Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 2-Amino-4-methylthiazole | HCID 74143 | — |
| Reactant | HCID 86634720 | HCID 86634720 | — |
| Catalyst | 1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine) | HCID 636044 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 24825976 | HCID 24825976 | 80.6% |
Reaction Steps
Using the method of Example 3, Step B, 4-methylthiazol-2-amine (25.2 mL, 10.1 mmol), ethyl 6-chloro-4-(naphthalen-1-yloxy)nicotinate (3.63 g, 11.1 mmol), potassium phosphate (2.35 g, 11.1 mmol), tris(dibenzylideneacetone)-dipalladium (0) (0.231 g, 0.252 mmol) and 4,5-bis(diphenylphosphino)-9,9-dimethyl-9H-xanthene (0.160 g, 0.277 mmol) were reacted in toluene (25 mL) and water (8 mL) to afford ethyl 6-(4-methylthiazol-2-ylamino)-4-(naphthalen-1-yloxy)nicotinate (3.30 g, 80.0% yield) as yellow solid. 1H NMR (CDCl3) δ 9.90 (bs, 1H), 8.91 (s, 1H), 7.97 (d, 1H), 7.91 (d, 1H), 7.77 (d, 1H), 7.53 (m, 1H), 7.47 (m, 1H), 7.43 (m, 1H), 7.14 (d, 1H), 6.18 (s, 1H), 5.90 (s, 1H), 4.37 (quart, 2H), 1.76 (s, 3H), 1.33 (t, 3H); Mass spectrum (apci) m/z=406 (100) (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08022222B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-75cd6cf08dd84fac860f92fd318cfcda |
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| Source note | uspto-grants-2011_09 |
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