tert-Butyl 4-(3-aminopropyl)piperidine-1-carboxylate

Name: tert-Butyl 4-(3-aminopropyl)piperidine-1-carboxylate
Brand: ChemScene
Availability: InStock
Rating: 5 (1 reviews)

CAS No. 150349-65-8
Cat. No. CS-0036303
Purity≥97%
MDL No.MFCD08234497

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Type	HazMat Fee
Excepted Quantity	$0.00
FedEx Limited Quantities Ground	$0.00
Hazmat Ground shipping	$50.00+
Inaccessible (Haz class 6.1 or 9), Domestic	$68.00+
Accessible (Haz class 3, 4, 5 or 8), Domestic	$158.00+
Inaccessible (Haz class 6.1 or 9), International	$108.00+
Accessible (Haz class 3, 4, 5 or 8), International	$238.00+

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tert-Butyl 4-(3-aminopropyl)piperidine-1-carboxylate|CS-0036303

Structure of 150349-65-8

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General Information

CAS No. 150349-65-8
Cat. No. CS-0036303
Purity ≥97%
MDL No. MFCD08234497
Storage 4°C, protect from light
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₁₃H₂₆N₂O₂
Molecular Weight 242.36
Synonym(s) None
SMILES O=C(OC(C)(C)C)N1CCC(CC1)CCCN

Description

tert-Butyl 4-(3-aminopropyl)piperidine-1-carboxylate features a piperidine core functionalized with a primary amine at the C3 position, enabling direct conjugation or further derivatization. The tert-butyl ester group provides stability and facilitates orthogonal deprotection under mild acidic conditions. This scaffold serves as a key intermediate in the synthesis of bioactive molecules, particularly within medicinal chemistry campaigns targeting G protein-coupled receptors.

Application

tert-Butyl 4-(3-aminopropyl)piperidine-1-carboxylate serves as a versatile bifunctional building block for medicinal chemistry and process development. The piperidine core provides a rigid, basic scaffold ideal for drug discovery, while the pendant primary amine enables conjugation via amidation, alkylation, or reductive amination. The tert-butyl carbamate group offers excellent bench stability and orthogonal protection, facilitating selective deprotection under mild acidic conditions. This compound functions as a key intermediate in the synthesis of bioactive molecules, particularly those requiring extended aliphatic linkers between pharmacophores.

Synthesis

Route1
- 946517-74-4
- ~94%
- In-stock
  
  150349-65-8
References
- RITCHER GEDEON NYRT Patent: WO2008/50168 A1, 2008 ; Location in patent: Page/Page column 29 ; WO 2008/050168 A1
Route2
- In-stock
  
  161975-20-8
- ~%
- In-stock
  
  150349-65-8
References
- US5494921 A1, ;

Safety Information

Download SDS

GHS Pictogram :	GHS No : GHS07,GHS05
Signal Word : Danger	UN#: 2735
Class : 8	Packing Group : Ⅱ
Hazard Statements : H302-H314-H335
Precautionary Statements : P260-P264-P270-P271-P280-P301+P310-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P310-P312-P330-P363-P403+P233-P405-P501

Quality Control

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Computational Chemistry Data

TPSA 55.56
LogP 2.3724
H_Acceptors 3
H_Donors 1
Rotatable_Bonds 3

Other Classifications

Building Blocks Functional Group Amine

Building Blocks Skeleton Aliphatic heterocycle compounds Piperidine compounds

Key Words

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tert-Butyl 4-(3-aminopropyl)piperidine-1-carboxylate

CAS No. 150349-65-8

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