2,6-Dimethyl-4-(3-nitro-phenyl)-1,4-dihydro-pyridine-3,5-dicarboxylic acid 3-{2-[4-(1-benzhydryl-piperidin-4-yl)-phenyl]-ethyl} ester 5-methyl ester

Base Information

Chemical Name:2,6-Dimethyl-4-(3-nitro-phenyl)-1,4-dihydro-pyridine-3,5-dicarboxylic acid 3-{2-[4-(1-benzhydryl-piperidin-4-yl)-phenyl]-ethyl} ester 5-methyl ester
CAS No.:126202-62-8
Molecular Formula:C₄₂H₄₃N₃O₆
Molecular Weight:685.82
Hs Code.:

2,6-Dimethyl-4-(3-nitro-phenyl)-1,4-dihydro-pyridine-3,5-dicarboxylic acid 3-{2-[4-(1-benzhydryl-piperidin-4-yl)-phenyl]-ethyl} ester 5-methyl ester

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Chemical Property of 2,6-Dimethyl-4-(3-nitro-phenyl)-1,4-dihydro-pyridine-3,5-dicarboxylic acid 3-{2-[4-(1-benzhydryl-piperidin-4-yl)-phenyl]-ethyl} ester 5-methyl ester

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Technology Process of 2,6-Dimethyl-4-(3-nitro-phenyl)-1,4-dihydro-pyridine-3,5-dicarboxylic acid 3-{2-[4-(1-benzhydryl-piperidin-4-yl)-phenyl]-ethyl} ester 5-methyl ester

There total 7 articles about 2,6-Dimethyl-4-(3-nitro-phenyl)-1,4-dihydro-pyridine-3,5-dicarboxylic acid 3-{2-[4-(1-benzhydryl-piperidin-4-yl)-phenyl]-ethyl} ester 5-methyl ester 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: 48.0%

: 134364-92-4
2-<4-(1-benzhydryl-4-piperidinyl)phenyl>ethyl alcohol

: 88712-56-5,125185-92-4
1,4-dihydro-2,6-dimethyl-3-methoxycarbonyl-4-(3-nitrophenyl)-pyridine-5-carboxylic acid chloride

: 126202-62-8
2,6-Dimethyl-4-(3-nitro-phenyl)-1,4-dihydro-pyridine-3,5-dicarboxylic acid 3-{2-[4-(1-benzhydryl-piperidin-4-yl)-phenyl]-ethyl} ester 5-methyl ester

Guidance literature:: In chloroform; N,N-dimethyl-formamide; at 4 - 5 ℃;
DOI:10.1248/cpb.39.91

Reference yield:

: 79849-46-0
4-(2-(tetrahydropyran-2-yloxy)ethyl)bromobenzene

: 126202-62-8
2,6-Dimethyl-4-(3-nitro-phenyl)-1,4-dihydro-pyridine-3,5-dicarboxylic acid 3-{2-[4-(1-benzhydryl-piperidin-4-yl)-phenyl]-ethyl} ester 5-methyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: 1) BuLi / 1) THF, hexane, -60 deg C, 30 min, 2) -60 deg C, 2.5h

2: 51 percent / 2:8 H₂SO₄-AcOH / Ambient temperature

3: 96 percent / H₂ / 10percent Pd/C / acetic acid; aq. HClO₄ / 65 - 70 °C

4: 73 percent / K₂CO₃ / dimethylformamide / Ambient temperature

5: 89 percent / K₂CO₃ / methanol / 1 h / Ambient temperature

6: 48 percent / CHCl₃; dimethylformamide / 4 - 5 °C

With n-butyllithium; sulfuric acid; hydrogen; potassium carbonate; acetic acid; palladium on activated charcoal; In methanol; perchloric acid; chloroform; acetic acid; N,N-dimethyl-formamide;
DOI:10.1248/cpb.39.91

Reference yield:

: 126202-71-9
2-<4-(1-benzyl-4-piperidinyll)phenyl>ethyl alcohol

: 126202-62-8
2,6-Dimethyl-4-(3-nitro-phenyl)-1,4-dihydro-pyridine-3,5-dicarboxylic acid 3-{2-[4-(1-benzhydryl-piperidin-4-yl)-phenyl]-ethyl} ester 5-methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 51 percent / 2:8 H₂SO₄-AcOH / Ambient temperature

2: 96 percent / H₂ / 10percent Pd/C / acetic acid; aq. HClO₄ / 65 - 70 °C

3: 73 percent / K₂CO₃ / dimethylformamide / Ambient temperature

4: 89 percent / K₂CO₃ / methanol / 1 h / Ambient temperature

5: 48 percent / CHCl₃; dimethylformamide / 4 - 5 °C

With sulfuric acid; hydrogen; potassium carbonate; acetic acid; palladium on activated charcoal; In methanol; perchloric acid; chloroform; acetic acid; N,N-dimethyl-formamide;
DOI:10.1248/cpb.39.91