Nitrogen → HCID 54079686, compound
Reaction equation
[CH3:1][O:2][C:3]1[C:9]2[S:10][CH:11]=[CH:12][C:8]=2[C:7](=[CH:13][C:14]([OH:16])=[O:15])[C:6]2[CH:17]=[CH:18][CH:19]=[CH:20][C:5]=2[CH:4]=1.[N+](=[CH2:23])=[N-].N#N>C(OCC)C>[CH3:23][O:15][C:14](=[O:16])[CH:13]=[C:7]1[C:8]2[CH:12]=[CH:11][S:10][C:9]=2[C:3]([O:2][CH3:1])=[CH:4][C:5]2[CH:20]=[CH:19][CH:18]=[CH:17][C:6]1=2Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
2 g of the product of example 2 are suspended in 20 ml ethyl ether and a freshly prepared solution of diazomethane is added at 0° C. until N2 evolution ceases. The solvent is evaporated off at 10° C. and the residue re-crystallised from ethanol to yield the title compound as a (Z,E) isomer mixture: m.p.=124°-125° C.
Workup
- customThe solvent is evaporated off at 10° C.
- customthe residue re-crystallised from ethanol
Sources & evidence
- ORD record
- ord-85c7899eaa2d4c29b5e743b92005e560
- Source dataset
- uspto-grants-1988_04
- Patent number
- US04740518
Reaction notes
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