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Potassium Carbonate → 4-{2-[2-(4-Chloro-phenyl)-5,6-difluoro-benzoimidazol-1-yl]-2-cyclohexyl-ethylsulfanyl}-benzoic acid methyl ester

HRID 417165
ノート
印刷プレビュー

反応式

HRID 417165 の反応式
[SH:1][C:2]1[CH:11]=[CH:10][C:5]([C:6]([O:8][CH3:9])=[O:7])=[CH:4][CH:3]=1.C(=O)([O-])[O-].[K+].[K+].[Cl:18][C:19]1[CH:24]=[CH:23][C:22]([C:25]2[N:29]([CH:30]([CH:40]3[CH2:45][CH2:44][CH2:43][CH2:42][CH2:41]3)[CH2:31]OC3C=CC=CC=3F)[C:28]3[CH:46]=[C:47]([F:51])[C:48]([F:50])=[CH:49][C:27]=3[N:26]=2)=[CH:21][CH:20]=1>CN(C)C=O>[CH3:9][O:8][C:6](=[O:7])[C:5]1[CH:4]=[CH:3][C:2]([S:1][CH2:31][CH:30]([N:29]2[C:28]3[CH:46]=[C:47]([F:51])[C:48]([F:50])=[CH:49][C:27]=3[N:26]=[C:25]2[C:22]2[CH:23]=[CH:24][C:19]([Cl:18])=[CH:20][CH:21]=2)[CH:40]2[CH2:41][CH2:42][CH2:43][CH2:44][CH2:45]2)=[CH:11][CH:10]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 11430Potassium CarbonateHCID 237573Methyl 4-sulfanylbenzoateHCID 461844412-(4-Chloro-phenyl)-1-[1-cyclohexyl-2-(2-fluoro-phenoxy)-ethyl]-5,6-difluoro-1H-benzoimidazole

生成物 1

HCID 666193434-{2-[2-(4-Chloro-phenyl)-5,6-difluoro-benzoimidazol-1-yl]-2-cyclohexyl-ethylsulfanyl}-benzoic acid methyl ester収率 65%

試薬・触媒・溶媒 1

HCID 6228
Dimethylformamide
溶媒

実験手順

To a solution of 74 mg (0.44 mmol) methyl 4-mercaptobenzoate in 3 ml N,N-dimethylformamide was added 61 mg (0.44 mmol) potassium carbonate at 0° C. The reaction mixture was stirred for 15 min. and then 200 mg (0.44 mmol) 1-(2-bromo-1-cyclohexyl-ethyl)-2-(4-chloro-phenyl)-5,6-difluoro-1H-benzoimidazole (Example 34, intermediate) was added at the same temperature. The cooling bath was removed and the reaction mixture stirred for 18 hours at room temperature. The reaction mixture was poured on 10% aqueous 30 ml citric acid and 30 ml ethyl acetate and the layers were separated. The aqueous layer was extracted a second time with 30 ml ethyl acetate. The combined organic layers were washed with 30 ml brine, dried over magnesium sulfate, filtered and concentrated under vacuum. The residue was purified by silica gel chromatography using a MPLC system (CombiFlash Companion, Isco Inc.) eluting with a gradient of n-heptane:ethyl acetate (100:0 to 70:30) to give the desired compound as a colorless solid (65%). MS (Turbo Spray) m/z=541.2 [M+H].

後処理

  1. customThe cooling bath was removed
  2. stirringthe reaction mixture stirred for 18 hours at room temperature
  3. additionThe reaction mixture was poured on 10% aqueous 30 ml citric acid and 30 ml ethyl acetate
  4. customthe layers were separated
  5. extractionThe aqueous layer was extracted a second time with 30 ml ethyl acetate
  6. washThe combined organic layers were washed with 30 ml brine
  7. dry with materialdried over magnesium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated under vacuum
  10. customThe residue was purified by silica gel chromatography
  11. washeluting with a gradient of n-heptane:ethyl acetate (100:0 to 70:30)

出典と根拠

ORDレコード
ord-f8ffa32bd1ce4279841018904f4d70a8
出典データセット
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08088930B2

反応ノート

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