1-Boc-4-(isopropylamino)piperidine

Name: 1-Boc-4-(isopropylamino)piperidine
Brand: ChemScene
Availability: InStock
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CAS No. 534595-51-2
Cat. No. CS-0154185
Purity≥97%
MDL No.MFCD07367732

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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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1-Boc-4-(isopropylamino)piperidine|CS-0154185

Structure of 534595-51-2

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General Information

CAS No. 534595-51-2
Cat. No. CS-0154185
Purity ≥97%
MDL No. MFCD07367732
Storage 4°C, protect from light
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₁₃H₂₆N₂O₂
Molecular Weight 242.36
Synonym(s) tert-butyl 4-[(1-methylethyl)amino]piperidine-1-carboxylate
SMILES CC(C)NC1CCN(CC1)C(=O)OC(C)(C)C

Description

1-Boc-4-(isopropylamino)piperidine features a protected piperidine core with a sterically hindered isopropylamino substituent, enabling stable incorporation into complex molecular architectures. This bench-stable derivative facilitates efficient synthesis of bioactive amines and serves as a key intermediate in medicinal chemistry campaigns requiring controlled nitrogen functionality.

Application

1-Boc-4-(isopropylamino)piperidine serves as a versatile building block in medicinal chemistry, enabling efficient access to piperidine-based scaffolds common in bioactive molecules. The Boc group provides stability and facilitates straightforward deprotection under mild acidic conditions. Its isopropylamino substituent offers favorable steric and electronic properties for target-directed synthesis, while the piperidine core supports diverse functionalization and coupling reactions in standard reductive amination and amide formation workflows.

Synthesis

Route1
- 79099-07-3
- 75-31-0
- ~41%
- In-stock
  
  534595-51-2
References
- RVX Therapeutics Inc.; McLure, Kevin G.; Young, Peter R. Patent: US2013/281399 A1, 2013 ; Location in patent: Paragraph 0521 ;
Route2
- 87120-72-7
- 67-64-1
- ~%
- In-stock
  
  534595-51-2
References
- US2003/199689 A1, ; Page/Page column 33 ;

Safety Information

Download SDS

GHS Pictogram :	GHS No : GHS07
Signal Word : Warning	UN#: N/A
Class : N/A	Packing Group : N/A
Hazard Statements : H317-H319
Precautionary Statements : P261-P264-P272-P280-P302+P352-P362+P364-P501

Quality Control

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Computational Chemistry Data

TPSA 41.57
LogP 2.3839
H_Acceptors 3
H_Donors 1
Rotatable_Bonds 2

Other Classifications

Building Blocks Functional Group Amine

Building Blocks Skeleton Aliphatic heterocycle compounds Piperidine compounds

Key Words

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1-Boc-4-(isopropylamino)piperidine

CAS No. 534595-51-2

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