Thiomorpholine → 1-(4-Thiomorpholin-4-yl-phenyl)-3-aza-bicyclo[3.1.0]hexane-3-carboxylic acid tert-butyl ester

HRID 1400049노트

반응식

HRID 1400049 반응식
[C:1]([O:5][C:6]([N:8]1[CH2:13][CH:12]2[C:10]([C:14]3[CH:19]=[CH:18][C:17](Br)=[CH:16][CH:15]=3)([CH2:11]2)[CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].CC(C)([O-])C.[Na+].[NH:27]1[CH2:32][CH2:31][S:30][CH2:29][CH2:28]1>C1(C)C=CC=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.[Pd].[Pd].C1C=CC(P(C2C(C3C(P(C4C=CC=CC=4)C4C=CC=CC=4)=CC=C4C=3C=CC=C4)=C3C(C=CC=C3)=CC=2)C2C=CC=CC=2)=CC=1>[C:1]([O:5][C:6]([N:8]1[CH2:13][CH:12]2[C:10]([C:14]3[CH:19]=[CH:18][C:17]([N:27]4[CH2:32][CH2:31][S:30][CH2:29][CH2:28]4)=[CH:16][CH:15]=3)([CH2:11]2)[CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2]

참가 물질

7

실험 절차

To a solution of 1-(4-bromo-phenyl)-3-aza-bicyclo[3.1.0]hexane-3-carboxylic acid tert-butyl ester (Intermediate I, 200 mg, 0.59 mmol) in anhydrous toluene (2 mL) were added Pd2(dba)3 (1.3 mg, 0.002 mmol), BINAP (2.8 mg, 0.004 mmol), sodium tert-butoxide (85 mg, 0.89 mmol) and thiomorpholine (0.07 mL, 0.65 mmol) at r.t. and reaction mixture was refluxed for 17 h. Reaction mixture was then concentrated and the crude product was purified by column chromatography (silica gel, 2:8 EtOAc:Pet. ether) to afford the title compound as viscous liquid (66 mg, 31%).

후처리

  1. customreaction mixture
  2. temperaturewas refluxed for 17 h
  3. customReaction mixture
  4. concentrationwas then concentrated
  5. customthe crude product was purified by column chromatography (silica gel, 2:8 EtOAc:Pet. ether)

출처 및 근거

ORD 기록
ord-979725f89ae649c893a00e8b3194cfee
출처 데이터셋
uspto-grants-2014_12
특허 번호
US08906913B2

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