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Chemical Structure| 108831-68-1 Chemical Structure| 108831-68-1

Structure of 108831-68-1

Chemical Structure| 108831-68-1

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Product Details of [ 108831-68-1 ]

CAS No. :108831-68-1
Formula : C8H7ClN2S
M.W : 198.67
SMILES Code : CC1=C(C)C2=C(Cl)N=CN=C2S1
MDL No. :MFCD00464832
InChI Key :HYOBKTVPACQCBR-UHFFFAOYSA-N
Pubchem ID :290212

Safety of [ 108831-68-1 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H319
Precautionary Statements:P305+P351+P338

Application In Synthesis of [ 108831-68-1 ]

* 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 [ 108831-68-1 ]

[ 108831-68-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 18593-44-7 ]
  • [ 108831-68-1 ]
YieldReaction ConditionsOperation in experiment
91% With trichlorophosphate;Reflux; General procedure: The different thieno[2,3-d]pyrimidin-4-one (6a-d or f-i) (1 eq.) and phosphoryl chloride (2.9 mL/mmoleq.) were refluxed for 8 h. The reaction mixture was then cooled in an ice-bath and carefully neutralised by the addition of aqueous saturated NaHCO3 solution. The resulting mixture was extracted with ethylacetate (15 mL/mmol eq.), the organic layer was separated, dried over MgSO4 and concentrated. The crude residue was purified by flash column chromatography eluting with n-hexane-EtOAc 100:0 v/vincreasing to n-hexane-EtOAc 85:15 v/v unless otherwise stated.
90.6% With thionyl chloride; In N,N-dimethyl-formamide; for 3.0h;Reflux; Take 1.8g (0.01mol) 5,6- dimethyl-thieno [2,3-d] pyrimidin -4 (3H) - one in 10ml of thionyl chloride, was added one drop of dimethyl formamide (DMF) was heated at reflux for 3 hours, monitored by TLC after completion of the reaction, the solvent was distilled off under reduced pressure to give a dark gray solid 1.8g, 90.6% yield, m.p. 112-113 .
80% With phosphorus pentachloride; trichlorophosphate; at 105℃; General procedure: A mixture of thienopyrimidinone (0.01 mol), POCl3 (11 mL) and PCl5 (1.5 g) was quickly heated to 105 C and boiled for 5-6 h. The solvent was evaporated. Dry product was dissolved in methylene chloride (12 mL) and neutralized by cold solution of NaOH (0.5 N). The organic phase was separated and dried over Na2SO4, filtered, and then solvent was evaporated in vacuum. The residue was crystallized from isopropyl alcohol. Yield 80%
 

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