Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 5-Chloro-2-methyl-1,8-naphthyridine | HCID 12266372 | — |
| Reactant | HCID 68459230 | HCID 68459230 | — |
| Product | HCID 68461764 | HCID 68461764 | — |
Reaction Steps
The product from Example 1d (18 mg, 0.085 mmol) was reacted in ethanol (1 mL) with the product from Example 153a (33 mg, 0.085 mmol) for 18 h following the procedure from Example 1g giving the crude title compound which was purified by HPLC with TFA providing the product as a trifluoroacetic acid salt (14 mg, 30%). 1H NMR (300 MHz, DMSO-d6) δ ppm: 0.97 (t, J=7.35 Hz, 3 H) 1.69-1.93 (m, 2 H) 2.02 (s, 3 H) 2.99 (t, J=6.99 Hz, 2 H) 3.75 (s, 3 H) 5.13 (s, 2 H) 6.29 (d, J=7.35 Hz, 1 H) 6.91 (dd, J=8.09, 2.57 Hz, 1 H) 6.95-7.05 (m, 2 H) 7.13 (d, J=8.82 Hz, 2 H) 7.16-7.24 (m, 2 H) 7.31 (t, J=8.09 Hz, 1 H) 7.38 (d, J=8.46 Hz, 1 H) 7.42 (d, J=8.82 Hz, 2 H) 7.80 (d, J=8.82 Hz, 1H) 8.35 (d, J=6.99 Hz, 1 H) 8.97 (d, J=8.82 Hz, 1 H) 9.97 (s, 1 H) 11.00 (s, 1 H) 14.36 (s,1H); MS (ESI+) m/z 565(M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07763731B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-f2c32f7868f74cdca66ea26c12fad332 |
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| Source note | uspto-grants-2010_07 |
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