tert-butyl 3-{3-fluoro-4-[(4-methyl-piperazin-1-yl)methyl]phenoxy}azetidine-1-carboxylate

Base Information

Chemical Name:tert-butyl 3-{3-fluoro-4-[(4-methyl-piperazin-1-yl)methyl]phenoxy}azetidine-1-carboxylate
CAS No.:1354792-53-2
Molecular Formula:C₂₀H₃₀FN₃O₃
Molecular Weight:379.475
Hs Code.:

Synonyms:tert-butyl 3-{3-fluoro-4-[(4-methyl-piperazin-1-yl)methyl]phenoxy}azetidine-1-carboxylate

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Chemical Property of tert-butyl 3-{3-fluoro-4-[(4-methyl-piperazin-1-yl)methyl]phenoxy}azetidine-1-carboxylate

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Technology Process of tert-butyl 3-{3-fluoro-4-[(4-methyl-piperazin-1-yl)methyl]phenoxy}azetidine-1-carboxylate

There total 4 articles about tert-butyl 3-{3-fluoro-4-[(4-methyl-piperazin-1-yl)methyl]phenoxy}azetidine-1-carboxylate 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: 45.0%

: 1354792-52-1
3-fluoro-4-[(4-methylpiperazin-1-yl)-methyl]phenol

: 141699-58-3
3-methanesulfonyloxy-azetidine-1-carboxylic acid tert-butyl ester

: 1354792-53-2
tert-butyl 3-{3-fluoro-4-[(4-methyl-piperazin-1-yl)methyl]phenoxy}azetidine-1-carboxylate

Guidance literature:: 3-fluoro-4-[(4-methylpiperazin-1-yl)-methyl]phenol; With sodium hydride; In N,N-dimethyl-formamide; mineral oil; for 0.5h; Inert atmosphere; Cooling with ice;

3-methanesulfonyloxy-azetidine-1-carboxylic acid tert-butyl ester; In N,N-dimethyl-formamide; mineral oil; at 80 ℃; for 144h;

Reference yield:

: 331-64-6
2-fluoro-4-methoxy-benzaldehyde

: 1354792-53-2
tert-butyl 3-{3-fluoro-4-[(4-methyl-piperazin-1-yl)methyl]phenoxy}azetidine-1-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1.1: 1,1-dichloroethane / 0.5 h / 20 °C

1.2: 20 °C

2.1: water; hydrogen bromide / 5 h / Reflux

3.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.5 h / Inert atmosphere; Cooling with ice

3.2: 144 h / 80 °C

With water; hydrogen bromide; sodium hydride; In 1,1-dichloroethane; N,N-dimethyl-formamide; mineral oil;

Reference yield:

: 109-01-3
1-methyl-piperazine

: 1354792-53-2
tert-butyl 3-{3-fluoro-4-[(4-methyl-piperazin-1-yl)methyl]phenoxy}azetidine-1-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1.1: 1,1-dichloroethane / 0.5 h / 20 °C

1.2: 20 °C

2.1: water; hydrogen bromide / 5 h / Reflux

3.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.5 h / Inert atmosphere; Cooling with ice

3.2: 144 h / 80 °C

With water; hydrogen bromide; sodium hydride; In 1,1-dichloroethane; N,N-dimethyl-formamide; mineral oil;