Butyryl chloride → 2-Propyl-6,7,8,9-tetrahydro-5H-[1,3]oxazolo[4,5-h][3]benzazepine
Reaction equation
[NH2:1][C:2]1[C:19]([OH:20])=[CH:18][C:5]2[CH2:6][CH2:7][N:8](C(OC(C)(C)C)=O)[CH2:9][CH2:10][C:4]=2[CH:3]=1.[C:21](Cl)(=O)[CH2:22][CH2:23][CH3:24]>>[CH2:22]([C:21]1[O:20][C:19]2[C:2]([N:1]=1)=[CH:3][C:4]1[CH2:10][CH2:9][NH:8][CH2:7][CH2:6][C:5]=1[CH:18]=2)[CH2:23][CH3:24]Participants
3
Procedure
The title compound was prepared as described in General Procedure 2 from 1,1-dimethylethyl 7-amino-8-hydroxy-1,2,4,5-tetrahydro-3H-3-benzazepine-3-carboxylate and butyryl chloride.
Sources & evidence
- ORD record
- ord-375a8b589f3a4aa6b943d5ab53c24507
- Source dataset
- uspto-grants-2011_08
- Patent number
- US07989444B2
Reaction notes
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