HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 22228179, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Diethyl cyanophosphonate | HCID 76257 | — |
| Reactant | 5-Amino-2-neopentyloxybenzonitrile | HCID 17822734 | — |
| Reactant | 1-(4-Fluorophenyl)-3-methyl-1H-pyrazole-5-carboxylic acid | HCID 22228066 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22228179 | HCID 22228179 | 11.6% |
Reaction Steps
1-(4-Fluorophenyl)-3-methylpyrazole-5-carboxylic acid (1.4 g), 5-amino-2-neopentyloxybenzonitrile (1.3 g), triethylamine (1.9 g) and diethyl cyanophosphate (1.6 g) were added to dimethylformamide (20 ml) and the mixture was stirred at room temperature for 1 h. The reaction mixture was added into water and extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate, after which the solvent was evaporated under reduced pressure. Methanol was added to the residue to allow crystallization. The crystals were recrystallized from hydrous methanol to give the title compound (0.3 g), melting point: 165° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07015218B1 |
| Source dataset | uspto-grants-2006_03 |
| ORD ID | ord-a06bda4d06714a99b501ddffb07fd5b5 |
| Source note | uspto-grants-2006_03 |