1-[2-methoxy-6-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)phenyl]isoquinoline

Base Information

Chemical Name:1-[2-methoxy-6-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)phenyl]isoquinoline
CAS No.:1360607-07-3
Molecular Formula:C₂₂H₂₄BNO₃
Molecular Weight:361.248
Hs Code.:

Synonyms:1-[2-methoxy-6-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)phenyl]isoquinoline

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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 1-[2-methoxy-6-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)phenyl]isoquinoline

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Technology Process of 1-[2-methoxy-6-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)phenyl]isoquinoline

There total 2 articles about 1-[2-methoxy-6-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)phenyl]isoquinoline 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: 88.0%

: 134948-96-2
1-(2-methoxyphenyl)isoquinoline

: 73183-34-3
bis(pinacol)diborane

: 1360607-07-3
1-[2-methoxy-6-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)phenyl]isoquinoline

Guidance literature:: With (1,5-cyclooctadiene)(methoxy)iridium(I) dimer; N,N-dibenzyl-N'-(pyridin-2-ylmethylene)hydrazine; 4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane; In tetrahydrofuran; at 50 ℃; for 7h; regioselective reaction; Inert atmosphere;
DOI:10.1002/anie.201104544

Reference yield: 88.0%

: 134948-96-2
1-(2-methoxyphenyl)isoquinoline

: 73183-34-3
bis(pinacol)diborane

: 25015-63-8
4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane

: 1360607-07-3
1-[2-methoxy-6-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)phenyl]isoquinoline

Guidance literature:: With cat. [Ir(μ-OCH3)(C8H12)]2/2-C5H4NCHNN(CH2C6H5)2; In tetrahydrofuran; Sonication; dried Schlenk tube charged with isoquinoline deriv. and diboron compd., added catalyst stock soln. (prepd. by sonication for 1 h) and pinacolborane, stirred at 50°C for 7 h; cooled to room temp., concd. to dryness, pptd. with hexane;
DOI:10.1002/anie.201104544