HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 22036855, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 11955792 | HCID 11955792 | — |
| Reactant | Chloromethyl formate | HCID 17803410 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 22036855 | HCID 22036855 | 46% |
Reaction Steps
0.19 g (0.50 mmol) of 2-(2-aminobenzimidazol-1-yl)-4,6-dimorpholino-1,3,5-triazine synthesized in (1) of the Example 6 and 60% sodium hydride (24 mg, 0.60 mmol) added to DMF (2 ml) were reacted at room temperature for 1 hour. The reaction mixture was added and reacted with 0.040 ml (0.55 mmol) of chloromethylformate at room temperature for 16 hours. The reaction solution was poured into water and extracted with methyl acetate. The organic layer was separated, 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 100 mg (yield: 46%) of the titled compound as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07071189B2 |
| Source dataset | uspto-grants-2006_07 |
| ORD ID | ord-eac1321f2c99465f8fa75f66bfd88b15 |
| Source note | uspto-grants-2006_07 |