3-phenyl-3-[4-[2-(5,6,7,8-tetrahydro[1,8]naphthyridin-2-yl)ethyl]indol-1-yl]propionic acid ethyl ester

Base Information

Chemical Name:3-phenyl-3-[4-[2-(5,6,7,8-tetrahydro[1,8]naphthyridin-2-yl)ethyl]indol-1-yl]propionic acid ethyl ester
CAS No.:912270-34-9
Molecular Formula:C₂₉H₃₁N₃O₂
Molecular Weight:453.584
Hs Code.:

Synonyms:3-phenyl-3-[4-[2-(5,6,7,8-tetrahydro[1,8]naphthyridin-2-yl)ethyl]indol-1-yl]propionic acid ethyl ester

Suppliers and Price of 3-phenyl-3-[4-[2-(5,6,7,8-tetrahydro[1,8]naphthyridin-2-yl)ethyl]indol-1-yl]propionic acid ethyl ester

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 3-phenyl-3-[4-[2-(5,6,7,8-tetrahydro[1,8]naphthyridin-2-yl)ethyl]indol-1-yl]propionic acid ethyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 3-phenyl-3-[4-[2-(5,6,7,8-tetrahydro[1,8]naphthyridin-2-yl)ethyl]indol-1-yl]propionic acid ethyl ester

There total 6 articles about 3-phenyl-3-[4-[2-(5,6,7,8-tetrahydro[1,8]naphthyridin-2-yl)ethyl]indol-1-yl]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: 48.0%

: 912270-33-8
7-[2-[1-(2-ethoxycarbonyl-1-phenylethyl)-1H-indol-4-yl]ethyl]-3,4-dihydro-2H-[1,8]naphthyridine-1-carboxylic acid tert-butyl ester

: 912270-34-9
3-phenyl-3-[4-[2-(5,6,7,8-tetrahydro[1,8]naphthyridin-2-yl)ethyl]indol-1-yl]propionic acid ethyl ester

Guidance literature:: With copper(II) bis(trifluoromethanesulfonate); In N,N-dimethyl-formamide; toluene; at 130 ℃; for 0.277778h; microwave irradiation;
DOI:10.1016/j.ejmech.2006.10.015

Reference yield:

: 912270-31-6
7-[2-(1H-indol-4-yl)vinyl]-3,4-dihydro-2H-[1,8]naphthyridine-1-carboxylic acid tert-butyl ester

: 912270-34-9
3-phenyl-3-[4-[2-(5,6,7,8-tetrahydro[1,8]naphthyridin-2-yl)ethyl]indol-1-yl]propionic acid ethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 58 percent / cesium carbonate / dimethylformamide / 1.5 h / 75 °C

2: 98 percent / H₂ / Pd-C / methanol / 20 h / 20 °C

3: 48 percent / copper(II) trifluoromethanesulfonate / toluene; dimethylformamide / 0.28 h / 130 °C / microwave irradiation

With hydrogen; copper(II) bis(trifluoromethanesulfonate); caesium carbonate; palladium on activated charcoal; In methanol; N,N-dimethyl-formamide; toluene;
DOI:10.1016/j.ejmech.2006.10.015

Reference yield:

: 912270-29-2
7-(2-iodoethyl)-3,4-dihydro-2H-[1,8]naphthyridine-1-carboxylic acid tert-butyl ester

: 912270-34-9
3-phenyl-3-[4-[2-(5,6,7,8-tetrahydro[1,8]naphthyridin-2-yl)ethyl]indol-1-yl]propionic acid ethyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 53 percent / potassium tert-butoxide / tetrahydrofuran / -78 - 20 °C

2: 63 percent / tri-o-tolylphosphine; triethylamine / Pd(OAc)2 / dimethylformamide / 0.3 h / 110 °C / microwave irradiation

3: 58 percent / cesium carbonate / dimethylformamide / 1.5 h / 75 °C

4: 98 percent / H₂ / Pd-C / methanol / 20 h / 20 °C

5: 48 percent / copper(II) trifluoromethanesulfonate / toluene; dimethylformamide / 0.28 h / 130 °C / microwave irradiation

With potassium tert-butylate; hydrogen; copper(II) bis(trifluoromethanesulfonate); caesium carbonate; triethylamine; tris-(o-tolyl)phosphine; palladium diacetate; palladium on activated charcoal; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; toluene; 2: Heck coupling;
DOI:10.1016/j.ejmech.2006.10.015