(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

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Chemical Name:(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
CAS No.:1432510-09-2
Molecular Formula:C₂₇H₃₁N₃O₄
Molecular Weight:461.561
Hs Code.:

Synonyms:(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

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Chemical Property of (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

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Technology Process of (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

There total 6 articles about (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 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: 60.0%

: 1432509-98-2
methyl 4-((2-(2-hydroxyethyl)-1-oxo-1,2,3,4-tetrahydropyrido[4,3-b]indol-5-yl)methyl)benzoate

: 23356-96-9
(S)-1-Pyrrolidin-2-yl-methanol

: 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

Guidance literature:: methyl 4-((2-(2-hydroxyethyl)-1-oxo-1,2,3,4-tetrahydropyrido[4,3-b]indol-5-yl)methyl)benzoate; With methanesulfonyl chloride; N-ethyl-N,N-diisopropylamine; In acetonitrile; at 20 ℃; for 0.0833333h;

(S)-1-Pyrrolidin-2-yl-methanol; In acetonitrile; at 50 ℃; for 0.5h;

Reference yield:

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

: 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

Guidance literature:: Multi-step reaction with 4 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

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

: 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

Guidance literature:: Multi-step reaction with 3 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

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