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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantSulfamideHCID 82267—
Reactant2-Amino-3-cyanopyridineHCID 818259—
SolventWaterHCID 962—
Product1H-pyrido[2,3-c][1,2,6]thiadiazin-4-amine-2,2-dioxideHCID 136295138—

Reaction Conditions

Temperature160 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633186B2
Source datasetuspto-grants-2014_01
ORD IDord-33c9b5c725284376ba9477343a50ed9a
Source noteuspto-grants-2014_01