4-[6-[3-(aminomethyl)phenyl]-1-ethyl-4-(1H-pyrrol-3-yl)-1H-imidazo[4,5-c]pyridin-2-yl]-1,2,5-oxadiazol-3-amine

Base Information

Chemical Name:4-[6-[3-(aminomethyl)phenyl]-1-ethyl-4-(1H-pyrrol-3-yl)-1H-imidazo[4,5-c]pyridin-2-yl]-1,2,5-oxadiazol-3-amine
CAS No.:913640-15-0
Molecular Formula:C₂₁H₂₀N₈O
Molecular Weight:400.443
Hs Code.:

Synonyms:4-[6-[3-(aminomethyl)phenyl]-1-ethyl-4-(1H-pyrrol-3-yl)-1H-imidazo[4,5-c]pyridin-2-yl]-1,2,5-oxadiazol-3-amine

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Chemical Property of 4-[6-[3-(aminomethyl)phenyl]-1-ethyl-4-(1H-pyrrol-3-yl)-1H-imidazo[4,5-c]pyridin-2-yl]-1,2,5-oxadiazol-3-amine

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Technology Process of 4-[6-[3-(aminomethyl)phenyl]-1-ethyl-4-(1H-pyrrol-3-yl)-1H-imidazo[4,5-c]pyridin-2-yl]-1,2,5-oxadiazol-3-amine

There total 8 articles about 4-[6-[3-(aminomethyl)phenyl]-1-ethyl-4-(1H-pyrrol-3-yl)-1H-imidazo[4,5-c]pyridin-2-yl]-1,2,5-oxadiazol-3-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: 91.0%

: 913642-18-9
4-(6-[3-(aminomethyl)phenyl]-1-ethyl-4-{1-[tris(1-methylethyl)silyl]-1H-pyrrol-3-yl}-1H-imidazo[4,5-c]pyridin-2-yl)-1,2,5-oxadiazol-3-amine

: 913640-15-0
4-[6-[3-(aminomethyl)phenyl]-1-ethyl-4-(1H-pyrrol-3-yl)-1H-imidazo[4,5-c]pyridin-2-yl]-1,2,5-oxadiazol-3-amine

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 25 ℃; for 2h;

Reference yield:

: 913642-07-6
2-bromo-N-ethyl-5-nitro-4-pyridinamine

: 913640-15-0
4-[6-[3-(aminomethyl)phenyl]-1-ethyl-4-(1H-pyrrol-3-yl)-1H-imidazo[4,5-c]pyridin-2-yl]-1,2,5-oxadiazol-3-amine

Guidance literature:: Multi-step reaction with 8 steps

1.1: hydrogenchloride; tin(ll) chloride / water / 0.75 h / 90 °C

1.2: pH ~ 10

2.1: 4-methyl-morpholine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 16 h / 20 °C

3.1: acetic acid / 24 h / 100 °C

4.1: acetic acid; sodium nitrite / 16 h / 20 °C

5.1: hydroxylamine; triethylamine / 1,4-dioxane / 16 h / 100 °C

6.1: potassium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,4-dioxane; water / 12 h / 70 °C

7.1: potassium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,4-dioxane; water / 12 h / 70 °C

8.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 2 h / 25 °C

With 4-methyl-morpholine; hydrogenchloride; tetrabutyl ammonium fluoride; hydroxylamine; potassium carbonate; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; tin(ll) chloride; sodium nitrite; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; 1,4-dioxane; water; N,N-dimethyl-formamide;

Reference yield:

: 4-{6-[3-(aminomethyl)phenyl]-4-chloro-1-ethyl-1H-imidazo[4,5-c]pyridin-2-yl}-1,2,5-oxadiazol-3-amine

: 913640-15-0
4-[6-[3-(aminomethyl)phenyl]-1-ethyl-4-(1H-pyrrol-3-yl)-1H-imidazo[4,5-c]pyridin-2-yl]-1,2,5-oxadiazol-3-amine

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,4-dioxane; water / 12 h / 70 °C

2: tetrabutyl ammonium fluoride / tetrahydrofuran / 2 h / 25 °C

With tetrabutyl ammonium fluoride; potassium carbonate; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; 1,4-dioxane; water;