Diisopropylethylamine → HCID 59451478, 화합물

HRID 1874949노트

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HRID 1874949 반응식
CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.[NH2:25][CH2:26][C:27]1[C:28]([F:44])=[C:29]([O:34][C:35]2[CH:36]=[C:37]([CH:40]=[C:41]([Cl:43])[CH:42]=2)[C:38]#[N:39])[C:30]([Cl:33])=[CH:31][CH:32]=1.[OH:45][CH2:46][CH2:47][O:48][C:49]1[CH:50]=[C:51]2[C:55](=[CH:56][CH:57]=1)[NH:54][C:53]([C:58](O)=[O:59])=[CH:52]2.CCN(C(C)C)C(C)C>O.CCOC(C)=O.CN(C=O)C>[Cl:33][C:30]1[CH:31]=[CH:32][C:27]([CH2:26][NH:25][C:58]([C:53]2[NH:54][C:55]3[C:51]([CH:52]=2)=[CH:50][C:49]([O:48][CH2:47][CH2:46][OH:45])=[CH:57][CH:56]=3)=[O:59])=[C:28]([F:44])[C:29]=1[O:34][C:35]1[CH:36]=[C:37]([C:38]#[N:39])[CH:40]=[C:41]([Cl:43])[CH:42]=1

참가 물질

8

실험 절차

HATU (0.026 g, 0.069 mmol) was added to a DMF (1 mL) solution of 3-{[3-(aminomethyl)-6-chloro-2-fluorophenyl]oxy}-5-chlorobenzonitrile (0.022 g, 0.069 mmol), 5-[(2-hydroxyethyl)oxy]-1H-indole-2-carboxylic acid (0.015 g, 0.069 mmol) and DIPEA (0.012 mL, 0.069 mmol). The reaction mixture was stirred for 2 h, poured into EtOAc and water and the layers separated. The organic layer was dried over MgSO4, filtered and the solvent evaporated. The residue was dissolved in MeOH and purification was accomplished by reverse-phase HPLC (water/acetonitrile with 0.1% TFA) to afford the title compound (0.013 g, 37%) as a white solid 1H NMR (400 MHz, DMSO-d6) δ ppm 11.44 (s, 1H), 8.96 (t, 1H), 7.80 (s, 1H), 7.44-7.54 (m, 3H), 7.37 (t, 1H), 7.28 (d, 1H), 7.05 (s, 2H), 6.83 (dd, 1H), 4.80 (t, 1H), 4.54 (d, 2H), 3.94 (t, 2H), 3.70 (q, 2H).

후처리

  1. customthe layers separated
  2. dry with materialThe organic layer was dried over MgSO4
  3. filtrationfiltered
  4. customthe solvent evaporated
  5. dissolutionThe residue was dissolved in MeOH
  6. custompurification

출처 및 근거

ORD 기록
ord-b24e5587e8ec4973b8de72a5a8666e24
출처 데이터셋
uspto-grants-2012_11
특허 번호
US08304419B2

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