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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1520007Generated: October 29, 2026

Sodium Hydroxide → HCID 86699006, compound

https://huagongshe.com/reaction/1520007

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSodium AzideHCID 33557—
ReactantSodium NitriteHCID 23668193—
Reactant1183808-98-1HCID 60892839—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventSulfuric AcidHCID 1118—
ProductHCID 86699006HCID 86699006—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cooled solution (0° C.) of 1-(2-Pyridin-4-yl-ethyl)-1H-pyrazol-4-ylamine (300 mg; 2.66 mmol; 1.0 eq.) in AcOH (2.0 mL) and H2SO4 (1.0 mL) was added dropwise a solution of sodium nitrite (220 mg; 3.19 mmol; 1.2 eq.) in water (1.50 mL) and the reaction mixture was stirred at 0° C. for 1 hour. A solution of sodium azide (207 mg; 3.2 mmol; 1.2 eq.) in water (1.5 mL) was then added dropwise at 0° C. and the reaction mixture was stirred at 0° C. for 2 hours. The reaction mixture was then poured into ice water, basified to pH=10-11 with NaOH (5N) and extracted with EtOAc (twice). Combined organic layers were washed with brine, dried over magnesium sulfate, filtered and concentrated to afford the title compound as a dark oil, which was used without further purification in the next step. MS (ESI+): 215.0 (purity 98.7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073892B2
Source datasetuspto-grants-2015_07
ORD IDord-3d820194128f4642bbb0b92a2b231e22
Source noteuspto-grants-2015_07