HCID 18781952, compound → HCID 18782006, compound
Reaction equation
C(S(C1N(CC(=O)CCC2C=CC=CC=2)C(=O)C1)=O)(C)(C)C.[CH2:23]([S:29]([CH:31]1[N:34]([CH2:35][C:36](=[O:45])[CH2:37][CH2:38][C:39]2[CH:44]=[CH:43][CH:42]=[CH:41][CH:40]=2)[C:33](=[O:46])[CH2:32]1)=[O:30])[CH2:24][CH2:25][CH2:26]CC.C1(CCCCCCNC(=O)CN2C(S(C)=O)CC2=O)C=CC=CC=1>>[CH2:23]([S:29]([CH:31]1[N:34]([CH2:35][C:36](=[O:45])[CH2:37][CH2:38][C:39]2[CH:40]=[CH:41][CH:42]=[CH:43][CH:44]=2)[C:33](=[O:46])[CH2:32]1)=[O:30])[CH2:24][CH2:25][CH3:26]Participants
4
Procedure
4-tert-Butylsulfinyl-1-(4-phenyl-2-oxobutyl)azetidin-2-one;4-n-Hexylsulfinyl-1-(4-phenyl-2-oxobutyl)azetidin-2-one;N-6-Phenylhexyl-(4-methylsulphinyl-2-oxoazetidin-1-yl)acetamide;
Sources & evidence
- ORD record
- ord-c37b66ec0af741f7a0a7a19d93db93d3
- Source dataset
- uspto-grants-2000_06
- Patent number
- US06071899
Reaction notes
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