6-(benzo[d]thiazol-6-ylamino)-4-(cyclopropylamino)-N-(4-hydroxy-4-methylcyclohexyl)nicotinamide

Base Information

Chemical Name:6-(benzo[d]thiazol-6-ylamino)-4-(cyclopropylamino)-N-(4-hydroxy-4-methylcyclohexyl)nicotinamide
CAS No.:1610018-01-3
Molecular Formula:C₂₃H₂₇N₅O₂S
Molecular Weight:437.566
Hs Code.:

Synonyms:6-(benzo[d]thiazol-6-ylamino)-4-(cyclopropylamino)-N-(4-hydroxy-4-methylcyclohexyl)nicotinamide

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Chemical Property of 6-(benzo[d]thiazol-6-ylamino)-4-(cyclopropylamino)-N-(4-hydroxy-4-methylcyclohexyl)nicotinamide

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Technology Process of 6-(benzo[d]thiazol-6-ylamino)-4-(cyclopropylamino)-N-(4-hydroxy-4-methylcyclohexyl)nicotinamide

There total 4 articles about 6-(benzo[d]thiazol-6-ylamino)-4-(cyclopropylamino)-N-(4-hydroxy-4-methylcyclohexyl)nicotinamide 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: 5.0%

: 533-30-2
1,3-benzothiazol-6-amine

: 1610021-15-2
6-chloro-4-(cyclopropylamino)-N-(4-hydroxy-4-methylcyclohexyl)nicotinamide

: 1610018-01-3
6-(benzo[d]thiazol-6-ylamino)-4-(cyclopropylamino)-N-(4-hydroxy-4-methylcyclohexyl)nicotinamide

Guidance literature:: 1,3-benzothiazol-6-amine; 6-chloro-4-(cyclopropylamino)-N-(4-hydroxy-4-methylcyclohexyl)nicotinamide; With sodium carbonate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; In 1,4-dioxane; for 0.166667h; Inert atmosphere;

With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; In 1,4-dioxane; at 110 ℃; for 18.1667h; Inert atmosphere;

Reference yield:

: 40296-46-6
ethyl 4,6-dichloronicotinate

: 1610018-01-3
6-(benzo[d]thiazol-6-ylamino)-4-(cyclopropylamino)-N-(4-hydroxy-4-methylcyclohexyl)nicotinamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl acetamide / 5 h / 90 °C

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

3.1: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 3 h / 20 °C

4.1: sodium carbonate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene / 1,4-dioxane / 0.17 h / Inert atmosphere

4.2: 18.17 h / 110 °C / Inert atmosphere

With lithium hydroxide monohydrate; water; sodium carbonate; N-ethyl-N,N-diisopropylamine; HATU; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; In 1,4-dioxane; N,N-dimethyl acetamide; N,N-dimethyl-formamide;

Reference yield:

: 1588424-59-2
ethyl 6-chloro-4-(cyclopropylamino)pyridine-3-carboxylate

: 1610018-01-3
6-(benzo[d]thiazol-6-ylamino)-4-(cyclopropylamino)-N-(4-hydroxy-4-methylcyclohexyl)nicotinamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: water; lithium hydroxide monohydrate / 1 h / 20 °C

2.1: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 3 h / 20 °C

3.1: sodium carbonate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene / 1,4-dioxane / 0.17 h / Inert atmosphere

3.2: 18.17 h / 110 °C / Inert atmosphere

With lithium hydroxide monohydrate; water; sodium carbonate; N-ethyl-N,N-diisopropylamine; HATU; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; In 1,4-dioxane; N,N-dimethyl-formamide;