Phenylacetylene → HCID 50913011, compound
Reaction equation
[N:1]1[N:5]2[CH:6]=[C:7](OS(C(F)(F)F)(=O)=O)[CH:8]=[CH:9][C:4]2=[CH:3][CH:2]=1.[C:18]1([C:24]#[CH:25])[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1>>[C:18]1([C:24]#[C:25][C:7]2[CH:8]=[CH:9][C:4]3[N:5]([N:1]=[CH:2][CH:3]=3)[CH:6]=2)[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1Participants
3
Procedure
The title compound, light yellow solid, MS: m/e=219.2 (M+H+), can be prepared in accordance with the general method of example 1 from trifluoro-methanesulfonic acid pyrazolo[1,5-a]pyridin-6-yl ester (example 33, step 2) and phenylacetylene.
Sources & evidence
- ORD record
- ord-bcb960b8dd234345bd1624b5c6a49fdc
- Source dataset
- uspto-grants-2013_11
- Patent number
- US08586581B2
Reaction notes
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