HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-[(Piperidin-4-yl)methyl]isoquinoline-5-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-(Aminomethyl)piperidine | HCID 23527 | — |
| Reactant | 5-Isoquinolinesulfonyl chloride | HCID 3371655 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[(Piperidin-4-yl)methyl]isoquinoline-5-sulfonamide | HCID 14623234 | — |
Reaction Steps
Dissolve 5.02 g of 4-aminomethylpiperidine and 22 g of triethylamine in 50 ml of dichloromethane. Add dropwise over 30 minutes 5.0 g of 5-isoquinoline sulfonyl chloride dissolved in 50 ml of dichloromethane while cooling the mixture in an ice bath. Stir at room temperature for 72 hours. Filter the reaction mixture and evaporate the filtrate. Chromatograph the residue over 400g of silica gel eluting with dichloromethane/methanol (9/1). Obtain the title compound by evaporating the appropriate fractions, as determined by thin layer chromatography. Dissolve the product in ethanol saturated with HCl and evaporate to obtain the title compound as the dihydrochloride salt. FAB MS (M+1)e =306.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04857301 |
| Source dataset | uspto-grants-1989_08 |
| ORD ID | ord-37c227ca22af461591368902b4fe82f4 |
| Source note | uspto-grants-1989_08 |