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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 880696Generated: October 30, 2026

Potassium tert-butoxide → N-[2,6-Dimethyl-4-(7-trifluoromethyl-3,4-dihydro-1H-isoquinolin-2-yl)-phenyl]-3,3-dimethyl-butanamide

https://huagongshe.com/reaction/880696

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium tert-butoxideHCID 23665647—
Reactant7-(Trifluoromethyl)-1,2,3,4-tetrahydroisoquinoline hydrochlorideHCID 44118286—
ReactantN-(4-Bromo-2,6-dimethyl-phenyl)-3,3-dimethyl-butanamideHCID 59741059—
SolventTolueneHCID 1140—
ProductN-[2,6-Dimethyl-4-(7-trifluoromethyl-3,4-dihydro-1H-isoquinolin-2-yl)-phenyl]-3,3-dimethyl-butanamideHCID 58097350—

Reaction Steps

Bis(dibenzylidineacetone)palladium (390 mg, 0.68 mmol) and (2′-dicyclohexyl phosphanyl-biphenyl-2-yl)-dimethylamine (800 mg, 2.0 mmol) were added to dry toluene (150 mL purged with argon) and stirred for 15 minutes under argon. Potassium tert-butoxide (4.75 g, 42.3 mmol), 7-trifluoromethyl-1,2,3,4-tetrahydro-isoquinoline hydrochloride salt (4.82 g, 20.3 mmol) and N-(4-Bromo-2,6-dimethyl-phenyl)-3,3-dimethyl-butanamide (5 g, 16.8 mmol) were then added and the reaction mixture was stirred at 80° C. overnight. The reaction mixture was then cooled to room temperature, filtered through silica gel, and recrystallized from toluene to afford the title compound as a solid. (5.94 g, 85%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993593B2
Source datasetuspto-grants-2015_03
ORD IDord-ef37906a337f4519b51d48ef7a0fe1a9
Source noteuspto-grants-2015_03