HCID 18960876, compound → HCID 18960923, compound
Reaction equation
[C:1]([OH:6])(=[O:5])[C:2]([OH:4])=[O:3].[CH2:7]([C:11]1[O:15][N:14]=[C:13]([C:16]2[CH2:17][NH:18][CH2:19][CH2:20][CH:21]=2)[CH:12]=1)CCC.[C:22](N1CCC(Cl)=C(C2C=C(CCCC)ON=2)C1)(=[O:29])C1C=CC=CC=1>>[C:1]([OH:6])(=[O:5])[C:2]([OH:4])=[O:3].[CH3:22][O:29][CH2:7][C:11]1[O:15][N:14]=[C:13]([C:16]2[CH2:17][NH:18][CH2:19][CH2:20][CH:21]=2)[CH:12]=1Participants
3
Procedure
3-(5-Butyl-3-isoxazolyl)-1,2,5,6-tetrahydropyridine oxalate starting from 1-benzoyl-4-chloro-3-(5-butyl-3-isoxazolyl)-1,2,5,6-tetrahydropyridine. M.p. 188°-91° C.
Sources & evidence
- ORD record
- ord-7b86bb37c0ae444db249861601335350
- Source dataset
- uspto-grants-1994_10
- Patent number
- US05356912
Reaction notes
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