HCID 23144648, compound → HCID 23144251, compound

HRID 337451Notes

Reaction equation

HRID 337451 reaction equation
[O:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[C:6]1[N:7]=[C:8]([NH:19]C(=O)OC(C)(C)C)[S:9][C:10]=1[C:11]([C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][N:14]=1)=[O:12]>FC(F)(F)C(O)=O>[N:14]1[CH:15]=[CH:16][CH:17]=[CH:18][C:13]=1[C:11]([C:10]1[S:9][C:8]([NH2:19])=[N:7][C:6]=1[C:2]1[O:1][CH:5]=[CH:4][CH:3]=1)=[O:12]

Participants

3

Procedure

Compound 185 (286 mg, 0.770 mmol) was dissolved in trifluoroacetic acid (2 mL), followed by stirring at room temperature for 1 hour. The reaction mixture was concentrated under reduced pressure, and ethyl acetate and a saturated aqueous solution of sodium hydrogencarbonate were added to the resulting residue, and the organic layer was separated. The organic layer was washed with a saturated aqueous solution of sodium chloride and dried over anhydrous magnesium sulfate, and then the solvent was distilled away under reduced pressure. The resulting residue was purified through silica gel column chromatography (hexane:ethyl acetate=1:4) to afford the entitled Compound 186 (208 mg, 99%).

Workup

  1. concentrationThe reaction mixture was concentrated under reduced pressure, and ethyl acetate
  2. additiona saturated aqueous solution of sodium hydrogencarbonate were added to the resulting residue
  3. customthe organic layer was separated
  4. washThe organic layer was washed with a saturated aqueous solution of sodium chloride
  5. dry with materialdried over anhydrous magnesium sulfate
  6. distillationthe solvent was distilled away under reduced pressure
  7. customThe resulting residue was purified through silica gel column chromatography (hexane:ethyl acetate=1:4)

Sources & evidence

ORD record
ord-24c9e7c13b8f472abfb482b82feb7a63
Source dataset
uspto-grants-2014_11
Patent number
US08889718B2

Reaction notes

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