Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium | HCID 223 | — |
| Reactant | HCID 66621372 | HCID 66621372 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 44181680 | HCID 44181680 | 22% |
Reaction Steps
Methyl 2-(3-(4-(cyclopropanecarbonyl)piperazine-1-carbonyl)phenyl)benzo[d]oxazole-7-carboxylate (130 mg, 0.33 mmol) was added to ammonium in methanol (10 mL) in a sealing tube and stirred at 25° C. for 3 days. The solvent was removed under reduced pressure. The crude product was purified by pre-HPLC to obtain 2-(3-(4-(cyclopropanecarbonyl)piperazine-1-carbonyl)phenyl)benzo[d]oxazole-7-carboxamide (30 mg, yield 22%). 1H-NMR (400 MHz, CD3OD) δ: 0.85-0.92 (m, 4H), 1.29 (m, 1H), 3.20-3.99 (m, 8H), 7.52-7.56 (t, J=8.0 Hz, 1H), 7.74-7.75 (m, 2H), 7.92-7.97 (m, 2H), 8.43-8.47 (m, 2H); LC-MS (ESI) m/z: 419 (M+1)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08088760B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-0586935728504534a0ae8c2c75a2e3e9 |
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| Source note | uspto-grants-2012_01 |
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