2-[2-({3-[(E)-2-(7-Chloro-quinolin-2-yl)-vinyl]-phenylamino}-methyl)-phenoxy]-propionic acid ethyl ester

Base Information

Chemical Name:2-[2-({3-[(E)-2-(7-Chloro-quinolin-2-yl)-vinyl]-phenylamino}-methyl)-phenoxy]-propionic acid ethyl ester
CAS No.:188699-80-1
Molecular Formula:C₂₉H₂₇ClN₂O₃
Molecular Weight:486.998
Hs Code.:

Synonyms:2-[2-({3-[(E)-2-(7-Chloro-quinolin-2-yl)-vinyl]-phenylamino}-methyl)-phenoxy]-propionic acid ethyl ester

Suppliers and Price of 2-[2-({3-[(E)-2-(7-Chloro-quinolin-2-yl)-vinyl]-phenylamino}-methyl)-phenoxy]-propionic acid ethyl ester

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

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Chemical Property of 2-[2-({3-[(E)-2-(7-Chloro-quinolin-2-yl)-vinyl]-phenylamino}-methyl)-phenoxy]-propionic acid ethyl ester

Chemical Property:

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

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Technology Process of 2-[2-({3-[(E)-2-(7-Chloro-quinolin-2-yl)-vinyl]-phenylamino}-methyl)-phenoxy]-propionic acid ethyl ester

There total 6 articles about 2-[2-({3-[(E)-2-(7-Chloro-quinolin-2-yl)-vinyl]-phenylamino}-methyl)-phenoxy]-propionic acid ethyl ester 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:

: 4965-33-7
2-methyl-7-chloroquinoline

: 188699-80-1
2-[2-({3-[(E)-2-(7-Chloro-quinolin-2-yl)-vinyl]-phenylamino}-methyl)-phenoxy]-propionic acid ethyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 78 percent / Ac₂O / 4.5 h / 130 °C

2: 94 percent / SnCl₂, HCl, AcOH / 1 h / 80 °C

3: diethyl ether / 2.5 h / Ambient temperature

4: NaBH₄, AcOH / ethanol / 12 h / Ambient temperature

5: K₂CO₃ / acetone / 40 h

With hydrogenchloride; sodium tetrahydroborate; acetic anhydride; potassium carbonate; acetic acid; tin(ll) chloride; In diethyl ether; ethanol; acetone;
DOI:10.1016/S0968-0896(96)00253-2

Reference yield:

: 99-61-6
3-nitro-benzaldehyde

: 188699-80-1
2-[2-({3-[(E)-2-(7-Chloro-quinolin-2-yl)-vinyl]-phenylamino}-methyl)-phenoxy]-propionic acid ethyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 78 percent / Ac₂O / 4.5 h / 130 °C

2: 94 percent / SnCl₂, HCl, AcOH / 1 h / 80 °C

3: diethyl ether / 2.5 h / Ambient temperature

4: NaBH₄, AcOH / ethanol / 12 h / Ambient temperature

5: K₂CO₃ / acetone / 40 h

With hydrogenchloride; sodium tetrahydroborate; acetic anhydride; potassium carbonate; acetic acid; tin(ll) chloride; In diethyl ether; ethanol; acetone;
DOI:10.1016/S0968-0896(96)00253-2

Reference yield:

: 158546-57-7
(E)-3-(2-(7-chloroquinolin-2-yl)vinyl)aniline

: 188699-80-1
2-[2-({3-[(E)-2-(7-Chloro-quinolin-2-yl)-vinyl]-phenylamino}-methyl)-phenoxy]-propionic acid ethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: diethyl ether / 2.5 h / Ambient temperature

2: NaBH₄, AcOH / ethanol / 12 h / Ambient temperature

3: K₂CO₃ / acetone / 40 h

With sodium tetrahydroborate; potassium carbonate; acetic acid; In diethyl ether; ethanol; acetone;
DOI:10.1016/S0968-0896(96)00253-2