Glycidyl tosylate → 3-(Pyrazolo[1,5-a]pyrid-4-yloxy)-1,2-epoxypropane
Reaction equation
[OH:1][C:2]1[C:3]2[N:4]([N:8]=[CH:9][CH:10]=2)[CH:5]=[CH:6][CH:7]=1.S(C1C=CC(C)=CC=1)(O[CH2:15][CH:16]1[O:18][CH2:17]1)(=O)=O>>[N:8]1[N:4]2[CH:5]=[CH:6][CH:7]=[C:2]([O:1][CH2:15][CH:16]3[O:18][CH2:17]3)[C:3]2=[CH:10][CH:9]=1Participants
3
Procedure
4-Hydroxypyrazolo[1,5-a]pyridine (5) as obtained by the above procedure is reacted, in the form of alkali metal salt, with glycidyl tosylate to give 3-(pyrazolo[1,5-a]pyrid-4-yloxy)-1,2-epoxypropane (6). The reaction is preferably carried out in a solvent such as dimethylformamide under an atmosphere of argon gas.
Sources & evidence
- ORD record
- ord-14df4bc3f46642bdae096f97f4d4fa6e
- Source dataset
- uspto-grants-1993_04
- Patent number
- US05202334
Reaction notes
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