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Chemical Structure| 13515-65-6 Chemical Structure| 13515-65-6

Structure of 13515-65-6

Chemical Structure| 13515-65-6

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Product Details of [ 13515-65-6 ]

CAS No. :13515-65-6
Formula : C4H9NS
M.W : 103.19
SMILES Code : CC(C)C(N)=S
MDL No. :MFCD07369538
InChI Key :NPCLRBQYESMUPD-UHFFFAOYSA-N
Pubchem ID :10909507

Safety of [ 13515-65-6 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 13515-65-6 ]

* 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 [ 13515-65-6 ]

[ 13515-65-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 13515-65-6 ]
  • [ 33142-21-1 ]
  • [ 62657-87-8 ]
  • 2
  • [ 13515-65-6 ]
  • [ 33142-21-1 ]
  • [ 165315-75-3 ]
YieldReaction ConditionsOperation in experiment
17% With magnesium sulfate; In ethanol; at 20℃; for 24h;Inert atmosphere; Reflux; [000241] Synthesis of ethyl 2-isopropylthiazole-5-carboxylate (294): To a stirred solution of compound 286 (3.05 g) in ethanol (60 mL) under argon atmosphere were added 2-methylpropanethioamide 293 (1.5 g, 14.56 mmol), dry magnesium sulfate (5 g) at RT and heated to reflux for 24 h. The reaction was monitored by TLC; after completion of the reaction, the volatiles were removed in vacuo. The residue was diluted with saturated sodium bicarbonate solution (100 mL), extracted with EtOAc (3 x 100 mL). The combined organic extracts were dried over sodium sulfate, filtered and concentrated in vacuo to obtain the crude. The crude was purified through flash column chromatography using 2% EtOAc/ hexanes to afford compound 294 (550 mg, 17%) as brown syrup. TLC: 10% EtOAc/ hexanes (R 0.5); 1H NMR (500 MHz, DMSO-d6) oe 8.31 (s, 1H), 4.30 (q, J= 7.0 Hz, 2H), 3.36-3.29 (m, 1H), 1.34 (d, J 6.9 Hz, 6H), 1.29 (t,J 7.1 Hz, 3H).
With magnesium sulfate; In ethanol; at 85℃; for 12h; Compound BB-4-1 (2.90 g, 19.26 mmol), BB-4-2 (1.45 g, 14.06 mmol) and MgSO4 (4.82 g, 40.06 mmol) were dissolved in ethanol (30 mL). The reaction mixture was heated to 85C and stirred for 12 hours. The reaction was quenched with saturated aqueous solution of sodium carbonate (30 mL), then the mixture was extracted with ethyl acetate (20 mL*3). The organic phases were combined, washed with saturated aqueous solution of sodium chloride (10 mL*2), and dried over anhydrous sodium sulfate, followed by filtration and removal of the solvent by evaporation under reduced pressure. The crude product was isolated by column chromatography to give BB-4-3. 1H NMR (400MHz, DMSO-d6) delta = 8.30 (s, 1H), 4.29 (q, J=7.2 Hz, 2H), 3.32 - 3.26 (m, 1H), 1.34 (d, J=6.9 Hz, 6H), 1.28 (t, J=7.1 Hz, 3H).
 

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