4-(2-Hydroxyphenyl)-semicarbazide hydrochloride → 5-Methoxy-2-[4-(2-hydroxyphenyl)-semicarbazono]indan-1,3-dione
Reaction equation
O.[CH3:2][O:3][C:4]1[CH:5]=[C:6]2[C:10](=[CH:11][CH:12]=1)[C:9](=[O:13])[C:8](=O)[C:7]2=[O:15].Cl.[OH:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][C:19]=1[NH:24][C:25](=[O:28])[NH:26][NH2:27]>>[CH3:2][O:3][C:4]1[CH:5]=[C:6]2[C:10](=[CH:11][CH:12]=1)[C:9](=[O:13])[C:8](=[N:27][NH:26][C:25]([NH:24][C:19]1[CH:20]=[CH:21][CH:22]=[CH:23][C:18]=1[OH:17])=[O:28])[C:7]2=[O:15]Participants
3
Procedure
5-methoxyindan-1,2,3-trione, monohydrate, 4-(2-hydroxyphenyl)-semicarbazide hydrochloride; reflux for 5 hours
Workup
- temperaturereflux for 5 hours
Sources & evidence
- ORD record
- ord-843b55a9d81348578af2b8af1e1a64a1
- Source dataset
- uspto-grants-1996_11
- Patent number
- US05571843
Reaction notes
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