HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1975938Generated: November 1, 2026
Water → 1,1-dioxo-3-(propan-2-ylamino)-4H-thieno[3,2-e][1,2,4]thiadiazine-6-carbonitrile
https://huagongshe.com/reaction/1975938
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 178418546 | HCID 178418546 | — |
| Reactant | HCID 178456992 | HCID 178456992 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1,1-dioxo-3-(propan-2-ylamino)-4H-thieno[3,2-e][1,2,4]thiadiazine-6-carbonitrile | HCID 178456998 | 2% |
Reaction Steps
To a solution of 6-bromo-3-isopropylamino-4H-thieno[3,2-e]-1,2,4-thiadiazine 1,1-dioxide (243 mg, 0.75 mmol) in dry N,N-dimethylformamide (2 ml) was added copper(I) cyanide (135 mg, 1.5 mmol) and the mixture was heated at 150° C. for 2 h under nitrogen. The dark mixture was allowed to cool to room temperature and water was added. The suspension was made basic by the addition of 1 N sodium hydroxide, filtered and the filtrate was acidified by the addition of 4 M hydrochloric acid. The resulting precipitate was purified by preparative hplc on a Source RPC 15 column using acetonitrile/water (20:80) with 0.1% TFA as eluent to afford 4 mg (2%) of the pure title compound; LC-MS: m/e 271 ((M+1)+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06225310B1 |
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| Source dataset | uspto-grants-2001_05 |
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| ORD ID | ord-b645fa9cc20247899fafa104d77ec6e0 |
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| Source note | uspto-grants-2001_05 |
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