HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 44360Erstellt: 23. Oktober 2026
2-Aminobenzonitrile → 4-amino-1H-2lambda6,1,3-benzothiadiazine-2,2-dione
https://huagongshe.com/de/reaction/44360
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 2-Aminobenzonitrile | HCID 72913 | — |
| Edukt | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Edukt | Sulfamide | HCID 82267 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 4-amino-1H-2lambda6,1,3-benzothiadiazine-2,2-dione | HCID 13330335 | — |
Reaktionsschritte
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) δ7.03 (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+).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08541421B2 |
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| Quelldatensatz | uspto-grants-2013_09 |
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| ORD ID | ord-f3956f9df4894fbd961f191eec64819d |
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| Quellennotiz | uspto-grants-2013_09 |
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