Technology Process of 4-chloro-3-(6,7-dimethoxy-2-oxo-1,2,3,4-tetrahydroquinoline-3-carboxamido)benzoic acid
There total 6 articles about 4-chloro-3-(6,7-dimethoxy-2-oxo-1,2,3,4-tetrahydroquinoline-3-carboxamido)benzoic acid which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
4-chloro-3-[(6,7-dimethoxy-2-oxo-1,2,3,4-tetrahydro-quinoline-3-carbonyl)-amino]-benzoic acid methyl ester;
With
water; lithium hydroxide;
In
tetrahydrofuran; methanol; dimethyl sulfoxide;
for 72h;
With
hydrogenchloride;
In
water;
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: acetic acid; iron / methanol / 1.5 h / 90 - 100 °C
2.1: water; lithium hydroxide / tetrahydrofuran; methanol / 1.5 h / 20 °C
2.2: Acidic conditions
3.1: triethylamine; HATU / N,N-dimethyl-formamide / 1.5 h / 20 °C
4.1: water; lithium hydroxide / dimethyl sulfoxide; tetrahydrofuran; methanol / 72 h
With
water; iron; acetic acid; triethylamine; HATU; lithium hydroxide;
In
tetrahydrofuran; methanol; dimethyl sulfoxide; N,N-dimethyl-formamide;
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: hydrogenchloride; water; sodium cyanoborohydride / ethanol
2.1: acetic acid; iron / methanol / 1.5 h / 90 - 100 °C
3.1: water; lithium hydroxide / tetrahydrofuran; methanol / 1.5 h / 20 °C
3.2: Acidic conditions
4.1: triethylamine; HATU / N,N-dimethyl-formamide / 1.5 h / 20 °C
5.1: water; lithium hydroxide / dimethyl sulfoxide; tetrahydrofuran; methanol / 72 h
With
hydrogenchloride; water; iron; sodium cyanoborohydride; acetic acid; triethylamine; HATU; lithium hydroxide;
In
tetrahydrofuran; methanol; ethanol; dimethyl sulfoxide; N,N-dimethyl-formamide;