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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289749Generated: October 29, 2026

Guanidine Hydrochloride → HCID 178470523, compound

https://huagongshe.com/reaction/2289749

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGuanidine HydrochlorideHCID 5742—
ReactantHCID 178470521HCID 178470521—
ReactantHCID 178512666HCID 178512666—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 178470523HCID 17847052321.8%

Reaction Conditions

Temperature40 °C

Reaction Steps

N-[(4-chloro-1-guanidino-7-isoquinolinyl)sulphonyl]cycloleucine trifluoroacetate ##STR48## NaH (1.12 g, 80% dispersion by wt in mineral oil, 37.3 mmol) was added portionwise to a stirred suspension of guanidine hydrochloride (5.85 g, 59.4 mmol) in DMSO (320 mL) and the mixture was heated at 30-50° C. under N2 for 30 min. N-[(1,4-Dichloro-1-guanidino-7-isoquinolinyl)sulphonyl]-cycloleucine ethyl ester (6.2 g, 14.9 mmol) was added in one portion and the mixture heated at 80° C. for 8 h. The cooled mixture concentrated in vacuo to ca. 160 mL and poured into water (800 mL). The aqueous mixture was extracted with EtOAc (4×150 mL) and the combined organic extracts were then washed with water, brine, dried (MgSO4) and evaporated in vacuo. The residue was purified by column chromatography upon silica gel using CH2Cl2 -MeOH-0.880NH3 (95:5:0.5 to 90:10:1) as eluant and then recrystallised from EtOAc to give N-[(4-chloro-1-guanidino-7-isoquinolinyl)sulphonyl]cyclo-leucine ethyl ester (1.43 g, 3.25 mmol) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06093731
Source datasetuspto-grants-2000_07
ORD IDord-b9b535b45a5146a19cbb88aa710dc0b2
Source noteuspto-grants-2000_07