ethyl 1-<(2'-cyanobiphenyl-4-yl)methyl>-2-mercapto-1H-benzimidazole-7-carboxylate

Base Information

Chemical Name:ethyl 1-<(2'-cyanobiphenyl-4-yl)methyl>-2-mercapto-1H-benzimidazole-7-carboxylate
CAS No.:139481-43-9
Molecular Formula:C₂₄H₁₉N₃O₂S
Molecular Weight:413.5
Hs Code.:

Synonyms:ethyl 1-<(2'-cyanobiphenyl-4-yl)methyl>-2-mercapto-1H-benzimidazole-7-carboxylate

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Chemical Property of ethyl 1-<(2'-cyanobiphenyl-4-yl)methyl>-2-mercapto-1H-benzimidazole-7-carboxylate

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Technology Process of ethyl 1-<(2'-cyanobiphenyl-4-yl)methyl>-2-mercapto-1H-benzimidazole-7-carboxylate

There total 9 articles about ethyl 1-<(2'-cyanobiphenyl-4-yl)methyl>-2-mercapto-1H-benzimidazole-7-carboxylate 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: 82.0%

: 140-89-6
potassium ethyl xanthogenate

: 136285-69-3
ethyl 3-amino-2-<<(2'-cyanobiphenyl-4-yl)methyl>amino>benzoate

: 139481-43-9
ethyl 1-<(2'-cyanobiphenyl-4-yl)methyl>-2-mercapto-1H-benzimidazole-7-carboxylate

Guidance literature:: In ethanol; for 8h; Heating;
DOI:10.1021/jm00067a016

Reference yield:

: 21606-04-2
methyl 2-carboxy-3-nitrobenzoate

: 139481-43-9
ethyl 1-<(2'-cyanobiphenyl-4-yl)methyl>-2-mercapto-1H-benzimidazole-7-carboxylate

Guidance literature:: Multi-step reaction with 8 steps

1: SOCl₂, DMF / toluene / 0.5 h / Heating

2: NaN₃ / acetone; H₂O / 1 h

3: 1.5 h / Heating

4: 85 percent / K₂CO₃ / acetonitrile / 4 h / Heating

5: 77 percent / 30percent ethanolic HCl / ethyl acetate / 1 h / Ambient temperature

6: 1.) FeCl₃*6H₂O, activated carbon, 2.) hydrazine monohydrate / 1.) MeOH, THF, reflux, 30 min, 2.) MeOH, THF, reflux, 14 h

7: 78 percent / ethanol / 1.5 h / Heating

8: 82 percent / ethanol / 8 h / Heating

With hydrogenchloride; thionyl chloride; sodium azide; potassium carbonate; pyrographite; hydrazine hydrate; N,N-dimethyl-formamide; In ethanol; water; ethyl acetate; acetone; toluene; acetonitrile;
DOI:10.1021/jm00067a016

Reference yield:

: 73833-13-3
acid chloride of 1-methylhydrogen-3-nitrophthalate

: 139481-43-9
ethyl 1-<(2'-cyanobiphenyl-4-yl)methyl>-2-mercapto-1H-benzimidazole-7-carboxylate

Guidance literature:: Multi-step reaction with 7 steps

1: NaN₃ / acetone; H₂O / 1 h

2: 1.5 h / Heating

3: 85 percent / K₂CO₃ / acetonitrile / 4 h / Heating

4: 77 percent / 30percent ethanolic HCl / ethyl acetate / 1 h / Ambient temperature

5: 1.) FeCl₃*6H₂O, activated carbon, 2.) hydrazine monohydrate / 1.) MeOH, THF, reflux, 30 min, 2.) MeOH, THF, reflux, 14 h

6: 78 percent / ethanol / 1.5 h / Heating

7: 82 percent / ethanol / 8 h / Heating

With hydrogenchloride; sodium azide; potassium carbonate; pyrographite; hydrazine hydrate; In ethanol; water; ethyl acetate; acetone; acetonitrile;
DOI:10.1021/jm00067a016