(4-(4-fluorophenyl)piperazin-1-yl)(2-morpholinoquinolin-6-yl)methanone

Base Information

Chemical Name:(4-(4-fluorophenyl)piperazin-1-yl)(2-morpholinoquinolin-6-yl)methanone
CAS No.:1637483-28-3
Molecular Formula:C₂₄H₂₅FN₄O₂
Molecular Weight:420.487
Hs Code.:

Synonyms:(4-(4-fluorophenyl)piperazin-1-yl)(2-morpholinoquinolin-6-yl)methanone

Suppliers and Price of (4-(4-fluorophenyl)piperazin-1-yl)(2-morpholinoquinolin-6-yl)methanone

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

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Chemical Property of (4-(4-fluorophenyl)piperazin-1-yl)(2-morpholinoquinolin-6-yl)methanone

Chemical Property:

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Technology Process of (4-(4-fluorophenyl)piperazin-1-yl)(2-morpholinoquinolin-6-yl)methanone

There total 5 articles about (4-(4-fluorophenyl)piperazin-1-yl)(2-morpholinoquinolin-6-yl)methanone 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: 77.0%

: 958333-34-1
2-(4-ethylpiperazin-1-yl)quinoline-6-carboxylic acid

: 2252-63-3
1-(4-Fluorophenyl)piperazine

: 1637483-28-3
(4-(4-fluorophenyl)piperazin-1-yl)(2-morpholinoquinolin-6-yl)methanone

Guidance literature:: With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine; In N,N-dimethyl-formamide; at 20 ℃; for 12h; Inert atmosphere;
DOI:10.1248/cpb.c13-00945

Reference yield:

: 327058-51-5
N-(4-bromophenyl)-(E)-3-ethoxyacrylamide

: 1637483-28-3
(4-(4-fluorophenyl)piperazin-1-yl)(2-morpholinoquinolin-6-yl)methanone

Guidance literature:: Multi-step reaction with 5 steps

1.1: sulfuric acid / 3 h / 0 - 20 °C / Inert atmosphere

2.1: trichlorophosphate / 6 h / 120 °C / Inert atmosphere

3.1: methanol / 90 °C / Inert atmosphere

4.1: n-butyllithium / tetrahydrofuran; hexane / 0.33 h / -78 °C / Inert atmosphere

4.2: 2 h / 0 - 20 °C / Inert atmosphere

5.1: O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine / N,N-dimethyl-formamide / 12 h / 20 °C / Inert atmosphere

With n-butyllithium; sulfuric acid; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine; trichlorophosphate; In tetrahydrofuran; methanol; hexane; N,N-dimethyl-formamide;
DOI:10.1248/cpb.c13-00945

Reference yield:

: 4-(6-bromoquinolin-2-yl)morpholine

: 1637483-28-3
(4-(4-fluorophenyl)piperazin-1-yl)(2-morpholinoquinolin-6-yl)methanone

Guidance literature:: Multi-step reaction with 2 steps

1.1: n-butyllithium / tetrahydrofuran; hexane / 0.33 h / -78 °C / Inert atmosphere

1.2: 2 h / 0 - 20 °C / Inert atmosphere

2.1: O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine / N,N-dimethyl-formamide / 12 h / 20 °C / Inert atmosphere

With n-butyllithium; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine; In tetrahydrofuran; hexane; N,N-dimethyl-formamide;
DOI:10.1248/cpb.c13-00945