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22276-95-5

22276-95-5 Structure

22276-95-5 Structure
IdentificationBack Directory
[Name]

5-Bromo-4-chloro-7H-pyrrolo[2,3-d]pyrimidine
[CAS]

22276-95-5
[Synonyms]

5-Bromo-4-chloro-7H-pyrro...
5-broMo-4-chloro-7H-pyrrolo[2
7-BroMo-6-chloro-7-deazapurine
4-chloro-5-bromo-7H-pyrrolo[2,3-d]pyrimidine
5-bromo-4-chloro-1H-pyrrolo[2,3-d]pyrimidine
5-Bromo-4-chloro-7H-pyrrolo[2,3-d]pyrimidine
7H-Pyrrolo[2,3-d]pyrimidine, 5-bromo-4-chloro-
5-Bromo-4-chloro-7H-pyrrolo[2,3-D]pyrimidine ,98%
7-bromo-5-chloro-2,4,9-triazabicyclo[4.3.0]nona-2,4,7,10-tetraene
[EINECS(EC#)]

1312995-182-4
[Molecular Formula]

C6H3BrClN3
[MDL Number]

MFCD09702029
[MOL File]

22276-95-5.mol
[Molecular Weight]

232.47
Chemical PropertiesBack Directory
[Melting point ]

221-225℃
[Boiling point ]

221.0±50.0 °C(Predicted)
[density ]

2.15±0.1 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,2-8°C
[form ]

solid
[pka]

9.43±0.20(Predicted)
[color ]

Yellow
[Water Solubility ]

Slightly soluble in water.
[InChI]

InChI=1S/C6H3BrClN3/c7-3-1-9-6-4(3)5(8)10-2-11-6/h1-2H,(H,9,10,11)
[InChIKey]

OXLMTRZWMHIZBY-UHFFFAOYSA-N
[SMILES]

C1=NC(Cl)=C2C(Br)=CNC2=N1
[CAS DataBase Reference]

22276-95-5
Safety DataBack Directory
[Symbol(GHS) ]

Skull and Crossbones (GHS06)
GHS06
[Signal word ]

Danger
[Hazard statements ]

H301
[Precautionary statements ]

P301+P310
[Hazard Codes ]

Xn
[Risk Statements ]

22
[RIDADR ]

2811
[WGK Germany ]

3
[HazardClass ]

6.1
[HazardClass ]

IRRITANT
[PackingGroup ]

[HS Code ]

2933599590
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Hydrochloric acid-->Phosphorus oxitrichloride-->Ethyl cyanoacetate-->N-Bromosuccinimide-->Sodium iodide-->Formamidine acetate-->Chloroacetaldehyde diethyl acetal-->4-Chloro-7H-pyrrolo[2,3-d]pyrimidine-->N,N-Dimethylformamide
[Preparation Products]

4-Chloro-7H-pyrrolo[2,3-d]pyrimidine-5-carbonitrile-->JAK3-IN-6
Hazard InformationBack Directory
[Uses]

It is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff.
[Synthesis]

4-chloro-7H-pyrrolo[2,3-d]pyrimidine (30 g/0.02 mol) was dissolved in 75 mL of chloroform, followed by added 3.5 g (0.02 mol) of N-bromosuccinamide. The resulting mixture was refluxed for 1 h. After cooling to room temperature, the precipitate was removed by filtration and dried under reduced pressure to afford 5-Bromo-4-chloro-7H-pyrrolo[2,3-d]pyrimidine.
5-Bromo-4-chloro-7H-pyrrolo[2,3-d]pyrimidine
[References]

[1] Organic Letters, 2003, vol. 5, # 20, p. 3587 - 3590
[2] Synthesis, 2011, # 9, p. 1442 - 1446
[3] Archiv der Pharmazie, 2016, vol. 349, # 5, p. 356 - 362
[4] European Journal of Medicinal Chemistry, 2017, vol. 138, p. 543 - 551
[5] Patent: CN107556318, 2018, A. Location in patent: Paragraph 0101-0103; 0106; 0107
Spectrum DetailBack Directory
[Spectrum Detail]

5-Bromo-4-chloro-7H-pyrrolo[2,3-d]pyrimidine(22276-95-5)1HNMR
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