3-[ethyl(1-methylpiperidin-4-yl)amino]-2-methyl-5-(trifluoromethyl)benzoic acid

Base Information

Chemical Name:3-[ethyl(1-methylpiperidin-4-yl)amino]-2-methyl-5-(trifluoromethyl)benzoic acid
CAS No.:1403595-18-5
Molecular Formula:C₁₇H₂₃F₃N₂O₂
Molecular Weight:344.377
Hs Code.:

Synonyms:3-[ethyl(1-methylpiperidin-4-yl)amino]-2-methyl-5-(trifluoromethyl)benzoic acid

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Chemical Property of 3-[ethyl(1-methylpiperidin-4-yl)amino]-2-methyl-5-(trifluoromethyl)benzoic acid

Chemical Property:

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Technology Process of 3-[ethyl(1-methylpiperidin-4-yl)amino]-2-methyl-5-(trifluoromethyl)benzoic acid

There total 4 articles about 3-[ethyl(1-methylpiperidin-4-yl)amino]-2-methyl-5-(trifluoromethyl)benzoic acid 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:

: 1403595-16-3
methyl 3-[ethyl(1-methylpiperidin-4-yl)amino]-2-methyl-5-(trifluoromethyl)benzoate

: 1403595-18-5
3-[ethyl(1-methylpiperidin-4-yl)amino]-2-methyl-5-(trifluoromethyl)benzoic acid

Guidance literature:: methyl 3-[ethyl(1-methylpiperidin-4-yl)amino]-2-methyl-5-(trifluoromethyl)benzoate; With water; sodium hydroxide; In methanol; at 50 ℃; for 3h;

With hydrogenchloride; In methanol; water; at 23 ℃; pH=5;

Reference yield:

: 13055-63-5
2-methyl-5-(trifluoromethyl)benzoic acid

: 1403595-18-5
3-[ethyl(1-methylpiperidin-4-yl)amino]-2-methyl-5-(trifluoromethyl)benzoic acid

Guidance literature:: Multi-step reaction with 7 steps

1.1: sodium carbonate / N,N-dimethyl-formamide / 4 h / 60 °C

2.1: hydrogen / palladium(II) hydroxide / methanol / 3 h

3.1: acetic acid; sodium tris(acetoxy)borohydride / dichloromethane / 20 h / 23 °C

4.1: acetic acid; sodium tris(acetoxy)borohydride / dichloromethane / 24 h / 23 °C

5.1: dichloromethane / 18 h / 20 °C

6.1: acetic acid; sodium tris(acetoxy)borohydride / dichloromethane / 60 h / 23 °C

7.1: sodium hydroxide; water / methanol / 3 h / 50 °C

7.2: 23 °C / pH 5

With water; hydrogen; sodium tris(acetoxy)borohydride; sodium carbonate; acetic acid; sodium hydroxide; palladium(II) hydroxide; In methanol; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 1396780-64-5
methyl 2-methyl-3-nitro-5-(trifluoromethyl)benzoate

: 1403595-18-5
3-[ethyl(1-methylpiperidin-4-yl)amino]-2-methyl-5-(trifluoromethyl)benzoic acid

Guidance literature:: Multi-step reaction with 6 steps

1.1: hydrogen / palladium(II) hydroxide / methanol / 3 h

2.1: acetic acid; sodium tris(acetoxy)borohydride / dichloromethane / 20 h / 23 °C

3.1: acetic acid; sodium tris(acetoxy)borohydride / dichloromethane / 24 h / 23 °C

4.1: dichloromethane / 18 h / 20 °C

5.1: acetic acid; sodium tris(acetoxy)borohydride / dichloromethane / 60 h / 23 °C

6.1: sodium hydroxide; water / methanol / 3 h / 50 °C

6.2: 23 °C / pH 5

With water; hydrogen; sodium tris(acetoxy)borohydride; acetic acid; sodium hydroxide; palladium(II) hydroxide; In methanol; dichloromethane;