HuagongsheHuagongshe Chemistry Print Report · For research reference only
7-Chloro-5-methylpyrazolo[1,5-a]pyrimidine → 7-[(3-Bromo-2-(2-cyanophenyl)benzofuran-5-yl)methylamino]-5-methylpyrazolo[1,5-a]pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 7-Chloro-5-methylpyrazolo[1,5-a]pyrimidine | HCID 10487287 | — |
| Reactant | 5-(Aminomethyl)-3-bromo-2-(2-cyanophenyl)benzofuran | HCID 19975970 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 7-[(3-Bromo-2-(2-cyanophenyl)benzofuran-5-yl)methylamino]-5-methylpyrazolo[1,5-a]pyrimidine | HCID 19975961 | — |
Reaction Steps
A solution of 1.7 g (10.1 mmol) 7-chloro-5-methylpyrazolo[1,5-a]pyrimidine (prepared according to Y. Makisumi, Chem. Pharm. Bull. 1962, 10, 620) and 3.27 g (10.0 mmol) 5-(aminomethyl)-3-bromo-2-(2-cyanophenyl)benzofuran (prepared according to WO 92/09600) in 50 ml dry ethanol was heated with reflux for 5 h. The title compound precipitated upon cooling to room temperature, was filtered with suction, and recrystallized from ethanol to give colorless crystals. yield: 3.5 g (76%), m.p. 210°-215° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05602137 |
| Source dataset | uspto-grants-1997_02 |
| ORD ID | ord-7b9c4cce776d47f8a7ce17c3a898c3b9 |
| Source note | uspto-grants-1997_02 |