7-(8-azabicyclo[3.2.1]oct-3-yl)-3-(3-methoxyphenyl)-2-pyridin-4-ylpyrazolo[1,5-a]pyrimidine

Base Information

Chemical Name:7-(8-azabicyclo[3.2.1]oct-3-yl)-3-(3-methoxyphenyl)-2-pyridin-4-ylpyrazolo[1,5-a]pyrimidine
CAS No.:1186332-14-8
Molecular Formula:C₂₅H₂₅N₅O
Molecular Weight:411.506
Hs Code.:

Synonyms:7-(8-azabicyclo[3.2.1]oct-3-yl)-3-(3-methoxyphenyl)-2-pyridin-4-ylpyrazolo[1,5-a]pyrimidine

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Chemical Property of 7-(8-azabicyclo[3.2.1]oct-3-yl)-3-(3-methoxyphenyl)-2-pyridin-4-ylpyrazolo[1,5-a]pyrimidine

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Technology Process of 7-(8-azabicyclo[3.2.1]oct-3-yl)-3-(3-methoxyphenyl)-2-pyridin-4-ylpyrazolo[1,5-a]pyrimidine

There total 8 articles about 7-(8-azabicyclo[3.2.1]oct-3-yl)-3-(3-methoxyphenyl)-2-pyridin-4-ylpyrazolo[1,5-a]pyrimidine 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: 33.0%

: 1186332-00-2
ethyl 3-(3-(3-methoxyphenyl)-2-(pyridin-4-yl)pyrazolo[1,5-a]pyrimidin-7-yl)-8-azabicyclo[3.2.1]octane-8-carboxylate

: 1186332-14-8
7-(8-azabicyclo[3.2.1]oct-3-yl)-3-(3-methoxyphenyl)-2-pyridin-4-ylpyrazolo[1,5-a]pyrimidine

Guidance literature:: With trimethylsilyl iodide; In chloroform; for 5h; Reflux;

Reference yield:

: 1134598-69-8
2-(3-methoxyphenyl)-3-oxo-3-pyridin-4-yl-propionitrile

: 1186332-14-8
7-(8-azabicyclo[3.2.1]oct-3-yl)-3-(3-methoxyphenyl)-2-pyridin-4-ylpyrazolo[1,5-a]pyrimidine

Guidance literature:: Multi-step reaction with 4 steps

1: trichlorophosphate / 18 h / 80 °C

2: hydrazine hydrate / ethanol / 6.5 h / Reflux

3: acetic acid / 2 h / 80 °C

4: trimethylsilyl iodide / chloroform / 5 h / Reflux

With trimethylsilyl iodide; hydrazine hydrate; acetic acid; trichlorophosphate; In ethanol; chloroform;

Reference yield:

: 32499-64-2
N-carbethoxytropinone

: 1186332-14-8
7-(8-azabicyclo[3.2.1]oct-3-yl)-3-(3-methoxyphenyl)-2-pyridin-4-ylpyrazolo[1,5-a]pyrimidine

Guidance literature:: Multi-step reaction with 5 steps

1: potassium tert-butylate / 1,2-dimethoxyethane; ethanol / 4 h / -10 - 20 °C

2: tetrahydrofuran; toluene / 3 h / 20 °C

3: 48 h / 110 °C

4: acetic acid / 2 h / 80 °C

5: trimethylsilyl iodide / chloroform / 5 h / Reflux

With trimethylsilyl iodide; potassium tert-butylate; acetic acid; In tetrahydrofuran; 1,2-dimethoxyethane; ethanol; chloroform; toluene;