Benzyl Bromide → HCID 18512036, compound

HRID 1370892Notes

Reaction equation

HRID 1370892 reaction equation
[CH3:1][C:2]1[C:7]([N+:8]([O-:10])=[O:9])=[CH:6][CH:5]=[CH:4][C:3]=1[NH:11][CH2:12][C:13]1[CH:30]=[CH:29][C:16]([O:17][C:18]2[CH:23]=[CH:22][C:21]([CH2:24][CH2:25][C:26]([OH:28])=[O:27])=[CH:20][CH:19]=2)=[CH:15][CH:14]=1.[CH2:31](Br)[C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1>>[CH2:31]([N:11]([CH2:12][C:13]1[CH:30]=[CH:29][C:16]([O:17][C:18]2[CH:23]=[CH:22][C:21]([CH2:24][CH2:25][C:26]([O:28][CH2:1][C:2]3[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=3)=[O:27])=[CH:20][CH:19]=2)=[CH:15][CH:14]=1)[C:3]1[CH:4]=[CH:5][CH:6]=[C:7]([N+:8]([O-:10])=[O:9])[C:2]=1[CH3:1])[C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1

Participants

3

Procedure

The product from example 98A and benzyl bromide were processed as described in Example 6B to provide the title compound.

Sources & evidence

ORD record
ord-818635eb708b4ed9bd578d6e451ecdab
Source dataset
uspto-grants-2003_06
Patent number
US06583180B2

Reaction notes

Loading…