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Chemical Structure| 1055974-00-9 Chemical Structure| 1055974-00-9

Structure of 1055974-00-9

Chemical Structure| 1055974-00-9

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Product Details of [ 1055974-00-9 ]

CAS No. :1055974-00-9
Formula : C13H16N2O3
M.W : 248.28
SMILES Code : CC1=NN(C(=O)OC(C)(C)C)C2=C1C=CC(O)=C2
MDL No. :MFCD24467331

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Application In Synthesis of [ 1055974-00-9 ]

* 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 [ 1055974-00-9 ]

[ 1055974-00-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1055974-00-9 ]
  • [ 101-06-4 ]
  • [ 1221179-36-7 ]
YieldReaction ConditionsOperation in experiment
With diamide; triphenylphosphine; In tetrahydrofuran; at 20℃; Reference Example 93Tert-butyl 6-(2-(dibenzylamino)ethoxy)-3-methylindazole-1-carboxylate Tert-butyl 6hydroxy-3-methylindazole-1-carboxylate (4.9962 g) that can be produced by the method described in Reference Example 60 or the like, and 2-(dibenzylamino)ethanol (5.0 mL; manufactured by Tokyo Chemical Industry Co., Ltd.) were dissolved in dehydrated THF (100 mL), and triphenylphosphine (10.5872 g; manufactured by Tokyo Chemical Industry Co., Ltd.) and TMAD (6.9197 g; manufactured by Masuda. Chemical Industries, Co., Ltd.) were added to the solution. The mixture was stirred overnight at room temperature. The reaction solution was filtered, and then the filtrate was concentrated under reduced pressure. Toluene was added to the resulting residue, and insoluble matters were filtered. Subsequently, the filtrate was concentrated under reduced pressure. The resulting residue was purified by column chromatography (?COLUMN-D?; n-hexane:ethyl acetate=90:10?75:25), and thus the title compound (9.6091 g) was obtained.1H-NMR (300 MHz, CDCl3); delta(ppm) 1.71(9H, s), 2.53(3H, s), 2.95(2H, t, J=5.8), 3.73(4H, s), 4.13(2H, t, J=5.8), 6.87(1H, dd, J=1.4, 8.7), 7.20-7.41(10H, m), 7.46(1H, d, J=8.7), 7.56(1H, d, J=1.4)LCMS: 472 [M+H]; Retention time: 2.04 minutes; LCMS condition: C
With diamide; triphenylphosphine; In tetrahydrofuran; at 20℃; tert-Butyl 6-hydroxy-3-methylindazole-1-carboxylate (4.9962 g), which can be manufactured by the method described in Reference Example 28 and the like, and 2-(dibenzylamino)ethanol (5.0 mL; made by Tokyo Chemical Industry Co., Ltd.) were dissolved in dehydrated THF (100 mL). Triphenyl phosphine (10.5872 g; made by Tokyo Chemical Industry Co., Ltd.) and TMAD (6.9197 g; made by Masuda Chemical Industry Co., Ltd) were added and [the contents] were stirred overnight at room temperature. After filtering the reaction solution, the filtrate was concentrated under reduced pressure. Toluene was added to the residue obtained. After filtering out the insoluble matter, the filtrate was concentrated under reduced pressure. The resulting residue was purified by column chromatography ('Column D;' n-hexane: ethyl acetate = 90:10?75:25), and the title compound (9.6091 g) was obtained. 1H-NMR (300MHz, CDCl3) ; delta (ppm) 1.71 (9H, s), 2.53 (3H, s), 2.95 (2H, t, J=5.8), 3.7 3 (4H, s), 4.13 (2H, t, J=5.8), 6.87 (1H, d d, J=1.4, 8.7), 7.20-7.41 (10H, m), 7.46 (1H, d. J=8.7), 7.56 (1H, d. J=1.4) LCMS: 472 [M + H]; Retention time: 2.04 min; LCMS conditions: C
 

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