HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → 2-(5,7-Dichloropyrazolo[1,5-a]pyrimidin-6-yl)ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-(5,7-Dichloropyrazolo[1,5-a]pyrimidin-6-yl)acetaldehyde | HCID 86613783 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(5,7-Dichloropyrazolo[1,5-a]pyrimidin-6-yl)ethanol | HCID 57526829 | 146.1% |
Reaction Steps
The above aldehyde (1.82 mmol) was dissolved in methanol (27 mL), and sodium borohydride (302 mg, 7.98 mmol) was added to this solution with ice-cooling. After this mixture was stirred for 30 min, aqueous ammonium chloride was added here. The resultant mixture was extracted with ethyl acetate, and the organic layer was washed with brine and dried over sodium sulfate. After the sodium sulfate was filtered off, the solvent was distilled off, and the residue was purified with column chromatography (15% ethyl acetate-hexane) to obtain the title compound (617 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07473694B2 |
| Source dataset | uspto-grants-2009_01 |
| ORD ID | ord-d0ee2f71c925443fb96d97d43f472a63 |
| Source note | uspto-grants-2009_01 |