Tolylboronic acid → HCID 58207240, compound
Reaction equation
Cl[C:2]1[N:7]2[N:8]=[C:9]([CH3:11])[CH:10]=[C:6]2[N:5]=[C:4]([NH2:12])[CH:3]=1.B(O)(O)[C:14]1[CH:15]=[CH:16][C:17]([CH3:20])=[CH:18][CH:19]=1>>[CH3:11][C:9]1[CH:10]=[C:6]2[N:5]=[C:4]([NH2:12])[CH:3]=[C:2]([C:14]3[CH:19]=[CH:18][C:17]([CH3:20])=[CH:16][CH:15]=3)[N:7]2[N:8]=1Participants
3
Procedure
The titled compound was prepared using a procedure analogous to that described in connection with Example 15 except that 7-chloro-2-methylpyrazolo[1,5-a]pyrimidin-5-amine (1J) and p-tolylboronic acid were used as starting materials.
Sources & evidence
- ORD record
- ord-cf1d3e73854b46c1b662f0f0213ede6e
- Source dataset
- uspto-grants-2014_12
- Patent number
- US08921358B2
Reaction notes
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