Benzyldihydronicotinamide → HCID 118557839, compound
Reaction equation
[Br-].[CH3:2][O:3][C:4]1[CH:5]=[C:6]2[C:10](=[CH:11][C:12]=1[O:13][CH3:14])[C:9](=[O:15])[CH:8]([CH2:16][C:17]1[CH:22]=[CH:21][N+:20]([CH2:23][C:24]3[CH:29]=[CH:28][CH:27]=[CH:26][C:25]=3[CH3:30])=[CH:19][C:18]=1[C:31]([NH:33][CH3:34])=[O:32])[CH2:7]2.C1C(C(N)=O)=CN(CC2C=CC=CC=2)C=C1>>[CH3:2][O:3][C:4]1[CH:5]=[C:6]2[C:10](=[CH:11][C:12]=1[O:13][CH3:14])[C:9](=[O:15])[CH:8]([CH2:16][CH:17]1[CH:22]=[CH:21][N:20]([CH2:23][C:24]3[CH:29]=[CH:28][CH:27]=[CH:26][C:25]=3[CH3:30])[CH:19]=[C:18]1[C:31]([NH:33][CH3:34])=[O:32])[CH2:7]2Participants
3
Procedure
The title compound 168 is prepared according to the procedure reported in Example 39.1 with compound 143 (89.1 mg, 0.2 mmol) and BNAH (1 equiv) as reactants. Pale yellow solid. (Yield 35.7 mg, 40%).
Sources & evidence
- ORD record
- ord-25201aa6ed2a4fb994310e1b59a18b8e
- Source dataset
- uspto-grants-2016_06
- Patent number
- US09376387B2
Reaction notes
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