4-Fluorobenzylamine → 9-(4-bromo-butyl)-9H-xanthene-9-carboxylic acid-4-fluoro-benzylamide
Reaction equation
[F:1][C:2]1[CH:9]=[CH:8][C:5]([CH2:6][NH2:7])=[CH:4][CH:3]=1.[Br:10][CH2:11][CH2:12][CH2:13][CH2:14][C:15]1([C:29](Cl)=[O:30])[C:28]2[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=2[O:22][C:21]2[C:16]1=[CH:17][CH:18]=[CH:19][CH:20]=2>>[F:1][C:2]1[CH:9]=[CH:8][C:5]([CH2:6][NH:7][C:29]([C:15]2([CH2:14][CH2:13][CH2:12][CH2:11][Br:10])[C:28]3[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=3[O:22][C:21]3[C:16]2=[CH:17][CH:18]=[CH:19][CH:20]=3)=[O:30])=[CH:4][CH:3]=1Participants
3
Procedure
Prepared analogously to Example 1 from 4-fluoro-benzylamine and 9-(4-bromo-butyl)-9H-xanthene-9-carboxylic acid chloride.
Sources & evidence
- ORD record
- ord-412619c146a24626a7540164cee36912
- Source dataset
- uspto-grants-2004_11
- Patent number
- US06821967B2
Reaction notes
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