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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1797627Generated: November 3, 2026

Water → HCID 60206162, compound

https://huagongshe.com/reaction/1797627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantButyl AcrylateHCID 8846—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 22175280HCID 22175280—
CatalystTetrabutylammonium ChlorideHCID 70681—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
ProductHCID 60206162HCID 6020616241%

Reaction Conditions

Temperature100 °C

Reaction Steps

A suspension of tert-butyl[2-isobutyl-4-(4-methylphenyl)-1-oxo-6-trifluoromethanesulfonyloxy-1,2-dihydro-3-isoquinolinyl]methylcarbamate (Example 182 (1)) (1.42 g, 2.5 mmol), butyl acrylate (0.54 ml, 3.8 mmol), sodium hydrogencarbonate (0.32 g, 3.81 mmol), tetrabutylammonium chloride (83 mg, 0.3 mmol) and palladium acetate (67 mg, 0.3 mmol) in N,N-dimethylformamide (30 ml) was stirred with heating at 100° C. under an argon atmosphere for 20 h. The reaction mixture was poured into water and extracted with ethyl acetate. After washing the extract with water, the extract was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to give butyl (E)-3-[3-[[(tert-butoxycarbonyl)amino]methyl]-2-isobutyl-4-(4-methylphenyl)-1-oxo-1,2-dihydro-6-isoquinolinyl]-2-propenate (0.56 g, 40.3%) as an amorphous.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07034039B2
Source datasetuspto-grants-2006_04
ORD IDord-460849c261b74936b690440a6081b6ee
Source noteuspto-grants-2006_04