Technology Process of C20H14ClN5OS
There total 8 articles about C20H14ClN5OS which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
Multi-step reaction with 2 steps
1: triethylamine; trichlorophosphate / acetonitrile / 100 °C
2: 1-methyl-pyrrolidin-2-one / 120 - 160 °C / Microwave irradiation
With
triethylamine; trichlorophosphate;
In
1-methyl-pyrrolidin-2-one; acetonitrile;
DOI:10.1016/j.bmcl.2012.02.099
- Guidance literature:
-
Multi-step reaction with 4 steps
1: 80 °C / Neat (no solvent)
2: hydrazine hydrate / acetic acid / 80 °C
3: triethylamine; trichlorophosphate / acetonitrile / 100 °C
4: 1-methyl-pyrrolidin-2-one / 120 - 160 °C / Microwave irradiation
With
hydrazine hydrate; triethylamine; trichlorophosphate;
In
1-methyl-pyrrolidin-2-one; acetic acid; acetonitrile;
DOI:10.1016/j.bmcl.2012.02.099
- Guidance literature:
-
Multi-step reaction with 5 steps
1: ammonium chloride; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / 1-methyl-pyrrolidin-2-one / 80 °C
2: 80 °C / Neat (no solvent)
3: hydrazine hydrate / acetic acid / 80 °C
4: triethylamine; trichlorophosphate / acetonitrile / 100 °C
5: 1-methyl-pyrrolidin-2-one / 120 - 160 °C / Microwave irradiation
With
ammonium chloride; benzotriazol-1-ol; hydrazine hydrate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; N-ethyl-N,N-diisopropylamine; trichlorophosphate;
In
1-methyl-pyrrolidin-2-one; acetic acid; acetonitrile;
DOI:10.1016/j.bmcl.2012.02.099