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7-(3,4-dimethoxyphenyl)-2-((3-(methoxymethyl)-3-methylpiperidin-1-yl)methyl)-5-methylthieno[3,2-c]pyridin-4(5H)-one hydrochloride

Base Information
  • Chemical Name:7-(3,4-dimethoxyphenyl)-2-((3-(methoxymethyl)-3-methylpiperidin-1-yl)methyl)-5-methylthieno[3,2-c]pyridin-4(5H)-one hydrochloride
  • CAS No.:1610521-69-1
  • Molecular Formula:C25H32N2O4S*ClH
  • Molecular Weight:493.067
  • Hs Code.:
7-(3,4-dimethoxyphenyl)-2-((3-(methoxymethyl)-3-methylpiperidin-1-yl)methyl)-5-methylthieno[3,2-c]pyridin-4(5H)-one hydrochloride

Synonyms:7-(3,4-dimethoxyphenyl)-2-((3-(methoxymethyl)-3-methylpiperidin-1-yl)methyl)-5-methylthieno[3,2-c]pyridin-4(5H)-one hydrochloride

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Chemical Property of 7-(3,4-dimethoxyphenyl)-2-((3-(methoxymethyl)-3-methylpiperidin-1-yl)methyl)-5-methylthieno[3,2-c]pyridin-4(5H)-one hydrochloride
Chemical Property:
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Technology Process of 7-(3,4-dimethoxyphenyl)-2-((3-(methoxymethyl)-3-methylpiperidin-1-yl)methyl)-5-methylthieno[3,2-c]pyridin-4(5H)-one hydrochloride

There total 9 articles about 7-(3,4-dimethoxyphenyl)-2-((3-(methoxymethyl)-3-methylpiperidin-1-yl)methyl)-5-methylthieno[3,2-c]pyridin-4(5H)-one hydrochloride 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:
Guidance literature:
3-(methoxymethyl)-3-methylpiperidine; 7-(3,4-dimethoxyphenyl)-5-methyl-4-oxo-4,5-dihydrothieno[3,2-c]pyridine-2-carbaldehyde; With sodium tris(acetoxy)borohydride; In 1,2-dichloro-ethane; at 85 ℃; for 24h; Inert atmosphere;
With hydrogenchloride; water;
Guidance literature:
Multi-step reaction with 5 steps
1.1: n-butyllithium / tetrahydrofuran; hexane / 2.5 h / -78 - -60 °C / Inert atmosphere
1.2: 1 h / -60 - 20 °C / Inert atmosphere
2.1: N-Bromosuccinimide / tetrahydrofuran / 24 h / 20 °C
3.1: caesium carbonate / tetrahydrofuran / 0.33 h / 20 °C
3.2: 20 °C
4.1: potassium carbonate; bis-triphenylphosphine-palladium(II) chloride / water; 1,2-dimethoxyethane / 0.5 h / 120 °C / Microwave irradiation
5.1: sodium tris(acetoxy)borohydride / 1,2-dichloro-ethane / 24 h / 85 °C / Inert atmosphere
With bis-triphenylphosphine-palladium(II) chloride; N-Bromosuccinimide; n-butyllithium; sodium tris(acetoxy)borohydride; potassium carbonate; caesium carbonate; In tetrahydrofuran; 1,2-dimethoxyethane; hexane; water; 1,2-dichloro-ethane;
Guidance literature:
Multi-step reaction with 4 steps
1.1: triethylamine / dichloromethane / 20 °C / Inert atmosphere
2.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 1 h / 20 °C / Sealed tube
2.2: 20 °C / Sealed tube
3.1: trifluoroacetic acid / dichloromethane / 1 h / 20 °C / Inert atmosphere
4.1: sodium tris(acetoxy)borohydride / 1,2-dichloro-ethane / 24 h / 85 °C / Inert atmosphere
With sodium tris(acetoxy)borohydride; sodium hydride; triethylamine; trifluoroacetic acid; In dichloromethane; 1,2-dichloro-ethane; N,N-dimethyl-formamide; mineral oil;
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