Hydrochloric Acid → HCID 68313298, compound

HRID 1914873Notes

Reaction equation

HRID 1914873 reaction equation
Cl.[F:2][C:3]1[C:4]([N+:24]([O-])=O)=[C:5]([O:22][CH3:23])[C:6]2[NH:10][C:9](=[O:11])[N:8]([C:12]3[CH:17]=[CH:16][C:15]([I:18])=[CH:14][C:13]=3[F:19])[C:7]=2[C:20]=1[F:21].C(OCC)(=O)C>C1COCC1.CCCCCC.[Zn]>[NH2:24][C:4]1[C:3]([F:2])=[C:20]([F:21])[C:7]2[N:8]([C:12]3[CH:17]=[CH:16][C:15]([I:18])=[CH:14][C:13]=3[F:19])[C:9](=[O:11])[NH:10][C:6]=2[C:5]=1[O:22][CH3:23]

Participants

7

Procedure

Concentrated HCl (2.5 mL) was added to a solution of 6,7-difluoro-1-(2-fluoro-4-iodo-phenyl)-4-methoxy-5-nitro-1,3-dihydro-benzoimidazol-2-one (1.6 g, 3.4 mmol) in THF (35 mL) and the resulting mixture was stirred for 5 min. This was followed by portion wise addition of zinc powder (2.2 g, 34 mmol) over a period of 30 minutes and stirring was continued for a further 30 minutes at room temperature. The reaction was monitored by TLC (60% ethyl acetate in hexane). The reaction mixture was concentrated and the concentrate was quenched with water and extracted with ethyl acetate. The organic layer was washed with brine and concentrated. The crude product was triturated with ether, filtered and the residue was dried to afford 1.4 g of the product (94.5% yield).

Workup

  1. stirringstirring
  2. waitwas continued for a further 30 minutes at room temperature
  3. concentrationThe reaction mixture was concentrated
  4. customthe concentrate was quenched with water
  5. extractionextracted with ethyl acetate
  6. washThe organic layer was washed with brine
  7. concentrationconcentrated
  8. customThe crude product was triturated with ether
  9. filtrationfiltered
  10. customthe residue was dried

Sources & evidence

ORD record
ord-8850ba81088046549b5591e701a7948a
Source dataset
uspto-grants-2013_12
Patent number
US08614239B2

Reaction notes

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