Ethanol → 1,2,4-Triazolo(3,4-a)phthalazine, 8-chloro-6-phenyl-
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[C:8]([NH:12][NH2:13])=[N:7][N:6]=[C:5]2[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1.[CH2:20](O)C>>[Cl:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[C:8]1=[N:12][N:13]=[CH:20][N:7]1[N:6]=[C:5]2[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1Participants
3
Procedure
The compound of the title is prepared by following essentially the same procedure outlined in example 114 above but using 6-chloro-4-phenyl-1-hydrazinophthalazine instead of 4-phenyl-1-hydrazinophthalazine. M.p. 189°-90° C. (from ethanol).
Workup
- customThe compound of the title is prepared
Sources & evidence
- ORD record
- ord-be0615fa61a64dd893fd5c94ad2f2b61
- Source dataset
- uspto-grants-1988_11
- Patent number
- US04788186
Reaction notes
Loading…