Benzylamine → HCID 69156391, compound
Reaction equation
[CH2:1]([N:8]1[C:17]([C:18](O)=[O:19])=[C:16]([C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)[C:15]2[C:10](=[CH:11][CH:12]=[C:13]([Br:27])[CH:14]=2)[C:9]1=[O:28])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH2:29]([NH2:36])[C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1>>[CH2:29]([NH:36][C:18]([C:17]1[N:8]([CH2:1][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)[C:9](=[O:28])[C:10]2[C:15]([C:16]=1[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)=[CH:14][C:13]([Br:27])=[CH:12][CH:11]=2)=[O:19])[C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1Participants
3
Procedure
The present compound was synthesized by a method similar to that in Example 249 and using 2-benzyl-6-bromo-1-oxo-4-phenyl-1,2-dihydroisoquinoline-3-carboxylic acid (250 mg) and benzylamine. Colorless crystals (210 mg).
Workup
- customThe present compound was synthesized by a method similar to that in Example 249
Sources & evidence
- ORD record
- ord-17f6fc1d3e9e49c0af6975534d87d5fa
- Source dataset
- uspto-grants-2008_07
- Patent number
- US07402595B2
Reaction notes
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