4-ethoxycarbonylmethyl-3'-nitro-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-5'-carboxylic acid

Base Information

Chemical Name:4-ethoxycarbonylmethyl-3'-nitro-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-5'-carboxylic acid
CAS No.:1314530-90-9
Molecular Formula:C₁₅H₁₉N₃O₆
Molecular Weight:337.332
Hs Code.:

Synonyms:4-ethoxycarbonylmethyl-3'-nitro-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-5'-carboxylic acid

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Chemical Property of 4-ethoxycarbonylmethyl-3'-nitro-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-5'-carboxylic acid

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Technology Process of 4-ethoxycarbonylmethyl-3'-nitro-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-5'-carboxylic acid

There total 1 articles about 4-ethoxycarbonylmethyl-3'-nitro-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-5'-carboxylic 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: 81.1%

: 59184-90-6
ethyl (piperidin-4-yl)acetate

: 7477-10-3
6-chloro-5-nitronicotinic acid

: 1314530-90-9
4-ethoxycarbonylmethyl-3'-nitro-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-5'-carboxylic acid

Guidance literature:: ethyl (piperidin-4-yl)acetate; 6-chloro-5-nitronicotinic acid; In N,N-dimethyl-formamide; at 130 ℃; for 1h; Microwave irradiation;

With hydrogenchloride; In water; N,N-dimethyl-formamide; pH=2;

Reference yield:

: 1314530-90-9
4-ethoxycarbonylmethyl-3'-nitro-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-5'-carboxylic acid

: 1314528-85-2
3'-(3-chloro-benzoylamino)-4-[2-(4-hydroxy-piperidin-1-yl)-2-oxo-ethyl]-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-5'-carboxylic acid

Guidance literature:: Multi-step reaction with 5 steps

1.1: triethylamine; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate / N,N-dimethyl-formamide / 1 h / 20 °C

2.1: hydrogen / 5%-palladium/activated carbon / ethanol

3.1: acetonitrile

4.1: lithium hydroxide / water; tetrahydrofuran; methanol

4.2: pH 2

5.1: triethylamine; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate / N,N-dimethyl-formamide / 3 h / 20 °C

With hydrogen; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; triethylamine; lithium hydroxide; 5%-palladium/activated carbon; In tetrahydrofuran; methanol; ethanol; water; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 1314530-90-9
4-ethoxycarbonylmethyl-3'-nitro-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-5'-carboxylic acid

: 1314530-93-2
[3'-(3-chloro-benzoylamino)-5'-cyclopropylcarbamoyl-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-4-yl]-acetic acid ethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate / N,N-dimethyl-formamide / 1 h / 20 °C

2: hydrogen / 5%-palladium/activated carbon / ethanol

3: acetonitrile

With hydrogen; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; triethylamine; 5%-palladium/activated carbon; In ethanol; N,N-dimethyl-formamide; acetonitrile;