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ChemicalBook--->CAS DataBase List--->98141-42-5

98141-42-5

98141-42-5 Structure

98141-42-5 Structure
IdentificationBack Directory
[Name]

4,6-dichloro-1-methyl-1H-pyrazolo[3,4-d]pyrimidine
[CAS]

98141-42-5
[Synonyms]

4,6-Dichloro-1-Methyl-1H-...
4,6-Dichloro-1-methyl-pyrazolo3,4-dpyrimidine
4,6-dichloro-1-methyl-1H-pyrazolo[3,4-d]pyrimidine
1H-Pyrazolo[3,4-d]pyriMidine, 4,6-dichloro-1-Methyl-
[Molecular Formula]

C6H4Cl2N4
[MDL Number]

MFCD09750213
[MOL File]

98141-42-5.mol
[Molecular Weight]

203.03
Chemical PropertiesBack Directory
[Boiling point ]

284℃
[density ]

1.76
[Fp ]

125℃
[storage temp. ]

Inert atmosphere,2-8°C
[pka]

-0.19±0.10(Predicted)
[Appearance]

Light yellow to light brown Solid
[InChI]

InChI=1S/C6H4Cl2N4/c1-12-5-3(2-9-12)4(7)10-6(8)11-5/h2H,1H3
[InChIKey]

TYMWHTJGWKSXRY-UHFFFAOYSA-N
[SMILES]

C1(Cl)=NC(Cl)=C2C=NN(C)C2=N1
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
[Hazard Codes ]

T
[Risk Statements ]

25
[Safety Statements ]

45
[RIDADR ]

UN2811
[HS Code ]

2933599590
Spectrum DetailBack Directory
[Spectrum Detail]

4,6-dichloro-1-methyl-1H-pyrazolo[3,4-d]pyrimidine(98141-42-5)1HNMR
Hazard InformationBack Directory
[Synthesis]

4,6-dichloro-1-methyl-1H-pyrazolo[3,4-d]pyrimidine is prepared by the reaction of Methylhydrazine and 2,4,6-trichloropyrimidine-5-carbaldehyde. The specific synthesis steps are as follows:
To a solution of 2,4,6-trichloropyrimidine-5-carbaldehyde (8 g, 37.84 mmol, 1.00 equiv) in ethanol (120 mL) was added a 40percent water solution of methylhydrazine (4 mL, 37.98 mmol, 1.00 equiv) and triethylamine (16 mL) at -78° C. The resulting mixture was stirred for 30 min at -78° C. and then 2 h at 0° C. After completion the reaction was concentrated under vacuum without heating. Then ethyl acetate was added and the solution was washed with saturated ammonium chloride solution. The organic layer was dried over anhydrous sodium sulfate and concentrated under vacuum without heating. The residue was purified by silica gel column chromatography eluting with ethyl acetate/petroleum ether (1:1) to afford 6 g (78percent) of 4,6-dichloro-1-methyl-1H-pyrazolo[3,4-d]pyrimidine as a white solid. LC-MS (ES, m/z): 203 [M+H]+.
4,6-dichloro-1-methyl-1H-pyrazolo[3,4-d]pyrimidine synthesis
[References]

[1] Patent: US2015/57260, 2015, A1. Location in patent: Paragraph 0414; 0415
[2] Patent: WO2015/25026, 2015, A1. Location in patent: Page/Page column 114
[3] Patent: WO2017/133664, 2017, A1. Location in patent: Page/Page column 83
[4] Patent: US2008/234262, 2008, A1. Location in patent: Page/Page column 83-84
[5] Patent: US2009/98086, 2009, A1. Location in patent: Page/Page column 59
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