HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 2-(5,7-Dichloropyrazolo[1,5-a]pyrimidin-6-yl)acetaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | Sodium periodate | HCID 23667635 | — |
| Reactant | 6-Allyl-5,7-dichloropyrazolo[1,5-a]pyrimidine | HCID 57526845 | — |
| Catalyst | Osmium Tetroxide | HCID 30318 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(5,7-Dichloropyrazolo[1,5-a]pyrimidin-6-yl)acetaldehyde | HCID 86613783 | — |
Reaction Steps
To a mixed solution of THF (24 mL) and water (6 mL) containing 6-allyl-5,7-dichloropyrazolo[1,5-a]pyrimidine (1.82 g, 7.89 mmol), sodium periodate (5.12 g, 23.9 mmol) and osmium tetraoxide (2.5w/v % in tert-butanol, 3 mL, 0.23 mmol) were added with ice-cooling. After this mixture was stirred at room temperature for 3 hr, aqueous sodium sulfite was added here. The resultant mixture was extracted with ethyl acetate and the organic layer was washed with aqueous sodium hydrogen carbonate and then brine and dried over sodium sulfate. After the sodium sulfate was filtered off, the solvent was distilled off to obtain 5,7-dichloro-6-(2-oxoethyl)pyrazolo[1,5-a]pyrimidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07473694B2 |
| Source dataset | uspto-grants-2009_01 |
| ORD ID | ord-4593c2454b6148dcb859fd46d5e0cbac |
| Source note | uspto-grants-2009_01 |