HCID 67192245, compound → HCID 59663080, compound

HRID 550707Notes

Reaction equation

HRID 550707 reaction equation
[Br:1][C:2]1[CH:3]=[N:4][C:5]2[N:6]([N:8]=[C:9]([C:11](N3CCC4C=CNC=4C3C)=[O:12])[CH:10]=2)[CH:7]=1.[CH3:23][CH:24]1[C:29]2[N:30]=[C:31]([C:33]([F:36])([F:35])[F:34])[O:32][C:28]=2[CH2:27][CH2:26][NH:25]1>>[Br:1][C:2]1[CH:3]=[N:4][C:5]2[N:6]([N:8]=[C:9]([C:11]([N:25]3[CH2:26][CH2:27][C:28]4[O:32][C:31]([C:33]([F:36])([F:34])[F:35])=[N:30][C:29]=4[CH:24]3[CH3:23])=[O:12])[CH:10]=2)[CH:7]=1

Participants

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 4-methyl-2-trifluoromethyl-4,5,6,7-tetrahydrooxazolo[4,5-c]pyridine to provide the title compound.

Sources & evidence

ORD record
ord-96351f2925e04486851825e940c95d5e
Source dataset
uspto-grants-2011_05
Patent number
US07947689B2

Reaction notes

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