(Bromomethyl)cyclobutane → (3S,5S)-3-(cyclobutylmethyl)-3-methyl-5-phenylmorpholin-2-one
Reaction equation
[CH3:1][C:2]1[C:3](=[O:14])[O:4][CH2:5][C@H:6]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[N:7]=1.Br[CH2:16][CH:17]1[CH2:20][CH2:19][CH2:18]1>>[CH:17]1([CH2:16][C@@:2]2([CH3:1])[C:3](=[O:14])[O:4][CH2:5][C@H:6]([C:8]3[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=3)[NH:7]2)[CH2:20][CH2:19][CH2:18]1Participants
3
Procedure
The title compound was prepared from (5S)-3-methyl-5-phenyl-5,6-dihydro-2H-1,4-oxazin-2-one (1 g, 5.28 mmol, see WO-A-02/051983) and (bromomethyl)cyclobutane according to the procedure outlined in Preparation 1. The total amount of compound synthesised was 0.445 g.
Workup
- customoutlined in Preparation 1
- customThe total amount of compound synthesised
Sources & evidence
- ORD record
- ord-9cf3e34bd58e492b831420bab5ba832d
- Source dataset
- uspto-grants-2009_11
- Patent number
- US07612226B2
Reaction notes
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