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Tetrahydrofuran → 7,7-Difluorooctahydropyrrolo[1,2-a]pyrazine

HRID 1013748
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HRID 1013748 반응식
[F:1][C:2]1([F:13])[CH2:12][N:5]2[C:6](=O)[CH2:7][NH:8][C:9](=O)[C@@H:4]2[CH2:3]1.C1COCC1.[H-].[Al+3].[Li+].[H-].[H-].[H-].[OH-].[Na+]>O>[F:13][C:2]1([F:1])[CH2:12][N:5]2[CH2:6][CH2:7][NH:8][CH2:9][CH:4]2[CH2:3]1
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참가 물질

6

반응물 4

HCID 8028TetrahydrofuranHCID 14798Sodium HydroxideHCID 21226445Aluminium lithium hydrideHCID 67316882(S)-7,7-difluoro-hexahydropyrrolo[1,2-a]pyrazine-1,4-dione

생성물 1

HCID 592158907,7-Difluorooctahydropyrrolo[1,2-a]pyrazine

시약·촉매·용매 1

HCID 962Water용매

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온도
0 °C

실험 절차

A pressure bottle was charged with (S)-7,7-difluoro-hexahydropyrrolo[1,2-a]pyrazine-1,4-dione (350 mg, 1841 μmol) and THF under nitrogen, and the solution was cooled to 0° C. under nitrogen. Lithium aluminum hydride (3681 μl, 3681 μmol) was added, the mixture was allowed to warm to RT, followed by heating at reflux for 3 h. 2 mL of water was carefully added, followed by 2 mL of 6N NaOH. After stirring for 10 min, the mixture was filtered through Celite and washed with EtOAc. The filtrate was concentrated. GC/MS: [M+H]=163.

후처리

  1. temperatureto warm to RT
  2. temperatureby heating
  3. temperatureat reflux for 3 h
  4. filtrationthe mixture was filtered through Celite
  5. washwashed with EtOAc
  6. concentrationThe filtrate was concentrated

출처 및 근거

ORD 기록
ord-3fb2f9710315455eb5e83854e0570d07
출처 데이터셋
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07981891B2

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