Sodium Carbonate → 5-(3,4-dimethoxy-phenyl)-3-phenyl-1H-pyrrolo[2,3-b]pyrazine

HRID 272057노트

반응식

HRID 272057 반응식
I[N:2]1[C:6]2[N:7]=[C:8]([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=3)[CH2:9][NH:10][C:5]=2[CH:4]=[CH:3]1.[CH3:17][O:18][C:19]1[CH:20]=[C:21](B(O)O)[CH:22]=[CH:23][C:24]=1[O:25][CH3:26].C(=O)([O-])[O-].[Na+].[Na+].C(=O)(O)[O-].[Na+]>Cl[Pd-2](Cl)(P(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)P(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.ClCCl.C(#N)C>[CH3:17][O:18][C:19]1[CH:20]=[C:21]([N:2]2[C:6]3[N:7]=[C:8]([C:11]4[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=4)[CH2:9][NH:10][C:5]=3[CH:4]=[CH:3]2)[CH:22]=[CH:23][C:24]=1[O:25][CH3:26]

참가 물질

8

반응물 4

HCID 10340Sodium CarbonateHCID 516892Sodium BicarbonateHCID 27347023,4-Dimethoxyphenylboronic acidHCID 686183675-iodo-3-phenyl-1H-pyrrolo[2,3-b]pyrazine

생성물 1

HCID 686173185-(3,4-dimethoxy-phenyl)-3-phenyl-1H-pyrrolo[2,3-b]pyrazine수율 27%

시약·촉매·용매 3

HCID 178418903HCID 178418903, 화합물촉매HCID 6342Acetonitrile용매HCID 6344Dichloromethane용매

실험 절차

50 mg (0.16 mmol) of 5-iodo-3-phenyl-1H-pyrrolo[2,3-b]pyrazine, 38 mg (0.20 mmol) of 3,4-dimethoxyphenylboronic acid and 6 mg (5 mol %) of dichlorobis(triphenylphosphino)palladium(II) were placed in a vial and 1 ml of acetonitrile and 1 ml of a 2 M aqueous solution of sodium carbonate were added and the mixture irradiated in a Personal Chemistry®® microwave reactor to 165° C. for 1200 sec. The resulting mixture was distributed between 15 ml of a saturated aqueous solution of sodium bicarbonate and 75 ml of dichloromethane. The organic phase was dried over sodium sulfate and evaporated. The crude was purified via flash chromatography on silica gel using a gradient of methanol in dichloromethane. The product isolated was crystallized from hot ethanol to afford 14 mg (43 μmol, 27% yield) of 5-(3,4-dimethoxy-phenyl)-3-phenyl-1H-pyrrolo[2,3-b]pyrazine as an orange powder. 1H-NMR (d6-DMSO) δ: 12.30 [1H] s, 8.92 [1H] s, 8.43 [1H] s, 8.35 [2H] d, 7.80 [1H] (m), 7.79 [1H] d(m), 7.46 [2H] dd, 7.25 [1H] dd(d), 7.13 [1H] d, 3.92 [3H] s, 3.84 [3H] s. MS: m/z 332 [MH+].

후처리

  1. additionwere added
  2. customthe mixture irradiated in a Personal Chemistry®® microwave reactor to 165° C. for 1200 sec
  3. dry with materialThe organic phase was dried over sodium sulfate
  4. customevaporated
  5. customThe crude was purified via flash chromatography on silica gel using a gradient of methanol in dichloromethane
  6. customThe product isolated
  7. customwas crystallized from hot ethanol

출처 및 근거

ORD 기록
ord-ef9de5f0b2334d6eb2726cfa64f4f10a
출처 데이터셋
uspto-grants-2008_11
특허 번호
US07452993B2

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