Technology Process of methyl 1-[(benzylcarbamoylmethyl)methylamino]-6,8-dichloro-isoquinoline-3-carboxylate
There total 10 articles about methyl 1-[(benzylcarbamoylmethyl)methylamino]-6,8-dichloro-isoquinoline-3-carboxylate which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
N-benzyl-2-methylaminoacetamide trifluoroacetate;
With
N-ethyl-N,N-diisopropylamine;
In
dimethyl sulfoxide;
for 0.0333333h;
methyl 1,6,8-trichloro-isoquinoline-3-carboxylate;
In
dimethyl sulfoxide;
at 95 ℃;
for 20h;
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: thionyl chloride / 3 h / 20 - 40 °C / Cooling with ice
2.1: ammonium carbonate; acetic acid / 14 h / 95 °C / Inert atmosphere
3.1: trichlorophosphate / 8 h / 100 °C / Inert atmosphere
4.1: N-ethyl-N,N-diisopropylamine / dimethyl sulfoxide / 0.03 h
4.2: 20 h / 95 °C
With
thionyl chloride; ammonium carbonate; acetic acid; N-ethyl-N,N-diisopropylamine; trichlorophosphate;
In
dimethyl sulfoxide;
- Guidance literature:
-
Multi-step reaction with 10 steps
1.1: potassium hydroxide / ethanol; water / 45 h / 110 °C
2.1: sulfuric acid; sodium nitrite / water / 2 h / 0 - 100 °C
3.1: N-Bromosuccinimide; dibenzoyl peroxide / tetrachloromethane / 17 h / Reflux
4.1: lithium hydroxide monohydrate / water / 4 h / Reflux
5.1: 24 h / 20 °C
6.1: hydrogenchloride / water; acetic acid / 3 h / 100 °C
7.1: thionyl chloride / 3 h / 20 - 40 °C / Cooling with ice
8.1: ammonium carbonate; acetic acid / 14 h / 95 °C / Inert atmosphere
9.1: trichlorophosphate / 8 h / 100 °C / Inert atmosphere
10.1: N-ethyl-N,N-diisopropylamine / dimethyl sulfoxide / 0.03 h
10.2: 20 h / 95 °C
With
hydrogenchloride; N-Bromosuccinimide; thionyl chloride; lithium hydroxide monohydrate; sulfuric acid; ammonium carbonate; acetic acid; N-ethyl-N,N-diisopropylamine; potassium hydroxide; sodium nitrite; trichlorophosphate; dibenzoyl peroxide;
In
tetrachloromethane; ethanol; water; acetic acid; dimethyl sulfoxide;