(3S,4R)-5-(3-Benzyloxymethyl-3H-imidazol-4-yl)-3-hydroxy-4-{(S)-3-methyl-2-[(S)-3-methyl-2-(3-methyl-butyrylamino)-butyrylamino]-butyrylamino}-pentanoic acid methyl ester

Base Information

Chemical Name:(3S,4R)-5-(3-Benzyloxymethyl-3H-imidazol-4-yl)-3-hydroxy-4-{(S)-3-methyl-2-[(S)-3-methyl-2-(3-methyl-butyrylamino)-butyrylamino]-butyrylamino}-pentanoic acid methyl ester
CAS No.:120849-35-6
Molecular Formula:C₃₂H₄₉N₅O₇
Molecular Weight:615.77
Hs Code.:

(3S,4R)-5-(3-Benzyloxymethyl-3H-imidazol-4-yl)-3-hydroxy-4-{(S)-3-methyl-2-[(S)-3-methyl-2-(3-methyl-butyrylamino)-butyrylamino]-butyrylamino}-pentanoic acid methyl ester

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Chemical Property of (3S,4R)-5-(3-Benzyloxymethyl-3H-imidazol-4-yl)-3-hydroxy-4-{(S)-3-methyl-2-[(S)-3-methyl-2-(3-methyl-butyrylamino)-butyrylamino]-butyrylamino}-pentanoic acid methyl ester

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Technology Process of (3S,4R)-5-(3-Benzyloxymethyl-3H-imidazol-4-yl)-3-hydroxy-4-{(S)-3-methyl-2-[(S)-3-methyl-2-(3-methyl-butyrylamino)-butyrylamino]-butyrylamino}-pentanoic acid methyl ester

There total 6 articles about (3S,4R)-5-(3-Benzyloxymethyl-3H-imidazol-4-yl)-3-hydroxy-4-{(S)-3-methyl-2-[(S)-3-methyl-2-(3-methyl-butyrylamino)-butyrylamino]-butyrylamino}-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:

: 79950-65-5,99310-01-7
N-[(1,1-dimethylethoxy)carbonyl]-3-[(phenylmethoxy)methyl]-L-histidine

: 120849-35-6
(3S,4R)-5-(3-Benzyloxymethyl-3H-imidazol-4-yl)-3-hydroxy-4-{(S)-3-methyl-2-[(S)-3-methyl-2-(3-methyl-butyrylamino)-butyrylamino]-butyrylamino}-pentanoic acid methyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: DMAP, DCC / CH₂Cl₂ / 24 h / Ambient temperature

2: acetonitrile / 0.5 h / 110 deg C bath temperature

3: NaBH₄, acetic acid / CH₂Cl₂ / 4 h / 0 °C

4: 88 percent / methanol / 0.25 h / Ambient temperature

5: 4 N HCl / dioxane / 0.75 h / Ambient temperature

6: 1.) DCC, 1-hydroxybenzotriazole 2.) diisopropylethylamine / 1.) CH₂Cl₂, DMF, 0 deg C, 2 h, 2 a.) 0 deg C, 3 h, 2 b.) r.t., overnight

With hydrogenchloride; dmap; sodium tetrahydroborate; benzotriazol-1-ol; acetic acid; N-ethyl-N,N-diisopropylamine; dicyclohexyl-carbodiimide; In 1,4-dioxane; methanol; dichloromethane; acetonitrile;
DOI:10.1021/jm00127a028

Reference yield:

: 120742-08-7
(S)-2-(3-Benzyloxymethyl-3H-imidazol-4-ylmethyl)-3-hydroxy-5-oxo-2,5-dihydro-pyrrole-1-carboxylic acid tert-butyl ester

: 120849-35-6
(3S,4R)-5-(3-Benzyloxymethyl-3H-imidazol-4-yl)-3-hydroxy-4-{(S)-3-methyl-2-[(S)-3-methyl-2-(3-methyl-butyrylamino)-butyrylamino]-butyrylamino}-pentanoic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: NaBH₄, acetic acid / CH₂Cl₂ / 4 h / 0 °C

2: 88 percent / methanol / 0.25 h / Ambient temperature

3: 4 N HCl / dioxane / 0.75 h / Ambient temperature

4: 1.) DCC, 1-hydroxybenzotriazole 2.) diisopropylethylamine / 1.) CH₂Cl₂, DMF, 0 deg C, 2 h, 2 a.) 0 deg C, 3 h, 2 b.) r.t., overnight

With hydrogenchloride; sodium tetrahydroborate; benzotriazol-1-ol; acetic acid; N-ethyl-N,N-diisopropylamine; dicyclohexyl-carbodiimide; In 1,4-dioxane; methanol; dichloromethane;
DOI:10.1021/jm00127a028

Reference yield:

: 120742-09-8
(4S,5S)-1-(tert-Butyloxycarbonyl)-4-hydroxy-5-<<3-(benzyloxymethyl)imidazol-4-yl>methyl>pyrrolidin-2-one

: 120849-35-6
(3S,4R)-5-(3-Benzyloxymethyl-3H-imidazol-4-yl)-3-hydroxy-4-{(S)-3-methyl-2-[(S)-3-methyl-2-(3-methyl-butyrylamino)-butyrylamino]-butyrylamino}-pentanoic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 88 percent / methanol / 0.25 h / Ambient temperature

2: 4 N HCl / dioxane / 0.75 h / Ambient temperature

3: 1.) DCC, 1-hydroxybenzotriazole 2.) diisopropylethylamine / 1.) CH₂Cl₂, DMF, 0 deg C, 2 h, 2 a.) 0 deg C, 3 h, 2 b.) r.t., overnight

With hydrogenchloride; benzotriazol-1-ol; N-ethyl-N,N-diisopropylamine; dicyclohexyl-carbodiimide; In 1,4-dioxane; methanol;
DOI:10.1021/jm00127a028