(+/-)-6-fluoro-7-piperazino-1-(2'-trans-phenylcyclopropyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid

Base Information

Chemical Name:(+/-)-6-fluoro-7-piperazino-1-(2'-trans-phenylcyclopropyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid
CAS No.:103477-57-2
Molecular Formula:C₂₃H₂₂FN₃O₃
Molecular Weight:407.444
Hs Code.:

Synonyms:(+/-)-6-fluoro-7-piperazino-1-(2'-trans-phenylcyclopropyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid

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Chemical Property of (+/-)-6-fluoro-7-piperazino-1-(2'-trans-phenylcyclopropyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid

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Technology Process of (+/-)-6-fluoro-7-piperazino-1-(2'-trans-phenylcyclopropyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid

There total 7 articles about (+/-)-6-fluoro-7-piperazino-1-(2'-trans-phenylcyclopropyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic 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: 64.0%

: 103477-56-1
(+/-)-7-<4-(ethoxycarbonyl)piperazino>-6-fluoro-1-(2'-trans-phenylcyclopropyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid ethyl piperazinecarboxylate salt

: 103477-57-2
(+/-)-6-fluoro-7-piperazino-1-(2'-trans-phenylcyclopropyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid

Guidance literature:: With potassium hydroxide; In ethanol; for 48h; Heating;
DOI:10.1021/jm00160a042

Reference yield:

: 155-09-9
trans-2-phenylcyclopropylamine

: 103477-57-2
(+/-)-6-fluoro-7-piperazino-1-(2'-trans-phenylcyclopropyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid

Guidance literature:: Multi-step reaction with 5 steps

1: CH₂Cl₂ / 0.5 h / Ambient temperature

2: 74 percent / NaH / tetrahydrofuran / 4 h / 70 °C

3: 93 percent / KOH / tetrahydrofuran; H₂O / 1.5 h / 65 - 70 °C

4: 76 percent / various solvent(s) / 18 h / 100 - 110 °C

5: 64 percent / 10percent aq. KOH / ethanol / 48 h / Heating

With potassium hydroxide; sodium hydride; In tetrahydrofuran; ethanol; dichloromethane; water;
DOI:10.1021/jm00160a042

Reference yield:

: 86483-51-4
ethyl 2,4-dichloro-5-fluoro-benzoyl-acetate

: 103477-57-2
(+/-)-6-fluoro-7-piperazino-1-(2'-trans-phenylcyclopropyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid

Guidance literature:: Multi-step reaction with 6 steps

1: acetic anhydride / 2 h / 110 °C

2: CH₂Cl₂ / 0.5 h / Ambient temperature

3: 74 percent / NaH / tetrahydrofuran / 4 h / 70 °C

4: 93 percent / KOH / tetrahydrofuran; H₂O / 1.5 h / 65 - 70 °C

5: 76 percent / various solvent(s) / 18 h / 100 - 110 °C

6: 64 percent / 10percent aq. KOH / ethanol / 48 h / Heating

With potassium hydroxide; acetic anhydride; sodium hydride; In tetrahydrofuran; ethanol; dichloromethane; water;
DOI:10.1021/jm00160a042