309956-78-3

  • Product Name(R)-3-(Boc-Amino)piperidine
  • Molecular FormulaC10H20N2O2
  • Molecular Weight200.281
  • Purity99%
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Product Details

Quick Details

  • CasNo: 309956-78-3
  • Molecular Formula: C10H20N2O2
  • Purity: 99%

Good Manufacturer In Bulk Supply (R)-3-(Boc-Amino)piperidine 309956-78-3

  • Molecular Formula:C10H20N2O2
  • Molecular Weight:200.281
  • Vapor Pressure:0.000854mmHg at 25°C 
  • Melting Point:121.0 to 125.0 °C 
  • Refractive Index:1.479 
  • Boiling Point:304.8 °C at 760 mmHg 
  • PKA:12.37±0.20(Predicted) 
  • Flash Point:138.2 °C 
  • PSA:50.36000 
  • Density:1.02 g/cm3 
  • LogP:1.98280 

(R)-3-(Boc-Amino)piperidine(Cas 309956-78-3) Usage

Solubility in organics

Soluble in methanol and ethanol.

Uses

(R)-3-(Boc-amino)piperidine is used as an organic chemical synthesis intermediate.

storage

Stable under recommended storage conditions. Incompatible with oxidizing agents.

Chemical Properties

White powder

IUPAC Name: tert-butyl N-[(3R)-piperidin-3-yl]carbamate  
Isomeric SMILES: CC(C)(C)OC(=O)N[C@@H]1CCCNC1  
InChIKey: WUOQXNWMYLFAHT-MRVPVSSYSA-N  
InChI: InChI=1S/C10H20N2O2/c1-10(2,3)14-9(13)12-8-5-4-6-11-7-8/h8,11H,4-7H2,1-3H3,(H,12,13)/t8-/m1/s1  

309956-78-3 Relevant articles

Convenient synthesis of (R)-3-[(tert -Butoxycarbonyl)amino]piperidine and (R)-3-[(tert -Butoxycarbonyl)amino]azepane

Kadyrov, Renat,Tok, Oleg L.

, p. 3573 - 3577 (2021/07/25)

When (R)-3-Boc-aminopiperidine as starting material with primary amine protected to avoid generating positional isomers impurities. So the synthetic route shown in Fig. 1 was …

Synthesis method of chiral 3-aminopiperidine and derivatives of 3-aminopiperidine

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Paragraph 0135-0136, (2019/09/17)

The invention relates to a synthesis met...

(R)- 3 - Boc - amino piperidine preparation method

-

Paragraph 0064; 0065; 0066; 0067; 0068; 0069; 0070, (2018/04/03)

The invention discloses a preparation me...

Amino-protected (R) - 3-amino-piperidine preparation method

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Paragraph 0062-0064, (2017/03/18)

During our investigation of the synthetic route for linagliptin via (R)-3-Boc-aminopiperidine, two process-related impurities were detected (Figure 2), which could also be found in …

309956-78-3 Process route

(R)-3-(tert-butoxycarbonylamino)piperidine-1-carboxylic acid benzyl ester
485820-12-0

(R)-3-(tert-butoxycarbonylamino)piperidine-1-carboxylic acid benzyl ester

(R)-piperidin-3-ylcarbamic acid tert-butyl ester
309956-78-3,172603-05-3

(R)-piperidin-3-ylcarbamic acid tert-butyl ester

Conditions
Conditions Yield
With palladium 10% on activated carbon; hydrogen; In methanol; water; at 35 - 40 ℃; for 2h; under 2250.23 - 3000.3 Torr; Time; Autoclave; Inert atmosphere;
95.4%
With hydrogen; palladium 10% on activated carbon; In ethanol; at 20 ℃; for 168h; under 760.051 Torr;
92%
In ethanol;
 
tert-butyl (R)-(+)-(N-benzylpiperidin-3-yl)carbamate
454713-13-4,216854-24-9

tert-butyl (R)-(+)-(N-benzylpiperidin-3-yl)carbamate

(R)-piperidin-3-ylcarbamic acid tert-butyl ester
309956-78-3,172603-05-3

(R)-piperidin-3-ylcarbamic acid tert-butyl ester

Conditions
Conditions Yield
With 5%-palladium/activated carbon; hydrogen; In ethanol; at 20 - 25 ℃; for 20h; under 150015 Torr;
97%
With palladium 10% on activated carbon; hydrogen; In methanol; at 45 ℃; for 2h; under 1140.08 Torr;
85%
With hydrogen; 10% palladium on activated carbon; In metahnol; at 20 ℃; for 24h;
 

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