Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 22176315 | HCID 22176315 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Catalyst | Ferrocene-1,1'-bis-(diphenylphosphine) | HCID 635956 | — |
| Product | HCID 22175826 | HCID 22175826 | 85.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07034039B2 |
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| Source dataset | uspto-grants-2006_04 |
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| ORD ID | ord-bd3684b184f74ce69522b90057d5791a |
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| Source note | uspto-grants-2006_04 |
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