HCID 90281393, compound → HCID 90281431, compound
Reaction equation
[Br:1][C:2]1[C:3]([C@@H:19]([NH:29][C:30](=[O:47])[CH2:31][N:32]2[C:36]3[C:37]([F:42])([F:41])[C@@H:38]4[CH2:40][C@@H:39]4[C:35]=3[C:34]([C:43]([F:46])([F:45])[F:44])=[N:33]2)[CH2:20][C:21]2[CH:26]=[C:25]([F:27])[CH:24]=[C:23]([F:28])[CH:22]=2)=[N:4][CH:5]=[C:6]([N:8]2C(=O)C3C(=CC=CC=3)C2=O)[CH:7]=1>C(O)C.O.NN>[NH2:8][C:6]1[CH:7]=[C:2]([Br:1])[C:3]([C@@H:19]([NH:29][C:30](=[O:47])[CH2:31][N:32]2[C:36]3[C:37]([F:42])([F:41])[C@@H:38]4[CH2:40][C@@H:39]4[C:35]=3[C:34]([C:43]([F:44])([F:45])[F:46])=[N:33]2)[CH2:20][C:21]2[CH:22]=[C:23]([F:28])[CH:24]=[C:25]([F:27])[CH:26]=2)=[N:4][CH:5]=1Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
To a mixture of Compound 41B (100 mg, 0.14 mmol) in 15 ml of ethanol, 0.05 ml of hydrazine monohydrate was added and the reaction mixture was stirred at room temperature for 10 min. The solvent was removed and the residue was purified by RP-HPLC eluting with acetonitrile/H2O (with 0.1% TFA) to afford the title product. MS (m/z) 592.20 [M+H]+.
Workup
- additionwas added
- customThe solvent was removed
- customthe residue was purified by RP-HPLC
- washeluting with acetonitrile/H2O (with 0.1% TFA)
Sources & evidence
- ORD record
- ord-b5efbb459f2144c8ae479edd2836d4ec
- Source dataset
- uspto-grants-2015_06
- Patent number
- US09050344B2
Reaction notes
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