(5S)-benzyl-5-(3,4-dihydroisoquinolin-2(1H)-yl-carbonyl)-3-[(1R)-1-phenylethyl]imidazolidine-2,4-dione

Base Information

Chemical Name:(5S)-benzyl-5-(3,4-dihydroisoquinolin-2(1H)-yl-carbonyl)-3-[(1R)-1-phenylethyl]imidazolidine-2,4-dione
CAS No.:1430105-06-8
Molecular Formula:C₂₈H₂₇N₃O₃
Molecular Weight:453.541
Hs Code.:

Synonyms:(5S)-benzyl-5-(3,4-dihydroisoquinolin-2(1H)-yl-carbonyl)-3-[(1R)-1-phenylethyl]imidazolidine-2,4-dione

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Chemical Property of (5S)-benzyl-5-(3,4-dihydroisoquinolin-2(1H)-yl-carbonyl)-3-[(1R)-1-phenylethyl]imidazolidine-2,4-dione

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Technology Process of (5S)-benzyl-5-(3,4-dihydroisoquinolin-2(1H)-yl-carbonyl)-3-[(1R)-1-phenylethyl]imidazolidine-2,4-dione

There total 5 articles about (5S)-benzyl-5-(3,4-dihydroisoquinolin-2(1H)-yl-carbonyl)-3-[(1R)-1-phenylethyl]imidazolidine-2,4-dione 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:

: 91-21-4
1,2,3,4-tetrahydroisoquinoline

: 1430105-05-7
lithium 4-benzyl-2,5-dioxo-1-[(1R)-1-phenylethyl]imidazolidine-4-carboxylate

: 1430104-75-8
(5R)-benzyl-5-(3,4-dihydroisoquinolin-2(1H)-yl-carbonyl)-3-[(1R)-1-phenylethyl]imidazolidine-2,4-dione

: 1430105-06-8
(5S)-benzyl-5-(3,4-dihydroisoquinolin-2(1H)-yl-carbonyl)-3-[(1R)-1-phenylethyl]imidazolidine-2,4-dione

Guidance literature:: With N-ethyl-N,N-diisopropylamine; HATU; In dichloromethane; for 18h;

Reference yield:

: 100-39-0
benzyl bromide

: 1430104-75-8
(5R)-benzyl-5-(3,4-dihydroisoquinolin-2(1H)-yl-carbonyl)-3-[(1R)-1-phenylethyl]imidazolidine-2,4-dione

: 1430105-06-8
(5S)-benzyl-5-(3,4-dihydroisoquinolin-2(1H)-yl-carbonyl)-3-[(1R)-1-phenylethyl]imidazolidine-2,4-dione

Guidance literature:: Multi-step reaction with 5 steps

1: sodium ethanolate / ethanol / 6 h

2: dichloromethane / 1 h

3: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 16.5 h / 0 - 20 °C

4: lithium hydroxide / tetrahydrofuran; methanol; water / 0.5 h

5: HATU; N-ethyl-N,N-diisopropylamine / dichloromethane / 18 h

With sodium ethanolate; N-ethyl-N,N-diisopropylamine; HATU; lithium hydroxide; In tetrahydrofuran; methanol; ethanol; dichloromethane; water; N,N-dimethyl-formamide;

Reference yield:

: 518314-53-9
2-(N-(tert-butoxycarbonyl)amino)-2-benzylpropanedioic diethyl ester

: 1430104-75-8
(5R)-benzyl-5-(3,4-dihydroisoquinolin-2(1H)-yl-carbonyl)-3-[(1R)-1-phenylethyl]imidazolidine-2,4-dione

: 1430105-06-8
(5S)-benzyl-5-(3,4-dihydroisoquinolin-2(1H)-yl-carbonyl)-3-[(1R)-1-phenylethyl]imidazolidine-2,4-dione

Guidance literature:: Multi-step reaction with 4 steps

1: dichloromethane / 1 h

2: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 16.5 h / 0 - 20 °C

3: lithium hydroxide / tetrahydrofuran; methanol; water / 0.5 h

4: HATU; N-ethyl-N,N-diisopropylamine / dichloromethane / 18 h

With N-ethyl-N,N-diisopropylamine; HATU; lithium hydroxide; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide;