ethyl{1-[2-(4-chlorophenyl)-2-oxo-ethylsulfanyl]-3-(4-methoxyphenyl)-3-oxo-propenylamino}acetate

Base Information

• Chemical Name: ethyl{1-[2-(4-chlorophenyl)-2-oxo-ethylsulfanyl]-3-(4-methoxyphenyl)-3-oxo-propenylamino}acetate
• CAS No.: 1228006-64-1
• Molecular Formula: C₂₂H₂₂ClNO₅S
• Molecular Weight: 447.939

Synonyms:ethyl{1-[2-(4-chlorophenyl)-2-oxo-ethylsulfanyl]-3-(4-methoxyphenyl)-3-oxo-propenylamino}acetate

Chemical Property of ethyl{1-[2-(4-chlorophenyl)-2-oxo-ethylsulfanyl]-3-(4-methoxyphenyl)-3-oxo-propenylamino}acetate

Chemical Property:

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Technology Process of ethyl{1-[2-(4-chlorophenyl)-2-oxo-ethylsulfanyl]-3-(4-methoxyphenyl)-3-oxo-propenylamino}acetate

There total 1 articles about ethyl{1-[2-(4-chlorophenyl)-2-oxo-ethylsulfanyl]-3-(4-methoxyphenyl)-3-oxo-propenylamino}acetate 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: 88.0%

ethyl 2-{[3-(4-methoxyphenyl)-3-oxopropanthioyl]amino}acetate (881891-99-2) + 4-chlorobenzoylmethyl bromide (536-38-9) → ethyl{1-[2-(4-chlorophenyl)-2-oxo-ethylsulfanyl]-3-(4-methoxyphenyl)-3-oxo-propenylamino}acetate (1228006-64-1)

Guidance literature:

ethyl 2-{[3-(4-methoxyphenyl)-3-oxopropanthioyl]amino}acetate; With potassium carbonate; In acetone; for 0.5h; Reflux;

4-chlorobenzoylmethyl bromide; In acetone; at 20 ℃; for 4h;

DOI:10.1002/jhet.334

Reference yield: 85.0%

ethyl{1-[2-(4-chlorophenyl)-2-oxo-ethylsulfanyl]-3-(4-methoxyphenyl)-3-oxo-propenylamino}acetate (1228006-64-1) → 3-(4-chloro-phenyl)-7-(4-methoxy-benzoyl)pyrrolo[2,1-b]thiazol-6-one (1228006-79-8)

Guidance literature:

With acetic acid; at 150 ℃; for 0.25h; regioselective reaction; Microwave irradiation;

DOI:10.1002/jhet.334

upstream raw materials:

ethyl 2-{[3-(4-methoxyphenyl)-3-oxopropanthioyl]amino}acetate

4-chlorobenzoylmethyl bromide

Downstream raw materials:

3-(4-chloro-phenyl)-7-(4-methoxy-benzoyl)pyrrolo[2,1-b]thiazol-6-one

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