Diazald → HCID 178486597, 화합물

HRID 2388590노트

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HRID 2388590 반응식
[OH-].[K+].[CH3:3]C1C=CC(S(N(N=O)C)(=O)=O)=CC=1.C(O)CO.CCOCC.[NH:26]1[C:30]2[CH:31]=[C:32]([N:35]3[CH:39]([C:40]4[CH:45]=[C:44]([F:46])[CH:43]=[C:42]([F:47])[C:41]=4[F:48])[C:38]([C:49]4[CH:54]=[CH:53][CH:52]=[CH:51][CH:50]=4)=[C:37]([OH:55])[C:36]3=[O:56])[CH:33]=[CH:34][C:29]=2[N:28]=[CH:27]1>CO.O>[NH:28]1[C:29]2[CH:34]=[CH:33][C:32]([N:35]3[CH:39]([C:40]4[CH:45]=[C:44]([F:46])[CH:43]=[C:42]([F:47])[C:41]=4[F:48])[C:38]([C:49]4[CH:54]=[CH:53][CH:52]=[CH:51][CH:50]=4)=[C:37]([O:55][CH3:3])[C:36]3=[O:56])=[CH:31][C:30]=2[N:26]=[CH:27]1

참가 물질

6

실험 절차

The compound was synthesized starting from KOH (10 eq in water), diazald (5 eq), ethylene glycol/Et2O (3/1 v/v), 1-(1H-benzo[d]imidazol-6-yl)-5-(2,3,5-trifluorophenyl)-3-hydroxy-4-phenyl-1H-pyrrol-2(5H)-one (0.230 g, 0.5 mmol, 1 eq) and MeOH/H2O (90/10 v/v); yield: 0.015 g (6.9%); MS m/z: 436.4 [M+H]+; 1H-NMR: (400 MHz, DMSO-D6) δ: 4.11 (s, 1H), 6.94 (s, 1H), 7.22-7.42 (m, 6H), 7.58-7.68 (m, 3H), 7.73-7.76 (m, 1H), 7.95 (s, 1H), 9.07 (s, 1H); HPLC (METHOD [A]): rt 15.38 min (82%)

후처리

  1. customThe compound was synthesized
  2. customrt 15.38 min (82%)

출처 및 근거

ORD 기록
ord-ae67d9e2827440df932a01b80c109987
출처 데이터셋
uspto-grants-2012_09
특허 번호
US08269019B2

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