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Cesium fluoride → Tert-butyl(4-(2,4-dimethyl-1,3-thiazol-5-yl)-2-{[3-(propylsulfonyl)phenyl]ethynyl}phenoxy)acetate

HRID 2390248
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HRID 2390248 반응식
[C:1]([O:5][C:6](=[O:30])[CH2:7][O:8][C:9]1[CH:14]=[CH:13][C:12](Br)=[CH:11][C:10]=1[C:16]#[C:17][C:18]1[CH:23]=[CH:22][CH:21]=[C:20]([S:24]([CH2:27][CH2:28][CH3:29])(=[O:26])=[O:25])[CH:19]=1)([CH3:4])([CH3:3])[CH3:2].[CH3:31][C:32]1[S:33][C:34](B2OC(C)(C)C(C)(C)O2)=[C:35]([CH3:37])[N:36]=1.[F-].[Cs+]>CCOC(C)=O.Cl[Pd](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>[C:1]([O:5][C:6](=[O:30])[CH2:7][O:8][C:9]1[CH:14]=[CH:13][C:12]([C:34]2[S:33][C:32]([CH3:31])=[N:36][C:35]=2[CH3:37])=[CH:11][C:10]=1[C:16]#[C:17][C:18]1[CH:23]=[CH:22][CH:21]=[C:20]([S:24]([CH2:27][CH2:28][CH3:29])(=[O:26])=[O:25])[CH:19]=1)([CH3:4])([CH3:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 25953Cesium fluorideHCID 185257002,4-Dimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,3-thiazoleHCID 56593972Tert-butyl(4-bromo-2-{[3-(propylsulfonyl)phenyl]ethynyl}phenoxy)acetate2회

생성물 1

HCID 58521912Tert-butyl(4-(2,4-dimethyl-1,3-thiazol-5-yl)-2-{[3-(propylsulfonyl)phenyl]ethynyl}phenoxy)acetate

시약·촉매·용매 2

HCID 178418476
HCID 178418476, 화합물
촉매
HCID 8857Ethyl Acetate용매

실험 절차

A solution of tert-butyl(4-bromo-2-{[3-(propylsulfonyl)phenyl]ethynyl}phenoxy)acetate (Intermediate 191; 100 mg; 0.20 mmol), 2,4-dimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,3-thiazole (73 mg; 0.30 mmol) was placed in a microwave vial and treated with caesium fluoride (93 mg; 0.61 mmol) and bis(triphenylphosphine)palladium(II) chloride (14 mg; 0.02 mmol). The tube was sealed and degased with N2 before adding dioxane (2 ml) and water (1 ml). The resulting reaction mixture was irradiated in a microwave reactor at 120° C. for 10 minutes. The reaction mixture was taken up in EtOAc and washed with water and brine. The organic phase was dried over MgSO4, filtered, concentrated and purified by flash column chromatography (silica), eluting with cyclohexane containing increasing amounts of EtOAc affording the title compound as a brown sticky solid (78 mg, 73%).

후처리

  1. customThe tube was sealed
  2. customdegased with N2
  3. additionbefore adding dioxane (2 ml) and water (1 ml)
  4. customThe resulting reaction mixture
  5. customwas irradiated in a microwave reactor at 120° C. for 10 minutes
  6. washwashed with water and brine
  7. dry with materialThe organic phase was dried over MgSO4
  8. filtrationfiltered
  9. concentrationconcentrated
  10. custompurified by flash column chromatography (silica)
  11. washeluting with cyclohexane containing
  12. temperatureincreasing amounts of EtOAc affording the title compound as a brown sticky solid (78 mg, 73%)

출처 및 근거

ORD 기록
ord-b77ffa87d825469aa34d047b41612afa
출처 데이터셋
uspto-grants-2012_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08273769B2

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