N-[4-(5-amino-1H-benzoimidazol-2-yl)-phenyl]-2-chloro-5-iodo-benzamide

Base Information

Chemical Name:N-[4-(5-amino-1H-benzoimidazol-2-yl)-phenyl]-2-chloro-5-iodo-benzamide
CAS No.:911211-62-6
Molecular Formula:C₂₀H₁₄ClIN₄O
Molecular Weight:488.715
Hs Code.:

<i>N</i>-[4-(5-amino-1<i>H</i>-benzoimidazol-2-yl)-phenyl]-2-chloro-5-iodo-benzamide

Synonyms:N-[4-(5-amino-1H-benzoimidazol-2-yl)-phenyl]-2-chloro-5-iodo-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-[4-(5-amino-1H-benzoimidazol-2-yl)-phenyl]-2-chloro-5-iodo-benzamide

Chemical Property:

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Technology Process of N-[4-(5-amino-1H-benzoimidazol-2-yl)-phenyl]-2-chloro-5-iodo-benzamide

There total 4 articles about N-[4-(5-amino-1H-benzoimidazol-2-yl)-phenyl]-2-chloro-5-iodo-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: 79.0%

: 911211-61-5
2-chloro-5-iodo-N-[4-(5-nitro-1H-benzoimidazol-2-yl)-phenyl]-benzamide

: 911211-62-6
N-[4-(5-amino-1H-benzoimidazol-2-yl)-phenyl]-2-chloro-5-iodo-benzamide

Guidance literature:: With tin(ll) chloride; In ethanol; ethyl acetate; Heating;
DOI:10.1016/j.bmcl.2006.07.056

Reference yield:

: 556-18-3,28107-09-7
4-aminobenzaldehyde

: 911211-62-6
N-[4-(5-amino-1H-benzoimidazol-2-yl)-phenyl]-2-chloro-5-iodo-benzamide

Guidance literature:: Multi-step reaction with 3 steps

1: 68 percent / pyridine / 115 °C

2: 67 percent / CH₂Cl₂ / 20 °C

3: 79 percent / SnCl₂ / ethanol; ethyl acetate / Heating

With pyridine; tin(ll) chloride; In ethanol; dichloromethane; ethyl acetate;
DOI:10.1016/j.bmcl.2006.07.056

Reference yield:

: 99-56-9
4-Nitrophenylene-1,2-diamine

: 911211-62-6
N-[4-(5-amino-1H-benzoimidazol-2-yl)-phenyl]-2-chloro-5-iodo-benzamide

Guidance literature:: Multi-step reaction with 3 steps

1: 68 percent / pyridine / 115 °C

2: 67 percent / CH₂Cl₂ / 20 °C

3: 79 percent / SnCl₂ / ethanol; ethyl acetate / Heating

With pyridine; tin(ll) chloride; In ethanol; dichloromethane; ethyl acetate;
DOI:10.1016/j.bmcl.2006.07.056