N-methyl-3-{1-[2-(5-methyl-3-trifluoromethyl-pyrazol-1-yl)-acetyl]-piperidin-4-yl}-N-(R)-1,2,3,4-tetrahydro-naphthalene-1-yl-benzamide

Base Information

Chemical Name:N-methyl-3-{1-[2-(5-methyl-3-trifluoromethyl-pyrazol-1-yl)-acetyl]-piperidin-4-yl}-N-(R)-1,2,3,4-tetrahydro-naphthalene-1-yl-benzamide
CAS No.:1263775-58-1
Molecular Formula:C₃₀H₃₃F₃N₄O₂
Molecular Weight:538.613
Hs Code.:

Synonyms:N-methyl-3-{1-[2-(5-methyl-3-trifluoromethyl-pyrazol-1-yl)-acetyl]-piperidin-4-yl}-N-(R)-1,2,3,4-tetrahydro-naphthalene-1-yl-benzamide

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Chemical Property of N-methyl-3-{1-[2-(5-methyl-3-trifluoromethyl-pyrazol-1-yl)-acetyl]-piperidin-4-yl}-N-(R)-1,2,3,4-tetrahydro-naphthalene-1-yl-benzamide

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Technology Process of N-methyl-3-{1-[2-(5-methyl-3-trifluoromethyl-pyrazol-1-yl)-acetyl]-piperidin-4-yl}-N-(R)-1,2,3,4-tetrahydro-naphthalene-1-yl-benzamide

There total 7 articles about N-methyl-3-{1-[2-(5-methyl-3-trifluoromethyl-pyrazol-1-yl)-acetyl]-piperidin-4-yl}-N-(R)-1,2,3,4-tetrahydro-naphthalene-1-yl-benzamide 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: 46.0%

: 1263776-13-1
3-{1-[2-(5-methyl-3-trifluoromethyl-pyrazol-1-yl)-acetyl]-piperidin-4-yl}-benzoic acid

: 114419-88-4
(R)-N-methyl-1,2,3,4-tetrahydronaphthalen-1-amine

: 1263775-58-1
N-methyl-3-{1-[2-(5-methyl-3-trifluoromethyl-pyrazol-1-yl)-acetyl]-piperidin-4-yl}-N-(R)-1,2,3,4-tetrahydro-naphthalene-1-yl-benzamide

Guidance literature:: 3-{1-[2-(5-methyl-3-trifluoromethyl-pyrazol-1-yl)-acetyl]-piperidin-4-yl}-benzoic acid; With N-ethyl-N,N-diisopropylamine; HATU; In N,N-dimethyl-formamide; at 20 ℃; for 0.25h;

(R)-N-methyl-1,2,3,4-tetrahydronaphthalen-1-amine; In N,N-dimethyl-formamide; at 20 ℃; for 2h;

Reference yield:

: 58313-23-8
3-iodobenzoic acid methyl ester

: 1263775-58-1
N-methyl-3-{1-[2-(5-methyl-3-trifluoromethyl-pyrazol-1-yl)-acetyl]-piperidin-4-yl}-N-(R)-1,2,3,4-tetrahydro-naphthalene-1-yl-benzamide

Guidance literature:: Multi-step reaction with 6 steps

1.1: sodium carbonate / bis-triphenylphosphine-palladium(II) chloride / 1,4-dioxane; water / 20 - 110 °C

2.1: hydrogen / palladium on activated charcoal / ethanol

3.1: hydrogenchloride / 1,4-dioxane / 20 °C

4.1: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 0.25 h / 20 °C

4.2: 20 °C

5.1: sodium hydroxide; water / methanol / 4 h / 20 °C

5.2: 20 °C

5.3: pH 1 - 2

6.1: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 0.25 h / 20 °C

6.2: 2 h / 20 °C

With hydrogenchloride; water; hydrogen; sodium carbonate; N-ethyl-N,N-diisopropylamine; HATU; sodium hydroxide; bis-triphenylphosphine-palladium(II) chloride; palladium on activated charcoal; In 1,4-dioxane; methanol; ethanol; water; N,N-dimethyl-formamide;

Reference yield:

: 782493-24-7
ethyl tert-butyl 4-(3-(ethoxycarbonyl)phenyl)-5,6-dihydropyridine-1(2H)-carboxylate

: 1263775-58-1
N-methyl-3-{1-[2-(5-methyl-3-trifluoromethyl-pyrazol-1-yl)-acetyl]-piperidin-4-yl}-N-(R)-1,2,3,4-tetrahydro-naphthalene-1-yl-benzamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: hydrogen / palladium on activated charcoal / ethanol

2.1: hydrogenchloride / 1,4-dioxane / 20 °C

3.1: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 0.25 h / 20 °C

3.2: 20 °C

4.1: sodium hydroxide; water / methanol / 4 h / 20 °C

4.2: 20 °C

4.3: pH 1 - 2

5.1: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 0.25 h / 20 °C

5.2: 2 h / 20 °C

With hydrogenchloride; water; hydrogen; N-ethyl-N,N-diisopropylamine; HATU; sodium hydroxide; palladium on activated charcoal; In 1,4-dioxane; methanol; ethanol; N,N-dimethyl-formamide;