HCID 67192245, compound → HCID 59663072, compound

HRID 550708Notes

Reaction equation

HRID 550708 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][O:24][C:25]1[O:26][C:27]2[CH2:32][CH2:31][NH:30][CH:29]([CH3:33])[C:28]=2[N:34]=1>>[Br:1][C:2]1[CH:3]=[N:4][C:5]2[N:6]([N:8]=[C:9]([C:11]([N:30]3[CH2:31][CH2:32][C:27]4[O:26][C:25]([O:24][CH3:23])=[N:34][C:28]=4[CH:29]3[CH3:33])=[O:12])[CH:10]=2)[CH:7]=1

Participants

3

Reactant 2

HCID 67192245HCID 67192245, compoundHCID 67195268HCID 67195268, compound

Product 1

HCID 59663072HCID 59663072, compound

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

Sources & evidence

ORD record
ord-808ca6f3cfbf4f50b975ffd6e1649998
Source dataset
uspto-grants-2011_05
Patent number
US07947689B2

Reaction notes

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