Methyl iodide → HCID 58545029, compound
Reaction equation
[C:1]([O-])([O-])=O.[K+].[K+].[CH2:7]([O:9][C:10](=[O:31])[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][N:17]([C:24]1[CH:29]=[CH:28][C:27]([OH:30])=[CH:26][N:25]=1)[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][N:19]=1)[CH3:8].CI.CCOC(C)=O>CN(C=O)C.[Cl-].[Na+].O>[CH2:7]([O:9][C:10](=[O:31])[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][N:17]([C:24]1[CH:29]=[CH:28][C:27]([O:30][CH3:1])=[CH:26][N:25]=1)[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][N:19]=1)[CH3:8]Participants
7
Conditions
- Temperature
- 50 °C
Procedure
K2CO3 (12 mg, 0.087 mmol) was added to compound II (20 mg, 0.058 mmol) in DMF (2 mL) at it under Ar(g). After 15 min CH3I (0.004 mL, 0.058 mmol) was added and the reaction was stirred at 50° C. for 3 h30. Brine (15 mL) and EtOAc (15 mL) were added, then the phases were separated, and the aqueous phase was extracted with EtOAc (2×5 mL). The organic phases were combined then dried over MgSO4, filtered, and subsequently evaporated under reduced pressure. The resulting residue was purified by silica gel column chromatography eluting with hexane/EtOAc (80:20 then 70:30) to furnish III as a colourless oil (11.65 mg, 56%).
Workup
- customthe phases were separated
- extractionthe aqueous phase was extracted with EtOAc (2×5 mL)
- dry with materialThe organic phases were combined then dried over MgSO4
- filtrationfiltered
- customsubsequently evaporated under reduced pressure
- customThe resulting residue was purified by silica gel column chromatography
- washeluting with hexane/EtOAc (80:20
Sources & evidence
- ORD record
- ord-ce16f395ff244c8ebb31971b98a32238
- Source dataset
- uspto-grants-2016_05
- Patent number
- US09340503B2
Reaction notes
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