Technology Process of (R)-methyl 7-((2-aminoethyl)amino)-14-cyclohexyl-7,8-dihydro-6H-benzo[2,3][1,5]oxazocino[5,4-a]indole-11-carboxylate
There total 11 articles about (R)-methyl 7-((2-aminoethyl)amino)-14-cyclohexyl-7,8-dihydro-6H-benzo[2,3][1,5]oxazocino[5,4-a]indole-11-carboxylate which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
trifluoroacetic acid;
In
dichloromethane;
at 20 ℃;
DOI:10.1021/jm1013105
- Guidance literature:
-
Multi-step reaction with 7 steps
1: caesium carbonate / 1,4-dioxane / 48 h / Reflux
2: pyridine / 20 °C
3: trimethylsilylazide; tetrabutylammonium triphenyldifluorosilicate / tetrahydrofuran / 56 h / 65 °C
4: palladium 10% on activated carbon; hydrogen / methanol / 4 h / 760.05 Torr
5: trimethyl orthoformate / 20 °C
6: sodium cyanoborohydride; acetic acid / methanol / 1 h / 20 °C
7: trifluoroacetic acid / dichloromethane / 20 °C
With
pyridine; trimethylsilylazide; palladium 10% on activated carbon; hydrogen; sodium cyanoborohydride; caesium carbonate; acetic acid; tetrabutylammonium triphenyldifluorosilicate; trifluoroacetic acid; trimethyl orthoformate;
In
tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane;
DOI:10.1021/jm1013105
- Guidance literature:
-
Multi-step reaction with 8 steps
1: cesium fluoride / N,N-dimethyl-formamide / 20 °C
2: caesium carbonate / 1,4-dioxane / 48 h / Reflux
3: pyridine / 20 °C
4: trimethylsilylazide; tetrabutylammonium triphenyldifluorosilicate / tetrahydrofuran / 56 h / 65 °C
5: palladium 10% on activated carbon; hydrogen / methanol / 4 h / 760.05 Torr
6: trimethyl orthoformate / 20 °C
7: sodium cyanoborohydride; acetic acid / methanol / 1 h / 20 °C
8: trifluoroacetic acid / dichloromethane / 20 °C
With
pyridine; trimethylsilylazide; palladium 10% on activated carbon; hydrogen; sodium cyanoborohydride; caesium carbonate; acetic acid; cesium fluoride; tetrabutylammonium triphenyldifluorosilicate; trifluoroacetic acid; trimethyl orthoformate;
In
tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm1013105