HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → HCID 22004680, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 1-Boc-4-(aminomethyl)piperidine | HCID 736817 | — |
| Reactant | Pyridine-2-sulfonyl Chloride | HCID 3787675 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22004680 | HCID 22004680 | 47.3% |
Reaction Steps
Pyridine (1.85 ml) was added to a stirred solution of 4-(aminomethyl)-1-(tert-butoxycarbonyl)piperidine (4.46 g) and pyridine-2-sulphonyl chloride (3.7 g) in dichloromethane (110 ml) at -10° C. under a nitrogen atmosphere. The reaction was then warmed to ambient temperature over 16 hours and poured into water (300 ml). The organic layer was separated and further washed with hydrochloric acid (1 M, 2×200 ml), saturated aqueous sodium bicarbonate solution (200 ml) and brine (200 ml). After drying over anhydrous magnesium sulphate, the solution was evaporated to dryness to afford N-{[1-(tert-butoxycarbonyl)-4-piperidyl]methyl}pyridine-2-sulphonamide (3.5 g) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06136825 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-0e4a699400ed47f6863108441c9fa01c |
| Source note | uspto-grants-2000_10 |