ethyl 2-[4-[1-[3-methoxy-4-[N'-(2-methylphenyl)ureido]phenylacetyl]-(2S)-pyrrolidinylcarbonyl]-1-piperazinyl]propionate

Base Information

Chemical Name:ethyl 2-[4-[1-[3-methoxy-4-[N'-(2-methylphenyl)ureido]phenylacetyl]-(2S)-pyrrolidinylcarbonyl]-1-piperazinyl]propionate
CAS No.:886447-27-4
Molecular Formula:C₃₁H₄₁N₅O₆
Molecular Weight:579.696
Hs Code.:

Synonyms:ethyl 2-[4-[1-[3-methoxy-4-[N'-(2-methylphenyl)ureido]phenylacetyl]-(2S)-pyrrolidinylcarbonyl]-1-piperazinyl]propionate

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Chemical Property of ethyl 2-[4-[1-[3-methoxy-4-[N'-(2-methylphenyl)ureido]phenylacetyl]-(2S)-pyrrolidinylcarbonyl]-1-piperazinyl]propionate

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Technology Process of ethyl 2-[4-[1-[3-methoxy-4-[N'-(2-methylphenyl)ureido]phenylacetyl]-(2S)-pyrrolidinylcarbonyl]-1-piperazinyl]propionate

There total 5 articles about ethyl 2-[4-[1-[3-methoxy-4-[N'-(2-methylphenyl)ureido]phenylacetyl]-(2S)-pyrrolidinylcarbonyl]-1-piperazinyl]propionate 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:

Reference yield: 27.0%

: 886447-24-1
ethyl 2-[4-((2S)-pyrrolidinylcarbonyl)-1-piperazinyl]propionate

: 181519-21-1
3-methoxy-4-[N'-(2-methylphenyl)ureido]phenylacetic acid

: 886447-27-4
ethyl 2-[4-[1-[3-methoxy-4-[N'-(2-methylphenyl)ureido]phenylacetyl]-(2S)-pyrrolidinylcarbonyl]-1-piperazinyl]propionate

Guidance literature:: With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In N,N-dimethyl-formamide; at 20 ℃; for 12h;
DOI:10.1016/j.bmc.2005.11.058

Reference yield:

: 824414-06-4
1-(ethoxycarbonyl-ethyl)piperazine

: 886447-27-4
ethyl 2-[4-[1-[3-methoxy-4-[N'-(2-methylphenyl)ureido]phenylacetyl]-(2S)-pyrrolidinylcarbonyl]-1-piperazinyl]propionate

Guidance literature:: Multi-step reaction with 3 steps

1: 58 percent / 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide HCl salt; HOBt; Et₃N / dimethylformamide / 12 h / 20 °C

2: 45 percent / TFA / CH₂Cl₂ / 12 h / 20 °C

3: 27 percent / 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide HCl salt; HOBt; Et₃N / dimethylformamide / 12 h / 20 °C

With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; trifluoroacetic acid; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2005.11.058

Reference yield:

: 886448-02-8
ethyl 2-(4-tert-butoxycarbonyl-1-piperazinyl)propionate

: 886447-27-4
ethyl 2-[4-[1-[3-methoxy-4-[N'-(2-methylphenyl)ureido]phenylacetyl]-(2S)-pyrrolidinylcarbonyl]-1-piperazinyl]propionate

Guidance literature:: Multi-step reaction with 4 steps

1: 44 percent / TFA / CH₂Cl₂ / 1 h

2: 58 percent / 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide HCl salt; HOBt; Et₃N / dimethylformamide / 12 h / 20 °C

3: 45 percent / TFA / CH₂Cl₂ / 12 h / 20 °C

4: 27 percent / 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide HCl salt; HOBt; Et₃N / dimethylformamide / 12 h / 20 °C

With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; trifluoroacetic acid; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2005.11.058