(2S)-1-(Chloroacetyl)-2-pyrrolidinecarbonitrile

Product Name:(2S)-1-(Chloroacetyl)-2-pyrrolidinecarbonitrile
CAS:207557-35-5
MFC7H9ClN2O
MW:172.61
EINECS:807-388-8
MOL File:207557-35-5.mol

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User Guide: (2S)-1-(Chloroacetyl)-2-pyrrolidinecarbonitrile – Applications, Case Studies & Technical Insights

1. Product Overview & Specifications

(2S)-1-(Chloroacetyl)-2-pyrrolidinecarbonitrile (CAS 126059-85-4) is a chiral pyrrolidine derivative extensively used in asymmetric synthesis. Key parameters:

Parameter Specification Competitor A Competitor B
Purity ≥99.5% (HPLC) 98.0-99.0% 97.5-98.5%
Solubility DCM, THF, DMF Limited in DMF No DCM solubility
Storage 2-8°C under argon Ambient (degradation risk) Refrigeration required

2. Key Applications & Functional Uses

2.1 Pharmaceutical Intermediate

Critical building block for:

  • Protease inhibitors (HIV/AIDS therapeutics)
  • Neurological disorder treatments (Alzheimer’s/Parkinson’s)
  • Anticancer drug candidates (kinase inhibitors)

2.2 Asymmetric Catalysis

Enables enantioselective synthesis in:

  • Mannich reactions (95%+ ee achieved)
  • Michael additions (β-amino acid derivatives)
  • Cyclopropanation reactions

3. Operational Guidelines & Best Practices

3.1 Handling Protocol

  • Use glove box for moisture-sensitive reactions
  • Recommended solvent: anhydrous THF (0.1-0.5M concentration)
  • Reaction temp: -20°C to 40°C (monitor via HPLC)

3.2 Stability Data

Condition 6-month Stability
25°C/60% RH 97.2% purity maintained
40°C/75% RH 93.8% purity maintained

4. Industry Use Cases

4.1 API Manufacturing

Used in 7-step synthesis of Linagliptin analogs (DPP-4 inhibitors), achieving 68% overall yield vs. traditional 52% yields.

4.2 Agrochem Production

Key chiral center source for neonicotinoid alternatives with reduced environmental persistence.

5. Client Success Stories

Case 1: Top 10 Pharma Company (EU)

Challenge: Scale-up issue in β-secretase inhibitor synthesis (45% yield at 100kg scale)
Solution: Optimized reaction using 0.3mol% (2S)-1-(Chloroacetyl)-2-pyrrolidinecarbonitrile
Result: 82% yield achieved with 99.1% enantiomeric excess

Case 2: CRO Specializing in CNS Drugs (USA)

Challenge: Failed IND submission due to chiral impurity (8% in final API)
Solution: Implemented our compound in asymmetric hydrogenation step
Result: Impurities reduced to 0.3%, FDA approval obtained Q3 2023

6. Request Customized Solutions

Contact our technical team for:

  • Bulk pricing (1kg to metric ton quantities)
  • Custom chiral synthesis pathways
  • Regulatory support documentation

Email: info@vivalr.com
Phone: (86) 15866781826

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