HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 711629Generated: October 25, 2026
2-Aminobenzonitrile → 4-amino-1H-2lambda6,1,3-benzothiadiazine-2,2-dione
https://huagongshe.com/reaction/711629
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Aminobenzonitrile | HCID 72913 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | Sulfamide | HCID 82267 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-amino-1H-2lambda6,1,3-benzothiadiazine-2,2-dione | HCID 13330335 | — |
Reaction Steps
A stirred mixture of 2-cyanoaniline (236 mg, 2.0 mmol), sulfamide (192 mg, 2.0 mmol) and DBU (304 mg, 2.0 mmol) was heated at 160° C. under nitrogen for 3 days. After cooling to room temperature, the reaction mixture was diluted with water and extracted three times with EtOAc. The aqueous layer was removed under vacuum and the residue was purified by chromatography on silica gel eluting with 10% MeOH in dichloromethane to give the title compound as a pale yellow solid. 1H NMR (400 MHz, DMSO-d6) δ 7.03 (dd, J=0.8, 8.0 Hz, 1H), 7.12 (dt, J=0.8, 8.0 Hz, 1H), 7.56 (dt, J=0.8, 8.0 Hz, 1H), 7.85 (dd, J=0.8, 8.0 Hz, 1H). MS 198 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09181276B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-f97924ee76fe4d0a874c52b815f8e5ba |
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| Source note | uspto-grants-2015_11 |
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