methyl 7-fluoro-6-iodo-1-methyl-4-oxo-2-phenyl-1,4-dihydroquinoline-3-carboxylate

Base Information

Chemical Name:methyl 7-fluoro-6-iodo-1-methyl-4-oxo-2-phenyl-1,4-dihydroquinoline-3-carboxylate
CAS No.:1439356-57-6
Molecular Formula:C₁₈H₁₃FINO₃
Molecular Weight:437.209
Hs Code.:

Synonyms:methyl 7-fluoro-6-iodo-1-methyl-4-oxo-2-phenyl-1,4-dihydroquinoline-3-carboxylate

Suppliers and Price of methyl 7-fluoro-6-iodo-1-methyl-4-oxo-2-phenyl-1,4-dihydroquinoline-3-carboxylate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Total 1 raw suppliers

Chemical Property of methyl 7-fluoro-6-iodo-1-methyl-4-oxo-2-phenyl-1,4-dihydroquinoline-3-carboxylate

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of methyl 7-fluoro-6-iodo-1-methyl-4-oxo-2-phenyl-1,4-dihydroquinoline-3-carboxylate

There total 5 articles about methyl 7-fluoro-6-iodo-1-methyl-4-oxo-2-phenyl-1,4-dihydroquinoline-3-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: 64.0%

: 1449290-97-4
C₁₀H₇F₂IO₃

: 21737-87-1
N-methyl benzimidoyl chloride

: 1439356-57-6
methyl 7-fluoro-6-iodo-1-methyl-4-oxo-2-phenyl-1,4-dihydroquinoline-3-carboxylate

Guidance literature:: C₁₀H₇F₂IO₃; N-methyl benzimidoyl chloride; With potassium carbonate; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 0 ℃; for 1h;

In N,N-dimethyl-formamide; at 110 ℃; for 1h;
DOI:10.1039/c3cc41690a

Reference yield:

: 161531-51-7
2,4-difluoro-5-iodobenzoic acid

: 1439356-57-6
methyl 7-fluoro-6-iodo-1-methyl-4-oxo-2-phenyl-1,4-dihydroquinoline-3-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1.1: thionyl chloride / 2 h / Reflux

2.1: triethylamine; magnesium chloride / acetonitrile / 10 - 50 °C / Inert atmosphere

2.2: 0 - 70 °C / Inert atmosphere

2.3: pH 5 - 6

3.1: potassium carbonate; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 1 h / 0 °C

3.2: 1 h / 110 °C

With thionyl chloride; potassium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; magnesium chloride; In N,N-dimethyl-formamide; acetonitrile;
DOI:10.1039/c3cc41690a

Reference yield:

: 2,4-difluoro-5-iodobenzoyl chloride

: 1439356-57-6
methyl 7-fluoro-6-iodo-1-methyl-4-oxo-2-phenyl-1,4-dihydroquinoline-3-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1.1: triethylamine; magnesium chloride / acetonitrile / 10 - 50 °C / Inert atmosphere

1.2: 0 - 70 °C / Inert atmosphere

1.3: pH 5 - 6

2.1: potassium carbonate; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 1 h / 0 °C

2.2: 1 h / 110 °C

With potassium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; magnesium chloride; In N,N-dimethyl-formamide; acetonitrile;
DOI:10.1039/c3cc41690a