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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1985490Generated: October 25, 2026

Potassium Carbonate → tert-Butyl 4-(3-oxo-3,4-dihydroisoquinolin-2(1H)-yl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1985490

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Amino-1-Boc-piperidineHCID 1268291—
ReactantMethyl 2-[2-(chloromethyl)phenyl]acetateHCID 9855748—
SolventAcetonitrileHCID 6342—
Producttert-Butyl 4-(3-oxo-3,4-dihydroisoquinolin-2(1H)-yl)piperidine-1-carboxylateHCID 5973189740%

Reaction Steps

Potassium carbonate (1.4 g, 10 mmol) was added to a solution of methyl 2-(2-(chloromethyl)phenyl)acetate (940 mg, 4.7 mmol) in acetonitrile (20 mL). 4-Amino-N-Boc-piperidine (1.13 g, 5.6 mmol) was added to the mixture. Reaction was heated at reflux for 1 hour. Mixture was cooled to room temperature and then filtered over celite. Filtrate was concentrated in vacuo. Residue was treated with toluene (29 mL). Acetic acid (1.5 ml) was added to the mixture. Reaction was heated at reflux for 2 hours. Mixture was concentrated in vacuo. Residue was treated with ethyl acetate (50 mL). Mixture was washed successively with aqueous sodium bicarbonate (2×30 mL), 1N hydrochloric acid (30 mL), and brine (20 mL). Organic layer was dried (magnesium sulfate), filtered and concentrated in vacuo. Silica gel chromatography gave the title compound as lightly colored oil in 40% yield. MS m/e (M+H)+=331.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07544680B2
Source datasetuspto-grants-2009_06
ORD IDord-6279c5282a174838b4a3bfb63b3b2c46
Source noteuspto-grants-2009_06