Methyl iodide → tert-Butyl [(1R,2S)-2-methoxy-2,3-dihydro-1H-inden-1-yl]carbamate
Reaction equation
[OH:1][C@H:2]1[CH2:10][C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C@H:3]1[NH:11][C:12](=[O:18])[O:13][C:14]([CH3:17])([CH3:16])[CH3:15].[O-2].[Ba+2].[OH-].[Ba+2].[OH-].I[CH3:25]>CN(C=O)C>[CH3:25][O:1][C@H:2]1[CH2:10][C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C@H:3]1[NH:11][C:12](=[O:18])[O:13][C:14]([CH3:15])([CH3:17])[CH3:16]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of tert-butyl [(1R,2S)-2-hydroxy-2,3-dihydro-1H-inden-1-yl]-carbamate (680. mg, 2.73 mmol), DMF (21.1), barium monoxide (5.02 g, 32.7 mmol), barium hydroxide (2.80 g, 16.4 mmol) and iodomethane (1.70 mL, 27.3 mmol) was stirred overnight. LC/MS showed no starting material. The reaction was quenched via addition of a saturated solution of NaHCO3 and was extracted with DCM. The organic layer was washed with H2O (3×), dried over sodium sulfate and concentrated in vacuo. The residue was purified via silica gel chromatography eluting with a gradient of 0 to 50% EtOAc in hexanes to afford the title compound (178 mg, 25%). LC/MS: Rt=1.24 min, ES+ 264 (AA standard).
Workup
- customThe reaction was quenched via addition of a saturated solution of NaHCO3
- extractionwas extracted with DCM
- washThe organic layer was washed with H2O (3×)
- dry with materialdried over sodium sulfate
- concentrationconcentrated in vacuo
- customThe residue was purified via silica gel chromatography
- washeluting with a gradient of 0 to 50% EtOAc in hexanes
Sources & evidence
- ORD record
- ord-8fb34a0c270b42a38a4cc2bd536b20b6
- Source dataset
- uspto-grants-2011_08
- Patent number
- US08008307B2
Reaction notes
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