HCID 18781964, compound → HCID 70276915, compound
Reaction equation
[CH3:1]S(C1N(CCCCC2C=CC=CC=2)C(=O)C1)=O.[C:19]1([CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][NH:31][C:32](=[O:47])[CH2:33][N:34]2[CH:37]([S:38]([CH2:40]CCCCC)=[O:39])[CH2:36][C:35]2=[O:46])[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1.OCCS(C1N(CC(=O)CCC2C=CC=CC=2)C(=O)C1)=O>>[C:19]1([CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][NH:31][C:32](=[O:47])[CH2:33][N:34]2[C@@H:37]([S:38]([CH3:40])=[O:39])[C@H:36]([CH3:1])[C:35]2=[O:46])[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=1Participants
4
Procedure
4-Methylsulfinyl-1-(4-phenylbutyl)-azetidin-2-one; N-(6-Phenylhexyl )-(4-n-hexylsulfinyl-2-oxoazetidin-1-yl )acetamide; 4-(2-Hydroxyethylsulphinyl)-N-(4-phenyl-2-oxobutyl)azetidin-2-one (Diastereoisomer 2);
Sources & evidence
- ORD record
- ord-2def6929cbfb448282bb21a4ee6a719d
- Source dataset
- uspto-grants-2000_06
- Patent number
- US06071899
Reaction notes
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