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90914-41-3

90914-41-3 Structure

90914-41-3 Structure
IdentificationBack Directory
[Name]

3-BROMO-4-CHLORO-1H-PYRAZOLO[3,4-D]PYRIMIDINE
[CAS]

90914-41-3
[Synonyms]

3-broMo-4-chloropyrazolo<3,4-d>pyriMidine
3-bromo-4-chloro-2H-pyrazolo[3,4-d]pyrimidine
3-BROMO-4-CHLORO-1H-PYRAZOLO[3,4-D]PYRIMIDINE
1H-Pyrazolo[3,4-d]pyriMidine, 3-broMo-4-chloro-
3-BROMO-4-CHLORO-1H-PYRAZOLO[3,4-D]PYRIMIDINE ISO 9001:2015 REACH
[Molecular Formula]

C5H2BrClN4
[MDL Number]

MFCD08276165
[MOL File]

90914-41-3.mol
[Molecular Weight]

233.45
Chemical PropertiesBack Directory
[Boiling point ]

270.3±50.0 °C(Predicted)
[density ]

2.41±0.1 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
[pka]

8.36±0.20(Predicted)
[Appearance]

Light yellow to yellow Solid
[InChI]

InChI=1S/C5H2BrClN4/c6-3-2-4(7)8-1-9-5(2)11-10-3/h1H,(H,8,9,10,11)
[InChIKey]

MDFHFCAMBZNSLV-UHFFFAOYSA-N
[SMILES]

C1=NC(Cl)=C2C(Br)=NNC2=N1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H332-H312-H302-H315-H319-H335
[Precautionary statements ]

P261-P271-P304+P340-P312-P264-P270-P301+P312-P330-P501-P280-P302+P352-P312-P322-P363-P501-P264-P280-P302+P352-P321-P332+P313-P362-P264-P280-P305+P351+P338-P337+P313P
[Hazard Codes ]

T
[Risk Statements ]

25
[Safety Statements ]

45
[RIDADR ]

UN2811
[HazardClass ]

IRRITANT
[HS Code ]

2933199090
Spectrum DetailBack Directory
[Spectrum Detail]

3-BROMO-4-CHLORO-1H-PYRAZOLO[3,4-D]PYRIMIDINE(90914-41-3)1HNMR
Hazard InformationBack Directory
[Synthesis]

4-Chloro-1H-pyrazolo[3,4-d]pyrimidine

5399-92-8

3-BROMO-4-CHLORO-1H-PYRAZOLO[3,4-D]PYRIMIDINE

90914-41-3

4-Chloro-1H-pyrazolo[3,4-d]pyrimidine (1.1 g, 7.1 mmol) was used as starting material and suspended in CHCl3 (50 mL). N-bromosuccinimide (NBS, 1.49 g, 8.4 mmol) was added to the suspension under stirring. The reaction mixture was stirred at room temperature for 5 h and subsequently cooled to 0°C. The resulting solid product was separated by vacuum filtration and washed with cold CHCl3. The solid product was dried over air and further purified by silica gel column chromatography (eluent: 50% EtOAc/hexanes) to afford finally 3-bromo-4-chloro-1H-pyrazolo[3,4-d]pyrimidine (1.3 g, 77% yield).

[References]

[1] Organic Letters, 2003, vol. 5, # 20, p. 3587 - 3590
[2] Patent: WO2005/51304, 2005, A2. Location in patent: Page/Page column 115-116
[3] Patent: WO2005/51304, 2005, A2. Location in patent: Page/Page column 115-116
[4] MedChemComm, 2018, vol. 9, # 8, p. 1340 - 1350
[5] Patent: WO2016/187723, 2016, A1. Location in patent: Page/Page column 51
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