N-(4,6-Diamino-2-{3-[(2-fluorophenyl)sulphanyl]-1H-indazol-1-yl}pyrimidin-5-yl)-3-methyl-butanamide

Base Information

Chemical Name:N-(4,6-Diamino-2-{3-[(2-fluorophenyl)sulphanyl]-1H-indazol-1-yl}pyrimidin-5-yl)-3-methyl-butanamide
CAS No.:1234572-63-4
Molecular Formula:C₂₂H₂₂FN₇OS
Molecular Weight:451.527
Hs Code.:

Synonyms:N-(4,6-Diamino-2-{3-[(2-fluorophenyl)sulphanyl]-1H-indazol-1-yl}pyrimidin-5-yl)-3-methyl-butanamide

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Chemical Property of N-(4,6-Diamino-2-{3-[(2-fluorophenyl)sulphanyl]-1H-indazol-1-yl}pyrimidin-5-yl)-3-methyl-butanamide

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Technology Process of N-(4,6-Diamino-2-{3-[(2-fluorophenyl)sulphanyl]-1H-indazol-1-yl}pyrimidin-5-yl)-3-methyl-butanamide

There total 5 articles about N-(4,6-Diamino-2-{3-[(2-fluorophenyl)sulphanyl]-1H-indazol-1-yl}pyrimidin-5-yl)-3-methyl-butanamide 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: 47.0%

: 1234572-51-0
2-{3-[(2-fluorophenyl)sulphanyl]-1H-indazol-1-yl}pyrimidine-4,5,6-triamine

: 108-12-3
isopentanoyl chloride

: 1234572-63-4
N-(4,6-Diamino-2-{3-[(2-fluorophenyl)sulphanyl]-1H-indazol-1-yl}pyrimidin-5-yl)-3-methyl-butanamide

Guidance literature:: With pyridine; at 0 - 20 ℃; for 18h;

Reference yield:

: 2557-78-0
2-fluorothiophenol

: 1234572-63-4
N-(4,6-Diamino-2-{3-[(2-fluorophenyl)sulphanyl]-1H-indazol-1-yl}pyrimidin-5-yl)-3-methyl-butanamide

Guidance literature:: Multi-step reaction with 4 steps

1: potassium carbonate / copper(l) iodide / isopropyl alcohol; ethylene glycol / 20 h / 130 °C

2: caesium carbonate / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; XPhos / N,N-dimethyl-formamide; toluene / 17 h / 90 °C / Inert atmosphere

3: hydrogen; pyridine / palladium 10% on activated carbon / 17 h / 20 °C / 2625.26 Torr

4: pyridine / 18 h / 0 - 20 °C

With pyridine; hydrogen; potassium carbonate; caesium carbonate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; copper(l) iodide; palladium 10% on activated carbon; XPhos; In ethylene glycol; N,N-dimethyl-formamide; isopropyl alcohol; toluene;

Reference yield:

: 66607-27-0
3-iodoindazole

: 1234572-63-4
N-(4,6-Diamino-2-{3-[(2-fluorophenyl)sulphanyl]-1H-indazol-1-yl}pyrimidin-5-yl)-3-methyl-butanamide

Guidance literature:: Multi-step reaction with 4 steps

1: potassium carbonate / copper(l) iodide / isopropyl alcohol; ethylene glycol / 20 h / 130 °C

2: caesium carbonate / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; XPhos / N,N-dimethyl-formamide; toluene / 17 h / 90 °C / Inert atmosphere

3: hydrogen; pyridine / palladium 10% on activated carbon / 17 h / 20 °C / 2625.26 Torr

4: pyridine / 18 h / 0 - 20 °C

With pyridine; hydrogen; potassium carbonate; caesium carbonate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; copper(l) iodide; palladium 10% on activated carbon; XPhos; In ethylene glycol; N,N-dimethyl-formamide; isopropyl alcohol; toluene;