HCID 67193042, compound → HCID 178421656, compound

HRID 550690Notes

Reaction equation

HRID 550690 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][NH:20][CH:21]=[C:15]4[CH:14]3[CH3:22])=[O:12])[CH:10]=2)[CH:7]=1.[NH:23]1[CH:27]=[N:26][N:25]=[N:24]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=[C:19]([C:27]5[NH:26][N:25]=[N:24][N:23]=5)[NH:20][CH:21]=[C:15]4[CH:14]3[CH3:22])=[O:12])[CH:10]=2)[CH:7]=1

Participants

3

Reactant 2

HCID 67193042HCID 67193042, compoundHCID 178418441HCID 178418441, compound

Product 1

HCID 178421656HCID 178421656, compound

Procedure

In close analogy to the procedure described in Example 52, (6-bromo-pyrazolo[1,5-a]pyrimidin-2-yl)-(4-methyl-2,4,6,7-tetrahydro-pyrrolo[3,4-c]pyridin-5-yl)-methanone is reacted with 1H tetrazole to provide the title compound.

Sources & evidence

ORD record
ord-eefe8c034c834b5396fc410c29f84061
Source dataset
uspto-grants-2011_05
Patent number
US07947689B2

Reaction notes

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