4-(4-phenoxyphenyl)-6-(piperidin-4-yl)-1H-pyrazolo[4,3-c]pyridin-3-amine

Base Information

Chemical Name:4-(4-phenoxyphenyl)-6-(piperidin-4-yl)-1H-pyrazolo[4,3-c]pyridin-3-amine
CAS No.:1266160-29-5
Molecular Formula:C₂₃H₂₃N₅O
Molecular Weight:385.469
Hs Code.:

Synonyms:4-(4-phenoxyphenyl)-6-(piperidin-4-yl)-1H-pyrazolo[4,3-c]pyridin-3-amine

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Chemical Property of 4-(4-phenoxyphenyl)-6-(piperidin-4-yl)-1H-pyrazolo[4,3-c]pyridin-3-amine

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Technology Process of 4-(4-phenoxyphenyl)-6-(piperidin-4-yl)-1H-pyrazolo[4,3-c]pyridin-3-amine

There total 10 articles about 4-(4-phenoxyphenyl)-6-(piperidin-4-yl)-1H-pyrazolo[4,3-c]pyridin-3-amine 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:

: 1266159-39-0
benzyl 4-(3-amino-4-(4-phenoxyphenyl)-1H-pyrazolo[4,3-c]pyridin-6-yl)-1-piperidinecarboxylate

: 1266160-29-5
4-(4-phenoxyphenyl)-6-(piperidin-4-yl)-1H-pyrazolo[4,3-c]pyridin-3-amine

Guidance literature:: benzyl 4-(3-amino-4-(4-phenoxyphenyl)-1H-pyrazolo[4,3-c]pyridin-6-yl)-1-piperidinecarboxylate; With hydrogenchloride; In methanol; for 3h; Reflux;

With sodium hydroxide; In H₂₀O (water); pH=11;

Reference yield:

: 498-94-2
isonipecotic acid

: 1266160-29-5
4-(4-phenoxyphenyl)-6-(piperidin-4-yl)-1H-pyrazolo[4,3-c]pyridin-3-amine

Guidance literature:: Multi-step reaction with 7 steps

1.1: sodium hydroxide / toluene; water / 4 h / 20 °C

2.1: oxalyl dichloride / dichloromethane; N,N-dimethyl-formamide / 1 h / 20 °C

3.1: diisopropylamine; n-butyllithium / hexane; tetrahydrofuran / -78 - 0 °C

4.1: ISOPROPYLAMIDE / 0.17 h / 250 °C / Microwave irradiation

5.1: trichlorophosphate / N,N-dimethyl-formamide / 0.83 h / 90 °C

6.1: hydrazine hydrate / N,N-dimethyl-formamide / 1.5 h / 110 °C

6.2: 1.5 h / 20 °C

7.1: hydrogenchloride / methanol / 3 h / Reflux

7.2: pH 11

With hydrogenchloride; n-butyllithium; oxalyl dichloride; hydrazine hydrate; diisopropylamine; sodium hydroxide; trichlorophosphate; In tetrahydrofuran; methanol; hexane; dichloromethane; ISOPROPYLAMIDE; water; N,N-dimethyl-formamide; toluene;

Reference yield:

: 167414-75-7
ethyl <1-(benzyloxycarbonyl)-4-piperidyl>-3-oxopropanoate

: 1266160-29-5
4-(4-phenoxyphenyl)-6-(piperidin-4-yl)-1H-pyrazolo[4,3-c]pyridin-3-amine

Guidance literature:: Multi-step reaction with 4 steps

1.1: ISOPROPYLAMIDE / 0.17 h / 250 °C / Microwave irradiation

2.1: trichlorophosphate / N,N-dimethyl-formamide / 0.83 h / 90 °C

3.1: hydrazine hydrate / N,N-dimethyl-formamide / 1.5 h / 110 °C

3.2: 1.5 h / 20 °C

4.1: hydrogenchloride / methanol / 3 h / Reflux

4.2: pH 11

With hydrogenchloride; hydrazine hydrate; trichlorophosphate; In methanol; ISOPROPYLAMIDE; N,N-dimethyl-formamide;