3-[2-(2-(2-(2-hydroxyethoxy)ethoxy)ethoxy)ethyl]-8-[4-(4-fluorophenyl)-4-oxobutyl]-1-phenyl-1,3,8-triazaspiro[4,5]decan-4-one

Base Information

Chemical Name:3-[2-(2-(2-(2-hydroxyethoxy)ethoxy)ethoxy)ethyl]-8-[4-(4-fluorophenyl)-4-oxobutyl]-1-phenyl-1,3,8-triazaspiro[4,5]decan-4-one
CAS No.:1446685-07-9
Molecular Formula:C₃₁H₄₂FN₃O₆
Molecular Weight:571.689
Hs Code.:

Synonyms:3-[2-(2-(2-(2-hydroxyethoxy)ethoxy)ethoxy)ethyl]-8-[4-(4-fluorophenyl)-4-oxobutyl]-1-phenyl-1,3,8-triazaspiro[4,5]decan-4-one

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Chemical Property of 3-[2-(2-(2-(2-hydroxyethoxy)ethoxy)ethoxy)ethyl]-8-[4-(4-fluorophenyl)-4-oxobutyl]-1-phenyl-1,3,8-triazaspiro[4,5]decan-4-one

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Technology Process of 3-[2-(2-(2-(2-hydroxyethoxy)ethoxy)ethoxy)ethyl]-8-[4-(4-fluorophenyl)-4-oxobutyl]-1-phenyl-1,3,8-triazaspiro[4,5]decan-4-one

There total 4 articles about 3-[2-(2-(2-(2-hydroxyethoxy)ethoxy)ethoxy)ethyl]-8-[4-(4-fluorophenyl)-4-oxobutyl]-1-phenyl-1,3,8-triazaspiro[4,5]decan-4-one 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: 76.0%

: 77544-60-6
p-toluenesulfonic acid 2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethyl ester

: 749-02-0
spiperone

: 1446685-07-9
3-[2-(2-(2-(2-hydroxyethoxy)ethoxy)ethoxy)ethyl]-8-[4-(4-fluorophenyl)-4-oxobutyl]-1-phenyl-1,3,8-triazaspiro[4,5]decan-4-one

Guidance literature:: With potassium hydroxide; In N,N-dimethyl-formamide; at 110 ℃; for 20h; Inert atmosphere;
DOI:10.1021/jo400646k

Reference yield:

: 1021-25-6
1-Phenyl-1,3,8-triaza-spiro[4.5]decan-4-one

: 1446685-07-9
3-[2-(2-(2-(2-hydroxyethoxy)ethoxy)ethoxy)ethyl]-8-[4-(4-fluorophenyl)-4-oxobutyl]-1-phenyl-1,3,8-triazaspiro[4,5]decan-4-one

Guidance literature:: Multi-step reaction with 2 steps

1: diisopropylamine / N,N-dimethyl-formamide / 17 h / 80 °C / Inert atmosphere

2: potassium hydroxide / N,N-dimethyl-formamide / 20 h / 110 °C / Inert atmosphere

With diisopropylamine; potassium hydroxide; In N,N-dimethyl-formamide;
DOI:10.1021/jo400646k

Reference yield:

: 112-60-7
Tetraethylene glycol

: 1446685-07-9
3-[2-(2-(2-(2-hydroxyethoxy)ethoxy)ethoxy)ethyl]-8-[4-(4-fluorophenyl)-4-oxobutyl]-1-phenyl-1,3,8-triazaspiro[4,5]decan-4-one

Guidance literature:: Multi-step reaction with 2 steps

1.1: dichloromethane / 0.5 h / 20 °C

1.2: 1.5 h / 0 - 20 °C

2.1: potassium hydroxide / N,N-dimethyl-formamide / 20 h / 110 °C / Inert atmosphere

With potassium hydroxide; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jo400646k