2-(2-Ethyl-8-(carbomethoxymethyloxy)-3-(m-methoxybenzyl)indolizine-1-yl)glyoxylamide

Base Information

Chemical Name:2-(2-Ethyl-8-(carbomethoxymethyloxy)-3-(m-methoxybenzyl)indolizine-1-yl)glyoxylamide
CAS No.:177557-59-4
Molecular Formula:C₂₃H₂₄N₂O₆
Molecular Weight:424.453
Hs Code.:

Synonyms:2-(2-Ethyl-8-(carbomethoxymethyloxy)-3-(m-methoxybenzyl)indolizine-1-yl)glyoxylamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 2-(2-Ethyl-8-(carbomethoxymethyloxy)-3-(m-methoxybenzyl)indolizine-1-yl)glyoxylamide

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Technology Process of 2-(2-Ethyl-8-(carbomethoxymethyloxy)-3-(m-methoxybenzyl)indolizine-1-yl)glyoxylamide

There total 10 articles about 2-(2-Ethyl-8-(carbomethoxymethyloxy)-3-(m-methoxybenzyl)indolizine-1-yl)glyoxylamide 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: 85.0%

: 96-32-2
bromoacetic acid methyl ester

: 177559-42-1
2-(2-ethyl-8-hydroxy-3-(m-methoxybenzyl)indolizine-1-yl)glyoxylamide

: 177557-59-4
2-(2-Ethyl-8-(carbomethoxymethyloxy)-3-(m-methoxybenzyl)indolizine-1-yl)glyoxylamide

Guidance literature:: With potassium carbonate; potassium iodide; In N,N-dimethyl-formamide; for 5h;
DOI:10.1021/jm960395q

Reference yield: 85.0%

: 177557-59-4
2-(2-Ethyl-8-(carbomethoxymethyloxy)-3-(m-methoxybenzyl)indolizine-1-yl)glyoxylamide

Guidance literature:

Reference yield:

: 1121-25-1,55780-69-3
2-methyl-3-pyridinol

: 177557-59-4
2-(2-Ethyl-8-(carbomethoxymethyloxy)-3-(m-methoxybenzyl)indolizine-1-yl)glyoxylamide

Guidance literature:: Multi-step reaction with 9 steps

1: 90 percent / KOH, tetrabutylammonium bromide / tetrahydrofuran / 1.5 h / Ambient temperature

2: 90.1 percent / ethyl acetate / 0.5 h / 70 °C

3: 79 percent / 1,8-diazabicyclo<5.4.0>undec-7-ene / benzene / 0.75 h / Heating

4: 77 percent / benzene / 4 h / Heating

5: NaBH₄, AlCl₃ / tetrahydrofuran / 0.75 h / Heating

6: tetrahydrofuran / 0 °C

7: aq. NH₄OH / tetrahydrofuran / Ambient temperature

8: 86 percent / H₂ / 10percent Pd/C / ethyl acetate

9: 85 percent / K₂CO₃, KI / dimethylformamide / 5 h

With potassium hydroxide; ammonium hydroxide; sodium tetrahydroborate; aluminium trichloride; tetrabutylammomium bromide; hydrogen; potassium carbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; potassium iodide; palladium on activated charcoal; In tetrahydrofuran; ethyl acetate; N,N-dimethyl-formamide; benzene;
DOI:10.1021/jm960395q