Methyl-carbamic acid 1-[6-(3,4-dichloro-phenyl)-pyridazin-3-yl]-piperidin-4-yl ester

Base Information

Chemical Name:Methyl-carbamic acid 1-[6-(3,4-dichloro-phenyl)-pyridazin-3-yl]-piperidin-4-yl ester
CAS No.:93182-05-9
Molecular Formula:C₁₇H₁₈Cl₂N₄O₂
Molecular Weight:381.262
Hs Code.:

Synonyms:Methyl-carbamic acid 1-[6-(3,4-dichloro-phenyl)-pyridazin-3-yl]-piperidin-4-yl ester

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Chemical Property of Methyl-carbamic acid 1-[6-(3,4-dichloro-phenyl)-pyridazin-3-yl]-piperidin-4-yl ester

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Technology Process of Methyl-carbamic acid 1-[6-(3,4-dichloro-phenyl)-pyridazin-3-yl]-piperidin-4-yl ester

There total 3 articles about Methyl-carbamic acid 1-[6-(3,4-dichloro-phenyl)-pyridazin-3-yl]-piperidin-4-yl 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: 89.0%

: 624-83-9
methyl isocyanate

: 93181-92-1
3-(4-hydroxypiperidino)-6-(3,4-dichlorophenyl)pyridazine

: 93182-05-9
Methyl-carbamic acid 1-[6-(3,4-dichloro-phenyl)-pyridazin-3-yl]-piperidin-4-yl ester

Guidance literature:: In tetrahydrofuran; for 144h; Heating;
DOI:10.1021/jm00153a011

Reference yield:

: 5382-16-1
4-HYDROXYPIPERIDINE

: 93182-05-9
Methyl-carbamic acid 1-[6-(3,4-dichloro-phenyl)-pyridazin-3-yl]-piperidin-4-yl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 80 percent / butan-1-ol / 3 h / Heating

2: 89 percent / tetrahydrofuran / 144 h / Heating

In tetrahydrofuran; butan-1-ol;
DOI:10.1021/jm00153a011

Reference yield:

: 58059-30-6
3-chloro-6-(3,4-dichlorophenyl)pyridazine

: 93182-05-9
Methyl-carbamic acid 1-[6-(3,4-dichloro-phenyl)-pyridazin-3-yl]-piperidin-4-yl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 80 percent / butan-1-ol / 3 h / Heating

2: 89 percent / tetrahydrofuran / 144 h / Heating

In tetrahydrofuran; butan-1-ol;
DOI:10.1021/jm00153a011