876690-37-8

Basic information

• Product Name: N-(8-quinolinyl)-1-benzofuran-2-carboxamide
• Synonyms: N-(8-quinolinyl)-1-benzofuran-2-carboxamide;N-(quinolin-8-yl)-1-benzofuran-2-carboxamide
• CAS NO: 876690-37-8
• Molecular Formula: C₁₈H₁₂N₂O₂
• Molecular Weight: 288.30008
• Mol File: 876690-37-8.mol

Chemical Properties

• Boiling Point: 409.7±20.0 °C(Predicted)
• Appearance: /
• Density: 1.356±0.06 g/cm3(Predicted)
• PKA: 11.09±0.43(Predicted)
• CAS DataBase Reference: N-(8-quinolinyl)-1-benzofuran-2-carboxamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(8-quinolinyl)-1-benzofuran-2-carboxamide(876690-37-8)
• EPA Substance Registry System: N-(8-quinolinyl)-1-benzofuran-2-carboxamide(876690-37-8)

Safety Data

• Hazardous Substances Data: 876690-37-8(Hazardous Substances Data)

Upstream product

• 578-66-5 8-amino quinoline 
• 41717-28-6 2-benzofuroyl chloride 
• 496-41-3 Benzofuran-2-carboxylic acid 

Relevant articles and documents

Synthesis of elaborate benzofuran‐2‐carboxamide derivatives through a combination of 8-aminoquinoline directed C–H arylation and transamidation chemistry

Herein, we present a short and highly modular synthetic route that involves 8-aminoquinoline directed C–H arylation and transamidation chemistry, and which enables access to a wide range of elaborate benzofuran‐2‐carboxamides. For the directed C–H arylation reactions, Pd catalysis was used to install a wide range of aryl and heteroaryl substituents at the C3 position of the benzofuran scaffold in high efficiency. Directing group cleavage and further diversification of the C3‐arylated benzofuran products were then achieved in a single synthetic operation through the utilization of a one‐pot, two‐step transamidation procedure, which proceeded via the intermediate N‐acyl‐Boc‐carbamates. Given the high efficiency and modularity of this synthetic strategy, it constitutes a very attractive method for generating structurally diverse collections of benzofuran derivatives for small molecule screening campaigns.

Directing Group-Assisted Copper(II)-Catalyzed ortho-Carbonylation to Benzamide using 2,2′-Azobisisobutyronitrile (AIBN)

An efficient copper-catalyzed regioselective C—H bond carbonylation of benzamides has been developed using 2,2′-azobisisobutyronitrile (AIBN) as traceless cyanating agent. The non-toxic and readily available AIBN was used for the carbonylative cyclization

Rh-Catalyzed, Regioselective, C-H Bond Functionalization: Access to Quinoline-Branched Amines and Dimers

Rh-catalyzed, chelation-induced, C-5 regioselective C-H functionalization of 8-amidoquinolines with a range of N-Boc aminals is reported for the first time. The addition of in situ generated imines to C(sp2)-H bonds afforded branched amines in