HCID 67192245, compound → HCID 178421613, compound

HRID 550688Notes

Reaction equation

HRID 550688 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]=[CH:20][NH: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[CH:19]=[CH:20][N:21]([C:27]5[NH:26][N:25]=[N:24][N:23]=5)[C:15]=4[CH:14]3[CH3:22])=[O:12])[CH:10]=2)[CH:7]=1

Participants

3

Reactant 2

HCID 67192245HCID 67192245, compoundHCID 178418441HCID 178418441, compound

Product 1

HCID 178421613HCID 178421613, compound

Procedure

In close analogy to the procedure described in Example 52, (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 1H tetrazole to provide the title compound.

Sources & evidence

ORD record
ord-422198b5bb374abc97874e8b5c0c60e9
Source dataset
uspto-grants-2011_05
Patent number
US07947689B2

Reaction notes

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