N₁-methyl-N₁-(2-morpholinoethyl)-N₃-(2-((2-phenylpyrimidin-5-yl)carbamoyl)-4-(piperidin-1-yl)phenyl)isophthalamide

Base Information

• Chemical Name: N₁-methyl-N₁-(2-morpholinoethyl)-N₃-(2-((2-phenylpyrimidin-5-yl)carbamoyl)-4-(piperidin-1-yl)phenyl)isophthalamide
• CAS No.: 1354652-65-5
• Molecular Formula: C₃₇H₄₁N₇O₄
• Molecular Weight: 647.777

Synonyms:N₁-methyl-N₁-(2-morpholinoethyl)-N₃-(2-((2-phenylpyrimidin-5-yl)carbamoyl)-4-(piperidin-1-yl)phenyl)isophthalamide

Chemical Property of N₁-methyl-N₁-(2-morpholinoethyl)-N₃-(2-((2-phenylpyrimidin-5-yl)carbamoyl)-4-(piperidin-1-yl)phenyl)isophthalamide

Chemical Property:

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Technology Process of N₁-methyl-N₁-(2-morpholinoethyl)-N₃-(2-((2-phenylpyrimidin-5-yl)carbamoyl)-4-(piperidin-1-yl)phenyl)isophthalamide

There total 10 articles about N₁-methyl-N₁-(2-morpholinoethyl)-N₃-(2-((2-phenylpyrimidin-5-yl)carbamoyl)-4-(piperidin-1-yl)phenyl)isophthalamide 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: 28.0%

3-(methyl-(2-morpholinoethyl)carbamoyl)benzoic acid (1354652-99-5) + 2-amino-N-(2-phenylpyrimidin-5-yl)-5-(piperidin-1-yl)benzamide (1354652-80-4) → N1-methyl-N1-(2-morpholinoethyl)-N3-(2-((2-phenylpyrimidin-5-yl)carbamoyl)-4-(piperidin-1-yl)phenyl)isophthalamide (1354652-65-5)

Guidance literature:

With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; at 25 ℃; for 4h;

Reference yield:

benzene 1,3-dicarboxylic acid monomethyl ester (1877-71-0) → N1-methyl-N1-(2-morpholinoethyl)-N3-(2-((2-phenylpyrimidin-5-yl)carbamoyl)-4-(piperidin-1-yl)phenyl)isophthalamide (1354652-65-5)

Guidance literature:

Multi-step reaction with 4 steps

1.1: oxalyl dichloride / N,N-dimethyl-formamide / dichloromethane / 1 h / 40 °C

2.1: triethylamine / dichloromethane / 3 h / 0 - 20 °C

3.1: water; lithium hydroxide monohydrate / tetrahydrofuran / 1 h / 25 °C

3.2: pH 2 - 3

4.1: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 4 h / 25 °C

With dmap; oxalyl dichloride; lithium hydroxide monohydrate; water; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; N,N-dimethyl-formamide; In tetrahydrofuran; dichloromethane;

Reference yield:

5-amino-2-phenylpyrimidine (59808-52-5) → N1-methyl-N1-(2-morpholinoethyl)-N3-(2-((2-phenylpyrimidin-5-yl)carbamoyl)-4-(piperidin-1-yl)phenyl)isophthalamide (1354652-65-5)

Guidance literature:

Multi-step reaction with 3 steps

1: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 25 °C

2: hydrogen / palladium on activated charcoal / ethyl acetate; ethanol / 2 h / 20 °C

3: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 4 h / 25 °C

With dmap; hydrogen; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; palladium on activated charcoal; In ethanol; dichloromethane; ethyl acetate;

upstream raw materials:

methyl-(2-morpholin-4-yl-ethyl)-amine

benzene 1,3-dicarboxylic acid monomethyl ester

5-amino-2-phenylpyrimidine

4-(2-AMINOETHYL)MORPHOLINE

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