ethyl {4-{2-{4-[(methylpyridin-2-ylmethylamino)methyl]-1H-benzimidazol-2-yl}phenylsulfamoyl}phenoxy}acetate

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Chemical Name:ethyl {4-{2-{4-[(methylpyridin-2-ylmethylamino)methyl]-1H-benzimidazol-2-yl}phenylsulfamoyl}phenoxy}acetate
CAS No.:760981-62-2
Molecular Formula:C₃₁H₃₁N₅O₅S
Molecular Weight:585.684
Hs Code.:

Synonyms:ethyl {4-{2-{4-[(methylpyridin-2-ylmethylamino)methyl]-1H-benzimidazol-2-yl}phenylsulfamoyl}phenoxy}acetate

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Chemical Property of ethyl {4-{2-{4-[(methylpyridin-2-ylmethylamino)methyl]-1H-benzimidazol-2-yl}phenylsulfamoyl}phenoxy}acetate

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Technology Process of ethyl {4-{2-{4-[(methylpyridin-2-ylmethylamino)methyl]-1H-benzimidazol-2-yl}phenylsulfamoyl}phenoxy}acetate

There total 6 articles about ethyl {4-{2-{4-[(methylpyridin-2-ylmethylamino)methyl]-1H-benzimidazol-2-yl}phenylsulfamoyl}phenoxy}acetate 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: 97.0%

: 21035-59-6
N-methyl-2-pyridinemethanamine

: 760981-55-3
ethyl {4-[2-(4-formyl-1H-benzimidazol-2-yl)phenylsulfamoyl]phenoxy}acetate

: 760981-62-2
ethyl {4-{2-{4-[(methylpyridin-2-ylmethylamino)methyl]-1H-benzimidazol-2-yl}phenylsulfamoyl}phenoxy}acetate

Guidance literature:: With sodium tris(acetoxy)borohydride; In 1,2-dichloro-ethane; for 2.5h;
DOI:10.1002/chem.200305299

Reference yield:

: 5344-90-1
2-Aminobenzyl alcohol

: 760981-62-2
ethyl {4-{2-{4-[(methylpyridin-2-ylmethylamino)methyl]-1H-benzimidazol-2-yl}phenylsulfamoyl}phenoxy}acetate

Guidance literature:: Multi-step reaction with 4 steps

1: pyridine / CH₂Cl₂ / 2 h / 20 °C

2: 36 percent / aq. Cu(OAc)2 / methanol; ethanol / 3 h / Heating

3: 86 percent / MnO₂ / CH₂Cl₂ / 20 °C

4: 97 percent / NaBH(OAc)3 / 1,2-dichloro-ethane / 2.5 h

With pyridine; manganese(IV) oxide; copper diacetate; sodium tris(acetoxy)borohydride; In methanol; ethanol; dichloromethane; 1,2-dichloro-ethane;
DOI:10.1002/chem.200305299

Reference yield:

: 2555-49-9
phenoxyacetic acid ethyl ester

: 760981-62-2
ethyl {4-{2-{4-[(methylpyridin-2-ylmethylamino)methyl]-1H-benzimidazol-2-yl}phenylsulfamoyl}phenoxy}acetate

Guidance literature:: Multi-step reaction with 5 steps

1: 78 percent / chlorosulfonic acid / CH₂Cl₂ / 3 h / 20 °C

2: pyridine / CH₂Cl₂ / 2 h / 20 °C

3: 36 percent / aq. Cu(OAc)2 / methanol; ethanol / 3 h / Heating

4: 86 percent / MnO₂ / CH₂Cl₂ / 20 °C

5: 97 percent / NaBH(OAc)3 / 1,2-dichloro-ethane / 2.5 h

With pyridine; chlorosulfonic acid; manganese(IV) oxide; copper diacetate; sodium tris(acetoxy)borohydride; In methanol; ethanol; dichloromethane; 1,2-dichloro-ethane;
DOI:10.1002/chem.200305299