3-{4-[(5-carbamimidoyl-benzofuran-2-carbonyl)-amino]-cyclohexyl}-propionic acid ethyl ester

Base Information

Chemical Name:3-{4-[(5-carbamimidoyl-benzofuran-2-carbonyl)-amino]-cyclohexyl}-propionic acid ethyl ester
CAS No.:789467-79-4
Molecular Formula:C₂₁H₂₇N₃O₄
Molecular Weight:385.463
Hs Code.:

Synonyms:3-{4-[(5-carbamimidoyl-benzofuran-2-carbonyl)-amino]-cyclohexyl}-propionic acid ethyl ester

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Chemical Property of 3-{4-[(5-carbamimidoyl-benzofuran-2-carbonyl)-amino]-cyclohexyl}-propionic acid ethyl ester

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Technology Process of 3-{4-[(5-carbamimidoyl-benzofuran-2-carbonyl)-amino]-cyclohexyl}-propionic acid ethyl ester

There total 5 articles about 3-{4-[(5-carbamimidoyl-benzofuran-2-carbonyl)-amino]-cyclohexyl}-propionic 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: 94.0%

: 174773-83-2
ethyl trans-3-[4-[5-(benzyloxycarbonylamidino)benzofuran-2-carboxamido]cyclohexyl]propionate

: 789467-79-4
3-{4-[(5-carbamimidoyl-benzofuran-2-carbonyl)-amino]-cyclohexyl}-propionic acid ethyl ester

Guidance literature:: With hydrogenchloride; hydrogen; palladium on activated charcoal; In ethanol; chloroform; at 20 ℃; for 14h;
DOI:10.1248/cpb.47.1694

Reference yield:

: 84102-75-0
5-cyanobenzo[b]furan-2-carboxylic acid

: 789467-79-4
3-{4-[(5-carbamimidoyl-benzofuran-2-carbonyl)-amino]-cyclohexyl}-propionic acid ethyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: HCl

2: NH₃ / ethanol

3: aq. NaOH / tetrahydrofuran

4: 76 percent / HOBt; EDI / dimethylformamide / 18 h / 20 °C

5: 94 percent / HCl; H₂ / 10 percent Pd/C / CHCl₃; ethanol / 14 h / 20 °C

With hydrogenchloride; sodium hydroxide; ammonia; hydrogen; benzotriazol-1-ol; palladium on activated charcoal; In tetrahydrofuran; ethanol; chloroform; N,N-dimethyl-formamide; 1: Pinner reaction / 2: aminolysis / 3: Acylation / 4: coupling / 5: Hydrogenolysis;
DOI:10.1248/cpb.47.1694

Reference yield:

: 174774-65-3
5-(benzyloxycarbonylamidino)-2-benzofurancarboxylic acid

: 789467-79-4
3-{4-[(5-carbamimidoyl-benzofuran-2-carbonyl)-amino]-cyclohexyl}-propionic acid ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 76 percent / HOBt; EDI / dimethylformamide / 18 h / 20 °C

2: 94 percent / HCl; H₂ / 10 percent Pd/C / CHCl₃; ethanol / 14 h / 20 °C

With hydrogenchloride; hydrogen; benzotriazol-1-ol; palladium on activated charcoal; In ethanol; chloroform; N,N-dimethyl-formamide; 1: coupling / 2: Hydrogenolysis;
DOI:10.1248/cpb.47.1694