5-(4-Cyano-phenylcarbamoyl)-5-(2,2,2-trifluoro-acetylamino)-pentanoic acid

Base Information

Chemical Name:5-(4-Cyano-phenylcarbamoyl)-5-(2,2,2-trifluoro-acetylamino)-pentanoic acid
CAS No.:80418-04-8
Molecular Formula:C₁₅H₁₄F₃N₃O₄
Molecular Weight:357.289
Hs Code.:

Synonyms:5-(4-Cyano-phenylcarbamoyl)-5-(2,2,2-trifluoro-acetylamino)-pentanoic acid

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Chemical Property of 5-(4-Cyano-phenylcarbamoyl)-5-(2,2,2-trifluoro-acetylamino)-pentanoic acid

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Technology Process of 5-(4-Cyano-phenylcarbamoyl)-5-(2,2,2-trifluoro-acetylamino)-pentanoic acid

There total 4 articles about 5-(4-Cyano-phenylcarbamoyl)-5-(2,2,2-trifluoro-acetylamino)-pentanoic acid 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: 32.0%

: trifluoroacetyl-α-DL-(α-aminoadipyl)-p-cyanoanilide δ-benzyl ester

: 80418-04-8
5-(4-Cyano-phenylcarbamoyl)-5-(2,2,2-trifluoro-acetylamino)-pentanoic acid

Guidance literature:: With hydrogen fluoride; methoxybenzene; at 0 ℃; for 0.5h;
DOI:10.1021/jm00346a013

Reference yield:

: trifluoroacetyl-DL-α-aminoadipic acid α-chloride δ-benzyl ester

: 80418-04-8
5-(4-Cyano-phenylcarbamoyl)-5-(2,2,2-trifluoro-acetylamino)-pentanoic acid

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / tetrahydrofuran / 0.5 h / Ambient temperature

2: 32 percent / HF, anisole / 0.5 h / 0 °C

With hydrogen fluoride; methoxybenzene; triethylamine; In tetrahydrofuran;
DOI:10.1021/jm00346a013

Reference yield:

: 2-(2,2,2-Trifluoro-acetylamino)-hexanedioic acid 6-benzyl ester

: 80418-04-8
5-(4-Cyano-phenylcarbamoyl)-5-(2,2,2-trifluoro-acetylamino)-pentanoic acid

Guidance literature:: Multi-step reaction with 3 steps

1: oxalyl chloride / Ambient temperature

2: triethylamine / tetrahydrofuran / 0.5 h / Ambient temperature

3: 32 percent / HF, anisole / 0.5 h / 0 °C

With oxalyl dichloride; hydrogen fluoride; methoxybenzene; triethylamine; In tetrahydrofuran;
DOI:10.1021/jm00346a013