4-(2-methoxy-4-nitrophenyl)-1-methyl-1H-pyrazole → 3-methoxy-4-(1-methyl-1H-pyrazol-4-yl)aniline

HRID 1855510ノート

反応式

HRID 1855510 の反応式
[CH3:1][O:2][C:3]1[CH:8]=[C:7]([N+:9]([O-])=O)[CH:6]=[CH:5][C:4]=1[C:12]1[CH:13]=[N:14][N:15]([CH3:17])[CH:16]=1.[H][H]>[Pd].CO>[CH3:1][O:2][C:3]1[CH:8]=[C:7]([NH2:9])[CH:6]=[CH:5][C:4]=1[C:12]1[CH:13]=[N:14][N:15]([CH3:17])[CH:16]=1

参加物

5

反応物 2

HCID 668604724-(2-methoxy-4-nitrophenyl)-1-methyl-1H-pyrazoleHCID 178418361HCID 178418361、化合物

生成物 1

HCID 584144723-methoxy-4-(1-methyl-1H-pyrazol-4-yl)aniline収率 100.3%

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 887Methanol溶媒

実験手順

A mixture of 4-(2-methoxy-4-nitro-phenyl)-1-methyl-1H-pyrazole (240 mg, 1.03 mmol) and palladium on carbon 10% (55 mg, 0.052 mmol) in methanol (15 mL) was stirred for 2 hours at under hydrogen atmosphere. The mixture was filtrated and the solvent evaporated to afford the title compound (210 mg, 100%) as a white solid. MS ISP (m/e): 204.3.0 [(M+H)+]. 1H NMR (CDCl3, 300 MHz): δ (ppm)=7.76 (s, 1H), 7.70 (s, 1H), 7.28 (d, 1H), 6.32 (d, 2H), 3.91 (s, 3H), 3.85 (s, 3H), 3.68 (s broad, 2H). Mp 129-131° C.

後処理

  1. filtrationThe mixture was filtrated
  2. customthe solvent evaporated

出典と根拠

ORDレコード
ord-9df6a4563e6e49baa2dd7041b5090aae
出典データセット
uspto-grants-2015_02
特許番号
US08962834B2

反応ノート

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