6-benzyloxy-3-amino-1,2,3,4-tetrahydro-9H-carbazole → 3-Amino-2,3,4,9-tetrahydro-1H-carbazol-6-ol

HRID 726384노트

반응식

HRID 726384 반응식
C([O:8][C:9]1[CH:10]=[C:11]2[C:19](=[CH:20][CH:21]=1)[NH:18][C:17]1[CH2:16][CH2:15][CH:14]([NH2:22])[CH2:13][C:12]2=1)C1C=CC=CC=1.[H][H]>C(O)C.[Ni]>[OH:8][C:9]1[CH:10]=[C:11]2[C:19](=[CH:20][CH:21]=1)[NH:18][C:17]1[CH2:16][CH2:15][CH:14]([NH2:22])[CH2:13][C:12]2=1

참가 물질

5

반응물 2

HCID 226113086-benzyloxy-3-amino-1,2,3,4-tetrahydro-9H-carbazoleHCID 178418361HCID 178418361, 화합물2회

생성물 1

HCID 153417413-Amino-2,3,4,9-tetrahydro-1H-carbazol-6-ol수율 56%

시약·촉매·용매 2

HCID 935Nickel촉매HCID 702Ethanol용매

실험 절차

To a solution of 0.871 gm (2.98 mMol) 6-benzyloxy-3-amino-1,2,3,4-tetrahydro-9H-carbazole in 200 mL ethanol were added about 2.0 gm Raney Nickel and hydrogen introduced to the reaction mixture under balloon pressure. After stirring for 18 hours at room temperature the balloon was refilled with hydrogen and the reaction stirred an additional 3 days at room temperature. The reaction mixture was filtered and the filtrate concentrated under reduced pressure to give a colorless solid. The residual solid was subjected to silica gel chromatography, eluting with 80:15:5 dichloromethane:menthanol:ammonium hydroxide. Fractions shown to contain product were combined and concentrated under reduced pressure to give 0.335 gm (56%) of the title compound.

후처리

  1. additionintroduced to the reaction mixture under balloon pressure
  2. stirringthe reaction stirred an additional 3 days at room temperature
  3. filtrationThe reaction mixture was filtered
  4. concentrationthe filtrate concentrated under reduced pressure
  5. customto give a colorless solid
  6. washeluting with 80:15:5 dichloromethane
  7. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-afebfb39ca394ce3a8ba64b4edca82a9
출처 데이터셋
uspto-grants-1998_01
특허 번호
US05708187

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