Lithium iodide → HCID 13127852, compound
Reaction equation
C(OC(NCCCCC#CCOC1C=CC=CC=1S([N:26]1[CH2:31][CH2:30][S:29][C:28]([CH3:33])([CH3:32])[CH:27]1[C:34]([O-:36])=[O:35])(=O)=O)=O)(C)(C)C.[I-].[Li+]>>[CH3:32][C:28]1([CH3:33])[S:29][CH2:30][CH2:31][NH:26][CH:27]1[C:34]([OH:36])=[O:35]Participants
3
Procedure
The methyl ester of methyl (3 S}[4 {[({7-[(tert-butoxycarbonyl)amino]-2-heptynyl}oxy)phenyl]sulfonyl}-2,2-dimethyl-3-thiomorpholine carboxylate was converted into the analogous carboxylic acid using lithium iodide according to the procedure of Example 250 to provide (3 S)-4-{[4-{7-[(tert-butoxycarbonyl)amino]-2-heptynyl)oxy)phenyl]sulfonyl}-2,2- dimethyl-3-thiomorpholine carboxylic acid as a white solid Electrospray Mass Spec: 541.2(M+H)+
Sources & evidence
- ORD record
- ord-b4b1bc3e0d4c4a189f8c938bf24ecea0
- Source dataset
- uspto-grants-2001_05
- Patent number
- US06225311B1
Reaction notes
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