Technology Process of C22H29N5
There total 9 articles about C22H29N5 which
guide to synthetic route it.
The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:
synthetic route:
- Guidance literature:
-
With
hydroxylamine hydrochloride; sodium acetate;
In
methanol;
at 20 ℃;
for 16h;
DOI:10.1016/j.bmcl.2011.02.098
- Guidance literature:
-
Multi-step reaction with 3 steps
1: N-ethyl-N,N-diisopropylamine / 1-methyl-pyrrolidin-2-one / 1 h / 80 °C
2: palladium diacetate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; sodium t-butanolate / 7 h / 95 °C
3: hydroxylamine hydrochloride; sodium acetate / methanol / 16 h / 20 °C
With
hydroxylamine hydrochloride; sodium acetate; palladium diacetate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; N-ethyl-N,N-diisopropylamine; sodium t-butanolate;
In
1-methyl-pyrrolidin-2-one; methanol;
2: Buchwald coupling;
DOI:10.1016/j.bmcl.2011.02.098
- Guidance literature:
-
Multi-step reaction with 2 steps
1: palladium diacetate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; sodium t-butanolate / 7 h / 95 °C
2: hydroxylamine hydrochloride; sodium acetate / methanol / 16 h / 20 °C
With
hydroxylamine hydrochloride; sodium acetate; palladium diacetate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; sodium t-butanolate;
In
methanol;
1: Buchwald coupling;
DOI:10.1016/j.bmcl.2011.02.098