Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Guanidine Hydrochloride | HCID 5742 | — |
| Reactant | HCID 16657954 | HCID 16657954 | — |
| Reactant | HCID 178479401 | HCID 178479401 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 178470522 | HCID 178470522 | 68% |
Reaction Steps
1-{[(4-Chloro-1-guanidino-7-isoquinolinyl)sulphonyl]amino}cyclobutanecarboxylic acid hydrochloride ##STR47## NaH (37 mg, 80% dispersion by wt in mineral oil, 1.24 mmol) was added in one portion to a stirred solution of guanidine hydrochloride (189 mg, 1.98 mmol) in DMSO (6 mL) and the mixture was heated at 60° C. under N2 for 30 min. Ethyl 1-{[(1,4-dichloro-7-isoquinolinyl)sulphonyl]amino)-cyclobutanecarboxylate (200 mg, 0.50 mmol) was added in one portion and the mixture heated at 80° C. for 10 h. The cooled mixture was poured into water, extracted with EtOAc (2×50 mL) and the combined organic extracts were dried (MgSO4) and evaporated in vacuo. The residue was purified by column chromatography upon silica gel using pentane-EtOAc (50:50 to 0:100) as eluant to give ethyl 1-{[(4-chloro-1-guanidino-7-isoquinolinyl)sulphonyl]amino)cyclobutanecarboxylate (150 mg, 0.34 mmol) as a yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06093731 |
|---|
| Source dataset | uspto-grants-2000_07 |
|---|
| ORD ID | ord-079bf1382f60463982000c23b880cac5 |
|---|
| Source note | uspto-grants-2000_07 |
|---|