Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 22179411 | HCID 22179411 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22179392 | HCID 22179392 | 22.7% |
Reaction Steps
A mixture of 3-(2-4-tolylethylamino)-5-chloro-6-methyl-1-(benzyloxycarbonylmethyl)pyrazinone (854 mg, 2.00 mmol), as prepared in the preceding step, potassium hydroxide (452 mg, 8.00 mmol), 10% palladium on carbon (254 mg) in tetrahydrofuran (20 mL), methanol (30 mL), and water (7 mL) was stirred under hydrogen balloon for three days. The mixture was filtered through Celite. The filtrate was adjusted to pH 2-4 with 10% HCl and concentrated to about 2 mL under reduced pressure. The white solid which precipitated from the solution was filtered, washed with a small amount of water, and dried to give the title compound (137 mg, 22.7%). 1H NMR (CDCl3) δ 7.20 (d, 2H, J=7.5 Hz), 7.10 (d, 2H, J=7.8 Hz), 6.70 (s, H), 4.71 (s, 2H), 2.87 (m, 2H), 2.50 (m, 2H), 2.26 (s, 3H), 2.15 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06476016B2 |
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| Source dataset | uspto-grants-2002_11 |
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| ORD ID | ord-282e455c37894cc08cfc65964fcb928b |
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| Source note | uspto-grants-2002_11 |
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