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

HRID 270632

Reaktionsgleichung

Reaktionsgleichung von HRID 270632
[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

Komponenten

5

Reaktionsbedingungen

Temperatur
70 °C

Versuchsvorschrift

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).

Aufarbeitung

  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

Quellen und Nachweise

ORD-Eintrag
ord-1fca4a96cc014ded9f6a1156ef705e5e
Quelldatensatz
uspto-grants-2008_11
Patentnummer
US07449575B2

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