2-(4-(aminomethyl)-3-methoxyphenyl)-N-((2-(4-methylpiperidin-1-yl)-6-(trifluoromethyl)pyridin-3-yl)methyl)propanamide

Base Information

Chemical Name:2-(4-(aminomethyl)-3-methoxyphenyl)-N-((2-(4-methylpiperidin-1-yl)-6-(trifluoromethyl)pyridin-3-yl)methyl)propanamide
CAS No.:1428790-31-1
Molecular Formula:C₂₄H₃₁F₃N₄O₂
Molecular Weight:464.531
Hs Code.:

Synonyms:2-(4-(aminomethyl)-3-methoxyphenyl)-N-((2-(4-methylpiperidin-1-yl)-6-(trifluoromethyl)pyridin-3-yl)methyl)propanamide

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Chemical Property of 2-(4-(aminomethyl)-3-methoxyphenyl)-N-((2-(4-methylpiperidin-1-yl)-6-(trifluoromethyl)pyridin-3-yl)methyl)propanamide

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Technology Process of 2-(4-(aminomethyl)-3-methoxyphenyl)-N-((2-(4-methylpiperidin-1-yl)-6-(trifluoromethyl)pyridin-3-yl)methyl)propanamide

There total 8 articles about 2-(4-(aminomethyl)-3-methoxyphenyl)-N-((2-(4-methylpiperidin-1-yl)-6-(trifluoromethyl)pyridin-3-yl)methyl)propanamide 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: 51.0%

: 1428790-30-0
tert-butyl 2-methoxy-4-(1-((2-(4-methylpiperidin-1-yl)-6-(trifluoromethyl)pyridin-3-yl)methylamino)-1-oxopropan-2-yl)benzylcarbamate

: 1428790-31-1
2-(4-(aminomethyl)-3-methoxyphenyl)-N-((2-(4-methylpiperidin-1-yl)-6-(trifluoromethyl)pyridin-3-yl)methyl)propanamide

Guidance literature:: With trifluoroacetic acid; In dichloromethane; at 0 - 23 ℃; for 4h;

Reference yield:

: 1428790-29-7
2-(4-cyano-3-methoxyphenyl)-N-((2-(4-methylpiperidin-1-yl)-6-(trifluoromethyl)pyridin-3-yl)methyl)propanamide

: 1428790-31-1
2-(4-(aminomethyl)-3-methoxyphenyl)-N-((2-(4-methylpiperidin-1-yl)-6-(trifluoromethyl)pyridin-3-yl)methyl)propanamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium tetrahydroborate; nickel(II) chloride hexahydrate / methanol / 1 h / 0 - 20 °C

1.2: 1 h

2.1: trifluoroacetic acid / dichloromethane / 4 h / 0 - 20 °C

With sodium tetrahydroborate; nickel(II) chloride hexahydrate; trifluoroacetic acid; In methanol; dichloromethane;

Reference yield:

: 91-23-6
2-Nitroanisole

: 1428790-31-1
2-(4-(aminomethyl)-3-methoxyphenyl)-N-((2-(4-methylpiperidin-1-yl)-6-(trifluoromethyl)pyridin-3-yl)methyl)propanamide

Guidance literature:: Multi-step reaction with 8 steps

1.1: potassium tert-butylate / N,N-dimethyl-formamide / 0.25 h / -30 - 20 °C

2.1: palladium 10% on activated carbon; hydrogen / tetrahydrofuran; ethanol / 15 h

3.1: sodium nitrite; potassium iodide

4.1: tetrakis(triphenylphosphine) palladium⁽⁰⁾ / N,N-dimethyl-formamide / 36 h / 120 °C

5.1: sodium hydroxide / tetrahydrofuran; water / 15 h / 20 °C

6.1: N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; benzotriazol-1-ol; triethylamine / acetonitrile / 15 h / 20 °C

7.1: sodium tetrahydroborate; nickel(II) chloride hexahydrate / methanol / 1 h / 0 - 20 °C

7.2: 1 h

8.1: trifluoroacetic acid / dichloromethane / 4 h / 0 - 20 °C

With sodium tetrahydroborate; tetrakis(triphenylphosphine) palladium⁽⁰⁾; nickel(II) chloride hexahydrate; palladium 10% on activated carbon; potassium tert-butylate; hydrogen; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; triethylamine; trifluoroacetic acid; potassium iodide; sodium hydroxide; sodium nitrite; In tetrahydrofuran; methanol; ethanol; dichloromethane; water; N,N-dimethyl-formamide; acetonitrile;