ethyl 3-(cyclopropylamino)-2-[(2-fluoro-5-iodophenyl)-carbonyl]-2-propenoate

Base Information

Chemical Name:ethyl 3-(cyclopropylamino)-2-[(2-fluoro-5-iodophenyl)-carbonyl]-2-propenoate
CAS No.:1253591-44-4
Molecular Formula:C₁₅H₁₅FINO₃
Molecular Weight:403.192
Hs Code.:

Synonyms:ethyl 3-(cyclopropylamino)-2-[(2-fluoro-5-iodophenyl)-carbonyl]-2-propenoate

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Chemical Property of ethyl 3-(cyclopropylamino)-2-[(2-fluoro-5-iodophenyl)-carbonyl]-2-propenoate

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Technology Process of ethyl 3-(cyclopropylamino)-2-[(2-fluoro-5-iodophenyl)-carbonyl]-2-propenoate

There total 3 articles about ethyl 3-(cyclopropylamino)-2-[(2-fluoro-5-iodophenyl)-carbonyl]-2-propenoate 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: 78.31%

: 697762-43-9
ethyl 3-(dimethylamino)-2-[(2-fluoro-5-iodophenyl)carbonyl]-2-propenoate

: 765-30-0
Cyclopropylamine

: 1253591-44-4
ethyl 3-(cyclopropylamino)-2-[(2-fluoro-5-iodophenyl)-carbonyl]-2-propenoate

Guidance literature:: In tetrahydrofuran; ethanol; at 20 ℃;

Reference yield:

: 124700-41-0
2-fluoro-5-iodobenzoic acid

: 1253591-44-4
ethyl 3-(cyclopropylamino)-2-[(2-fluoro-5-iodophenyl)-carbonyl]-2-propenoate

Guidance literature:: Multi-step reaction with 3 steps

1: thionyl chloride / Reflux

2: triethylamine / toluene / Reflux

3: ethanol; diethyl ether / 20 °C

With thionyl chloride; triethylamine; In diethyl ether; ethanol; toluene;
DOI:10.1016/j.bmc.2014.05.028

Reference yield:

: 186584-73-6
2-fluoro-5-iodobenzoyl chloride

: 1253591-44-4
ethyl 3-(cyclopropylamino)-2-[(2-fluoro-5-iodophenyl)-carbonyl]-2-propenoate

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / toluene / Reflux

2: ethanol; diethyl ether / 20 °C

With triethylamine; In diethyl ether; ethanol; toluene;
DOI:10.1016/j.bmc.2014.05.028