Technology Process of 9,10,11-trimethoxy-6-toluenesulfonyl-6,7-dihydro-5H-dibenzo[c,e]azepine-2,3-diol
There total 6 articles about 9,10,11-trimethoxy-6-toluenesulfonyl-6,7-dihydro-5H-dibenzo[c,e]azepine-2,3-diol which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
N-(3,4-dihydroxybenzyl)-4-methyl-N-(3,4,5-trimethoxybenzyl)benzenesulfonamide;
With
[bis(acetoxy)iodo]benzene;
In
1,2-dimethoxyethane;
at 0 ℃;
for 0.5h;
Inert atmosphere;
With
methanesulfonic acid;
In
1,2-dimethoxyethane;
at 0 ℃;
for 1h;
Inert atmosphere;
DOI:10.1055/s-0032-1316559
- Guidance literature:
-
Multi-step reaction with 2 steps
1.1: acetic acid; triethylamine tris(hydrogen fluoride) / tetrahydrofuran / 20 °C / Inert atmosphere
2.1: [bis(acetoxy)iodo]benzene / 1,2-dimethoxyethane / 0.5 h / 0 °C / Inert atmosphere
2.2: 1 h / 0 °C / Inert atmosphere
With
[bis(acetoxy)iodo]benzene; acetic acid; triethylamine tris(hydrogen fluoride);
In
tetrahydrofuran; 1,2-dimethoxyethane;
DOI:10.1055/s-0032-1316559
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: lithium aluminium tetrahydride / diethyl ether / 2 h / 20 °C / Inert atmosphere
2.1: triethylamine / dichloromethane / 0 - 20 °C / Inert atmosphere
3.1: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 20 °C / Inert atmosphere
4.1: acetic acid; triethylamine tris(hydrogen fluoride) / tetrahydrofuran / 20 °C / Inert atmosphere
5.1: [bis(acetoxy)iodo]benzene / 1,2-dimethoxyethane / 0.5 h / 0 °C / Inert atmosphere
5.2: 1 h / 0 °C / Inert atmosphere
With
lithium aluminium tetrahydride; [bis(acetoxy)iodo]benzene; di-isopropyl azodicarboxylate; acetic acid; triethylamine tris(hydrogen fluoride); triethylamine; triphenylphosphine;
In
tetrahydrofuran; 1,2-dimethoxyethane; diethyl ether; dichloromethane;
DOI:10.1055/s-0032-1316559