HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → HCID 58256406, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | HCID 67151542 | HCID 67151542 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 58256406 | HCID 58256406 | 6.7% |
Reaction Steps
Isoquinoline-5-sulfonic acid [4-((S)-3-amino-4-hydroxy-butyl)-phenyl]-amide (109 mg) was dissolved in methanol (3 ml) at room temperature before addition of sodium acetate (72.2 mg) and a solution of cyanogen bromide (40.4 mg) in methanol (1 ml) dropwise. The reaction mixture was stirred at room temperature for 36 hours, then aqueous ammonia 25% was added (55 μl) and stirring was continued for an another hour. The solvent was evaporated in vacuo and the residue purified by Isco chromatography (column: Silicycle Si-Amine, AcOEt) to give isoquinoline-5-sulfonic acid {4-[2-((S)-2-amino-4,5-dihydro-oxazol-4-yl)-ethyl]-phenyl}-amide (7.8 mg) as a yellow solid. Description. MS (ISP): 397.2 ([M+H]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08354441B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-fc3612a97c024f3db31c4103959c0ce1 |
| Source note | uspto-grants-2013_01 |