Hydrogen Bromide → HCID 178516493, compound
Reaction equation
Br.C[O:3][C:4]1[CH:9]=[CH:8][N:7]=[C:6]([C:10]2[CH:11]=[N:12][N:13]3[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=23)[N:5]=1>>[N:12]1[N:13]2[CH:18]=[CH:17][CH:16]=[CH:15][C:14]2=[C:10]([C:6]2[N:5]=[C:4]([OH:3])[CH:9]=[CH:8][N:7]=2)[CH:11]=1Participants
3
Conditions
- Temperature
- 100 °C
Procedure
48% Aqueous hydrogen bromide (19.50 mL) was added to 3-(4-methoxypyrimidin-2-yl) pyrazolo[1,5-a]pyridine (Preparation 4a, 0.30 g, 1.32 mmol) and the resulting mixture was heated to 100° C. with stirring. After 3 hours, the mixture was cooled and the resultant precipitate was filtered and dried in vacuo to give the title compound (0.28 g, 99%) as the hydrobromide salt.
Workup
- temperaturethe mixture was cooled
- filtrationthe resultant precipitate was filtered
- customdried in vacuo
Sources & evidence
- ORD record
- ord-625c7ff4699a489280a8c607c82d84bc
- Source dataset
- uspto-grants-2015_12
- Patent number
- US09206183B2
Reaction notes
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