4-((8-fluoro-2-(2-(4-(hydroxymethyl)piperidin-1-yl)ethyl)-1-oxo-1,2,3,4-tetrahydropyrido[4,3-b]indol-5-yl)methyl)-N-hydroxybenzamide

Base Information

Chemical Name:4-((8-fluoro-2-(2-(4-(hydroxymethyl)piperidin-1-yl)ethyl)-1-oxo-1,2,3,4-tetrahydropyrido[4,3-b]indol-5-yl)methyl)-N-hydroxybenzamide
CAS No.:1432508-83-2
Molecular Formula:C₂₇H₃₁FN₄O₄
Molecular Weight:494.566
Hs Code.:

Synonyms:4-((8-fluoro-2-(2-(4-(hydroxymethyl)piperidin-1-yl)ethyl)-1-oxo-1,2,3,4-tetrahydropyrido[4,3-b]indol-5-yl)methyl)-N-hydroxybenzamide

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Chemical Property of 4-((8-fluoro-2-(2-(4-(hydroxymethyl)piperidin-1-yl)ethyl)-1-oxo-1,2,3,4-tetrahydropyrido[4,3-b]indol-5-yl)methyl)-N-hydroxybenzamide

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Technology Process of 4-((8-fluoro-2-(2-(4-(hydroxymethyl)piperidin-1-yl)ethyl)-1-oxo-1,2,3,4-tetrahydropyrido[4,3-b]indol-5-yl)methyl)-N-hydroxybenzamide

There total 7 articles about 4-((8-fluoro-2-(2-(4-(hydroxymethyl)piperidin-1-yl)ethyl)-1-oxo-1,2,3,4-tetrahydropyrido[4,3-b]indol-5-yl)methyl)-N-hydroxybenzamide 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: 40.0%

: 1432510-15-0
methyl 4-((8-fluoro-2-(2-(4-(hydroxymethyl)piperidin-1-yl)ethyl)-1-oxo-1,2,3,4-tetrahydropyrido[4,3-b]indol-5-yl)methyl)benzoate

: 1432508-83-2
4-((8-fluoro-2-(2-(4-(hydroxymethyl)piperidin-1-yl)ethyl)-1-oxo-1,2,3,4-tetrahydropyrido[4,3-b]indol-5-yl)methyl)-N-hydroxybenzamide

Guidance literature:: With hydroxylamine; potassium hydroxide; In methanol; water; at 20 ℃; for 1h;

Reference yield:

: 2417-72-3
Methyl 4-(bromomethyl)benzoate

: 1432508-83-2
4-((8-fluoro-2-(2-(4-(hydroxymethyl)piperidin-1-yl)ethyl)-1-oxo-1,2,3,4-tetrahydropyrido[4,3-b]indol-5-yl)methyl)-N-hydroxybenzamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: caesium carbonate / acetonitrile / 3 h / Reflux

2.1: sodium hydride; 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone / N,N-dimethyl-formamide / 16 h / 20 °C

3.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 1 h / 20 °C

4.1: N-ethyl-N,N-diisopropylamine; methanesulfonyl chloride / acetonitrile / 0.08 h / 20 °C

4.2: 0.5 h / 50 °C

5.1: potassium hydroxide; hydroxylamine / methanol / 1 h / 20 °C

With 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone; tetrabutyl ammonium fluoride; hydroxylamine; sodium hydride; caesium carbonate; methanesulfonyl chloride; N-ethyl-N,N-diisopropylamine; potassium hydroxide; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 128487-04-7
8-fluoro-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indol-1-one

: 1432508-83-2
4-((8-fluoro-2-(2-(4-(hydroxymethyl)piperidin-1-yl)ethyl)-1-oxo-1,2,3,4-tetrahydropyrido[4,3-b]indol-5-yl)methyl)-N-hydroxybenzamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: caesium carbonate / acetonitrile / 3 h / Reflux

2.1: sodium hydride; 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone / N,N-dimethyl-formamide / 16 h / 20 °C

3.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 1 h / 20 °C

4.1: N-ethyl-N,N-diisopropylamine; methanesulfonyl chloride / acetonitrile / 0.08 h / 20 °C

4.2: 0.5 h / 50 °C

5.1: potassium hydroxide; hydroxylamine / methanol / 1 h / 20 °C

With 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone; tetrabutyl ammonium fluoride; hydroxylamine; sodium hydride; caesium carbonate; methanesulfonyl chloride; N-ethyl-N,N-diisopropylamine; potassium hydroxide; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; acetonitrile;