N-[2-[4-(1-amino-1-methylethyl)-1-piperidinyl]-3-fluorophenyl]-4-(2-methyl-4-pyridinyl)-1H-imidazole-2-carboxamide

Base Information

Chemical Name:N-[2-[4-(1-amino-1-methylethyl)-1-piperidinyl]-3-fluorophenyl]-4-(2-methyl-4-pyridinyl)-1H-imidazole-2-carboxamide
CAS No.:1350916-78-7
Molecular Formula:C₂₄H₂₉FN₆O
Molecular Weight:436.532
Hs Code.:

Synonyms:N-[2-[4-(1-amino-1-methylethyl)-1-piperidinyl]-3-fluorophenyl]-4-(2-methyl-4-pyridinyl)-1H-imidazole-2-carboxamide

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Chemical Property of N-[2-[4-(1-amino-1-methylethyl)-1-piperidinyl]-3-fluorophenyl]-4-(2-methyl-4-pyridinyl)-1H-imidazole-2-carboxamide

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Technology Process of N-[2-[4-(1-amino-1-methylethyl)-1-piperidinyl]-3-fluorophenyl]-4-(2-methyl-4-pyridinyl)-1H-imidazole-2-carboxamide

There total 9 articles about N-[2-[4-(1-amino-1-methylethyl)-1-piperidinyl]-3-fluorophenyl]-4-(2-methyl-4-pyridinyl)-1H-imidazole-2-carboxamide 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:

: 1350918-32-9
N-(2-(4-(2-aminopropan-2-yl)piperidin-1-yl)-3-fluorophenyl)-4-(2-methylpyridin-4-yl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazole-2-carboxamide

: 1350916-78-7
N-[2-[4-(1-amino-1-methylethyl)-1-piperidinyl]-3-fluorophenyl]-4-(2-methyl-4-pyridinyl)-1H-imidazole-2-carboxamide

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; methanol; at 25 ℃; for 3h;

Reference yield:

: 530116-33-7
tert-butyl 4-(1-amino-1-methylethyl)piperidine-1-carboxylate

: 1350916-78-7
N-[2-[4-(1-amino-1-methylethyl)-1-piperidinyl]-3-fluorophenyl]-4-(2-methyl-4-pyridinyl)-1H-imidazole-2-carboxamide

Guidance literature:: Multi-step reaction with 7 steps

1.1: potassium carbonate / diethyl ether; water / 0 - 25 °C

2.1: trifluoroacetic acid / dichloromethane / 4 h / 25 °C

3.1: N-ethyl-N,N-diisopropylamine / acetonitrile / 80 °C

4.1: acetic acid; iron / 20 °C

4.2: 0.17 h

5.1: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 20 °C

6.1: hydrogen / palladium 10% on activated carbon / ethyl acetate / 20 °C

7.1: hydrogenchloride / 1,4-dioxane; methanol / 3 h / 25 °C

With hydrogenchloride; hydrogen; iron; potassium carbonate; acetic acid; N-ethyl-N,N-diisopropylamine; HATU; trifluoroacetic acid; palladium 10% on activated carbon; In 1,4-dioxane; methanol; diethyl ether; dichloromethane; water; ethyl acetate; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 1350918-25-0
ethyl 4-(2-methylpyridin-4-yl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazole-2-carboxylate

: 1350916-78-7
N-[2-[4-(1-amino-1-methylethyl)-1-piperidinyl]-3-fluorophenyl]-4-(2-methyl-4-pyridinyl)-1H-imidazole-2-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1: sodium hydroxide; methanol / 20 °C

2: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 20 °C

3: hydrogen / palladium 10% on activated carbon / ethyl acetate / 20 °C

4: hydrogenchloride / 1,4-dioxane; methanol / 3 h / 25 °C

With hydrogenchloride; methanol; hydrogen; N-ethyl-N,N-diisopropylamine; HATU; sodium hydroxide; palladium 10% on activated carbon; In 1,4-dioxane; methanol; ethyl acetate; N,N-dimethyl-formamide;