HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113630Generated: November 1, 2026
Potassium Carbonate → 6-Methyl-3'-trifluoromethyl-[2,2']bipyridinyl-5-carbonitrile
https://huagongshe.com/reaction/2113630
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Methylboronic Acid | HCID 139377 | — |
| Reactant | 6-Chloro-3'-trifluoromethyl-[2,2']bipyridinyl-5-carbonitrile | HCID 58628189 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-Methyl-3'-trifluoromethyl-[2,2']bipyridinyl-5-carbonitrile | HCID 58628191 | — |
Reaction Steps
In a sealed tube, dissolve 6-chloro-3′-trifluoromethyl-[2,2′]bipyridinyl-5-carbonitrile (242 mg, 0.853 mmol), CH3B(OH)2 (300 mg, 5.10 mmol), K2CO3 (1.6 g, 12 mmol), and Pd(PPh3)4 in a solution of dioxane (10 mL) and H2O (2 mL). Bubble argon through the mixture for 30 minutes and seal. Heat the mixture at 115° C. overnight. Cool the mixture to room temperature. Add H2O (20 mL) and extract with EtOAc (3×20 mL). Combine the organic extracts and wash with brine (60 mL). Dry the organic layer over Na2SO4 and remove the solvent under reduced pressure. Purify the crude product using silica gel chromatography eluting with EtOAc/hexane (1:1) to yield the title compound. MS 264.07 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07432275B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-6fee241b24664faa8a6bba38cc01b94c |
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| Source note | uspto-grants-2008_10 |
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