HCID 67191013, compound → HCID 24897246, compound

HRID 550703Notes

Reaction equation

HRID 550703 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]4C=[CH:20][NH:21][C:15]=4[CH:14]3[CH3:22])=[O:12])[CH:10]=2)[CH:7]=1.CC1C2N=C[O:32]C=2CCN1>>[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:32][CH:20]=[N:21][C:15]=4[CH:14]3[CH3:22])=[O:12])[CH:10]=2)[CH:7]=1

Participants

3

Reactant 2

HCID 67191013HCID 67191013, compoundHCID 67192245HCID 67192245, compound

Product 1

HCID 24897246HCID 24897246, 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 4-methyl-4,5,6,7-tetrahydro-oxazolo[4,5-c]pyridine to provide the title compound.

Sources & evidence

ORD record
ord-683a54264ae243f68fbaafd6f0534b39
Source dataset
uspto-grants-2011_05
Patent number
US07947689B2

Reaction notes

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