HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 527294Generated: October 27, 2026
4-(Pyrimidin-2-yloxy)benzaldehyde → HCID 178513720, compound
https://huagongshe.com/reaction/527294
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-(Pyrimidin-2-yloxy)benzaldehyde | HCID 2763562 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 5-amino-3-((3-chlorophenyl)amino)-1H-pyrazole-4-carboxamide | HCID 86698956 | — |
| Catalyst | Piperidine | HCID 8082 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178513720 | HCID 178513720 | 30% |
Reaction Steps
5-amino-3-((3-chlorophenyl)amino)-1H-pyrazole-4-carboxamide (100 mg) was then suspended in EtOH (4 mL) and 4-(pyrimidin-2-yloxy)benzaldehyde (80 mg, 1 eq.) and piperidine (1 drop) were added. Stirred at reflux until intermediate was absent (HPLC). After reaction was complete (18 hrs) it was brought to room temperature and filtered to obtain product as a yellow powder. Powder was washed with EtOH. Product was allowed to dry under vacuum for 1 hr (104 mg, 60% yield). Resulting imine (104 mg) was suspended in 5 mL MeOH and sodium borohydride (10 eq, 100 mg) was added. HPLC confirmed reaction was complete (absence of imine). After completion (1 hr), precipitate was filtered to obtain D32 as a light yellow powder. Product was washed with deionized water to remove excess sodium borohydride. Product was allowed to dry under vacuum for 18 hrs. 31 mg (30% yield) of final product was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09346792B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-1799764781a94b3693fdbc117941c4db |
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| Source note | uspto-grants-2016_05 |
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