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4-Iodopyridine → HCID 86680495、化合物

HRID 2205548
ノート
印刷プレビュー

反応式

HRID 2205548 の反応式
I[C:2]1[CH:7]=[CH:6][N:5]=[CH:4][CH:3]=1.[Li]CCCC.[F:13][C:14]1[CH:19]=[CH:18][C:17]([C:20]2[CH:24]=[C:23]([C:25](=O)[CH3:26])[O:22][N:21]=2)=[CH:16][CH:15]=1>C1COCC1>[F:13][C:14]1[CH:15]=[CH:16][C:17]([C:20]2[CH:24]=[C:23]([CH:25]([C:2]3[CH:7]=[CH:6][N:5]=[CH:4][CH:3]=3)[CH3:26])[O:22][N:21]=2)=[CH:18][CH:19]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 6094924-IodopyridineHCID 228319891-(3-(4-Fluorophenyl)isoxazol-5-yl)ethanoneHCID 178418339Butyllithium

生成物 1

HCID 86680495HCID 86680495、化合物収率 30.8%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

To a stirred solution of 4-iodopyridine (0.3 g, 1.463 mmol) in THF (10 mL) was added n-BuLi (0.6 mL, 0.96 mmol) at −78° C. and stirred for 10 min. A solution of 1-(3-(4-fluorophenyl)isoxazol-5-yl)ethanone (0.1 g, 0.484 mmol) in THF (5 mL) was added to the reaction and the mixture stirred at −78° C. for 2 h. The reaction was quenched with saturated ammonium chloride solution (10 mL) and diluted with ethyl acetate (50 mL). The organic layer was separated, washed with saturated ammonium chloride (3×150 mL) followed by brine solution (2×20 mL). The organic layer was dried over sodium sulfate, filtered and concentrated under reduced pressure to obtain crude product. The crude product was purified by column chromatography (100-200μ silica gel; 50% ethyl acetate in hexane) to obtain 3-(4-fluorophenyl)-5-(1-(pyridin-4-yl)ethyl)isoxazole as off-white solid (0.04 g, 29% yield). 1H NMR (400 MHz, DMSO-d6): δ 8.55 (d, 2H), 7.91 (dd, 2H), 7.46 (d, 2H), 7.32 (t, 2H), 6.81 (s, 1H), 7.04 (s, 1H), 1.86 (s, 3H); LC-MS m/z calculated for [M+H]+285.10. found 285.1.

後処理

  1. stirringthe mixture stirred at −78° C. for 2 h
  2. customThe reaction was quenched with saturated ammonium chloride solution (10 mL)
  3. additiondiluted with ethyl acetate (50 mL)
  4. customThe organic layer was separated
  5. washwashed with saturated ammonium chloride (3×150 mL)
  6. dry with materialThe organic layer was dried over sodium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated under reduced pressure
  9. customto obtain crude product
  10. customThe crude product was purified by column chromatography (100-200μ silica gel; 50% ethyl acetate in hexane)

出典と根拠

ORDレコード
ord-277cdc5759ab4ccdbde6fa9998971963
出典データセット
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09371316B2

反応ノート

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