N-[(1-aza-15-crown-5)-yl-carbamoyl]ethyl-2-nitro-3-benzyloxy-4-methylbenzamide

Base Information

Chemical Name:N-[(1-aza-15-crown-5)-yl-carbamoyl]ethyl-2-nitro-3-benzyloxy-4-methylbenzamide
CAS No.:1235452-62-6
Molecular Formula:C₂₈H₃₇N₃O₉
Molecular Weight:559.616
Hs Code.:

Synonyms:N-[(1-aza-15-crown-5)-yl-carbamoyl]ethyl-2-nitro-3-benzyloxy-4-methylbenzamide

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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 N-[(1-aza-15-crown-5)-yl-carbamoyl]ethyl-2-nitro-3-benzyloxy-4-methylbenzamide

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Technology Process of N-[(1-aza-15-crown-5)-yl-carbamoyl]ethyl-2-nitro-3-benzyloxy-4-methylbenzamide

There total 2 articles about N-[(1-aza-15-crown-5)-yl-carbamoyl]ethyl-2-nitro-3-benzyloxy-4-methylbenzamide 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: 92.0%

: 339187-21-2
N-β-alanyl-4-methyl-3-benzyloxy-2-nitrobenzamide

: 66943-05-3
1,4,7,10-tetraoxa-15-azacyclopentadecane

: 1235452-62-6
N-[(1-aza-15-crown-5)-yl-carbamoyl]ethyl-2-nitro-3-benzyloxy-4-methylbenzamide

Guidance literature:: With N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline; In 1,4-dioxane; at 20 ℃; Inert atmosphere;
DOI:10.1134/S1070363210040213

Reference yield:

: 7536-35-8
2-nitro-3-benzyloxy-4-methylbenzoyl chloride

: 1235452-62-6
N-[(1-aza-15-crown-5)-yl-carbamoyl]ethyl-2-nitro-3-benzyloxy-4-methylbenzamide

Guidance literature:: Multi-step reaction with 2 steps

2: N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline / 1,4-dioxane / 20 °C / Inert atmosphere

With N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline; In 1,4-dioxane; 1: Schotten-Baumann reaction;
DOI:10.1134/S1070363210040213