HCID 67192245, compound → HCID 59663094, compound
Reaction equation
[Br:1][C:2]1[CH:3]=[N:4][C:5]2[N:6]([N:8]=[C:9]([C:11]([N:13]3[CH2:18][CH2:17][C:16]4[CH:19]=[CH:20][NH:21][C:15]=4[CH:14]3[CH3:22])=[O:12])[CH:10]=2)[CH:7]=1.CC1[O:25]C2CCNC(C)C=2N=1>>[Br:1][C:2]1[CH:3]=[N:4][C:5]2[N:6]([N:8]=[C:9]([C:11]([N:13]3[CH2:18][CH2:17][C:16]4[O:25][C:20]([CH3:19])=[N:21][C:15]=4[CH:14]3[CH3:22])=[O:12])[CH:10]=2)[CH:7]=1Participants
3
Procedure
(6-Bromo-pyrazolo[1,5-a]pyrimidin-2-yl)-(7-methyl-1,4,5,7-tetrahydro-pyrrolo[2,3-c]pyridin-6-yl)-methanone is reacted with 2,4-dimethyl-4,5,6,7-tetrahydro-oxazolo[4,5-c]pyridine to provide the title compound.
Sources & evidence
- ORD record
- ord-c66fe77d24f1441b9ce31bddf4c1c7fd
- Source dataset
- uspto-grants-2011_05
- Patent number
- US07947689B2
Reaction notes
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