HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → HCID 21248374, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | HCID 13747168 | HCID 13747168 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21248374 | HCID 21248374 | — |
Reaction Steps
The title compound was prepared from 7-(2-hydroxyethyl-amino)-5-methyl-1H-pyrazolo[4,3-b]pyridine (2 g) and benzoyl chloride by the general method of Example 4 without the addition of methanol. The crude reaction mixture was poured into a large excess of water and extracted with ethyl acetate (×3). The combined organic layers were washed with water (×2), dried with anhydrous sodium sulphate, filtered and evaporated to dryness. The resulting intermediate dibenzoylated compound was recrystallized from carbon tetrachloride/60°-80° C. petrol to give a pale yellow solid, m.p. 136°-138° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04818754 |
| Source dataset | uspto-grants-1989_04 |
| ORD ID | ord-145283af0e7d4ce29dd99739618a62d3 |
| Source note | uspto-grants-1989_04 |