Diisopropylethylamine → 2-(4-{2-[2-(4-Chloro-phenyl)-5,6-difluoro-benzoimidazol-1-yl]-2-cyclohexyl-acetylamino}-3-fluoro-phenoxy)-2-methyl-propionic acid ethyl ester

HRID 1161342ノート

反応式

HRID 1161342 の反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[N:12]([CH:13]([CH:27]3[CH2:32][CH2:31][CH2:30][CH2:29][CH2:28]3)[C:14]([NH:16][CH2:17][C@H:18]3CC[C@H](C(O)=O)C[CH2:19]3)=[O:15])[C:11]3[CH:33]=[CH:34][C:35]([F:37])=[CH:36][C:10]=3[N:9]=2)=[CH:4][CH:3]=1.[F:38][P-](F)(F)(F)(F)F.N1(OC(N(C)C)=[N+](C)C)C2N=CC=CC=2N=N1.C(N(C(C)C)C(C)C)C.[CH2:71]([O:73][C:74](=[O:87])[C:75]([O:78][C:79]1C=CC(N)=[C:81]([F:86])[CH:80]=1)([CH3:77])[CH3:76])[CH3:72]>CN(C)C=O.C(OCC)(=O)C>[CH2:71]([O:73][C:74](=[O:87])[C:75]([O:78][C:79]1[CH:19]=[CH:18][C:17]([NH:16][C:14](=[O:15])[CH:13]([N:12]2[C:11]3[CH:33]=[C:34]([F:38])[C:35]([F:37])=[CH:36][C:10]=3[N:9]=[C:8]2[C:5]2[CH:4]=[CH:3][C:2]([Cl:1])=[CH:7][CH:6]=2)[CH:27]2[CH2:32][CH2:31][CH2:30][CH2:29][CH2:28]2)=[C:81]([F:86])[CH:80]=1)([CH3:77])[CH3:76])[CH3:72]

参加物

7

反応物 4

HCID 81531DiisopropylethylamineHCID 9886157Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 671309762-(4-Amino-3-fluoro-phenoxy)-2-methyl-propionic acid ethyl esterHCID 178523387HCID 178523387、化合物2 回

生成物 1

HCID 686460602-(4-{2-[2-(4-Chloro-phenyl)-5,6-difluoro-benzoimidazol-1-yl]-2-cyclohexyl-acetylamino}-3-fluoro-phenoxy)-2-methyl-propionic acid ethyl ester収率 40%

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide溶媒HCID 8857Ethyl Acetate溶媒

実験手順

To the solution of 0.2 g (0.49 mmol) [2-(4-chloro-phenyl)-5,6-difluoro-benzoimidazol-1-yl]-cyclohexyl-acetic acid (example 22, intermediate c)) in 3 ml N,N-dimethylformamide, 0.21 g (0.55 mmol) O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate, 0.42 ml (0.32 g, 2.5 mmol) N-ethyldiisopropylamine and 0.13 g (0.54 mmol) 2-(4-amino-3-fluoro-phenoxy)-2-methyl-propionic acid ethyl ester were added. After 18 h the reaction mixture was poured on water and ethyl acetate, the phases were separated, the organic layer was washed twice with water followed by brine and dried over magnesium sulfate. After filtration the residue was purified by column chromatography on silica gel to give 0.12 g (40%) of the desired compound as light yellow foam.

後処理

  1. customthe phases were separated
  2. washthe organic layer was washed twice with water
  3. dry with materialdried over magnesium sulfate
  4. filtrationAfter filtration the residue
  5. customwas purified by column chromatography on silica gel

出典と根拠

ORDレコード
ord-10c6f0bbb8ab4367a0ce48505b93e9ea
出典データセット
uspto-grants-2010_10
特許番号
US07816540B2

反応ノート

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