1,1'-Carbonyldiimidazole → N-(3-methoxy-benzyl)-N-methyl-2-(3,5-dichlorophenyl)-2-(phenylsulfanyl)-acetamide

HRID 1666301

Reaktionsgleichung

Reaktionsgleichung von HRID 1666301
[Cl:1][C:2]1[CH:3]=[C:4]([CH:9]([S:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[C:10]([OH:12])=O)[CH:5]=[C:6]([Cl:8])[CH:7]=1.C(N1C=CN=C1)(N1C=CN=C1)=O.[CH3:32][NH:33][CH2:34][C:35]1[CH:40]=[CH:39][CH:38]=[C:37]([O:41][CH3:42])[CH:36]=1>ClCCl>[CH3:42][O:41][C:37]1[CH:36]=[C:35]([CH:40]=[CH:39][CH:38]=1)[CH2:34][N:33]([CH3:32])[C:10](=[O:12])[CH:9]([C:4]1[CH:5]=[C:6]([Cl:8])[CH:7]=[C:2]([Cl:1])[CH:3]=1)[S:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1

Komponenten

5

Versuchsvorschrift

A solution of 2-(3,5-dichlorophenyl)-2-(phenyl-sulfanyl)acetic acid (1.65 g) in dichloromethane (50 ml) was treated with 1,1′-carbonyldiimidazole (0.90 g) at room temperature for 2 hours. A solution of N-methyl-3-methoxy-benzylamine (1.0 g) in dichloromethane (15 ml) was added and the stirring was continued for one hour. The reaction mixture was washed with aqueous hydrochloric acid (1M, 50 ml) and aqueous sodium hydroxide (1M, 50 ml). The organic phase was dried and concentrated to dryness leaving crude N-(3-methoxy-benzyl)-N-methyl-2-(3,5-dichlorophenyl)-2-(phenylsulfanyl)-acetamide (1.8 g) as a viscous oil.

Aufarbeitung

  1. washThe reaction mixture was washed with aqueous hydrochloric acid (1M, 50 ml) and aqueous sodium hydroxide (1M, 50 ml)
  2. customThe organic phase was dried
  3. concentrationconcentrated to dryness

Quellen und Nachweise

ORD-Eintrag
ord-2bfcea556a594983b140437c4a5c38c2
Quelldatensatz
uspto-grants-2011_10
Patentnummer
US08044067B2

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