3-Iodopyridine → 3-(3,4-Difluorophenylethynyl)-pyridine
Reaction equation
I[C:2]1[CH:3]=[N:4][CH:5]=[CH:6][CH:7]=1.[C:8]([C:10]1[CH:15]=[CH:14][C:13]([F:16])=[C:12]([F:17])[CH:11]=1)#[CH:9]>>[F:17][C:12]1[CH:11]=[C:10]([C:8]#[C:9][C:2]2[CH:3]=[N:4][CH:5]=[CH:6][CH:7]=2)[CH:15]=[CH:14][C:13]=1[F:16]Participants
3
Procedure
Prepare essentially as described in EXAMPLE 46 using 3-iodopyridine (445 mg, 2.17 mmol) and 4-ethynyl-1,2-difluorobenzene, (prepared essentially as described in PREPARATION 14), (300 mg, 2.17 mmol) to give the title compound (87.6 mg, 21%).
Workup
- customPrepare essentially
- custom(prepared essentially
- customas described in PREPARATION 14), (300 mg, 2.17 mmol)
Sources & evidence
- ORD record
- ord-27867171597e4d74b16c6691679ff754
- Source dataset
- uspto-grants-2011_03
- Patent number
- US07915424B2
Reaction notes
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