HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 247575Generated: October 26, 2026
Ethylenediamine → N-(2-Aminoethyl)isoquinoline-5-sulfonamide
https://huagongshe.com/reaction/247575
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylenediamine | HCID 3301 | — |
| Reactant | 5-Isoquinolinesulfonyl chloride | HCID 3371655 | — |
| Reactant | Chloroform methanol | HCID 21584188 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | N-(2-Aminoethyl)isoquinoline-5-sulfonamide | HCID 3544 | 66% |
Reaction Steps
In 200 ml of chloroform was dissolved 12.0 g of 1,2-diaminoethane, and to the solution was added dropwise 100 ml of a chloroform solution containing 4.55 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 then the reaction solution was extracted with a 10% aqueous hydrochloric acid solution. The pH of the aqueous layer was adjusted to 10 with a 10% aqueous sodium hydroxide solution, and the aqueous layer was extracted with chloroform. The chloroform layer extracted was washed with water and dried with anhydrous potassium carbonate. Then the chloroform was distilled from the chloroform layer, and the residue obtained was subjected to a column chromatography [silica gel: 200 g; developing solvent: 2% methanol/chloroform (volume ratio)] to give 3.3 g of N-(2-aminoethyl)-5-isoquinolinesulfonamide as an oily substace in a yield of 66%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04709032 |
|---|
| Source dataset | uspto-grants-1987_11 |
|---|
| ORD ID | ord-845614edcf494f7ba5f129e53db8d5d2 |
|---|
| Source note | uspto-grants-1987_11 |
|---|