(6'-bromo-3'-nitro-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-4-yl)-acetic acid ethyl ester

Base Information

Chemical Name:(6'-bromo-3'-nitro-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-4-yl)-acetic acid ethyl ester
CAS No.:1314531-24-2
Molecular Formula:C₁₄H₁₈BrN₃O₄
Molecular Weight:372.219
Hs Code.:

Synonyms:(6'-bromo-3'-nitro-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-4-yl)-acetic acid ethyl ester

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Chemical Property of (6'-bromo-3'-nitro-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-4-yl)-acetic acid ethyl ester

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Technology Process of (6'-bromo-3'-nitro-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-4-yl)-acetic acid ethyl ester

There total 1 articles about (6'-bromo-3'-nitro-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-4-yl)-acetic acid ethyl 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: 75.7%

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

: 55304-80-8
2,6-dibromo-3-nitropyridine

: 1314531-24-2
(6'-bromo-3'-nitro-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-4-yl)-acetic acid ethyl ester

Guidance literature:: With triethylamine; In ethanol; at 20 ℃;

Reference yield:

: 1314531-24-2
(6'-bromo-3'-nitro-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-4-yl)-acetic acid ethyl ester

: 1314530-63-6
N-[4-(tert-butylcarbamoyl-methyl)-6'-methanesulfonyl-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-3'-yl]-3-chloro-benzamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: N,N`-dimethylethylenediamine; copper(II) bis(trifluoromethanesulfonate) / dimethyl sulfoxide / 1 h / 115 °C / Microwave irradiation

2.1: hydrogen / palladium 10% on activated carbon / ethanol / 20 °C

3.1: N-ethyl-N,N-diisopropylamine / acetonitrile / 1 h / 80 °C

4.1: lithium hydroxide / water; tetrahydrofuran / 20 °C

4.2: pH 2

5.1: triethylamine; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate / N,N-dimethyl-formamide / 2 h / 20 °C

With hydrogen; copper(II) bis(trifluoromethanesulfonate); O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; triethylamine; N-ethyl-N,N-diisopropylamine; lithium hydroxide; N,N`-dimethylethylenediamine; palladium 10% on activated carbon; In tetrahydrofuran; ethanol; water; dimethyl sulfoxide; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 1314531-24-2
(6'-bromo-3'-nitro-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-4-yl)-acetic acid ethyl ester

: 1314531-27-5
[3'-(3-chloro-benzoylamino)-6'-methanesulfonyl-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-4-yl]-acetic acid ethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: N,N`-dimethylethylenediamine; copper(II) bis(trifluoromethanesulfonate) / dimethyl sulfoxide / 1 h / 115 °C / Microwave irradiation

2: hydrogen / palladium 10% on activated carbon / ethanol / 20 °C

3: N-ethyl-N,N-diisopropylamine / acetonitrile / 1 h / 80 °C

With hydrogen; copper(II) bis(trifluoromethanesulfonate); N-ethyl-N,N-diisopropylamine; N,N`-dimethylethylenediamine; palladium 10% on activated carbon; In ethanol; dimethyl sulfoxide; acetonitrile;