Technology Process of N-(3-amino-9H-β-carbolin-8-yl)benzamide
There total 9 articles about N-(3-amino-9H-β-carbolin-8-yl)benzamide which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
palladium 10% on activated carbon; hydrazine hydrate;
In
methanol;
for 5h;
Reflux;
Inert atmosphere;
DOI:10.1016/j.bmcl.2012.03.077
- Guidance literature:
-
Multi-step reaction with 11 steps
1: hydrazine hydrate / pentan-1-ol / 7 h / Reflux; Inert atmosphere
2: hydrogenchloride; sodium nitrite / water / 2 h / 0 °C / Inert atmosphere
3: acetic acid / water / 1 h / Reflux; Inert atmosphere
4: chloroform / 0.5 h / 40 °C / Inert atmosphere
5: sodium nitrate; trifluoroacetic acid / 18 h / 0 - 20 °C / Inert atmosphere
6: hydrogenchloride / water / 12 h / Reflux; Inert atmosphere
7: acetic acid / methanol / 4 h / 20 °C / pH 4 / Inert atmosphere
8: sodium cyanoborohydride / methanol / 1 h / 20 °C / Inert atmosphere
9: hydrogenchloride; tin(II) chloride dihdyrate / methanol; water / 48 h / 0 - 20 °C / Inert atmosphere
10: dmap / chloroform / 24 h / 20 °C / Inert atmosphere
11: palladium 10% on activated carbon; hydrazine hydrate / methanol / 5 h / Reflux; Inert atmosphere
With
hydrogenchloride; dmap; sodium nitrate; tin(II) chloride dihdyrate; palladium 10% on activated carbon; sodium cyanoborohydride; hydrazine hydrate; acetic acid; trifluoroacetic acid; sodium nitrite;
In
methanol; pentan-1-ol; chloroform; water;
3: Curtius rearrangement;
DOI:10.1016/j.bmcl.2012.03.077
- Guidance literature:
-
Multi-step reaction with 4 steps
1: sodium cyanoborohydride / methanol / 1 h / 20 °C / Inert atmosphere
2: hydrogenchloride; tin(II) chloride dihdyrate / methanol; water / 48 h / 0 - 20 °C / Inert atmosphere
3: dmap / chloroform / 24 h / 20 °C / Inert atmosphere
4: palladium 10% on activated carbon; hydrazine hydrate / methanol / 5 h / Reflux; Inert atmosphere
With
hydrogenchloride; dmap; tin(II) chloride dihdyrate; palladium 10% on activated carbon; sodium cyanoborohydride; hydrazine hydrate;
In
methanol; chloroform; water;
DOI:10.1016/j.bmcl.2012.03.077