Potassium Carbonate → HCID 54111344, compound
Reaction equation
C(=O)([O-])[O-].[K+].[K+].[CH2:7]([C:15]1[CH:16]=[N:17][C:18]([C:21]2[CH:26]=[CH:25][C:24]([OH:27])=[CH:23][CH:22]=2)=[N:19][CH:20]=1)[CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14].Cl[CH2:29][CH:30]([OH:43])[CH2:31][O:32][CH2:33][CH2:34][O:35][CH2:36][CH2:37][O:38][CH2:39][CH2:40][CH2:41][CH3:42]>CN(C)C=O.O>[CH2:7]([C:15]1[CH:20]=[N:19][C:18]([C:21]2[CH:26]=[CH:25][C:24]([O:27][CH2:29][C@@H:30]([OH:43])[CH2:31][O:32][CH2:33][CH2:34][O:35][CH2:36][CH2:37][O:38][CH2:39][CH2:40][CH2:41][CH3:42])=[CH:23][CH:22]=2)=[N:17][CH:16]=1)[CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14]Participants
Procedure
Potassium carbonate (2.1 g, 15.7 mmol) was added to a solution of 5-octyl-2-(4-hydroxyphenyl)pyrimidine (3.0 g, 10.5 mmol) and 1-chloro-3-(2-(2-butoxyethoxy)ethoxy)-2-propanol (2.7 g, 10.5 mmol) in N,N-dimethylformamide (100 ml). The resulting mixture was stirred at reflux temperature for 18 hours and then cooled to ambient temperature. The mixture was diluted with water (100 ml) and was extracted with three 100 ml aliquots of diethyl ether. The extracts were dried (over MgSO4), filtered, and concentrated to give crude product as an oil. 5-octyl-2-[4-((S)-2-hydroxy-3-(2-(2-(butoxy)ethoxy)ethoxy)propoxy)phenyl]pyrimidine was then isolated by chromatography. The chiral (S)-hydroxy compound (3.5 g, 7.5 mmol) was treated with diethylaminosulfur trifluoride (5.3 g, 15 mmol) to produce Comparative Example 1.
Workup
- temperatureat reflux temperature for 18 hours
- extractionwas extracted with three 100 ml aliquots of diethyl ether
- dry with materialThe extracts were dried (over MgSO4)
- filtrationfiltered
- concentrationconcentrated
- customto give crude product as an oil
Sources & evidence
- ORD record
- ord-c3b2bb6d7e7f47898fde290622a44508
- Source dataset
- uspto-grants-1999_10
- Patent number
- US05972241
Reaction notes
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