Acetyl 2-hydroxy-1, 3-diaminoalkanes
An alkyl, radical technology, applied in the field of acetyl 2-hydroxy-1, which can solve the problem of effective treatment methods that do not suspend, prevent or reverse the progression of Alzheimer's disease, etc.
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Embodiment 1
[0854] Embodiment 1: the preparation of 7-bromo-1-tetralinone
[0855]
[0856] 7-Bromo-1-tetralinone was prepared following the procedure described in Cornelius, L.A.M.; Combs, D.W. Synthetic Communications 1994, 24, 2777-2788. The above isomers were separated using flash chromatography on silica gel (BiotageFlash 75, eluent solvent 20 / 1 hexane:MTBE) to yield 5-bromo-1-tetralinone (11.59 g, 51%) and 7-bromo-1 - Tetralinone (9.45 g, 42%).
Embodiment 2
[0858] Embodiment 2: the preparation of (R)-7-ethyltetralin-1-alcohol
[0859]
[0860] See generally: Jones, T.K.; Mohan, J.J.; Xavier, L.C.; Blacklock, T.J.; Mathre, D.J.; Sohar, P.; , 56, 763-769. More specifically, 7-ethyl-1-tetralinone (2.29 g, 13.1 mmol) was placed in a 100 mL round bottom flask and dissolved in anhydrous THF (40 mL). Activated 4mm molecular sieves were added and the mixture was aged for 2 hours before cannula transfer to a 250 mL three necked round bottom flask equipped with a dropping funnel, thermometer and nitrogen inlet. The solution was cooled to -25°C and 1M (S)-tetrahydro-1-methyl-3,3-diphenyl-1H,3H-pyrollo[1 ,2-c][1,3,2]oxazaborole. The source of oxazoborole is Aldrich, cat. No. 45, 770-1, "(S)-2-Methyl-CBS-oxazaborolidine". The use of S-promoters generates R-alcohols. According to the aforementioned references, the use of 5 mol% oxazaborolidine catalyst gave comparable results.
[0861] A solution of borane-dimethylsulfide (0.70 g, 0.8...
Embodiment 3
[0862] Example 3: (S)-7-ethyl-1,2,3,4-tetrahydro-1-naphthylamine hydrochloride
[0863]
[0864] See generally: Rover, S.; Adam. G..; Cesura, A.M.; Galley, G.; Jenck, F.; -1338. Their authors reported a slight decrease in yield by partial formation of dihydronaphthalene through removal of the hydroxyl moiety.
[0865] More specifically, a solution of (R)-7-ethyltetralin-1-ol (1.77 g, 10.1 mmol) in toluene (25 mL) was cooled in an ice bath and treated with diphenylphosphoryl azide ( DPPA, 3.3 g, 2.7 mL, 12 mmol). A solution of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU, 1.8 g, 1.8 mL, 12 mmol) in toluene (8 mL) was added over 20 minutes, and the mixture was heated at 0° C. Stir for 2 hours and 16 hours at room temperature. The mixture was filtered through a pad of silica gel (elution 6:1 hexane / ethyl acetate) to remove the precipitate and the volatiles were removed in vacuo to give crude S-azide as an oily residue. This material was used directly in the next step without f...
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