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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289753Generated: October 26, 2026

Water → HCID 178499191, compound

https://huagongshe.com/reaction/2289753

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantGuanidine HydrochlorideHCID 5742—
ReactantMethyl 1-{[(1,4-dichloro-7-isoquinolinyl)sulphonyl]amino}-cyclohexanecarboxylateHCID 16658027—
ReactantHCID 178479403HCID 178479403—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 178499191HCID 1784991915.8%

Reaction Conditions

Temperature60 °C

Reaction Steps

1-{[(4-Chloro-1-guanidino-7-isoquinolinyl)sulphonyl]amino}cyclohexanecarboxylic acid hydrochloride ##STR54## NaH (22.3 mg, 80% dispersion by wt in mineral oil, 0.743 mmol) was added in one portion to a stirred solution of guanidine hydrochloride (117 mg, 1.98 mmol) in DMSO (5 mL) and the mixture was heated at 50-70° C. under N2 for 25 min. Methyl 1-{[(1,4-dichloro-7-isoquinolinyl)sulphonyl]amino}-cyclohexanecarboxylate (124 mg, 0.30 mmol) was added in one portion and the mixture heated at 80° C. for 8 h. The cooled mixture was poured into water (50 mL), extracted with EtOAc (2×50 mL) and the combined organic extracts were washed with water, brine, dried (MgSO4) and evaporated in vacuo. The residue was crystallised from a minimum of hot EtOAc to give methyl 1-{[(4-chloro-1-guanidino-7-isoquinolinyl)sulphonyl]amino}cyclohexanecarboxylate (12 mg, 0.043 mmol) as yellow solid. Evaporation of the mother liquors and trituration of the residue with Et2O gave a second crop (7 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06093731
Source datasetuspto-grants-2000_07
ORD IDord-93568fb32c9d426faa1cc4ef8da2bb0f
Source noteuspto-grants-2000_07