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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2390771Generated: October 29, 2026

Trifluoroborane-methyl sulfide → HCID 44517769, compound

https://huagongshe.com/reaction/2390771

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroborane-methyl sulfideHCID 11137191—
ReactantHCID 66868286HCID 66868286—
SolventDichloromethaneHCID 6344—
ProductHCID 44517769HCID 4451776945%

Reaction Steps

To anhydrous dichloromethane (5 mL) was added [4-[6-(2(S)-hydroxypropylamino)-2-pyridin-3-yl-pyrimidin-4-yl]-3-(3-methoxy-5-ethylphenyl)pyrazol-1-yl]acetonitrile (150 mg, 0.33 mmol) and boron trifluoride-dimethylsulfide (344 μL, 3.27 mmol) under nitrogen atmosphere. The reaction mixture was stirred for 12 hours at room temperature under nitrogen atmosphere. After completion of the demethylation, the solvent was removed by vacuum distillation, and the reaction mixture was dissolved, extracted with ethyl acetate, washed with brine, dried over anhydrous magnesium sulfate, and concentrated through vacuum distillation. Column chromatography gave the title compound (64.89 mg, 45%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273880B2
Source datasetuspto-grants-2012_09
ORD IDord-60b4e2b843ed46bd98e067167132db10
Source noteuspto-grants-2012_09