HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → N-(2-Aminoethyl)-1-chloroisoquinoline-5-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-Chloro-isoquinoline-5-sulfonic acid (2-amino-ethyl)-amide hydrochloride | HCID 86610926 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(2-Aminoethyl)-1-chloroisoquinoline-5-sulfonamide | HCID 13730021 | 90.2% |
Reaction Steps
A 5N NaOH solution (0.937 mL) is added slowly to a stirred suspension of 1-chloro-isoquinoline-5-sulfonic acid (2-amino-ethyl)-amide hydrochloride (1.51 g, 4.69 mmol) in THF (20 mL)/CH3OH (20 mL) at ambient temperature to form a clear solution. After concentration in vacuo, the tan solid is suspended in EtOAc/CH3OH and sonicated for a few minutes. The mixture is filtered and concentrated to give 1.21 g (4.23 mmol, 90% yield) of the title compound as a tan powder. ESIMS: m/z 286 [(M+H)+, 35Cl], 288 [(M+H)+, 37Cl].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07414063B2 |
| Source dataset | uspto-grants-2008_08 |
| ORD ID | ord-2390295f1cec464faaf21eb06cee041a |
| Source note | uspto-grants-2008_08 |