Sodium hydride → HCID 19956392, compound
Reaction equation
[CH2:1]([N:4]([C:39]([O:41][C:42]([CH3:45])([CH3:44])[CH3:43])=[O:40])[CH2:5][CH2:6][CH2:7][N:8]([C:32]([O:34][C:35]([CH3:38])([CH3:37])[CH3:36])=[O:33])[CH2:9]/[CH:10]=[CH:11]/[CH2:12][N:13]([C:25]([O:27][C:28]([CH3:31])([CH3:30])[CH3:29])=[O:26])[CH2:14][CH2:15][CH2:16][NH:17][C:18]([O:20][C:21]([CH3:24])([CH3:23])[CH3:22])=[O:19])[CH:2]=[CH2:3].[H-].[Na+].[CH2:48](I)[CH2:49][CH3:50]>CN(C=O)C>[CH2:50]([N:17]([C:18]([O:20][C:21]([CH3:22])([CH3:23])[CH3:24])=[O:19])[CH2:16][CH2:15][CH2:14][N:13]([C:25]([O:27][C:28]([CH3:31])([CH3:29])[CH3:30])=[O:26])[CH2:12]/[CH:11]=[CH:10]/[CH2:9][N:8]([C:32]([O:34][C:35]([CH3:38])([CH3:37])[CH3:36])=[O:33])[CH2:7][CH2:6][CH2:5][N:4]([CH2:1][CH2:2][CH3:3])[C:39]([O:41][C:42]([CH3:45])([CH3:44])[CH3:43])=[O:40])[CH:49]=[CH2:48]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 0.7 g (1.092 mmol) of (E)-1-allyl-1,5,10,14-tetra-BOC-1,5,10,14-tetraazatetradec-7-ene (see Example 2a) in 9.4 ml of DMF there are added, with stirring, 0.087 g (2.175 mmol) of sodium hydride dispersion (approx. 60%) and, after 5 min., 0.212 ml (2.176 mmol) of propyl iodide. The reaction mixture is stirred for 15 h at room temperature; a further 0.043 g (1.075 mmol) of sodium hydride dispersion (approx. 60%) and 0.106 ml (1.088 mmol) of propyl iodide are added, and the mixture is stirred for a further 96 h at 20° C. and is then concentrated by evaporation in vacuo. Working up analogously to Example 1a) yields the oily title compound, Rf value=0.46 (silica gel/ethyl acetate:hexane (2:3)).
Workup
- stirringThe reaction mixture is stirred for 15 h at room temperature
- stirringthe mixture is stirred for a further 96 h at 20° C.
- concentrationis then concentrated by evaporation in vacuo
Sources & evidence
- ORD record
- ord-9b1601d6a83a4c5c810a1a58890f690d
- Source dataset
- uspto-grants-1997_05
- Patent number
- US05627215
Reaction notes
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