HuagongsheHuagongshe Chemistry Print Report · For research reference only
4,5-Dimethyl-1,2-phenylenediamine → HCID 178428586, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4,5-Dimethyl-1,2-phenylenediamine | HCID 76635 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 178521133 | HCID 178521133 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178428586 | HCID 178428586 | 83.9% |
Reaction Steps
Method A A stirred solution of 4,5-dimethylphenylenediamine (4.32 g) and diisopropylethylamine (30 ml) in dichloromethane (200 ml) was treated with 4-nitropyrazole-3-carboxylic chloride (5 g) portionwise at 0° C. The reaction mixture was warmed to ambient temperature and stirred for 30 minutes. The solvent was removed in vacuo and the oily residue was partitioned between ethyl acetate and water. The organic layer was dried over magnesium sulfate and concentrated. The residual oil was re-crystallised from ethyl acetate and methanol (10%) to give 4-nitro-1H-pyrazole-3-carboxylic acid (2-amino-4,5-dimethylphenyl)amide (6.58 g) as an orange solid. LC-MS (METHOD B): RT=2.36 minutes, 276.09 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06897208B2 |
| Source dataset | uspto-grants-2005_05 |
| ORD ID | ord-634480a3c7ce4d0db19dd41c7ebe537b |
| Source note | uspto-grants-2005_05 |