HuagongsheHuagongshe Chemistry Print Report · For research reference only
Malononitrile → HCID 178509169, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Malononitrile | HCID 8010 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | 1H-Indazol-5-amine | HCID 88012 | — |
| Reactant | HCID 21955021 | HCID 21955021 | — |
| Product | HCID 178509169 | HCID 178509169 | 63% |
Reaction Steps
4-[(1H-Indazol-5-yl)hydrazono]-4H-pyrazole-3,5-diamine was prepared using 2-[(1H-indazol-5-yl)hydrazono]malononitrile (0.105 g, 0.5 mmol) which was derived from 5-aminoindazole (0.133 g, 1.0 mmol) and malononitrile (1.5 mmol) in a manner similar to that described in Example 2, and hydrazine hydrate. The resulting solid was isolated by filtration, washed with ethanol, and dried to yield 0.076 g (63%) of the title compound as a brown solid; 1H NMR (ppm, 200 MHz, DMSO-d6) δ 6.0 (br s, 4H), 7.50 (d, 1H), 7.94 (d, 1H), 8.0 (s, 1H), 8.08 (s, 1H), 10.68 (br s, 1H), 13.08 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07875728B2 |
| Source dataset | uspto-grants-2011_01 |
| ORD ID | ord-9d6e8f119dc241af9e64256a0ea9295f |
| Source note | uspto-grants-2011_01 |