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Chemical Structure| 182198-35-2 Chemical Structure| 182198-35-2

Structure of 182198-35-2

Chemical Structure| 182198-35-2

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Product Details of [ 182198-35-2 ]

CAS No. :182198-35-2
Formula : C12H7ClN2S
M.W : 246.72
SMILES Code : ClC1=C(C(C2=CC=CC=C2)=CS3)C3=NC=N1
MDL No. :MFCD00218029

Safety of [ 182198-35-2 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H312-H315-H319-H332-H335
Precautionary Statements:P233-P260-P261-P264-P270-P271-P280-P301+P312-P302+P352-P304-P304+P340-P305+P351+P338-P312-P321-P322-P330-P332+P313-P337+P313-P340-P362-P363-P403-P403+P233-P405-P501

Application In Synthesis of [ 182198-35-2 ]

* 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 [ 182198-35-2 ]

[ 182198-35-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 25602-68-0 ]
  • [ 182198-35-2 ]
  • [ 1437774-75-8 ]
YieldReaction ConditionsOperation in experiment
0.099 g With triethylamine; In ethanol; at 70℃; i) 8-(5-phenylthieno[2,3-d]pyrimidin-4-yl)-8-azabicyclo[3.2.1]octan-3-oneA mixture of 4-chloro-5-phenyl-thieno[2,3-d]pyrimidine (1.00 g, 4.05 mmol), <strong>[25602-68-0]nortropinone hydrochloride</strong> (0.983 g, 6.08 mmol) and triethylamine (1.71 mL, 12.2 mmol) in THF (20 mL) was heated to 70 °C overnight. Ethanol (20 mL) was added and the mixture was heated to 70 °C for 3 hr. Further batches of <strong>[25602-68-0]nortropinone hydrochloride</strong> (0.983 g, 6.08 mmol) and triethylamine (1.71 mL, 12.2 mmol) were added and the mixture was heated to 70 °C overnight. Further batches of <strong>[25602-68-0]nortropinone hydrochloride</strong> (0.983 g, 6.08 mmol) and triethylamine (1.71 mL, 12.2 mmol) were added and the mixture was heated to 70 °C over 3 nights. It was cooled to room temperature and diluted with dichloromethane (40 mL) and water (40 mL). The layers were separated and the aqueous was extracted with dichloromethane (2 x 40 mL). The combined organic layers were washed with brine (1 x 40 mL), filtered through a hydrophobic frit and evaporated to give a brown oil. Mass: 3.21 g. This was purified by silica chromatography (100 g cartridge; eluent petrol / ethyl acetate 0 to 40percent). Fractions corresponding to the main peak were combined and evaporated to give 8-(5- phenylthieno[2,3-d]pyrimidin-4-yl)-8-azabicyclo[3.2.1]octan-3-one as a white solid (0.99 g). LCMS RT = 4.43 min. M+l = 336.
0.99 g With triethylamine; In tetrahydrofuran; ethanol; at 70℃; i) 8-(5-phenylthieno[2,3-d]pyrimidin-4-yl)-8-azabicyclo[3.2.1]octan-3-one A mixture of 4-chloro-5-phenyl-thieno[2,3-d]pyrimidine (1.00 g, 4.05 mmol), <strong>[25602-68-0]nortropinone hydrochloride</strong> (0.983 g, 6.08 mmol) and triethylamine (1.71 mL, 12.2 mmol) in THF (20 mL) was heated to 70° C. overnight. Ethanol (20 mL) was added and the mixture was heated to 70° C. for 3 hr. Further batches of <strong>[25602-68-0]nortropinone hydrochloride</strong> (0.983 g, 6.08 mmol) and triethylamine (1.71 mL, 12.2 mmol) were added and the mixture was heated to 70° C. overnight. Further batches of <strong>[25602-68-0]nortropinone hydrochloride</strong> (0.983 g, 6.08 mmol) and triethylamine (1.71 mL, 12.2 mmol) were added and the mixture was heated to 70° C. over 3 nights. It was cooled to room temperature and diluted with dichloromethane (40 mL) and water (40 mL). The layers were separated and the aqueous was extracted with dichloromethane (2*40 mL). The combined organic layers were washed with brine (1*40 mL), filtered through a hydrophobic frit and evaporated to give a brown oil. Mass: 3.21 g. This was purified by silica chromatography (100 g cartridge; eluent petrol/ethyl acetate 0 to 40percent). Fractions corresponding to the main peak were combined and evaporated to give 8-(5-phenylthieno[2,3-d]pyrimidin-4-yl)-8-azabicyclo[3.2.1]octan-3-one as a white solid (0.99 g). LCMS RT=4.43 min. M+1=336. The following compounds were synthesised according to the method described using the appropriate starting materials: 1-(5-phenylthieno[2,3-d]pyrimidin-4-yl)piperidin-4-one
  • 2
  • [ 25602-68-0 ]
  • [ 182198-35-2 ]
  • [ 1437773-66-4 ]
 

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