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(Diethylamino)sulfur trifluoride → HCID 67499044, 화합물

HRID 2197592
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HRID 2197592 반응식
[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
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참가 물질

4

반응물 2

HCID 123472(Diethylamino)sulfur trifluorideHCID 578033298-(1,3-Thiazol-2-yl)-1,4-dioxaspiro[4.5]decan-8-ol

생성물 1

HCID 67499044HCID 67499044, 화합물수율 82.1%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

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온도
-78 °C

실험 절차

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)+.

후처리

  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

출처 및 근거

ORD 기록
ord-698cbd008a22479fb03b874a6f534e05
출처 데이터셋
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08338603B2

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