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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 880674Generated: October 26, 2026

Dimethylamine → n-[4-(6-Chloro-3,4-dihydro-1h-isoquinolin-2-yl)-2,6-dimethyl-phenyl]-3,3-dimethylbutanamide

https://huagongshe.com/reaction/880674

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
Reactant6-Chloro-1,2,3,4-Tetrahydroisoquinoline HydrochlorideHCID 12595084—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantN-(4-Bromo-2,6-dimethyl-phenyl)-3,3-dimethyl-butanamideHCID 59741059—
SolventTolueneHCID 1140—
Productn-[4-(6-Chloro-3,4-dihydro-1h-isoquinolin-2-yl)-2,6-dimethyl-phenyl]-3,3-dimethylbutanamideHCID 24937081—

Reaction Steps

Bis(dibenzylidineacetone)palladium (2 mg, 0.0035 mmol) and 2′-dicyclohexylphosphanyl-biphenyl-2-yl)-dimethylamine (3.3 mg, 0.0084 mmol) were added to dry toluene (5 mL purged with argon) and stirred for 15 minutes under argon. Potassium tert-butoxide (188 mg, 1.7 mmol), 6-chloro-1,2,3,4-tetrahydro isoquinoline hydrochloride salt (165 mg, 0.8 mmol), and N-(4-bromo-2,6-dimethylphenyl)-3,3-dimethylbutanamide (200 mg, 0.67 mmol) were then added, and the reaction mixture was stirred at 80° C. overnight. The reaction mixture was then cooled to room temperature and filtered through silica gel. Purification by preparative thin layer chromatography afforded the title compound as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993593B2
Source datasetuspto-grants-2015_03
ORD IDord-acc41914cd3f4b08bc453d2c44301d73
Source noteuspto-grants-2015_03