(5-((2-(2-methylpyridin-3-yl)phenoxy)methyl)-4,5-dihydroisoxazol-3-yl)methanamine hydrochloride

Base Information

Chemical Name:(5-((2-(2-methylpyridin-3-yl)phenoxy)methyl)-4,5-dihydroisoxazol-3-yl)methanamine hydrochloride
CAS No.:1620294-42-9
Molecular Formula:C₁₇H₁₉N₃O₂*ClH
Molecular Weight:333.818
Hs Code.:

Synonyms:(5-((2-(2-methylpyridin-3-yl)phenoxy)methyl)-4,5-dihydroisoxazol-3-yl)methanamine hydrochloride

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

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Chemical Property of (5-((2-(2-methylpyridin-3-yl)phenoxy)methyl)-4,5-dihydroisoxazol-3-yl)methanamine hydrochloride

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Technology Process of (5-((2-(2-methylpyridin-3-yl)phenoxy)methyl)-4,5-dihydroisoxazol-3-yl)methanamine hydrochloride

There total 2 articles about (5-((2-(2-methylpyridin-3-yl)phenoxy)methyl)-4,5-dihydroisoxazol-3-yl)methanamine hydrochloride 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: 96.0%

: 1620294-40-7
tert-butyl ((5-((2-(2-methylpyridin-3-yl)phenoxy)methyl)-4,5-dihydroisoxazol-3-yl)methyl)carbamate

: 1620294-42-9
(5-((2-(2-methylpyridin-3-yl)phenoxy)methyl)-4,5-dihydroisoxazol-3-yl)methanamine hydrochloride

Guidance literature:: With hydrogenchloride; In diethyl ether; at 0 - 20 ℃; for 12h; Inert atmosphere;

Reference yield:

: 1012084-56-8
2-methyl-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-pyridine

: 1620294-98-5
tert-butyl ((5-((2-bromophenoxy)methyl)-4,5-dihydroisoxazol-3-yl)methyl)carbamate

: 1620294-42-9
(5-((2-(2-methylpyridin-3-yl)phenoxy)methyl)-4,5-dihydroisoxazol-3-yl)methanamine hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / 1,4-dioxane; water / 16 h / 90 °C / Sealed tube; Inert atmosphere

2: hydrogenchloride / diethyl ether / 12 h / 0 - 20 °C / Inert atmosphere

With hydrogenchloride; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; potassium carbonate; In 1,4-dioxane; diethyl ether; water; 1: |Suzuki Coupling;