methyl 2-((2,6-dichlorophenyl)amino)-7,7-dimethyl-7,8-dihydro-1H-benzofuro[4,5-d]imidazole-5-carboxylate

Base Information

Chemical Name:methyl 2-((2,6-dichlorophenyl)amino)-7,7-dimethyl-7,8-dihydro-1H-benzofuro[4,5-d]imidazole-5-carboxylate
CAS No.:1374298-22-2
Molecular Formula:C₁₉H₁₇Cl₂N₃O₃
Molecular Weight:406.268
Hs Code.:

Synonyms:methyl 2-((2,6-dichlorophenyl)amino)-7,7-dimethyl-7,8-dihydro-1H-benzofuro[4,5-d]imidazole-5-carboxylate

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Chemical Property of methyl 2-((2,6-dichlorophenyl)amino)-7,7-dimethyl-7,8-dihydro-1H-benzofuro[4,5-d]imidazole-5-carboxylate

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Technology Process of methyl 2-((2,6-dichlorophenyl)amino)-7,7-dimethyl-7,8-dihydro-1H-benzofuro[4,5-d]imidazole-5-carboxylate

There total 6 articles about methyl 2-((2,6-dichlorophenyl)amino)-7,7-dimethyl-7,8-dihydro-1H-benzofuro[4,5-d]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: 55.0%

: 1374298-19-7
methyl 4, 5-diamino-2,2-dimethyl-2,3-dihydrobenzofuran-7-carboxylate

: 6590-95-0
2,6-dichlorophenylisothiocyanate

: 1374298-22-2
methyl 2-((2,6-dichlorophenyl)amino)-7,7-dimethyl-7,8-dihydro-1H-benzofuro[4,5-d]imidazole-5-carboxylate

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In acetonitrile; at 20 ℃; for 24h;
DOI:10.1016/j.bmcl.2017.10.062

Reference yield:

: 65-49-6
4-Aminosalicylic acid

: 1374298-22-2
methyl 2-((2,6-dichlorophenyl)amino)-7,7-dimethyl-7,8-dihydro-1H-benzofuro[4,5-d]imidazole-5-carboxylate

Guidance literature:: Multi-step reaction with 7 steps

1.1: ethanol / Reflux

2.1: sodium nitrite; trifluoroacetic acid / 2 h / -5 - 0 °C

3.1: sulfuric acid / Reflux

4.1: potassium carbonate / N,N-dimethyl-formamide / 0.5 h / 80 °C

4.2: 9 h / 80 °C

5.1: aluminum (III) chloride / dichloromethane / 18 h / -70 - 20 °C

6.1: iron; hydrogenchloride / water; methanol / 2 h / 0 - 20 °C

7.1: N-ethyl-N,N-diisopropylamine / acetonitrile / 24 h / 20 °C

With hydrogenchloride; aluminum (III) chloride; sulfuric acid; iron; potassium carbonate; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; sodium nitrite; In methanol; ethanol; dichloromethane; water; N,N-dimethyl-formamide; acetonitrile; 5.1: |Claisen Rearrangement;
DOI:10.1016/j.bmcl.2017.10.062

Reference yield:

: 1374298-18-6
methyl 4-amino-2,2-dimethyl-5-nitro-2,3-dihydrobenzofuran-7-carboxylate

: 1374298-22-2
methyl 2-((2,6-dichlorophenyl)amino)-7,7-dimethyl-7,8-dihydro-1H-benzofuro[4,5-d]imidazole-5-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: iron; hydrogenchloride / water; methanol / 2 h / 0 - 20 °C

2: N-ethyl-N,N-diisopropylamine / acetonitrile / 24 h / 20 °C

With hydrogenchloride; iron; N-ethyl-N,N-diisopropylamine; In methanol; water; acetonitrile;
DOI:10.1016/j.bmcl.2017.10.062