HCID 86630689, compound → HCID 86703037, compound

HRID 1851214Notes

Reaction equation

HRID 1851214 reaction equation
[CH3:1][C:2]1[CH:24]=[C:5]2[N:6]=[C:7]([C:16]3[CH:23]=[CH:22][C:19]([CH:20]=[O:21])=[CH:18][CH:17]=3)[C:8]([C:10]3[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=3)=[CH:9][N:4]2[N:3]=1.[CH:25]1(C2C=C(N)NN=2)C[CH2:26]1>>[CH:1]1([C:2]2[CH:24]=[C:5]3[N:6]=[C:7]([C:16]4[CH:23]=[CH:22][C:19]([CH:20]=[O:21])=[CH:18][CH:17]=4)[C:8]([C:10]4[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=4)=[CH:9][N:4]3[N:3]=2)[CH2:26][CH2:25]1

Participants

3

Reactant 2

HCID 86630689HCID 86630689, compoundHCID 178507266HCID 178507266, compound

Product 1

HCID 86703037HCID 86703037, compound

Procedure

This compound was prepared in a manner according to 4-(2-methyl-6-phenylpyrazolo[1,5-a]pyrimidin-5-yl)benzaldehyde by using 3-cyclopropyl-1H-pyrazol-5 amine in the first step.

Workup

  1. customThis compound was prepared in a manner

Sources & evidence

ORD record
ord-133d0b92a7f34d7cbda85468b893dc0c
Source dataset
uspto-grants-2015_02
Patent number
US08957064B2

Reaction notes

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