Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1049197Generated: November 1, 2026

Sodium borohydride → HCID 178513718, compound

https://huagongshe.com/reaction/1049197

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant4-{[5-(Trifluoromethyl)pyridin-2-yl]oxy}benzaldehydeHCID 26985700—
Reactant5-amino-3-((3-chlorophenyl)amino)-1H-pyrazole-4-carboxamideHCID 86698956—
CatalystPiperidineHCID 8082—
SolventEthanolHCID 702—
ProductHCID 178513718HCID 17851371870%

Reaction Steps

5-amino-3-((3-chlorophenyl)amino)-1H-pyrazole-4-carboxamide (300 mg) was suspended in EtOH (5 mL) and 4-[{5-(Trifluoromethyl)pyridin-2-yl}oxy]benzaldehyde (318 mg, 1 eq.) and piperidine (3 drops) 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 (360 mg, 60% yield). Resulting imine (360 mg) was suspended in 10 mL MeOH and sodium borohydride (10 eq., 272 mg) was added. HPLC confirmed reaction was complete (absence of imine). After completion (1 hr), precipitate was filtered to obtain D33 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. 255 mg (70% yield) of final product was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382237B2
Source datasetuspto-grants-2016_07
ORD IDord-8e24deac4b1a4d6686a46a11ab8925ca
Source noteuspto-grants-2016_07