HCID 67192245, compound → HCID 59663088, compound

HRID 550705Notes

Reaction equation

HRID 550705 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.[Cl:23][C:24]1[O:25][C:26]2[CH2:31][CH2:30][NH:29][CH:28]([CH3:32])[C:27]=2[N:33]=1>>[Br:1][C:2]1[CH:3]=[N:4][C:5]2[N:6]([N:8]=[C:9]([C:11]([N:29]3[CH2:30][CH2:31][C:26]4[O:25][C:24]([Cl:23])=[N:33][C:27]=4[CH:28]3[CH3:32])=[O:12])[CH:10]=2)[CH:7]=1

Participants

3

Reactant 2

HCID 67192245HCID 67192245, compoundHCID 67195273HCID 67195273, compound

Product 1

HCID 59663088HCID 59663088, 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-chloro-4-methyl-4,5,6,7-tetrahydrooxazolo[4,5-c]pyridine to provide the title compound.

Sources & evidence

ORD record
ord-cdc7958d748043dcb3844ceed69387f3
Source dataset
uspto-grants-2011_05
Patent number
US07947689B2

Reaction notes

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