1410130-06-1

Basic information

• Product Name: C₂₅H₃₄N₂O₆S
• Synonyms: C₂₅H₃₄N₂O₆S
• CAS NO: 1410130-06-1
• Molecular Weight: 490.621
• Mol File: 1410130-06-1.mol

Chemical Properties

• CAS DataBase Reference: C₂₅H₃₄N₂O₆S(CAS DataBase Reference)
• NIST Chemistry Reference: C₂₅H₃₄N₂O₆S(1410130-06-1)
• EPA Substance Registry System: C₂₅H₃₄N₂O₆S(1410130-06-1)

Safety Data

• Hazardous Substances Data: 1410130-06-1(Hazardous Substances Data)

Upstream product

• 1293324-03-4 tert-butyl (2-bromo-4-methylbenzyl)carbamate 
• 1410131-60-0 C₁₂H₁₇NO₄S 

Downstream Products

• 1410131-10-0 3-(3,4-dimethoxyphenylethyl)-9-methyl-3,4,6,10b-tetrahydro-1H-[1,2,4]thiadiazino[5,4-a]isoindole 2,2-dioxide 
• 1410131-09-7 3-(3,4-dimethoxyphenylethyl)-9-methyl-6,10b-dihydro-1H-[1,2,4]thiadiazino[5,4-a]isoindol-4(3H)-one 2,2-dioxide 

Relevant articles and documents

Synthesis of an isoindoline-annulated, tricyclic sultam library via microwave-assisted, continuous-flow organic synthesis (MACOS)

A microwave-assisted, continuous-flow organic synthesis (MACOS) protocol for the synthesis of an isoindoline-annulated, tricyclic sultam library, utilizing a Heck-aza-Michael (HaM) strategy, is reported. This sequence involves a Heck reaction on vinylsulfonamides with batch microwave heating followed by a one-pot, sequential intramolecular aza-Michael cyclization/Boc-deprotection using MACOS. Subsequent cyclization with either 1,1-carbonyldiimidazole or chloromethyl pivalate using MACOS provided an array of tricyclic sultams. This efficient three-step protocol requires only a few hours to produce the target sultams starting from simple starting materials. Using this strategy, a 38-member library of isoindoline-annulated sultams was generated in good to excellent overall yields (53-87%). Georg Thieme Verlag Stuttgart · New York.