HCID 9847914, compound → HCID 22626725, compound

HRID 277949Notes

Reaction equation

HRID 277949 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]([Cl:29])=[C:25]([Cl: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]([Cl:29])=[C:25]([Cl:30])[CH:24]=1

Participants

3

Reactant 1

HCID 9847914HCID 9847914, compound

Product 1

HCID 22626725HCID 22626725, compound

Reagents, catalysts & solvents 1

HCID 8857Ethyl AcetateSolvent

Procedure

The 2-trifluoroacetamido-3-(3,4-dichlorophenyl)-6-benzoyl-imidazo[1,2-a]pyridine (9.91 g, 20.8 mmol) was converted to product in a manner substantially analogous to Example 67 to yield 7.17 g. (90.4%). EA, MS(FD).

Workup

  1. customto yield 7.17 g

Sources & evidence

ORD record
ord-600da960ea804e7a85a418241de6f55b
Source dataset
uspto-grants-2002_03
Patent number
US06358971B1

Reaction notes

Loading…