Dichloromethane → Phenylmethyl 4-{5-amino-6-[(methylamino)carbonyl]pyrazin-2-yl}benzoate

HRID 646686노트

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HRID 646686 반응식
[NH2:1][C:2]1[C:3]([C:9]([NH:11][CH3:12])=[O:10])=[N:4][C:5](Br)=[CH:6][N:7]=1.[CH2:13]([O:20][C:21]([C:23]1[CH:28]=[CH:27][C:26](B(O)O)=[CH:25][CH:24]=1)=[O:22])[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1.C(N(CC)CC)C.ClCCl>CN(C=O)C>[NH2:1][C:2]1[N:7]=[CH:6][C:5]([C:26]2[CH:27]=[CH:28][C:23]([C:21]([O:20][CH2:13][C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)=[O:22])=[CH:24][CH:25]=2)=[N:4][C:3]=1[C:9]([NH:11][CH3:12])=[O:10]

참가 물질

6

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온도
85 °C

실험 절차

To a stirred mixture of 3-amino-6-bromo-N-methyl-2-pyrazinecarboxamide (0.577 g, 2.5 mmol), 4-benzyloxycarbonylphenylboronic acid (0.768 g, 3.0 mmol), triethylamine (1.01 g, 10 mmol) in 10 mL of DMF was added [1,1′-bis(diphenylphosphino)-ferrocene]dichloropalladium(II) complex with dichloromethane (1:1), (20.4 mg, 0.025 mmol). The stirred mixture was warmed to 80-90° C. for 12 h and then concentrated on a rotary evaporator under reduced pressure. The residue was dissolved in 50 mL of EtOAc, washed with brine (30 mL). The organic layer was filtered through celite, and then dried over anhydrous sodium sulfate. Filtration, concentration and column chromatography on silica EtOAc) gave a solid (450 mg, 59.7% yield). 1H NMR (400 MHz; DMSO-d6): 8.91 (s, 1H); 8.84 (br s, 1H); 8.33 (d, 2H); 8.02 (d, 2H); 7.30-7.48 (m, 5H); 5.38 (s, 2H); 2.86 (s, 3M); MS (EI) for C20H15N4O3: 363 (MH+).

후처리

  1. concentrationconcentrated on a rotary evaporator under reduced pressure
  2. dissolutionThe residue was dissolved in 50 mL of EtOAc
  3. washwashed with brine (30 mL)
  4. filtrationThe organic layer was filtered through celite
  5. dry with materialdried over anhydrous sodium sulfate
  6. filtrationFiltration, concentration and column chromatography on silica EtOAc)

출처 및 근거

ORD 기록
ord-d326b60a4af646aa98e463b402cc2bcb
출처 데이터셋
uspto-grants-2010_04
특허 번호
US07704995B2

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