HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3-Butanediamine → N-(2-amino-1-methylpropyl)-5-isoquinolinesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3-Butanediamine | HCID 136362 | — |
| Reactant | 5-Isoquinolinesulfonyl chloride | HCID 3371655 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | N-(2-amino-1-methylpropyl)-5-isoquinolinesulfonamide | HCID 20159892 | 80% |
Reaction Steps
In 100 ml of chloroform was dissolved 12.9 g of 2,3-diaminobutane and to the solution was added dropwise 10 ml of a chloroform solution containing 4.0 g of 5-isoquinolinesulfonyl chloride under cooling with ice. After the dropwise addition of the chloroform solution, the mixed solution was stirred at a temperature of 20° C. to 25° C. for two hours, and the reaction mixture solution was washed with water and dried with anhydrous sodium carbonate. The chloroform was distilled therefrom under reduced pressure, and the residue thus obtained was subjected to a column chromatography [silica gel: 160 g; solvent: chloroform] to give 3.92 g of N-(2-amino-1-methylpropyl)-5-isoquinolinesulfonamide in a yield of 80%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04634770 |
| Source dataset | uspto-grants-1987_01 |
| ORD ID | ord-7c19baa7d1c445cba8ab5daebd50addf |
| Source note | uspto-grants-1987_01 |