Ethylenediamine → N-(2-Aminoethyl)-2-[4-[2-(2,3,6,9-tetrahydro-1,3-dipropyl-2,6-dioxo-1H-purin-8-yl)propyl]phenoxy]-acetamide
Reaction equation
[CH2:1]([N:4]1[C:12](=[O:13])[C:11]2[N:10]=[C:9]([CH:14]([CH3:27])[CH2:15][C:16]3[CH:26]=[CH:25][C:19]([O:20][CH2:21][C:22](O)=[O:23])=[CH:18][CH:17]=3)[NH:8][C:7]=2[N:6]([CH2:28][CH2:29][CH3:30])[C:5]1=[O:31])[CH2:2][CH3:3].ON1C(=O)CCC1=O.Cl.CN(C)CCCN=C=NCC.[CH2:52]([NH2:55])[CH2:53][NH2:54]>CN(C)C=O.CO.C(Cl)(Cl)Cl>[NH2:54][CH2:53][CH2:52][NH:55][C:22](=[O:23])[CH2:21][O:20][C:19]1[CH:25]=[CH:26][C:16]([CH2:15][CH:14]([C:9]2[NH:8][C:7]3[N:6]([CH2:28][CH2:29][CH3:30])[C:5](=[O:31])[N:4]([CH2:1][CH2:2][CH3:3])[C:12](=[O:13])[C:11]=3[N:10]=2)[CH3:27])=[CH:17][CH:18]=1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 3
Procedure
Dissolve 2-[4-[2-(2,3,6,9-tetrahydro-1,3-dipropyl-2,6-dioxo-1H-purin-8-yl)propyl]phenoxy]acetic acid (800 mg, 1.87 mmol) in dimethylformamide (20 mL) and treat with N-hydroxysuccinimide (215 mg, 1.87 mmol) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (751 mg, 3.92 mmol). Stir for 1 hour and add to a stirring solution of ethylenediamine (20 mL of a 10% solution in methanol). Stir for 1 hour and dilute with chloroform (600 mL). Separate the organic phase, wash with 5% sodium carbonate (200 mL), then brine (300 mL). Dry (MgSO4) and evaporate the solvent in vacuo. Purify by radial chromatography (5→10% methanol/chloroform with 1% ammonium hydroxide) and recrystallize (10% isopropanol/hexane) to give the title compound (364 mg); mp 143-44° C.
Workup
- stirringStir for 1 hour
- customSeparate the organic phase
- washwash with 5% sodium carbonate (200 mL)
- dry with materialDry (MgSO4)
- customevaporate the solvent in vacuo
- customPurify by radial chromatography (5→10% methanol/chloroform with 1% ammonium hydroxide)
- customrecrystallize (10% isopropanol/hexane)
Sources & evidence
- ORD record
- ord-366adbd27c1b4e4190d30a261cfba53e
- Source dataset
- uspto-grants-1993_05
- Patent number
- US05208240
Reaction notes
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