5-[4-(2H-pyrazol-3-yl)phenoxy]-2-pyrrolidin-1-ylmethyl-1H-benzoimidazole

Base Information

Chemical Name:5-[4-(2H-pyrazol-3-yl)phenoxy]-2-pyrrolidin-1-ylmethyl-1H-benzoimidazole
CAS No.:1541185-01-6
Molecular Formula:C₂₁H₂₁N₅O
Molecular Weight:359.431
Hs Code.:

Synonyms:5-[4-(2H-pyrazol-3-yl)phenoxy]-2-pyrrolidin-1-ylmethyl-1H-benzoimidazole

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Chemical Property of 5-[4-(2H-pyrazol-3-yl)phenoxy]-2-pyrrolidin-1-ylmethyl-1H-benzoimidazole

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Technology Process of 5-[4-(2H-pyrazol-3-yl)phenoxy]-2-pyrrolidin-1-ylmethyl-1H-benzoimidazole

There total 3 articles about 5-[4-(2H-pyrazol-3-yl)phenoxy]-2-pyrrolidin-1-ylmethyl-1H-benzoimidazole 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:

: C₂₇H₃₅N₅O₂Si

: 1541185-01-6
5-[4-(2H-pyrazol-3-yl)phenoxy]-2-pyrrolidin-1-ylmethyl-1H-benzoimidazole

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; at 50 ℃; for 1h;

Reference yield:

: 1541188-13-9
4-{4-[2-(2-trimethylsilanylethoxymethyl)-2H-pyrazol-3-yl]phenoxy}benzene-1,2-diamine

: 1541185-01-6
5-[4-(2H-pyrazol-3-yl)phenoxy]-2-pyrrolidin-1-ylmethyl-1H-benzoimidazole

Guidance literature:: Multi-step reaction with 3 steps

1.1: bromo-tris(1-pyrrolidinyl)phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / dichloromethane / 0.33 h / 25 °C

1.2: 16 h / 25 °C

2.1: acetic acid / 0.33 h / 110 °C

3.1: hydrogenchloride / 1,4-dioxane / 1 h / 50 °C

With hydrogenchloride; acetic acid; N-ethyl-N,N-diisopropylamine; bromo-tris(1-pyrrolidinyl)phosphonium hexafluorophosphate; In 1,4-dioxane; dichloromethane;

Reference yield:

: 37386-15-5
2-(pyrrolidin-1-yl)acetic acid

: 1541185-01-6
5-[4-(2H-pyrazol-3-yl)phenoxy]-2-pyrrolidin-1-ylmethyl-1H-benzoimidazole

Guidance literature:: Multi-step reaction with 3 steps

1.1: bromo-tris(1-pyrrolidinyl)phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / dichloromethane / 0.33 h / 25 °C

1.2: 16 h / 25 °C

2.1: acetic acid / 0.33 h / 110 °C

3.1: hydrogenchloride / 1,4-dioxane / 1 h / 50 °C

With hydrogenchloride; acetic acid; N-ethyl-N,N-diisopropylamine; bromo-tris(1-pyrrolidinyl)phosphonium hexafluorophosphate; In 1,4-dioxane; dichloromethane;