HCID 14254887, compound → HCID 20032923, compound
Reaction equation
[N:1]1([C:6]2[CH:11]=[CH:10][C:9]([C:12]3[CH2:13][CH2:14][C:15](=[O:18])[NH:16][N:17]=3)=[CH:8][N:7]=2)[CH:5]=[CH:4][N:3]=[CH:2]1>O1CCOCC1>[N:1]1([C:6]2[CH:11]=[CH:10][C:9]([C:12]3[CH:13]=[CH:14][C:15](=[O:18])[NH:16][N:17]=3)=[CH:8][N:7]=2)[CH:5]=[CH:4][N:3]=[CH:2]1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
2 g. (8.3 mmole) of the compound prepared in Example 2 were boiled in 250 ml. dioxan with 50 g. pyrolusite for 5 hours, filtered off with suction and the filtrate concentrated until it crystallised. After recrystallisation from ethanol, there was obtained 1 g. of the title compound; m.p. 300° C.
Workup
- filtrationfiltered off with suction
- concentrationthe filtrate concentrated until it
- customcrystallised
- customAfter recrystallisation from ethanol
- customthere was obtained 1 g
Sources & evidence
- ORD record
- ord-5a3642c97d8a4b84a1e5ead68b7d9900
- Source dataset
- uspto-grants-1989_07
- Patent number
- US04847251
Reaction notes
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