Triethylamine → 4-[N-[1-[N-(benzofuran-2-ylcarbonyl)amino]cyclohexanecarbonyl]amino]-1-[2-(tetrazol-1-yl)phenyl]piperidin-3-one

HRID 1392397노트

반응식

HRID 1392397 반응식
[O:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[CH:3]=[C:2]1[C:10]([NH:12][C:13]1([C:19]([NH:21][CH:22]2[CH2:27][CH2:26][N:25]([C:28]3[CH:33]=[CH:32][CH:31]=[CH:30][C:29]=3[N:34]3[CH:38]=[N:37][N:36]=[N:35]3)[CH2:24][CH:23]2[OH:39])=[O:20])[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]1)=[O:11].C(N(CC)CC)C>CS(C)=O.C(OCC)(=O)C>[O:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[CH:3]=[C:2]1[C:10]([NH:12][C:13]1([C:19]([NH:21][CH:22]2[CH2:27][CH2:26][N:25]([C:28]3[CH:33]=[CH:32][CH:31]=[CH:30][C:29]=3[N:34]3[CH:38]=[N:37][N:36]=[N:35]3)[CH2:24][C:23]2=[O:39])=[O:20])[CH2:14][CH2:15][CH2:16][CH2:17][CH2:18]1)=[O:11]

참가 물질

5

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온도
0 °C

실험 절차

To the solution of 4-[N-[1-[N-(benzofuran-2-ylcarbonyl)amino]cyclohexanecarbonyl]amino]-1-[2-(tetrazol-1-yl)phenyl]piperidin-3-ol (0.6 g) obtained in Step 1 in 10 ml of dimethylsulfoxide, was added 0.48 ml of triethylamine (3.4 mmol). The reaction mixture was cooled to 0° C. Pyridine-SO3 complex (0.54 g, 3.4 mmol) was added to the reaction mixture, which was then stirred for about 2 hours at room temperature. The reaction mixture was diluted with 50 ml of ethyl acetate and washed with brine. The resulting organic layer was dried and concentrated on sodium sulfate. The resulting residue was filtered and dried to give 0.4 g of the titled compound.

후처리

  1. additionPyridine-SO3 complex (0.54 g, 3.4 mmol) was added to the reaction mixture, which
  2. washwashed with brine
  3. customThe resulting organic layer was dried
  4. concentrationconcentrated on sodium sulfate
  5. filtrationThe resulting residue was filtered
  6. customdried

출처 및 근거

ORD 기록
ord-cfb7e0780cd1443fb3d34eedd06fa22a
출처 데이터셋
uspto-grants-2008_03
특허 번호
US07342027B2

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