7-[[3-(aminomethyl)-3-phenyl]-1-pyrrolidinyl]-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid

Base Information

Chemical Name:7-[[3-(aminomethyl)-3-phenyl]-1-pyrrolidinyl]-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid
CAS No.:124563-02-6
Molecular Formula:C₂₄H₂₃F₂N₃O₃
Molecular Weight:439.462
Hs Code.:

Synonyms:7-[[3-(aminomethyl)-3-phenyl]-1-pyrrolidinyl]-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid

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Chemical Property of 7-[[3-(aminomethyl)-3-phenyl]-1-pyrrolidinyl]-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid

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Technology Process of 7-[[3-(aminomethyl)-3-phenyl]-1-pyrrolidinyl]-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid

There total 5 articles about 7-[[3-(aminomethyl)-3-phenyl]-1-pyrrolidinyl]-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid 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: 89.0%

: 124562-99-8
3-phenyl-3-pyrrolidinemethanamine

: 94695-52-0
1-cyclopropyl-6,7,8-trifluoro-4-oxo-1,4-dihydroquinolin-3-carboxylic acid

: 124563-02-6
7-[[3-(aminomethyl)-3-phenyl]-1-pyrrolidinyl]-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid

Guidance literature:: With triethylamine; In acetonitrile; 1.) reflux, 3 h, 2.) room temp., 18 h;
DOI:10.1021/jm00164a060

Reference yield:

: 124562-96-5
3-phenyl-1-(phenylmethyl)-3-pyrrolidinemethanamine

: 124563-02-6
7-[[3-(aminomethyl)-3-phenyl]-1-pyrrolidinyl]-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid

Guidance literature:: Multi-step reaction with 2 steps

1: H₂ / 20percent Pd/C / methanol / 24 h / 25 °C / 2585.7 Torr

2: 89 percent / Et₃N / acetonitrile / 1.) reflux, 3 h, 2.) room temp., 18 h

With hydrogen; triethylamine; palladium on activated charcoal; In methanol; acetonitrile;
DOI:10.1021/jm00164a060

Reference yield:

: 124562-93-2
3-phenyl-1-(phenylmethyl)-3-pyrrolidinecarboxamide

: 124563-02-6
7-[[3-(aminomethyl)-3-phenyl]-1-pyrrolidinyl]-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid

Guidance literature:: Multi-step reaction with 3 steps

1: LiAlH₄ / tetrahydrofuran / 1.) room temp., overnight, 2.) reflux, 2 h

2: H₂ / 20percent Pd/C / methanol / 24 h / 25 °C / 2585.7 Torr

3: 89 percent / Et₃N / acetonitrile / 1.) reflux, 3 h, 2.) room temp., 18 h

With lithium aluminium tetrahydride; hydrogen; triethylamine; palladium on activated charcoal; In tetrahydrofuran; methanol; acetonitrile;
DOI:10.1021/jm00164a060