Hydrazine → HCID 19973161, compound
Reaction equation
[C:1]1([C:7]2[N:8]([N:12]3C(=O)C4C(=CC=CC=4)C3=O)[CH:9]=[CH:10][CH:11]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.NN>C(O)C>[C:1]1([C:7]2[N:8]([NH2:12])[CH:9]=[CH:10][CH:11]=2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a stirred suspension consisting of 2-(2-phenyl-1H-pyrrol-1-yl)-1H-isoindol-1,3(2H)dione (7.2 g) in abs. ethanol (150 ml) was added hydrazine (3.9 ml) at room temperature. The reaction mixture was warmed to reflux for 2 hours and allowed to cool to room temperature overnight. The solid by-product was filtered and washed with ether. The combined filtrates were concentrated in vacuo to give an oil which solidified on standing. Recrystallization from ether afforded 3.9 g of the product as a solid, m.p. 80°-82° C.
Workup
- temperatureThe reaction mixture was warmed
- temperatureto reflux for 2 hours
- filtrationThe solid by-product was filtered
- washwashed with ether
- concentrationThe combined filtrates were concentrated in vacuo
- customto give an oil which
- customRecrystallization from ether
Sources & evidence
- ORD record
- ord-c3081f8d155d491fb1822af9bc442845
- Source dataset
- uspto-grants-1997_02
- Patent number
- US05605925
Reaction notes
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