Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 1H-1-Benzazepine-2,5-dione, 3-methoxy- | HCID 10750663 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 19704915 | HCID 19704915 | — |
Reaction Steps
2,5-Dihydro-2,5-dioxo-3-methoxy-1H-benz[b]azepine (0.4 g) was treated with 80 mL of liquid anhydrous ammonia chilled to -78° C. The mixture was sealed in a pressure vessel and warmed to 23° C. for 18 hours. The excess ammonia was evaporated to give a solid. The solid was dissolved in hot methanol (120 mL); the solution was filtered and evaporated to 60 mL; and crystallization was initiated by cooling the solution in an ice bath. The solid was filtered, washed (cold methanol) and dried under vacuum (25° C., 15 Pa) to give the title compound (0.28 g); mp 295.2-296.5° C. (dec); NMR: 11.38 )s,1, NH), 8.09 dd,1, J=8.2, 1.6), 7.54 (m,1), 7.44 (dd,1, J=8.2, 1.6), 7.21 (m,1), 6.23 (s,1). Analysis for C10H8N2O2 : Calculated: C, 63.82; H, 4.28; N, 14.89; Found: C, 63.80; H, 4.41; N, 14.87.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05492905 |
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| Source dataset | uspto-grants-1996_02 |
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| ORD ID | ord-87fffdd130084745a63963c60bd7950c |
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| Source note | uspto-grants-1996_02 |
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