HuagongsheHuagongshe Chemistry Print Report · For research reference only
N5-(2-methylpropyl)4-nitrotetrazolo[1,5-a][1,7]naphthyridin-5-amine → N5-(2-methylpropyl)tetrazolo[1,5-a][1,7]naphthyridin-4,5-diamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N5-(2-methylpropyl)4-nitrotetrazolo[1,5-a][1,7]naphthyridin-5-amine | HCID 12015802 | — |
| Reactant | Sodium hydrogen sulphide | HCID 86586439 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | N5-(2-methylpropyl)tetrazolo[1,5-a][1,7]naphthyridin-4,5-diamine | HCID 12015803 | 90.8% |
Reaction Steps
N5-(2-Methylpropyl)-4-nitrotetrazolo[1,5-a][1,7]naphthyridin-5-amine (1.5 g, 5.22 mmol) was suspended in acetic acid (75 mL). An excess of sodium hydrogen sulfide was dissolved in a minimum of water and added to the suspension. The reaction mixture turned red and all of the material went into solution. The reaction mixture was extracted twice with dichloromethane (150 mL). The extracts were combined, washed with water, dried over magnesium sulfate, filtered and concentrated under vacuum to provide 1.22 g of N5-(2-methylpropyl)tetrazolo[1,5-a][1,7]naphthyridin-4,5-diamine as a light yellow solid, m.p. 203-204.5° C. Analysis: Calculated for: C12H15N7: %C, 56.02; %H, 5.88; %N, 38.11; Found: %C, 55.68; %H, 5.81; %N, 37.74.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06624172B2 |
| Source dataset | uspto-grants-2003_09 |
| ORD ID | ord-f455f0bd59c64ca8845cc3ff8e311886 |
| Source note | uspto-grants-2003_09 |