Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 21221013 | HCID 21221013 | — |
| Product | HCID 57085494 | HCID 57085494 | — |
Reaction Steps
Trifluoroacetic acid (10 ml) was added to a solution of N-[(1-tert-butoxycarbonyl-4-piperidyl)methyl]pyridine-3-carboxamide (1.56 g) in dichloromethane (25 ml) and the mixture stirred for 2 hours then the solvent was removed in vacuo. The residue was dissolved in dry acetonitrile (10 ml) and potassium carbonate (5.0 g) was added, followed by a solution of (R)-7-chloro-1,4-benzodioxan-2-ylmethyl 4-toluenesulphonate (1.7 g) in dry acetonitrile (15 ml), and the mixture was stirred and heated under reflux for 6 hours. The cooled mixture was poured into water then extracted with dichloromethane (2×100 ml). The combined extracts were washed with brine (100 ml), dried over magnesium sulphate, and the solvent removed in vacuo. The residue was purified by flash chromatography over silica eluting with a 20:1 mixture of dichloromethane and methanol. Appropriate fractions were combined and the solvent removed in vacuo to give (S)-N-{[1-(8-chloro-1,4-benzodioxan-2-ylmethyl)-4-piperidyl]methyl}pyridine-3-carboxamide (1.04 g) as a colourless solid m.p. 52-54° C. [α]D -35.3° (c=1.024, methanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05935973 |
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| Source dataset | uspto-grants-1999_08 |
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| ORD ID | ord-c13717a3418a4a2995b000475a84f712 |
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| Source note | uspto-grants-1999_08 |
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