Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | HCID 22285039 | HCID 22285039 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 9813880 | HCID 9813880 | 4% |
Reaction Steps
A mixture of 1-methyl-4-chlorobenzo(g)imidazo(4,5-c)quinoline (Preparation 19 in Example 11) (130 mg, 0.49 mmol) and MeNH2 (2.0M/THF, 1.5 mL, 2.92 mmol) was heated in a pressure tube at 80° C. for 18 hours. After the reaction mixture was cooled to RT, it was diluted with EtOAc (100 mL), washed with sat'd NaCO3 (50 mL), and brine. The organic layer was dried over MgSO4, filtered and evaporated in vacuo. The crude material was submitted to flash chromatography (5% MeOH/EtOAc) affording the title compound as a pale white solid (5.2 mg, 4%). 1H NMR (CDCl3): 8.44 (s, 1H), 8.35 (s, 1H), 7.94 (d, J=8.3, 1H), 7.90 (d, J=8.3, 1H), 7.72 (s, 1H), 7.46 (m, 1H), 7.40 (m, 1H), 5.95 (b, 1H), 4.28 (s, 3H), 3.31 (s, 3H). (ESI) m/z (M+H)+=263.14. Inhibition of IKK-1 activity was measured using the assay of Example 2, where the inhibitory potential of the compound of Example 16 resulted in an IC50 of 0.80 μM.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06869956B2 |
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| Source dataset | uspto-grants-2005_03 |
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| ORD ID | ord-ca5a513ca78845a0bcdadc5a66158457 |
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| Source note | uspto-grants-2005_03 |
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