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Sodium Carbonate → N6-(4-{[2-(trifluoromethyl)pyridin-4-yl]oxy}phenyl)-4,5'-bipyrimidine-2,6-diamine

HRID 729984
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HRID 729984 반응식
C[C:2]1C=CC=[C:4](C)[C:3]=1[C:9]1[N:14]=[C:13]([NH2:15])[N:12]=[C:11]([NH:16][C:17]2[CH:22]=[CH:21][C:20]([O:23][C:24]3[CH:29]=[CH:28][N:27]=[C:26]([C:30]([F:33])([F:32])[F:31])[CH:25]=3)=[CH:19][CH:18]=2)[CH:10]=1.[N:34]1C=C(B(O)O)C=[N:36][CH:35]=1.C(=O)([O-])[O-].[Na+].[Na+]>CN(C=O)C>[F:32][C:30]([F:33])([F:31])[C:26]1[CH:25]=[C:24]([O:23][C:20]2[CH:19]=[CH:18][C:17]([NH:16][C:11]3[N:12]=[C:13]([NH2:15])[N:14]=[C:9]([C:3]4[CH:4]=[N:34][CH:35]=[N:36][CH:2]=4)[CH:10]=3)=[CH:22][CH:21]=2)[CH:29]=[CH:28][N:27]=1
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참가 물질

5

반응물 3

HCID 10340Sodium CarbonateHCID 2795193(Pyrimidin-5-yl)boronic acidHCID 118449986-(2,6-dimethylphenyl)-N4-(4-{[2-(trifluoromethyl) pyridin-4-yl]oxy}phenyl)pyrimidine-2,4-diamine

생성물 1

HCID 11845000N6-(4-{[2-(trifluoromethyl)pyridin-4-yl]oxy}phenyl)-4,5'-bipyrimidine-2,6-diamine수율 23%

시약·촉매·용매 1

HCID 6228
Dimethylformamide
용매

실험 절차

A suspension of 6-chloro-N4-(4-{[2-(trifluoromethyl)pyridin-4-yl]oxy}phenyl)pyrimidine-2,4-diamine (150 mg, 0.39 mmol, see example 335), pyrimidin-5-ylboronic acid (97.37 mg, 0.79 mmol), tetrakis(triphenylphosphin)palladium(0) (45.41 mg, 0.04 mmol), sodium carbonate (208.23 mg, 1.96 mmol) in 2.5 mil of anhydrous DMF was degassed for 10 min. The mixture was reacted under microwave condition at 180° C. for 20 min. The reaction mixture was filtered and concentrated. The residue was extracted with EtOAc (6 ml) and washed with 1 M NaOH solution (1 mL×2) and water (1 mL×3). The organic layer was dried to furnish 129 mg of the crude product. The crude product was purified by prep-TLC (Hex:EtOAc=2:8) to give 38 mg (23%) of the title compound as a yellow solid. 1H NMR (CD3OD): δ 9.28 (s, 2H), 9.20 (s, 1H), 8.54 (d, 1H), 7.88 (d, 2H), 7.32 (d, 1H), 7.15 (m, 3H), 6.56 (s, 1H) ppm; MS ES 426 (M+H)+, calc. 426, RT=2.35 min; TLC (Hexane:EtOAc=1:9) Rf=0.25.

후처리

  1. customwas degassed for 10 min
  2. customThe mixture was reacted under microwave condition at 180° C. for 20 min
  3. filtrationThe reaction mixture was filtered
  4. concentrationconcentrated
  5. extractionThe residue was extracted with EtOAc (6 ml)
  6. washwashed with 1 M NaOH solution (1 mL×2) and water (1 mL×3)
  7. customThe organic layer was dried
  8. customto furnish 129 mg of the crude product
  9. customThe crude product was purified by prep-TLC (Hex:EtOAc=2:8)

출처 및 근거

ORD 기록
ord-e612fd65131542c58fc53f7ae8c9b6c5
출처 데이터셋
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07582646B2

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