N-methyl-N-(trimethylsilyl)trifluoroacetamide → 2-[[[1-(2-Amino-4-thiazolyl)-2-[[1-[[[[3-[[(1,4-dihydro-6,7-dihydroxy-4-oxo-3-quinolinyl)carbonyl]amino]-2-oxo-1-imidazolidinyl]sulfonyl]amino]carbonyl]-2-oxo-3-azetidinyl]amino]-2-oxoethylidene]amino]oxy]-2-methylpropanoic acid, diphenylmethyl ester

HRID 868149노트

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HRID 868149 반응식
[OH:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][C:11]=1[OH:12])[NH:8][CH:7]=[C:6]([C:13]([NH:15][N:16]1[CH2:20][CH2:19][N:18]([S:21]([NH:24][C:25]([N:27]3[CH2:30][CH:29]([NH:31][C:32](=[O:41])OCC4C=CC=CC=4)[C:28]3=[O:42])=[O:26])(=[O:23])=[O:22])[C:17]1=[O:43])=[O:14])[CH2:5]2.CN([Si](C)(C)C)C(=[O:51])C(F)(F)F.[NH2:56][C:57]1[S:58][CH:59]=[C:60](/[C:62](=[N:66]/[O:67][C:68]([CH3:86])([CH3:85])[C:69]([O:71][CH:72]([C:79]2[CH:84]=[CH:83][CH:82]=[CH:81][CH:80]=2)[C:73]2[CH:78]=[CH:77][CH:76]=[CH:75][CH:74]=2)=[O:70])/C(O)=O)[N:61]=1>CN(C)C=O.[Pd]>[NH2:56][C:57]1[S:58][CH:59]=[C:60]([C:62](=[N:66][O:67][C:68]([CH3:86])([CH3:85])[C:69]([O:71][CH:72]([C:79]2[CH:84]=[CH:83][CH:82]=[CH:81][CH:80]=2)[C:73]2[CH:74]=[CH:75][CH:76]=[CH:77][CH:78]=2)=[O:70])[C:32]([NH:31][CH:29]2[CH2:30][N:27]([C:25]([NH:24][S:21]([N:18]3[CH2:19][CH2:20][N:16]([NH:15][C:13]([C:6]4[C:5](=[O:51])[C:4]5[C:9](=[CH:10][C:11]([OH:12])=[C:2]([OH:1])[CH:3]=5)[NH:8][CH:7]=4)=[O:14])[C:17]3=[O:43])(=[O:23])=[O:22])=[O:26])[C:28]2=[O:42])=[O:41])[N:61]=1

참가 물질

6

실험 절차

To a solution of [1-[[[[3-[[(1,4-dihydro-6,7-dihydroxy-3-quinolinyl)carbonyl]amino]-2-oxo-1-imidazolidinyl]sulfonyl]amino]carbonyl]-2-oxo-3-azetidinyl]carbamic acid, phenylmethyl ester (3.35 g, 5.3 mmol) in 60 ml of N,N-dimethylformamide, N-methyl-N-trimethylsilyl trifluoroacetamide (5.28 g, 26.5 mmol) was added. After 30 minutes, 1.68 g of palladium on carbon was added, and the mixture was hydrogenolyzed for 1 hour. The catalyst was removed by filtration and the filtrate added to a solution of (Z)-2-amino-α-[[2-(diphenylmethoxy)-1,1-dimethyl-2-oxoethoxy]imino]-4-thiazoleacetic acid, 1-benzotriazole ester (2.96 g, 5.3 mmol) in 30 ml of N,N-dimethylformamide. After stirring for 20 hours, the solvent was distilled off and the residue triturated with 60 ml of water and 75 ml of ethyl acetate. The resulting crystals were filtered off, washed with water and dried in vacuo to give 3.27 g of the title compound.

후처리

  1. waitthe mixture was hydrogenolyzed for 1 hour
  2. customThe catalyst was removed by filtration
  3. distillationthe solvent was distilled off
  4. customthe residue triturated with 60 ml of water and 75 ml of ethyl acetate
  5. filtrationThe resulting crystals were filtered off
  6. washwashed with water
  7. customdried in vacuo

출처 및 근거

ORD 기록
ord-a63c0aea668a424c99324d7eb3442978
출처 데이터셋
uspto-grants-1988_10
특허 번호
US04777252

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