HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 552485Generated: October 30, 2026
Sodium Carbonate → 4-(3-Fluoro-phenyl)-6-methyl-pyridine-2-carboxylic acid (4-methyl-thiazol-2-yl)-amide
https://huagongshe.com/reaction/552485
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 3-Fluorophenylboronic acid | HCID 2733986 | — |
| Reactant | HCID 25208982 | HCID 25208982 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-(3-Fluoro-phenyl)-6-methyl-pyridine-2-carboxylic acid (4-methyl-thiazol-2-yl)-amide | HCID 25209414 | 71% |
Reaction Steps
To a suspension of 150 mg (0.48 mmol) of 4-Bromo-6-methyl-pyridine-2-carboxylic acid (4-methyl-thiazol-2-yl)-amide, 71 mg (0.5 mmol, 1.05 equiv.) of 3-Fluorophenyl-boronic acid in 2 ml of dioxane were added 0.5 ml of 2M sodium carbonate solution and the mixture was purged with Argon for 10 min. Then 25 mg (0.096 mmol, 0.2 equiv.) of Triphenylphosphine and 10.8 mg (0.048 mmol, 0.1 equiv.) of Palladium acetate were added and the mixture was stirred under Argon atmosphere for 24 h at 90° C. The reaction was allowed to cool to r.t., taken up in two times in ethyl acetate and evaporated to dryness. The residue was separated by flash chromatography on silicagel (heptane/ethyl acetate 4:1) to yield the title compound (111 mg, 71%) as a yellow solid, MS (ISP): m/e=328.0 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07951824B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-7b4b6f8c219549e3baa96fd0b71e4735 |
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| Source note | uspto-grants-2011_05 |
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