(2S,4S,5S)-5-{(S)-2-[(S)-1-Benzyl-2-(4-methoxymethoxy-piperidin-1-yl)-2-oxo-ethylamino]-hexanoylamino}-6-cyclohexyl-4-hydroxy-2-isopropyl-hexanoic acid [2-(2-benzyloxy-ethylamino)-2-methyl-propyl]-amide

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Chemical Name:(2S,4S,5S)-5-{(S)-2-[(S)-1-Benzyl-2-(4-methoxymethoxy-piperidin-1-yl)-2-oxo-ethylamino]-hexanoylamino}-6-cyclohexyl-4-hydroxy-2-isopropyl-hexanoic acid [2-(2-benzyloxy-ethylamino)-2-methyl-propyl]-amide
CAS No.:161316-45-6
Molecular Formula:C₅₀H₈₁N₅O₇
Molecular Weight:864.222
Hs Code.:

(2S,4S,5S)-5-{(S)-2-[(S)-1-Benzyl-2-(4-methoxymethoxy-piperidin-1-yl)-2-oxo-ethylamino]-hexanoylamino}-6-cyclohexyl-4-hydroxy-2-isopropyl-hexanoic acid [2-(2-benzyloxy-ethylamino)-2-methyl-propyl]-amide

Synonyms:(2S,4S,5S)-5-{(S)-2-[(S)-1-Benzyl-2-(4-methoxymethoxy-piperidin-1-yl)-2-oxo-ethylamino]-hexanoylamino}-6-cyclohexyl-4-hydroxy-2-isopropyl-hexanoic acid [2-(2-benzyloxy-ethylamino)-2-methyl-propyl]-amide

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Chemical Property of (2S,4S,5S)-5-{(S)-2-[(S)-1-Benzyl-2-(4-methoxymethoxy-piperidin-1-yl)-2-oxo-ethylamino]-hexanoylamino}-6-cyclohexyl-4-hydroxy-2-isopropyl-hexanoic acid [2-(2-benzyloxy-ethylamino)-2-methyl-propyl]-amide

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Technology Process of (2S,4S,5S)-5-{(S)-2-[(S)-1-Benzyl-2-(4-methoxymethoxy-piperidin-1-yl)-2-oxo-ethylamino]-hexanoylamino}-6-cyclohexyl-4-hydroxy-2-isopropyl-hexanoic acid [2-(2-benzyloxy-ethylamino)-2-methyl-propyl]-amide

There total 5 articles about (2S,4S,5S)-5-{(S)-2-[(S)-1-Benzyl-2-(4-methoxymethoxy-piperidin-1-yl)-2-oxo-ethylamino]-hexanoylamino}-6-cyclohexyl-4-hydroxy-2-isopropyl-hexanoic acid [2-(2-benzyloxy-ethylamino)-2-methyl-propyl]-amide 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: 29.0%

: 60656-87-3
benzyloxyacetoaldehyde

: 142708-25-6
(2S,4S,5S)-5-{(S)-2-[(S)-1-Benzyl-2-(4-methoxymethoxy-piperidin-1-yl)-2-oxo-ethylamino]-hexanoylamino}-6-cyclohexyl-4-hydroxy-2-isopropyl-hexanoic acid (2-amino-2-methyl-propyl)-amide

: 161316-45-6
(2S,4S,5S)-5-{(S)-2-[(S)-1-Benzyl-2-(4-methoxymethoxy-piperidin-1-yl)-2-oxo-ethylamino]-hexanoylamino}-6-cyclohexyl-4-hydroxy-2-isopropyl-hexanoic acid [2-(2-benzyloxy-ethylamino)-2-methyl-propyl]-amide

Guidance literature:: With sodium acetate; sodium cyanoborohydride; acetic acid; In isopropyl alcohol; pH 6.0; 1.) 0 deg C, 6 h, 2.) RT, 14 h;
DOI:10.1021/jm00045a003

Reference yield:

: 124032-36-6
(3S,5S)-5-[(1S)-1-(t-butoxycarbonyl)amino-2-cyclohexylethyl]-3-isopropyldihydrofuran-2(3H)-one

: 161316-45-6
(2S,4S,5S)-5-{(S)-2-[(S)-1-Benzyl-2-(4-methoxymethoxy-piperidin-1-yl)-2-oxo-ethylamino]-hexanoylamino}-6-cyclohexyl-4-hydroxy-2-isopropyl-hexanoic acid [2-(2-benzyloxy-ethylamino)-2-methyl-propyl]-amide

Guidance literature:: Multi-step reaction with 4 steps

1: 42 percent / glacial acetic acid / 1.) 50 deg C, 48 h, 2.) 55 deg C, 5 d

2: trifluoroacetic acid / CH₂Cl₂ / 4.5 h / 0 °C

3: HOBt hydrate, 4-methylmorpholine, EDC / dimethylformamide / 1.) -23 deg C, 4 h, 2.) RT, 18 h

4: 29 percent / HOAc, NaOAc, NaBH₃CN / propan-2-ol / pH 6.0; 1.) 0 deg C, 6 h, 2.) RT, 14 h

With 4-methyl-morpholine; sodium acetate; sodium cyanoborohydride; benzotriazol-1-ol; acetic acid; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; trifluoroacetic acid; In dichloromethane; N,N-dimethyl-formamide; isopropyl alcohol;
DOI:10.1021/jm00045a003

Reference yield:

: 140660-69-1
(2S,4S)-3-aza-2-butyl-4-<<4-(1,3-dioxabutyl)piperidin-1-yl>carbonyl>-5-phenylpentanoic acid

: 161316-45-6
(2S,4S,5S)-5-{(S)-2-[(S)-1-Benzyl-2-(4-methoxymethoxy-piperidin-1-yl)-2-oxo-ethylamino]-hexanoylamino}-6-cyclohexyl-4-hydroxy-2-isopropyl-hexanoic acid [2-(2-benzyloxy-ethylamino)-2-methyl-propyl]-amide

Guidance literature:: Multi-step reaction with 2 steps

1: HOBt hydrate, 4-methylmorpholine, EDC / dimethylformamide / 1.) -23 deg C, 4 h, 2.) RT, 18 h

2: 29 percent / HOAc, NaOAc, NaBH₃CN / propan-2-ol / pH 6.0; 1.) 0 deg C, 6 h, 2.) RT, 14 h

With 4-methyl-morpholine; sodium acetate; sodium cyanoborohydride; benzotriazol-1-ol; acetic acid; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; In N,N-dimethyl-formamide; isopropyl alcohol;
DOI:10.1021/jm00045a003