Ammonium formate → 2-(4-Amino-2-fluorobenzamido)acetic acid

HRID 1399442Notes

Reaction equation

HRID 1399442 reaction equation
[F:1][C:2]1[CH:14]=[C:13]([N+:15]([O-])=O)[CH:12]=[CH:11][C:3]=1[C:4]([NH:6][CH2:7][C:8]([OH:10])=[O:9])=[O:5].C([O-])=O.[NH4+]>CO.[Zn]>[NH2:15][C:13]1[CH:12]=[CH:11][C:3]([C:4]([NH:6][CH2:7][C:8]([OH:10])=[O:9])=[O:5])=[C:2]([F:1])[CH:14]=1

Participants

5

Procedure

To a solution of 2-(2-fluoro-4-nitrobenzamido)acetic acid (100 mg, 0.413 mmol) in methanol (15 mL) was added successively zinc dust (270 mg, 4.132 mmol) and ammonium formate (260 mg, 4.132 mmol) at rt. The reaction mixture was stirred at rt for 15 min. The reaction mixture was filtered and washed with methanol (2×5 mL). The residue obtained after evaporation of the solvents was diluted with water (5 mL) and acidified with AcOH (3 mL). The solution was extracted with EtOAc (3×50 mL) and the combined organic layer was dried over anhyd Na2SO4. The solution was filtered and evaporated the solvent. The residue was chromatographed over silica gel column using chloroform:methanol (70:30) as eluents to give the product as a white color solid (59 mg, 67%), mp 190-194° C.

Workup

  1. filtrationThe reaction mixture was filtered
  2. washwashed with methanol (2×5 mL)
  3. customThe residue obtained
  4. customafter evaporation of the solvents
  5. additionwas diluted with water (5 mL)
  6. extractionThe solution was extracted with EtOAc (3×50 mL)
  7. dry with materialthe combined organic layer was dried over anhyd Na2SO4
  8. filtrationThe solution was filtered
  9. customevaporated the solvent
  10. customThe residue was chromatographed over silica gel column

Sources & evidence

ORD record
ord-3dbdedf424db4f1d869b8a10ae749a53
Source dataset
uspto-grants-2014_12
Patent number
US08906344B2

Reaction notes

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