HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(difluoromethyl)-1H-1,3-benzodiazole → 2-(6-Amino-2-difluoromethylbenzimidazol-1-yl)-4,6-dimorpholinopyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(difluoromethyl)-1H-1,3-benzodiazole | HCID 597703 | — |
| Reactant | 2-(2-Difluoromethyl-6-nitrobenzimidazol-1-yl)-4,6-dimorpholinopyrimidine | HCID 22036868 | — |
| Reactant | 2-(2-Difluoromethyl-5-nitrobenzimidazol-1-yl)-4,6-dimorpholinopyrimidine | HCID 22036886 | — |
| Product | 2-(6-Amino-2-difluoromethylbenzimidazol-1-yl)-4,6-dimorpholinopyrimidine | HCID 22036899 | 88% |
Reaction Steps
In accordance with the procedure of the Example 1 except that 2-difluoromethylbenzimidazole in (1) of the Example 1 was replaced by 2-difluoro-6-nitrobenzimidazole, a mixture of 2-(2-difluoromethyl-5-nitrobenzimidazol-1-yl)-4,6-dimorpholinopyrimidine with 2-(2-difluoromethyl-6-nitrobenzimidazol-1-yl)-4,6-dimorpholinopyrimidine was obtained. In accordance with the procedure of (3) of the Example 8, using 0.92 g (2.0 mmol) of this mixture, 0.76 g (yield: 88%) of the titled compound was obtained as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07071189B2 |
| Source dataset | uspto-grants-2006_07 |
| ORD ID | ord-ded3e55de6ba4c58b7ab83aa957d0d54 |
| Source note | uspto-grants-2006_07 |