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Chemical Structure| 876191-56-9 Chemical Structure| 876191-56-9

Structure of 876191-56-9

Chemical Structure| 876191-56-9

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Product Details of [ 876191-56-9 ]

CAS No. :876191-56-9
Formula : C9H14N2O2S
M.W : 214.29
SMILES Code : O=C(OC(C)(C)C)NC1=CSN=C1C
MDL No. :MFCD11499025

Safety of [ 876191-56-9 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of [ 876191-56-9 ]

* 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 [ 876191-56-9 ]

[ 876191-56-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 15903-66-9 ]
  • [ 75-65-0 ]
  • [ 876191-56-9 ]
YieldReaction ConditionsOperation in experiment
97% With diphenylphosphoranyl azide; triethylamine;Heating / reflux; To a solution of <strong>[15903-66-9]3-methyl-isothiazole-4-carboxylic acid</strong> (method 33) (14.8 g, 103 mmol) in anhydrous t-BuOH (100 mL) triethyl amine (10.5 g, 104 mmol) was added followed by the dropwise addition of diphenylphosphoryl azide (28.6 g, 104 mmol) and the resulting mixture was heated at reflux overnight after which the TLC showed the complete disappearance of the starting material. The reaction mixture was cooled to room temperature and poured into ice cold water (500 mL). The aqueous layer was extracted with ether (3*100 mL) and the combined organic layers were washed with satd, NaHCO3 (100 mL), brine (100 mL) and dried (Na2SO4). Concentration of the ether solution provided the crude product, which was purified by column chromatography to get the pure product as light brown crystals. Yield 21.4 g (97%). Having the following properties 1H NMR (300 MHz) δ 1.53 (s, 9H), 2.40 (s, 3H), 6.50 (s, 1H), 8.66 (s, 1H).
74% With diphenyl phosphoryl azide; N-ethyl-N,N-diisopropylamine; at 90℃; for 12h;Inert atmosphere; To a solution of <strong>[15903-66-9]3-methyl-1,2-thiazole-4-carboxylic acid</strong> (390 mg, 2.72 mmol) in tert- butanol (20 ml) under N2 were added DPPA (750 mg, 2.72 mmol) and DIPEA (0.71 ml, 4.09 mmol). The RM was heated at 90 C for 12 h. The solution was concentrated under reduced and the resulting residue purified by column chromatography (silica, 9- 17 % EtOAc in petrol) to give the title compound as a yellow solid. Y = 74 %. LCMS (ESI): m/z: [M+H]+ = 215.0.
 

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