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Chemical Structure| 154650-88-1 Chemical Structure| 154650-88-1

Structure of 154650-88-1

Chemical Structure| 154650-88-1

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Product Details of [ 154650-88-1 ]

CAS No. :154650-88-1
Formula : C9H7NO2S
M.W : 193.22
SMILES Code : O=C(C1=CC2=CC=CN=C2S1)OC
MDL No. :MFCD12025885

Safety of [ 154650-88-1 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 154650-88-1 ]

* 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 [ 154650-88-1 ]

[ 154650-88-1 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 154650-88-1 ]
  • [ 59944-76-2 ]
YieldReaction ConditionsOperation in experiment
85% With hydrogenchloride; sodium hydroxide; In methanol; water; C101 (0.700 g, 3.63 mmol) is dissolved in MeOH (15 mL) and 3 mL H2O. 2N NaOH (1.82 mL, 3.63 mmol) is added drop-wise, and the reaction is stirred at rt for 24 h. The reaction is concentrated in vacuo, and H2O (40 mL) is added to dissolve the residue. The resulting solution is acidified to pH 4 using concentrated HCl, and the precipitate is isolated by filtration, yielding thieno[2,3-b]pyridine-2-carboxylic acid (C102) as a white powder (85% yield). MS (EI) for C8H5NO2S, M/z: 179 (M)+.
85% With hydrogenchloride; sodium hydroxide; In methanol; water; C101 (0.700 g, 3.63 mmol) is dissolved in MeOH (15 mL) and 3 mL water. 2N NaOH (1.82 mL, 3.63 mmol) is added drop-wise, and the reaction is stirred at rt for 24 h. The reaction is concentrated in vacuo, and water (40 mL) is added to dissolve the residue. The resulting solution is acidified to pH 4 using concentrated HCl, and the precipitate is isolated by filtration, yielding thieno[2,3-b]pyridine-2-carboxylic acid (C102) as a white powder (85% yield). MS (EI) for C8H5NO2S, m/z: 179 (M)+.
78% With water; sodium hydroxide; In methanol; at 20℃; for 5h; Thieno[2,3-b]pyridine-2-carboxylic acid (147-C). To a solution of compound 147-B (0.508 g, 2.63 mmol) in a mixture of MeOH (15 mL) and H2O (3 mL) was added 3N NaOH (1.9 mL, 5.66 mmol) and the reaction mixture was stirred at ambient temperature for 5 h. The solvent was evaporated under reduced pressure, the residue dissolved in H2O, and acidified with 1N HCl. The precipitate was filtered, washed with H2O, and dried under vacuum to afford compound 147-C as a white solid (0.366 g, 78%). MS: m/z 180.0 (MH+).
  • 2
  • [ 154650-88-1 ]
  • [ 53174-98-4 ]
 

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