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

Base Information

Chemical Name:{4-[6-((S)-1-tert-butoxycarbonylamino-2-phenyl-ethyl)-3-dimethylaminomethyl-pyridazin-4-yl]-phenyl}-carbamic acid methyl ester
CAS No.:1187648-79-8
Molecular Formula:C₂₈H₃₅N₅O₄
Molecular Weight:505.617
Hs Code.:

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

There total 7 articles about {4-[6-((S)-1-tert-butoxycarbonylamino-2-phenyl-ethyl)-3-dimethylaminomethyl-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: 47.0%

: 1187648-78-7
{4-[6-((S)-1-tert-butoxycarbonylamino-2-phenyl-ethyl)-3-chloromethyl-pyridazin-4-yl]-phenyl}-carbamic acid methyl ester

: 124-40-3
dimethyl amine

: 1187648-79-8
{4-[6-((S)-1-tert-butoxycarbonylamino-2-phenyl-ethyl)-3-dimethylaminomethyl-pyridazin-4-yl]-phenyl}-carbamic acid methyl ester

Guidance literature:: With potassium hydroxide; In 1,4-dioxane; at 20 ℃; for 1.5h; Inert atmosphere;

Reference yield:

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

: 1187648-79-8
{4-[6-((S)-1-tert-butoxycarbonylamino-2-phenyl-ethyl)-3-dimethylaminomethyl-pyridazin-4-yl]-phenyl}-carbamic acid methyl ester

Guidance literature:: Multi-step reaction with 7 steps

1: hydrogen / palladium 10% on activated carbon / methanol

2: triethylamine / dichloromethane / 0 °C

3: pyridine / 5.25 h / 0 - 20 °C

4: N-ethyl-N,N-diisopropylamine / 1,1'-bis-(diphenylphosphino)ferrocene; palladium diacetate / N,N-dimethyl-formamide / 4 h / 55 °C

5: sodium tetrahydroborate; calcium chloride / ethanol / -10 - 20 °C

6: sulfuryl dichloride / chloroform / 1.18 h / 0 - 20 °C

7: potassium hydroxide / 1,4-dioxane / 1.5 h / 20 °C / Inert atmosphere

With pyridine; sodium tetrahydroborate; sulfuryl dichloride; hydrogen; triethylamine; N-ethyl-N,N-diisopropylamine; calcium chloride; potassium hydroxide; 1,1'-bis-(diphenylphosphino)ferrocene; palladium 10% on activated carbon; palladium diacetate; In 1,4-dioxane; methanol; ethanol; dichloromethane; chloroform; N,N-dimethyl-formamide;

Reference yield:

: 1187648-26-5
(S)-tert-butyl 1-(5-(4-aminophenyl)-6-oxo-1,6-dihydropyridazin-3-yl)-2-phenylethylcarbamate

: 1187648-79-8
{4-[6-((S)-1-tert-butoxycarbonylamino-2-phenyl-ethyl)-3-dimethylaminomethyl-pyridazin-4-yl]-phenyl}-carbamic acid methyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: triethylamine / dichloromethane / 0 °C

2: pyridine / 5.25 h / 0 - 20 °C

3: N-ethyl-N,N-diisopropylamine / 1,1'-bis-(diphenylphosphino)ferrocene; palladium diacetate / N,N-dimethyl-formamide / 4 h / 55 °C

4: sodium tetrahydroborate; calcium chloride / ethanol / -10 - 20 °C

5: sulfuryl dichloride / chloroform / 1.18 h / 0 - 20 °C

6: potassium hydroxide / 1,4-dioxane / 1.5 h / 20 °C / Inert atmosphere

With pyridine; sodium tetrahydroborate; sulfuryl dichloride; triethylamine; N-ethyl-N,N-diisopropylamine; calcium chloride; potassium hydroxide; 1,1'-bis-(diphenylphosphino)ferrocene; palladium diacetate; In 1,4-dioxane; ethanol; dichloromethane; chloroform; N,N-dimethyl-formamide;