1-(2-iodophenyl)-N-methyl-N-(3-p-toluenesulfonyloxypropyl)-3-isoquinolinecarboxamine

Base Information

Chemical Name:1-(2-iodophenyl)-N-methyl-N-(3-p-toluenesulfonyloxypropyl)-3-isoquinolinecarboxamine
CAS No.:1044196-27-1
Molecular Formula:C₂₇H₂₅IN₂O₄S
Molecular Weight:600.477
Hs Code.:

Synonyms:1-(2-iodophenyl)-N-methyl-N-(3-p-toluenesulfonyloxypropyl)-3-isoquinolinecarboxamine

Suppliers and Price of 1-(2-iodophenyl)-N-methyl-N-(3-p-toluenesulfonyloxypropyl)-3-isoquinolinecarboxamine

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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-iodophenyl)-N-methyl-N-(3-p-toluenesulfonyloxypropyl)-3-isoquinolinecarboxamine

Chemical Property:

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Technology Process of 1-(2-iodophenyl)-N-methyl-N-(3-p-toluenesulfonyloxypropyl)-3-isoquinolinecarboxamine

There total 1 articles about 1-(2-iodophenyl)-N-methyl-N-(3-p-toluenesulfonyloxypropyl)-3-isoquinolinecarboxamine 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: 35.0%

: 1-(2-iodophenyl)-N-methyl-N-(3-hydroxypropyl)-3-isoquinolinecarboxamine

: 98-59-9
p-toluenesulfonyl chloride

: 1044196-27-1
1-(2-iodophenyl)-N-methyl-N-(3-p-toluenesulfonyloxypropyl)-3-isoquinolinecarboxamine

Guidance literature:: With triethylamine; In dichloromethane; at 0 ℃; for 4h;
DOI:10.1016/j.bmc.2008.04.046

Reference yield:

: 1044196-27-1
1-(2-iodophenyl)-N-methyl-N-(3-p-toluenesulfonyloxypropyl)-3-isoquinolinecarboxamine

: 215922-66-0
C₂₀H₁₈⁽¹⁸⁾FIN₂O

Guidance literature:: With [¹⁸F]-potassium fluoride; potassium carbonate; [2.2.2]cryptande; In dimethyl sulfoxide; at 120 ℃; for 0.166667h;
DOI:10.1016/j.bmc.2008.04.046