2-(4-carboxycyclohexylamino)-5-nitro-N-(1,3-benzodioxol-5-ylmethyl)benzamide

Base Information

Chemical Name:2-(4-carboxycyclohexylamino)-5-nitro-N-(1,3-benzodioxol-5-ylmethyl)benzamide
CAS No.:247568-42-9
Molecular Formula:C₂₂H₂₃N₃O₇
Molecular Weight:441.441
Hs Code.:

Synonyms:2-(4-carboxycyclohexylamino)-5-nitro-N-(1,3-benzodioxol-5-ylmethyl)benzamide

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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-(4-carboxycyclohexylamino)-5-nitro-N-(1,3-benzodioxol-5-ylmethyl)benzamide

Chemical Property:

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Technology Process of 2-(4-carboxycyclohexylamino)-5-nitro-N-(1,3-benzodioxol-5-ylmethyl)benzamide

There total 79 articles about 2-(4-carboxycyclohexylamino)-5-nitro-N-(1,3-benzodioxol-5-ylmethyl)benzamide 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:

: 874-89-5
4-Cyanobenzyl alcohol

: 247568-42-9
2-(4-carboxycyclohexylamino)-5-nitro-N-(1,3-benzodioxol-5-ylmethyl)benzamide

Guidance literature:: Multi-step reaction with 6 steps

3: hydrazine hydrate / ethanol

6: tetrahydrofuran; methanol

With hydrazine hydrate; In tetrahydrofuran; methanol; ethanol;

Reference yield:

1N-sodium hydroxide: 1N-sodium hydroxide

: 247568-41-8
2-[4-(methoxycarbonyl)cyclohexylamino]-5-nitro-N-(1,3-benzodioxol-5-ylmethyl)benzamide

: 247568-42-9
2-(4-carboxycyclohexylamino)-5-nitro-N-(1,3-benzodioxol-5-ylmethyl)benzamide

Guidance literature:: In tetrahydrofuran; methanol;

Reference yield:

: 196194-41-9
ethyl 3-methoxy-4-(2-methoxyethoxy)benzoate

: 247568-42-9
2-(4-carboxycyclohexylamino)-5-nitro-N-(1,3-benzodioxol-5-ylmethyl)benzamide

Guidance literature:: Multi-step reaction with 7 steps

2: N-methyl-acetamide; dichloromethane

3: trichlorophosphate / pyridine

4: tetrahydrofuran; ethyl acetate

7: tetrahydrofuran; methanol

With trichlorophosphate; In tetrahydrofuran; pyridine; N-methyl-acetamide; methanol; dichloromethane; ethyl acetate;