HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dichloroethane → N-(1H-Pyrazol-4-yl)-5-(m-tolyl)oxazole-4-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 1H-pyrazol-4-amine | HCID 78035 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 5-(m-Tolyl)oxazole-4-carboxylic acid | HCID 29923092 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(1H-Pyrazol-4-yl)-5-(m-tolyl)oxazole-4-carboxamide | HCID 68283740 | — |
Reaction Steps
To a solution of 5-(m-tolyl)oxazole-4-carboxylic acid (11.18 g) in DCM (65 mL), HOBT (11.15 g, 0.083 mol) and EDC (15.8 g, 0.083 mol) was added at 0° C. This suspension was stirred at this temperature for 10 min, then it was added to a suspension was of 1H-pyrazol-4-amine (5.48 g) and DIPEA (17.65 mL) in DCM (50 mL). The resulting mixture was allowed to warm to rt and was stirred at rt for 18 h. Percipitation of the desired compound was obtained by the addition of water. The solid was filtered and dried to yield the title compound. LC-MS conditions B: tR=0.63 min, [M+H]+=269.13.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09303023B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-8a558551a3c84f9bb3688e4d7ee08375 |
| Source note | uspto-grants-2016_04 |