Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Perchloric Acid | HCID 24247 | — |
| Reactant | HCID 11681258 | HCID 11681258 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 11616429 | HCID 11616429 | — |
Reaction Steps
Pd/C (0.015 g, 10% w/w) and catalytic amount of perchloric acid was added to a solution of compound of Example 40 (0.11 g, 0.3 mmol) in acetic acid (60 mL). The reaction mixture was subjected to hydrogenation at 100 psi of hydrogen at 65° C. for 6.5 h. The reaction mixture was cooled to 25° C. and filtered through high flow bed. The filtrate was concentrated, diluted with water and extracted with ethyl acetate. The combined organic layer was washed with water, brine, concentrated and purified using flash chromatography (silica gel, ethyl acetate and pet. ether 60-80° C.) to obtain the title compound. Yield: 0.05 g (47%); 1H NMR (CDCl3, 300 MHz): δ 3.90 (s, 3H, OCH3), 4.32 (s, 2H, CH2), 5.21 (s, 2H, CH2) 7.38 (m, 5H, Ar), 8.09 (d, 1H, Ar), 8.61 (s, 1H, Ar); MS: m/e (Cl) 303 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07964631B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-bea402ea57fb4168bd7a040cc89840ce |
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| Source note | uspto-grants-2011_06 |
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