N-(13-cyclohexyl-11-oxo-3,6,9-trioxa-12-azatetradecyl)-1-(4-methoxybenzyl)-3-(1-(4-methoxybenzyl)-3-(1-(4-methoxybenzyl)-3-nitro-1H-pyrazole-5-carboxamido)-1H-pyrazole-5-carboxamido)-1H-pyrazole-5-carboxamide

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Chemical Name:N-(13-cyclohexyl-11-oxo-3,6,9-trioxa-12-azatetradecyl)-1-(4-methoxybenzyl)-3-(1-(4-methoxybenzyl)-3-(1-(4-methoxybenzyl)-3-nitro-1H-pyrazole-5-carboxamido)-1H-pyrazole-5-carboxamido)-1H-pyrazole-5-carboxamide
CAS No.:1282034-90-5
Molecular Formula:C₅₂H₆₃N₁₁O₁₂
Molecular Weight:1034.14
Hs Code.:

N-(13-cyclohexyl-11-oxo-3,6,9-trioxa-12-azatetradecyl)-1-(4-methoxybenzyl)-3-(1-(4-methoxybenzyl)-3-(1-(4-methoxybenzyl)-3-nitro-1H-pyrazole-5-carboxamido)-1H-pyrazole-5-carboxamido)-1H-pyrazole-5-carboxamide

Synonyms:N-(13-cyclohexyl-11-oxo-3,6,9-trioxa-12-azatetradecyl)-1-(4-methoxybenzyl)-3-(1-(4-methoxybenzyl)-3-(1-(4-methoxybenzyl)-3-nitro-1H-pyrazole-5-carboxamido)-1H-pyrazole-5-carboxamido)-1H-pyrazole-5-carboxamide

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Chemical Property of N-(13-cyclohexyl-11-oxo-3,6,9-trioxa-12-azatetradecyl)-1-(4-methoxybenzyl)-3-(1-(4-methoxybenzyl)-3-(1-(4-methoxybenzyl)-3-nitro-1H-pyrazole-5-carboxamido)-1H-pyrazole-5-carboxamido)-1H-pyrazole-5-carboxamide

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Technology Process of N-(13-cyclohexyl-11-oxo-3,6,9-trioxa-12-azatetradecyl)-1-(4-methoxybenzyl)-3-(1-(4-methoxybenzyl)-3-(1-(4-methoxybenzyl)-3-nitro-1H-pyrazole-5-carboxamido)-1H-pyrazole-5-carboxamido)-1H-pyrazole-5-carboxamide

There total 6 articles about N-(13-cyclohexyl-11-oxo-3,6,9-trioxa-12-azatetradecyl)-1-(4-methoxybenzyl)-3-(1-(4-methoxybenzyl)-3-(1-(4-methoxybenzyl)-3-nitro-1H-pyrazole-5-carboxamido)-1H-pyrazole-5-carboxamido)-1H-pyrazole-5-carboxamide 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: 75.0%

: 1282034-88-1
1-(1-(4-methoxybenzyl)-3-(1-(4-methoxybenzyl)-3-(1-(4-methoxybenzyl)-3-nitro-1H-pyrazole-5-carboxamido)-1H-pyrazole-5-carboxamido)-1H-pyrazole-5-yl)-1-oxo-5,8,11-trioxa-2-azatridecan-13-oic acid

: 5913-13-3
[(1R)-1-cyclohexylethyl]amine

: 1282034-90-5
N-(13-cyclohexyl-11-oxo-3,6,9-trioxa-12-azatetradecyl)-1-(4-methoxybenzyl)-3-(1-(4-methoxybenzyl)-3-(1-(4-methoxybenzyl)-3-nitro-1H-pyrazole-5-carboxamido)-1H-pyrazole-5-carboxamido)-1H-pyrazole-5-carboxamide

Guidance literature:: With 2-chloro-1-methyl-pyridinium iodide; N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃; Inert atmosphere;
DOI:10.1021/ja107675n

Reference yield:

: 1282034-86-9
1-(1-(4-methoxybenzyl)-3-(1-(4-methoxybenzyl)-3-(1-(4-methoxybenzyl)-3-nitro-1H-pyrazole-5-carboxamido)-1H-pyrazole-5-carboxamido)-1H-pyrazole-5-yl)-1-oxo-5,8,11-trioxa-2-azatridecan-13-oic acid ethyl ester

: 1282034-90-5
N-(13-cyclohexyl-11-oxo-3,6,9-trioxa-12-azatetradecyl)-1-(4-methoxybenzyl)-3-(1-(4-methoxybenzyl)-3-(1-(4-methoxybenzyl)-3-nitro-1H-pyrazole-5-carboxamido)-1H-pyrazole-5-carboxamido)-1H-pyrazole-5-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: methanol; water; lithium hydroxide / tetrahydrofuran / 48 h / 20 °C

2: 2-chloro-1-methyl-pyridinium iodide; N-ethyl-N,N-diisopropylamine / dichloromethane / 20 °C / Inert atmosphere

With methanol; 2-chloro-1-methyl-pyridinium iodide; water; N-ethyl-N,N-diisopropylamine; lithium hydroxide; In tetrahydrofuran; dichloromethane;
DOI:10.1021/ja107675n

Reference yield:

: 1282034-69-8
1-(4-methoxybenzyl)-3-(1-(4-methoxybenzyl)-3-(1-(4-methoxybenzyl)-3-nitro-1H-pyrazole-5-carboxamido)-1H-pyrazole-5-carboxamido)-1H-pyrazole-5-carboxylic acid

: 1282034-90-5
N-(13-cyclohexyl-11-oxo-3,6,9-trioxa-12-azatetradecyl)-1-(4-methoxybenzyl)-3-(1-(4-methoxybenzyl)-3-(1-(4-methoxybenzyl)-3-nitro-1H-pyrazole-5-carboxamido)-1H-pyrazole-5-carboxamido)-1H-pyrazole-5-carboxamide

Guidance literature:: Multi-step reaction with 3 steps

1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane

2: methanol; water; lithium hydroxide / tetrahydrofuran / 48 h / 20 °C

3: 2-chloro-1-methyl-pyridinium iodide; N-ethyl-N,N-diisopropylamine / dichloromethane / 20 °C / Inert atmosphere

With methanol; 2-chloro-1-methyl-pyridinium iodide; water; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; lithium hydroxide; In tetrahydrofuran; dichloromethane;
DOI:10.1021/ja107675n