[6-(4-tert-Butyl-benzyl)-3-oxo-1-thioxo-1H-pyrrolo[1,2-c]imidazol-2-yl]-acetic acid ethyl ester

Base Information

Chemical Name:[6-(4-tert-Butyl-benzyl)-3-oxo-1-thioxo-1H-pyrrolo[1,2-c]imidazol-2-yl]-acetic acid ethyl ester
CAS No.:147434-39-7
Molecular Formula:C₂₁H₂₄N₂O₃S
Molecular Weight:384.499
Hs Code.:

Synonyms:[6-(4-tert-Butyl-benzyl)-3-oxo-1-thioxo-1H-pyrrolo[1,2-c]imidazol-2-yl]-acetic acid ethyl ester

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Chemical Property of [6-(4-tert-Butyl-benzyl)-3-oxo-1-thioxo-1H-pyrrolo[1,2-c]imidazol-2-yl]-acetic acid ethyl ester

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Technology Process of [6-(4-tert-Butyl-benzyl)-3-oxo-1-thioxo-1H-pyrrolo[1,2-c]imidazol-2-yl]-acetic acid ethyl ester

There total 7 articles about [6-(4-tert-Butyl-benzyl)-3-oxo-1-thioxo-1H-pyrrolo[1,2-c]imidazol-2-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: 54.0%

: 147434-06-8
[6-(4-tert-Butyl-benzyl)-1,3-dioxo-1H-pyrrolo[1,2-c]imidazol-2-yl]-acetic acid ethyl ester

: 147434-39-7
[6-(4-tert-Butyl-benzyl)-3-oxo-1-thioxo-1H-pyrrolo[1,2-c]imidazol-2-yl]-acetic acid ethyl ester

Guidance literature:: With tetraphosphorus decasulfide; In 1,4-dioxane; for 8h; Heating;
DOI:10.1016/0223-5234(93)90016-8

Reference yield:

: 2199-43-1
ethyl 1H-pyrrole-2-carboxylate

: 147434-39-7
[6-(4-tert-Butyl-benzyl)-3-oxo-1-thioxo-1H-pyrrolo[1,2-c]imidazol-2-yl]-acetic acid ethyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: 31 percent / AlCl₃ / CH₂Cl₂ / 2 h / Heating

2: 70 percent / triethylsilane / trifluoroacetic acid / 16 h / Ambient temperature

3: 90 percent / 2 N aq. NaOH / ethanol / 2 h / Heating

4: 88 percent / diethyl phosphorocyanidate, Et₃N / dimethylformamide / 24 h / Ambient temperature

5: 79 percent / 0.67 h / 150 °C

6: 54 percent / P₂S₅ / dioxane / 8 h / Heating

With triethylsilane; sodium hydroxide; aluminium trichloride; tetraphosphorus decasulfide; diethyl cyanophosphonate; triethylamine; In 1,4-dioxane; ethanol; dichloromethane; N,N-dimethyl-formamide; trifluoroacetic acid;
DOI:10.1016/0223-5234(93)90016-8

Reference yield:

: 147433-62-3
4-(4-tert-Butyl-benzyl)-1H-pyrrole-2-carboxylic acid

: 147434-39-7
[6-(4-tert-Butyl-benzyl)-3-oxo-1-thioxo-1H-pyrrolo[1,2-c]imidazol-2-yl]-acetic acid ethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 88 percent / diethyl phosphorocyanidate, Et₃N / dimethylformamide / 24 h / Ambient temperature

2: 79 percent / 0.67 h / 150 °C

3: 54 percent / P₂S₅ / dioxane / 8 h / Heating

With tetraphosphorus decasulfide; diethyl cyanophosphonate; triethylamine; In 1,4-dioxane; N,N-dimethyl-formamide;
DOI:10.1016/0223-5234(93)90016-8