N-{(R)-2-[5-(3-fluoro-1H-indazol-5-yl)pyridin-3-ylamino]-2-phenylethyl}isobutyramide

Base Information

Chemical Name:N-{(R)-2-[5-(3-fluoro-1H-indazol-5-yl)pyridin-3-ylamino]-2-phenylethyl}isobutyramide
CAS No.:1613639-16-9
Molecular Formula:C₂₄H₂₄FN₅O
Molecular Weight:417.486
Hs Code.:

Synonyms:N-{(R)-2-[5-(3-fluoro-1H-indazol-5-yl)pyridin-3-ylamino]-2-phenylethyl}isobutyramide

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Chemical Property of N-{(R)-2-[5-(3-fluoro-1H-indazol-5-yl)pyridin-3-ylamino]-2-phenylethyl}isobutyramide

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Technology Process of N-{(R)-2-[5-(3-fluoro-1H-indazol-5-yl)pyridin-3-ylamino]-2-phenylethyl}isobutyramide

There total 7 articles about N-{(R)-2-[5-(3-fluoro-1H-indazol-5-yl)pyridin-3-ylamino]-2-phenylethyl}isobutyramide 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:

: 1613639-46-5
3-fluoro-5-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-1H-indazole

: 1613639-59-0
N-[(R)-2-(5-bromopyridin-3-ylamino)-2-phenylethyl]isobutyramide

: 1613639-16-9
N-{(R)-2-[5-(3-fluoro-1H-indazol-5-yl)pyridin-3-ylamino]-2-phenylethyl}isobutyramide

Guidance literature:: With potassium carbonate; In 1,4-dioxane; water; at 100 ℃; for 2h; Microwave irradiation; Inert atmosphere;

Reference yield:

: 875-74-1
(R)-phenylglycine

: 1613639-16-9
N-{(R)-2-[5-(3-fluoro-1H-indazol-5-yl)pyridin-3-ylamino]-2-phenylethyl}isobutyramide

Guidance literature:: Multi-step reaction with 5 steps

1: L-proline; potassium carbonate; copper(l) iodide / dimethyl sulfoxide / 12 h / 100 °C / Inert atmosphere

2: triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran / 0 - 20 °C / Inert atmosphere

3: hydrazine hydrate / ethanol / 1 h / 80 °C / Inert atmosphere

4: N-ethyl-N,N-diisopropylamine / dichloromethane / 0 - 20 °C / Inert atmosphere

5: potassium carbonate / 1,4-dioxane; water / 2 h / 100 °C / Microwave irradiation; Inert atmosphere

With copper(l) iodide; potassium carbonate; hydrazine hydrate; N-ethyl-N,N-diisopropylamine; triphenylphosphine; L-proline; diethylazodicarboxylate; In tetrahydrofuran; 1,4-dioxane; ethanol; dichloromethane; water; dimethyl sulfoxide; 2: |Mitsunobu Displacement;

Reference yield:

: 625-92-3
3,5-dibromopyridine

: 1613639-16-9
N-{(R)-2-[5-(3-fluoro-1H-indazol-5-yl)pyridin-3-ylamino]-2-phenylethyl}isobutyramide

Guidance literature:: Multi-step reaction with 5 steps

1: L-proline; potassium carbonate; copper(l) iodide / dimethyl sulfoxide / 12 h / 100 °C / Inert atmosphere

2: triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran / 0 - 20 °C / Inert atmosphere

3: hydrazine hydrate / ethanol / 1 h / 80 °C / Inert atmosphere

4: N-ethyl-N,N-diisopropylamine / dichloromethane / 0 - 20 °C / Inert atmosphere

5: potassium carbonate / 1,4-dioxane; water / 2 h / 100 °C / Microwave irradiation; Inert atmosphere

With copper(l) iodide; potassium carbonate; hydrazine hydrate; N-ethyl-N,N-diisopropylamine; triphenylphosphine; L-proline; diethylazodicarboxylate; In tetrahydrofuran; 1,4-dioxane; ethanol; dichloromethane; water; dimethyl sulfoxide; 2: |Mitsunobu Displacement;