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Chemical Structure| 18774-50-0 Chemical Structure| 18774-50-0

Structure of 18774-50-0

Chemical Structure| 18774-50-0

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Product Details of [ 18774-50-0 ]

CAS No. :18774-50-0
Formula : C9H7NO2S
M.W : 193.22
SMILES Code : O=C(C1=C(N)SC2=CC=CC=C21)O

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Application In Synthesis of [ 18774-50-0 ]

* 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 [ 18774-50-0 ]

[ 18774-50-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 7311-95-7 ]
  • [ 18774-50-0 ]
YieldReaction ConditionsOperation in experiment
95% To a solution of 2-amino-benzo[b]thiophene-3-carboxylic acid ethyl ester (5.24 g, 23.6 mmol) in ethanol-tetrahydrofuran (1:1, 60.0 mL) was added 2 M aqueous sodium hydroxide solution (60.0 mL) at room temperature, and the mixture was refluxed for 8 h. After the removing solvents in vacuo, the residue was added water and 2 M aqueous hydrochloric acid solution to adjusted pH 5.0. The resulting precipitate was obtained by filtration, washed with water and dried in vacuo to give 22 (4.34 g, 95%) as a pink powder. 1H NMR (600 MHz, DMSO-d6): δ 7.00-7.07 (1H, m), 7.18-7.25 (1H, m), 7.58 (1H, d, J = 7.3 Hz), 7.92 (2H, br s), 7.95-8.02 (1H, m), 12.28 (1H, br s); MS (ESI): m/z 191 [M-H]+.
13% With potassium hydroxide; ethanol; water; for 0.333333h;Heating / reflux; Ethyl 2-amino-1-benzothiophene-3-carboxylate (obtained according to procedures described in Hallas, G.; Towns, A.D., Dyes and Pigments (1997), 35,219-237) (10 g, 40.0 mmol) was suspended in ethanol (100 ml_), and heated to reflux. A solution of potassium hydroxide (KOH, 8.4 g) in water (100 ml_) was added over the period of 10 minutes. The reaction mixture was refluxed for another 10 minutes, cooled to room temperature, and filtered. The collected solid was washed with water to pH neutral to give the title compound as a brown solid (1.0 g, 13.0 % yield). ESMS [M+H]+m/z 194.2.
An aq. solution of NaOH (IM, 20 mL) was added to a solution of ethyl 2-amino-l- benzothiophene-3-carboxylate (0.66 g, 3.00 mmol) in dioxane (10 mL) and the reaction mixture was heated at 1000C for 2 h. The reaction mixture was concentrated in vacuo to leave an aqueous residue and then a 2M aq. solution of HCl was added such that the pH = 4 to give a precipitate. The mixture was filtered and the collected solid was washed with water to give the crude title compound (0.42 g, 72%). 1H NMR (400 MHz, DMSO/DMSO-d6)* ) δ 12.25 (s, IH), 7.95 (d, IH), 7.89 (s, 2H), 7.56 (d, IH), 7.22-7.17 (m, IH), 7.04-6.99 (m, IH); m/z (M-H)" 192.2.
 

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