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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1405102Generated: October 31, 2026

Sodium borohydride → HCID 178513739, compound

https://huagongshe.com/reaction/1405102

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 178513738HCID 178513738—
SolventMethanolHCID 887—
ProductHCID 178513739HCID 178513739—

Reaction Steps

5-((4-hydroxybenzylidene)amino)-3-((4-nitrophenyl)amino)-1H-pyrazole-4-carboxamide (5.0 g) was suspended in 350 mL of MeOH and sodium borohydride was added until bubbling ceased. HPLC confirmed reaction was complete (absence of imine). Once completed (1 hr), precipitate was filtered to obtain 5-((4-hydroxybenzyl)amino)-3-((4-nitrophenyl)amino)-1H-pyrazole-4-carboxamide as an off white to light yellow powder. Product was washed with deionized water to remove excess sodium borohydride. Product was allowed to dry under vacuum for 18 hrs. 4.80 g (95% yield) of final product was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916555B2
Source datasetuspto-grants-2014_12
ORD IDord-567e0a2cff9c492ab3041a6aa0258723
Source noteuspto-grants-2014_12