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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1797639Generated: October 30, 2026

Methanol → HCID 22175826, compound

https://huagongshe.com/reaction/1797639

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
ReactantHCID 22176315HCID 22176315—
Catalystpalladium(II) acetateHCID 167845—
CatalystFerrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
ProductHCID 22175826HCID 2217582685.9%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixed solution of tert-butyl[4-(4-chlorophenyl)-2-isobutyl-1-oxo-6-trifluoromethanesulfonyloxy-1,2-dihydro-3-isoquinolinyl]methylcarbamate (2.35 g, 4 mmol), 1,1′-bis(diphenylphosphino)ferrocene (0.11 g, 0.2 mmol), triethylamine (0.6 ml, 4.4 mmol) and palladium acetate (45 mg, 0.2 mmol) in tetrahydrofuran (20 ml)-methanol (20 ml) was stirred with heating at 100° C. under a carbon monoxide atmosphere at 5 atm for 2 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-(4-chlorophenyl)-2-isobutyl-1-oxo-1,2-dihydro-6-isoquinolinecarboxylate (1.71 g, 85.9%) as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07034039B2
Source datasetuspto-grants-2006_04
ORD IDord-bd3684b184f74ce69522b90057d5791a
Source noteuspto-grants-2006_04