Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 5-Hydrazino-1,3-dimethyl-4-nitro-1H-pyrazole | HCID 3537257 | — |
| Reactant | 7,8-dimethoxy-3,4-dihydro-1H-1-benzazepine-2,5-dione | HCID 23000064 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 136591214 | HCID 136591214 | 12.2% |
Reaction Steps
1,3-Dimethyl-4-nitro-1H-pyrazol-5-yl-hydrazine (0.073 g, 0.4 mmol) was added to a suspension of 7,8-dimethoxy-1H-[1]benzazepin-2,5(3H, 4H)-dione (0.100 g, 0.4 mmol) in acetic acid (5 ml) with stirring under argon. The mixture was heated at 70° C. for 2 days, cooled and water (5 ml) added. The precipitate was then filtered off to give the title compound as a yellow solid (0.019 g, yield 11.5%); 1H-NMR (DMSO-d6, 300 MHz): δ (ppm)=12.8 (v br s; 1 H), 9.59 (s; 1H), 7.2 (s; 1H), 6.63 (s; 1H), 3.96 (s; 3H), 3.75-3.77 (s, 6H), 3.05 (br t, 2H), 2.57 (br t, 2H), 2.35 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07767664B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-2783a0d68f0c44529a4618bec0d1722f |
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| Source note | uspto-grants-2010_08 |
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