Thiophenol → HCID 53652081, compound
Reaction equation
[N+:1]([C:4]1[C:13]([O:14][CH2:15][CH2:16][CH2:17][CH2:18]Br)=[CH:12][CH:11]=[C:10]2[C:5]=1[CH:6]=[CH:7][C:8](=[O:20])[NH:9]2)([O-:3])=[O:2].[C:21]1([SH:27])[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1>>[N+:1]([C:4]1[C:13]([O:14][CH2:15][CH2:16][CH2:17][CH2:18][S:27][C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)=[CH:12][CH:11]=[C:10]2[C:5]=1[CH:6]=[CH:7][C:8](=[O:20])[NH:9]2)([O-:3])=[O:2]Participants
3
Procedure
Prepared analogous to Example 122 from 5-nitro-6-(4-bromo-butoxy)-carbostyril [m.p. 250° C., prepared by nitration of 6-(4-bromo-butoxy)-3,4-dihydro-carbostyril] and thiophenol.
Sources & evidence
- ORD record
- ord-163a80ab8d724703b96119af53e62f17
- Source dataset
- uspto-grants-1982_05
- Patent number
- US04329347
Reaction notes
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