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Ammonium formate → (Octahydropyrrolo[1,2-a]pyrazin-8a-yl)methanol

HRID 421209
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HRID 421209 반응식
C1(C[N:8]2[CH2:13][CH2:12][N:11]3[CH2:14][CH2:15][CH2:16][C:10]3([CH2:17][OH:18])[CH2:9]2)C=CC=CC=1.C([O-])=O.[NH4+]>CO.[Pd]>[CH2:9]1[NH:8][CH2:13][CH2:12][N:11]2[CH2:14][CH2:15][CH2:16][C:10]12[CH2:17][OH:18]
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참가 물질

5

반응물 2

HCID 2723923Ammonium formateHCID 59215761[2-(phenylmethyl)hexahydropyrrolo[1,2-a]pyrazin-8a(6H)-yl]methanol

생성물 1

HCID 45122045(Octahydropyrrolo[1,2-a]pyrazin-8a-yl)methanol수율 105.1%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

To a solution of [2-(phenylmethyl)hexahydropyrrolo[1,2-a]pyrazin-8a(6H)-yl]methanol (D66, 180 mg) in anhydrous methanol (5 mL) under a Nitrogen atmosphere at rt, ammonium formate (475 mg) and palladium (10% on carbon, 13 mg) were added. The resulting suspension was heated at reflux temperature for 3.5 hours, then allowed to cool to r.t. and filtered over Celite. The organic extract was dried and concentrated in vacuo to give the desired compound (120 mg) as orange waxy solid.

후처리

  1. temperatureThe resulting suspension was heated
  2. temperatureat reflux temperature for 3.5 hours
  3. filtrationfiltered over Celite
  4. extractionThe organic extract
  5. customwas dried
  6. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-e79ee58d489b4fad9709b3b7fcd306ce
출처 데이터셋
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08097618B2

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