Benzylamine → HCID 22180445, compound
Reaction equation
[CH2:1]([NH2:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Br:9][CH2:10][CH2:11][CH2:12][CH2:13][C:14]1([C:27](Cl)=[O:28])[C:26]2[CH:25]=[CH:24][CH:23]=[CH:22][C:21]=2[C:20]2[C:15]1=[CH:16][CH:17]=[CH:18][CH:19]=2>>[CH2:1]([NH:8][C:27]([C:14]1([CH2:13][CH2:12][CH2:11][CH2:10][Br:9])[C:26]2[CH:25]=[CH:24][CH:23]=[CH:22][C:21]=2[C:20]2[C:15]1=[CH:16][CH:17]=[CH:18][CH:19]=2)=[O:28])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Participants
3
Procedure
Prepared analogously to Example 1c from benzylamine and 9-(4-bromo-butyl)-9H-fluorene-9-carboxylic acid chloride.
Sources & evidence
- ORD record
- ord-eae0bf599b994456b6c0f086acc688dc
- Source dataset
- uspto-grants-2004_11
- Patent number
- US06821967B2
Reaction notes
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