HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 48979Generated: October 28, 2026
Acetonitrile → HCID 20634277, compound
https://huagongshe.com/reaction/48979
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Sodium Dithionite | HCID 24489 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 5-Nitro-3-(3-methylpyrazol-1-yl)-1,2-benzisothiazole | HCID 20634278 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 20634277 | HCID 20634277 | — |
Reaction Steps
A mixture of 5-nitro-3-(3-methylpyrazol-1-yl)-1,2-benzisothiazole (3.12 g, 12.0 mmol), sodium bicarbonate (2.00 g, 23.8 mmol), acetonitrile and water is stirred one hour at 70° C. and treated with sodium hydrosulfite (8.70 g, 50.0 mmol) in portions. The resultant mixture is stirred overnight at reflux, cooled to room temperature and diluted with ethyl acetate. The organic layer is dried over anhydrous magnesium sulfate and concentrated in vacuo. The residue is washed with a mixture of methylene chloride and ethyl acetate. The organic layer is decanted to afford the title compound as a viscous brown oil which is identified by NMR spectral analysis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06706663B2 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-4820fec84905457887f6c476a3246362 |
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| Source note | uspto-grants-2004_03 |
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