2-((2-chloro-6-fluorophenyl)amino)-1,7,7-trimethyl-7,8-dihydro-1H-benzofuro-[4,5-d]imidazole-5-carboxylic acid

Base Information

Chemical Name:2-((2-chloro-6-fluorophenyl)amino)-1,7,7-trimethyl-7,8-dihydro-1H-benzofuro-[4,5-d]imidazole-5-carboxylic acid
CAS No.:1374298-71-1
Molecular Formula:C₁₉H₁₇ClFN₃O₃
Molecular Weight:389.814
Hs Code.:

Synonyms:2-((2-chloro-6-fluorophenyl)amino)-1,7,7-trimethyl-7,8-dihydro-1H-benzofuro-[4,5-d]imidazole-5-carboxylic acid

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Chemical Property of 2-((2-chloro-6-fluorophenyl)amino)-1,7,7-trimethyl-7,8-dihydro-1H-benzofuro-[4,5-d]imidazole-5-carboxylic acid

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Technology Process of 2-((2-chloro-6-fluorophenyl)amino)-1,7,7-trimethyl-7,8-dihydro-1H-benzofuro-[4,5-d]imidazole-5-carboxylic acid

There total 9 articles about 2-((2-chloro-6-fluorophenyl)amino)-1,7,7-trimethyl-7,8-dihydro-1H-benzofuro-[4,5-d]imidazole-5-carboxylic acid 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: 70.0%

: 1374298-75-5
methyl 2-((2-chloro-6-fluorophenyl)amino)-1,7,7-trimethyl-7,8-dihydro-1H-benzofuro[4,5-d]imidazole-5-carboxylate

: 1374298-71-1
2-((2-chloro-6-fluorophenyl)amino)-1,7,7-trimethyl-7,8-dihydro-1H-benzofuro-[4,5-d]imidazole-5-carboxylic acid

Guidance literature:: With sodium hydroxide; In water; at 20 - 60 ℃;
DOI:10.1016/j.bmcl.2018.02.048

Reference yield:

: 65-49-6
4-Aminosalicylic acid

: 1374298-71-1
2-((2-chloro-6-fluorophenyl)amino)-1,7,7-trimethyl-7,8-dihydro-1H-benzofuro-[4,5-d]imidazole-5-carboxylic acid

Guidance literature:: Multi-step reaction with 8 steps

1.1: ethanol / Reflux

1.2: 2 h / -5 - 0 °C

2.1: sulfuric acid / Reflux

3.1: potassium carbonate / N,N-dimethyl-formamide / 3 h / 80 °C

4.1: N,N-dimethyl-aniline / 1.5 h / Reflux

4.2: 100 °C

5.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 3 h / 0 - 20 °C

6.1: iron / methanol / 0 °C

6.2: 2 h / 20 °C

7.1: acetonitrile / 24 h / 20 °C

7.2: 20 °C

8.1: sodium hydroxide / water / 20 - 60 °C

With sulfuric acid; iron; sodium hydride; potassium carbonate; N,N-dimethyl-aniline; sodium hydroxide; In methanol; ethanol; water; N,N-dimethyl-formamide; acetonitrile; mineral oil;
DOI:10.1016/j.bmcl.2018.02.048

Reference yield:

: 106125-55-7
methyl 4-amino-2-hydroxy-5-nitrobenzoate

: 1374298-71-1
2-((2-chloro-6-fluorophenyl)amino)-1,7,7-trimethyl-7,8-dihydro-1H-benzofuro-[4,5-d]imidazole-5-carboxylic acid

Guidance literature:: Multi-step reaction with 6 steps

1.1: potassium carbonate / N,N-dimethyl-formamide / 3 h / 80 °C

2.1: N,N-dimethyl-aniline / 1.5 h / Reflux

2.2: 100 °C

3.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 3 h / 0 - 20 °C

4.1: iron / methanol / 0 °C

4.2: 2 h / 20 °C

5.1: acetonitrile / 24 h / 20 °C

5.2: 20 °C

6.1: sodium hydroxide / water / 20 - 60 °C

With iron; sodium hydride; potassium carbonate; N,N-dimethyl-aniline; sodium hydroxide; In methanol; water; N,N-dimethyl-formamide; acetonitrile; mineral oil;
DOI:10.1016/j.bmcl.2018.02.048