Technology Process of C23H27ClN6O3
There total 8 articles about C23H27ClN6O3 which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine;
In
N,N-dimethyl-formamide;
at 20 ℃;
for 2.5 - 5h;
Product distribution / selectivity;
- Guidance literature:
-
Multi-step reaction with 6 steps
1: sodium hydroxide; water / methanol / 20 °C
2: hydrogen; platinum(IV) oxide / methanol
3: triethylamine / tetrahydrofuran / -78 °C
4: ammonia / methanol
5: bis-[(trifluoroacetoxy)iodo]benzene; pyridine / acetonitrile; water
6: N-ethyl-N,N-diisopropylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide
With
pyridine; platinum(IV) oxide; ammonia; water; hydrogen; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; N-ethyl-N,N-diisopropylamine; bis-[(trifluoroacetoxy)iodo]benzene; sodium hydroxide;
In
tetrahydrofuran; methanol; water; N,N-dimethyl-formamide; acetonitrile;
5: |Hofmann Rearrangement;
DOI:10.1016/j.bmcl.2015.11.089
- Guidance literature:
-
Multi-step reaction with 7 steps
1: triethylamine; palladium diacetate / acetonitrile / 24 h / 85 °C
2: sodium hydroxide; water / methanol / 20 °C
3: hydrogen; platinum(IV) oxide / methanol
4: triethylamine / tetrahydrofuran / -78 °C
5: ammonia / methanol
6: bis-[(trifluoroacetoxy)iodo]benzene; pyridine / acetonitrile; water
7: N-ethyl-N,N-diisopropylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide
With
pyridine; platinum(IV) oxide; ammonia; water; hydrogen; palladium diacetate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; N-ethyl-N,N-diisopropylamine; bis-[(trifluoroacetoxy)iodo]benzene; sodium hydroxide;
In
tetrahydrofuran; methanol; water; N,N-dimethyl-formamide; acetonitrile;
1: |Heck Reaction / 6: |Hofmann Rearrangement;
DOI:10.1016/j.bmcl.2015.11.089