Methylamine → N-Methyl-2-(1-methyl-1H-pyrazol-4-yl)ethan-1-amine

HRID 385889

反応式

HRID 385889 の反応式
Cl[CH2:2][CH2:3][C:4]1[CH:5]=[N:6][N:7]([CH3:9])[CH:8]=1.[CH3:10][NH2:11]>>[CH3:10][NH:11][CH2:2][CH2:3][C:4]1[CH:5]=[N:6][N:7]([CH3:9])[CH:8]=1

参加物

3

実験手順

To neat 4-(2-chloroethyl)-1-methyl-1H-pyrazole (50 g, 0.24 mol) was added a 25% aqueous solution of methylamine (1.15 L, 7.21 mol). The mixture was placed into an autoclave at 60° C. for 15 h. The resulting mixture was concentrated in vacuo, treated with aqueous solution of NaOH and extracted with DCM. The combined organic layers were concentrated in vacuo and purified by vacuum distillation to afford the title compound. b.p. 89-90° C./2 mm Hg.

後処理

  1. concentrationThe resulting mixture was concentrated in vacuo
  2. additiontreated with aqueous solution of NaOH
  3. extractionextracted with DCM
  4. concentrationThe combined organic layers were concentrated in vacuo
  5. distillationpurified by vacuum distillation

出典と根拠

ORDレコード
ord-6e4fd895a7144b869cd4b77e9541f4cc
出典データセット
uspto-grants-2013_02
特許番号
US08367706B2

関連ノート

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