1-(2-Amino-6-{[2-({2-[1-(cyclopropylmethyl)piperidin-4-yl]-7-(2,4-dichlorophenyl)-[1,2,4]triazolo[1,5-c]pyrimidin-5-yl}amino)ethyl]amino}pyridin-3-yl)-2,2,2-trifluoroethanone

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Chemical Name:1-(2-Amino-6-{[2-({2-[1-(cyclopropylmethyl)piperidin-4-yl]-7-(2,4-dichlorophenyl)-[1,2,4]triazolo[1,5-c]pyrimidin-5-yl}amino)ethyl]amino}pyridin-3-yl)-2,2,2-trifluoroethanone
CAS No.:1196678-17-7
Molecular Formula:C₂₉H₃₀Cl₂F₃N₉O
Molecular Weight:648.518
Hs Code.:

1-(2-Amino-6-{[2-({2-[1-(cyclopropylmethyl)piperidin-4-yl]-7-(2,4-dichlorophenyl)-[1,2,4]triazolo[1,5-c]pyrimidin-5-yl}amino)ethyl]amino}pyridin-3-yl)-2,2,2-trifluoroethanone

Synonyms:1-(2-Amino-6-{[2-({2-[1-(cyclopropylmethyl)piperidin-4-yl]-7-(2,4-dichlorophenyl)-[1,2,4]triazolo[1,5-c]pyrimidin-5-yl}amino)ethyl]amino}pyridin-3-yl)-2,2,2-trifluoroethanone

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Chemical Property of 1-(2-Amino-6-{[2-({2-[1-(cyclopropylmethyl)piperidin-4-yl]-7-(2,4-dichlorophenyl)-[1,2,4]triazolo[1,5-c]pyrimidin-5-yl}amino)ethyl]amino}pyridin-3-yl)-2,2,2-trifluoroethanone

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Technology Process of 1-(2-Amino-6-{[2-({2-[1-(cyclopropylmethyl)piperidin-4-yl]-7-(2,4-dichlorophenyl)-[1,2,4]triazolo[1,5-c]pyrimidin-5-yl}amino)ethyl]amino}pyridin-3-yl)-2,2,2-trifluoroethanone

There total 13 articles about 1-(2-Amino-6-{[2-({2-[1-(cyclopropylmethyl)piperidin-4-yl]-7-(2,4-dichlorophenyl)-[1,2,4]triazolo[1,5-c]pyrimidin-5-yl}amino)ethyl]amino}pyridin-3-yl)-2,2,2-trifluoroethanone 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: 48.0%

: 1-{2-amino-6-[(2-aminoethyl)amino]pyridin-3-yl}-2,2,2-trifluoroethanone hydrochloride

: 1196678-38-2
5-Chloro-2-[1-(cyclopropylmethyl)piperidin-4-yl]-7-(2,4-dichlorophenyl)[1,2,4]triazolo[1,5-c]-pyrimidine

: 1196678-17-7
1-(2-Amino-6-{[2-({2-[1-(cyclopropylmethyl)piperidin-4-yl]-7-(2,4-dichlorophenyl)-[1,2,4]triazolo[1,5-c]pyrimidin-5-yl}amino)ethyl]amino}pyridin-3-yl)-2,2,2-trifluoroethanone

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dimethyl sulfoxide; at 130 ℃; for 0.5h; Microwave irradiation;

Reference yield:

: 6574-98-7
2,4-dichlorobenzylnitrile

: 1196678-17-7
1-(2-Amino-6-{[2-({2-[1-(cyclopropylmethyl)piperidin-4-yl]-7-(2,4-dichlorophenyl)-[1,2,4]triazolo[1,5-c]pyrimidin-5-yl}amino)ethyl]amino}pyridin-3-yl)-2,2,2-trifluoroethanone

Guidance literature:: Multi-step reaction with 7 steps

1.1: diisopropylamine; n-butyllithium / hexane; tetrahydrofuran / -70 - -60 °C / Inert atmosphere

1.2: 16.33 h / -70 - 20 °C

2.1: ethanol; sodium / ethanol / 4 h / Reflux

3.1: 1-methyl-pyrrolidin-2-one / 3 h / 150 °C

4.1: hydrogenchloride / 1,4-dioxane / 3 h / 20 °C

5.1: potassium carbonate / N,N-dimethyl-formamide / 16 h / 80 °C

6.1: trichlorophosphate; N-benzyl-N,N,N-triethylammonium chloride / 2.5 h / 120 °C

6.2: pH 7

7.1: N-ethyl-N,N-diisopropylamine / dimethyl sulfoxide / 0.5 h / 130 °C / Microwave irradiation

With hydrogenchloride; n-butyllithium; ethanol; N-benzyl-N,N,N-triethylammonium chloride; sodium; potassium carbonate; diisopropylamine; N-ethyl-N,N-diisopropylamine; trichlorophosphate; In tetrahydrofuran; 1,4-dioxane; 1-methyl-pyrrolidin-2-one; ethanol; hexane; dimethyl sulfoxide; N,N-dimethyl-formamide;

Reference yield:

: 159603-71-1
t-butyl N-(6-chloro-2-pyridinyl)carbamate

: 1196678-17-7
1-(2-Amino-6-{[2-({2-[1-(cyclopropylmethyl)piperidin-4-yl]-7-(2,4-dichlorophenyl)-[1,2,4]triazolo[1,5-c]pyrimidin-5-yl}amino)ethyl]amino}pyridin-3-yl)-2,2,2-trifluoroethanone

Guidance literature:: Multi-step reaction with 4 steps

1.1: n-butyllithium / tetrahydrofuran / -50 - 0 °C

1.2: 1 h / -40 °C

2.1: N-ethyl-N,N-diisopropylamine / dimethyl sulfoxide / 0.5 h / 90 °C / Microwave irradiation

3.1: hydrogenchloride / 1,4-dioxane / 20 h

4.1: N-ethyl-N,N-diisopropylamine / dimethyl sulfoxide / 0.5 h / 130 °C / Microwave irradiation

With hydrogenchloride; n-butyllithium; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; 1,4-dioxane; dimethyl sulfoxide;