5-(4-(3-(aminomethyl)phenyl)piperidine-1-carbonyl)-2-hydroxy-N-methoxybenzamide trifluoroacetate

Base Information

Chemical Name:5-(4-(3-(aminomethyl)phenyl)piperidine-1-carbonyl)-2-hydroxy-N-methoxybenzamide trifluoroacetate
CAS No.:1411991-93-9
Molecular Formula:C₂HF₃O₂*C₂₁H₂₅N₃O₄
Molecular Weight:497.471
Hs Code.:

Synonyms:5-(4-(3-(aminomethyl)phenyl)piperidine-1-carbonyl)-2-hydroxy-N-methoxybenzamide trifluoroacetate

Suppliers and Price of 5-(4-(3-(aminomethyl)phenyl)piperidine-1-carbonyl)-2-hydroxy-N-methoxybenzamide trifluoroacetate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 5-(4-(3-(aminomethyl)phenyl)piperidine-1-carbonyl)-2-hydroxy-N-methoxybenzamide trifluoroacetate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 5-(4-(3-(aminomethyl)phenyl)piperidine-1-carbonyl)-2-hydroxy-N-methoxybenzamide trifluoroacetate

There total 2 articles about 5-(4-(3-(aminomethyl)phenyl)piperidine-1-carbonyl)-2-hydroxy-N-methoxybenzamide trifluoroacetate 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:

: 1411992-93-2
tert-butyl (3-(1-(4-hydroxy-3-(methoxycarbamoyl)benzoyl)piperidin-4-yl)benzyl)carbamate

: 76-05-1
trifluoroacetic acid

: 1411991-93-9
5-(4-(3-(aminomethyl)phenyl)piperidine-1-carbonyl)-2-hydroxy-N-methoxybenzamide trifluoroacetate

Guidance literature:: tert-butyl (3-(1-(4-hydroxy-3-(methoxycarbamoyl)benzoyl)piperidin-4-yl)benzyl)carbamate; With hydrogenchloride; In methanol; at 20 ℃; for 12h;

trifluoroacetic acid;

Reference yield:

: 1411992-89-6
4-hydroxy-3-(methoxycarbamoyl)benzoic acid

: 725228-49-9
tert-butyl 3-(piperidin-4-yl)benzylcarbamate

: 1411991-93-9
5-(4-(3-(aminomethyl)phenyl)piperidine-1-carbonyl)-2-hydroxy-N-methoxybenzamide trifluoroacetate

Guidance literature:: Multi-step reaction with 2 steps

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

2: hydrogenchloride / methanol / 12 h / 20 °C

With hydrogenchloride; dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In methanol; dichloromethane;