpholino-1,3,5-triazine (320 mg, 1.0 mmol) dissolved in DMF (20 ml) was added with potassium carbonate (430 mg, 3.2 mmol) and cis-2,6-dimethylmorpholine (140 mg, 1.2 mmol) and stirred at room temperature for 45 minutes. The reaction mixture was condensed under reduced pressure and the obtained residue was added with dichloromethane and water and shaken for mixing. The separated organic layer was washed with water and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure and the residue was purified by silica gel column chromatography to obtain 360 mg (yield: 90%) of the titled compound as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06251900B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-123ffe505673438aae8d2c6fca113a2c |
| Source note | uspto-grants-2001_06 |