(2S,4R)-4-hydroxy-N-(2-hydroxy-4-(4-methylthiazol-5-yl) benzyl)-1-((R)-3-methyl-2-(1-oxoisoindolin-2-yl)butanoyl)pyrrolidine-2-carboxamide

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Chemical Name:(2S,4R)-4-hydroxy-N-(2-hydroxy-4-(4-methylthiazol-5-yl) benzyl)-1-((R)-3-methyl-2-(1-oxoisoindolin-2-yl)butanoyl)pyrrolidine-2-carboxamide
CAS No.:1448188-71-3
Molecular Formula:C₂₉H₃₂N₄O₅S
Molecular Weight:548.663
Hs Code.:

Synonyms:(2S,4R)-4-hydroxy-N-(2-hydroxy-4-(4-methylthiazol-5-yl) benzyl)-1-((R)-3-methyl-2-(1-oxoisoindolin-2-yl)butanoyl)pyrrolidine-2-carboxamide

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Chemical Property of (2S,4R)-4-hydroxy-N-(2-hydroxy-4-(4-methylthiazol-5-yl) benzyl)-1-((R)-3-methyl-2-(1-oxoisoindolin-2-yl)butanoyl)pyrrolidine-2-carboxamide

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Technology Process of (2S,4R)-4-hydroxy-N-(2-hydroxy-4-(4-methylthiazol-5-yl) benzyl)-1-((R)-3-methyl-2-(1-oxoisoindolin-2-yl)butanoyl)pyrrolidine-2-carboxamide

There total 7 articles about (2S,4R)-4-hydroxy-N-(2-hydroxy-4-(4-methylthiazol-5-yl) benzyl)-1-((R)-3-methyl-2-(1-oxoisoindolin-2-yl)butanoyl)pyrrolidine-2-carboxamide 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: 66.0%

: (2S,4R)-4-hydroxy-N-[[2-hydroxy-4-(4-methylthiazol-5-yl)phenyl]methyl]pyrrolidine-2-carboxamide hydrochloride

: 180923-77-7
(R)-3-methyl-2-(1-oxoisoindolin-2-yl)butanoic acid

: 1448188-71-3
(2S,4R)-4-hydroxy-N-(2-hydroxy-4-(4-methylthiazol-5-yl) benzyl)-1-((R)-3-methyl-2-(1-oxoisoindolin-2-yl)butanoyl)pyrrolidine-2-carboxamide

Guidance literature:: With N-ethyl-N,N-diisopropylamine; HATU; In N,N-dimethyl-formamide; at 20 ℃; for 0.5h;

Reference yield: 66.0%

: (2S,4R)-4-Hydroxy-N-(2-hydroxy-4-(4-methylthiazol-5-yl)benzyl)pyrrolidine-2-carboxamide hydrochloride

: 180923-77-7
(R)-3-methyl-2-(1-oxoisoindolin-2-yl)butanoic acid

: 1448188-71-3
(2S,4R)-4-hydroxy-N-(2-hydroxy-4-(4-methylthiazol-5-yl) benzyl)-1-((R)-3-methyl-2-(1-oxoisoindolin-2-yl)butanoyl)pyrrolidine-2-carboxamide

Guidance literature:: With N-ethyl-N,N-diisopropylamine; HATU; In N,N-dimethyl-formamide; at 20 ℃; for 0.5h;

Reference yield:

: 288067-35-6
4-bromo-2-hydroxy-benzonitrile

: 1448188-71-3
(2S,4R)-4-hydroxy-N-(2-hydroxy-4-(4-methylthiazol-5-yl) benzyl)-1-((R)-3-methyl-2-(1-oxoisoindolin-2-yl)butanoyl)pyrrolidine-2-carboxamide

Guidance literature:: Multi-step reaction with 5 steps

1: palladium diacetate; potassium acetate / 1-methyl-pyrrolidin-2-one / 3 h / 110 °C / Inert atmosphere

2: lithium aluminium tetrahydride / tetrahydrofuran / 1 h / 50 °C

3: N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 1 h / 20 °C / Cooling

4: hydrogenchloride / dichloromethane; methanol; 1,4-dioxane / 20 °C

5: N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 0.5 h / 20 °C

With hydrogenchloride; lithium aluminium tetrahydride; potassium acetate; palladium diacetate; N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In tetrahydrofuran; 1,4-dioxane; 1-methyl-pyrrolidin-2-one; methanol; dichloromethane; N,N-dimethyl-formamide;