tert-butyl 4-((4-bromo-3-chlorobenzyl)(methyl)amino)-4-oxobutylcarbamate

Base Information

Chemical Name:tert-butyl 4-((4-bromo-3-chlorobenzyl)(methyl)amino)-4-oxobutylcarbamate
CAS No.:1338327-17-5
Molecular Formula:C₁₇H₂₄BrClN₂O₃
Molecular Weight:419.746
Hs Code.:

Synonyms:tert-butyl 4-((4-bromo-3-chlorobenzyl)(methyl)amino)-4-oxobutylcarbamate

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Chemical Property of tert-butyl 4-((4-bromo-3-chlorobenzyl)(methyl)amino)-4-oxobutylcarbamate

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Technology Process of tert-butyl 4-((4-bromo-3-chlorobenzyl)(methyl)amino)-4-oxobutylcarbamate

There total 3 articles about tert-butyl 4-((4-bromo-3-chlorobenzyl)(methyl)amino)-4-oxobutylcarbamate 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: 46.1%

: 57294-38-9
N-(tert-butoxycarbonyl)-4-aminobutanoic acid

: 1338326-96-7
1-(4-bromo-3-chlorophenyl)-N-methylmethanamine

: 1338327-17-5
tert-butyl 4-((4-bromo-3-chlorobenzyl)(methyl)amino)-4-oxobutylcarbamate

Guidance literature:: With N-ethyl-N,N-diisopropylamine; HATU; In N,N-dimethyl-formamide; at 18 - 25 ℃; for 20h; Inert atmosphere;

Reference yield:

: 120077-69-2
3-chloro4-bromo-benzaldehyde

: 1338327-17-5
tert-butyl 4-((4-bromo-3-chlorobenzyl)(methyl)amino)-4-oxobutylcarbamate

Guidance literature:: Multi-step reaction with 3 steps

1: acetic acid; sodium tris(acetoxy)borohydride / tetrahydrofuran / 4 h / 18 - 25 °C / Inert atmosphere

2: sodium tetrahydroborate / methanol / 2 h / 18 - 25 °C / Inert atmosphere

3: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 20 h / 18 - 25 °C / Inert atmosphere

With sodium tetrahydroborate; sodium tris(acetoxy)borohydride; acetic acid; N-ethyl-N,N-diisopropylamine; HATU; In tetrahydrofuran; methanol; N,N-dimethyl-formamide;

Reference yield:

: 1338326-97-8
(Z)-N-(4-bromo-3-chlorobenzylidene)methanamine

: 1338327-17-5
tert-butyl 4-((4-bromo-3-chlorobenzyl)(methyl)amino)-4-oxobutylcarbamate

Guidance literature:: Multi-step reaction with 2 steps

1: sodium tetrahydroborate / methanol / 2 h / 18 - 25 °C / Inert atmosphere

2: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 20 h / 18 - 25 °C / Inert atmosphere

With sodium tetrahydroborate; N-ethyl-N,N-diisopropylamine; HATU; In methanol; N,N-dimethyl-formamide;