N¹-Aethoxycarbonyl-N²-(2-methyl-4-phenyl-1,2,3,4-tetrahydroisochinol-8-yl)-S-aethylisothioharnstoff

Base Information

Chemical Name:N¹-Aethoxycarbonyl-N²-(2-methyl-4-phenyl-1,2,3,4-tetrahydroisochinol-8-yl)-S-aethylisothioharnstoff
CAS No.:80947-22-4
Molecular Formula:C₂₂H₂₇N₃O₂S
Molecular Weight:397.541
Hs Code.:

N<sup>1</sup>-Aethoxycarbonyl-N<sup>2</sup>-(2-methyl-4-phenyl-1,2,3,4-tetrahydroisochinol-8-yl)-S-aethylisothioharnstoff

Synonyms:N¹-Aethoxycarbonyl-N²-(2-methyl-4-phenyl-1,2,3,4-tetrahydroisochinol-8-yl)-S-aethylisothioharnstoff

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Chemical Property of N¹-Aethoxycarbonyl-N²-(2-methyl-4-phenyl-1,2,3,4-tetrahydroisochinol-8-yl)-S-aethylisothioharnstoff

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Technology Process of N¹-Aethoxycarbonyl-N²-(2-methyl-4-phenyl-1,2,3,4-tetrahydroisochinol-8-yl)-S-aethylisothioharnstoff

There total 2 articles about N¹-Aethoxycarbonyl-N²-(2-methyl-4-phenyl-1,2,3,4-tetrahydroisochinol-8-yl)-S-aethylisothioharnstoff 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:

: 24526-64-5
nomifensine

: 80947-22-4
N¹-Aethoxycarbonyl-N²-(2-methyl-4-phenyl-1,2,3,4-tetrahydroisochinol-8-yl)-S-aethylisothioharnstoff

Guidance literature:: Multi-step reaction with 2 steps

1: 61.5 g / CH₂Cl₂ / 2 h / Ambient temperature

2: 7.1 g / potassium carbonate / acetone / 24 h

With potassium carbonate; In dichloromethane; acetone;