Water → HCID 59556157, compound
Reaction equation
C([Li])CCC.[S:6]1[CH:10]=[CH:9][N:8]=[C:7]1[NH:11][C:12](=[O:15])[O:13][CH3:14].[CH2:16]1[O:26][C:19]2([CH2:24][CH2:23][C:22](=[O:25])[CH2:21][CH2:20]2)[O:18][CH2:17]1.O>C1COCC1.CCOC(C)=O>[OH:25][C:22]1([C:10]2[S:6][C:7]([NH:11][C:12](=[O:15])[O:13][CH3:14])=[N:8][CH:9]=2)[CH2:23][CH2:24][C:19]2([O:18][CH2:17][CH2:16][O:26]2)[CH2:20][CH2:21]1Participants
Procedure
A solution of n-butyllithium (10.0 mL of 1.6 M solution in hexane, 15.93 mmol) was added to methyl 1,3-thiazol-2-ylcarbamate (1.05 g, 6.64 mmol) in THF (10 mL) at −78° C. with stirring under N2. After being stirred at −78° C. for 1 h, a solution of 1,4-cyclohexanedione mono-ethylene ketal (1.84 g, 11.75 mmol) in THF (10 mL) was added to the lithiated compound solution via syringe at −78° C. The reaction mixture was allowed to warm to room temperature slowly and stirred overnight. water and EtOAc were added. The aqueous layer was extracted with EtOAc (3×). The combined organic layers were washed with saturated NaCl, dried (MgSO4), concentrated and flash chromatographed (50% EtOAc/hexane to 75% EtOAc/hexane) to give 0.744 g of the title compound in 51% yield. MS (EI) calcd: (M+H)+=315.1; found: 315.0.
Workup
- stirringAfter being stirred at −78° C. for 1 h
- stirringstirred overnight
- extractionThe aqueous layer was extracted with EtOAc (3×)
- washThe combined organic layers were washed with saturated NaCl
- dry with materialdried (MgSO4)
- concentrationconcentrated
- customflash chromatographed (50% EtOAc/hexane to 75% EtOAc/hexane)
Sources & evidence
- ORD record
- ord-4b897e569e7e4ebea48acb09fa7ec1b3
- Source dataset
- uspto-grants-2010_11
- Patent number
- US07834021B2
Reaction notes
Loading…