HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 471569Generated: October 26, 2026
1,8-Diazabicyclo(5.4.0)undec-7-ene → 1H-pyrido[2,3-c][1,2,6]thiadiazin-4-amine-2,2-dioxide
https://huagongshe.com/reaction/471569
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | Sulfamide | HCID 82267 | — |
| Reactant | 2-Amino-3-cyanopyridine | HCID 818259 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1H-pyrido[2,3-c][1,2,6]thiadiazin-4-amine-2,2-dioxide | HCID 136295138 | — |
Reaction Steps
A stirred mixture of 2-aminonicotinonitrile (238 mg, 2.0 mmol), sulfamide (192 mg, 2.0 mmol), and 1 mL of DBU was heated at 160° C. under nitrogen overnight. After it was cooled down to room temperature, the reaction mixture was diluted with water, and extracted three times with EtOAc. The aqueous layer was dried down under vacuum, and the residue was purified by chromatography on silica gel eluting with 15% MeOH in dichloromethane to give the title compound as a yellow solid. 1H NMR (400 MHz, DMSO-d6) δ 6.87 (t, J=5.6 Hz, 1H), 7.95 (brs, 2H), 8.22 (d, J=5.2 Hz, 1H), 8.39-8.37 (m, 1H), 12.58 (brs, 1H). MS 199 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08633186B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-33c9b5c725284376ba9477343a50ed9a |
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| Source note | uspto-grants-2014_01 |
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