Tetrahydrofuran → HCID 59750392, compound

HRID 748404Notes

Reaction equation

HRID 748404 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]1

Participants

5

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

  1. concentrationconcentrated under reduced pressure
  2. additionTrifluoroacetic acid (5 ml) was added to the residue
  3. stirringthe mixture was stirred at room temperature for 1 hr
  4. washThe fractions eluted with hexane-ethyl acetate (1:1
  5. customv/v) were collected
  6. concentrationconcentrated
  7. 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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