Pyridine → 6-Benzyloxy-3-dimethlamino-1,2,3,4-tetrahydrocarbazole

HRID 365252노트

반응식

HRID 365252 반응식
[CH3:1][N:2]([CH3:10])[CH:3]1[CH2:8][CH2:7][C:6](=O)[CH2:5][CH2:4]1.Cl.[CH2:12]([O:19][C:20]1[CH:25]=[CH:24][C:23]([NH:26]N)=[CH:22][CH:21]=1)[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.N1C=CC=CC=1>C(O)C.O>[CH2:12]([O:19][C:20]1[CH:25]=[C:24]2[C:23](=[CH:22][CH:21]=1)[NH:26][C:6]1[CH2:7][CH2:8][CH:3]([N:2]([CH3:10])[CH3:1])[CH2:4][C:5]2=1)[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1

참가 물질

6

반응물 3

HCID 1049PyridineHCID 3016725(4-(Benzyloxy)phenyl)hydrazine monohydrochlorideHCID 103745454-(Dimethylamino)cyclohexan-1-one

생성물 1

HCID 128917786-Benzyloxy-3-dimethlamino-1,2,3,4-tetrahydrocarbazole수율 24.9%

시약·촉매·용매 2

HCID 702Ethanol용매HCID 962Water용매2회

실험 절차

To a solution of 3.78 gm (26.8 mMol) 4-dimethylamino-1-cyclohexanone and 6.69 gm (26.8 mMol) 4-benzyloxyphenylhydrazine hydrochloride in 50 mL ethanol were added 2.17 mL (26.8 mMol) pyridine. To this solution were added 5×10 mL portions of water and the reaction mixture then stored at 0° C. for 18 hours. The reaction mixture was then diluted with an additional 50 mL of water and the mixture extracted well with dichloromethane. The combined organic extracts were dried over sodium sulfate and the volatiles removed under reduced pressure. The residual oil was subjected to flash silica gel chromatography, eluting with 9:1 chloroform:methanol. Fractions shown to contain the desired product were combined and concentrated under reduced pressure to give 2.14 gm (24.9%) of the title compound.

후처리

  1. extractionthe mixture extracted well with dichloromethane
  2. dry with materialThe combined organic extracts were dried over sodium sulfate
  3. customthe volatiles removed under reduced pressure
  4. washeluting with 9:1 chloroform
  5. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-950aa7b0e5f34a3cbc6373c32c31c471
출처 데이터셋
uspto-grants-2000_10
특허 번호
US06126932

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