(S)-2-{4-[(1-Oxo-1,2-dihydro-isoquinolin-7-ylmethyl)-prop-2-ynyl-amino]-benzoylamino}-pentanedioic acid diethyl ester

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Chemical Name:(S)-2-{4-[(1-Oxo-1,2-dihydro-isoquinolin-7-ylmethyl)-prop-2-ynyl-amino]-benzoylamino}-pentanedioic acid diethyl ester
CAS No.:133933-21-8
Molecular Formula:C₂₉H₃₁N₃O₆
Molecular Weight:517.582
Hs Code.:

Synonyms:(S)-2-{4-[(1-Oxo-1,2-dihydro-isoquinolin-7-ylmethyl)-prop-2-ynyl-amino]-benzoylamino}-pentanedioic acid diethyl ester

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Chemical Property of (S)-2-{4-[(1-Oxo-1,2-dihydro-isoquinolin-7-ylmethyl)-prop-2-ynyl-amino]-benzoylamino}-pentanedioic acid diethyl ester

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Technology Process of (S)-2-{4-[(1-Oxo-1,2-dihydro-isoquinolin-7-ylmethyl)-prop-2-ynyl-amino]-benzoylamino}-pentanedioic acid diethyl ester

There total 6 articles about (S)-2-{4-[(1-Oxo-1,2-dihydro-isoquinolin-7-ylmethyl)-prop-2-ynyl-amino]-benzoylamino}-pentanedioic acid diethyl ester 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:

: 76858-72-5
diethyl N-(4-(prop-2-ynylamino)benzoyl)-L-glutamate

: 133933-20-7
7-(bromomethyl)-2-<(pivaloyloxy)methyl>isoquinolin-1-(2H)-one

: 133933-21-8
(S)-2-{4-[(1-Oxo-1,2-dihydro-isoquinolin-7-ylmethyl)-prop-2-ynyl-amino]-benzoylamino}-pentanedioic acid diethyl ester

Guidance literature:: With magnesium oxide; In N,N-dimethyl acetamide; at 90 - 100 ℃; for 18h;
DOI:10.1021/jm00113a011

Reference yield:

: 26829-47-0
7-methylisoquinolin-1(2H)-one

: 133933-21-8
(S)-2-{4-[(1-Oxo-1,2-dihydro-isoquinolin-7-ylmethyl)-prop-2-ynyl-amino]-benzoylamino}-pentanedioic acid diethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 80 percent / K₂CO₃ / tetrahydrofuran / 96 h / Heating

2: 44 percent / 1,3-dibromo-5,5-dimethylhydantoin (DDH), benzoyl peroxide / CCl₄ / 24 h / Heating; Irradiation

3: MgO / N,N-dimethyl-acetamide / 18 h / 90 - 100 °C

With Perbenzoic acid; 1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione; magnesium oxide; potassium carbonate; In tetrahydrofuran; tetrachloromethane; N,N-dimethyl acetamide;
DOI:10.1021/jm00113a011

Reference yield:

: 133933-18-3
N-(3-toluoyl)aminoacetaldehyde dimethyl acetal

: 133933-21-8
(S)-2-{4-[(1-Oxo-1,2-dihydro-isoquinolin-7-ylmethyl)-prop-2-ynyl-amino]-benzoylamino}-pentanedioic acid diethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 39 percent / H₂SO₄ / 72 h / 25 °C

2: 80 percent / K₂CO₃ / tetrahydrofuran / 96 h / Heating

3: 44 percent / 1,3-dibromo-5,5-dimethylhydantoin (DDH), benzoyl peroxide / CCl₄ / 24 h / Heating; Irradiation

4: MgO / N,N-dimethyl-acetamide / 18 h / 90 - 100 °C

With Perbenzoic acid; 1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione; sulfuric acid; magnesium oxide; potassium carbonate; In tetrahydrofuran; tetrachloromethane; N,N-dimethyl acetamide;
DOI:10.1021/jm00113a011