C₂₆H₃₄Cl₂N₂O₃

Base Information

Chemical Name:C₂₆H₃₄Cl₂N₂O₃
CAS No.:1201823-94-0
Molecular Formula:C₂₆H₃₄Cl₂N₂O₃
Molecular Weight:493.474
Hs Code.:

C<sub>26</sub>H<sub>34</sub>Cl<sub>2</sub>N<sub>2</sub>O<sub>3</sub>

Synonyms:C₂₆H₃₄Cl₂N₂O₃

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Chemical Property of C₂₆H₃₄Cl₂N₂O₃

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Technology Process of C₂₆H₃₄Cl₂N₂O₃

There total 13 articles about C₂₆H₃₄Cl₂N₂O₃ 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:

: 1091599-69-7
tert-butyl 4-{2-[6-(bromomethyl)-3,5-dichloro-2-oxopyridin-1(2H)-yl]ethyl}benzoate

: 369633-59-0
(2S)-2-propylpyrrolidine

: 1201823-94-0
C₂₆H₃₄Cl₂N₂O₃

Guidance literature:: In 1-methyl-pyrrolidin-2-one; at 140 ℃; for 0.166667h; Irradiation with microwave;

Reference yield:

: 675-10-5
4-hydroxy-6-methyl-2-pyron

: 1201823-94-0
C₂₆H₃₄Cl₂N₂O₃

Guidance literature:: Multi-step reaction with 9 steps

1.1: sodium hydroxide / water / 0.25 h / 20 °C

1.2: 24 h / 80 °C

1.3: 0.5 h

2.1: sulfuric acid / 4 h / Heating; Reflux

3.1: pyridine / 3 h / 5 °C

4.1: hydrogen; N-ethyl-N,N-diisopropylamine / palladium 10% on activated carbon / ethyl acetate; water

5.1: N-chloro-succinimide; acetic acid / water / 20 - 70 °C

6.1: sodium hydroxide; water / tetrahydrofuran; methanol / 4 h / 70 °C

7.1: dmap / tetrahydrofuran / 60 °C

8.1: 2,2'-azobis(isobutyronitrile); N-Bromosuccinimide / tetrachloromethane / 1 h / Reflux

9.1: 1-methyl-pyrrolidin-2-one / 0.17 h / 140 °C / Irradiation with microwave

With pyridine; dmap; N-chloro-succinimide; N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); sulfuric acid; water; hydrogen; acetic acid; N-ethyl-N,N-diisopropylamine; sodium hydroxide; palladium 10% on activated carbon; In tetrahydrofuran; 1-methyl-pyrrolidin-2-one; methanol; tetrachloromethane; water; ethyl acetate;

Reference yield:

: 60531-36-4
4-(2-amino-ethyl)-benzoic acid hydrochloride

: 1201823-94-0
C₂₆H₃₄Cl₂N₂O₃

Guidance literature:: Multi-step reaction with 9 steps

1.1: sodium hydroxide / water / 0.25 h / 20 °C

1.2: 24 h / 80 °C

1.3: 0.5 h

2.1: sulfuric acid / 4 h / Heating; Reflux

3.1: pyridine / 3 h / 5 °C

4.1: hydrogen; N-ethyl-N,N-diisopropylamine / palladium 10% on activated carbon / ethyl acetate; water

5.1: N-chloro-succinimide; acetic acid / water / 20 - 70 °C

6.1: sodium hydroxide; water / tetrahydrofuran; methanol / 4 h / 70 °C

7.1: dmap / tetrahydrofuran / 60 °C

8.1: 2,2'-azobis(isobutyronitrile); N-Bromosuccinimide / tetrachloromethane / 1 h / Reflux

9.1: 1-methyl-pyrrolidin-2-one / 0.17 h / 140 °C / Irradiation with microwave

With pyridine; dmap; N-chloro-succinimide; N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); sulfuric acid; water; hydrogen; acetic acid; N-ethyl-N,N-diisopropylamine; sodium hydroxide; palladium 10% on activated carbon; In tetrahydrofuran; 1-methyl-pyrrolidin-2-one; methanol; tetrachloromethane; water; ethyl acetate;