Sodium hydride → tert-Butyl{1-[2-(7,8-difluoro-2-oxoquinoxalin-1(2H)-yl)ethyl]piperidin-4-yl}carbamate
Reaction equation
[F:1][C:2]1[C:11]([F:12])=[C:10]2[C:5]([N:6]=[CH:7][C:8](=[O:13])[NH:9]2)=[CH:4][CH:3]=1.[H-].[Na+].CS(O[CH2:21][CH2:22][N:23]1[CH2:28][CH2:27][CH:26]([NH:29][C:30]([O:32][C:33]([CH3:36])([CH3:35])[CH3:34])=[O:31])[CH2:25][CH2:24]1)(=O)=O.C(OC(=O)NC1CCN(CCN2C3C(=CC=C(OC)C=3)C=CC2=O)CC1)(C)(C)C>C(OCC)(=O)C>[C:33]([O:32][C:30](=[O:31])[NH:29][CH:26]1[CH2:27][CH2:28][N:23]([CH2:22][CH2:21][N:9]2[C:10]3[C:5](=[CH:4][CH:3]=[C:2]([F:1])[C:11]=3[F:12])[N:6]=[CH:7][C:8]2=[O:13])[CH2:24][CH2:25]1)([CH3:36])([CH3:35])[CH3:34]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
7,8-Difluoroquinoxalin-2(1H)-one (Intermediate 155—a mixture of regioisomers containing 30% 5,6-difluoroquinoxalin-2(1H)-one, 1.0 g, 5.50 mmol) was deprotonated with sodium hydride (60% in oil, 0.26 g, 6.60 mmol) and alkylated with 2-{4-[(tert-butoxycarbonyl)amino]piperidin-1-yl}ethyl methanesulfonate (Intermediate 6) (6.6 mmol) as described for Intermediate 2. Chromatography on silica gel with 70-100% ethyl acetate in hexanes gave 320 mg of the product as a colorless solid.
Sources & evidence
- ORD record
- ord-4fbbd7339c944307b97206fdece1072c
- Source dataset
- uspto-grants-2012_02
- Patent number
- US08124602B2
Reaction notes
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