Potassium Carbonate → 3-(6-{7-[2-(1-tert-Butoxycarbonyl-pyrrolidin-2-yl)-3H-imidazol-4-yl]-dibenzothiophen-3-yl}-1H-benzoimidazol-2-yl)-2-aza-bicyclo[2.2.1]heptane-2-carboxylic acid tert-butyl ester

HRID 79816ノート

反応式

HRID 79816 の反応式
C(OC(N1CC2CC1C(C1N(C3C=CC4C5C=CC([C:32]6[NH:33][C:34]([CH:37]7[CH2:41][CH2:40][CH2:39][N:38]7[C:42]([O:44][C:45]([CH3:48])([CH3:47])[CH3:46])=[O:43])=[N:35][CH:36]=6)=CC=5SC=4C=3)C3C=CC=CC=3N=1)C2)=O)(C)(C)C.C(OC(N1CCCC1C1NC([C:71]2[CH:72]=[CH:73][C:74]3[C:78]4[CH:79]=[CH:80][C:81](Br)=[CH:82][C:77]=4[S:76][C:75]=3[CH:84]=2)=CN=1)=O)(C)(C)C.[C:85]([O:89][C:90]([N:92]1[CH:97]([C:98]2[NH:102][C:101]3[CH:103]=[C:104](B4OC(C)(C)C(C)(C)O4)[CH:105]=[CH:106][C:100]=3[N:99]=2)[CH:96]2[CH2:116][CH:93]1[CH2:94][CH2:95]2)=[O:91])([CH3:88])([CH3:87])[CH3:86].C(=O)([O-])[O-].[K+].[K+]>COCCOC.C(OCC)(=O)C.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2].C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[C:85]([O:89][C:90]([N:92]1[CH:97]([C:98]2[NH:102][C:101]3[CH:103]=[C:104]([C:81]4[CH:80]=[CH:79][C:78]5[C:74]6[CH:73]=[CH:72][C:71]([C:32]7[NH:33][C:34]([CH:37]8[CH2:41][CH2:40][CH2:39][N:38]8[C:42]([O:44][C:45]([CH3:46])([CH3:47])[CH3:48])=[O:43])=[N:35][CH:36]=7)=[CH:84][C:75]=6[S:76][C:77]=5[CH:82]=4)[CH:105]=[CH:106][C:100]=3[N:99]=2)[CH:96]2[CH2:116][CH:93]1[CH2:94][CH2:95]2)=[O:91])([CH3:88])([CH3:86])[CH3:87]

参加物

9

反応条件

温度
80 °C

実験手順

3-(6-{(7-[2-(1-tert-Butoxycarbonyl-pyrrolidin-2-yl)-3H-imidazol-4-yl]-dibenzothiophen-3-yl}-1H-benzoimidazol-2-yl)-2-aza-bicyclo[2.2.1]heptane-2-carboxylic acid tert-butyl ester: A mixture of 2-[5-(7-Bromo-dibenzothiophen-3-yl)-1H-imidazol-2-yl]-pyrrolidine-1-carboxylic acid tert-butyl ester (300 mg, 0.48 mmol, 1 eq.), 3-[6-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)-1H-benzoimidazol-2-yl]-2-aza-bicyclo[2.2.1]heptane-2-carboxylic acid tert-butyl ester (1.1 eq., 530 mg), [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (3%, 12 mg), tetrakis(triphenylphosphine)palladium (3%, 17 mg) and 2N potassium carbonate aqueous solution (3.3 eq., 0.8 mL) in 2 mL DME was heated to 80° C. under Argon for 5 hours. The reaction mixture was cooled and diluted in ethyl acetate and washed with saturated sodium bicarbonate solution. The organic layer dried (MgSO4), concentrated and purified by flash column chromatography (silica gel, 20 to 100% ethyl acetate/hexane) to give a yellow foam 3-(6-{7-[2-(1-tert-Butoxycarbonyl-pyrrolidin-2-yl)-3H-imidazol-4-yl]-dibenzothiophen-3-yl}-1H-benzoimidazol-2-yl)-2-aza-bicyclo[2.2.1]heptane-2-carboxylic acid tert-butyl ester (245 mg, yield 70%). LCMS-ESI−: calc'd for C42H46N6O4S: 730.92. Found: 731.2 (M+H+).

後処理

  1. temperatureThe reaction mixture was cooled
  2. washwashed with saturated sodium bicarbonate solution
  3. dry with materialThe organic layer dried (MgSO4)
  4. concentrationconcentrated
  5. custompurified by flash column chromatography (silica gel, 20 to 100% ethyl acetate/hexane)

出典と根拠

ORDレコード
ord-61f07669998140b792305a0229647db8
出典データセット
uspto-grants-2014_09
特許番号
US08841278B2

反応ノート

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