Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1049163Generated: November 3, 2026

Sodium borohydride → HCID 178513739, compound

https://huagongshe.com/reaction/1049163

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 numberUS09382237B2
Source datasetuspto-grants-2016_07
ORD IDord-901f7b2e68864038829d8c50500b6020
Source noteuspto-grants-2016_07