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Sodium Carbonate → HCID 90389673、化合物

HRID 59765
ノート
印刷プレビュー

反応式

HRID 59765 の反応式
[I:1][C:2]1[C:3](N)=[N:4][CH:5]=[CH:6][C:7]=1[O:8][CH3:9].[H+].[B-](F)(F)(F)[F:13].N([O-])=O.[Na+].C([O-])([O-])=O.[Na+].[Na+]>O>[F:13][C:3]1[C:2]([I:1])=[C:7]([O:8][CH3:9])[CH:6]=[CH:5][N: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

6

反応物 4

HCID 10340Sodium CarbonateHCID 28118Tetrafluoroboric acidHCID 23668193Sodium NitriteHCID 242292063-Iodo-4-methoxypyridin-2-amine

生成物 1

HCID 90389673HCID 90389673、化合物

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
-20 °C

実験手順

To a cold (−20° C.), stirred suspension of the 3-iodo-4-methoxypyridin-2-amine (2.5 g, 10 mmol) in HBF4 (70 mL, 470 mmol) was added an aqueous solution of NaNO2 (1.67 M, 6 mL, 10 mmol) over 20 min. The reaction turned green and then brown in color. The mixture was stirred at 0° C. for 3 h. The reaction was then carefully poured into a cold (0° C.) saturated solution of Na2CO3 (50 g) in H2O (100 mL). The layer was then extracted with EtOAc (×3). The combined organic layers were dried over anhydrous MgSO4, filtered, and concentrated under vacuum to leave a residue which was purified by column chromatography on silica gel (elution with 5:1 to 2:1 hexanes:ethyl acetate) to yield 2-fluoro-3-iodo-4-methoxypyridine as a light yellow solid.

後処理

  1. stirringThe mixture was stirred at 0° C. for 3 h
  2. extractionThe layer was then extracted with EtOAc (×3)
  3. dry with materialThe combined organic layers were dried over anhydrous MgSO4
  4. filtrationfiltered
  5. concentrationconcentrated under vacuum
  6. customto leave a residue which
  7. customwas purified by column chromatography on silica gel (elution with 5:1 to 2:1 hexanes:ethyl acetate)

出典と根拠

ORDレコード
ord-940df2b609564ca49e67ea9a7eb5af63
出典データセット
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09440952B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート