HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2216625Generated: October 29, 2026
(4H,6H,7H-pyrazolo(3,2-c)(1,4)oxazin-2-yl)methanol → 6,7-dihydro-4H-pyrazolo(5,1-c)(1,4)oxazine-2-carbaldehyde
https://huagongshe.com/reaction/2216625
Participants
| Role | Name | HCID | Charge |
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| Reactant | (4H,6H,7H-pyrazolo(3,2-c)(1,4)oxazin-2-yl)methanol | HCID 11845787 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 6,7-dihydro-4H-pyrazolo(5,1-c)(1,4)oxazine-2-carbaldehyde | HCID 11845422 | 76.1% |
Reaction Steps
To a solution of 6,7-dihydro-4H-pyrazolo[5,1-c][1,4]oxazin-2-ylmethanol (1.08 g, 7.0 mmol) in 1,2-dichloroethane (30 ml) was added 5.4 g of activated manganese dioxide at room temperature with stirring. The mixture was heated to 60° C. for 1 hr and then stirred at room temperature for 16 hr. The final mixture was filtered through a column of silica gel topped with celite. The filter pad was eluted with methylene chloride, followed by ethyl acetate. The ethyl acetate eluent was evaporated and the residue triturated with to give 0.81 g of a white solid; mp 91° C.; MS (ESI) m/z 153.2 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07112582B2 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-2f1403f954c749eebf82b97d520390e1 |
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| Source note | uspto-grants-2006_09 |
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