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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1525417Generated: October 27, 2026

Hydrochloric Acid → 2-(4-chloro-3,5-diphenyl-1H-pyrazolo[3,4-c]pyridazin-1-yl)acetic acid

https://huagongshe.com/reaction/1525417

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium NitriteHCID 23668193—
Reactantsodium 2-(5-amino-3-phenyl-4-(phenylethynyl)-1H-pyrazol-1-yl)acetateHCID 70982572—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product2-(4-chloro-3,5-diphenyl-1H-pyrazolo[3,4-c]pyridazin-1-yl)acetic acidHCID 66575782—

Reaction Steps

A suspension of sodium 2-(5-amino-3-phenyl-4-(phenylethynyl)-1H-pyrazol-1-yl)acetate (2 g, 6.0 mmol) in diethylether (10 mL) and concentrated HCl (50 mL) was cooled at −15° C. before sodium nitrite (0.62 g, 8.0 mmol) in water (5 mL) was added dropwise. The solution was allowed to warm up to room temperature and left stirring for further 18 h. The reaction mixture was carefully quenched with an aqueous solution of Na2CO3 at 10° C., until pH basic, and then extracted EtOAc, backwashed with water then brine, dried (MgSO4) and concentrated in vacuo. The resultant residue was purified using chromatography (silica gel, gradient 2 to 10% diethylether/CH2Cl2) yielding Compound 47 as a yellow foam (580 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09079909B2
Source datasetuspto-grants-2015_07
ORD IDord-75d7989a25ff4850904b84b12955a48e
Source noteuspto-grants-2015_07