HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-[2-(N-methyl-N-benzylamino)ethyl]-5-isoquinolinesulfonamide → N-(2-(Methylamino)ethyl)-5-isoquinolinesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-[2-(N-methyl-N-benzylamino)ethyl]-5-isoquinolinesulfonamide | HCID 20254295 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(2-(Methylamino)ethyl)-5-isoquinolinesulfonamide | HCID 3540 | 64% |
Reaction Steps
In 100 ml of ethanol was dissolved 2.0 g of N-[2-(N-methyl-N-benzylamino)ethyl]-5-isoquinolinesulfonamide, i.e., Compound (65) as obtained in Example 16, and to the solution was added 0.2 g of 10% palladium-carbon. Then the solution was vigorously stirred at a temperature of 20° C. to 25° C. in a hydrogen stream of 2.0 to 2.5 atm. for 5 hours. After the palladium-carbon was separated from the reaction solution by filtration, the reaction solution was concentrated to dryness to give 0.95 g of N-(2-methylaminoethyl)-5-isoquinolinesulfonamide, i.e., Compound (14) in a yield of 64%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04560755 |
| Source dataset | uspto-grants-1985_12 |
| ORD ID | ord-76f004a48c194523a2321bb9c0334e83 |
| Source note | uspto-grants-1985_12 |