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Tetrahydrofuran → HCID 86680495、化合物

HRID 2406480
ノート
印刷プレビュー

反応式

HRID 2406480 の反応式
I[C:2]1[CH:7]=[CH:6][N:5]=[CH:4][CH:3]=1.[Li][CH2:9][CH2:10][CH2:11][CH3:12].[F:13][C:14]1[CH:19]=[CH:18][C:17]([C:20]2ON=C(C(=O)C)[N:21]=2)=[CH:16][CH:15]=1.C1C[O:31]CC1>>[F:13][C:14]1[CH:15]=[CH:16][C:17]([C:20]2[CH:9]=[C:10]([CH:11]([C:2]3[CH:7]=[CH:6][N:5]=[CH:4][CH:3]=3)[CH3:12])[O:31][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 4

HCID 8028Tetrahydrofuran2 回HCID 6094924-IodopyridineHCID 82283232HCID 82283232、化合物HCID 178418339Butyllithium

生成物 1

HCID 86680495HCID 86680495、化合物収率 29%

実験手順

To a stirred solution of 4-iodopyridine (0.29 g, 0.463 mmol) in THF (30 mL) at −78° C. was added n-BuLi (2.4 mL, 3.9 mmol) and the mixture was stirred for 10 min. 1-(5-(4-Fluorophenyl)-1,2,4-oxadiazol-3-yl)ethanone (0.5 g, 2.79 mmol) in THF (5 mL) was then added to reaction, which was then stirred at −78° C. for 2 h. The reaction was then quenched with saturated ammonium chloride solution (10 mL) and diluted with ethyl acetate (50 mL). The organic layer was separated, washed with ammonium chloride solution (3×150 mL) followed by brine solution (2×20 mL), 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 and 30% ethyl acetate in hexane) to obtain 3-(4-fluorophenyl)-5-(1-(pyridin-4-yl)ethyl)isoxazole as off-white solid (0.06 g, 29% yield). 1H NMR (400 MHz, CDCl3): δ 8.60 (d, 2H), 8.11 (dd, 2H), 7.48 (d, 2H), 7.19 (t, 2H), 3.40 (s, 1H), 1.99 (s, 3H); LC-MS m/z calculated for [M+H]+ 286.09, found 286.2.

後処理

  1. stirringwas then stirred at −78° C. for 2 h
  2. customThe reaction was then quenched with saturated ammonium chloride solution (10 mL)
  3. additiondiluted with ethyl acetate (50 mL)
  4. customThe organic layer was separated
  5. washwashed with ammonium chloride solution (3×150 mL)
  6. dry with materialdried 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 and 30% ethyl acetate in hexane)

出典と根拠

ORDレコード
ord-0d732098d55a4eacb4ab9ec2158f6cf9
出典データセット
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08809372B2

反応ノート

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