Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | trans-2-(4-Fluorophenyl)vinylboronic acid | HCID 5706776 | — |
| Reactant | 2-(6-Iodo-pyrazin-2-yl)-4-methyl-thiazole-5-carboxylic acid benzylamide | HCID 73213269 | — |
| Catalyst | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Solvent | Dimethyl Ether | HCID 8254 | — |
| Product | HCID 24954328 | HCID 24954328 | 60% |
Reaction Steps
To a solution of 2-(6-iodo-pyrazin-2-yl)-4-methyl-thiazole-5-carboxylic acid benzylamide (100 mg, 0.23 mmol, 1.0 equiv) in dimethyl ether (1 mL) was added Na2CO3 (49 mg, 0.46 mmol, 2.0 equiv), trans-2-(4-fluorophenyl)vinyl boronic acid (95 mg, 0.57 mmol, 2.5 equiv), PdCl2(dppf) (17 mg, 0.02 mmol, 0.1 equiv) and water (0.1 mL) in a sealed tube. The reaction vessel was immersed in an oil bath preheated to 100° C. After stirring for 1 hr, the reaction mixture was cooled and the solvent was removed in vacuo. The crude product was purified by column chromatography [SiO2, methanol/dichloromethane, 0:100 to 5:95, v/v] and recrystallization (methanol/pentane) to give 2-{6-[(E)-2-(4-fluoro-phenyl)-vinyl]-pyrazin-2-yl}-4-methyl-thiazole-5-carboxylic acid benzylamide (59 mg, 60%). 1H NMR (400 MHz, CD2Cl2) δ 9.17 (s, 1H), 8.63 (s, 1H), 7.81 (d, J=16.0 Hz, 1H), 7.61-7.64 (m, 2H), 7.27-7.37 (m, 5H), 7.09-7.13 (m, 3H), 6.23 (bs, 1H), 4.61 (d, J=8.0 Hz, 2H), 2.74 (s, 3H); HRMS (M+H)+=431.13.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08314138B2 |
|---|
| Source dataset | uspto-grants-2012_11 |
|---|
| ORD ID | ord-57a6647f4e354f64b2207464867d4e8c |
|---|
| Source note | uspto-grants-2012_11 |
|---|