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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416585Generated: November 2, 2026

Dichloromethane → HCID 86759565, compound

https://huagongshe.com/reaction/2416585

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 22631312HCID 22631312—
Reactantbenzyl (4R)-4-t-butoxycarbonylamino-5-chloropentanoateHCID 86588383—
CatalystTetrabutylammonium IodideHCID 67553—
SolventDimethylformamideHCID 6228—
ProductHCID 86759565HCID 86759565—

Reaction Conditions

Temperature70 °C

Reaction Steps

8.81 g (27 mmol) of 1-amino-7-hydroxyisoquinoline monohydrobromide was dissolved in 120 ml of DMF. 14.0 g (41 mmol) of benzyl (4R)-4-t-butoxycarbonylamino-5-chloropentanoate, 11.2 g (81.0 mmol) of potassium carbonate and 9.96 g (27 mmol) of tetrabutylammonium iodide were added to the obtained solution, and they were stirred at 70° C. for 3 days. After the treatment with dichloromethane as the extraction solvent in an ordinary manner, the obtained crude product was purified by the silica gel column chromatography to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06825181B1
Source datasetuspto-grants-2004_11
ORD IDord-489b8aa5a3cf45859ffddb56a79f4d1e
Source noteuspto-grants-2004_11