2-Aminoimidazole → HCID 86703038, compound

HRID 1851216Notes

Reaction equation

HRID 1851216 reaction equation
[S:1]1[CH:5]=[CH:4][C:3]([C:6]2[C:7]([C:15]3[CH:22]=[CH:21][C:18]([CH:19]=[O:20])=[CH:17][CH:16]=3)=[N:8][C:9]3[N:10](N=CC=3)[CH:11]=2)=[CH:2]1.NC1[NH:25][CH:26]=[CH:27]N=1>>[S:1]1[CH:5]=[CH:4][C:3]([C:6]2[C:7]([C:15]3[CH:16]=[CH:17][C:18]([CH:19]=[O:20])=[CH:21][CH:22]=3)=[N:8][C:9]3[N:10]([CH:27]=[CH:26][N:25]=3)[CH:11]=2)=[CH:2]1

Participants

3

Reactant 2

HCID 821402-AminoimidazoleHCID 86630690HCID 86630690, compound

Product 1

HCID 86703038HCID 86703038, compound

Procedure

This compound was prepared in a manner according to 4-(6-thiophen-3-yl-pyrazolo[1,5-a]pyrimidin-5-yl)-benzaldehyde by using 2-aminoimidazole in the first step.

Workup

  1. customThis compound was prepared in a manner

Sources & evidence

ORD record
ord-a2025b25f2984bd59c40a703233a9e31
Source dataset
uspto-grants-2015_02
Patent number
US08957064B2

Reaction notes

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