Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | HCID 66605740 | HCID 66605740 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 66604278 | HCID 66604278 | 87% |
Reaction Steps
A mixture of methyl 7-methoxy-2-(piperidin-1-yl)-5H-pyrido[3,2-b]indole-4-carboxylate (15 mg, 0.044 mmol) and 7 N NH3 in MeOH (1.5 mL) in a sealed microwave tube was heated at 75° C. for 40 h. Removal of solvent to afford 7-methoxy-2-(piperidin-1-yl)-5H-pyrido[3,2-b]indole-4-carboxamide (14 mg, 0.038 mmol, 87% yield) as a solid. MS (ESI) m/z 325.1 (M+H). 1H NMR (500 MHz, MeOD) δ ppm 8.04 (1H, d, J=8.85 Hz), 7.21 (1H, s), 7.06 (1H, d, J=2.14 Hz), 6.82 (1H, dd, J=8.70, 2.29 Hz), 3.91 (3H, s), 3.49-3.62 (4H, m), 1.74-1.82 (4H, m), 1.66-1.73 (2H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08815840B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-222efc7a67ad47ad8dc7f7258c1d3892 |
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| Source note | uspto-grants-2014_08 |
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