1-(2-amino-2-methylpropyl)-3-(2-fluoro-4-(piperidin-4-ylmethyl)phenyl)urea

Base Information

Chemical Name:1-(2-amino-2-methylpropyl)-3-(2-fluoro-4-(piperidin-4-ylmethyl)phenyl)urea
CAS No.:1299488-12-2
Molecular Formula:C₁₇H₂₇FN₄O
Molecular Weight:322.426
Hs Code.:

Synonyms:1-(2-amino-2-methylpropyl)-3-(2-fluoro-4-(piperidin-4-ylmethyl)phenyl)urea

Suppliers and Price of 1-(2-amino-2-methylpropyl)-3-(2-fluoro-4-(piperidin-4-ylmethyl)phenyl)urea

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 1-(2-amino-2-methylpropyl)-3-(2-fluoro-4-(piperidin-4-ylmethyl)phenyl)urea

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 1-(2-amino-2-methylpropyl)-3-(2-fluoro-4-(piperidin-4-ylmethyl)phenyl)urea

There total 5 articles about 1-(2-amino-2-methylpropyl)-3-(2-fluoro-4-(piperidin-4-ylmethyl)phenyl)urea 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:

: 1299488-11-1
tert-butyl 4-(4-(3-(2-amino-2-methylpropyl)ureido)-3-fluorobenzyl)piperidine-1-carboxylate

: 1299488-12-2
1-(2-amino-2-methylpropyl)-3-(2-fluoro-4-(piperidin-4-ylmethyl)phenyl)urea

Guidance literature:: With trifluoroacetic acid; In dichloromethane; at 20 ℃; for 3h;

Reference yield:

: 131858-37-2
4-(bromomethyl)-2-fluoro-1-nitrobenzene

: 1299488-12-2
1-(2-amino-2-methylpropyl)-3-(2-fluoro-4-(piperidin-4-ylmethyl)phenyl)urea

Guidance literature:: Multi-step reaction with 5 steps

1.1: 4 h / 140 °C

2.1: sodium hydride / tetrahydrofuran; oil / 4 h

3.1: potassium fluoride / palladium diacetate / tetrahydrofuran / 1 h / 20 °C / Sealed tube; Inert atmosphere

4.1: tetrahydrofuran / 1 h / 20 °C

4.2: 20 °C

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

With potassium fluoride; sodium hydride; trifluoroacetic acid; palladium diacetate; In tetrahydrofuran; dichloromethane; oil;

Reference yield:

: 1132941-95-7
3-fluoro-4-nitrobenzyl phosphonate

: 1299488-12-2
1-(2-amino-2-methylpropyl)-3-(2-fluoro-4-(piperidin-4-ylmethyl)phenyl)urea

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium hydride / tetrahydrofuran; oil / 4 h

2.1: potassium fluoride / palladium diacetate / tetrahydrofuran / 1 h / 20 °C / Sealed tube; Inert atmosphere

3.1: tetrahydrofuran / 1 h / 20 °C

3.2: 20 °C

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

With potassium fluoride; sodium hydride; trifluoroacetic acid; palladium diacetate; In tetrahydrofuran; dichloromethane; oil;