1H-Imidazole, 1-hexyl- → HCID 178444702, compound

HRID 1943310Notes

Reaction equation

HRID 1943310 reaction equation
[CH2:1]([N:7]1[CH:11]=[CH:10][N:9]=[CH:8]1)[CH2:2][CH2:3][CH2:4][CH2:5][CH3:6].[Br:12][CH2:13][C:14]1[CH:19]=[CH:18][C:17]([C:20]2[O:21][C:22]([C:25]3[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=3)=[CH:23][N:24]=2)=[CH:16][CH:15]=1>>[Br-:12].[CH2:1]([N+:7]1[CH:11]=[CH:10][N:9]([CH2:13][C:14]2[CH:15]=[CH:16][C:17]([C:20]3[O:21][C:22]([C:25]4[CH:26]=[CH:27][CH:28]=[CH:29][CH:30]=4)=[CH:23][N:24]=3)=[CH:18][CH:19]=2)[CH:8]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH3:6]

Participants

3

Reactant 2

HCID 30156601H-Imidazole, 1-hexyl-HCID 122501072-(4-bromomethyl-phenyl)-5-phenyl-oxazole

Product 1

HCID 178444702HCID 178444702, compound

Procedure

The experimental procedure is identical to the procedure for compound la (1-hexylimidazole [2-5] 0.787 g, 5.2 mmol, 2-(4-bromomethyl-phenyl)-5-phenyl-oxazole 1.390 g, 4.4 mmol).

Sources & evidence

ORD record
ord-212621a54050470f8152a46c94b3f72b
Source dataset
uspto-grants-2013_03
Patent number
US08389940B2

Reaction notes

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