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1-BENZYL-2,3-DIHYDRO-1H-PYRROLO[2,3-B]QUINOLIN-4-YLAMINE

Base Information Edit
  • Chemical Name:1-BENZYL-2,3-DIHYDRO-1H-PYRROLO[2,3-B]QUINOLIN-4-YLAMINE
  • CAS No.:135882-37-0
  • Molecular Formula:C18H17N3
  • Molecular Weight:275.353
  • Hs Code.:
  • Mol file:135882-37-0.mol
1-BENZYL-2,3-DIHYDRO-1H-PYRROLO[2,3-B]QUINOLIN-4-YLAMINE

Synonyms:1-Benzyl-2,3-dihydro-1H-pyrrolo[2,3-b]quinolin-4-ylamine;4-amino-1-benzyl-2,3-dihydro-1H-pyrrolo[2,3-b]quinoline;AH-357/02177012;

Suppliers and Price of 1-BENZYL-2,3-DIHYDRO-1H-PYRROLO[2,3-B]QUINOLIN-4-YLAMINE
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
Total 2 raw suppliers
Chemical Property of 1-BENZYL-2,3-DIHYDRO-1H-PYRROLO[2,3-B]QUINOLIN-4-YLAMINE Edit
Chemical Property:
  • Melting Point:174 - 176 °C (ethanol) 
  • PSA:42.15000 
  • LogP:4.02590 
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 1-BENZYL-2,3-DIHYDRO-1H-PYRROLO[2,3-B]QUINOLIN-4-YLAMINE

There total 3 articles about 1-BENZYL-2,3-DIHYDRO-1H-PYRROLO[2,3-B]QUINOLIN-4-YLAMINE 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:
Guidance literature:
With lithium diisopropyl amide; In tetrahydrofuran; cyclohexane; at -35 - -10 ℃;
DOI:10.1021/jm0303204
Guidance literature:
Multi-step reaction with 2 steps
1.1: phosphorus oxychloride; SnCl4 / CHCl3; tetrahydrofuran / 1.5 h / 20 °C
1.2: 91 percent / CHCl3; tetrahydrofuran / 5 h / 50 °C
2.1: 39 percent / lithium diisopropylamine / tetrahydrofuran; cyclohexane / -35 - -10 °C
With tin(IV) chloride; lithium diisopropyl amide; trichlorophosphate; In tetrahydrofuran; chloroform; cyclohexane;
DOI:10.1021/jm0303204
Guidance literature:
Multi-step reaction with 2 steps
1.1: phosphorus oxychloride; SnCl4 / CHCl3; tetrahydrofuran / 1.5 h / 20 °C
1.2: 91 percent / CHCl3; tetrahydrofuran / 5 h / 50 °C
2.1: 39 percent / lithium diisopropylamine / tetrahydrofuran; cyclohexane / -35 - -10 °C
With tin(IV) chloride; lithium diisopropyl amide; trichlorophosphate; In tetrahydrofuran; chloroform; cyclohexane;
DOI:10.1021/jm0303204
upstream raw materials:

1-benzyl-2-pyrrolidone

anthranilic acid nitrile

Downstream raw materials:

PGP-4008

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