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(Diethylamino)sulfur trifluoride → (rac)-7-fluoro-2-phenoxymethyl-6,7-dihydro-5H-pyrazolo[1,5-a]pyrazin-4-one

HRID 2046186
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HRID 2046186 반응식
CCN(S(F)(F)[F:7])CC.O[CH:11]1[N:16]2[N:17]=[C:18]([CH2:20][O:21][C:22]3[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=3)[CH:19]=[C:15]2[C:14](=[O:28])[NH:13][CH2:12]1>C(Cl)Cl>[F:7][CH:11]1[N:16]2[N:17]=[C:18]([CH2:20][O:21][C:22]3[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=3)[CH:19]=[C:15]2[C:14](=[O:28])[NH:13][CH2:12]1
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참가 물질

4

반응물 2

HCID 123472(Diethylamino)sulfur trifluorideHCID 67973603(rac)-7-hydroxy-2-phenoxymethyl-6,7-dihydro-5H-pyrazolo[1,5-a]pyrazin-4-one

생성물 1

HCID 67973614(rac)-7-fluoro-2-phenoxymethyl-6,7-dihydro-5H-pyrazolo[1,5-a]pyrazin-4-one수율 102.7%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

DAST (0.035 mL, 0.29 mmol) was added to a solution of (rac)-7-hydroxy-2-phenoxymethyl-6,7-dihydro-5H-pyrazolo[1,5-a]pyrazin-4-one (50 mg, 0.19 mmol) in DCM (0.5 mL) at −10° C. The mixture was stirred at room temperature for 15 minutes. Then quenched with a 1N solution of HCl and extracted with DCM. The organic layer was separated, dried (Na2SO4), filtered and the solvent evaporated in vacuo to yield (rac)-7-fluoro-2-phenoxymethyl-6,7-dihydro-5H-pyrazolo[1,5-a]pyrazin-4-one (51 mg, quantitative) as light brown solid that was used without further purification.

후처리

  1. customThen quenched with a 1N solution of HCl
  2. extractionextracted with DCM
  3. customThe organic layer was separated
  4. dry with materialdried (Na2SO4)
  5. filtrationfiltered
  6. customthe solvent evaporated in vacuo

출처 및 근거

ORD 기록
ord-9b5bb7b95acb4274abb85477336f243d
출처 데이터셋
uspto-grants-2013_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08592422B2

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