HCID 21434082, compound → HCID 178474350, compound
Reaction equation
Cl.[C:2]([NH:5][C:6]1[CH:7]=[C:8]([NH2:13])[CH:9]=[C:10]([OH:12])[CH:11]=1)(=[O:4])[CH3:3].[C:14]([C:17]1[C:18](=[O:28])[O:19][C:20]([OH:27])=[C:21]([C:24](=O)[CH3:25])[C:22]=1[OH:23])(=[O:16])[CH3:15]>>[C:2]([NH:5][C:6]1[CH:11]=[C:10]([OH:12])[CH:9]=[C:8]([NH:13][C:24](=[C:21]2[C:22]([OH:23])=[C:17]([C:14](=[O:16])[CH3:15])[C:18](=[O:28])[O:19][C:20]2=[O:27])[CH3:25])[CH:7]=1)(=[O:4])[CH3:3]Participants
3
Procedure
Similarly reaction of 5-acetamido-3-aminophenol hydrochloride with 3,5-diacetyl-4,6-dihydroxy-2H-pyran-2-one as described above furnishes 3-[1-(5-acetamido-3-hydroxyphenylamino)ethylidene]-5-acetyl-4-hydroxy-2H-pyran-2,6(3H)-dione.
Sources & evidence
- ORD record
- ord-cc97b36826f44bc1bf5263d78d145e9b
- Source dataset
- uspto-grants-1977_05
- Patent number
- US04025642
Reaction notes
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