1383717-12-1

Basic information

• Product Name: C₁₄H₂₀ClN₃O₄S
• Synonyms: C₁₄H₂₀ClN₃O₄S
• CAS NO: 1383717-12-1
• Molecular Weight: 361.849
• Mol File: 1383717-12-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₁₄H₂₀ClN₃O₄S(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₄H₂₀ClN₃O₄S(1383717-12-1)
• EPA Substance Registry System: C₁₄H₂₀ClN₃O₄S(1383717-12-1)

Safety Data

• Hazardous Substances Data: 1383717-12-1(Hazardous Substances Data)

Upstream product

• 17200-29-2 5-chloro-benzoxazole 
• 95-85-2 2-hydroxy-5-chloro-aniline 
• 1383717-11-0 methanesulfonic acid 2-[(5-chloro-benzooxazol-2-yl)-(3-oxo-butyl)amino]ethyl ester 
• 1383717-09-6 C₁₃H₁₅ClN₂O₃ 
• 1356342-15-8 2-[(5-chloro-1,3-benzoxazol-2-yl)amino]ethanol 
• 1251033-26-7 2-bromo-5-chlorobenzo[d]oxazole 

Relevant articles and documents

Enantioselective synthesis of a dual orexin receptor antagonist

A concise, enantioselective synthesis of the potent dual orexin inhibitor suvorexant (1) is reported. Key features of the synthesis include a mild copper-catalyzed amination, a highly chemoselective conjugate addition, and a tandem enantioselective transamination/seven-membered ring annulation. The synthesis requires inexpensive starting materials and only four linear steps for completion.