N-[[5-[1-(2-imidazol-1-ylethyl)indazol-3-yl]-1,2,4-oxadiazol-3-yl]methyl]benzamide

Base Information

Chemical Name:N-[[5-[1-(2-imidazol-1-ylethyl)indazol-3-yl]-1,2,4-oxadiazol-3-yl]methyl]benzamide
CAS No.:1309060-58-9
Molecular Formula:C₂₂H₁₉N₇O₂
Molecular Weight:413.439
Hs Code.:

Synonyms:N-[[5-[1-(2-imidazol-1-ylethyl)indazol-3-yl]-1,2,4-oxadiazol-3-yl]methyl]benzamide

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Chemical Property of N-[[5-[1-(2-imidazol-1-ylethyl)indazol-3-yl]-1,2,4-oxadiazol-3-yl]methyl]benzamide

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Technology Process of N-[[5-[1-(2-imidazol-1-ylethyl)indazol-3-yl]-1,2,4-oxadiazol-3-yl]methyl]benzamide

There total 4 articles about N-[[5-[1-(2-imidazol-1-ylethyl)indazol-3-yl]-1,2,4-oxadiazol-3-yl]methyl]benzamide 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: 18.0%

: 1309060-47-6
[5-[1-(2-imidazol-1-ylethyl)indazol-3-yl]-1,2,4-oxadiazol-3-yl]methanamine

: 65-85-0,8013-63-6
benzoic acid

: 1309060-58-9
N-[[5-[1-(2-imidazol-1-ylethyl)indazol-3-yl]-1,2,4-oxadiazol-3-yl]methyl]benzamide

Guidance literature:: benzoic acid; With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In N,N-dimethyl-formamide; at 20 ℃; for 0.5h; Inert atmosphere;

[5-[1-(2-imidazol-1-ylethyl)indazol-3-yl]-1,2,4-oxadiazol-3-yl]methanamine; In N,N-dimethyl-formamide; Inert atmosphere;
DOI:10.1021/jm401881q

Reference yield:

: 1151512-98-9
3-[3-tert-butoxycarbonylaminomethyl-1,2,4-oxadiazol-5-yl]indazole

: 1309060-58-9
N-[[5-[1-(2-imidazol-1-ylethyl)indazol-3-yl]-1,2,4-oxadiazol-3-yl]methyl]benzamide

Guidance literature:: Multi-step reaction with 3 steps

1: caesium carbonate / N,N-dimethyl-formamide / 0.5 h / 20 °C / Inert atmosphere

2: trifluoroacetic acid; water; chlorotriisopropylsilane / 20 °C

3: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 0.5 h / 20 °C / Inert atmosphere

With chlorotriisopropylsilane; water; caesium carbonate; N-ethyl-N,N-diisopropylamine; HATU; trifluoroacetic acid; In N,N-dimethyl-formamide;

Reference yield:

: 1151512-97-8
tert-butyl 2-(1H-indazole-3-carbonyloxyimino)-2-aminoethylcarbamate

: 1309060-58-9
N-[[5-[1-(2-imidazol-1-ylethyl)indazol-3-yl]-1,2,4-oxadiazol-3-yl]methyl]benzamide

Guidance literature:: Multi-step reaction with 4 steps

1: sodium acetate / N,N-dimethyl-formamide / 0.33 h / 140 °C / Microwave irradiation

2: caesium carbonate / N,N-dimethyl-formamide / 0.5 h / 20 °C / Inert atmosphere

3: trifluoroacetic acid; water; chlorotriisopropylsilane / 20 °C

4: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 0.5 h / 20 °C / Inert atmosphere

With chlorotriisopropylsilane; water; sodium acetate; caesium carbonate; N-ethyl-N,N-diisopropylamine; HATU; trifluoroacetic acid; In N,N-dimethyl-formamide;