(4-(3-(aminomethyl)phenyl)piperidin-1-yl)(4-((hydroxydimethylsilyl)methoxy)phenyl)methanone

Base Information

Chemical Name:(4-(3-(aminomethyl)phenyl)piperidin-1-yl)(4-((hydroxydimethylsilyl)methoxy)phenyl)methanone
CAS No.:1431289-58-5
Molecular Formula:C₂₂H₃₀N₂O₃Si
Molecular Weight:398.577
Hs Code.:

Synonyms:(4-(3-(aminomethyl)phenyl)piperidin-1-yl)(4-((hydroxydimethylsilyl)methoxy)phenyl)methanone

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Chemical Property of (4-(3-(aminomethyl)phenyl)piperidin-1-yl)(4-((hydroxydimethylsilyl)methoxy)phenyl)methanone

Chemical Property:

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Technology Process of (4-(3-(aminomethyl)phenyl)piperidin-1-yl)(4-((hydroxydimethylsilyl)methoxy)phenyl)methanone

There total 6 articles about (4-(3-(aminomethyl)phenyl)piperidin-1-yl)(4-((hydroxydimethylsilyl)methoxy)phenyl)methanone 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:

: 1431289-56-3
tert-butyl 3-(1-(4-((hydroxydimethylsilyl)methoxy)benzoyl)piperidin-4-yl)benzylcarbamate

: 1431289-58-5
(4-(3-(aminomethyl)phenyl)piperidin-1-yl)(4-((hydroxydimethylsilyl)methoxy)phenyl)methanone

Guidance literature:: With trifluoroacetic acid; In dichloromethane; at 20 ℃; for 12h;

Reference yield:

: C₁₃H₂₀O₄Si

: 1431289-58-5
(4-(3-(aminomethyl)phenyl)piperidin-1-yl)(4-((hydroxydimethylsilyl)methoxy)phenyl)methanone

Guidance literature:: Multi-step reaction with 3 steps

1: lithium hydroxide; water / tetrahydrofuran

2: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; dmap / dichloromethane / 12 h / 20 °C

3: trifluoroacetic acid / dichloromethane / 12 h / 20 °C

With dmap; water; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; trifluoroacetic acid; lithium hydroxide; In tetrahydrofuran; dichloromethane;

Reference yield:

: 99-76-3,156291-94-0
methyl 4-hydroxylbenzoate

: 1431289-58-5
(4-(3-(aminomethyl)phenyl)piperidin-1-yl)(4-((hydroxydimethylsilyl)methoxy)phenyl)methanone

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium carbonate / acetone / 0.25 h / 20 °C

1.2: 72 h / 60 °C

2.1: lithium hydroxide; water / tetrahydrofuran / 24 h / 20 °C

3.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; dmap / dichloromethane / 12 h / 20 °C

4.1: trifluoroacetic acid / dichloromethane / 12 h / 20 °C

With dmap; water; potassium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; trifluoroacetic acid; lithium hydroxide; In tetrahydrofuran; dichloromethane; acetone;