Sodium Carbonate → HCID 67285003, compound
Reaction equation
[NH2:1][C:2]1[CH:14]=[CH:13][C:5]2[O:6][CH2:7][CH2:8][N:9](C(=O)C)[C:4]=2[CH:3]=1.Br[CH2:16][CH2:17][O:18][CH2:19][CH2:20]Br.C([O-])([O-])=O.[Na+].[Na+].[OH-].[K+]>O.CO>[O:18]1[CH2:19][CH2:20][N:1]([C:2]2[CH:14]=[CH:13][C:5]3[O:6][CH2:7][CH2:8][NH:9][C:4]=3[CH:3]=2)[CH2:16][CH2:17]1Participants
Conditions
- Temperature
- 150 °C
Procedure
A mixture of 1-(6-amino-2H-benzo[b][1,4]oxazin-4(3H)-yl)ethanone (0.5832 g, 3.03 mmol), 1-bromo-2-(2-bromoethoxy)ethane (0.774 g, 3.34 mmol), MeOH (3 mL), and Na2CO3 (0.6432 g, 6.07 mmol) in a pressure vessel was stirred at 150° C. After 1.5 h, the mixture was cooled to rt. To the cooled mixture was added a solution of KOH (1.1066 g, 19.72 mmol) in water (2 mL) and the mixture was stirred at 55° C. After 1 h, the mixture was cooled to rt, poured into ice water (50 mL), and extracted with EtOAc (50 mL×2). The combined organics were washed with brine (50 mL×2), dried over Na2SO4, filtered, and concentrated under reduced pressure to give a violet solid. The violet solid was purified by column chromatography on a silica gel column using 0 to 100% gradient of EtOAc in hexane as eluent to give 6-morpholino-3,4-dihydro-2H-benzo[b][1,4]-oxazine as a white solid: Mass Spectrum (ESI) m/e=221.2 (M+1).
Workup
- temperaturethe mixture was cooled to rt
- stirringthe mixture was stirred at 55° C
- waitAfter 1 h
- temperaturethe mixture was cooled to rt
- extractionextracted with EtOAc (50 mL×2)
- washThe combined organics were washed with brine (50 mL×2)
- dry with materialdried over Na2SO4
- filtrationfiltered
- concentrationconcentrated under reduced pressure
- customto give a violet solid
- customThe violet solid was purified by column chromatography on a silica gel column
Sources & evidence
- ORD record
- ord-b7b6e3480c0e44b69dfa3bbd0da0496e
- Source dataset
- uspto-grants-2014_07
- Patent number
- US08765940B2
Reaction notes
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