Lithium iodide → HCID 22645076, compound
Reaction equation
C[O:2][C:3]([CH:5]1[C:10]([CH3:12])([CH3:11])[S:9][CH2:8][CH2:7][N:6]1[S:13]([C:16]1[CH:21]=[CH:20][C:19]([O:22][CH2:23][C:24]#[C:25][CH2:26][CH2:27][CH2:28][NH:29][C:30]([O:32][C:33]([CH3:36])([CH3:35])[CH3:34])=[O:31])=[CH:18][CH:17]=1)(=[O:15])=[O:14])=[O:4].[I-].[Li+]>C(OCC)(=O)C>[C:33]([O:32][C:30]([NH:29][CH2:28][CH2:27][CH2:26][C:25]#[C:24][CH2:23][O:22][C:19]1[CH:20]=[CH:21][C:16]([S:13]([N:6]2[CH2:7][CH2:8][S:9][C:10]([CH3:12])([CH3:11])[CH:5]2[C:3]([OH:4])=[O:2])(=[O:15])=[O:14])=[CH:17][CH:18]=1)=[O:31])([CH3:36])([CH3:34])[CH3:35]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 0.764 g (1.41 mmol) of methyl-4-{[4-({6-[(tert-butoxycarbonyl)amino]-2-hexynyl}oxy)pheny]sulfonyl}-2,2-dimethyl-3-thiomorpholinecarboxylate and 3.77 g (28.2 mmol) of lithium iodide in 30 mL of ethyl acetate was heated to reflux for 18 h. The resulting reaction was acidified, washed with water, an aqueous solution of Na2S2O3, brine, dried over MgSO4, filtered and concentrated in vacuo. The residue was chromatographed on silica gel eluting with 0.5% methanol/dichloromethane to provide 0.417 g (56%) of 4-{[4-({6-[(tert-butoxycarbonyl)amino]-2-hexynyl}oxy)phenyl]sulfonyl}-2,2-dimethyl-3-thiomorpholine carboxylic acid as a white solid. Electrospray Mass Spec: 527.2(M+H)+
Workup
- temperatureto reflux for 18 h
- customThe resulting reaction
- washwashed with water
- dry with materialan aqueous solution of Na2S2O3, brine, dried over MgSO4
- filtrationfiltered
- concentrationconcentrated in vacuo
- customThe residue was chromatographed on silica gel eluting with 0.5% methanol/dichloromethane
Sources & evidence
- ORD record
- ord-105edccc05be4cbca5d067306f2b213d
- Source dataset
- uspto-grants-2004_11
- Patent number
- US06812227B2
Reaction notes
Loading…