(E)-(S)-4-[(S)-2-((S)-2-Benzyloxycarbonylamino-4-methyl-pentanoylamino)-3-(4-hydroxymethyl-phenyl)-propionylamino]-6-(trityl-carbamoyl)-hex-2-enoic acid ethyl ester

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Chemical Name:(E)-(S)-4-[(S)-2-((S)-2-Benzyloxycarbonylamino-4-methyl-pentanoylamino)-3-(4-hydroxymethyl-phenyl)-propionylamino]-6-(trityl-carbamoyl)-hex-2-enoic acid ethyl ester
CAS No.:1026128-56-2
Molecular Formula:C₅₂H₅₈N₄O₈
Molecular Weight:867.055
Hs Code.:

(E)-(S)-4-[(S)-2-((S)-2-Benzyloxycarbonylamino-4-methyl-pentanoylamino)-3-(4-hydroxymethyl-phenyl)-propionylamino]-6-(trityl-carbamoyl)-hex-2-enoic acid ethyl ester

Synonyms:(E)-(S)-4-[(S)-2-((S)-2-Benzyloxycarbonylamino-4-methyl-pentanoylamino)-3-(4-hydroxymethyl-phenyl)-propionylamino]-6-(trityl-carbamoyl)-hex-2-enoic acid ethyl ester

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Chemical Property of (E)-(S)-4-[(S)-2-((S)-2-Benzyloxycarbonylamino-4-methyl-pentanoylamino)-3-(4-hydroxymethyl-phenyl)-propionylamino]-6-(trityl-carbamoyl)-hex-2-enoic acid ethyl ester

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Technology Process of (E)-(S)-4-[(S)-2-((S)-2-Benzyloxycarbonylamino-4-methyl-pentanoylamino)-3-(4-hydroxymethyl-phenyl)-propionylamino]-6-(trityl-carbamoyl)-hex-2-enoic acid ethyl ester

There total 15 articles about (E)-(S)-4-[(S)-2-((S)-2-Benzyloxycarbonylamino-4-methyl-pentanoylamino)-3-(4-hydroxymethyl-phenyl)-propionylamino]-6-(trityl-carbamoyl)-hex-2-enoic acid ethyl 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:

: 103882-09-3,62129-44-6
N-Boc-4-I-Phe-OH

: 1026128-56-2
(E)-(S)-4-[(S)-2-((S)-2-Benzyloxycarbonylamino-4-methyl-pentanoylamino)-3-(4-hydroxymethyl-phenyl)-propionylamino]-6-(trityl-carbamoyl)-hex-2-enoic acid ethyl ester

Guidance literature:: Multi-step reaction with 9 steps

1: 87 percent / 1,3-dicyclohexylcarbodiimide, 4-(dimethylamino)pyridine / CH₂Cl₂ / 6 h / 23 °C

2: 83 percent / 2,6-di-tert-butyl-4-methylphenol, Pd(PPh₃)4 / dioxane / 6 h / 80 °C

3: 61 percent / aq. OsO₄, N-methylmorpholine N-oxide / acetone / 3 h / 23 °C

4: aq. NaIO₄ / diethyl ether / 2 h / 23 °C

5: 74 percent / NaBH₄ / ethanol / 0.33 h / 0 °C

6: 93 percent / H₂ / Pd/C / ethyl acetate / 6 h / 23 °C

7: HOBT, NMM, EDC / CH₂Cl₂ / 23 °C

8: HCl / dioxane / 23 °C

9: HOBT, NMM, EDC / CH₂Cl₂ / 23 °C

With 4-methyl-morpholine; hydrogenchloride; dmap; sodium tetrahydroborate; sodium periodate; osmium(VIII) oxide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; 2,6-di-tert-butyl-4-methyl-phenol; hydrogen; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; 4-methylmorpholine N-oxide; dicyclohexyl-carbodiimide; palladium on activated charcoal; In 1,4-dioxane; diethyl ether; ethanol; dichloromethane; ethyl acetate; acetone;
DOI:10.1021/jm9800696

Reference yield:

: 129150-58-9
benzyl Boc-4-iodophenylalanine

: 1026128-56-2
(E)-(S)-4-[(S)-2-((S)-2-Benzyloxycarbonylamino-4-methyl-pentanoylamino)-3-(4-hydroxymethyl-phenyl)-propionylamino]-6-(trityl-carbamoyl)-hex-2-enoic acid ethyl ester

Guidance literature:: Multi-step reaction with 8 steps

1: 83 percent / 2,6-di-tert-butyl-4-methylphenol, Pd(PPh₃)4 / dioxane / 6 h / 80 °C

2: 61 percent / aq. OsO₄, N-methylmorpholine N-oxide / acetone / 3 h / 23 °C

3: aq. NaIO₄ / diethyl ether / 2 h / 23 °C

4: 74 percent / NaBH₄ / ethanol / 0.33 h / 0 °C

5: 93 percent / H₂ / Pd/C / ethyl acetate / 6 h / 23 °C

6: HOBT, NMM, EDC / CH₂Cl₂ / 23 °C

7: HCl / dioxane / 23 °C

8: HOBT, NMM, EDC / CH₂Cl₂ / 23 °C

With 4-methyl-morpholine; hydrogenchloride; sodium tetrahydroborate; sodium periodate; osmium(VIII) oxide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; 2,6-di-tert-butyl-4-methyl-phenol; hydrogen; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; 4-methylmorpholine N-oxide; palladium on activated charcoal; In 1,4-dioxane; diethyl ether; ethanol; dichloromethane; ethyl acetate; acetone;
DOI:10.1021/jm9800696

Reference yield:

: 211186-18-4
(S)-benzyl 2-((tert-butoxycarbonyl)amino)-3-(4-vinylphenyl)propanoate

: 1026128-56-2
(E)-(S)-4-[(S)-2-((S)-2-Benzyloxycarbonylamino-4-methyl-pentanoylamino)-3-(4-hydroxymethyl-phenyl)-propionylamino]-6-(trityl-carbamoyl)-hex-2-enoic acid ethyl ester

Guidance literature:: Multi-step reaction with 7 steps

1: 61 percent / aq. OsO₄, N-methylmorpholine N-oxide / acetone / 3 h / 23 °C

2: aq. NaIO₄ / diethyl ether / 2 h / 23 °C

3: 74 percent / NaBH₄ / ethanol / 0.33 h / 0 °C

4: 93 percent / H₂ / Pd/C / ethyl acetate / 6 h / 23 °C

5: HOBT, NMM, EDC / CH₂Cl₂ / 23 °C

6: HCl / dioxane / 23 °C

7: HOBT, NMM, EDC / CH₂Cl₂ / 23 °C

With 4-methyl-morpholine; hydrogenchloride; sodium tetrahydroborate; sodium periodate; osmium(VIII) oxide; hydrogen; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; 4-methylmorpholine N-oxide; palladium on activated charcoal; In 1,4-dioxane; diethyl ether; ethanol; dichloromethane; ethyl acetate; acetone;
DOI:10.1021/jm9800696