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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289734Generated: October 31, 2026

Potassium Carbonate → HCID 178451266, compound

https://huagongshe.com/reaction/2289734

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl bromoacetateHCID 79177—
ReactantHCID 178451316HCID 178451316—
ReactantHCID 178479407HCID 178479407—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 178451266HCID 17845126657.6%

Reaction Conditions

Temperature23 °C

Reaction Steps

N-(Carboxymethyl)-N-[(4-chloro-1-guanidino-7-isoquinolinyl)sulphonyl]glycine hydrochloride ##STR31## Anhydrous K2CO3 (88 mg, 0.64 mmol) and then t-butyl bromoacetate (56 μL, 0.38 mmol) were added to a stirred solution of N-[(4-chloro-1-guanidino-7-isoquinolinyl)sulphonyl]glycine t-butyl ester (132 mg, 0.33 mmol) in DMF (2.0 mL) and the mixture was stirred at 23° C. for 18 h. The mixture was diluted with EtOAc (300 mL), washed with brine (150 mL), water (200 mL), dried (MgSO4) and evaporated in vacuo. The residue was purified by column chromatography upon silica gel using pentane-EtOAc (80:20 to 50:50) as eluant to give N-(t-butoxycarbonylmethyl)-N-[(4-chloro-1-guanidino-7-isoquinolinyl)sulphonyl]glycine t-butyl ester (101 mg, 0.19 mmol) as a pale yellow foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06093731
Source datasetuspto-grants-2000_07
ORD IDord-319e8c9e0d5049299f20110f1252277c
Source noteuspto-grants-2000_07