Potassium Carbonate → HCID 59643068, 화합물

HRID 2251087노트

반응식

HRID 2251087 반응식
[CH3:1][N:2]1[C:6]([NH:7][C:8]2[C:13]([CH:14]=O)=[CH:12][N:11]=[C:10]([S:16][CH3:17])[N:9]=2)=[CH:5][C:4]([CH3:18])=[N:3]1.Br[CH2:20][C:21]([C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][C:24]=1[Cl:29])=[O:22].C(=O)([O-])[O-].[K+].[K+].N12CCCN=C1CCCCC2>CN(C=O)C.CCOC(C)=O.[NH4+].[Cl-]>[Cl:29][C:24]1[CH:25]=[CH:26][CH:27]=[CH:28][C:23]=1[C:21]([C:20]1[N:7]([C:6]2[N:2]([CH3:1])[N:3]=[C:4]([CH3:18])[CH:5]=2)[C:8]2[N:9]=[C:10]([S:16][CH3:17])[N:11]=[CH:12][C:13]=2[CH:14]=1)=[O:22]

참가 물질

8

반응물 4

HCID 11430Potassium CarbonateHCID 811841,8-Diazabicyclo(5.4.0)undec-7-eneHCID 27357852-Bromo-2'-chloroacetophenoneHCID 59643093HCID 59643093, 화합물

생성물 1

HCID 59643068HCID 59643068, 화합물

시약·촉매·용매 3

HCID 6228Dimethylformamide용매HCID 8857Ethyl Acetate용매HCID 25517Ammonium Chloride용매

실험 절차

To a solution of 4-(2,5-dimethyl-2H-pyrazol-3-ylamino)-2-methylsulfanyl-pyrimidine-5-carbaldehyde, 18, (0.25 g, 0.95 mmol) in DMF (4 mL) is added 2-bromo-1-(2-chloro-phenyl)-ethanone (0.33 g, 1.42 mmol) and potassium carbonate (0.26 g, 1.90 mmol). The reaction mixture is stirred at room temp for 21 hours after which the reaction solution is diluted with EtOAc and washed three times with aqueous saturated NH4Cl. The organic phase is washed with brine, dried (MgSO4), filtered, concentrated in vacuo and the resulting residue is dissolved in DMF (6 mL) and 1,8-diazabicyclo[5.4.0]undec-7-ene (0.28 mL, 1.90 mmol) is added to the reaction. After stirring the reaction at room temp for 3 hours, the mixture is diluted with aqueous saturated NH4Cl solution and extracted with EtOAc. The organic phase is washed with brine, dried (MgSO4), filtered, concentrated in vacuo, and the resulting residue is purified over silica (33% EtOAc//hexanes) to afford 0.14 g of the desired product: 1H NMR (300 MHz, CDCl3) δ 8.92 (s, 1H), 7.52-7.35 (m, 4H), 7.00 (s, 1H), 6.14 (s, 1H), 3.67 (s, 3H), 2.55 (s, 3H), 2.37 (s, 3H); ESI+ MS: m/z (rel intensity) 398.0 (100, M++H).

후처리

  1. washwashed three times with aqueous saturated NH4Cl
  2. washThe organic phase is washed with brine
  3. dry with materialdried (MgSO4)
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo
  6. dissolutionthe resulting residue is dissolved in DMF (6 mL)
  7. stirringAfter stirring
  8. customthe reaction at room temp for 3 hours
  9. extractionextracted with EtOAc
  10. washThe organic phase is washed with brine
  11. dry with materialdried (MgSO4)
  12. filtrationfiltered
  13. concentrationconcentrated in vacuo
  14. customthe resulting residue is purified over silica (33% EtOAc//hexanes)

출처 및 근거

ORD 기록
ord-423bb7b1c18b46cdab06be425836fb59
출처 데이터셋
uspto-grants-2008_01
특허 번호
US07319102B1

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