2-amino-3-phenylisoquinolinium trifluoroacetate

Base Information

Chemical Name:2-amino-3-phenylisoquinolinium trifluoroacetate
CAS No.:1353561-10-0
Molecular Formula:C₂F₃O₂*C₁₅H₁₃N₂
Molecular Weight:334.298
Hs Code.:

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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 2-amino-3-phenylisoquinolinium trifluoroacetate

Chemical Property:

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Technology Process of 2-amino-3-phenylisoquinolinium trifluoroacetate

There total 3 articles about 2-amino-3-phenylisoquinolinium trifluoroacetate 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: 52.0%

: 1353561-02-0
tert-butoxycarbonyl (3-phenylisoquinolinium-2-yl)amide

: 76-05-1
trifluoroacetic acid

: 1353561-10-0
2-amino-3-phenylisoquinolinium trifluoroacetate

Guidance literature:: In dichloromethane; at 20 ℃; for 3h;
DOI:10.1055/s-0030-1260219

Reference yield:

: 1353561-15-5
C₂₀H₂₀N₂O₂

: 1353561-10-0
2-amino-3-phenylisoquinolinium trifluoroacetate

Guidance literature:: Multi-step reaction with 2 steps

1: silver trifluoromethanesulfonate / acetonitrile / 3 h / 80 °C / Inert atmosphere

2: dichloromethane / 3 h / 20 °C

With silver trifluoromethanesulfonate; In dichloromethane; acetonitrile;
DOI:10.1055/s-0030-1260219

Reference yield:

: 59046-72-9
o-(phenylethynyl)benzaldehyde

: 1353561-10-0
2-amino-3-phenylisoquinolinium trifluoroacetate

Guidance literature:: Multi-step reaction with 3 steps

1: acetonitrile / 5 h / 80 °C

2: silver trifluoromethanesulfonate / acetonitrile / 3 h / 80 °C / Inert atmosphere

3: dichloromethane / 3 h / 20 °C

With silver trifluoromethanesulfonate; In dichloromethane; acetonitrile;
DOI:10.1055/s-0030-1260219