Spermidine → HCID 86704359, compound
Reaction equation
[C:1]([O:10][CH2:11][CH3:12])(=[O:9])/[CH:2]=[CH:3]\[C:4]([O:6][CH2:7][CH3:8])=[O:5].[NH2:13][CH2:14][CH2:15][CH2:16][CH2:17][NH:18][CH2:19][CH2:20][CH2:21][NH2:22]>C1COCC1>[O:9]=[C:1]([CH2:2][CH:3]([C:4]([O:6][CH2:7][CH3:8])=[O:5])[NH:22][CH2:21][CH2:20][CH2:19][NH:18][CH2:17][CH2:16][CH2:15][CH2:14][NH:13][CH:2]([C:1]([O:10][CH2:11][CH3:12])=[O:9])[CH2:3][C:4]([O:6][CH2:7][CH3:8])=[O:5])[O:10][CH2:11][CH3:12]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 60 °C
Procedure
11.9 g (69 mmol) of diethyl maleate were added to a solution of 5 g (34.5 mmol) of spermidine in 5 ml of THF. The reaction mixture was stirred for 3 days at 60° C. After removing the solvent in vacuo, the product was obtained quantitatively as a yellow liquid.
Workup
- customAfter removing the solvent in vacuo
- customthe product was obtained quantitatively as a yellow liquid
Sources & evidence
- ORD record
- ord-a2973cd677db45f79d2518b4041bf0e7
- Source dataset
- uspto-grants-2016_08
- Patent number
- US09421298B2
Reaction notes
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