Reaktion #1583822

ord-3c6fb5aa64a04031be8f901393fca0da

Reaktionsgleichung

CCn1nc(-c2ccc(Cl)cc2)nc1CC(=O)O
[3-(4-chlorophenyl)-1-ethyl-1H-1,2,4-triazol-5-yl]acetic acid
CN(C)C=O
DMF
O=C(Cl)C(=O)Cl
oxalyl chloride
CCn1nc(-c2ccc(Cl)cc2)nc1CC(=O)Cl
[3-(4-chlorophenyl)-1-ethyl-1H-1,2,4-triazol-5-yl]acetyl chloride

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONare added dropwise
  2. 2
    Einengenconcentrated under reduced pressure

Vorschrift

1.2 mmol (318 mg) of [3-(4-chlorophenyl)-1-ethyl-1H-1,2,4-triazol-5-yl]acetic acid and 0.1 mmol (7 mg) of DMF are dissolved in 5 ml of anhydrous dichloromethane 1.3 mmol of oxalyl chloride (163 mg) in 3 ml of anhydrous dichloromethane are added dropwise. The solution is stirred at room temperature for 8 h and then concentrated under reduced pressure. The [3-(4-chlorophenyl)-1-ethyl-1H-1,2,4-triazol-5-yl]acetyl chloride obtained in this manner is processed further in crude form.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09198432B2uspto-grants-2015_12