(1-adamantyl)carbonyloxymethyl 4-(1-hydroxy-1-methylethyl)-2-propyl-1-{4-[2-(1-trityltetrazol-5-yl)phenyl]phenylmethyl}imidazole-5-carboxylate

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Chemical Name:(1-adamantyl)carbonyloxymethyl 4-(1-hydroxy-1-methylethyl)-2-propyl-1-{4-[2-(1-trityltetrazol-5-yl)phenyl]phenylmethyl}imidazole-5-carboxylate
CAS No.:1304676-48-9
Molecular Formula:C₅₅H₅₆N₆O₅
Molecular Weight:881.087
Hs Code.:

(1-adamantyl)carbonyloxymethyl 4-(1-hydroxy-1-methylethyl)-2-propyl-1-{4-[2-(1-trityltetrazol-5-yl)phenyl]phenylmethyl}imidazole-5-carboxylate

Synonyms:(1-adamantyl)carbonyloxymethyl 4-(1-hydroxy-1-methylethyl)-2-propyl-1-{4-[2-(1-trityltetrazol-5-yl)phenyl]phenylmethyl}imidazole-5-carboxylate

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Chemical Property of (1-adamantyl)carbonyloxymethyl 4-(1-hydroxy-1-methylethyl)-2-propyl-1-{4-[2-(1-trityltetrazol-5-yl)phenyl]phenylmethyl}imidazole-5-carboxylate

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Technology Process of (1-adamantyl)carbonyloxymethyl 4-(1-hydroxy-1-methylethyl)-2-propyl-1-{4-[2-(1-trityltetrazol-5-yl)phenyl]phenylmethyl}imidazole-5-carboxylate

There total 4 articles about (1-adamantyl)carbonyloxymethyl 4-(1-hydroxy-1-methylethyl)-2-propyl-1-{4-[2-(1-trityltetrazol-5-yl)phenyl]phenylmethyl}imidazole-5-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: 95.4%

: 761404-85-7
4-(1-hydroxy-1-methylethyl)-2-propyl-1-(4-(2-(1-(triphenylmethyl)tetrazol-5-yl)phenyl)phenyl)methylimidazole-5-carboxylic acid

: 1304676-48-9
(1-adamantyl)carbonyloxymethyl 4-(1-hydroxy-1-methylethyl)-2-propyl-1-{4-[2-(1-trityltetrazol-5-yl)phenyl]phenylmethyl}imidazole-5-carboxylate

Guidance literature:: 4-(1-hydroxy-1-methylethyl)-2-propyl-1-(4-(2-(1-(triphenylmethyl)tetrazol-5-yl)phenyl)phenyl)methylimidazole-5-carboxylic acid; With potassium carbonate; potassium iodide; In N,N-dimethyl acetamide; at 20 ℃; for 0.5h;

(1-adamantyl)carbonyloxymethyl halide; In N,N-dimethyl acetamide; at 70 ℃; for 2h;
DOI:10.1016/j.ejmech.2011.05.019

Reference yield:

: 144690-33-5
ethyl 4-(2-hydroxypropan-2-yl)-2-propyl-1-({2'-[1-(triphenylmethyl)-1H-1,2,3,4-tetrazol-5-yl]-[1,1'-biphenyl]-4-yl}methyl)-1H-imidazole-5-carboxylate

: 1304676-48-9
(1-adamantyl)carbonyloxymethyl 4-(1-hydroxy-1-methylethyl)-2-propyl-1-{4-[2-(1-trityltetrazol-5-yl)phenyl]phenylmethyl}imidazole-5-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1.1: potassium hydroxide / water; isopropyl alcohol / 4 h / 60 °C

2.1: potassium carbonate; potassium iodide / N,N-dimethyl acetamide / 0.5 h / 20 °C

2.2: 2 h / 70 °C

With potassium carbonate; potassium iodide; potassium hydroxide; In N,N-dimethyl acetamide; water; isopropyl alcohol;
DOI:10.1016/j.ejmech.2011.05.019

Reference yield:

: 144689-93-0
ethyl 4-(2-hydroxypropan-2-yl)-2-propyl-1H-imidazole-5-carboxylate

: 1304676-48-9
(1-adamantyl)carbonyloxymethyl 4-(1-hydroxy-1-methylethyl)-2-propyl-1-{4-[2-(1-trityltetrazol-5-yl)phenyl]phenylmethyl}imidazole-5-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1.1: potassium carbonate / N,N-dimethyl acetamide; acetone / 10 h / Reflux

2.1: potassium hydroxide / water; isopropyl alcohol / 4 h / 60 °C

3.1: potassium carbonate; potassium iodide / N,N-dimethyl acetamide / 0.5 h / 20 °C

3.2: 2 h / 70 °C

With potassium carbonate; potassium iodide; potassium hydroxide; In N,N-dimethyl acetamide; water; isopropyl alcohol; acetone;
DOI:10.1016/j.ejmech.2011.05.019