4'-fluoro-N-[6-fluoro-3-(1-pyrrolidinylmethyl)-7-quinolinyl]-[1,1'-biphenyl]-4-carboxamide

Base Information

Chemical Name:4'-fluoro-N-[6-fluoro-3-(1-pyrrolidinylmethyl)-7-quinolinyl]-[1,1'-biphenyl]-4-carboxamide
CAS No.:521070-97-3
Molecular Formula:C₂₇H₂₃F₂N₃O
Molecular Weight:443.496
Hs Code.:

Synonyms:4'-fluoro-N-[6-fluoro-3-(1-pyrrolidinylmethyl)-7-quinolinyl]-[1,1'-biphenyl]-4-carboxamide

Suppliers and Price of 4'-fluoro-N-[6-fluoro-3-(1-pyrrolidinylmethyl)-7-quinolinyl]-[1,1'-biphenyl]-4-carboxamide

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 4'-fluoro-N-[6-fluoro-3-(1-pyrrolidinylmethyl)-7-quinolinyl]-[1,1'-biphenyl]-4-carboxamide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 4'-fluoro-N-[6-fluoro-3-(1-pyrrolidinylmethyl)-7-quinolinyl]-[1,1'-biphenyl]-4-carboxamide

There total 7 articles about 4'-fluoro-N-[6-fluoro-3-(1-pyrrolidinylmethyl)-7-quinolinyl]-[1,1'-biphenyl]-4-carboxamide 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: 53.0%

: 521070-96-2
4-bromo-N-[6-fluoro-3-(1-pyrrolidinylmethyl)-7-quinolinyl]benzamide

: 1765-93-1
4-fluoroboronic acid

: 521070-97-3
4'-fluoro-N-[6-fluoro-3-(1-pyrrolidinylmethyl)-7-quinolinyl]-[1,1'-biphenyl]-4-carboxamide

Guidance literature:: With tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium carbonate; In 1,2-dimethoxyethane; at 85 ℃; for 5h; Inert atmosphere;
DOI:10.1021/jm201596h

Reference yield:

: 521074-15-7
N-[3-(chloromethyl)-6-fluoro-7-quinolinyl]acetamide hydrochloride

: 521070-97-3
4'-fluoro-N-[6-fluoro-3-(1-pyrrolidinylmethyl)-7-quinolinyl]-[1,1'-biphenyl]-4-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1: potassium carbonate / acetonitrile / 2 h / 80 °C

2: hydrogenchloride / 1 h / 100 °C

3: N,N-dimethyl acetamide / 5 h

4: tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium carbonate / 1,2-dimethoxyethane / 5 h / 85 °C / Inert atmosphere

With hydrogenchloride; tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium carbonate; potassium carbonate; In 1,2-dimethoxyethane; N,N-dimethyl acetamide; acetonitrile; 4: Suzuki coupling;
DOI:10.1021/jm201596h

Reference yield:

: C₁₂H₉FN₂O₂

: 521070-97-3
4'-fluoro-N-[6-fluoro-3-(1-pyrrolidinylmethyl)-7-quinolinyl]-[1,1'-biphenyl]-4-carboxamide

Guidance literature:: Multi-step reaction with 6 steps

1: sodium tetrahydroborate / ethanol / 3 h / 20 °C / Cooling with ice

2: thionyl chloride / 2 h / 20 °C

3: potassium carbonate / acetonitrile / 2 h / 80 °C

4: hydrogenchloride / 1 h / 100 °C

5: N,N-dimethyl acetamide / 5 h

6: tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium carbonate / 1,2-dimethoxyethane / 5 h / 85 °C / Inert atmosphere

With hydrogenchloride; sodium tetrahydroborate; tetrakis(triphenylphosphine) palladium⁽⁰⁾; thionyl chloride; sodium carbonate; potassium carbonate; In 1,2-dimethoxyethane; ethanol; N,N-dimethyl acetamide; acetonitrile; 6: Suzuki coupling;
DOI:10.1021/jm201596h