(+/-) ethyl 2-[(3-{4-chlorophenylsulfonylamino}-1-{3-[(E)-2-(7-chloro-2-quinolyl)vinyl]phenyl}propyl)thio]acetate

Base Information

Chemical Name:(+/-) ethyl 2-[(3-{4-chlorophenylsulfonylamino}-1-{3-[(E)-2-(7-chloro-2-quinolyl)vinyl]phenyl}propyl)thio]acetate
CAS No.:904916-18-3
Molecular Formula:C₃₀H₂₈Cl₂N₂O₄S₂
Molecular Weight:615.601
Hs Code.:

Synonyms:(+/-) ethyl 2-[(3-{4-chlorophenylsulfonylamino}-1-{3-[(E)-2-(7-chloro-2-quinolyl)vinyl]phenyl}propyl)thio]acetate

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Chemical Property of (+/-) ethyl 2-[(3-{4-chlorophenylsulfonylamino}-1-{3-[(E)-2-(7-chloro-2-quinolyl)vinyl]phenyl}propyl)thio]acetate

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Technology Process of (+/-) ethyl 2-[(3-{4-chlorophenylsulfonylamino}-1-{3-[(E)-2-(7-chloro-2-quinolyl)vinyl]phenyl}propyl)thio]acetate

There total 6 articles about (+/-) ethyl 2-[(3-{4-chlorophenylsulfonylamino}-1-{3-[(E)-2-(7-chloro-2-quinolyl)vinyl]phenyl}propyl)thio]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: 82.0%

: 904916-17-2
(+/-)-4-chloro-N-(3-chloro-3-{3-[(E)-2-(7-chloro-2-quinolyl)vinyl]phenyl}propyl)benzenesulfonamide

: 623-51-8
ethyl 2-sulfanylacetate

: 904916-18-3
(+/-) ethyl 2-[(3-{4-chlorophenylsulfonylamino}-1-{3-[(E)-2-(7-chloro-2-quinolyl)vinyl]phenyl}propyl)thio]acetate

Guidance literature:: With N,N'-dimethylimidazolinone; caesium carbonate; at 40 ℃; for 12h;
DOI:10.1248/cpb.54.603

Reference yield:

: 203940-08-3
1-{3-[(E)-2-(7-chloro-2-quinolyl)vinyl]phenyl}propenone

: 904916-18-3
(+/-) ethyl 2-[(3-{4-chlorophenylsulfonylamino}-1-{3-[(E)-2-(7-chloro-2-quinolyl)vinyl]phenyl}propyl)thio]acetate

Guidance literature:: Multi-step reaction with 4 steps

1: 58 percent / potassium tert-butoxide / dioxane; benzene / 10 h / 80 °C

2: 90 percent / sodium borohydride / tetrahydrofuran; ethanol / 1 h / 20 °C

3: 100 percent / thionyl chloride / 1,2-dichloro-ethane / 5 h / 20 °C

4: 82 percent / cesium carbonate; N,N'-dimethylimidazolinone / 12 h / 40 °C

With sodium tetrahydroborate; thionyl chloride; N,N'-dimethylimidazolinone; potassium tert-butylate; caesium carbonate; In tetrahydrofuran; 1,4-dioxane; ethanol; 1,2-dichloro-ethane; benzene; 1: Michael addition;
DOI:10.1248/cpb.54.603

Reference yield:

: 203940-38-9
(+/-)-4-chloro-N-(3-{3-[(E)-2-(7-chloro-2-quinolyl)vinyl]phenyl}-3-hydroxypropyl)benzenesulfonamide

: 904916-18-3
(+/-) ethyl 2-[(3-{4-chlorophenylsulfonylamino}-1-{3-[(E)-2-(7-chloro-2-quinolyl)vinyl]phenyl}propyl)thio]acetate

Guidance literature:: Multi-step reaction with 2 steps

1: 100 percent / thionyl chloride / 1,2-dichloro-ethane / 5 h / 20 °C

2: 82 percent / cesium carbonate; N,N'-dimethylimidazolinone / 12 h / 40 °C

With thionyl chloride; N,N'-dimethylimidazolinone; caesium carbonate; In 1,2-dichloro-ethane;
DOI:10.1248/cpb.54.603