Trifluoroacetic acid → Ethyl 2-[2-(2,4-difluorophenylamino)-5-fluoro-6-methoxynicotinoyl]acetate

HRID 232462Notes

Reaction equation

HRID 232462 reaction equation
[F:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[NH:9][C:10]1[N:39]=[C:38]([O:40][CH3:41])[C:37]([F:42])=[CH:36][C:11]=1[C:12]([CH:14](C(OCC)=O)[C:15]([O:17][CH:18](C1C=CC=CC=1)[C:19]1C=CC=CC=1)=[O:16])=[O:13].FC(F)(F)C(O)=O.C(OC(C)C)(C)C>C1(OC)C=CC=CC=1>[F:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[NH:9][C:10]1[N:39]=[C:38]([O:40][CH3:41])[C:37]([F:42])=[CH:36][C:11]=1[C:12]([CH2:14][C:15]([O:17][CH2:18][CH3:19])=[O:16])=[O:13]

Participants

5

Procedure

In 2 ml of anisole was dissolved 200 mg of diphenylmethyl ethyl 2-(2,4-difluorophenylamino)-5-fluoro-6-methoxynicotinoylmalonate, and 2 ml of trifluoroacetic acid was added thereto with ice-cooling, after which the resulting mixture was subjected to reaction at the same temperature for 10 minutes. The solvent was removed by distillation under reduced pressure, and to the crystalline material thus obtained was added 2 ml of diisopropyl ether, after which crystals were collected by filtration to obtain 120 mg (yield 94.3%) of ethyl 2-[2-(2,4-difluorophenylamino)-5-fluoro-6-methoxynicotinoyl]acetate.

Workup

  1. additionwas added
  2. temperaturewith ice-cooling
  3. customafter which the resulting mixture was subjected to reaction at the same temperature for 10 minutes
  4. customThe solvent was removed by distillation under reduced pressure
  5. customto the crystalline material thus obtained
  6. filtrationafter which crystals were collected by filtration

Sources & evidence

ORD record
ord-757d374aa8a8419ca670e09bc07e9a8f
Source dataset
uspto-grants-1989_07
Patent number
US04851535

Reaction notes

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