HCID 9824750, compound → HCID 22626654, compound

HRID 277948Notes

Reaction equation

HRID 277948 reaction equation
FC(F)(F)C([NH:5][C:6]1[N:7]=[C:8]2[CH:13]=[CH:12][C:11]([C:14](=[O:21])[C:15]3[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=3)=[CH:10][N:9]2[C:22]=1[C:23]1[CH:28]=[CH:27][C:26]([F:29])=[C:25]([F:30])[CH:24]=1)=O>CC(=O)OCC>[NH2:5][C:6]1[N:7]=[C:8]2[CH:13]=[CH:12][C:11]([C:14](=[O:21])[C:15]3[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=3)=[CH:10][N:9]2[C:22]=1[C:23]1[CH:28]=[CH:27][C:26]([F:29])=[C:25]([F:30])[CH:24]=1

Participants

3

Procedure

The 2-trifluoroacetamido-3-(3,4-difluorophenyl)-6-benzoyl-imidazo[1,2-a]pyridine (7.44 g, 16.7 mmol) was converted to product in a manner substantially analogous to Example 67 to yield 5.09 g. (87.2%). EA, MS(FD).

Workup

  1. customto yield 5.09 g

Sources & evidence

ORD record
ord-d0889260dc1d4b14ab8a75d19e062d69
Source dataset
uspto-grants-2002_03
Patent number
US06358971B1

Reaction notes

Loading…