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Ethylene Glycol → 1-(Difluoromethyl)-7-[(2,3-difluorophenyl)sulfanyl]-1-methyl-1,2,3,4-tetrahydro[1]benzofuro[2,3-c]pyridine

HRID 1616878
ノート
印刷プレビュー

反応式

HRID 1616878 の反応式
[F:1][CH:2]([F:18])[C:3]1([CH3:17])[C:8]2[O:9][C:10]3[CH:15]=[C:14](I)[CH:13]=[CH:12][C:11]=3[C:7]=2[CH2:6][CH2:5][NH:4]1.[F:19][C:20]1[C:25]([F:26])=[CH:24][CH:23]=[CH:22][C:21]=1[S:27][Si](C(C)C)(C(C)C)C(C)C.[F-].[Cs+].C(O)CO.CN(C=O)C>[Cu]I>[F:1][CH:2]([F:18])[C:3]1([CH3:17])[C:8]2[O:9][C:10]3[CH:15]=[C:14]([S:27][C:21]4[CH:22]=[CH:23][CH:24]=[C:25]([F:26])[C:20]=4[F:19])[CH:13]=[CH:12][C:11]=3[C:7]=2[CH2:6][CH2:5][NH:4]1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 5

HCID 174Ethylene GlycolHCID 6228DimethylformamideHCID 25953Cesium fluorideHCID 67322878(2,3-Difluorophenylsulfanyl)-triisopropylsilaneHCID 673233061-difluoromethyl-7-iodo-1-methyl-1,2,3,4-tetrahydro-benzofuro[2,3-C]pyridine

生成物 1

HCID 67323415
1-(Difluoromethyl)-7-[(2,3-difluorophenyl)sulfanyl]-1-methyl-1,2,3,4-tetrahydro[1]benzofuro[2,3-c]pyridine
収率 135.5%

試薬・触媒・溶媒 1

HCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)触媒

反応条件

温度
105 °C

実験手順

Into a Schlenk flask equipped with a magnetic stir bar was added 1-difluoromethyl-7-iodo-1-methyl-1,2,3,4-tetrahydro-benzofuro[2,3-C]pyridine (enantiomer 1, 100 mg, 0.30 mmol), (2,3-difluorophenylsulfanyl)-triisopropylsilane (125 mg, 0.43 mmol), CsF (189 mg, 1.24 mmol), CuI (25 mg, 0.13 mmol), ethylene glycol (85 μL, 1.5 mmol) and anhydrous DMF (3 mL, 0.30 mmol). The Schlenck flask was evacuated and flushed with argon three times. The reaction mixture was heated at 105° C. under argon for 17 h. Upon cooling, the reaction was diluted with DCM, filtered through celite and solvent was evaporated. Purification using preparative TLC (2000 micron silica gfel plate; elution with 15% EtOAc in dichloromethane) afforded 155 mg of product as a viscous, pale oil. MS m/z: 382 [M+H]+.

後処理

  1. customInto a Schlenk flask equipped with a magnetic stir bar
  2. customThe Schlenck flask was evacuated
  3. customflushed with argon three times
  4. temperatureUpon cooling
  5. additionthe reaction was diluted with DCM
  6. filtrationfiltered through celite and solvent
  7. customwas evaporated
  8. customPurification
  9. washTLC (2000 micron silica gfel plate; elution with 15% EtOAc in dichloromethane)

出典と根拠

ORDレコード
ord-3380e2749444467abff963aa8ef3d12e
出典データセット
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08765779B2

反応ノート

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