Tetrahydrofuran → HCID 59750392, compound
Reaction equation
[O:1]=[C:2]1[C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][C:6]=2[S:5][C:4]([C:12]2[N:17]=[C:16]([CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][C:24]([O:26]CC[Si](C)(C)C)=[O:25])[CH:15]=[CH:14][CH:13]=2)=[N:3]1.[F-].C([N+](CCCC)(CCCC)CCCC)CCC.O1CCCC1>CN(C)C=O>[O:1]=[C:2]1[C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][C:6]=2[S:5][C:4]([C:12]2[N:17]=[C:16]([CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][C:24]([OH:26])=[O:25])[CH:15]=[CH:14][CH:13]=2)=[N:3]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
2-(Trimethylsilyl)ethyl 7-[6-(4-oxo-4H-1,3-benzothiazin-2-yl)-2-pyridyl]heptanoate (0.50 g, 1.1 mmol) was dissolved in N,N-dimethylformamide (4 ml), and 1.0 M tetrabutylammonium fluoride solution in tetrahydrofuran (2.6 ml, 2.6 mmol) was added thereto. The reaction mixture was stirred for 30 minutes and concentrated under reduced pressure. Trifluoroacetic acid (5 ml) was added to the residue, and the mixture was stirred at room temperature for 1 hr. The reaction mixture was subjected to a silica gel (40 g) column chromatography. The fractions eluted with hexane-ethyl acetate (1:1, v/v) were collected and concentrated. The residue was recrystallized from ethanol-hexane to give the titled compound (0.24 g, 61%) as white crystals.
Workup
- concentrationconcentrated under reduced pressure
- additionTrifluoroacetic acid (5 ml) was added to the residue
- stirringthe mixture was stirred at room temperature for 1 hr
- washThe fractions eluted with hexane-ethyl acetate (1:1
- customv/v) were collected
- concentrationconcentrated
- customThe residue was recrystallized from ethanol-hexane
Sources & evidence
- ORD record
- ord-7efacc25dcc44066acc7ec58cd68b03f
- Source dataset
- uspto-grants-2008_07
- Patent number
- US07399759B2
Reaction notes
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