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(Diethylamino)sulfur trifluoride → HCID 90203658、化合物

HRID 1480204
ノート
印刷プレビュー

反応式

HRID 1480204 の反応式
[Cl:1][C:2]1[C:7]([C:8]2(O)[CH2:11][O:10][CH2:9]2)=[CH:6][N:5]=[C:4]([C:13]#[N:14])[CH:3]=1.CCN(S(F)(F)[F:21])CC>ClCCl>[Cl:1][C:2]1[C:7]([C:8]2([F:21])[CH2:11][O:10][CH2:9]2)=[CH:6][N:5]=[C:4]([C:13]#[N:14])[CH:3]=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

4

反応物 2

HCID 123472(Diethylamino)sulfur trifluorideHCID 90204051HCID 90204051、化合物

生成物 1

HCID 90203658HCID 90203658、化合物収率 90%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
-75 °C

実験手順

To a solution of 4-chloro-5-(3-hydroxyoxetan-3-yl)pyridine-2-carbonitrile (example 123b, 2.0 g, 9.5 mmol) in dry dichloromethane (50 ml) under an argon atmosphere cooled down to −75° C. was added DAST (1.61 g, 1.32 ml, 9.97 mmol). The reaction was stirred at −75° C. for 15 min, then let to warm up to 0° C. and stirred at 0° C. for 1 hour. The reaction was then quenched by addition of a 2M aqueous solution of sodium carbonate. The bi-phasic mixture was stirred at room temperature for 15 minutes, poured into a separatory funnel and extraction was carried out. The organic phase was dried over sodium sulfate and evaporated down to dryness. The crude material was purified by flash chromatography on silica eluting with a heptane/ethyl acetate gradient to yield the title compound (1.81 g, 90%). MS (ESI, m/z): 213.0 (M+H+).

後処理

  1. temperatureto warm up to 0° C.
  2. stirringstirred at 0° C. for 1 hour
  3. customThe reaction was then quenched by addition of a 2M aqueous solution of sodium carbonate
  4. stirringThe bi-phasic mixture was stirred at room temperature for 15 minutes
  5. additionpoured into a separatory funnel
  6. extractionextraction
  7. dry with materialThe organic phase was dried over sodium sulfate
  8. customevaporated down to dryness
  9. customThe crude material was purified by flash chromatography on silica eluting with a heptane/ethyl acetate gradient

出典と根拠

ORDレコード
ord-2f9f600c43674b1a9a2aff50cc8f3e9e
出典データセット
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09409866B2

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