Methanol → 8-chloro-N-[4-(ethylsulfonyl)-2-oxobutyl]dibenz[b,f][1,4]oxazepin-10(11H)-carboxamide
Reaction equation
[Cl:1][C:2]1[CH:24]=[CH:23][C:5]2[O:6][C:7]3[CH:22]=[CH:21][CH:20]=[CH:19][C:8]=3[CH2:9][N:10]([C:11]([NH:13][CH2:14][C:15](=[O:18])[CH:16]=[CH2:17])=[O:12])[C:4]=2[CH:3]=1.[CH2:25]([SH:27])[CH3:26].N1CCCCC1.[OH-:34].C([N+](C)(C)C)C1C=CC=CC=1.C[OH:47]>C(Cl)Cl>[Cl:1][C:2]1[CH:24]=[CH:23][C:5]2[O:6][C:7]3[CH:22]=[CH:21][CH:20]=[CH:19][C:8]=3[CH2:9][N:10]([C:11]([NH:13][CH2:14][C:15](=[O:18])[CH2:16][CH2:17][S:27]([CH2:25][CH3:26])(=[O:47])=[O:34])=[O:12])[C:4]=2[CH:3]=1Participants
7
Reactant 5
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 8-chloro-N-(2-oxo-3-butenyl)dibenz[b,f][1,4]oxazepin-10(11H)-carboxamide (1.00 gram), ethanethiol (0.23 mL), piperidine (0.092 mL), and N-benzyltrimethylammonium hydroxide (0,092 mL) in methylene chloride (16 mL) and methanol (4 mL) was stirred at room temperature for 5 hours. The reaction was diluted with methylene chloride (100 mL), washed with 100 mL each of 1N HCl (two times), water, saturated aqueous sodium bicarbonate, and brine, dried over MgSO4, and evaporated in vacuo. The crude product was purified by flash chromatography through silica gel 60 (350 mL) using 92:8 methylene chloride: ethyl acetate to yield a colorless oil. The yield of the title compound was 0.38 gram. (32%).
Workup
- washwashed with 100 mL each of 1N HCl (two times), water, saturated aqueous sodium bicarbonate, and brine
- dry with materialdried over MgSO4
- customevaporated in vacuo
- customThe crude product was purified by flash chromatography through silica gel 60 (350 mL)
- customethyl acetate to yield a colorless oil
Sources & evidence
- ORD record
- ord-2b5c76fc8da44789b35dde5a24f94aed
- Source dataset
- uspto-grants-1995_01
- Patent number
- US05382578
Reaction notes
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