1-(Bromomethyl)-3-chlorobenzene → HCID 68705060, compound

HRID 1988846Notes

Reaction equation

HRID 1988846 reaction equation
[CH2:1]([O:3][C:4]1[CH:22]=[CH:21][CH:20]=[CH:19][C:5]=1[CH2:6][O:7][C:8]1[CH:13]=[CH:12][N:11]=[C:10]2[C:14]([CH3:18])=[C:15]([CH3:17])[NH:16][C:9]=12)[CH3:2].[Cl:23][C:24]1[CH:25]=[C:26]([CH:29]=[CH:30][CH:31]=1)[CH2:27]Br>>[ClH:23].[Cl:23][C:24]1[CH:25]=[C:26]([CH:29]=[CH:30][CH:31]=1)[CH2:27][N:16]1[C:9]2[C:10](=[N:11][CH:12]=[CH:13][C:8]=2[O:7][CH2:6][C:5]2[CH:19]=[CH:20][CH:21]=[CH:22][C:4]=2[O:3][CH2:1][CH3:2])[C:14]([CH3:18])=[C:15]1[CH3:17]

Participants

3

Reactant 2

HCID 698381-(Bromomethyl)-3-chlorobenzeneHCID 687022847-[(2-Ethoxyphenyl)methoxy]-2,3-dimethyl-1H-pyrrolo[3,2-b]pyridine

Product 1

HCID 68705060HCID 68705060, compoundYield 79.8%

Procedure

In accordance with the same procedures as in Step 2 of Example 33, except for using 7-(2-ethoxybenzyloxy)-2,3-dimethyl-1H-pyrrolo[3,2-b]pyridine prepared in Step 2 and 3-chlorobenzyl bromide, the titled compound was obtained as a white solid. (Yield: 79.8%)

Sources & evidence

ORD record
ord-1a9eca2fb9314c67a3884fcf41f0d1bb
Source dataset
uspto-grants-2010_01
Patent number
US07642269B2

Reaction notes

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