Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | 2-Methylpyridine-3-boronic acid | HCID 20111647 | — |
| Reactant | HCID 58203842 | HCID 58203842 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Product | HCID 58204233 | HCID 58204233 | — |
Reaction Steps
To a solution of 9-Chloro-2-(1-isopropyl-1H-imidazol-2-yl)-4,5-dihydro-6-oxa-1-thia-10-aza-benzo[e]azulene (63 mg, 0.18 mmol), Potassium acetate (60.2 mg, 0.613 mmol), 2-methylpyridine-3-boronic acid, (32.2 mg, 0.235 mmol) and Tetrakis(triphenylphosphine)palladium(0) (28 mg, 0.024 mmol) in Acetonitrile (2 mL, 30 mmol) and Water (2 mL, 100 mmol) was degassed. The reaction was heated in the microwave at 140° C. for 20 minutes. The reaction was cooled to r.t., then extract with ethyl acetate. The combined organics were concentrated and purified by reverse phase HPLC to give 304. MS: (ESI+)=403.1. 1H NMR (400 MHz, DMSO) δ 8.55-8.47 (m, 1H), 7.86 (d, J=7.7 Hz, 1H), 7.54 (d, J=8.3 Hz, 1H), 7.50-7.43 (m, 2H), 7.36 (dd, J=7.7, 4.9 Hz, 1H), 7.29 (s, 1H), 7.00 (s, 1H), 4.82 (dt, J=13.3, 6.5 Hz, 1H), 4.43 (t, J=4.6 Hz, 2H), 2.65 (s, 3H), 1.44 (d, J=6.6 Hz, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09175009B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-ca573c3722cf4639933b960547a7d425 |
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| Source note | uspto-grants-2015_11 |
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