Technology Process of 7-[[4-[(2,6-dimethylphenyl)amino]benzoyl]methylamino]Heptanoic acid methyl ester
There total 7 articles about 7-[[4-[(2,6-dimethylphenyl)amino]benzoyl]methylamino]Heptanoic acid methyl ester which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
caesium carbonate;
tris-(dibenzylideneacetone)dipalladium(0); 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene;
In
toluene;
at 100 ℃;
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: sodium tris(acetoxy)borohydride / 1,2-dichloro-ethane / 4 h / 20 °C
1.2: 20 °C
2.1: carbonochloridic acid 1-chloro-ethyl ester / 1,2-dichloro-ethane / 10.03 h / 0 °C / Reflux
2.2: 1 h / Reflux
3.1: N-ethyl-N,N-diisopropylamine; HATU / dichloromethane / 4 h / 20 °C
4.1: caesium carbonate / 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; tris-(dibenzylideneacetone)dipalladium(0) / toluene / 100 °C
With
carbonochloridic acid 1-chloro-ethyl ester; sodium tris(acetoxy)borohydride; caesium carbonate; N-ethyl-N,N-diisopropylamine; HATU;
tris-(dibenzylideneacetone)dipalladium(0); 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene;
In
dichloromethane; 1,2-dichloro-ethane; toluene;
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: thionyl chloride / -10 - 20 °C
2.1: sodium tris(acetoxy)borohydride / 1,2-dichloro-ethane / 4 h / 20 °C
2.2: 20 °C
3.1: carbonochloridic acid 1-chloro-ethyl ester / 1,2-dichloro-ethane / 10.03 h / 0 °C / Reflux
3.2: 1 h / Reflux
4.1: N-ethyl-N,N-diisopropylamine; HATU / dichloromethane / 4 h / 20 °C
5.1: caesium carbonate / 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; tris-(dibenzylideneacetone)dipalladium(0) / toluene / 100 °C
With
thionyl chloride; carbonochloridic acid 1-chloro-ethyl ester; sodium tris(acetoxy)borohydride; caesium carbonate; N-ethyl-N,N-diisopropylamine; HATU;
tris-(dibenzylideneacetone)dipalladium(0); 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene;
In
dichloromethane; 1,2-dichloro-ethane; toluene;