benzyl 4-{2-[7-fluoro-3-(propan-2-yl)-1H-indazol-1-yl]-1H-imidazol-5-yl}piperidine-1-carboxylate

Base Information

Chemical Name:benzyl 4-{2-[7-fluoro-3-(propan-2-yl)-1H-indazol-1-yl]-1H-imidazol-5-yl}piperidine-1-carboxylate
CAS No.:1415741-33-1
Molecular Formula:C₂₆H₂₈FN₅O₂
Molecular Weight:461.539
Hs Code.:

Synonyms:benzyl 4-{2-[7-fluoro-3-(propan-2-yl)-1H-indazol-1-yl]-1H-imidazol-5-yl}piperidine-1-carboxylate

Suppliers and Price of benzyl 4-{2-[7-fluoro-3-(propan-2-yl)-1H-indazol-1-yl]-1H-imidazol-5-yl}piperidine-1-carboxylate

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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 benzyl 4-{2-[7-fluoro-3-(propan-2-yl)-1H-indazol-1-yl]-1H-imidazol-5-yl}piperidine-1-carboxylate

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of benzyl 4-{2-[7-fluoro-3-(propan-2-yl)-1H-indazol-1-yl]-1H-imidazol-5-yl}piperidine-1-carboxylate

There total 2 articles about benzyl 4-{2-[7-fluoro-3-(propan-2-yl)-1H-indazol-1-yl]-1H-imidazol-5-yl}piperidine-1-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:

: 1415741-32-0
7-fluoro-3-(propan-2-yl)-1H-indazole-1-carboximidamide

: 816464-47-8
benzyl 4-(2-bromoacetyl)piperidine-1-carboxylate

: 1415741-33-1
benzyl 4-{2-[7-fluoro-3-(propan-2-yl)-1H-indazol-1-yl]-1H-imidazol-5-yl}piperidine-1-carboxylate

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 19h;

Reference yield:

: 1415739-96-6
7-fluoro-N'-hydroxy-3-(propan-2-yl)-1H-indazole-1-carboximidamide

: 1415741-33-1
benzyl 4-{2-[7-fluoro-3-(propan-2-yl)-1H-indazol-1-yl]-1H-imidazol-5-yl}piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: acetic anhydride; hydrogen / 5%-palladium/activated carbon / acetic acid / 5 h / 20 °C / 760.05 Torr

2: potassium carbonate / N,N-dimethyl-formamide / 19 h / 20 °C

With hydrogen; acetic anhydride; potassium carbonate; 5%-palladium/activated carbon; In acetic acid; N,N-dimethyl-formamide;