4-(((3-(3-(trifluoromethoxy)phenyl)pyrazolo[1,5-a]pyrimidin-5-yl)amino)methyl)tetrahydro-2H-thiopyran 1,1-dioxide

Base Information

Chemical Name:4-(((3-(3-(trifluoromethoxy)phenyl)pyrazolo[1,5-a]pyrimidin-5-yl)amino)methyl)tetrahydro-2H-thiopyran 1,1-dioxide
CAS No.:1361951-33-8
Molecular Formula:C₁₉H₁₉F₃N₄O₃S
Molecular Weight:440.446
Hs Code.:

Synonyms:4-(((3-(3-(trifluoromethoxy)phenyl)pyrazolo[1,5-a]pyrimidin-5-yl)amino)methyl)tetrahydro-2H-thiopyran 1,1-dioxide

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Chemical Property of 4-(((3-(3-(trifluoromethoxy)phenyl)pyrazolo[1,5-a]pyrimidin-5-yl)amino)methyl)tetrahydro-2H-thiopyran 1,1-dioxide

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Technology Process of 4-(((3-(3-(trifluoromethoxy)phenyl)pyrazolo[1,5-a]pyrimidin-5-yl)amino)methyl)tetrahydro-2H-thiopyran 1,1-dioxide

There total 6 articles about 4-(((3-(3-(trifluoromethoxy)phenyl)pyrazolo[1,5-a]pyrimidin-5-yl)amino)methyl)tetrahydro-2H-thiopyran 1,1-dioxide 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: 29.0%

: 476660-77-2
[(1,1-dioxotetrahydro-2H-thiopyran-4-yl)methyl]amine

: 1361951-79-2
5-chloro-3-(3-(trifluoromethoxy)phenyl)pyrazolo[1,5-a]pyrimidine

: 1361951-33-8
4-(((3-(3-(trifluoromethoxy)phenyl)pyrazolo[1,5-a]pyrimidin-5-yl)amino)methyl)tetrahydro-2H-thiopyran 1,1-dioxide

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In isopropyl alcohol; at 150 ℃; for 12h; Microwave irradiation;
DOI:10.1021/ml500300c

Reference yield:

: 108307-56-8
2-[3-(trifluoromethoxy)phenyl]ethanenitrile

: 1361951-33-8
4-(((3-(3-(trifluoromethoxy)phenyl)pyrazolo[1,5-a]pyrimidin-5-yl)amino)methyl)tetrahydro-2H-thiopyran 1,1-dioxide

Guidance literature:: Multi-step reaction with 5 steps

1: N-ethyl-N,N-diisopropylamine / 4 h / Reflux

2: hydrazine hydrate; acetic acid / ethanol / 16 h / Reflux

3: sodium ethanolate / ethanol / 16 h / Reflux

4: trichlorophosphate / Reflux

5: N-ethyl-N,N-diisopropylamine / isopropyl alcohol / 12 h / 150 °C / Microwave irradiation

With hydrazine hydrate; sodium ethanolate; acetic acid; N-ethyl-N,N-diisopropylamine; trichlorophosphate; In ethanol; isopropyl alcohol;
DOI:10.1021/ml500300c

Reference yield:

: 1361951-71-4
3-(dimethylamino)-2-(3-(trifluoromethoxy)phenyl)acrylonitrlle

: 1361951-33-8
4-(((3-(3-(trifluoromethoxy)phenyl)pyrazolo[1,5-a]pyrimidin-5-yl)amino)methyl)tetrahydro-2H-thiopyran 1,1-dioxide

Guidance literature:: Multi-step reaction with 4 steps

1: hydrazine hydrate; acetic acid / ethanol / 16 h / Reflux

2: sodium ethanolate / ethanol / 16 h / Reflux

3: trichlorophosphate / Reflux

4: N-ethyl-N,N-diisopropylamine / isopropyl alcohol / 12 h / 150 °C / Microwave irradiation

With hydrazine hydrate; sodium ethanolate; acetic acid; N-ethyl-N,N-diisopropylamine; trichlorophosphate; In ethanol; isopropyl alcohol;
DOI:10.1021/ml500300c