Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 5-Chloro-2-methyl-1,8-naphthyridine | HCID 12266372 | — |
| Reactant | HCID 68456665 | HCID 68456665 | — |
| Product | HCID 68458469 | HCID 68458469 | — |
Reaction Steps
The product from Example 1d (18 mg, 0.085 mmol) was reacted in ethanol (1 mL) with the product from Example 236a (35 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 (22 mg, 37%). 1H NMR (300 MHz, DMSO-d6) δ ppm: 0.97 (t, J=7.35 Hz, 3 H) 1.75-1.93 (m, 2 H), 2.02 (s, 3 H), 2.99 (t, J=7.54 Hz, 2 H), 3.86 (s, 3 H) 5.26 (s, 2 H) 6.30 (d, J=6.99 Hz, 1 H) 7.14 (d, J=8.82 Hz, 2 H), 7.17-7.27 (m, 2 H), 7.37 (d, J=8.46 Hz, 1 H), 7.42 (d, J=8.82 Hz, 2 H), 7.59 (d, J=8.46 Hz, 2 H), 7.80 (d, J=8.46 Hz, 1 H) 7.99 (d, J=8.09 Hz, 2 H), 8.36 (d, J=7.35 Hz, 1 H), 8.97 (d, J=8.46 Hz, 1 H) 9.98 (s, 1 H), 11.01 (s, 1 H), 14.38 (s, 1 H); MS (ESI+) m/z 593(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-426aa4b9c7c84a6eaddd9cb91f9e621c |
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| Source note | uspto-grants-2010_07 |
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