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(Diethylamino)sulfur trifluoride → HCID 67499044、化合物

HRID 2197592
ノート
印刷プレビュー

反応式

HRID 2197592 の反応式
[S:1]1[CH:5]=[CH:4][N:3]=[C:2]1[C:6]1(O)[CH2:15][CH2:14][C:9]2([O:13][CH2:12][CH2:11][O:10]2)[CH2:8][CH2:7]1.C(N(S(F)(F)[F:23])CC)C>C(Cl)Cl>[F:23][C:6]1([C:2]2[S:1][CH:5]=[CH:4][N:3]=2)[CH2:15][CH2:14][C:9]2([O:13][CH2:12][CH2:11][O:10]2)[CH2:8][CH2:7]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 578033298-(1,3-Thiazol-2-yl)-1,4-dioxaspiro[4.5]decan-8-ol

生成物 1

HCID 67499044HCID 67499044、化合物収率 82.1%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
-78 °C

実験手順

To a −78° C. solution of the product of Example 27A (4.53 g, 17.77 mmol) in methylene chloride (50 mL) was added diethylaminosulfur trifluoride (DAST) (4.18 g, 3.97 mL, 30.0 mmol). The reaction mixture was stirred at −78° C. for four hours, then allowed to warm to ambient temperature, and stirred overnight. The reaction mixture was then cooled to 0° C., quenched with saturated aqueous sodium bicarbonate, and extracted with methylene chloride. The organic layer was separated and concentrated. The resulting residue was chromatographed on silica gel, eluting with 0%-15% ethyl acetate-hexane to obtain the title compound (3.55 g, 78%). 1H NMR (300 MHz, DMSO-d6) δ ppm 7.83 (m, 1H), 7.79 (m, 1H), 3.92 (s, 4H), 2.41-2.07 (m, 4H), 1.91-1.63 (m, 4H). MS (DCI) m/z 244 (M+H)+.

後処理

  1. temperatureto warm to ambient temperature
  2. stirringstirred overnight
  3. temperatureThe reaction mixture was then cooled to 0° C.
  4. customquenched with saturated aqueous sodium bicarbonate
  5. extractionextracted with methylene chloride
  6. customThe organic layer was separated
  7. concentrationconcentrated
  8. customThe resulting residue was chromatographed on silica gel
  9. washeluting with 0%-15% ethyl acetate-hexane

出典と根拠

ORDレコード
ord-698cbd008a22479fb03b874a6f534e05
出典データセット
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08338603B2

反応ノート

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