Acetic Acid → (6R,9R)-6-(2,3-difluorophenyl)-3-(dimethylamino)-6,7,8,9-tetrahydro-5H-cyclohepta[b]pyridin-9-ol

HRID 1666147노트

반응식

HRID 1666147 반응식
[C:1]([BH3-])#[N:2].[Na+].N[C:6]1[CH:7]=[C:8]2[CH2:16][C@H:15]([C:17]3[CH:22]=[CH:21][CH:20]=[C:19]([F:23])[C:18]=3[F:24])[CH2:14][CH2:13][C@@H:12]([OH:25])[C:9]2=[N:10][CH:11]=1.C=O.[C:28](O)(=O)C>C(#N)C>[F:24][C:18]1[C:19]([F:23])=[CH:20][CH:21]=[CH:22][C:17]=1[C@@H:15]1[CH2:14][CH2:13][C@@H:12]([OH:25])[C:9]2=[N:10][CH:11]=[C:6]([N:2]([CH3:1])[CH3:28])[CH:7]=[C:8]2[CH2:16]1

참가 물질

6

실험 절차

SODIUM CYANOBOROHYDRIDE (242 mg, 3.86 mmol) was added to the Acetonitrile (2 mL) solution of (6R,9R)-3-amino-6-(2,3-difluorophenyl)-6,7,8,9-tetrahydro-5H-cyclohepta[b]pyridin-9-ol (56 mg, 0.193 mmol) and FORMALDEHYDE (1 mL, 13.43 mmol) at rt. The reaction was stirred at room temperature for 4 hours. ACETIC ACID (0.5 mL, 8.73 mmol) was added to the reaction mixture (Caution: heat generation was observed to cause acetonitrile reflux) and the reaction was stirred overnight. Volatile was removed mostly via vacuum and the crude was added NaOH (1N), extracted with ethyl acetate twice. The ethyl acetate layer was dried (Na2SO4), filtered and concentrated. Flash column by methanol in CH2Cl2 from 0 to 4% gave the desired product (27.6 mg, 45%). MS(ESI)[M+H+]=319.35.

후처리

  1. stirringthe reaction was stirred overnight
  2. customVolatile was removed mostly via vacuum
  3. additionthe crude was added NaOH (1N)
  4. extractionextracted with ethyl acetate twice
  5. dry with materialThe ethyl acetate layer was dried (Na2SO4)
  6. filtrationfiltered
  7. concentrationconcentrated

출처 및 근거

ORD 기록
ord-2fcf233feb8c4ac38af882f8c19a9f9d
출처 데이터셋
uspto-grants-2011_10
특허 번호
US08044043B2

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