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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1797548Generated: November 2, 2026

Water → HCID 22175943, compound

https://huagongshe.com/reaction/1797548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
ReactantHCID 22176047HCID 22176047—
Catalystpalladium(II) acetateHCID 167845—
CatalystFerrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
SolventMethanolHCID 887—
ProductHCID 22175943HCID 2217594392.5%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixed solution of tert-butyl[4-(2-fluorophenyl)-2-isobutyl-1-oxo-6-trifluoromethanesulfonyloxy-1,2-dihydro-3-isoquinolinyl]methylcarbamate (2.86 g, 5 mmol), 1,1′-bis(diphenylphosphino)ferrocene (0.14 g, 0.25 mmol), triethylamine (0.77 mL, 5.5 mmol) and palladium acetate (56 mg, 0.25 mmol) in tetrahydrofuran (20 mL) and methanol (20 mL) was stirred with heating at 100° C. under a carbon monoxide atmosphere at 5 atm for 1 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 methyl 3-[[(tert-butoxycarbonyl)amino]methyl]-4-(2-fluorophenyl)-2-isobutyl-1-oxo-1,2-dihydro-6-isoquinolinecarboxylate (2.23 g, 92.5%) as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07034039B2
Source datasetuspto-grants-2006_04
ORD IDord-092e5a23ce7447eb98323a5da619bea8
Source noteuspto-grants-2006_04