Triethylamine → HCID 23533346, 화합물

HRID 1795345노트

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HRID 1795345 반응식
CN1CCN(C2C=C[C:11]3[C:12](C=2)=[CH:13][CH:14]=[C:15]2[C:20]=3[O:19][C:18]([C:21]([NH:23][C:24]3[CH:29]=[CH:28][C:27]([N:30]4[CH2:35][CH2:34][O:33][CH2:32][CH2:31]4)=[CH:26][CH:25]=3)=[O:22])=[CH:17][C:16]2=[O:36])CC1.C1C=CC2N(O)N=NC=2C=1.CN([C:51]([O:55]N1N=NC2C=CC=CC1=2)=[N+](C)C)C.[B-](F)(F)(F)F.[CH2:70]([N:72]([CH2:75]C)[CH2:73][CH3:74])[CH3:71].COC1C=C([N:85]2CCOCC2)C=CC=1N>CN(C)C1C=CN=CC=1.CN(C)C=O.C(OCC)(=O)C>[CH3:51][O:55][C:29]1[CH:28]=[C:27]([N:30]2[CH2:31][CH2:32][O:33][CH2:34][CH2:35]2)[CH:26]=[CH:25][C:24]=1[NH:23][C:21]([C:18]1[O:19][C:20]2[C:15]([C:16](=[O:36])[CH:17]=1)=[CH:14][CH:13]=[CH:12][C:11]=2[N:85]1[CH2:74][CH2:73][N:72]([CH3:75])[CH2:70][CH2:71]1)=[O:22]

참가 물질

9

실험 절차

8-(4-Methyl-piperazin-1-yl)-4-oxo-4H-chromene-2-carboxylic acid hydrochloride (Reference Example 1) (0.10 g, 0.35mmol), HOBt (0.10 g, 0.7 mmol), TBTU (0.225 g, 0.7 mmol), 4-(dimethylamino) pyridine (0.01 g, catalytic amount), triethylamine (0.15 mL, 1.04 mmol), and commercially available 2-methoxy-4-morpholin-4-yl-phenylamine (SALOR) (0.08 g, 0.38 mmol) were dissolved in dimethylformamide (2.5 mL) and stirred at room temperature overnight. Ethyl acetate (150 mL) was added and the resulting mixture was washed with water (3×50 mL), dried (Na2SO4), filtered, concentrated under vacuum and triturated with ether to yield a yellow solid (85 mg, 54%). LCMS: m/z=480.3

후처리

  1. washthe resulting mixture was washed with water (3×50 mL)
  2. dry with materialdried (Na2SO4)
  3. filtrationfiltered
  4. concentrationconcentrated under vacuum
  5. customtriturated with ether

출처 및 근거

ORD 기록
ord-6f88d9d14fba437bb0cebe63ad367868
출처 데이터셋
uspto-grants-2006_04
특허 번호
US07026314B2

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