ethyl [4-[(4R)-benzyloxy-1-tert-butoxycarbonyl-(2S)-pyrrolidinylcarbonyl]-1-piperazinyl]acetate

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Chemical Name:ethyl [4-[(4R)-benzyloxy-1-tert-butoxycarbonyl-(2S)-pyrrolidinylcarbonyl]-1-piperazinyl]acetate
CAS No.:886447-81-0
Molecular Formula:C₂₅H₃₇N₃O₆
Molecular Weight:475.585
Hs Code.:

Synonyms:ethyl [4-[(4R)-benzyloxy-1-tert-butoxycarbonyl-(2S)-pyrrolidinylcarbonyl]-1-piperazinyl]acetate

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of ethyl [4-[(4R)-benzyloxy-1-tert-butoxycarbonyl-(2S)-pyrrolidinylcarbonyl]-1-piperazinyl]acetate

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Technology Process of ethyl [4-[(4R)-benzyloxy-1-tert-butoxycarbonyl-(2S)-pyrrolidinylcarbonyl]-1-piperazinyl]acetate

There total 1 articles about ethyl [4-[(4R)-benzyloxy-1-tert-butoxycarbonyl-(2S)-pyrrolidinylcarbonyl]-1-piperazinyl]acetate 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: 100.0%

: 40350-83-2,54631-82-2,54631-81-1
(2S,4R)-4-(benzyloxy)-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxylic acid

: 40004-08-8
1-(Ethoxycarbonylmethyl)piperazine

: 886447-81-0
ethyl [4-[(4R)-benzyloxy-1-tert-butoxycarbonyl-(2S)-pyrrolidinylcarbonyl]-1-piperazinyl]acetate

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

Reference yield: 94.0%

: 886447-81-0
ethyl [4-[(4R)-benzyloxy-1-tert-butoxycarbonyl-(2S)-pyrrolidinylcarbonyl]-1-piperazinyl]acetate

: 886447-37-6
ethyl [4-[(4R)-benzyloxy-(2S)-pyrrolidinylcarbonyl]-1-piperazinyl]acetate

Guidance literature:: With trifluoroacetic acid; In dichloromethane; at 20 ℃; for 12h;
DOI:10.1016/j.bmc.2005.11.058

Reference yield:

: 886447-81-0
ethyl [4-[(4R)-benzyloxy-1-tert-butoxycarbonyl-(2S)-pyrrolidinylcarbonyl]-1-piperazinyl]acetate

: [4-((2S,4R)-4-Hydroxy-1-{2-[3-methoxy-4-(3-o-tolyl-ureido)-phenyl]-acetyl}-pyrrolidine-2-carbonyl)-piperazin-1-yl]-acetic acid

Guidance literature:: Multi-step reaction with 4 steps

1: 94 percent / TFA / CH₂Cl₂ / 12 h / 20 °C

2: 72 percent / 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide HCl salt; HOBt; Et₃N / tetrahydrofuran / 12 h / 20 °C

3: 100 percent / NaOH / tetrahydrofuran; methanol / 5 h / Heating

4: 58 percent / hydrogen / Pd(OH)2/C / ethanol / 72 h / 20 °C

With sodium hydroxide; hydrogen; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; trifluoroacetic acid; palladium dihydroxide; In tetrahydrofuran; methanol; ethanol; dichloromethane;
DOI:10.1016/j.bmc.2005.11.058