HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 639060Generated: October 26, 2026
Dimethyl Sulfide → 7-Chloro-3-oxo-3,4-dihydro-2H-pyrido[3,2-b][1,4]oxazine-6-carbaldehyde
https://huagongshe.com/reaction/639060
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfide | HCID 1068 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 7-Chloro-6-((E)-styryl)-4H-pyrido[3,2-b][1,4]oxazin-3-one | HCID 68563867 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 7-Chloro-3-oxo-3,4-dihydro-2H-pyrido[3,2-b][1,4]oxazine-6-carbaldehyde | HCID 57486872 | 68% |
Reaction Steps
7-Chloro-6-((E)-styryl)-4H-pyrido[3,2-b][1,4]oxazin-3-one (8.0 g, 27.9 mmole) was dissolved in a mixture of DMF (400 mL) and methanol (40 mL), and the solution was cooled to −78° C. Ozone was bubbled through the solution with stirring for 45 minutes, then the excess ozone was removed by bubbling oxygen through the solution for 30 min. Dimethylsulfide (21 mL, 279 mmole) was added to the solution, and the reaction was stirred at −78° C. for 3 hr, then at room temperature overnight. The solvent was removed in vacuo, and the residue was triturated with Et2O (150 mL). The collected solid was washed with additional Et2O and dried to afford a white solid (4 g, 68%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07691850B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-fc22bd498b15429ba53c6cfc43e6e3a8 |
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| Source note | uspto-grants-2010_04 |
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