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Chemical Structure| 76872-68-9 Chemical Structure| 76872-68-9

Structure of 76872-68-9

Chemical Structure| 76872-68-9

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Product Details of [ 76872-68-9 ]

CAS No. :76872-68-9
Formula : C7H7ClN2S
M.W : 186.66
SMILES Code : CC(S1)=CC2=C1CN=C(Cl)N2

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Application In Synthesis of [ 76872-68-9 ]

* 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 [ 76872-68-9 ]

[ 76872-68-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 35265-82-8 ]
  • [ 76872-68-9 ]
YieldReaction ConditionsOperation in experiment
88% With sodium tetrahydroborate; ethanol; In tetrahydrofuran; at 0 - 20℃; for 16.0h; 2,4-Dichloro-6-methylthieno[3,2-d]pyrimidine (10 g, 45.6 mmol) was dissolved in a mixed solution of tetrahydrofuran(100 mL) and ethanol (100 mL), the reaction solution was cooled to 0C, sodium borohydride (12.5 g, 198mmol) was added in batches. The reaction mixture was allowed to warm to room temperature and stirring was continuedfor 16 hours. The reaction mixture was diluted with water (500 mL) and then the pH was adjusted to 7 with 1 N aqueoushydrochloric acid solution. The aqueous phase was extracted with ethyl acetate (150 mL 3 3). The organic phase waswashed successively with water (100 mL x 3) and brine (100 mL), dried over anhydrous sodium sulfate, filtered and thefiltrate was concentrated under reduced pressure to delivera white solid45-e (7.5g, yield: 88%). This product was usedwithout further purification. LC-MS (ESI): m/z = 187 [M+H]+.
With sodium tetrahydroborate; ethanol; In tetrahydrofuran; at 0 - 20℃; for 16.0h; 2,4-Dichloro-6-methylthieno[3,2-d]pyrimidine (10 g, 45.6 mmol) was dissolved in tetrahydrofuran (100 mL) and ethanol (100 mL). The reaction solution was cooled to 0 C. and sodium borohydride (12.5 g, 198 mmol) was added in portions. The reaction solution was warmed to room temperature and stirred for further 16 hours, then diluted with water (500 mL) and adjusted to pH=7 with 1N aqueous hydrochloric acid solution. The aqueous phase was extracted with ethyl acetate (150 mL*3). The organic phase was washed with water (100 mL*3) and brine (100 mL) successively, dried over anhydrous sodium sulfate, filtered and the filtrate was concentrated under reduced pressure to give 31-e as a white solid (7.5 g, yield 88%) which was used without further purification. LC-MS (ESI): m/z=187[M+H]+.
 

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