tert-butyl 3-(2'-(((4'-chloro-[1,1'-biphenyl]-4-yl)amino)methyl)-2-methyl-[1,1'-biphenyl]-4-ylcarboxamido)propanoate

Base Information

Chemical Name:tert-butyl 3-(2'-(((4'-chloro-[1,1'-biphenyl]-4-yl)amino)methyl)-2-methyl-[1,1'-biphenyl]-4-ylcarboxamido)propanoate
CAS No.:1414931-62-6
Molecular Formula:C₃₄H₃₅ClN₂O₃
Molecular Weight:555.116
Hs Code.:

Synonyms:tert-butyl 3-(2'-(((4'-chloro-[1,1'-biphenyl]-4-yl)amino)methyl)-2-methyl-[1,1'-biphenyl]-4-ylcarboxamido)propanoate

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Chemical Property of tert-butyl 3-(2'-(((4'-chloro-[1,1'-biphenyl]-4-yl)amino)methyl)-2-methyl-[1,1'-biphenyl]-4-ylcarboxamido)propanoate

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Technology Process of tert-butyl 3-(2'-(((4'-chloro-[1,1'-biphenyl]-4-yl)amino)methyl)-2-methyl-[1,1'-biphenyl]-4-ylcarboxamido)propanoate

There total 4 articles about tert-butyl 3-(2'-(((4'-chloro-[1,1'-biphenyl]-4-yl)amino)methyl)-2-methyl-[1,1'-biphenyl]-4-ylcarboxamido)propanoate 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:

: 135-68-2
4-(4-chlorophenyl)aniline

: 1414931-61-5
tert-butyl 3-(2'-formyl-2-methyl-[1,1'-biphenyl]-4-ylcarboxamido)propanoate

: 1414931-62-6
tert-butyl 3-(2'-(((4'-chloro-[1,1'-biphenyl]-4-yl)amino)methyl)-2-methyl-[1,1'-biphenyl]-4-ylcarboxamido)propanoate

Guidance literature:: With sodium tris(acetoxy)borohydride; acetic acid; In 1,2-dichloro-ethane; at 20 ℃; for 16h;

Reference yield:

: 7697-28-1
4-bromo-3-methylbenzoic acid

: 1414931-62-6
tert-butyl 3-(2'-(((4'-chloro-[1,1'-biphenyl]-4-yl)amino)methyl)-2-methyl-[1,1'-biphenyl]-4-ylcarboxamido)propanoate

Guidance literature:: Multi-step reaction with 3 steps

1: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 16 h / 20 °C

2: potassium carbonate / dichloro[1,1'-bis(di-t-butylphosphino)ferrocene]palladium(II) / 1,4-dioxane; water / 3 h / 85 °C

3: acetic acid; sodium tris(acetoxy)borohydride / 1,2-dichloro-ethane / 16 h / 20 °C

With sodium tris(acetoxy)borohydride; potassium carbonate; acetic acid; N-ethyl-N,N-diisopropylamine; HATU; dichloro[1,1'-bis(di-t-butylphosphino)ferrocene]palladium(II); In 1,4-dioxane; water; 1,2-dichloro-ethane; N,N-dimethyl-formamide;

Reference yield:

: 58620-93-2
tert-butyl 3-aminopropanoate hydrochloride

: 1414931-62-6
tert-butyl 3-(2'-(((4'-chloro-[1,1'-biphenyl]-4-yl)amino)methyl)-2-methyl-[1,1'-biphenyl]-4-ylcarboxamido)propanoate

Guidance literature:: Multi-step reaction with 3 steps

1: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 16 h / 20 °C

2: potassium carbonate / dichloro[1,1'-bis(di-t-butylphosphino)ferrocene]palladium(II) / 1,4-dioxane; water / 3 h / 85 °C

3: acetic acid; sodium tris(acetoxy)borohydride / 1,2-dichloro-ethane / 16 h / 20 °C

With sodium tris(acetoxy)borohydride; potassium carbonate; acetic acid; N-ethyl-N,N-diisopropylamine; HATU; dichloro[1,1'-bis(di-t-butylphosphino)ferrocene]palladium(II); In 1,4-dioxane; water; 1,2-dichloro-ethane; N,N-dimethyl-formamide;