Phenoxyacetyl chloride → HCID 11444815, 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.[O:27]([CH2:34][C:35](Cl)=[O:36])[C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1.[NH2:38][C:39]1[CH:51]=[CH:50][C:42]2[O:43]C(C)(C)[O:45][C:46](=[O:47])[C:41]=2[CH:40]=1>>[OH:43][C:42]1[CH:50]=[CH:51][C:39]([N:38]([C:35](=[O:36])[CH2:34][O:27][C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=2)[CH2:17][C:18]2[CH:26]=[CH:25][C:21]([C:22]([NH:13][CH2:12][C:11]3[CH:10]=[CH:9][C:8]([O:1][C:2]4[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=4)=[CH:15][CH:14]=3)=[O:23])=[CH:20][CH:19]=2)=[CH:40][C:41]=1[C:46]([OH:47])=[O:45]Participants
5
Procedure
The title compound was prepared following the procedure A using 4-phenoxybenzylamine, 4-(chloromethyl)benzoyl chloride, phenoxyacetyl chloride and 6-amino-2,2-dimethyl-4H-1,3-benzodioxin-4-one. M+(ESI): 603.1
Sources & evidence
- ORD record
- ord-f9e5314b21014f6e9d22b5885513f96a
- Source dataset
- uspto-grants-2008_04
- Patent number
- US07365225B2
Reaction notes
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