HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 896152Generated: October 29, 2026
Water → 7-Nitro-4-methyl-4H-benzo[1,4]thiazin-3-one
https://huagongshe.com/reaction/896152
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 7-Nitro-2H-benzo[b][1,4]thiazin-3(4H)-one | HCID 370121 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 7-Nitro-4-methyl-4H-benzo[1,4]thiazin-3-one | HCID 21877780 | 90% |
Reaction Steps
To a stirred suspension of 3,4-dihydro-7-nitro-2H-1,4-benzothiazin-3-one (Step 2, 4.7 g, 22.3 mmol) and potassium carbonate (3.70 g, 26.8 mmol) in dry DMF (40 mL) in an ice bath is added iodomethane (4.16 mL, 66.8 mmol). The reaction mixture is taken out of the ice bath and heated at 50° C. for 1-2h. The resulting mixture is allowed to cool down. Water (35 mL) and ice are added and the precipitate is filtered off and washed with water (10 mL). The resulting solid is dried under high vacuum to give the title compound as a yellow solid (4.5 g, 90%), MS m/z 225.5 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06919329B2 |
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| Source dataset | uspto-grants-2005_07 |
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| ORD ID | ord-ba540ac30dbf49f8bb88a0cb7cfb69fa |
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| Source note | uspto-grants-2005_07 |
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