[3-(5-amino-3-methyl-3,6-dihydro-2H-[1,4]oxazin-3-yl)-phenyl]-(6-bromo-1-methyl-1H-indazol-3-yl)-amine

Base Information

Chemical Name:[3-(5-amino-3-methyl-3,6-dihydro-2H-[1,4]oxazin-3-yl)-phenyl]-(6-bromo-1-methyl-1H-indazol-3-yl)-amine
CAS No.:1429869-66-8
Molecular Formula:C₁₉H₂₀BrN₅O
Molecular Weight:414.305
Hs Code.:

Synonyms:[3-(5-amino-3-methyl-3,6-dihydro-2H-[1,4]oxazin-3-yl)-phenyl]-(6-bromo-1-methyl-1H-indazol-3-yl)-amine

Suppliers and Price of [3-(5-amino-3-methyl-3,6-dihydro-2H-[1,4]oxazin-3-yl)-phenyl]-(6-bromo-1-methyl-1H-indazol-3-yl)-amine

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 [3-(5-amino-3-methyl-3,6-dihydro-2H-[1,4]oxazin-3-yl)-phenyl]-(6-bromo-1-methyl-1H-indazol-3-yl)-amine

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of [3-(5-amino-3-methyl-3,6-dihydro-2H-[1,4]oxazin-3-yl)-phenyl]-(6-bromo-1-methyl-1H-indazol-3-yl)-amine

There total 8 articles about [3-(5-amino-3-methyl-3,6-dihydro-2H-[1,4]oxazin-3-yl)-phenyl]-(6-bromo-1-methyl-1H-indazol-3-yl)-amine 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:

: 1429869-68-0
5-[3-(6-bromo-1-methyl-1H-indazol-3-ylamino)-phenyl]-5-methyl-morpholine-3-thione

: 1429869-66-8
[3-(5-amino-3-methyl-3,6-dihydro-2H-[1,4]oxazin-3-yl)-phenyl]-(6-bromo-1-methyl-1H-indazol-3-yl)-amine

Guidance literature:: With tert.-butylhydroperoxide; ammonium hydroxide; In methanol; water; at 20 ℃; for 20h;

Reference yield:

: 1262858-65-0
(RS)-2-amino-2-(3-bromo-phenyl)-propionic acid hydrochloride

: 1429869-66-8
[3-(5-amino-3-methyl-3,6-dihydro-2H-[1,4]oxazin-3-yl)-phenyl]-(6-bromo-1-methyl-1H-indazol-3-yl)-amine

Guidance literature:: Multi-step reaction with 6 steps

1: sodium tetrahydroborate; boron trifluoride diethyl etherate / tetrahydrofuran / 72 h / 0 - 20 °C

2: potassium carbonate / dichloromethane / 3 h / 0 - 20 °C

3: potassium tert-butylate; tert-butyl alcohol / 0.5 h / Reflux

4: XPhos; potassium phosphate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / water; toluene / 20 h / 120 °C / Inert atmosphere

5: Lawessons reagent / toluene / 2 h / 120 °C / Reflux

6: tert.-butylhydroperoxide; ammonium hydroxide / water; methanol / 20 h / 20 °C

With Lawessons reagent; tert.-butylhydroperoxide; ammonium hydroxide; sodium tetrahydroborate; potassium phosphate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; boron trifluoride diethyl etherate; potassium tert-butylate; potassium carbonate; tert-butyl alcohol; XPhos; In tetrahydrofuran; methanol; dichloromethane; water; toluene;

Reference yield:

: 1262858-66-1
rac-N-[1-(3-bromophenyl)-2-hydroxy-1-methylethyl]-2-chloroacetamide

: 1429869-66-8
[3-(5-amino-3-methyl-3,6-dihydro-2H-[1,4]oxazin-3-yl)-phenyl]-(6-bromo-1-methyl-1H-indazol-3-yl)-amine

Guidance literature:: Multi-step reaction with 4 steps

1: potassium tert-butylate; tert-butyl alcohol / 0.5 h / Reflux

2: XPhos; potassium phosphate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / water; toluene / 20 h / 120 °C / Inert atmosphere

3: Lawessons reagent / toluene / 2 h / 120 °C / Reflux

4: tert.-butylhydroperoxide; ammonium hydroxide / water; methanol / 20 h / 20 °C

With Lawessons reagent; tert.-butylhydroperoxide; ammonium hydroxide; potassium phosphate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; potassium tert-butylate; tert-butyl alcohol; XPhos; In methanol; water; toluene;