(S)-3-(benzyloxy)-N-methyl-2-(4-nitro-N-(3-phenylprop-2-yn-1-yl)phenylsulfonamido)propanamide

Base Information

Chemical Name:(S)-3-(benzyloxy)-N-methyl-2-(4-nitro-N-(3-phenylprop-2-yn-1-yl)phenylsulfonamido)propanamide
CAS No.:1386995-61-4
Molecular Formula:C₂₆H₂₅N₃O₆S
Molecular Weight:507.567
Hs Code.:

Synonyms:(S)-3-(benzyloxy)-N-methyl-2-(4-nitro-N-(3-phenylprop-2-yn-1-yl)phenylsulfonamido)propanamide

Suppliers and Price of (S)-3-(benzyloxy)-N-methyl-2-(4-nitro-N-(3-phenylprop-2-yn-1-yl)phenylsulfonamido)propanamide

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Chemical Property of (S)-3-(benzyloxy)-N-methyl-2-(4-nitro-N-(3-phenylprop-2-yn-1-yl)phenylsulfonamido)propanamide

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Technology Process of (S)-3-(benzyloxy)-N-methyl-2-(4-nitro-N-(3-phenylprop-2-yn-1-yl)phenylsulfonamido)propanamide

There total 5 articles about (S)-3-(benzyloxy)-N-methyl-2-(4-nitro-N-(3-phenylprop-2-yn-1-yl)phenylsulfonamido)propanamide 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:

: 591-50-4
iodobenzene

: 1386995-59-0
(S)-3-(benzyloxy)-N-methyl-2-(4-nitro-N-(prop-2-yn-1-yl)-phenylsulfonamido)propanamide

: 1386995-61-4
(S)-3-(benzyloxy)-N-methyl-2-(4-nitro-N-(3-phenylprop-2-yn-1-yl)phenylsulfonamido)propanamide

Guidance literature:: With copper(l) iodide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; triethylamine; In tetrahydrofuran; at 50 ℃; for 7h; Inert atmosphere;
DOI:10.1039/c2ob25111f

Reference yield:

: 1386995-58-9
(S)-3-(benzyloxy)-N-methyl-2-(4-nitrophenylsulfonamido)propanamide

: 1386995-61-4
(S)-3-(benzyloxy)-N-methyl-2-(4-nitro-N-(3-phenylprop-2-yn-1-yl)phenylsulfonamido)propanamide

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / N,N-dimethyl-formamide / 17.5 h / 0 - 20 °C / Inert atmosphere

2: copper(l) iodide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; triethylamine / tetrahydrofuran / 7 h / 50 °C / Inert atmosphere

With copper(l) iodide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; potassium carbonate; triethylamine; In tetrahydrofuran; N,N-dimethyl-formamide; 1: Sonogashira coupling / 2: Sonogashira coupling;
DOI:10.1039/c2ob25111f

Reference yield:

: 1386995-54-5
(S)-methyl 3-(benzyloxy)-2-(4-nitrophenylsulfonamido)propanoate

: 1386995-61-4
(S)-3-(benzyloxy)-N-methyl-2-(4-nitro-N-(3-phenylprop-2-yn-1-yl)phenylsulfonamido)propanamide

Guidance literature:: Multi-step reaction with 3 steps

1: water / 18 h / 20 °C

2: potassium carbonate / N,N-dimethyl-formamide / 17.5 h / 0 - 20 °C / Inert atmosphere

3: copper(l) iodide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; triethylamine / tetrahydrofuran / 7 h / 50 °C / Inert atmosphere

With copper(l) iodide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; potassium carbonate; triethylamine; In tetrahydrofuran; water; N,N-dimethyl-formamide; 2: Sonogashira coupling / 3: Sonogashira coupling;
DOI:10.1039/c2ob25111f