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4-(1H-Pyrazol-4-yl)-7-[[2-(trimethylsilyl)ethoxy]methyl]-7H-pyrrolo[2,3-d]pyrimidine
[CAS# 941685-27-4]

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Identification
Classification Pharmaceutical intermediate >> Heterocyclic compound intermediate >> Pyrimidine compound
Name 4-(1H-Pyrazol-4-yl)-7-[[2-(trimethylsilyl)ethoxy]methyl]-7H-pyrrolo[2,3-d]pyrimidine
Synonyms 4-(7-{[2-(trimethylsilyl)ethoxy]methyl}-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazole
Molecular Structure CAS # 941685-27-4, 4-(1H-Pyrazol-4-yl)-7-[[2-(trimethylsilyl)ethoxy]methyl]-7H-pyrrolo[2,3-d]pyrimidine, 4-(7-{[2-(trimethylsilyl)ethoxy]methyl}-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazole
Molecular Formula C15H21N5OSi
Molecular Weight 315.45
CAS Registry Number 941685-27-4
EC Number 801-232-2
SMILES C[Si](C)(C)CCOCN1C=CC2=C(N=CN=C21)C3=CNN=C3
Properties
Solubility Insoluble (1.0E-3 g/L) (25 ºC), Calc.*
Density 1.20±0.1 g/cm3 (20 ºC 760 Torr), Calc.*
Index of Refraction 1.607, Calc.*
Boiling Point 501.8±50.0 ºC (760 mmHg), Calc.*
Flash Point 257.3±30.1 ºC, Calc.*
* Calculated using Advanced Chemistry Development (ACD/Labs) Software.
Safety Data
Hazard Symbols symbol   GHS07 Warning    Details
Hazard Statements H302    Details
Precautionary Statements P280-P305+P351+P338    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Acute toxicityAcute Tox.4H302
Acute toxicityAcute Tox.4H332
Acute toxicityAcute Tox.4H312
SDS Available
up Discovory and Applicatios
4-(1H-Pyrazol-4-yl)-7-[[2-(trimethylsilyl)ethoxy]methyl]-7H-pyrrolo[2,3-d]pyrimidine is a complex organic compound that belongs to the class of pyrrolo[2,3-d]pyrimidine derivatives. This compound consists of several functional groups, including a pyrazole ring, a pyrrolo[2,3-d]pyrimidine structure, and a trimethylsilyl group. These structural features contribute to its unique chemical properties, which have been explored in the context of drug development and chemical synthesis.

The synthesis of 4-(1H-Pyrazol-4-yl)-7-[[2-(trimethylsilyl)ethoxy]methyl]-7H-pyrrolo[2,3-d]pyrimidine is typically achieved through various organic reactions that involve the construction of the pyrimidine core, pyrazole ring, and the introduction of the trimethylsilyl group. These methods ensure that the compound is synthesized in a controlled and efficient manner, making it accessible for use in various chemical applications.

This compound has gained attention for its potential application in medicinal chemistry. The pyrrolo[2,3-d]pyrimidine structure is known to possess bioactivity, particularly in the development of small molecule inhibitors that can target specific enzymes and proteins. The presence of the pyrazole group and the trimethylsilyl ether can influence the compound’s ability to interact with biological targets, enhancing its potential as a therapeutic agent. Although specific applications in drug development are still under investigation, pyrrolo[2,3-d]pyrimidine derivatives have been shown to exhibit properties that could be useful in treating a variety of diseases, particularly cancers and neurodegenerative disorders.

Additionally, the trimethylsilyl group in the structure plays a critical role in improving the compound’s solubility and stability, which are essential factors for its bioavailability and efficacy in pharmaceutical formulations. This functional group also contributes to the compound’s ability to cross biological membranes, which is a crucial characteristic for drugs designed to act within living organisms.

The use of 4-(1H-Pyrazol-4-yl)-7-[[2-(trimethylsilyl)ethoxy]methyl]-7H-pyrrolo[2,3-d]pyrimidine in material science is another potential application. Its structural features, particularly the ability of the pyrazole and pyrimidine rings to interact with different materials, open up possibilities for the development of new functional materials, such as molecular sensors or catalysts.

Overall, 4-(1H-Pyrazol-4-yl)-7-[[2-(trimethylsilyl)ethoxy]methyl]-7H-pyrrolo[2,3-d]pyrimidine is a promising compound with potential applications in medicinal chemistry, material science, and other areas. Its structural characteristics and bioactivity make it a subject of ongoing research, with its applications likely to expand as further studies are conducted. The compound’s functional groups contribute to its versatility, making it a valuable candidate for drug development and other industrial applications.
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