Methyl iodide → HCID 13687902, compound
Reaction equation
[CH3:1][O:2][C:3](=[O:37])[C:4]([NH:35][NH2:36])([CH3:34])[CH2:5][C:6]1[CH:11]=[CH:10][C:9]([O:12][CH:13]2C3C(=CC=CC=3)C(=O)O2)=[C:8]([O:23][CH:24]2C3C(=CC=CC=3)C(=O)O2)[CH:7]=1.IC>>[CH3:1][O:2][C:3](=[O:37])[C:4]([NH:35][NH2:36])([CH3:34])[CH2:5][C:6]1[CH:11]=[CH:10][C:9]([O:12][CH3:13])=[C:8]([O:23][CH3:24])[CH:7]=1Participants
3
Procedure
Following the procedure for preparation of compound 119, and substituting bromophthalide with iodomethane, provided the title compound 120. 1H NMR (CD3OD, 400 MHz): 1.44 (s, 3H), 3.00 (dd, 2H), 3.80 (2 s, 6H), 4.77 (s, 3H), 6.71–6.86 (m, 3H). MS (ESI) m/z 269.33 (M+H+).
Sources & evidence
- ORD record
- ord-b0b30c9780484853a05c4e011cf5246f
- Source dataset
- uspto-grants-2006_09
- Patent number
- US07101912B2
Reaction notes
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