2-氨基吡唑并[1,5-a]嘧啶-3-羧酸乙酯

2-氨基吡唑并[1,5-a]嘧啶-3-羧酸乙酯 - Names and Identifiers

Name	ethyl 2-aminopyrazolo[1,5-a]pyrimidine-3-carboxylate
Synonyms	ethyl 2-aminopyrazolo[1,5-a]pyrimidine-3-carboxylate 2-Aminopyrazolo[1,5-a]pyrimidine-3-carboxylic acid ethyl ester Pyrazolo[1,5-a]pyrimidine-3-carboxylic acid, 2-amino-, ethyl ester
CAS	1260169-02-5

2-氨基吡唑并[1,5-a]嘧啶-3-羧酸乙酯 - Physico-chemical Properties

Molecular Formula	C9H10N4O2
Molar Mass	206.2013
Storage Condition	under inert gas (nitrogen or Argon) at 2–8 °C

2-氨基吡唑并[1,5-a]嘧啶-3-羧酸乙酯 - Introduction

ethyl 2-aminopyrazolo[1,5-a]pyrimidine-3-carboxylate is an organic compound with the chemical formula C9H8N4O2.

The compound has the following properties:
-Appearance: Colorless or light yellow solid
-Melting point: approximately 118-120 ° C
-Solubility: Soluble in most common organic solvents, such as ethanol, dichloromethane and dimethyl sulfoxide

ethyl 2-aminopyrazolo[1,5-a]pyrimidine-3-carboxylate has certain applications in the field of drug research:
-Drug activity: As a drug precursor, it can be used to synthesize biologically active compounds, such as anti-inflammatory drugs, anti-tumor drugs, etc.
-Antibacterial activity: Studies have shown that the compound has certain antibacterial activity and has an inhibitory effect on the growth of certain bacteria.

The preparation method of the compound generally includes the following steps:
1. Synthesis of pyrazolo [1,5-a] Pyrimidine structure: Pyrazole and pyrimidine groups are connected through a series of organic synthesis reactions.
2. Amination reaction: by reacting the synthesized pyrazolo [1,5-a] Pyrimidine structure with an amination reagent, an amino group is introduced.
3. Carboxylation reaction: Finally, the carboxylation reagent reacts with the amination product to introduce carboxylic acid groups and generate ethyl 2-aminopyrazolo[1,5-a]pyrimidine-3-carboxylate.

Safety information about this compound, according to laboratory conditions and use, should follow general chemical safety procedures, such as wearing laboratory safety equipment (such as gloves, goggles, etc.), avoid inhalation, contact with skin, or swallowing. When handling this compound, refer to the relevant safety data sheet for detailed safety information. At the same time, please store the compound in an airtight container, away from fire and oxidizing agents, and avoid direct sunlight.

Last Update：2024-04-09 21:11:58