(2S)-1-(Chloroacetyl)-2-pyrrolidinecarbonitrile CAS#207557-35-5

1.Key Pharmaceutical Intermediate: (2S)-1-(Chloroacetyl)-2-pyrrolidinecarbonitrile is an important chemical building block widely used as a core intermediate in pharmaceutical synthesis.

2.Essential Raw Material for Vildagliptin Production: It serves as a key starting material for the manufacture of Vildagliptin, a prescription drug used in the treatment of Type 2 diabetes.

3.High Purity Solid Form: The product is available as a white to light-yellow solid, offering consistent physical characteristics for chemical processing and synthesis applications.

4.Valuable Role in Drug Development: With its specific molecular structure, it provides an effective foundation for constructing pharmaceutical compounds and supporting advanced medicinal chemistry research.

Product Description

(2S)-1-(Chloroacetyl)-2-pyrrolidinecarbonitrile (CAS#207557-35-5) is an important chemical building block used in pharmaceutical synthesis. It appears as a white to light-yellow solid and is mainly utilized as a key raw material for the production of Vildagliptin, a prescription drug indicated for the treatment of Type 2 diabetes.

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Properties

Melting point 52-53 °C
Boiling point 363.1±37.0 °C(Predicted)
density 1.27±0.1 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
solubility Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly)
form Solid
pka-4.65±0.40(Predicted)
color Pale Yellow to Light Brown
Stability:Hygroscopic
HS Code 2933998090

Product Application

(2S)-1-(Chloroacetyl)-2-pyrrolidinecarbonitrile, also known as (2S)-N-chloroacetyl-2-cyanotetrahydropyrrole, is a key synthetic intermediate of Vildagliptin and is primarily used in the preparation of this pharmaceutical compound.

In the synthesis process, L-prolinamide is used as the starting material, with THF as the solvent and K₂CO₃ as an acid-binding agent to perform a chloroacetylation reaction, producing (S)-1-(2-chloroacetyl)-2-pyrrolidine carboxamide. The amide group is then converted into a nitrile group through a dehydration cyanation reaction using TFAA, resulting in the intermediate (2S)-N-chloroacetyl-2-cyanotetrahydropyrrole.

Subsequently, DCM is used as the solvent, K₂CO₃ serves as the acid-binding agent, and the intermediate undergoes a condensation reaction with 3-amino-1-adamantanol. After purification by column chromatography, Vildagliptin is obtained.

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