5-methoxy-2-[1-(4-methoxybenzyl)-1H-indazol-3-yl]-N-[3-(trifluoromethyl)pyridin-4-yl]pyrimidin-4-amine

Base Information

Chemical Name:5-methoxy-2-[1-(4-methoxybenzyl)-1H-indazol-3-yl]-N-[3-(trifluoromethyl)pyridin-4-yl]pyrimidin-4-amine
CAS No.:1429746-86-0
Molecular Formula:C₂₆H₂₁F₃N₆O₂
Molecular Weight:506.487
Hs Code.:

Synonyms:5-methoxy-2-[1-(4-methoxybenzyl)-1H-indazol-3-yl]-N-[3-(trifluoromethyl)pyridin-4-yl]pyrimidin-4-amine

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Chemical Property of 5-methoxy-2-[1-(4-methoxybenzyl)-1H-indazol-3-yl]-N-[3-(trifluoromethyl)pyridin-4-yl]pyrimidin-4-amine

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of 5-methoxy-2-[1-(4-methoxybenzyl)-1H-indazol-3-yl]-N-[3-(trifluoromethyl)pyridin-4-yl]pyrimidin-4-amine

There total 5 articles about 5-methoxy-2-[1-(4-methoxybenzyl)-1H-indazol-3-yl]-N-[3-(trifluoromethyl)pyridin-4-yl]pyrimidin-4-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: 3.73%

: 1429747-36-3
5-methoxy-2-[1-(4-methoxybenzyl)-1H-indazol-3-yl]pyrimidin-4-amine

: 1060801-89-9
4-bromo-3-(trifluoromethyl)pyridine

: 1429746-86-0
5-methoxy-2-[1-(4-methoxybenzyl)-1H-indazol-3-yl]-N-[3-(trifluoromethyl)pyridin-4-yl]pyrimidin-4-amine

Guidance literature:: With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; sodium t-butanolate; In N,N-dimethyl-formamide; at 100 ℃; for 24h; Inert atmosphere;

Reference yield:

: 50264-88-5
indazole-3-carbonitrile

: 1429746-86-0
5-methoxy-2-[1-(4-methoxybenzyl)-1H-indazol-3-yl]-N-[3-(trifluoromethyl)pyridin-4-yl]pyrimidin-4-amine

Guidance literature:: Multi-step reaction with 4 steps

1: caesium carbonate / N,N-dimethyl-formamide / 18 h / 20 °C / Inert atmosphere

2: sodium methylate; ammonium chloride; acetic acid / methanol / 23 h / 20 - 50 °C / Inert atmosphere

3: piperidine / i-Amyl alcohol / 72 h / 100 °C / Inert atmosphere

4: tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; sodium t-butanolate / N,N-dimethyl-formamide / 24 h / 100 °C / Inert atmosphere

With piperidine; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; sodium methylate; ammonium chloride; caesium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; acetic acid; sodium t-butanolate; In methanol; i-Amyl alcohol; N,N-dimethyl-formamide;

Reference yield:

: 1429747-31-8
1-(4-methoxybenzyl)-1H-indazole-3-carboximidamide

: 1429746-86-0
5-methoxy-2-[1-(4-methoxybenzyl)-1H-indazol-3-yl]-N-[3-(trifluoromethyl)pyridin-4-yl]pyrimidin-4-amine

Guidance literature:: Multi-step reaction with 2 steps

1: piperidine / i-Amyl alcohol / 72 h / 100 °C / Inert atmosphere

2: tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; sodium t-butanolate / N,N-dimethyl-formamide / 24 h / 100 °C / Inert atmosphere

With piperidine; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; sodium t-butanolate; In i-Amyl alcohol; N,N-dimethyl-formamide;