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Methanol → 1,3-Dihydro-1-methyl-3-[4-(5-methyl-1H-imidazol-1-yl)-2-butynyl]-2H-imidazol-2-one

HRID 846654
ノート
印刷プレビュー

反応式

HRID 846654 の反応式
Br[CH2:2][C:3]#[C:4][CH2:5][N:6]1[CH:10]=[CH:9][N:8]([CH3:11])[C:7]1=[O:12].C([N:16]1[CH:20]=[C:19]([CH3:21])[N:18]=[CH:17]1)(=O)C.CO>C(#N)C>[CH3:11][N:8]1[CH:9]=[CH:10][N:6]([CH2:5][C:4]#[C:3][CH2:2][N:18]2[C:19]([CH3:21])=[CH:20][N:16]=[CH:17]2)[C:7]1=[O:12]
参加物反応条件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 887MethanolHCID 109534921-Acetyl-4-methylimidazoleHCID 150655461-(4-bromo-2-butynyl)-1,3-dihydro-3-methyl-2H-imidazol-2-one

生成物 1

HCID 150655801,3-Dihydro-1-methyl-3-[4-(5-methyl-1H-imidazol-1-yl)-2-butynyl]-2H-imidazol-2-one収率 79.6%

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

反応条件

温度
85 °C

実験手順

A mixture of 1-(4-bromo-2-butynyl)-1,3-dihydro-3-methyl-2H-imidazol-2-one (4.12 g, 0.018 mol) and 1-acetyl-4-methylimidazole (4.47 g, 0.036 mol) in acetonitrile (6 mL) was heated in an oil bath (bath temperature 85° C.) for 1 hr. Methanol (20 mL) was added and, after 1 hr, the solvents were removed and the residue was partitioned between ethyl acetate and 4N NaOH solution. The ethyl acetate was removed and the residual oil was chromatographed on silica gel using methanol:chloroform as eluant to give 3.3 g of product.

後処理

  1. customthe solvents were removed
  2. customthe residue was partitioned between ethyl acetate and 4N NaOH solution
  3. customThe ethyl acetate was removed
  4. customthe residual oil was chromatographed on silica gel

出典と根拠

ORDレコード
ord-3dfa2bada05a46e387658623f86b5387
出典データセット
uspto-grants-1992_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05137905

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート