(S)-N-hydroxy-4-((2-(2-(2-(hydroxymethyl)pyrrolidin-1-yl)ethyl)-1-oxo-1,2,3,4-tetrahydropyrido[4,3-b]indol-5-yl)methyl)benzamide

Base Information

Chemical Name:(S)-N-hydroxy-4-((2-(2-(2-(hydroxymethyl)pyrrolidin-1-yl)ethyl)-1-oxo-1,2,3,4-tetrahydropyrido[4,3-b]indol-5-yl)methyl)benzamide
CAS No.:1432508-78-5
Molecular Formula:C₂₆H₃₀N₄O₄
Molecular Weight:462.549
Hs Code.:

Synonyms:(S)-N-hydroxy-4-((2-(2-(2-(hydroxymethyl)pyrrolidin-1-yl)ethyl)-1-oxo-1,2,3,4-tetrahydropyrido[4,3-b]indol-5-yl)methyl)benzamide

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Chemical Property of (S)-N-hydroxy-4-((2-(2-(2-(hydroxymethyl)pyrrolidin-1-yl)ethyl)-1-oxo-1,2,3,4-tetrahydropyrido[4,3-b]indol-5-yl)methyl)benzamide

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Technology Process of (S)-N-hydroxy-4-((2-(2-(2-(hydroxymethyl)pyrrolidin-1-yl)ethyl)-1-oxo-1,2,3,4-tetrahydropyrido[4,3-b]indol-5-yl)methyl)benzamide

There total 7 articles about (S)-N-hydroxy-4-((2-(2-(2-(hydroxymethyl)pyrrolidin-1-yl)ethyl)-1-oxo-1,2,3,4-tetrahydropyrido[4,3-b]indol-5-yl)methyl)benzamide 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%

: 1432510-09-2
(S)-methyl 4-((2-(2-(2-(hydroxymethyl)pyrrolidin-1-yl)ethyl)-1-oxo-1,2,3,4-tetrahydropyrido[4,3-b]indol-5-yl)methyl)benzoate

: 1432508-78-5
(S)-N-hydroxy-4-((2-(2-(2-(hydroxymethyl)pyrrolidin-1-yl)ethyl)-1-oxo-1,2,3,4-tetrahydropyrido[4,3-b]indol-5-yl)methyl)benzamide

Guidance literature:: With hydroxylamine hydrochloride; hydroxylamine; potassium hydroxide; In methanol; water; at 20 ℃; for 0.5h;

Reference yield:

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

: 1432508-78-5
(S)-N-hydroxy-4-((2-(2-(2-(hydroxymethyl)pyrrolidin-1-yl)ethyl)-1-oxo-1,2,3,4-tetrahydropyrido[4,3-b]indol-5-yl)methyl)benzamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: caesium carbonate / acetonitrile / 1 h / Reflux

2.1: sodium hydride; 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone / N,N-dimethyl-formamide / 16 h / 0 - 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: hydroxylamine hydrochloride; potassium hydroxide; hydroxylamine / methanol; water / 0.5 h / 20 °C

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

Reference yield:

: 1432509-96-0
methyl 4-((1-oxo-1,2,3,4-tetrahydropyrido[4,3-b]indol-5-yl)methyl)benzoate

: 1432508-78-5
(S)-N-hydroxy-4-((2-(2-(2-(hydroxymethyl)pyrrolidin-1-yl)ethyl)-1-oxo-1,2,3,4-tetrahydropyrido[4,3-b]indol-5-yl)methyl)benzamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium hydride; 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone / N,N-dimethyl-formamide / 16 h / 0 - 20 °C

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

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

3.2: 0.5 h / 50 °C

4.1: hydroxylamine hydrochloride; potassium hydroxide; hydroxylamine / methanol; water / 0.5 h / 20 °C

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