Reaction #1668094

ord-3aef10c45d4d42bea70f6fdf6a07af18

Reaction equation

NNc1c(Cl)cc(Cl)cc1Cl
2,4,6-trichloro phenylhydrazine
Nc1cc([N+](=O)[O-])ccc1Cl
2-chloro-5-nitroaniline
COc1ccc([N+](=O)[O-])cc1N
2-methoxy-5-nitroaniline
CCOC(=O)C=C(OCC)OCC
β,β-diethoxyacrylic acid ethyl ester
CCCCCCCCCCCCCC(=O)Nc1ccc(OC)c(Nc2cc(=O)n(-c3c(Cl)cc(Cl)cc3Cl)[nH]2)c1
desired product
CCCCCCCCCCCCCC(=O)Nc1ccc(OC)c(Nc2cc(=O)n(-c3c(Cl)cc(Cl)cc3Cl)[nH]2)c1
1-(2,4,6-Trichlorophenyl)-3-(2-methoxy-5-n-tetradecanoylaminoanilino)-5-pyrazolone

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Otherin Synthesis Example 1

Procedure

Using the same procedure as Method (a) in Synthesis Example 1, in place of 2-chloro-5-nitroaniline, 2-methoxy-5-nitroaniline was reacted with β,β-diethoxyacrylic acid ethyl ester and then the reaction product was further reacted with 2,4,6-trichloro phenylhydrazine to give the desired product having a melting point of 254°C.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US03935015uspto-grants-1976_01