N-(tert-butoxycarbonylaminoheptyl)-5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3-carboxamide

Base Information

Chemical Name:N-(tert-butoxycarbonylaminoheptyl)-5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3-carboxamide
CAS No.:1440337-67-6
Molecular Formula:C₂₉H₃₅Cl₃N₄O₃
Molecular Weight:593.981
Hs Code.:

Synonyms:N-(tert-butoxycarbonylaminoheptyl)-5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3-carboxamide

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Chemical Property of N-(tert-butoxycarbonylaminoheptyl)-5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3-carboxamide

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Technology Process of N-(tert-butoxycarbonylaminoheptyl)-5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3-carboxamide

There total 3 articles about N-(tert-butoxycarbonylaminoheptyl)-5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3-carboxamide 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:

: 99733-18-3
N-(tert-butoxycarbonyl)-1,7-heptanediamine

: 168273-05-0
5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3-carbonyl chloride

: 1440337-67-6
N-(tert-butoxycarbonylaminoheptyl)-5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3-carboxamide

Guidance literature:: With triethylamine; In dichloromethane; at 0 - 20 ℃; for 18h;
DOI:10.1002/ardp.201200392

Reference yield:

: 158941-22-1
ethyl 1-(2,4-dichlorophenyl)-4-methyl-5-(4-chlorophenyl)-1H-pyrazole-3-carboxylate

: 1440337-67-6
N-(tert-butoxycarbonylaminoheptyl)-5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3-carboxamide

Guidance literature:: Multi-step reaction with 3 steps

1: sodium hydroxide; water / ethanol / 3 h / 20 °C

2: thionyl chloride / toluene / 3 h / Reflux

3: triethylamine / dichloromethane / 18 h / 0 - 20 °C

With thionyl chloride; water; triethylamine; sodium hydroxide; In ethanol; dichloromethane; toluene;
DOI:10.1002/ardp.201200392

Reference yield:

: 162758-35-2
rimonabant acid

: 1440337-67-6
N-(tert-butoxycarbonylaminoheptyl)-5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: thionyl chloride / toluene / 3 h / Reflux

2: triethylamine / dichloromethane / 18 h / 0 - 20 °C

With thionyl chloride; triethylamine; In dichloromethane; toluene;
DOI:10.1002/ardp.201200392