Benzyl Bromide → HCID 118557824, compound

HRID 2207229Notes

Reaction equation

HRID 2207229 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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