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Chemical Structure| 1110642-47-1 Chemical Structure| 1110642-47-1

Structure of 1110642-47-1

Chemical Structure| 1110642-47-1

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Product Details of [ 1110642-47-1 ]

CAS No. :1110642-47-1
Formula : C28H38BNO5
M.W : 479.42
SMILES Code : O=C(O1)N([C@@H](C)C2=CC=C(B3OC(C)(C)C(C)(C)O3)C=C2)CC[C@@]1(C4=CC=CC=C4)CC(C)(C)O

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* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 1110642-47-1 ]

[ 1110642-47-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 356560-80-0 ]
  • [ 1110642-47-1 ]
  • [ 1236325-03-3 ]
YieldReaction ConditionsOperation in experiment
63.5% With caesium carbonate;bis-triphenylphosphine-palladium(II) chloride; In 1,4-dioxane; water; for 2h;Reflux; Inert atmosphere; EXAMPLE 3(S)-3-((S)-l -(4-([1 ,2,4]triazolo[l ,5-a]pyridin-6-yl)phenyl)ethyl)-6-(2-hydroxy-2- methylpropyl)-6-phenyl- 1 ,3-oxazinan-2-one To a solution of (S)-6-(2-hydroxy-2-methylpropyl)-6-phenyl-3-((S)-l-(4- (4,4,5,5- tetramethyl-1 ,3,2-dioxaborolan-2-yl)phenyl)ethyl)-l ,3-oxazinan-2-one (300 mg, 0.63 mmol) and 6-bromo-[l,2,4]triazolo[l,5-a]pyridine (149 mg, 0.75 mmol) in dry 1,4-dioxane (15 mL) were added 2M aq Cs2CO3 (2 mL) and Pd(PPh3)Cl2 (40 mg, 0.056 mmol). After addition, the mixture was heated to reflux for 2 h under N2 atmosphere. The solid was filtered off and diluted with water (50 mL) and EtOAc (100 mL), the mixture was extracted with EA (3x50 mL). The combined organic layer was washed with brine (100 mL), dried over Na2SO4, filtered, and concentrated to dryness. The residue was purified by prep TLC to afford (S)-3-((S)-l-(4-([l,2,4]triazolo[l,5- a]pyridin-6-yl)phenyl)ethyl)-6-(2-hydroxy-2-methylpropyl)-6-phenyl- 1 ,3 -oxazinan-2- one (188 mg, yield: 63.5%). LC-MS Method tR = 1.18 min, m/z = 471, 418; 1H NMR (CDCl3): deltal.05 (s, 3H), 1.12 (s, 3H), 1.49-1.51 (m, 3H), 2.15-2.18 (m, 2H), 2.21-2.23 (m, IH), 2.32-2.37 (m, IH), 2.82-2.87 (m, IH), 3.01-3.06 (m, IH), 5.63-5.68 (m, IH), 7.01-7.06 (m, 2H), 7.19-7.22 (m, 3H), 7.29-7.32 (m, 3H), 7.33-7.36 (m, 2H),7.36-7.38 (m, IH), 7.75-7.78 (m, IH), 7.11-7.13 (m, IH), 8.79 (s, IH).
63.5% With bis-triphenylphosphine-palladium(II) chloride; caesium carbonate; In 1,4-dioxane; water; for 2h;Inert atmosphere; Reflux; To a solution of (S)-6-(2-hydroxy-2-methylpropyl)-6-phenyl-3-((S)-1-(4-(4,4,5,5- tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)ethyl)-1,3-oxazinan-2-one (18, 300 mg, 0.63 mmol) and <strong>[356560-80-0]6-bromo-[1,2,4]triazolo[1,5-a]pyridine</strong> (149 mg, 0.75 mmol) in dry 1,4-dioxane (15 mL) were added 2M aq Cs2CO3 (2 mL) and Pd(PPh3)Cl2 (40 mg, 0.056 mmol). After addition, the mixture was heated to reflux for 2 h under N2 atmosphere. The solid was filtered off and diluted with water (50 mL) and EtOAc (100 mL), the mixture was extracted with EA (3×50 mL). The combined organic layer was washed with brine (100 mL), dried over Na2SO4, filtered, and concentrated to dryness. The residue was purified by prep TLC to afford (S)-3-((S)-1-(4-([1,2,4]triazolo[1,5-a]pyridin-6-yl)phenyl)ethyl)-6-(2-hydroxy-2-methylpropyl)-6-phenyl-1,3-oxazinan-2-one (12m, 188 mg, yield: 63.5%). LC-MS Method tR = 1.18 min, m/z = 471, 418; 1H NMR (CDCl3): delta1.05 (s, 3H), 1.12 (s, 3H), 1.49-1.51 (m, 3H), 2.15-2.18 (m, 2H), 2.21-2.23 (m, 1H), 2.32-2.37 (m, 1H), 2.82-2.87 (m, 1H), 3.01-3.06 (m, 1H), 5.63-5.68 (m, 1H), 7.01-7.06 (m, 2H), 7.19-7.22 (m, 3H), 7.29-7.32 (m, 3H), 7.33-7.36 (m, 2H),7.36-7.38 (m, 1H), 7.75-7.78 (m, 1H), 7.11-7.13 (m, 1H), 8.79 (s, 1H).
 

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