HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chlorobenzaldehyde → HCID 178513733, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chlorobenzaldehyde | HCID 7726 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 5-amino-3-(pyridin-3-ylamino)-1H-pyrazole-4-carboxamide | HCID 86698959 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178513733 | HCID 178513733 | 55% |
Reaction Steps
5-amino-3-(pyridin-3-ylamino)-1H-pyrazole-4-carboxamide (1.0 g) was suspended in 10 mL of ethanol and 4-chlorobenzaldehyde (644 mg, 1.0 eq.) and piperidine (0.10 eq, 39 μL) was added. Stirred the reaction at reflux until starting material was absent and confirmed by HPLC. After reaction was complete (18 hrs) it was brought to room temperature and filtered to obtain 5-((4-chlorobenzylidene)amino)-3-(pyridin-3-ylamino)-1H-pyrazole-4-carboxamide as a yellow to orange powder. The product was washed with ethanol to remove any excess 4-chlorobenzaldehyde. Product was allowed to dry under vacuum for 1 hr (850 mg, 55% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08916555B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-f158658a435249d6b2ef95bd73971d20 |
| Source note | uspto-grants-2014_12 |