Acetic Acid → HCID 19940142, compound

HRID 1493521Notes

Reaction equation

HRID 1493521 reaction equation
C=O.[C:3](O)(=O)C.[CH2:7]([NH:10][CH2:11][CH:12]=[CH2:13])[CH:8]=[CH2:9].[S:14]1[CH:18]=[CH:17][CH:16]=[C:15]1[C:19]1[NH:20][C:21]([C:24]2[S:25][CH:26]=[CH:27][CH:28]=2)=[CH:22][CH:23]=1>C(O)C>[CH2:7]([N:10]([CH2:3][C:22]1[CH:23]=[C:19]([C:15]2[S:14][CH:18]=[CH:17][CH:16]=2)[NH:20][C:21]=1[C:24]1[S:25][CH:26]=[CH:27][CH:28]=1)[CH2:11][CH:12]=[CH2:13])[CH:8]=[CH2:9]

Participants

6

Procedure

Paraformaldehyde (9.1 mg, 0.3 mmol) was added to a solution of acetic acid (0.33 mL, 0.71 mmol) and diallylamine (0.32 mmol) in 1 mL of ethanol. After stirring at room temperature for a few minutes, 2.5-dithienylpyrrole (0.3 mmol) was then added all at once. The reaction mixture was then allowed to stir at 60° for 19 hours. The reaction solvent was evaporated under reduced pressure, and the crude product was taken up with ethyl acetate. The organic layer was then washed with water (10 mL) and brine (10 mL). The aqueous layer was extracted with chloroform (10 mL). The combined organic layers were then dried over anhydrous magnesium sulfate, filtered and the solvent was removed under pressure. The crude product was purified on 50 g of silica gel. Elution with hexane-ethyl acetate (5:1), gave 67 mg (65%) of title compound.

Workup

  1. stirringto stir at 60° for 19 hours
  2. customThe reaction solvent was evaporated under reduced pressure
  3. washThe organic layer was then washed with water (10 mL) and brine (10 mL)
  4. extractionThe aqueous layer was extracted with chloroform (10 mL)
  5. dry with materialThe combined organic layers were then dried over anhydrous magnesium sulfate
  6. filtrationfiltered
  7. customthe solvent was removed under pressure
  8. customThe crude product was purified on 50 g of silica gel
  9. washElution with hexane-ethyl acetate (5:1)

Sources & evidence

ORD record
ord-08d9929bce2f4aa89c9ff063b907382c
Source dataset
uspto-grants-1991_06
Patent number
US05021586

Reaction notes

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