6-[cyclohexyl(cyclopropylmethyl)amino]-N-[4-(1H-1,2,4-triazol-1-ylmethyl)phenyl]pyrimidine-4-carboxamide

Base Information

Chemical Name:6-[cyclohexyl(cyclopropylmethyl)amino]-N-[4-(1H-1,2,4-triazol-1-ylmethyl)phenyl]pyrimidine-4-carboxamide
CAS No.:1114591-75-1
Molecular Formula:C₂₄H₂₉N₇O
Molecular Weight:431.541
Hs Code.:

Synonyms:6-[cyclohexyl(cyclopropylmethyl)amino]-N-[4-(1H-1,2,4-triazol-1-ylmethyl)phenyl]pyrimidine-4-carboxamide

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Chemical Property of 6-[cyclohexyl(cyclopropylmethyl)amino]-N-[4-(1H-1,2,4-triazol-1-ylmethyl)phenyl]pyrimidine-4-carboxamide

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Technology Process of 6-[cyclohexyl(cyclopropylmethyl)amino]-N-[4-(1H-1,2,4-triazol-1-ylmethyl)phenyl]pyrimidine-4-carboxamide

There total 5 articles about 6-[cyclohexyl(cyclopropylmethyl)amino]-N-[4-(1H-1,2,4-triazol-1-ylmethyl)phenyl]pyrimidine-4-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:

: 1114592-08-3
6-[cyclohexyl(cyclopropylmethyl)amino]pyrimidine-4-carboxylic acid

: 119192-10-8
4-(1H-1,2,4-triazol-1-ylmethyl)aniline

: 1114591-75-1
6-[cyclohexyl(cyclopropylmethyl)amino]-N-[4-(1H-1,2,4-triazol-1-ylmethyl)phenyl]pyrimidine-4-carboxamide

Guidance literature:: With CF₃O₃S^(1-)*C₅H₅NPol⁽¹⁺⁾; triethylamine; In dichloromethane; at 20 ℃; for 24h; divinylbenzene

Reference yield:

: 1114592-06-1
methyl 2-chloro-6-[cyclohexyl(cyclopropylmethyl)amino]pyrimidine-4-carboxylate

: 1114591-75-1
6-[cyclohexyl(cyclopropylmethyl)amino]-N-[4-(1H-1,2,4-triazol-1-ylmethyl)phenyl]pyrimidine-4-carboxamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: ammonium formate / palladium 10% on activated carbon / water; isopropyl alcohol / 0.75 h / 20 °C

2.1: lithium hydroxide; water / tetrahydrofuran; ethanol / 1 h / 20 °C

2.2: pH 6

3.1: CF₃O₃S^(1-)*C₅H₅NPol⁽¹⁺⁾; triethylamine / dichloromethane / 24 h / 20 °C

With lithium hydroxide; CF₃O₃S^(1-)*C₅H₅NPol⁽¹⁺⁾; water; ammonium formate; triethylamine; palladium 10% on activated carbon; In tetrahydrofuran; ethanol; dichloromethane; water; isopropyl alcohol;

Reference yield:

: 99175-39-0
cyclohexyl-cyclopropylmethyl-amine; hydrochloride

: 1114591-75-1
6-[cyclohexyl(cyclopropylmethyl)amino]-N-[4-(1H-1,2,4-triazol-1-ylmethyl)phenyl]pyrimidine-4-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: triethylamine / tetrahydrofuran / 48 h / 0 - 20 °C

2.1: ammonium formate / palladium 10% on activated carbon / water; isopropyl alcohol / 0.75 h / 20 °C

3.1: lithium hydroxide; water / tetrahydrofuran; ethanol / 1 h / 20 °C

3.2: pH 6

4.1: CF₃O₃S^(1-)*C₅H₅NPol⁽¹⁺⁾; triethylamine / dichloromethane / 24 h / 20 °C

With lithium hydroxide; CF₃O₃S^(1-)*C₅H₅NPol⁽¹⁺⁾; water; ammonium formate; triethylamine; palladium 10% on activated carbon; In tetrahydrofuran; ethanol; dichloromethane; water; isopropyl alcohol;