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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588589Generated: October 31, 2026

Triethylamine → HCID 178477817, compound

https://huagongshe.com/reaction/588589

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBromineHCID 24408—
ReactantSodium BicarbonateHCID 516892—
Reactant4-chloro-5-phenyl-1H-pyrazolo[3,4-c]pyridazineHCID 86717263—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
ProductHCID 178477817HCID 17847781746.8%

Reaction Steps

A mixture of 4-chloro-5-phenyl-1H-pyrazolo[3,4-c]pyridazine (155 mg, 0.67 mmol), bromine (51 μL, 1 mmol) and triethylamine (98 μL, 0.7 mmol) in chloroform (4 mL) was stirred at room temperature for 1 h. Additional bromine (25 μL) and chloroform (4 mL) were added and the reaction mixture was stirred at room temperature for 4 h. Further bromine (25 μL) and triethylamine (98 μL) were added and the reaction mixture was stirred at room temperature for 16 h. The reaction mixture was diluted with CH2Cl2 and a sodium bicarbonate solution. The aqueous phase was extracted with CH2Cl2 and the combined organic phases were dried (phase separator cartridge) and concentrated in vacuo. The resultant residue was purified using chromatography (silica gel, ethyl acetate/isohexane 0:1 to 1:1), to provide Compound Ibb as a solid (97 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227976B2
Source datasetuspto-grants-2016_01
ORD IDord-e3eb881d2d574f1ea26f62d4adbe150b
Source noteuspto-grants-2016_01