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Diisopropylethylamine → 4-(4'-Methoxy-biphenyl-4-ylcarbamoyl) 5-methyl-furan-2-carboxylic acid

HRID 460046
ノート
印刷プレビュー

反応式

HRID 460046 の反応式
C[O:2][C:3]([C:5]1[O:6][C:7]([CH3:13])=[C:8]([C:10]([OH:12])=O)[CH:9]=1)=[O:4].F[P-](F)(F)(F)(F)F.N1(OC(N(C)C)=[N+](C)C)C2N=CC=CC=2N=N1.C(N(C(C)C)CC)(C)C.[CH3:47][O:48][C:49]1[CH:54]=[CH:53][C:52]([C:55]2[CH:60]=[CH:59][C:58]([NH2:61])=[CH:57][CH:56]=2)=[CH:51][CH:50]=1>CN(C)C=O.C(OCC)(=O)C>[CH3:47][O:48][C:49]1[CH:50]=[CH:51][C:52]([C:55]2[CH:60]=[CH:59][C:58]([NH:61][C:10]([C:8]3[CH:9]=[C:5]([C:3]([OH:2])=[O:4])[O:6][C:7]=3[CH3:13])=[O:12])=[CH:57][CH:56]=2)=[CH:53][CH:54]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 81531DiisopropylethylamineHCID 27595644-Amino-4'-methoxybiphenylHCID 9886157Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 184446775-(Methoxycarbonyl)-2-methylfuran-3-carboxylic acid

生成物 1

HCID 184445754-(4'-Methoxy-biphenyl-4-ylcarbamoyl) 5-methyl-furan-2-carboxylic acid

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide溶媒HCID 8857Ethyl Acetate溶媒

実験手順

To a solution of 5-methyl-furan-2,4-dicarboxylic acid-2-methyl ester (23) (100 mg) in N,N-dimethylformamide (3.0 mL) was added O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (228 mg), diisopropylethylamine (0.56 mL) and 4′-methoxy-biphenyl-4-ylamine (120 mg). The resulting solution was stirred at room temperature for 2 hours. The reaction mixture was diluted with ethyl acetate (20 mL) and washed successively with water (2×20 mL), 0.1 M hydrochloric acid (20 mL), water (20 mL), saturated sodium hydrogen carbonate (10 mL) and brine (10 mL). This solution was dried and concentrated in vacuo. The residue (170 mg) was dissolved in dichloromethane (5 mL), treated with triethylamine (0.3 mL) and a scavenger resin PS-TsCl (0.6 g) and the mixture shaken for 3 hours at room temperature. The reaction mixture was filtered and concentrated in-vacuo. The residue was dissolved in methanol/tetrahydrofuran (1:3 by volume) (20 mL), treated with 1.0 M aqueous lithium hydroxide solution (2.0 mL) and allowed to stir at room temperature for 4 hours. The pH of the reaction mixture was adjusted to between pH 4 and pH 5 by careful addition of 1.0 M hydrochloric acid (1.0 mL) and partly concentrated in vacuo.

後処理

  1. washwashed successively with water (2×20 mL), 0.1 M hydrochloric acid (20 mL), water (20 mL), saturated sodium hydrogen carbonate (10 mL) and brine (10 mL)
  2. customThis solution was dried
  3. concentrationconcentrated in vacuo
  4. dissolutionThe residue (170 mg) was dissolved in dichloromethane (5 mL)
  5. additiontreated with triethylamine (0.3 mL)
  6. stirringa scavenger resin PS-TsCl (0.6 g) and the mixture shaken for 3 hours at room temperature
  7. filtrationThe reaction mixture was filtered
  8. concentrationconcentrated in-vacuo
  9. dissolutionThe residue was dissolved in methanol/tetrahydrofuran (1:3 by volume) (20 mL)
  10. additiontreated with 1.0 M aqueous lithium hydroxide solution (2.0 mL)
  11. stirringto stir at room temperature for 4 hours
  12. additionThe pH of the reaction mixture was adjusted to between pH 4 and pH 5 by careful addition of 1.0 M hydrochloric acid (1.0 mL)
  13. concentrationpartly concentrated in vacuo

出典と根拠

ORDレコード
ord-c7e7c1a692f643899207c73959a9ead0
出典データセット
uspto-grants-2007_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07196089B2

反応ノート

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