Cesium carbonate → 2-[[2-[(1,3-dimethylpyrazol-4-yl)amino]-5-(trifluoromethyl)-4-pyridyl]amino]-N-methoxy-benzamide

HRID 1045947

반응식

HRID 1045947 반응식
CC1(C)C2C=CC=C(P(C3C=CC=CC=3)C3C=CC=CC=3)C=2OC2C1=CC=CC=2P(C1C=CC=CC=1)C1C=CC=CC=1.[NH2:43][C:44]1[CH:54]=[CH:53][CH:52]=[CH:51][C:45]=1[C:46]([NH:48][O:49][CH3:50])=[O:47].[CH3:55][N:56]1[CH:60]=[C:59]([NH:61][C:62]2[CH:67]=[C:66](I)[C:65]([C:69]([F:72])([F:71])[F:70])=[CH:64][N:63]=2)[C:58]([CH3:73])=[N:57]1.C(=O)([O-])[O-].[Cs+].[Cs+]>C([O-])(=O)C.[Pd+2].C([O-])(=O)C.C(OC)(C)(C)C.O1CCOCC1>[CH3:55][N:56]1[CH:60]=[C:59]([NH:61][C:62]2[CH:67]=[C:66]([NH:43][C:44]3[CH:54]=[CH:53][CH:52]=[CH:51][C:45]=3[C:46]([NH:48][O:49][CH3:50])=[O:47])[C:65]([C:69]([F:71])([F:70])[F:72])=[CH:64][N:63]=2)[C:58]([CH3:73])=[N:57]1

참가 물질

8

반응물 4

HCID 10796Cesium carbonateHCID 6360441,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 123927072-Amino-N-methoxybenzamideHCID 56951658N-(1,3-dimethylpyrazol-4-yl)-4-iodo-5-(trifluoromethyl)pyridin-2-amine

생성물 1

HCID 569514332-[[2-[(1,3-dimethylpyrazol-4-yl)amino]-5-(trifluoromethyl)-4-pyridyl]amino]-N-methoxy-benzamide수율 69.6%

시약·촉매·용매 3

HCID 167845palladium(II) acetate촉매HCID 15413tert-Butyl methyl ether용매HCID 312751,4-Dioxane용매

반응 조건

온도
100 °C

실험 절차

9,9-dimethyl-4,5-bis(diphenylphosphino)xanthene (0.303 g, 0.52 mmol), palladium(II) acetate (0.059 g, 0.26 mmol), 2-amino-N-methoxybenzamide (1.479 g, 8.90 mmol), N-(1,3-dimethylpyrazol-4-yl)-4-iodo-5-(trifluoromethyl)pyridin-2-amine (2 g, 5.23 mmol) and cesium carbonate (3.41 g, 10.47 mmol) were weighed out in a round bottom flask. Dioxane (60 mL) was added and argon was bubbled through the mixture for 10 minutes. The suspension was stirred at 100° C. overnight. The reaction mixture was allowed to cool to room temperature with stirring, diluted with DCM and MeOH. Silica gel was added and the mixture was concentrated. The crude product was purified by flash chromatography on silica gel (150 g) eluting with 0 to 5% MeOH in EtOAc/DCM (1:1). The solvent was evaporated to dryness, giving. 35 mL of tBuOMe was added and the resulting solution was stirred at room temperature for 3 hours. The resulting precipitate was collected by filtration, washed with tBuOMe and dried to a constant weight to afford the title compound (1.53 g, 3.64 mmol, 69.5%) as a white solid. This solid was taken up into a minimum of acetonitrile, heated to 100° C. and more acetonitrile was added until complete solubilisation was achieved. The solution was filtered and left to cool to room temperature overnight. The resulting crystals were collected by filtration and dried to constant weight under high vacuum (7.10−2 mbar) at 50° C. for 1 hour, to give the title compound (1.2 g, 2.63 mmol, 50.2%) as a crystalline white solid.

후처리

  1. customargon was bubbled through the mixture for 10 minutes
  2. temperatureto cool to room temperature
  3. stirringwith stirring
  4. additiondiluted with DCM and MeOH
  5. additionSilica gel was added
  6. concentrationthe mixture was concentrated
  7. customThe crude product was purified by flash chromatography on silica gel (150 g)
  8. washeluting with 0 to 5% MeOH in EtOAc/DCM (1:1)
  9. customThe solvent was evaporated to dryness
  10. customgiving
  11. stirringthe resulting solution was stirred at room temperature for 3 hours
  12. filtrationThe resulting precipitate was collected by filtration
  13. washwashed with tBuOMe
  14. customdried to a constant weight

출처 및 근거

ORD 기록
ord-d68a7bea55ac4316b7c67f180b850863
출처 데이터셋
uspto-grants-2013_10
특허 번호
US08569298B2

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