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(Diethylamino)sulfur trifluoride → HCID 90203658, 화합물

HRID 1480204
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HRID 1480204 반응식
[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
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참가 물질

4

반응물 2

HCID 123472(Diethylamino)sulfur trifluorideHCID 90204051HCID 90204051, 화합물

생성물 1

HCID 90203658HCID 90203658, 화합물수율 90%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

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온도
-75 °C

실험 절차

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+).

후처리

  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

출처 및 근거

ORD 기록
ord-2f9f600c43674b1a9a2aff50cc8f3e9e
출처 데이터셋
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09409866B2

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