2-(1,4-Diazepan-1-yl)ethan-1-ol → HCID 57541158, compound

HRID 545368

Reaction equation

HRID 545368 reaction equation
[CH2:1]([C:7]1[CH:8]=[C:9]([C:13]2[N:17]([CH3:18])[C:16]([C:19]([OH:21])=O)=[C:15]([I:22])[N:14]=2)[CH:10]=[CH:11][CH:12]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH3:6].[N:23]1([CH2:30][CH2:31][OH:32])[CH2:29][CH2:28][CH2:27][NH:26][CH2:25][CH2:24]1>>[CH2:1]([C:7]1[CH:8]=[C:9]([C:13]2[N:17]([CH3:18])[C:16]([C:19]([N:26]3[CH2:27][CH2:28][CH2:29][N:23]([CH2:30][CH2:31][OH:32])[CH2:24][CH2:25]3)=[O:21])=[C:15]([I:22])[N:14]=2)[CH:10]=[CH:11][CH:12]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH3:6]

Participants

3

Reactant 2

HCID 27365502-(1,4-Diazepan-1-yl)ethan-1-olHCID 671332392-(3-Hexyl-phenyl)-5-iodo-3-methyl-3H-imidazole-4-carboxylic acid2×

Product 1

HCID 57541158HCID 57541158, compound

Procedure

In analogy to the procedure described for example 1, 2-(3-hexyl-phenyl)-5-iodo-3-methyl-3H-imidazole-4-carboxylic acid (intermediate 1) and 2-[1,4]diazepan-1-yl-ethanol gave the title compound as light yellow oil. MS: 539.3 (MH+).

Sources & evidence

ORD record
ord-7eeb171285dd47cda16ab654bf1006ba
Source dataset
uspto-grants-2011_05
Patent number
US07935707B2

Linked notes

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