Technology Process of C12H16BrN3O2S
There total 4 articles about C12H16BrN3O2S 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
tris-(2-carboxyethyl)-phosphine hydrochloride;
In
water; dimethyl sulfoxide;
at 25 ℃;
for 0.333333h;
Darkness;
DOI:10.1021/jm2016182
- Guidance literature:
-
Multi-step reaction with 4 steps
1: hydrogenchloride; water / Reflux
2: benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 0 - 20 °C
3: hydrazine hydrate / methanol / 2.5 h / Reflux
4: tris-(2-carboxyethyl)-phosphine hydrochloride / water; dimethyl sulfoxide / 0.33 h / 25 °C / Darkness
With
hydrogenchloride; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; water; tris-(2-carboxyethyl)-phosphine hydrochloride; hydrazine hydrate; N-ethyl-N,N-diisopropylamine;
In
tetrahydrofuran; methanol; water; dimethyl sulfoxide;
DOI:10.1021/jm2016182
- Guidance literature:
-
Multi-step reaction with 5 steps
1: sodium acetate; acetic anhydride / Reflux
2: hydrogenchloride; water / Reflux
3: benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 0 - 20 °C
4: hydrazine hydrate / methanol / 2.5 h / Reflux
5: tris-(2-carboxyethyl)-phosphine hydrochloride / water; dimethyl sulfoxide / 0.33 h / 25 °C / Darkness
With
hydrogenchloride; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; water; sodium acetate; tris-(2-carboxyethyl)-phosphine hydrochloride; acetic anhydride; hydrazine hydrate; N-ethyl-N,N-diisopropylamine;
In
tetrahydrofuran; methanol; water; dimethyl sulfoxide;
DOI:10.1021/jm2016182