N-(5-chloropyridin-2-yl)-2-[((4-((2-aminoimidazol-1-yl)methyl)-3-chlorothiophen-2-yl)carbonyl)amino]-3-methoxy-5-chlorobenzamide

Base Information

Chemical Name:N-(5-chloropyridin-2-yl)-2-[((4-((2-aminoimidazol-1-yl)methyl)-3-chlorothiophen-2-yl)carbonyl)amino]-3-methoxy-5-chlorobenzamide
CAS No.:229336-78-1
Molecular Formula:C₂₂H₁₇Cl₃N₆O₃S
Molecular Weight:551.84
Hs Code.:

Synonyms:N-(5-chloropyridin-2-yl)-2-[((4-((2-aminoimidazol-1-yl)methyl)-3-chlorothiophen-2-yl)carbonyl)amino]-3-methoxy-5-chlorobenzamide

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Chemical Property of N-(5-chloropyridin-2-yl)-2-[((4-((2-aminoimidazol-1-yl)methyl)-3-chlorothiophen-2-yl)carbonyl)amino]-3-methoxy-5-chlorobenzamide

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Technology Process of N-(5-chloropyridin-2-yl)-2-[((4-((2-aminoimidazol-1-yl)methyl)-3-chlorothiophen-2-yl)carbonyl)amino]-3-methoxy-5-chlorobenzamide

There total 6 articles about N-(5-chloropyridin-2-yl)-2-[((4-((2-aminoimidazol-1-yl)methyl)-3-chlorothiophen-2-yl)carbonyl)amino]-3-methoxy-5-chlorobenzamide 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: 87.0%

: 7720-39-0
1H-imidazol-2-amine

: 229335-21-1
3-chloro-N-[4-chloro-2-[[(5-chloro-2-pyridinyl)amino]carbonyl]-6-methoxyphenyl]-4-chloromethyl-2-thiophenecarboxamide

: 229336-78-1
N-(5-chloropyridin-2-yl)-2-[((4-((2-aminoimidazol-1-yl)methyl)-3-chlorothiophen-2-yl)carbonyl)amino]-3-methoxy-5-chlorobenzamide

Guidance literature:: In N,N-dimethyl-formamide; at 0 - 20 ℃;
DOI:10.1021/jm070125f

Reference yield:

: 4920-80-3
3-methoxy-2-nitrobenzoic acid

: 229336-78-1
N-(5-chloropyridin-2-yl)-2-[((4-((2-aminoimidazol-1-yl)methyl)-3-chlorothiophen-2-yl)carbonyl)amino]-3-methoxy-5-chlorobenzamide

Guidance literature:: Multi-step reaction with 6 steps

1: 100 percent / oxalyl chloride; DMF / CH₂Cl₂ / 16 h / 20 °C

2: 97 percent / pyridine / 4-dimethylaminopyridine / 20 °C

3: 88 percent / aq. sodium hydrosulfite / tetrahydrofuran; dioxane

4: 90 percent / N-chlorosuccinimide / benzene / 24 h / 50 - 55 °C

5: 85 percent / pyridine / CH₂Cl₂ / 0 - 20 °C

6: 87 percent / dimethylformamide / 0 - 20 °C

With pyridine; sodium disulfite; N-chloro-succinimide; oxalyl dichloride; N,N-dimethyl-formamide; dmap; In tetrahydrofuran; 1,4-dioxane; dichloromethane; N,N-dimethyl-formamide; benzene;
DOI:10.1021/jm070125f

Reference yield:

: 15865-57-3
2-nitro-3-methoxybenzoyl chloride

: 229336-78-1
N-(5-chloropyridin-2-yl)-2-[((4-((2-aminoimidazol-1-yl)methyl)-3-chlorothiophen-2-yl)carbonyl)amino]-3-methoxy-5-chlorobenzamide

Guidance literature:: Multi-step reaction with 5 steps

1: 97 percent / pyridine / 4-dimethylaminopyridine / 20 °C

2: 88 percent / aq. sodium hydrosulfite / tetrahydrofuran; dioxane

3: 90 percent / N-chlorosuccinimide / benzene / 24 h / 50 - 55 °C

4: 85 percent / pyridine / CH₂Cl₂ / 0 - 20 °C

5: 87 percent / dimethylformamide / 0 - 20 °C

With pyridine; sodium disulfite; N-chloro-succinimide; dmap; In tetrahydrofuran; 1,4-dioxane; dichloromethane; N,N-dimethyl-formamide; benzene;
DOI:10.1021/jm070125f