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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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(Diethylamino)sulfur trifluoride → 1-Piperidineacetonitrile, 4-fluoro-

HRID 1359849
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HRID 1359849 반응식
CCN(S(F)(F)[F:7])CC.O[CH:11]1[CH2:16][CH2:15][N:14]([CH2:17][C:18]#[N:19])[CH2:13][CH2:12]1>C(Cl)Cl>[F:7][CH:11]1[CH2:16][CH2:15][N:14]([CH2:17][C:18]#[N:19])[CH2:13][CH2:12]1
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참가 물질

4

반응물 2

HCID 123472(Diethylamino)sulfur trifluorideHCID 111054492-(4-Hydroxypiperidin-1-YL)acetonitrile

생성물 1

HCID 181800121-Piperidineacetonitrile, 4-fluoro-수율 71%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

DAST (4.36 mL, 33 mmol) was added to a solution of (4-hydroxy-piperidin-1-yl)-acetonitrile (4.25 g, 30 mmol) in DCM (80 mL) at −30° C., the mixture was then stirred at rt for overnight. The reaction was cooled to −30° C. and quenched with methanol (10 mL) for 30 mins. The organic layer was then washed with NaHCO3 and dried. The residue was purified on a silica gel column to give 3 g (71%) of (4-fluoro-piperidin-1-yl)-acetonitrile.

후처리

  1. temperatureThe reaction was cooled to −30° C.
  2. customquenched with methanol (10 mL) for 30 mins
  3. washThe organic layer was then washed with NaHCO3
  4. customdried
  5. customThe residue was purified on a silica gel column

출처 및 근거

ORD 기록
ord-40242723da6d462587b2a23680811fda
출처 데이터셋
uspto-grants-2003_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06599902B2

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