1575701-42-6

Basic information

• Product Name: 4-methyl-N-(quinolin-8-ylmethyl)benzenesulfonamide
• Synonyms: 4-methyl-N-(quinolin-8-ylmethyl)benzenesulfonamide
• CAS NO: 1575701-42-6
• Molecular Weight: 312.392
• Mol File: 1575701-42-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 4-methyl-N-(quinolin-8-ylmethyl)benzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: 4-methyl-N-(quinolin-8-ylmethyl)benzenesulfonamide(1575701-42-6)
• EPA Substance Registry System: 4-methyl-N-(quinolin-8-ylmethyl)benzenesulfonamide(1575701-42-6)

Safety Data

• Hazardous Substances Data: 1575701-42-6(Hazardous Substances Data)

Upstream product

• 127-65-1 chloroamine-T 
• 611-32-5 8-methylquinoline 
• 71996-32-2 N-(5λ⁴-dibenzo[b,d]thiophen-5-ylidene)-4-methylbenzenesulfonamide 
• 55962-05-5 [N-(p-tolylsulfonyl)imino]phenyliodinane 
• 70-55-3 toluene-4-sulfonamide 
• 941-55-9 4-toluenesulfonyl azide 

Relevant articles and documents

Rhodium(III)-catalyzed C(sp3)-H amidation of 8-methylquinolines with amides at room temperature

Here we disclose a Rh(III)-catalyzed chelation-assisted C(sp3)-H activation of 8-methylquinolines, which can enable intermolecular amidation using commercially available, reliable amides as the amidating reagent to provide an efficient route to

Chelation-Assisted Rhodium-Catalyzed Direct Amidation with Amidobenziodoxolones: C(sp2)-H, C(sp3)-H, and Late-Stage Functionalizations

Air-stable and convenient amidobenziodoxolones as an amidating reagent were disclosed to enable direct amidation on a wide range of C(sp2)-H bonds of (hetero)arenes and alkenes, as well as unactivated C(sp3)-H bonds under RhIII catalysis. The approach to access 49 examples of structurally diverse amides is featured by mild conditions, complete chemoselectivity and regioselectivity, broad substrate scope (not limited to strongly heterocyclic coordinating groups), and tolerance of valuable functional substituents, such as unprotected amine and hydroxyl groups. The synthetic applicability of this protocol is also demonstrated by late-stage functionalization of biologically important scaffolds.