(3-((R)-2-((R)-2-((2-carbamoyl-4-iodophenyl)amino)-1-hydroxy-2-oxoethyl)-3-oxomorpholin-4-yl)-1H-pyrazol-1-yl)methyl pivalate

Base Information

Chemical Name:(3-((R)-2-((R)-2-((2-carbamoyl-4-iodophenyl)amino)-1-hydroxy-2-oxoethyl)-3-oxomorpholin-4-yl)-1H-pyrazol-1-yl)methyl pivalate
CAS No.:1616070-63-3
Molecular Formula:C₂₂H₂₆IN₅O₇
Molecular Weight:599.382
Hs Code.:

Synonyms:(3-((R)-2-((R)-2-((2-carbamoyl-4-iodophenyl)amino)-1-hydroxy-2-oxoethyl)-3-oxomorpholin-4-yl)-1H-pyrazol-1-yl)methyl pivalate

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Chemical Property of (3-((R)-2-((R)-2-((2-carbamoyl-4-iodophenyl)amino)-1-hydroxy-2-oxoethyl)-3-oxomorpholin-4-yl)-1H-pyrazol-1-yl)methyl pivalate

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Technology Process of (3-((R)-2-((R)-2-((2-carbamoyl-4-iodophenyl)amino)-1-hydroxy-2-oxoethyl)-3-oxomorpholin-4-yl)-1H-pyrazol-1-yl)methyl pivalate

There total 4 articles about (3-((R)-2-((R)-2-((2-carbamoyl-4-iodophenyl)amino)-1-hydroxy-2-oxoethyl)-3-oxomorpholin-4-yl)-1H-pyrazol-1-yl)methyl pivalate 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:

: 1616070-62-2
(R)-2-hydroxy-2-((R)-3-oxo-4-(1-((pivaloyloxy)methyl)-1H-pyrazol-3-yl)morpholin-2-yl)acetic acid

: 32658-67-6
2-amino-5-iodoanthranilamide

: 1616070-63-3
(3-((R)-2-((R)-2-((2-carbamoyl-4-iodophenyl)amino)-1-hydroxy-2-oxoethyl)-3-oxomorpholin-4-yl)-1H-pyrazol-1-yl)methyl pivalate

Guidance literature:: With 1-hydroxy-7-aza-benzotriazole; 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 N,N-dimethyl-formamide;

Reference yield:

: 1616070-60-0
(3-iodo-1H-pyrazol-1-yl)methyl pivalate

: 1616070-63-3
(3-((R)-2-((R)-2-((2-carbamoyl-4-iodophenyl)amino)-1-hydroxy-2-oxoethyl)-3-oxomorpholin-4-yl)-1H-pyrazol-1-yl)methyl pivalate

Guidance literature:: Multi-step reaction with 3 steps

1.1: potassium phosphate / 1,4-dioxane / 0.08 h

1.2: 0.33 h

1.3: 3 h / 50 - 85 °C

2.1: trifluoroacetic acid / 0.75 h

3.1: N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; 1-hydroxy-7-aza-benzotriazole; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide

With potassium phosphate; 1-hydroxy-7-aza-benzotriazole; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In 1,4-dioxane; N,N-dimethyl-formamide;

Reference yield:

: 18997-19-8
Chloromethyl pivalate

: 1616070-63-3
(3-((R)-2-((R)-2-((2-carbamoyl-4-iodophenyl)amino)-1-hydroxy-2-oxoethyl)-3-oxomorpholin-4-yl)-1H-pyrazol-1-yl)methyl pivalate

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium hydride / tetrahydrofuran / 0.5 h / -10 °C

1.2: 1 h / -10 °C

2.1: potassium phosphate / 1,4-dioxane / 0.08 h

2.2: 0.33 h

2.3: 3 h / 50 - 85 °C

3.1: trifluoroacetic acid / 0.75 h

4.1: N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; 1-hydroxy-7-aza-benzotriazole; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide

With potassium phosphate; 1-hydroxy-7-aza-benzotriazole; sodium hydride; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In tetrahydrofuran; 1,4-dioxane; N,N-dimethyl-formamide;