Basic information Safety Supplier Related

5-chloro-3-methylsulfanyl-2,4,9-triazabicyclo[4.3.0]nona-2,4,7,10-tetraene

Basic information Safety Supplier Related

5-chloro-3-methylsulfanyl-2,4,9-triazabicyclo[4.3.0]nona-2,4,7,10-tetraene Basic information

Product Name:
5-chloro-3-methylsulfanyl-2,4,9-triazabicyclo[4.3.0]nona-2,4,7,10-tetraene
Synonyms:
  • 5-chloro-3-methylsulfanyl-2,4,9-triazabicyclo[4.3.0]nona-2,4,7,10-tetraene
  • 4-chloro-7H-pyrrolo[2,3-d]pyrimidin-5-amine
  • 7H-Pyrrolo[2,3-D]pyrimidine, 4-chloro-2-(methylthio)-
  • Inchi=1/C7H6cln3S/C1-12-7-10-5(8)4-2-3-9-6(4)11-7/H2-3H,1H3,(H,9,10,11
  • 4-Chloro-2-methylsulfanyl-7H-pyrrolo[2,3-d]pyrimidine
  • 4-chloro-2-(Methylthio)-7H-pyrrolo[2
  • 4-Chloro-2-(Methylthio)-7H-pyrrolo[2,3-D]pyriMidin
  • 2-(Methylthio)-4-chloropyrrolo<2,3-d>pyriMidine
CAS:
57564-94-0
MF:
C7H6ClN3S
MW:
199.66
Product Categories:
  • Heterocycle-Pyrimidine series
  • CHIRAL CHEMICALS
Mol File:
57564-94-0.mol
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5-chloro-3-methylsulfanyl-2,4,9-triazabicyclo[4.3.0]nona-2,4,7,10-tetraene Chemical Properties

Boiling point:
342.1±52.0 °C(Predicted)
Density 
1.59
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
pka
10.01±0.20(Predicted)
Appearance
Off-white to light yellow Solid
InChI
InChI=1S/C7H6ClN3S/c1-12-7-10-5(8)4-2-3-9-6(4)11-7/h2-3H,1H3,(H,9,10,11)
InChIKey
WEGGBXZHIWVHOI-UHFFFAOYSA-N
SMILES
C1(SC)=NC(Cl)=C2C=CNC2=N1
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Safety Information

Hazard Codes 
T
Risk Statements 
25
Safety Statements 
45
RIDADR 
2811
WGK Germany 
3
HazardClass 
6.1
PackingGroup 
HS Code 
2933998090
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5-chloro-3-methylsulfanyl-2,4,9-triazabicyclo[4.3.0]nona-2,4,7,10-tetraene Usage And Synthesis

Synthesis

67831-83-8

57564-94-0

General procedure for the synthesis of 4-chloro-2-(methylthio)-7H-pyrrolo[2,3-d]pyrimidines from 2-methylthio-4-hydroxy-7H-pyrrolo[2,3-d]pyrimidines: triclosan (5 mL, 53.7 mmol) and triethylamine (0.2 mL, 1.43 mmol) were added to 2-methylthio-7H-pyrrolo[2,3-d]pyrimidin-4-yl alcohol (0.10 g, 0.55 mmol). The reaction mixture was heated to reflux at 130 °C for 4 h and subsequently cooled to room temperature. Excess trichlorophosphate was removed by distillation under reduced pressure. Ice water was carefully added to the residue and the suspension was extracted with ether (3 x 20 mL). The organic phases were combined, washed with distilled water (10 mL), dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The crude product was purified by column chromatography (Florisil, 100-200 mesh), using diethyl ether as eluent, to give the pure 4-chloro-2-methylthio-7H-pyrrolo[2,3-d]pyrimidine in 77% yield (literature value 43%). Melting point: 207-209°C. 1H NMR (CDCl3): δ 2.67 (s, 3H, SCH3), 6.56-6.59 (m, 1H, H-5), 7.21-7.23 (m, 1H, H-6). IR (KBr) cm-1: 3412 (NH), 3122 (CH), 1614 (C=C). Mass Spectrometry (MS): m/z [M+1]+ 201. Calculated values for elemental analysis (C7H6N3ClS): C 42.11, H 3.03, N 21.05, S 16.06; measured values: C 42.29, H 3.38, N 21.14, S 16.36.

References

[1] Bioorganic and Medicinal Chemistry, 2012, vol. 20, # 22, p. 6770 - 6789
[2] European Journal of Medicinal Chemistry, 2017, vol. 127, p. 369 - 378

5-chloro-3-methylsulfanyl-2,4,9-triazabicyclo[4.3.0]nona-2,4,7,10-tetraeneSupplier

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