Basic information Uses Safety Supplier Related
ChemicalBook >  Product Catalog >  Pharmaceutical intermediates >  Heterocyclic compound >  Pyrimidines >  Thiophene pyrimidine >  2,4-dichloro-6,7-dihydrothieno[3,2-d]pyrimidine

2,4-dichloro-6,7-dihydrothieno[3,2-d]pyrimidine

Basic information Uses Safety Supplier Related

2,4-dichloro-6,7-dihydrothieno[3,2-d]pyrimidine Basic information

Product Name:
2,4-dichloro-6,7-dihydrothieno[3,2-d]pyrimidine
Synonyms:
  • 2,4-dichloro-6,7-dihydrothieno[3,2-d]pyrimidine
  • 2,4-Dichloro-6,7-dihyrothieno[3,2-d]pyrimidine
  • 7-dihydrothieno[3
  • tert-butyl 3-BroMo-6
  • 2,4-Dichloro-6,7-dihydro-thieno[3,2-
  • 2,4-dichloro-6H,7H-thieno[3,2-d]pyrimidine
  • 2,4-Dichloro-6,7-dihydrothieno[3,2-d]pyrimidi...
  • Thieno[3,2-d]pyrimidine, 2,4-dichloro-6,7-dihydro-
CAS:
74901-69-2
MF:
C6H4Cl2N2S
MW:
207.08
Product Categories:
  • Heterocycle-Pyrimidine series
  • CHIRAL CHEMICALS
Mol File:
74901-69-2.mol
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2,4-dichloro-6,7-dihydrothieno[3,2-d]pyrimidine Chemical Properties

Boiling point:
329.4±42.0 °C(Predicted)
Density 
1.613±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
-2.53±0.20(Predicted)
Appearance
Off-white to light yellow Solid
InChI
InChI=1S/C6H4Cl2N2S/c7-5-4-3(1-2-11-4)9-6(8)10-5/h1-2H2
InChIKey
CUVQFHMQHBMFCI-UHFFFAOYSA-N
SMILES
C1(Cl)=NC(Cl)=C2SCCC2=N1
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22-36
Safety Statements 
26
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2,4-dichloro-6,7-dihydrothieno[3,2-d]pyrimidine Usage And Synthesis

Uses

2,4-Dichloro-6,7-dihydrothiophene[3,2-D]pyrimidine is a pyrimidine organic compound that can be used as a pharmaceutical intermediate.

Synthesis

913581-92-7

74901-69-2

General procedure for the synthesis of 2,4-dichloro-6,7-dihydrothieno[3,2-d]pyrimidine (VII) from 6,7-dihydrothieno[3,2-d]pyrimidine-2,4-diol (VI): 2.4 g (14.1 mmol) of 6,7-dihydrothieno[3,2-d]pyrimidine-2,4-diol (VI) was suspended in 14 mL of phosphorus oxychloride and added with 4.5 mL (28.2 mmol) of diethylaniline and the mixture was stirred at 80 °C for 22 hours. Upon completion of the reaction, it was cooled to room temperature and the reaction mixture was slowly poured into ice water, the precipitate formed was collected by filtration and washed with cold water. The resulting precipitate was dissolved in dichloromethane and the water was removed by a phase separator. The organic phase was concentrated to dryness under reduced pressure to give 2.5 g of the target product VII in 85% yield.

References

[1] Organic Process Research and Development, 2016, vol. 20, # 5, p. 982 - 988
[2] Patent: WO2006/111549, 2006, A1. Location in patent: Page/Page column 61; 59; 65; 68; 69; 72; 74; 76; 84
[3] Patent: US2007/259846, 2007, A1. Location in patent: Page/Page column 30; 31
[4] Patent: WO2013/26797, 2013, A1. Location in patent: Page/Page column 24-25
[5] Patent: US2013/150341, 2013, A1. Location in patent: Paragraph 0364; 0365; 0366; 0367

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