Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (+-)-Anabasine | HCID 2181 | — |
| Reactant | N-Acetylsulfanilyl chloride | HCID 8481 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 659759 | HCID 659759 | — |
Reaction Steps
A 842 mg portion of 4-(acetylamino)benzene sulfonyl chloride was added under ice-cooling to a pyridine solution (10 ml) of 3-(piperidin-2-yl)pyridine and stirred at room temperature for 2 hours. The solvent was concentrated under a reduced pressure, and the thus obtained residue was mixed with ethyl acetate and then washed with water, 1 M hydrochloric acid and saturated brine. This was dried with anhydrous sodium sulfate and then concentrated under a reduced pressure, and the thus obtained residue was purified by a silica gel column chromatography using chloroform:methanol (98:2) as the elution solvent, thereby obtaining 1.00 g of N-(4-{[2-(pyridin-3-yl)piperidin-1-yl]sulfonyl}phenyl)acetamide as a yellow foamy substance. FAB-MS (Pos): 360 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08101580B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-904f5c4003ce488d90e1ef8479457482 |
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| Source note | uspto-grants-2012_01 |
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