Reaktion #89942

ord-3b92ce2d54f94a298ff3bbf4bdd5e07d

Reaktionsgleichung

COCCOc1cc(C(N)=O)c(N)cc1OC
2-amino-4-methoxy-5-(2-methoxyethoxyl)benzamide
c1ccncc1
pyridine
O=C(Cl)c1cccc([N+](=O)[O-])c1
3-nitrobenzoyl chloride
COCCOc1cc(C(N)=O)c(Nc2cccc([N+](=O)[O-])c2)cc1OC
desired product
COCCOc1cc(C(N)=O)c(Nc2cccc([N+](=O)[O-])c2)cc1OC
4-Methoxy-5-(2-methoxyethoxy)-(3-nitrophenyl)aminobenzamide

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Einengenwas concentrated in vacuo

Vorschrift

To a mixture of 2-amino-4-methoxy-5-(2-methoxyethoxyl)benzamide (1.78 g, 7.40 mmol) and pyridine (2.40 mL, 29.6 mmol) in CHCl3 (40 mL) was added 3-nitrobenzoyl chloride (1.44 g, 7.8 mmol). The mixture was stirred at RT for 2.5 h upon which the mixture was concentrated in vacuo to give the desired product, which was used directly in the next step without purification.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09440961B2uspto-grants-2016_09