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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 418541Generated: October 30, 2026

Hydrochloric Acid → (R)-2-(3-Fluoro-4-(trifluoromethyl)phenyl)-N-(6-methyl-1-oxo-2-(1-(piperazin-1-yl)propan-2-yl)-1,2-dihydroisoquinolin-5-yl)acetamide

https://huagongshe.com/reaction/418541

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
Reactant1,4-DioxaneHCID 31275—
Reactant(R)-tert-Butyl 4-(2-(5-(2-(3-fluoro-4-(trifluoromethyl)phenyl)acetamido)-6-methyl-1-oxoisoquinolin-2(1H)-yl)propyl)piperazine-1-carboxylateHCID 66648918—
Product(R)-2-(3-Fluoro-4-(trifluoromethyl)phenyl)-N-(6-methyl-1-oxo-2-(1-(piperazin-1-yl)propan-2-yl)-1,2-dihydroisoquinolin-5-yl)acetamideHCID 25014311—

Reaction Steps

To a solution of (R)-tert-butyl 4-(2-(5-(2-(3-fluoro-4-(trifluoromethyl)phenyl)acetamido)-6-methyl-1-oxoisoquinolin-2(1H)-yl)propyl)piperazine-1-carboxylate (100 mg, 0.0002 mol) in methanol (6 mL, 0.1 mol) was added 4M hydrogen chloride in 1,4-dioxane(6 mL, 0.02 mol) at 0° C. The mixture was stirred at room temperature overnight. The volatiles were removed under reduced pressure and the residue was purified by reverse phase preparative HPLC to afford the desired product as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093265B2
Source datasetuspto-grants-2012_01
ORD IDord-336ad487365a4416b86023af9511be97
Source noteuspto-grants-2012_01