(1S,2R)-2-(4-(2,6-dichlorobenzamido)pyridin-2-ylcarbamoyl)cyclopropanecarboxylic acid

Base Information

• Chemical Name: (1S,2R)-2-(4-(2,6-dichlorobenzamido)pyridin-2-ylcarbamoyl)cyclopropanecarboxylic acid
• CAS No.: 1258294-23-3
• Molecular Formula: C₁₇H₁₃Cl₂N₃O₄
• Molecular Weight: 394.214

Synonyms:(1S,2R)-2-(4-(2,6-dichlorobenzamido)pyridin-2-ylcarbamoyl)cyclopropanecarboxylic acid

Chemical Property of (1S,2R)-2-(4-(2,6-dichlorobenzamido)pyridin-2-ylcarbamoyl)cyclopropanecarboxylic acid

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Technology Process of (1S,2R)-2-(4-(2,6-dichlorobenzamido)pyridin-2-ylcarbamoyl)cyclopropanecarboxylic acid

There total 3 articles about (1S,2R)-2-(4-(2,6-dichlorobenzamido)pyridin-2-ylcarbamoyl)cyclopropanecarboxylic acid 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%

2,6-dichloro-N-(2-(2,4-dioxo-3-azabicyclo[3.1.0]hexan-3-yl)pyridin-4-yl)benzamide (1258298-13-3) → (1S,2R)-2-(4-(2,6-dichlorobenzamido)pyridin-2-ylcarbamoyl)cyclopropanecarboxylic acid (1258294-23-3) + (1R,2S)-2-(4-(2,6-dichlorobenzamido)pyridin-2-ylcarbamoyl)cyclopropanecarboxylic acid (1258294-24-4)

Guidance literature:

With lithium hydroxide; In tetrahydrofuran; at 20 ℃; for 2h;

DOI:10.1021/jm400266t

Reference yield:

N-(2-aminopyridin-4-yl)-2,6-dichlorobenzamide (1258291-83-6) → (1S,2R)-2-(4-(2,6-dichlorobenzamido)pyridin-2-ylcarbamoyl)cyclopropanecarboxylic acid (1258294-23-3) + (1R,2S)-2-(4-(2,6-dichlorobenzamido)pyridin-2-ylcarbamoyl)cyclopropanecarboxylic acid (1258294-24-4)

Guidance literature:

Multi-step reaction with 2 steps

1: 1,4-dioxane / 4 h / 90 °C / Inert atmosphere

2: lithium hydroxide / tetrahydrofuran / 2 h / 20 °C

With lithium hydroxide; In tetrahydrofuran; 1,4-dioxane;

DOI:10.1021/jm400266t

Reference yield:

3-oxabicyclo[3.1.0]hexane-2,4-dione (5617-74-3) → (1S,2R)-2-(4-(2,6-dichlorobenzamido)pyridin-2-ylcarbamoyl)cyclopropanecarboxylic acid (1258294-23-3) + (1R,2S)-2-(4-(2,6-dichlorobenzamido)pyridin-2-ylcarbamoyl)cyclopropanecarboxylic acid (1258294-24-4)

Guidance literature:

Multi-step reaction with 2 steps

1: 1,4-dioxane / 4 h / 90 °C / Inert atmosphere

2: lithium hydroxide / tetrahydrofuran / 2 h / 20 °C

With lithium hydroxide; In tetrahydrofuran; 1,4-dioxane;

DOI:10.1021/jm400266t

upstream raw materials:

2,6-dichloro-N-(2-(2,4-dioxo-3-azabicyclo[3.1.0]hexan-3-yl)pyridin-4-yl)benzamide

N-(2-aminopyridin-4-yl)-2,6-dichlorobenzamide

3-oxabicyclo[3.1.0]hexane-2,4-dione

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