Water → HCID 22713342, compound
Reaction equation
FC1C=CC([C:8]2[CH:13]=[C:12]([S:14]([C:17]3[CH:22]=[CH:21][C:20](C)=[C:19](C4C=CC(F)=CC=4)[CH:18]=3)(=[O:16])=[O:15])[CH:11]=[CH:10][C:9]=2[CH3:31])=CC=1.[O:32]1[C:36]2([CH2:41][CH2:40][NH:39][CH2:38][CH2:37]2)[O:35][CH2:34][CH2:33]1.C(=O)([O-])[O-].[K+].[K+].O>CN1C(=O)N(C)CCC1>[C:9]1([CH3:31])[CH:10]=[CH:11][C:12]([S:14]([C:17]2[CH:22]=[CH:21][C:20]([N:39]3[CH2:40][CH2:41][C:36]4([O:35][CH2:34][CH2:33][O:32]4)[CH2:37][CH2:38]3)=[CH:19][CH:18]=2)(=[O:15])=[O:16])=[CH:13][CH:8]=1Participants
6
Procedure
To a solution of 4-fluorophenyl-4-tolylsulfone (1.25 g, 5 mmol) in N,N′-dimethylpropyleneurea (5 ml) was added 1,4-dioxa-8-aza-spiro[4.5]decane (0.88 g, 6 mmol), and potassium carbonate (0.83 g, 6 mmol). The mixture was stirred at room temperature for 4 h and then heated at 70° C. for 18 h. An additional 0.22 g of 1,4-dioxa-8-aza-spiro[4.5]decane was added, and the reaction was continued for 1 day. The mixture was cooled to room temperature, and treated with water. The resulting suspension was filtered, and the precipitate washed with water and methanol, and dried in vacuo to give 1.80 g of a white solid; m.p. 164-165° C.; MS (ES) m/z 373.9 (MH+); HRMS (EI) Calcd. for C20H23NO4S (M+): 373.1348, Found: 373.1342.
Workup
- temperatureheated at 70° C. for 18 h
- waitthe reaction was continued for 1 day
- temperatureThe mixture was cooled to room temperature
- filtrationThe resulting suspension was filtered
- washthe precipitate washed with water and methanol
- customdried in vacuo
Sources & evidence
- ORD record
- ord-6ac78cfb74324262892458ffa3141107
- Source dataset
- uspto-grants-2004_06
- Patent number
- US06743787B2
Reaction notes
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