Acetyl chloride → HCID 11398115, compound
Reaction equation
[O:1]([C:8]1[CH:15]=[CH:14][C:11]([CH2:12][NH2:13])=[CH:10][CH:9]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Cl[CH2:17][C:18]1[CH:26]=[CH:25][C:21]([C:22](Cl)=[O:23])=[CH:20][CH:19]=1.[C:27](Cl)(=[O:29])[CH3:28].[NH2:31][C:32]1[CH:44]=[CH:43][C:35]2[O:36]C(C)(C)[O:38][C:39](=[O:40])[C:34]=2[CH:33]=1>>[C:27]([N:31]([CH2:17][C:18]1[CH:26]=[CH:25][C:21]([C:22]([NH:13][CH2:12][C:11]2[CH:10]=[CH:9][C:8]([O:1][C:2]3[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=3)=[CH:15][CH:14]=2)=[O:23])=[CH:20][CH:19]=1)[C:32]1[CH:44]=[CH:43][C:35]([OH:36])=[C:34]([CH:33]=1)[C:39]([OH:40])=[O:38])(=[O:29])[CH3:28]Participants
5
Procedure
The title compound was prepared following the procedure A using 4-phenoxybenzylamine, 4-(chloromethyl)benzoyl chloride, acetyl chloride and 6-amino-2,2-dimethyl-4H-1,3-benzodioxin-4-one. M+(ESI): 511.1
Sources & evidence
- ORD record
- ord-9e1fcd904b854893979c93ec186c8067
- Source dataset
- uspto-grants-2008_04
- Patent number
- US07365225B2
Reaction notes
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