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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 511825Generated: November 2, 2026

Hydrochloric Acid → (NE,R)-N-[[5-[(2-fluorophenyl)methoxy]-2-pyridinyl]methylidene]-2-methylpropane-2-sulfinamide

https://huagongshe.com/reaction/511825

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiisobutylaluminum hydrideHCID 14487—
ReactantSodium BicarbonateHCID 516892—
Reactanttert-Butylsulfinamide, (R)-(+)-HCID 10964479—
ReactantHCID 67290985HCID 67290985—
CatalystCopper SulfateHCID 24462—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product(NE,R)-N-[[5-[(2-fluorophenyl)methoxy]-2-pyridinyl]methylidene]-2-methylpropane-2-sulfinamideHCID 8745787236%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of Reactant 5-(2-fluorobenzyloxy)picolinonitrile (690 mg, 3.0 mmol) in dichloromethane (20 mL) was added DIBAL-H (3.7 mL, 3.6 mmol, 0.99 M) at −78° C. After being stirred at −78° C. for 4 hours, methanol (2 mL) was added to the mixture. 1N hydrochloric acid (0.5 mL) was added to the mixture at room temperature. The mixture was stirred at room temperature for 1 hour. Sat. sodium bicarbonate aqueous solution was added to the mixture until the pH was neutrized. The organic layer was extracted with dichloromethane, dried over sodium sulfate and concentrated in vacuo. The residue was dissolved in dichloromethane (20 mL). Copper(II) sulfate (1.2 g, 7.6 mmol) followed by (R)-(+)-2-methyl-2-propanesulfinamide (370 mg, 3.0 mmol) were added to the mixture respectively and the mixture was stirred for overnight at room temperature. The reaction mixture was filtrated off through a pad of Celite and the filtrate was concentrated in vacuo. The residue was purified by column chromatography on silica gel eluting with hexane/ethyl acetate (2:1 (v/v)) to give 360 mg (36% yield) of the title compound as a colorless oil:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09101616B2
Source datasetuspto-grants-2015_08
ORD IDord-f07bac2f0bbe4f6ca873d9d81206f310
Source noteuspto-grants-2015_08