Methyl Methacrylate → HCID 57777462, compound
Reaction equation
C([O:8][C:9]1[CH:14]=[C:13](I)[CH:12]=[CH:11][C:10]=1[N:16]1[S:20](=[O:22])(=[O:21])[N:19](CC[Si](C)(C)C)[C:18](=[O:29])[CH2:17]1)C1C=CC=CC=1.[C:30]([O:35][CH3:36])(=[O:34])[C:31]([CH3:33])=[CH2:32]>>[CH3:36][O:35][C:30](=[O:34])[CH:31]([CH3:33])[CH2:32][C:13]1[CH:12]=[CH:11][C:10]([N:16]2[CH2:17][C:18](=[O:29])[NH:19][S:20]2(=[O:21])=[O:22])=[C:9]([OH:8])[CH:14]=1Participants
3
Procedure
The title compound is prepared from 5-(2-benzyloxy-4-iodo-phenyl)-1,1-dioxo-2-(2-trimethylsilanylethyl)-1,2,5-thiadiazolidin-3-one and methyl methacrylate analogous to Example 133. (M+1)+=343. HPLC retention time=0.99 min (Method 14).
Sources & evidence
- ORD record
- ord-cd8195e624b445c08d6ff6303591ebb9
- Source dataset
- uspto-grants-2011_12
- Patent number
- US08084448B2
Reaction notes
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