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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2373218Generated: October 30, 2026

Triethylamine → HCID 86602401, compound

https://huagongshe.com/reaction/2373218

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHCID 11688198HCID 11688198—
SolventWaterHCID 962—
ProductHCID 86602401HCID 8660240178.7%

Reaction Steps

To a mixture of [1-ethyl-6-(methoxymethyl)-4-(5-methyl-3-pyridyl)-1H-pyrazolo[3,4-b]pyridin-5-yl]methanol (110 mg), Et3N (0.29 ml) in N,N-dimethylsulfoxide (3 ml) was added sulfur trioxide-pyridine complex (168 mg) at room temperature and the mixture was stirred at room temperature for 1 hour. The reaction mixture was diluted with water and extracted with EtOAc. The organic layer was washed with saturated aqueous ammonium chloride, saturated aqueous NaHCO3, water, brine, dried over anhydrous MgSO4 and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel eluting with a mixture of EtOAc and n-hexane(3:1) to give 1-ethyl-6-(methoxymethyl)-4-(5-methyl-3-pyridyl)-1H-pyrazolo[3,4-b]pyridine-5-carbaldehyde (86 mg) as a white crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07459451B2
Source datasetuspto-grants-2008_12
ORD IDord-9eb622de1a38483d8ce4312c8ea10da1
Source noteuspto-grants-2008_12