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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | tert-Butylsulfinamide, (R)-(+)- | HCID 10964479 | — |
| Reactant | HCID 67290985 | HCID 67290985 | — |
| Catalyst | Copper Sulfate | HCID 24462 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (NE,R)-N-[[5-[(2-fluorophenyl)methoxy]-2-pyridinyl]methylidene]-2-methylpropane-2-sulfinamide | HCID 87457872 | 36% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09101616B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-f07bac2f0bbe4f6ca873d9d81206f310 |
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| Source note | uspto-grants-2015_08 |
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