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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2366953Generated: November 4, 2026

Potassium Carbonate → HCID 52934565, compound

https://huagongshe.com/reaction/2366953

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Methylphenyl boronic acidHCID 2733267—
Reactant1-Methylethyl((cis)-1-acetyl-6-bromo-2-methyl-1,2,3,4-tetrahydro-4-quinolinyl)carbamateHCID 52935020—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
ProductHCID 52934565HCID 5293456593%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 1-methylethyl[(2S,4R)-1-acetyl-6-bromo-2-methyl-1,2,3,4-tetrahydro-4-quinolinyl]carbamate (for a preparation see Example 4) (25 mg, 0.068 mmol), (2-methylphenyl)boronic acid (11.97 mg, 0.088 mmol), potassium carbonate (28.1 mg, 0.203 mmol) and tetrakis(triphenylphosphine)palladium(0) (3.91 mg, 3.39 μmol) in ethanol (1 mL) and toluene (1 mL) was degassed under house vacuum and quenched several times with nitrogen, and then was heated at 100° C. for 30 min before being cooled to room temperature. The mixture was filtered through celite and the insoluble washed with EtOH. Most of the solvent was concentrated in vacuo. Purification of the residue by flash chromatography on silica gel (gradient: 30 to 60% AcOEt in hexanes) gave 1-methylethyl [(2S,4R)-1-acetyl-2-methyl-6-(2-methylphenyl)-1,2,3,4-tetrahydro-4-quinolinyl]carbamate (24 mg, 0.063 mmol, 93%) as a colourless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697725B2
Source datasetuspto-grants-2014_04
ORD IDord-83a2c24e80824337a16bf0d68d092bce
Source noteuspto-grants-2014_04