Technology Process of HCl*Phe-Phe-Gly-Phe-Met-NH2
There total 9 articles about HCl*Phe-Phe-Gly-Phe-Met-NH2 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
hydrogenchloride; acetic acid;
for 0.5h;
- Guidance literature:
-
Multi-step reaction with 5 steps
1: 72 percent / 1.) triethylamine (TEA), 2.) N-hydroxybenztriazole (HOBt), N,N'-dicyclohexylcarbodiimide (DCC) / dimethylformamide / 16 h
2: 76 percent / methanolic NH3 / 48 h / Ambient temperature
3: 95 percent / 4 M HCl / ethyl acetate / 0.25 h / Ambient temperature
4: 78 percent / 1.) triethylamine (TEA), 2.) N-hydroxybenztriazole (HOBt), N,N'-dicyclohexylcarbodiimide (DCC) / dimethylformamide / 16 h / Ambient temperature
5: 79 percent / 4 M HCl, acetic acid / 0.5 h
With
hydrogenchloride; ammonia; benzotriazol-1-ol; acetic acid; triethylamine; dicyclohexyl-carbodiimide;
In
ethyl acetate; N,N-dimethyl-formamide;
- Guidance literature:
-
Multi-step reaction with 3 steps
1: 95 percent / 4 M HCl / ethyl acetate / 0.25 h / Ambient temperature
2: 78 percent / 1.) triethylamine (TEA), 2.) N-hydroxybenztriazole (HOBt), N,N'-dicyclohexylcarbodiimide (DCC) / dimethylformamide / 16 h / Ambient temperature
3: 79 percent / 4 M HCl, acetic acid / 0.5 h
With
hydrogenchloride; benzotriazol-1-ol; acetic acid; triethylamine; dicyclohexyl-carbodiimide;
In
ethyl acetate; N,N-dimethyl-formamide;