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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289747Generated: October 30, 2026

Water → HCID 178470522, compound

https://huagongshe.com/reaction/2289747

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantGuanidine HydrochlorideHCID 5742—
ReactantHCID 16657954HCID 16657954—
ReactantHCID 178479401HCID 178479401—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 178470522HCID 17847052268%

Reaction Conditions

Temperature60 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06093731
Source datasetuspto-grants-2000_07
ORD IDord-079bf1382f60463982000c23b880cac5
Source noteuspto-grants-2000_07