(S)-2-[(S)-3-((S)-5-Benzyloxycarbonylamino-2-tert-butoxycarbonylamino-pentanoylamino)-2-hydroxy-butyrylamino]-4-methyl-pentanoic acid methyl ester

Base Information

Chemical Name:(S)-2-[(S)-3-((S)-5-Benzyloxycarbonylamino-2-tert-butoxycarbonylamino-pentanoylamino)-2-hydroxy-butyrylamino]-4-methyl-pentanoic acid methyl ester
CAS No.:373604-97-8
Molecular Formula:C₂₉H₄₆N₄O₉
Molecular Weight:594.706
Hs Code.:

(S)-2-[(S)-3-((S)-5-Benzyloxycarbonylamino-2-tert-butoxycarbonylamino-pentanoylamino)-2-hydroxy-butyrylamino]-4-methyl-pentanoic acid methyl ester

Synonyms:(S)-2-[(S)-3-((S)-5-Benzyloxycarbonylamino-2-tert-butoxycarbonylamino-pentanoylamino)-2-hydroxy-butyrylamino]-4-methyl-pentanoic acid methyl ester

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Chemical Property of (S)-2-[(S)-3-((S)-5-Benzyloxycarbonylamino-2-tert-butoxycarbonylamino-pentanoylamino)-2-hydroxy-butyrylamino]-4-methyl-pentanoic acid methyl ester

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Technology Process of (S)-2-[(S)-3-((S)-5-Benzyloxycarbonylamino-2-tert-butoxycarbonylamino-pentanoylamino)-2-hydroxy-butyrylamino]-4-methyl-pentanoic acid methyl ester

There total 4 articles about (S)-2-[(S)-3-((S)-5-Benzyloxycarbonylamino-2-tert-butoxycarbonylamino-pentanoylamino)-2-hydroxy-butyrylamino]-4-methyl-pentanoic acid methyl 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: 91.6%

: 276888-31-4
2-[2-(5-benzyloxycarbonylamino-2-tert-butoxycarbonylamino-pentanoyloxy)-3-(9H-fluoren-9-ylmethoxycarbonylamino)-butyrylamino]-4-methyl-pentanoic acid methyl ester

: 373604-97-8
(S)-2-[(S)-3-((S)-5-Benzyloxycarbonylamino-2-tert-butoxycarbonylamino-pentanoylamino)-2-hydroxy-butyrylamino]-4-methyl-pentanoic acid methyl ester

Guidance literature:: With diethylamine; In dichloromethane; at 20 ℃; for 12h;
DOI:10.1016/S0040-4039(01)01287-4

Reference yield:

: 54259-27-7
(S)-methyl 2-formamido-4-methylpentanoate

: 373604-97-8
(S)-2-[(S)-3-((S)-5-Benzyloxycarbonylamino-2-tert-butoxycarbonylamino-pentanoylamino)-2-hydroxy-butyrylamino]-4-methyl-pentanoic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 86 percent / Cl₃COOCCl; NMM / CH₂Cl₂ / -40 - -15 °C

2: 74.5 percent / CH₂Cl₂ / 96 h / 0 - 20 °C

3: 91.6 percent / Et₂NH / CH₂Cl₂ / 12 h / 20 °C

With 4-methyl-morpholine; diethylamine; trichloromethyl chloroformate; In dichloromethane; 1: Ugi dehydration reaction / 2: Passerini reaction;
DOI:10.1016/S0040-4039(01)01287-4

Reference yield:

: 7517-19-3
methyl (L)-leucinate hydrochloride

: 373604-97-8
(S)-2-[(S)-3-((S)-5-Benzyloxycarbonylamino-2-tert-butoxycarbonylamino-pentanoylamino)-2-hydroxy-butyrylamino]-4-methyl-pentanoic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: HCOONa / 70 °C

1.2: 70 percent / Ac₂O / 0 - 20 °C

2.1: 86 percent / Cl₃COOCCl; NMM / CH₂Cl₂ / -40 - -15 °C

3.1: 74.5 percent / CH₂Cl₂ / 96 h / 0 - 20 °C

4.1: 91.6 percent / Et₂NH / CH₂Cl₂ / 12 h / 20 °C

With 4-methyl-morpholine; sodium formate; diethylamine; trichloromethyl chloroformate; In dichloromethane; 2.1: Ugi dehydration reaction / 3.1: Passerini reaction;
DOI:10.1016/S0040-4039(01)01287-4