Dimethylformamide → methyl N-(4-cyanophenyl)-N-[4-amino-6-[(2,6-dichlorophenyl)methyl]-1,3,5-triazin-2-yl]glycine

HRID 25051

反応式

HRID 25051 の反応式
[H-].[Na+].[NH2:3][C:4]1[N:9]=[C:8]([CH2:10][C:11]2[C:16]([Cl:17])=[CH:15][CH:14]=[CH:13][C:12]=2[Cl:18])[N:7]=[C:6]([NH:19][C:20]2[CH:27]=[CH:26][C:23]([C:24]#[N:25])=[CH:22][CH:21]=2)[N:5]=1.C[O:29][C:30](=[O:33])[CH2:31]Cl.[CH3:34]N(C=O)C>>[CH3:34][CH:31]([C:30]([OH:29])=[O:33])[N:19]([C:20]1[CH:21]=[CH:22][C:23]([C:24]#[N:25])=[CH:26][CH:27]=1)[C:6]1[N:5]=[C:4]([NH2:3])[N:9]=[C:8]([CH2:10][C:11]2[C:16]([Cl:17])=[CH:15][CH:14]=[CH:13][C:12]=2[Cl:18])[N:7]=1

参加物

5

反応条件

温度
70 °C

実験手順

A solution of sodium hydride (0.00195 mol) in DMF (7 ml) was added to compound (1) (0.00186 mol) and the resulting solution was stirred for 5 minutes under argon. Then, chloroacetic acid methyl ester (0.0186 mol) was added and the reaction mixture was heated to 70° C. for 19 hours. The reaction mixture was then quenched with water and the resulting solid was filtered off. The residue was treated with hot ACN, then filtered while still hot. The residue from the cooled filtrate was recrystallized from 1,4-dioxane. The precipitate was filtered off, yielding 0.16 g (19.4%) of methyl N-(4-cyanophenyl)-N-[4-amino-6-[(2,6-dichlorophenyl)methyl]-1,3,5-triazin-2-yl]glycine (compound 39).

後処理

  1. customThe reaction mixture was then quenched with water
  2. filtrationthe resulting solid was filtered off
  3. additionThe residue was treated with hot ACN
  4. filtrationfiltered while still hot
  5. customThe residue from the cooled filtrate was recrystallized from 1,4-dioxane
  6. filtrationThe precipitate was filtered off

出典と根拠

ORDレコード
ord-aec5bb57d76b45cbac751505cdb98cb7
出典データセット
uspto-grants-2005_02
特許番号
US06858609B2

関連ノート

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