Hydrochloric Acid → HCID 86605520, compound
Reaction equation
FC(F)(F)C(O)=O.C(OC(=O)[N:17]([CH2:20][CH2:21][CH2:22][N:23]([CH3:25])[CH3:24])[CH2:18][CH3:19])C1C=CC=CC=1.[ClH:27].[H][H]>C(O)C.[Pd]>[ClH:27].[ClH:27].[CH2:18]([NH:17][CH2:20][CH2:21][CH2:22][N:23]([CH3:25])[CH3:24])[CH3:19]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
To a solution of (3-dimethylaminopropyl)-ethyl-carbamic acid benzyl ester trifluoroacetate (0.84 g, 2.2 mmol) in ethanol (30 mL) and concentrated hydrochloric acid (0.5 mL, 6 mmol) was added palladium on carbon (10%, 50 mg). The suspension was shaken under 50 psi hydrogen. When the consumption of hydrogen was observed to have ceased, the mixture was filtered through a pad of diatomaceous earth and then concentrated under reduced pressure to give N′-ethyl-N,N-dimethylpropane-1,3-diamine dihydrochloride (400 mg, 89%) as a white solid. MS (ES+): m/z (M+H)=131.3 to a suspension of the N′-ethyl-N,N-dimethylpropane-1,3-diamine dihydrochloride (0.26 g, 1.3 mmol) in dichloromethane (5 mL) was added triethylamine (0.51 mL, 3.9 mmol). After stirring for 10 minutes, the mixture was treated with 17-hydroxywortmannin (0.28 g, 0.65 mmol). After stirring overnight at room temperature, the mixture was concentrated under reduced pressure and then purified by reverse-phase HPLC (employing a gradient elution of 5% acetonitrile/95% water to 95% acetonitrile over 45 minutes). The title compound was obtained as a rust-colored solid (11.6 mg). MS(ES+): m/z (M+H)=561.4.
Workup
- customWhen the consumption of hydrogen
- filtrationthe mixture was filtered through a pad of diatomaceous earth
- concentrationconcentrated under reduced pressure
Sources & evidence
- ORD record
- ord-c62bb290a3e44caa8ca2ff3509caf7ad
- Source dataset
- uspto-grants-2010_02
- Patent number
- US07666901B2
Reaction notes
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