Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | (Pyridin-4-yl)boronic acid | HCID 2734379 | — |
| Reactant | HCID 86652757 | HCID 86652757 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water 1,2-dimethoxyethane | HCID 18180031 | — |
| Product | HCID 44176975 | HCID 44176975 | 50.3% |
Reaction Steps
A mixture of benzothiazol-5-yl-(6-chloro-pyrazin-2-yl)-amine (0.06 g, 0.228 mmol), pyridine-4-boronic acid (0.043 g, 0.342 mmol), sodium carbonate (0.124 g, 1.14 mmol) and tetrakis(triphenylphosphine)palladium(0) (0.013 g, 0.0114 mmol) in DME:water (3:2, 5 mL) was heated at reflux for 22 h. The reaction mixture was concentrated under reduced pressure and the residue obtained was extracted with dichloromethane. The organic layer was washed with water, brine, dried over sodium sulfate and concentrated. The crude product was purified by flash chromatography (5% methanol in CH2Cl2 as eluent) to yield N-(6-pyridin-4-ylpyrazin-2-yl)-1,3-benzothiazol-5-amine (0.035 g, 50%) as a yellow solid. 1H NMR (CD3OD) δ 9.31 (s, 1H), 8.98 (d, J=2.02 Hz, 1H), 8.75-8.74 (d, J=5.31 Hz, 2H), 8.64 (s, 1H), 8.31 (s, 1H), 8.24-8.22 (d, J=5.99 Hz, 2H), 8.06-8.04 (d, J=8.77 Hz, 1H), 7.74-7.71 (dd, J=10.73, 2.01 Hz, 1H); MS (API-ES/Positive); m/z: 306 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08436171B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-7c9232eafbe04377b2f6c6198c9a1b90 |
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| Source note | uspto-grants-2013_05 |
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