1,4-Difluoro-2-iodobenzene → 2-tert-Butyl-6-(2,5-difluoro-phenylethynyl)-pyrazolo[1,5-a]pyrimidine
Reaction equation
[C:1]([C:5]1[CH:15]=[C:8]2[N:9]=[CH:10][C:11]([C:13]#[CH:14])=[CH:12][N:7]2[N:6]=1)([CH3:4])([CH3:3])[CH3:2].[F:16][C:17]1[CH:22]=[CH:21][C:20]([F:23])=[CH:19][C:18]=1I>>[C:1]([C:5]1[CH:15]=[C:8]2[N:9]=[CH:10][C:11]([C:13]#[C:14][C:21]3[CH:22]=[C:17]([F:16])[CH:18]=[CH:19][C:20]=3[F:23])=[CH:12][N:7]2[N:6]=1)([CH3:4])([CH3:3])[CH3:2]Participants
3
Procedure
The title compound, a white solid, MS: m/e=312.2 (M+H+), can be prepared in accordance with the general method of example 1 from 2-tert-butyl-6-ethynyl-pyrazolo[1,5-a]pyrimidine (example 21, step 2) and 1,4-difluoro-2-iodobenzene.
Sources & evidence
- ORD record
- ord-b498815e5d914f19bdcb57cb35ac8df1
- Source dataset
- uspto-grants-2015_01
- Patent number
- US08933094B2
Reaction notes
Loading…