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Chemical Structure| 861905-31-9 Chemical Structure| 861905-31-9

Structure of 861905-31-9

Chemical Structure| 861905-31-9

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Product Details of [ 861905-31-9 ]

CAS No. :861905-31-9
Formula : C16H24BNO3
M.W : 289.18
SMILES Code : CC1(C)C(C)(C)OB(C2=C(C)C=CC(C(NCC)=O)=C2)O1

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Application In Synthesis of [ 861905-31-9 ]

* 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 [ 861905-31-9 ]

[ 861905-31-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 261953-36-0 ]
  • [ 861905-31-9 ]
  • N-ethyl-3-(1H-indazol-6-yl)-4-methylbenzamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
With sodium hydrogencarbonate;tetrakis(triphenylphosphine) palladium(0); In water; isopropyl alcohol; at 150℃; for 0.5h;Microwave irradiation; A stirred mixture of 6-iodo-1H-indazole (0.45g), N-ethyl-4-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide (Intermediate 18, 0.54g) tetrakis(triphenylphosphine)palladium(0) (0.05g) and aqueous sodium hydrogen carbonate (1M, 1ml) in isopropanol (10ml) was heated at 150C for 30min in a microwave oven . The reaction mixture was poured into water (50ml) and extracted with ethyl acetate (3x25ml). The extracts w ere w ashed with w ater (25ml) d ried (Na2SO4) a nd oncentrated u nder v acuum. The residual oil was purified by column chromatography on silica (50g) eluting with ether/ ethyl acetate (7:3) to give the title compound as a pale yellow foam (0.25g). LC-MS: Rt 2.7min.
With sodium hydrogencarbonate;tetrakis(triphenylphosphine) palladium(0); In water; isopropyl alcohol; at 150℃; for 0.5h; Intermediate 12: N-Ethyl-3- (1H-indazol-6-yl)-4-methvibenzamide; A stirred mixture of 6-iodo-1 H-indazole (0.45g), N-ethyl-4-methyl-3- (4, 4,5, 5- tetramethyl-1, 3, 2-dioxaborolan-2-yi) benzamide (Intermediate 10, 0. 54g) tetrakis (triphenylphosphine) palladium (0) (0.05g) and aqueous sodium hydrogen carbonate (1M, 1ml) in isopropanol (10ml) was heated at 150C for 30min in a microwave oven. The reaction mixture was poured into water (50ml) and extracted with ethyl acetate (3x25ml). The extracts were washed with water (25ml) d ried (Na2SO4) a nd concentrated u nder vacuum. The residual oil was purified by column chromatography on silica (50g) eluting with ether/ ethyl acetate (7: 3) to give the title compound as a pale yellow foam (0.25g). LC-MS: Rt 2.7min
 

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