HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → N-benzyl-3-bromo-1-methyl-4-nitro-1H-pyrazol-5-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | 3,5-Dibromo-1-methyl-4-nitro-1H-pyrazole | HCID 22918638 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-benzyl-3-bromo-1-methyl-4-nitro-1H-pyrazol-5-amine | HCID 22918628 | 81% |
Reaction Steps
2 g (7.02 mmoles) of 3,5-dibromo-1-methyl-4-nitropyrazole are heated in a solution of 11 g (0.1 mole) of benzylamine in 50 ml ethanol for 10 hours at boiling temperature. After cooling, the reaction mixture is poured on 100 ml water, the separated product is filtered and washed with water (20 ml). After vacuum drying, 1.76 g (81 percent of theory) of 5-benzylamino-3-bromo-1-methyl-4-nitropyrazole are obtained in the form of yellow needles with a melting point of 133° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05663366 |
| Source dataset | uspto-grants-1997_09 |
| ORD ID | ord-a8dce0c8917b4cbc91406509daf86791 |
| Source note | uspto-grants-1997_09 |