7-[3-((S)-2-Amino-3-phenyl-propionylamino)-pyrrolidin-1-yl]-1-cyclopropyl-6-fluoro-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid; hydrochloride

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Chemical Name:7-[3-((S)-2-Amino-3-phenyl-propionylamino)-pyrrolidin-1-yl]-1-cyclopropyl-6-fluoro-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid; hydrochloride
CAS No.:122536-63-4
Molecular Formula:3C₂₆H₂₇FN₄O₄*4ClH
Molecular Weight:1581.41
Hs Code.:

7-[3-((S)-2-Amino-3-phenyl-propionylamino)-pyrrolidin-1-yl]-1-cyclopropyl-6-fluoro-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid; hydrochloride

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Chemical Property of 7-[3-((S)-2-Amino-3-phenyl-propionylamino)-pyrrolidin-1-yl]-1-cyclopropyl-6-fluoro-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid; hydrochloride

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Technology Process of 7-[3-((S)-2-Amino-3-phenyl-propionylamino)-pyrrolidin-1-yl]-1-cyclopropyl-6-fluoro-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid; hydrochloride

There total 5 articles about 7-[3-((S)-2-Amino-3-phenyl-propionylamino)-pyrrolidin-1-yl]-1-cyclopropyl-6-fluoro-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid; hydrochloride 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:

: 13734-34-4
N-tert-butoxycarbonyl-L-phenylalanine

: 122536-63-4,122537-09-1,140412-59-5,140412-60-8
7-[3-((S)-2-Amino-3-phenyl-propionylamino)-pyrrolidin-1-yl]-1-cyclopropyl-6-fluoro-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid; hydrochloride

Guidance literature:: Multi-step reaction with 5 steps

1: N-methylporpholine / CH₂Cl₂ / 0.08 h / -20 - -10 °C

2: N-methylmorpholine / CH₂Cl₂ / 0.5 h / -10 °C

3: H₂ / 20percent Pd/C / methanol / 3 h / 24.5 - 25.5 °C / 2518.5 - 2668.5 Torr

4: Et₃N / acetonitrile / 4 h / Heating

5: 1.0 M aq. HCl / ethanol / 1.) RT, 1 h, 2.) reflux, 2 h

With 4-methyl-morpholine; hydrogenchloride; N-methylporpholine; hydrogen; triethylamine; palladium on activated charcoal; In methanol; ethanol; dichloromethane; acetonitrile;
DOI:10.1021/jm00088a011

Reference yield:

: 67729-36-6,60398-40-5
Boc-Phe-O-COO-isoBu

: 122536-63-4,122537-09-1,140412-59-5,140412-60-8
7-[3-((S)-2-Amino-3-phenyl-propionylamino)-pyrrolidin-1-yl]-1-cyclopropyl-6-fluoro-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid; hydrochloride

Guidance literature:: Multi-step reaction with 4 steps

1: N-methylmorpholine / CH₂Cl₂ / 0.5 h / -10 °C

2: H₂ / 20percent Pd/C / methanol / 3 h / 24.5 - 25.5 °C / 2518.5 - 2668.5 Torr

3: Et₃N / acetonitrile / 4 h / Heating

4: 1.0 M aq. HCl / ethanol / 1.) RT, 1 h, 2.) reflux, 2 h

With 4-methyl-morpholine; hydrogenchloride; hydrogen; triethylamine; palladium on activated charcoal; In methanol; ethanol; dichloromethane; acetonitrile;
DOI:10.1021/jm00088a011

Reference yield:

: 3-((S)-2-tert-Butoxycarbonylamino-3-phenyl-propionylamino)-pyrrolidine-1-carboxylic acid benzyl ester

: 122536-63-4,122537-09-1,140412-59-5,140412-60-8
7-[3-((S)-2-Amino-3-phenyl-propionylamino)-pyrrolidin-1-yl]-1-cyclopropyl-6-fluoro-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid; hydrochloride

Guidance literature:: Multi-step reaction with 3 steps

1: H₂ / 20percent Pd/C / methanol / 3 h / 24.5 - 25.5 °C / 2518.5 - 2668.5 Torr

2: Et₃N / acetonitrile / 4 h / Heating

3: 1.0 M aq. HCl / ethanol / 1.) RT, 1 h, 2.) reflux, 2 h

With hydrogenchloride; hydrogen; triethylamine; palladium on activated charcoal; In methanol; ethanol; acetonitrile;
DOI:10.1021/jm00088a011