N-(2-(butylamino)-1-(1H-imidazol-4-yl)-2-oxoethyl)-2-iodo-N-(4-methoxybenzyl)benzamide

Base Information

Chemical Name:N-(2-(butylamino)-1-(1H-imidazol-4-yl)-2-oxoethyl)-2-iodo-N-(4-methoxybenzyl)benzamide
CAS No.:1586800-09-0
Molecular Formula:C₂₄H₂₇IN₄O₃
Molecular Weight:546.408
Hs Code.:

Synonyms:N-(2-(butylamino)-1-(1H-imidazol-4-yl)-2-oxoethyl)-2-iodo-N-(4-methoxybenzyl)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 N-(2-(butylamino)-1-(1H-imidazol-4-yl)-2-oxoethyl)-2-iodo-N-(4-methoxybenzyl)benzamide

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Technology Process of N-(2-(butylamino)-1-(1H-imidazol-4-yl)-2-oxoethyl)-2-iodo-N-(4-methoxybenzyl)benzamide

There total 1 articles about N-(2-(butylamino)-1-(1H-imidazol-4-yl)-2-oxoethyl)-2-iodo-N-(4-methoxybenzyl)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: 46.0%

: 2769-64-4
n-butyl isonitrile

: 88-67-5
2-Iodobenzoic acid

: 2393-23-9
4-methoxy-benzylamine

: 3034-50-2
4⁽⁵⁾formylimidazole

: 1586800-09-0
N-(2-(butylamino)-1-(1H-imidazol-4-yl)-2-oxoethyl)-2-iodo-N-(4-methoxybenzyl)benzamide

Guidance literature:: With sodium sulfate; In methanol; at 20 ℃; Sealed tube;
DOI:10.1016/j.tetlet.2014.02.023

Reference yield: 60.0%

: 1586800-09-0
N-(2-(butylamino)-1-(1H-imidazol-4-yl)-2-oxoethyl)-2-iodo-N-(4-methoxybenzyl)benzamide

: 1586800-27-2
N-butyl-5-(4-methoxybenzyl)-6-oxo-5,6-dihydro-4H-benzo[f]imidazo[1,5-a][1,4]diazepine-4-carboxamide

Guidance literature:: With copper(l) iodide; caesium carbonate; In dimethyl sulfoxide; at 100 ℃; for 0.5h; Sealed tube; Microwave irradiation;
DOI:10.1016/j.tetlet.2014.02.023