Water → HCID 57285323, compound
Reaction equation
[CH3:1][N:2]1[C:7](=[O:8])[CH:6]=[CH:5][C:4]([O:9][C@H:10]2[C@@:15]([OH:17])([CH3:16])[C:14]([CH3:19])([CH3:18])[O:13][C:12]3[CH:20]=[CH:21][C:22]([S:24]([C:27]4[CH:32]=[CH:31][C:30]([O:33]C)=[C:29]([O:35]C)[CH:28]=4)(=[O:26])=[O:25])=[CH:23][C:11]2=3)=[N:3]1.O>ClCCl.B(Br)(Br)Br>[CH3:1][N:2]1[C:7](=[O:8])[CH:6]=[CH:5][C:4]([O:9][C@H:10]2[C@@:15]([OH:17])([CH3:16])[C:14]([CH3:19])([CH3:18])[O:13][C:12]3[CH:20]=[CH:21][C:22]([S:24]([C:27]4[CH:32]=[CH:31][C:30]([OH:33])=[C:29]([OH:35])[CH:28]=4)(=[O:26])=[O:25])=[CH:23][C:11]2=3)=[N:3]1Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
(3S,4R)-3,4-Dihydro-4-(2,3-dihydro-2-methyl-3-oxopyridazin-6-yl)oxy-6-(3,4-dimethoxyphenyl)sulphonyl-3-hydroxy-2,2,3-trimethyl-2H-benzo[b]pyran (0.50 g) (see Preparation 26) was dissolved in dichloromethane (12 ml) (under a nitrogen atmosphere) and boron tribromide (4 ml of a 1 M solution in dichloromethane) was added. The mixture was stirred at room temperature for one hour and a precipitate was formed. Water (20 ml) and dichloromethane (15 ml) were added, an insoluble gum formed and the solvents were decanted off. The gum was then chromatographed on silica using 1:9 methanol:dichloromethane as the eluent to yield (3S,4R)-3,4-dihydro-4-(2,3-dihydro-2-methyl-3-oxopyridazin-6-yl)oxy-6-(3,4-dihydroxyphenyl)sulphonyl-3-hydroxy-2,2,3-trimethyl-2H-benzo[b]pyran (0.33 g) as a white foam which was then triturated with diethyl ether and dried to give a white solid.
Workup
- additionwas added
- customa precipitate was formed
- customan insoluble gum formed
- customthe solvents were decanted off
- customThe gum was then chromatographed on silica using 1:9 methanol
Sources & evidence
- ORD record
- ord-acc4df06b0bf48c6941123d0ea348ba2
- Source dataset
- uspto-grants-2000_06
- Patent number
- US06071938
Reaction notes
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