Benzyl Bromide → HCID 118557824, compound
Reaction equation
[C:1]([C:4]1[CH:5]=[N:6][CH:7]=[CH:8][C:9]=1[CH2:10][CH:11]1[CH2:19][C:18]2[C:13](=[CH:14][C:15]([O:22][CH3:23])=[C:16]([O:20][CH3:21])[CH:17]=2)[C:12]1=[O:24])(=[O:3])[CH3:2].[CH2:25]([Br:32])[C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1>>[Br-:32].[C:1]([C:4]1[CH:5]=[N+:6]([CH2:25][C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)[CH:7]=[CH:8][C:9]=1[CH2:10][CH:11]1[CH2:19][C:18]2[C:13](=[CH:14][C:15]([O:22][CH3:23])=[C:16]([O:20][CH3:21])[CH:17]=2)[C:12]1=[O:24])(=[O:3])[CH3:2]Participants
3
Procedure
The title compound 33 is prepared according to the procedure reported in Example 38.1 with compound 32 (46 mg, 0.14 mmol) and benzyl bromide (34 μL, 0.28 mmol) as reactants. White solid. (Yield 62.3 mg, 91%).
Sources & evidence
- ORD record
- ord-101324ceee5b4b6e9e54959727f689f9
- Source dataset
- uspto-grants-2016_06
- Patent number
- US09376387B2
Reaction notes
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