Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 4-Methoxybenzenesulfonyl chloride | HCID 7401 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 11000970 | HCID 11000970 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21971879 | HCID 21971879 | 28.9% |
Reaction Steps
Triethylamine (0.62 ml) was added to a solution of (S)-4-(aminomethyl)-1-(7-chloro-1,4-benzodioxan-2-ylmethyl)piperidine (0.44 g) and 4-methoxybenzene-sulphonyl chloride (0.61 g) in dichloromethane (22 ml) under nitrogen. The reaction was stirred for 20 hours, diluted with dichloromethane (100 ml) and washed with water (100 ml) and brine (100 ml). After drying over anhydrous magnesium sulphate, the mixture was concentrated under reduced pressure to afford an orange oil. Purification by flash chromatography on silica gel eluting with a 20:1 mixture of dichloromethane and methanol gave a colourless gum. Trituration with diethyl ether (20 ml) yielded (S)-(-)-N-{[1-(7-chloro-1,4-benzodioxan-2-ylmethyl)-4-piperidyl]-methyl}-4-methoxybenzenesulphonamide as a white solid (0.20 g); m.p. 130-131° C., [α]D22.5 28.9° (c=0.51, CH2Cl2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06136825 |
|---|
| Source dataset | uspto-grants-2000_10 |
|---|
| ORD ID | ord-5ef8bb81794c40179fda4414f2219810 |
|---|
| Source note | uspto-grants-2000_10 |
|---|