1-{3-[5-(1-methyl-1H-pyrazol-4-yl)-1H-pyrrolo[2,3-b]pyridin-3-yl]-isoxazol-5-yl}-1-phenylethanol

Base Information

Chemical Name:1-{3-[5-(1-methyl-1H-pyrazol-4-yl)-1H-pyrrolo[2,3-b]pyridin-3-yl]-isoxazol-5-yl}-1-phenylethanol
CAS No.:1379669-42-7
Molecular Formula:C₂₂H₁₉N₅O₂
Molecular Weight:385.425
Hs Code.:

Synonyms:1-{3-[5-(1-methyl-1H-pyrazol-4-yl)-1H-pyrrolo[2,3-b]pyridin-3-yl]-isoxazol-5-yl}-1-phenylethanol

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Chemical Property of 1-{3-[5-(1-methyl-1H-pyrazol-4-yl)-1H-pyrrolo[2,3-b]pyridin-3-yl]-isoxazol-5-yl}-1-phenylethanol

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Technology Process of 1-{3-[5-(1-methyl-1H-pyrazol-4-yl)-1H-pyrrolo[2,3-b]pyridin-3-yl]-isoxazol-5-yl}-1-phenylethanol

There total 5 articles about 1-{3-[5-(1-methyl-1H-pyrazol-4-yl)-1H-pyrrolo[2,3-b]pyridin-3-yl]-isoxazol-5-yl}-1-phenylethanol 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:

: 1379670-76-4
tert-butyl 3-(4-methoxymethoxy-4-phenylpent-2-ynoyl)-5-(1-methyl-1H-pyrazol-4-yl)-1H-pyrrolo[2,3-b]pyridine-1-carboxylate

: 1379669-42-7
1-{3-[5-(1-methyl-1H-pyrazol-4-yl)-1H-pyrrolo[2,3-b]pyridin-3-yl]-isoxazol-5-yl}-1-phenylethanol

Guidance literature:: tert-butyl 3-(4-methoxymethoxy-4-phenylpent-2-ynoyl)-5-(1-methyl-1H-pyrazol-4-yl)-1H-pyrrolo[2,3-b]pyridine-1-carboxylate; With hydroxylamine hydrochloride; triethylamine; In ethanol; at 80 ℃; for 120h;

With hydrogenchloride; In methanol; at 55 ℃; for 0.5h;

Reference yield:

: 918522-51-7
5-(1-methyl-1H-pyrazol-4-yl)-1H-pyrrolo[2,3-b]-pyridine

: 1379669-42-7
1-{3-[5-(1-methyl-1H-pyrazol-4-yl)-1H-pyrrolo[2,3-b]pyridin-3-yl]-isoxazol-5-yl}-1-phenylethanol

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium hydroxide; iodine / N,N-dimethyl-formamide / 1.5 h / 20 °C

2.1: triethylamine; dmap / dichloromethane / 4 h / 20 °C

3.1: caesium carbonate; copper(l) iodide; palladium diacetate; tri-tert-butyl phosphine / acetonitrile; toluene / 0.08 h / 80 °C

4.1: triethylamine; hydroxylamine hydrochloride / ethanol / 120 h / 80 °C

4.2: 0.5 h / 55 °C

With dmap; copper(l) iodide; tri-tert-butyl phosphine; hydroxylamine hydrochloride; iodine; palladium diacetate; caesium carbonate; triethylamine; potassium hydroxide; In ethanol; dichloromethane; N,N-dimethyl-formamide; toluene; acetonitrile;

Reference yield:

: 1093676-98-2
3-iodo-5-(1-methyl-1H-pyrazol-4-yl)-1H-pyrrolo[2,3-b]pyridine

: 1379669-42-7
1-{3-[5-(1-methyl-1H-pyrazol-4-yl)-1H-pyrrolo[2,3-b]pyridin-3-yl]-isoxazol-5-yl}-1-phenylethanol

Guidance literature:: Multi-step reaction with 3 steps

1.1: triethylamine; dmap / dichloromethane / 4 h / 20 °C

2.1: caesium carbonate; copper(l) iodide; palladium diacetate; tri-tert-butyl phosphine / acetonitrile; toluene / 0.08 h / 80 °C

3.1: triethylamine; hydroxylamine hydrochloride / ethanol / 120 h / 80 °C

3.2: 0.5 h / 55 °C

With dmap; copper(l) iodide; tri-tert-butyl phosphine; hydroxylamine hydrochloride; palladium diacetate; caesium carbonate; triethylamine; In ethanol; dichloromethane; toluene; acetonitrile;