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Chemical Structure| 1736-72-7 Chemical Structure| 1736-72-7

Structure of 1736-72-7

Chemical Structure| 1736-72-7

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Product Details of [ 1736-72-7 ]

CAS No. :1736-72-7
Formula : C8H7F3N2S
M.W : 220.22
SMILES Code : NC(=S)NC1=CC=C(C=C1)C(F)(F)F
MDL No. :MFCD00041189

Safety of [ 1736-72-7 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H301
Precautionary Statements:P501-P270-P264-P301+P310+P330-P405
Class:6.1
UN#:2811
Packing Group:

Application In Synthesis of [ 1736-72-7 ]

* 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 [ 1736-72-7 ]

[ 1736-72-7 ] Synthesis Path-Downstream   1~2

  • 2
  • [ 1736-72-7 ]
  • [ 33142-21-1 ]
  • [ 1095824-45-5 ]
YieldReaction ConditionsOperation in experiment
69.63% In ethanol; for 16h;Heating / reflux; A RT solution of V.1 (10 g, 45.45 mmol) in ethanol (100 mL) was treated with V.2 (10.26 g, 68.18 mmol, Plouvier, B.; Bailly, C.; Houssin, R.; Henichart, J. P. Heterocycles 1991, 32, 693-701), and the reaction mixture was heated at reflux for 16 hr. The ethanol solvent was distilled off and the residue was dissolved in EtOAc. The organic layer was washed with sodium bicarbonate solution, water, and brine, dried over anhydrous Na2SO4, filtered, and concentrated under vacuum. Purification by flash column chromatography (SiO2, 100% hexane to 12% EtOAc-Hexane) afforded V.3 as a yellow solid (10 g, 69.63%). 1HNMR (CDCl3, 200 MHz) delta 9.3-9.4 (br s, 1H, D2O exchangeable), 8.0 (s, 1H), 7.6-7.7 (d, 2H), 7.3-7.4 (d, 2H), 4.2-4.4 (q, 2H), 1.3-1.4 (t, 3H); m/z: 317 [M+1].
69.63% In ethanol; at 20℃;Reflux; A room temperature solution of [4- (trifluoromethyl)-phenyl]thiourea (1O g, 45.45 mmol) in ethanol (100 mL) was treated with G.2 (10.26 g, 68.18 mmol, Plouvier, B.; Bailly, C; Houssin, R.; Henichart, J. P. Heterocycles 1991, 32, 693-701), and the reaction mixture was heated at reflux for 16 hr. The ethanol solvent was distilled off and the residue was dissolved in EtOAc. The organic layer was washed with sodium bicarbonate solution, water, and brine, dried over anhydrous Na2SO^ filtered, and concentrated under vacuum. Purification by flash column chromatography (SiO2, 100% hexane to 12% EtOAc/Hexane) afforded compound 189.1 as a yellow solid (1Og, 69.63%). 1H NMR (CDCl3, 200 MHz) delta 9.3-9.4 (br s, 1H, D2O exchangeable), 8.0 ( s, 1H), 7.6-7.7 (d, 2H), 7.3-7.4 (d, 2H), 4.2-4.4 (q, 2H), 1.3-1.4 (m, 3H); LCMS m/z = 317 [M+l].
 

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