Benzyl Bromide → HCID 70981397, compound
Reaction equation
[CH2:1]([N:5]1[C:10](=[O:11])[CH:9]=[C:8]2[C:12]([CH3:16])([CH3:15])[CH2:13][NH:14][C:7]2=[CH:6]1)[CH:2]([CH3:4])[CH3:3].[CH2:17](Br)[C:18]1C=CC=C[CH:19]=1>>[CH2:1]([N:5]1[C:10](=[O:11])[CH:9]=[C:8]2[C:12]([CH3:16])([CH3:15])[CH2:13][NH:14][C:7]2=[CH:6]1)[C:2]1[CH:4]=[CH:19][CH:18]=[CH:17][CH:3]=1Participants
3
Procedure
Prepared in an analogous method to 6-isobutyl-3,3-dimethyl-1,2,3,6-tetrahydro-pyrrolo[2,3-c]pyridin-5-one using benzyl bromide instead of 3-bromo-2-methylpropene and omitting the hydrogenation step (see Preparations 128 and 130).
Sources & evidence
- ORD record
- ord-5050fb030f9544d3a72a94fd2cde5ed1
- Source dataset
- uspto-grants-2015_04
- Patent number
- US09018214B2
Reaction notes
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