2-Bromobenzaldehyde → HCID 178468898, compound

HRID 489419Notes

Reaction equation

HRID 489419 reaction equation
[Br:1][C:2]1[CH:9]=[CH:8][CH:7]=[CH:6][C:3]=1[CH:4]=O.[NH2:10][C:11]1[CH:15]=[CH:14][NH:13][N:12]=1.[C:16]([CH2:21][C:22]([O:24][CH2:25][CH3:26])=[O:23])(=O)[CH:17]([CH3:19])[CH3:18]>>[Br:1][C:2]1[CH:9]=[CH:8][CH:7]=[CH:6][C:3]=1[CH:4]1[C:21]([C:22]([O:24][CH2:25][CH3:26])=[O:23])=[C:16]([CH:17]([CH3:19])[CH3:18])[NH:10][C:11]2=[N:12][NH:13][CH:14]=[C:15]12

Participants

4

Reactant 3

HCID 811292-BromobenzaldehydeHCID 81583Ethyl isobutyrylacetateHCID 178418806HCID 178418806, compound

Product 1

HCID 178468898HCID 178468898, compound

Procedure

The title compound was prepared from 2-bromobenzaldehyde, 3-aminopyrazole and ethyl isobutyrylacetate in the same manner as in Example 275.

Sources & evidence

ORD record
ord-6076fcef71fe4bc489d922efd4b2e911
Source dataset
uspto-grants-2005_12
Patent number
US06977262B2

Reaction notes

Loading…