2-Bromoethyl methyl ether → HCID 86745335, compound

HRID 1461614Notes

Reaction equation

HRID 1461614 reaction equation
[C:1]([NH:4][C:5]1[C:6]([I:35])=[C:7]([C:24]([NH:26][CH2:27][CH:28]([CH2:30][CH:31]([OH:34])[CH2:32][OH:33])[OH:29])=[O:25])[C:8]([I:23])=[C:9]([C:21]=1[I:22])[C:10]([NH:12][CH2:13][CH:14]([CH2:16][CH:17]([OH:20])[CH2:18][OH:19])[OH:15])=[O:11])(=[O:3])[CH3:2].[CH3:36][O:37][CH2:38][CH2:39]Br>>[OH:34][CH:31]([CH2:32][OH:33])[CH2:30][CH:28]([OH:29])[CH2:27][NH:26][C:24](=[O:25])[C:7]1[C:6]([I:35])=[C:5]([N:4]([CH2:39][CH2:38][O:37][CH3:36])[C:1](=[O:3])[CH3:2])[C:21]([I:22])=[C:9]([C:10]([NH:12][CH2:13][CH:14]([CH2:16][CH:17]([OH:20])[CH2:18][OH:19])[OH:15])=[O:11])[C:8]=1[I:23]

Participants

3

Reactant 2

HCID 809722-Bromoethyl methyl etherHCID 86745334HCID 86745334, compound

Product 1

HCID 86745335HCID 86745335, compound

Procedure

This compound is prepared from 5-acetamido-N,N'-bis[(2,3-dihydroxypropyl)-2-hydroxyethyl]-2,4,6-triiodoisophthalamide, prepared as in Example 2, Step B, with 2-bromoethyl methyl ether (BrCH2CH2OCH3) in the same manner as described in Example 8.

Sources & evidence

ORD record
ord-e9f00ae73c44481ea0576b9d63aedc91
Source dataset
uspto-grants-1991_12
Patent number
US05075502

Reaction notes

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