{4-[6-((S)-1-tert-butoxycarbonylamino-2-phenyl-ethyl)-3-chloro-pyridazin-4-yl]-phenyl}-carbamic acid methyl ester

Base Information

Chemical Name:{4-[6-((S)-1-tert-butoxycarbonylamino-2-phenyl-ethyl)-3-chloro-pyridazin-4-yl]-phenyl}-carbamic acid methyl ester
CAS No.:1187648-53-8
Molecular Formula:C₂₅H₂₇ClN₄O₄
Molecular Weight:482.967
Hs Code.:

Synonyms:{4-[6-((S)-1-tert-butoxycarbonylamino-2-phenyl-ethyl)-3-chloro-pyridazin-4-yl]-phenyl}-carbamic acid methyl ester

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Chemical Property of {4-[6-((S)-1-tert-butoxycarbonylamino-2-phenyl-ethyl)-3-chloro-pyridazin-4-yl]-phenyl}-carbamic acid methyl ester

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Technology Process of {4-[6-((S)-1-tert-butoxycarbonylamino-2-phenyl-ethyl)-3-chloro-pyridazin-4-yl]-phenyl}-carbamic acid methyl ester

There total 7 articles about {4-[6-((S)-1-tert-butoxycarbonylamino-2-phenyl-ethyl)-3-chloro-pyridazin-4-yl]-phenyl}-carbamic acid methyl ester 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: 84.0%

: 24424-99-5
di-tert-butyl dicarbonate

: {4-[6-((S)-1-amino-2-phenyl-ethyl)-3-chloro-pyridazin-4-yl]-phenyl}-carbamic acid methyl ester trifluoroacetate

: 1187648-53-8
{4-[6-((S)-1-tert-butoxycarbonylamino-2-phenyl-ethyl)-3-chloro-pyridazin-4-yl]-phenyl}-carbamic acid methyl ester

Guidance literature:: With triethylamine; In acetonitrile; at 60 ℃; for 3h;

Reference yield: 84.0%

: 24424-99-5
di-tert-butyl dicarbonate

: C₂₀H₁₉ClN₄O₂

: 1187648-53-8
{4-[6-((S)-1-tert-butoxycarbonylamino-2-phenyl-ethyl)-3-chloro-pyridazin-4-yl]-phenyl}-carbamic acid methyl ester

Guidance literature:: With triethylamine; In acetonitrile;
DOI:10.1016/j.bmcl.2018.02.049

Reference yield:

: 1187648-25-4
(S)-tert-butyl 1-(5-(4-nitrophenyl)-6-oxo-1,6-dihydropyridazin-3-yl)-2-phenylethylcarbamate

: 1187648-53-8
{4-[6-((S)-1-tert-butoxycarbonylamino-2-phenyl-ethyl)-3-chloro-pyridazin-4-yl]-phenyl}-carbamic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: zinc; ammonium chloride / methanol

2: pyridine / dichloromethane / 1 h / 0 °C

3: trichlorophosphate / acetonitrile; chloroform / 3 h / 65 °C

4: triethylamine / acetonitrile

With pyridine; ammonium chloride; triethylamine; zinc; trichlorophosphate; In methanol; dichloromethane; chloroform; acetonitrile;
DOI:10.1016/j.bmcl.2018.02.049