HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 178513739, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 178513738 | HCID 178513738 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178513739 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08916555B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-567e0a2cff9c492ab3041a6aa0258723 |
| Source note | uspto-grants-2014_12 |