(S)-3-[4-benzyloxy-3-(4-{(S)-2-[(S)-1-tert-butoxycarbonyl-2-(4-hydroxy-phenyl)ethylcarbamoyl]-2-dibenzylaminoethyl}phenoxy)phenyl]-2-(tritylamino)-propionic acid benzyl ester

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Chemical Name:(S)-3-[4-benzyloxy-3-(4-{(S)-2-[(S)-1-tert-butoxycarbonyl-2-(4-hydroxy-phenyl)ethylcarbamoyl]-2-dibenzylaminoethyl}phenoxy)phenyl]-2-(tritylamino)-propionic acid benzyl ester
CAS No.:903523-85-3
Molecular Formula:C₇₈H₇₅N₃O₈
Molecular Weight:1182.47
Hs Code.:

(S)-3-[4-benzyloxy-3-(4-{(S)-2-[(S)-1-tert-butoxycarbonyl-2-(4-hydroxy-phenyl)ethylcarbamoyl]-2-dibenzylaminoethyl}phenoxy)phenyl]-2-(tritylamino)-propionic acid benzyl ester

Synonyms:(S)-3-[4-benzyloxy-3-(4-{(S)-2-[(S)-1-tert-butoxycarbonyl-2-(4-hydroxy-phenyl)ethylcarbamoyl]-2-dibenzylaminoethyl}phenoxy)phenyl]-2-(tritylamino)-propionic acid benzyl ester

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Chemical Property of (S)-3-[4-benzyloxy-3-(4-{(S)-2-[(S)-1-tert-butoxycarbonyl-2-(4-hydroxy-phenyl)ethylcarbamoyl]-2-dibenzylaminoethyl}phenoxy)phenyl]-2-(tritylamino)-propionic acid benzyl ester

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Technology Process of (S)-3-[4-benzyloxy-3-(4-{(S)-2-[(S)-1-tert-butoxycarbonyl-2-(4-hydroxy-phenyl)ethylcarbamoyl]-2-dibenzylaminoethyl}phenoxy)phenyl]-2-(tritylamino)-propionic acid benzyl ester

There total 7 articles about (S)-3-[4-benzyloxy-3-(4-{(S)-2-[(S)-1-tert-butoxycarbonyl-2-(4-hydroxy-phenyl)ethylcarbamoyl]-2-dibenzylaminoethyl}phenoxy)phenyl]-2-(tritylamino)-propionic acid benzyl 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:

: (S)-2-Dibenzylamino-3-(4-iodo-phenyl)-propionic acid methyl ester

: 903523-85-3
(S)-3-[4-benzyloxy-3-(4-{(S)-2-[(S)-1-tert-butoxycarbonyl-2-(4-hydroxy-phenyl)ethylcarbamoyl]-2-dibenzylaminoethyl}phenoxy)phenyl]-2-(tritylamino)-propionic acid benzyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 87 percent / Cs₂CO₃ / CuI; N,N-dimethylglycine hydrochloride / dioxane / 30 h / 90 °C

2: LiOH / tetrahydrofuran; methanol; H₂O / 0.5 h / 0 °C

3: 404 mg / EDCl; HOAt; i-Pr₂NEt / dimethylformamide / 14 h / 0 - 20 °C

With lithium hydroxide; 1-hydroxy-7-aza-benzotriazole; caesium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; copper(l) iodide; N,N-dimethylglycine hydrochoride; In tetrahydrofuran; 1,4-dioxane; methanol; water; N,N-dimethyl-formamide;
DOI:10.1021/jo0606960

Reference yield:

: 903523-81-9
(S)-3-(4-benzyloxy-3-hydroxyphenyl)-2-(tritylamino)propionic acid benzyl ester

: 903523-85-3
(S)-3-[4-benzyloxy-3-(4-{(S)-2-[(S)-1-tert-butoxycarbonyl-2-(4-hydroxy-phenyl)ethylcarbamoyl]-2-dibenzylaminoethyl}phenoxy)phenyl]-2-(tritylamino)-propionic acid benzyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 87 percent / Cs₂CO₃ / CuI; N,N-dimethylglycine hydrochloride / dioxane / 30 h / 90 °C

2: LiOH / tetrahydrofuran; methanol; H₂O / 0.5 h / 0 °C

3: 404 mg / EDCl; HOAt; i-Pr₂NEt / dimethylformamide / 14 h / 0 - 20 °C

With lithium hydroxide; 1-hydroxy-7-aza-benzotriazole; caesium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; copper(l) iodide; N,N-dimethylglycine hydrochoride; In tetrahydrofuran; 1,4-dioxane; methanol; water; N,N-dimethyl-formamide;
DOI:10.1021/jo0606960

Reference yield:

: (S)-2-Amino-3-(4-benzyloxy-3-hydroxy-phenyl)-propionic acid benzyl ester; compound with trifluoro-acetic acid

: 903523-85-3
(S)-3-[4-benzyloxy-3-(4-{(S)-2-[(S)-1-tert-butoxycarbonyl-2-(4-hydroxy-phenyl)ethylcarbamoyl]-2-dibenzylaminoethyl}phenoxy)phenyl]-2-(tritylamino)-propionic acid benzyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 6.6 g / Et₃N / dimethylformamide / 4 h

2: 87 percent / Cs₂CO₃ / CuI; N,N-dimethylglycine hydrochloride / dioxane / 30 h / 90 °C

3: LiOH / tetrahydrofuran; methanol; H₂O / 0.5 h / 0 °C

4: 404 mg / EDCl; HOAt; i-Pr₂NEt / dimethylformamide / 14 h / 0 - 20 °C

With lithium hydroxide; 1-hydroxy-7-aza-benzotriazole; caesium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; N-ethyl-N,N-diisopropylamine; copper(l) iodide; N,N-dimethylglycine hydrochoride; In tetrahydrofuran; 1,4-dioxane; methanol; water; N,N-dimethyl-formamide;
DOI:10.1021/jo0606960