Pyridine → Pyridine, 3-(4-aminobutyl)-
Reaction equation
P12(SP3(SP(SP(S3)(S1)=S)(=S)S2)=S)=[S:2].[Br:15][C:16]1[C:17]2[C:18]3[C:22](=[CH:23][CH:24]=1)[NH:21][C:20](=O)[C:19]=3[CH:26]=[CH:27][CH:28]=2.[N:29]1C=CC=CC=1>>[N:21]1[CH:28]=[CH:27][CH:26]=[C:19]([CH2:18][CH2:22][CH2:23][CH2:24][NH2:29])[CH:20]=1.[Br:15][C:16]1[C:17]2[C:18]3[C:22](=[CH:23][CH:24]=1)[N:21]=[C:20]([SH:2])[C:19]=3[CH:26]=[CH:27][CH:28]=2Participants
5
Procedure
4-(3-Pyridinyl)butylamine was prepared by the procedure described in Helv. Chim. Acta. 65 1868-1883 (1982). 6-Bromobenz(cd)indol-2-thiol was prepared by the action of P2S5 upon 6-bromobenz(cd)indol-2-one in refluxing pyridine.
Sources & evidence
- ORD record
- ord-16cea23ece1a42acb1ada6a611c11f22
- Source dataset
- uspto-grants-1992_01
- Patent number
- US05081131
Reaction notes
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