HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 642360Generated: October 26, 2026
Cesium carbonate → 2-(3-Chloro-4-fluoro-phenyl)-4-{[(2,4-dimethoxy-benzyl)-ethoxycarbonylmethyl-amino]-methyl}-thiazole-5-carboxylic acid ethyl ester
https://huagongshe.com/reaction/642360
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 3-Chloro-4-fluorophenylboronic Acid (contains varying amounts of Anhydride) | HCID 2734660 | — |
| Reactant | 2-Bromo-4-{[(2,4-dimethoxy-benzyl)-ethoxycarbonylmethyl-amino]-methyl}-thiazole-5-carboxylic acid ethyl ester | HCID 68426454 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-(3-Chloro-4-fluoro-phenyl)-4-{[(2,4-dimethoxy-benzyl)-ethoxycarbonylmethyl-amino]-methyl}-thiazole-5-carboxylic acid ethyl ester | HCID 68428455 | 56.6% |
Reaction Steps
A mixture of 2-bromo-4-{[(2,4-dimethoxy-benzyl)-ethoxycarbonylmethyl-amino]-methyl}-thiazole-5-carboxylic acid ethyl ester (1.04 g, 2.08 mmole), 3-chloro-4-fluorophenylboronic acid (726 mg, 4.16 mmole), cesium carbonate (2.04 g, 6.25 mmole) and tetrakis(triphenylphosphine)palladium (241 mg, 0.21 mmole) in dioxane (7 ml) was refluxed for 16 h before it was cooled to room temperature, quenched with water and filtered. The filtrate was partitioned between ethyl acetate and water. The organic layer was washed with brine, dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with a gradient of ethyl acetate and hexanes to give the title compound as a yellow oil (649 mg). MS: (+) m/z 551.26 (M+H+)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07696223B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-8fde0a2b07044225a8f16573286f6793 |
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| Source note | uspto-grants-2010_04 |
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