3-{[5-(Adamantan-1-yloxymethyl)-2-cyclohexyl-1H-imidazole-4-carbonyl]-amino}-benzoic Acid Benzyl Ester

Base Information

Chemical Name:3-{[5-(Adamantan-1-yloxymethyl)-2-cyclohexyl-1H-imidazole-4-carbonyl]-amino}-benzoic Acid Benzyl Ester
CAS No.:269071-43-4
Molecular Formula:C₃₅H₄₁N₃O₄
Molecular Weight:567.728
Hs Code.:

Synonyms:3-{[5-(Adamantan-1-yloxymethyl)-2-cyclohexyl-1H-imidazole-4-carbonyl]-amino}-benzoic Acid Benzyl Ester

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Chemical Property of 3-{[5-(Adamantan-1-yloxymethyl)-2-cyclohexyl-1H-imidazole-4-carbonyl]-amino}-benzoic Acid Benzyl Ester

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Technology Process of 3-{[5-(Adamantan-1-yloxymethyl)-2-cyclohexyl-1H-imidazole-4-carbonyl]-amino}-benzoic Acid Benzyl Ester

There total 7 articles about 3-{[5-(Adamantan-1-yloxymethyl)-2-cyclohexyl-1H-imidazole-4-carbonyl]-amino}-benzoic Acid Benzyl 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: 65.5%

: 269071-42-3
5-(Adamantan-1-yloxymethyl)-2-cyclohexyl-1H-imidazole-4-carboxylic Acid

: 80787-43-5
3-aminobenzoic acid benzyl ester

: 269071-43-4
3-{[5-(Adamantan-1-yloxymethyl)-2-cyclohexyl-1H-imidazole-4-carbonyl]-amino}-benzoic Acid Benzyl Ester

Guidance literature:: In ethyl acetate;

Reference yield: 65.5%

: 269071-41-2
5-(Adamantan-1-yl-oxymethyl)-2-cyclohexyl-1H-imidazole-4-carboxylic acid benzyl ester

: 80787-43-5
3-aminobenzoic acid benzyl ester

: 269071-43-4
3-{[5-(Adamantan-1-yloxymethyl)-2-cyclohexyl-1H-imidazole-4-carbonyl]-amino}-benzoic Acid Benzyl Ester

Guidance literature:: In ethyl acetate;

Reference yield:

: (adamantan-1-yloxy)-acetyl chloride

: 269071-43-4
3-{[5-(Adamantan-1-yloxymethyl)-2-cyclohexyl-1H-imidazole-4-carbonyl]-amino}-benzoic Acid Benzyl Ester

Guidance literature:: Multi-step reaction with 5 steps

1: 105.6 g / N,O-trimethylsilylacetamide / benzene / 16 h / 20 °C

2: 80 percent / OXONE; (C₄H₉)4NBr / CH₂Cl₂ / 48 h / 20 °C

3: NH₄OAc; AcOH / 2 h / 70 °C

4: H₂ / Pd/C / tetrahydrofuran; methanol

5: 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride; 4-(dimethylamino)pyridine; 1-hydroxybenzotriazole / dimethylformamide / 72 h / 20 °C

With dmap; Oxone; N,O-bis-(trimethylsilyl)-acetamide; ammonium acetate; tetrabutylammomium bromide; hydrogen; benzotriazol-1-ol; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide; benzene;
DOI:10.1021/jm0490686