Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416591Generated: October 31, 2026

Dichloromethane → HCID 86759566, compound

https://huagongshe.com/reaction/2416591

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantPotassium CarbonateHCID 11430—
ReactantN-Boc-2-chloroethylamineHCID 3795708—
ReactantHCID 22631323HCID 22631323—
SolventAcetic AcidHCID 176—
SolventHydrogen BromideHCID 260—
ProductHCID 86759566HCID 86759566—

Reaction Conditions

Temperature140 °C

Reaction Steps

10.4 g (26.7 mmol) of benzyl-(6-iodo-7-methoxyisoquinoline-1-yl)amine was dissolved in a mixture of 8 ml of acetic acid and 40 ml of hydrobromic acid, and the obtained solution was stirred at 140° C. overnight. The solvent was evaporated, and the residue was dissolved in 50 ml of DMF. 14.6 g (65.2 mmol) of t-butyl (2-chloroethyl)carbamate and 4.95 g (163 mmol) of potassium carbonate were added to the obtained solution, and they were stirred at 70° C. overnight. 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-b5583d9f791a45c0be443de05d2d5d5a
Source noteuspto-grants-2004_11