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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1823931Generated: October 30, 2026

1-Phenyl-1,2-propanedione → 3-(5-methyl-4-phenyl-1H-imidazol-2-yl)-3,4-dihydro-1H-isoquinoline

https://huagongshe.com/reaction/1823931

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Phenyl-1,2-propanedioneHCID 11363—
ReactantAmmonium HydroxideHCID 14923—
ReactantAmmonium AcetateHCID 517165—
Reactanttert-Butyl 3-formyl-3,4-dihydroisoquinoline-2(1H)-carboxylateHCID 12190329—
SolventAcetic AcidHCID 176—
Product3-(5-methyl-4-phenyl-1H-imidazol-2-yl)-3,4-dihydro-1H-isoquinolineHCID 21914142—

Reaction Steps

3-Formyl-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester (1.83 g, 7 mmol) was combined with AcOH (25 mL) to which was immediately added 1-phenyl-propane-1,2-dione (3.11 g, 21 mmol) and NH4OAc (13.49 g, 175 mmol). The reaction mixture was then placed on a steam bath and heated under an argon atmosphere for 20 minutes. The reaction mixture was cooled in an ice bath and then added to an ice slurry (44 g). The resulting mixture was basified by addition of concentrated NH4OH (50 mL) and then extracted twice with diethyl ether (150 mL each). The combined organic phases were dried over MgSO4, filtered and concentrated to yield crude product. This material was purified by preparative HPLC to yield the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07041681B2
Source datasetuspto-grants-2006_05
ORD IDord-7647c46102f94ab582024f138e0c065e
Source noteuspto-grants-2006_05