Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | HCID 18697932 | HCID 18697932 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | HCID 18697937 | HCID 18697937 | — |
Reaction Steps
A suspension of 4-(2-(4-benzyloxycarbonylpiperazin-1-yl)pyrid-5-yl)-N-(2-ethylbenzoxazol-5-yl)-2-pyrimidineamine (100 mg, 0.19 mmol) and 10% palladium on charcoal (30 mg) in ethanol (25 ml) was stirred under an atmosphere of hydrogen at 50° for 2 h, then filtered through Celite® and evaporated. The residue was subjected to column chromatography (silica, 0.88 ammonia solution-methanol-dichloromethane, 1:5:94) to afford the title compound (25 mg) as a white solid m.p. 174-176°. δH (CDCl3) 1.15 (3H, t, J 7.2 Hz), 1.45 (3H, t, J 7.6 Hz), 2.49 (2H, q, J 7.2 Hz), 2.58 (4H, m), 2.96 (2H, q, J 7.6 Hz), 3.71 (4H, m), 6.71 (1H, d, J 9.0 Hz), 7.04 (1H, d, J 5.3 Hz), 7.40 (1H, br s), 7.41 (1H, d, J 8.7 Hz), 7.49 (1H, dd, J 2.1, 8.7 Hz), 8.09 (1H, d, J 2.1 Hz), 8.20 (1H, dd, J 2.4, 9.0 Hz), 8.36 (1H, d, J 5.3 Hz) and 8.87 (1H, d, J 2.1 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06093716 |
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| Source dataset | uspto-grants-2000_07 |
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| ORD ID | ord-27ba9795a77144c38343fca9211e8263 |
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| Source note | uspto-grants-2000_07 |
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