(5-benzyl-3-methyl-2-thioxo-2,3-dihydro-1H-imidazol-4-yl)-acetic acid ethyl ester

Base Information

Chemical Name:(5-benzyl-3-methyl-2-thioxo-2,3-dihydro-1H-imidazol-4-yl)-acetic acid ethyl ester
CAS No.:869113-78-0
Molecular Formula:C₁₅H₁₈N₂O₂S
Molecular Weight:290.386
Hs Code.:

(5-benzyl-3-methyl-2-thioxo-2,3-dihydro-1<i>H</i>-imidazol-4-yl)-acetic acid ethyl ester

Synonyms:(5-benzyl-3-methyl-2-thioxo-2,3-dihydro-1H-imidazol-4-yl)-acetic acid ethyl ester

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Chemical Property of (5-benzyl-3-methyl-2-thioxo-2,3-dihydro-1H-imidazol-4-yl)-acetic acid ethyl ester

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Technology Process of (5-benzyl-3-methyl-2-thioxo-2,3-dihydro-1H-imidazol-4-yl)-acetic acid ethyl ester

There total 3 articles about (5-benzyl-3-methyl-2-thioxo-2,3-dihydro-1H-imidazol-4-yl)-acetic acid ethyl ester 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: 80.0%

: 556-61-6
methyl thioisocyanate

: (S)-4-Amino-3-oxo-5-phenyl-pentanoic acid ethyl ester; hydrochloride

: 869113-78-0
(5-benzyl-3-methyl-2-thioxo-2,3-dihydro-1H-imidazol-4-yl)-acetic acid ethyl ester

Guidance literature:: With triethylamine; In ethanol; for 12h; Heating;
DOI:10.1016/j.tetlet.2005.08.138

Reference yield:

: 13734-34-4
N-tert-butoxycarbonyl-L-phenylalanine

: 869113-78-0
(5-benzyl-3-methyl-2-thioxo-2,3-dihydro-1H-imidazol-4-yl)-acetic acid ethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 95 percent / CDI; MgCl₂

2: 100 percent / HCl (satd.) / ethyl acetate / 1 h / 20 °C

3: 80 percent / triethylamine / ethanol / 12 h / Heating

With hydrogenchloride; triethylamine; 1,1'-carbonyldiimidazole; magnesium chloride; In ethanol; ethyl acetate;
DOI:10.1016/j.tetlet.2005.08.138

Reference yield:

: 112271-08-6
(4S)-40<(tertibutyloxycarbonyl)amino>-3-oxo-5-phenylpentanoic acid ethyl ester

: 869113-78-0
(5-benzyl-3-methyl-2-thioxo-2,3-dihydro-1H-imidazol-4-yl)-acetic acid ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 100 percent / HCl (satd.) / ethyl acetate / 1 h / 20 °C

2: 80 percent / triethylamine / ethanol / 12 h / Heating

With hydrogenchloride; triethylamine; In ethanol; ethyl acetate;
DOI:10.1016/j.tetlet.2005.08.138