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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723837Generated: October 26, 2026

Phenylhydrazine → HCID 178518862, compound

https://huagongshe.com/reaction/1723837

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylhydrazineHCID 7516—
ReactantHydrazineHCID 9321—
ReactantNicotinoyl chlorideHCID 82604—
Reactant1H-pyrazolo(3,4-b)pyridineHCID 2755850—
Reactant2-Chloronicotinoyl chlorideHCID 2774541—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductHCID 178518862HCID 178518862—

Reaction Steps

Scheme 4 depicts the synthesis of the 1H-pyrazolo[3,4-b]pyridine q. A nicotinoylchloride k (e.g., 2-chloronicotinoyl chloride) is reacted with a hydrazine m (e.g., phenylhydrazine) and a base such as triethylamine in a solvent such as anhydrous methylene chloride to give o (e.g., 1-phenyl-1H-pyrazolo[3,4-b]pyridin-3-ol). The compound o is then cyclized by heating at 175° C. to provide p. p is reacted as in the transformation of d to g in Scheme 1 to provide q.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07485636B2
Source datasetuspto-grants-2009_02
ORD IDord-04791b4fb7df49afb20a6caf7d8afbb9
Source noteuspto-grants-2009_02