Cas no 895132-31-7 (1-Boc-4-Cyano-4-(Cyclopropylmethyl)-Piperidine)

1-Boc-4-Cyano-4-(Cyclopropylmethyl)-Piperidine is a versatile intermediate in organic synthesis, particularly valuable for the preparation of pharmacologically active compounds. The Boc (tert-butoxycarbonyl) group provides excellent protection for the piperidine nitrogen, enabling selective functionalization under mild conditions. The cyano and cyclopropylmethyl substituents at the 4-position enhance its utility in constructing complex heterocyclic frameworks, often found in drug discovery. This compound exhibits high stability and compatibility with a range of reaction conditions, making it a reliable building block for medicinal chemistry applications. Its well-defined structure and purity ensure consistent performance in multi-step synthetic routes, particularly in the development of CNS-targeting and antiviral agents.
1-Boc-4-Cyano-4-(Cyclopropylmethyl)-Piperidine structure
895132-31-7 structure
Product Name:1-Boc-4-Cyano-4-(Cyclopropylmethyl)-Piperidine
CAS No:895132-31-7
MF:C15H24N2O2
MW:264.363264083862
MDL:MFCD11849800
CID:1942321
Update Time:2025-06-23

1-Boc-4-Cyano-4-(Cyclopropylmethyl)-Piperidine Chemical and Physical Properties

Names and Identifiers

    • 1-Boc-4-Cyano-4-(Cyclopropylmethyl)-Piperidine
    • 1,1-Dimethylethyl 4-cyano-4-(cyclopropylmethyl)-1-piperidinecarboxylate (ACI)
    • tert-Butyl 4-cyano-4-(cyclopropylmethyl)piperidine-1-carboxylate
    • MDL: MFCD11849800
    • Inchi: 1S/C15H24N2O2/c1-14(2,3)19-13(18)17-8-6-15(11-16,7-9-17)10-12-4-5-12/h12H,4-10H2,1-3H3
    • InChI Key: ILNVEWHRASLBNI-UHFFFAOYSA-N
    • SMILES: N#CC1(CCN(C(OC(C)(C)C)=O)CC1)CC1CC1

1-Boc-4-Cyano-4-(Cyclopropylmethyl)-Piperidine Pricemore >>

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1-Boc-4-Cyano-4-(Cyclopropylmethyl)-Piperidine Production Method

Production Method 1

Reaction Conditions
1.1 Reagents: Potassium bis(trimethylsilyl)amide Solvents: Tetrahydrofuran ;  cooled; 40 °C; 2 h, 40 °C
Reference
Design, synthesis and in vitro activity of quinazolone glycine transporter-1 inhibitors
Jiang, Neng; Jiang, Jian-qin; Shen, Jian-hua, Zhongguo Yaoke Daxue Xuebao, 2012, 43(3), 199-203

Production Method 2

Reaction Conditions
1.1 Reagents: Lithium bis(trimethylsilyl)amide Solvents: Tetrahydrofuran ;  25 °C
1.2 -
Reference
Discovery of GlyT1 inhibitors with improved pharmacokinetic properties
Wolkenberg, Scott E.; Zhao, Zhijian; Wisnoski, David D.; Leister, William H.; O'Brien, Julie; et al, Bioorganic & Medicinal Chemistry Letters, 2009, 19(5), 1492-1495

1-Boc-4-Cyano-4-(Cyclopropylmethyl)-Piperidine Raw materials

1-Boc-4-Cyano-4-(Cyclopropylmethyl)-Piperidine Preparation Products

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