Sodium Hydroxide → HCID 131723613, compound
Reaction equation
[CH3:1][O:2][P:3]([CH2:7][NH:8][S:9]([C:12]1[S:13][CH:14]=[CH:15][CH:16]=1)(=[O:11])=[O:10])(=[O:6])[O:4]C.[OH-].[Na+:18]>>[Na+:18].[CH3:1][O:2][P:3]([CH2:7][NH:8][S:9]([C:12]1[S:13][CH:14]=[CH:15][CH:16]=1)(=[O:11])=[O:10])(=[O:4])[O-:6]Participants
3
Procedure
The diester (vii) was treated with sodium hydroxide according to the procedure described in Example 46, step 5, to produce the title compound: 1H NMR (300 MHz, CD3OD) δH 7.65 (dd, J=4.8, 1.2 Hz, 1H), 7.62 (dd, J=3.6, 1.2 Hz, 1H), 7.15 (dd, J=4.8, 3.6 Hz, 1H), 3.55 (d, J=9.3 Hz, 3H), 3.04 (d, J=13.8 Hz, 2H); 31P NMR: (121 MHz, CD3OD) δP 17.60; 13C NMR (75 MHz, CD3OD) δC 141.77, 132.98, 132.90, 128.43, 52.02, 40.11, (d, J=147.2 Hz).
Sources & evidence
- ORD record
- ord-c21cbee426e343029755b3564888022c
- Source dataset
- uspto-grants-2005_07
- Patent number
- US06921756B2
Reaction notes
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