6,7-dimethoxy-2-(trifluoroacetyl)-1-[2-(trifluoroacetylamino)phenyl]-1,2,3,4-tetrahydroisoquinoline

Base Information

• Chemical Name: 6,7-dimethoxy-2-(trifluoroacetyl)-1-[2-(trifluoroacetylamino)phenyl]-1,2,3,4-tetrahydroisoquinoline
• CAS No.: 247128-62-7
• Molecular Formula: C₂₁H₁₈F₆N₂O₄
• Molecular Weight: 476.375
• Mol file: 247128-62-7.mol

Synonyms:6,7-dimethoxy-2-(trifluoroacetyl)-1-[2-(trifluoroacetylamino)phenyl]-1,2,3,4-tetrahydroisoquinoline

Chemical Property of 6,7-dimethoxy-2-(trifluoroacetyl)-1-[2-(trifluoroacetylamino)phenyl]-1,2,3,4-tetrahydroisoquinoline

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 6,7-dimethoxy-2-(trifluoroacetyl)-1-[2-(trifluoroacetylamino)phenyl]-1,2,3,4-tetrahydroisoquinoline

There total 3 articles about 6,7-dimethoxy-2-(trifluoroacetyl)-1-[2-(trifluoroacetylamino)phenyl]-1,2,3,4-tetrahydroisoquinoline 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: 72.0%

trifluoroacetic anhydride (407-25-0) + N-[2-(3,4-dimethoxyphenyl)ethyl]-2-(trifluoroacetylamino)benzylidenimine → 6,7-dimethoxy-2-(trifluoroacetyl)-1-[2-(trifluoroacetylamino)phenyl]-1,2,3,4-tetrahydroisoquinoline (247128-62-7)

Guidance literature:

at 80 ℃; for 24h;

DOI:10.1021/jm980434t

Reference yield:

2,2,2-trifluoro-N-(2-formylphenyl)acetamide (6203-15-2) → 6,7-dimethoxy-2-(trifluoroacetyl)-1-[2-(trifluoroacetylamino)phenyl]-1,2,3,4-tetrahydroisoquinoline (247128-62-7)

Guidance literature:

Multi-step reaction with 2 steps

1: 78 percent / pyridine; 4 Angstroem sieves / 36 h / Heating

2: 72 percent / 24 h / 80 °C

With pyridine; 4 A molecular sieve; 1: Condensation / 2: Pictet-Spengler cyclization;

DOI:10.1021/jm980434t

Reference yield:

2-(3,4-dimethoxyphenyl)-ethylamine (120-20-7) → 6,7-dimethoxy-2-(trifluoroacetyl)-1-[2-(trifluoroacetylamino)phenyl]-1,2,3,4-tetrahydroisoquinoline (247128-62-7)

Guidance literature:

Multi-step reaction with 2 steps

1: 78 percent / pyridine; 4 Angstroem sieves / 36 h / Heating

2: 72 percent / 24 h / 80 °C

With pyridine; 4 A molecular sieve; 1: Condensation / 2: Pictet-Spengler cyclization;

DOI:10.1021/jm980434t

upstream raw materials:

trifluoroacetic anhydride

2,2,2-trifluoro-N-(2-formylphenyl)acetamide

2-(3,4-dimethoxyphenyl)-ethylamine

Downstream raw materials:

1-(2-aminophenyl)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline