3-Fluoro-5-iodopicolinonitrile → Methyl 2-(6-cyano-5-fluoropyridin-3-yl)-6-fluorobenzoate

HRID 1374162ノート

反応式

HRID 1374162 の反応式
[F:1][C:2]1[C:3]([C:9]#[N:10])=[N:4][CH:5]=[C:6](I)[CH:7]=1.[F:11][C:12]1[C:13]([C:20]([O:22][CH3:23])=[O:21])=[C:14]([Zn]I)[CH:15]=[CH:16][CH:17]=1>C1COCC1>[C:9]([C:3]1[N:4]=[CH:5][C:6]([C:14]2[CH:15]=[CH:16][CH:17]=[C:12]([F:11])[C:13]=2[C:20]([O:22][CH3:23])=[O:21])=[CH:7][C:2]=1[F:1])#[N:10]

参加物

4

反応物 2

HCID 210758683-Fluoro-5-iodopicolinonitrileHCID 178498692HCID 178498692、化合物

生成物 1

HCID 21075884Methyl 2-(6-cyano-5-fluoropyridin-3-yl)-6-fluorobenzoate

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

A solution of 3-fluoro-5-iodopyridine-2-carbonitrile (1.08 g, 3.87 mmol) in 10 mL of THF and palladium tetrakistriphenylphosphine (0.18 g, 0.16 mmol) was added to a solution of [3-fluoro-2-(methoxycarbonyl)phenyl](iodo)zinc (prepared from methyl 2-fluoro-6-iodobenzoate and Reike Zinc) in 20 mL of THF via cannula. The mixture was heated to reflux for one hour, cooled, and partitioned between ethyl acetate and water. The organic extract was washed with brine, dried over MgSO4, filtered and concentrated under vacuum. The residue was subjected to silica gel chromatography eluted with 0–20% ethyl acetate in hexanes to provide methyl 2-(6-cyano-5-fluoropyridin-3-yl)-6-fluorobenzoate that gave proton NMR spectra consistent with theory.

後処理

  1. temperatureThe mixture was heated
  2. temperatureto reflux for one hour
  3. temperaturecooled
  4. custompartitioned between ethyl acetate and water
  5. extractionThe organic extract
  6. washwas washed with brine
  7. dry with materialdried over MgSO4
  8. filtrationfiltered
  9. concentrationconcentrated under vacuum
  10. washeluted with 0–20% ethyl acetate in hexanes

出典と根拠

ORDレコード
ord-bc86ad7b1b81453584731b89221b3090
出典データセット
uspto-grants-2007_01
特許番号
US07163951B2

反応ノート

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