(2S,4S)-tert-butyl 2-(5-(4-bromophenyl)-1H-imidazol-2-yl)-4-(methylthio)pyrrolidine-1-carboxylate

Base Information

Chemical Name:(2S,4S)-tert-butyl 2-(5-(4-bromophenyl)-1H-imidazol-2-yl)-4-(methylthio)pyrrolidine-1-carboxylate
CAS No.:1373164-85-2
Molecular Formula:C₁₉H₂₄BrN₃O₂S
Molecular Weight:438.388
Hs Code.:

Synonyms:(2S,4S)-tert-butyl 2-(5-(4-bromophenyl)-1H-imidazol-2-yl)-4-(methylthio)pyrrolidine-1-carboxylate

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Chemical Property of (2S,4S)-tert-butyl 2-(5-(4-bromophenyl)-1H-imidazol-2-yl)-4-(methylthio)pyrrolidine-1-carboxylate

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Technology Process of (2S,4S)-tert-butyl 2-(5-(4-bromophenyl)-1H-imidazol-2-yl)-4-(methylthio)pyrrolidine-1-carboxylate

There total 8 articles about (2S,4S)-tert-butyl 2-(5-(4-bromophenyl)-1H-imidazol-2-yl)-4-(methylthio)pyrrolidine-1-carboxylate 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: 98.0%

: C₁₉H₂₄BrNO₅S

: 1373164-85-2
(2S,4S)-2-[4-(4-bromo-phenyl)-1H-imidazol-2-yl]-4-methylsulfanyl-pyrrolidine-1-carboxylic acid tert-butyl ester

Guidance literature:: With ammonium acetate; In toluene; at 100 ℃;

Reference yield:

: C₁₉H₂₄BrNO₅S

: 1373164-85-2
(2S,4S)-tert-butyl 2-(5-(4-bromophenyl)-1H-imidazol-2-yl)-4-(methylthio)pyrrolidine-1-carboxylate

Guidance literature:: With ammonium acetate; In toluene; at 110 ℃;

Reference yield:

: 74844-91-0
1-tert-butyl 2-methyl (2S,4R)-4-hydroxy-1,2-pyrrolidinedicarboxylate

: 1373164-85-2
(2S,4S)-tert-butyl 2-(5-(4-bromophenyl)-1H-imidazol-2-yl)-4-(methylthio)pyrrolidine-1-carboxylate

Guidance literature:: Multi-step reaction with 5 steps

1: pyridine / 0 - 20 °C

2: N,N-dimethyl-formamide / 20 °C

3: lithium hydroxide; water / methanol / 20 °C

4: N-ethyl-N,N-diisopropylamine / acetonitrile / 18 h / 20 °C

5: ammonium acetate / toluene / 110 °C

With pyridine; ammonium acetate; water; N-ethyl-N,N-diisopropylamine; lithium hydroxide; In methanol; N,N-dimethyl-formamide; toluene; acetonitrile;