(R)-(4-(4-(4-(2-(isopropylsulfonyl)phenylamino)pyrazolo[1,5-a][1,3,5]triazin-2-ylamino)-5-methoxy-2-methylphenyl)piperidin-1-yl)(morpholin-3-yl)methanone

Base Information

Chemical Name:(R)-(4-(4-(4-(2-(isopropylsulfonyl)phenylamino)pyrazolo[1,5-a][1,3,5]triazin-2-ylamino)-5-methoxy-2-methylphenyl)piperidin-1-yl)(morpholin-3-yl)methanone
CAS No.:1190115-55-9
Molecular Formula:C₃₂H₄₀N₈O₅S
Molecular Weight:648.786
Hs Code.:

(R)-(4-(4-(4-(2-(isopropylsulfonyl)phenylamino)pyrazolo[1,5-a][1,3,5]triazin-2-ylamino)-5-methoxy-2-methylphenyl)piperidin-1-yl)(morpholin-3-yl)methanone

Synonyms:(R)-(4-(4-(4-(2-(isopropylsulfonyl)phenylamino)pyrazolo[1,5-a][1,3,5]triazin-2-ylamino)-5-methoxy-2-methylphenyl)piperidin-1-yl)(morpholin-3-yl)methanone

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Chemical Property of (R)-(4-(4-(4-(2-(isopropylsulfonyl)phenylamino)pyrazolo[1,5-a][1,3,5]triazin-2-ylamino)-5-methoxy-2-methylphenyl)piperidin-1-yl)(morpholin-3-yl)methanone

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Technology Process of (R)-(4-(4-(4-(2-(isopropylsulfonyl)phenylamino)pyrazolo[1,5-a][1,3,5]triazin-2-ylamino)-5-methoxy-2-methylphenyl)piperidin-1-yl)(morpholin-3-yl)methanone

There total 5 articles about (R)-(4-(4-(4-(2-(isopropylsulfonyl)phenylamino)pyrazolo[1,5-a][1,3,5]triazin-2-ylamino)-5-methoxy-2-methylphenyl)piperidin-1-yl)(morpholin-3-yl)methanone 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:

: 1190115-60-6
(R)-tert-butyl 3-(4-(4-(4-(2-(isopropylsulfonyl)phenylamino)pyrazolo[1,5-a][1,3,5]triazin-2-ylamino)-5-methoxy-2-methylphenyl)piperidine-1-carbonyl)morpholine-4-carboxylate

: 1190115-55-9
(R)-(4-(4-(4-(2-(isopropylsulfonyl)phenylamino)pyrazolo[1,5-a][1,3,5]triazin-2-ylamino)-5-methoxy-2-methylphenyl)piperidin-1-yl)(morpholin-3-yl)methanone

Guidance literature:: (R)-tert-butyl 3-(4-(4-(4-(2-(isopropylsulfonyl)phenylamino)pyrazolo[1,5-a][1,3,5]triazin-2-ylamino)-5-methoxy-2-methylphenyl)piperidine-1-carbonyl)morpholine-4-carboxylate; With hydrogenchloride; In 1,4-dioxane; at 20 ℃; for 0.5h;

With sodium hydrogencarbonate; In water;

Reference yield:

: 2-methoxy-5-methyl-4-(piperidin-4-yl)aniline trifluoroacetate

: 1190115-55-9
(R)-(4-(4-(4-(2-(isopropylsulfonyl)phenylamino)pyrazolo[1,5-a][1,3,5]triazin-2-ylamino)-5-methoxy-2-methylphenyl)piperidin-1-yl)(morpholin-3-yl)methanone

Guidance literature:: Multi-step reaction with 3 steps

1: trifluoroacetic acid / isopropyl alcohol / 3 h / 150 °C

2: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide

3: hydrogenchloride / 1,4-dioxane / 0.5 h / 20 °C

With hydrogenchloride; N-ethyl-N,N-diisopropylamine; HATU; trifluoroacetic acid; In 1,4-dioxane; N,N-dimethyl-formamide; isopropyl alcohol;

Reference yield:

: 1190115-52-6
N-(2-(isopropylsulfonyl)phenyl)-2-(methylthio)pyrazolo[1,5-a][1,3,5]triazine

: 1190115-55-9
(R)-(4-(4-(4-(2-(isopropylsulfonyl)phenylamino)pyrazolo[1,5-a][1,3,5]triazin-2-ylamino)-5-methoxy-2-methylphenyl)piperidin-1-yl)(morpholin-3-yl)methanone

Guidance literature:: Multi-step reaction with 4 steps

1: 3-chloro-benzenecarboperoxoic acid / 1,2-dichloro-ethane / 0 - 20 °C

2: trifluoroacetic acid / isopropyl alcohol / 3 h / 150 °C

3: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide

4: hydrogenchloride / 1,4-dioxane / 0.5 h / 20 °C

With hydrogenchloride; N-ethyl-N,N-diisopropylamine; 3-chloro-benzenecarboperoxoic acid; HATU; trifluoroacetic acid; In 1,4-dioxane; 1,2-dichloro-ethane; N,N-dimethyl-formamide; isopropyl alcohol;