188111-79-7

  • Product Name:(R)-1-Boc-3-Aminopiperidine
  • Molecular Formula:C10H20N2O2
  • Purity:99%
  • Molecular Weight:200.281
Inquiry

Product Details

Quality manufacturer supply (R)-1-Boc-3-Aminopiperidine 188111-79-7 in stock with high standard

  • Molecular Formula:C10H20N2O2
  • Molecular Weight:200.281
  • Vapor Pressure:0.00456mmHg at 25°C 
  • Refractive Index:1.4730 
  • Boiling Point:277.3 °C at 760 mmHg 
  • PKA:10.35±0.20(Predicted) 
  • Flash Point:121.5 °C 
  • PSA:55.56000 
  • Density:1.041g/cm3 
  • LogP:1.98280 

(R)-1-Boc-3-Aminopiperidine(Cas 188111-79-7) Usage

General Description

(R)-3-Amino-1-Boc-piperidine can be used as a precursor for the preparation of dipeptidyl peptidase IV inhibitors like linagliptin, alogliptin, and other antidiabetic agents.

InChI:InChI=1/C10H20N2O2/c1-10(2,3)14-9(13)12-6-4-5-8(11)7-12/h8H,4-7,11H2,1-3H3/t8-/m0/s1

188111-79-7 Relevant articles

Asymmetric synthesis of a high added value chiral amine using immobilized ω-transaminases

Petri, Antonella,Colonna, Valeria,Piccolo, Oreste

, p. 60 - 66 (2019)

Chiral N-heterocyclic molecules and in p...

Application of asymmetric hydrogenation in synthesis of Trelagliptin intermediate

-

Paragraph 0014, (2018/09/21)

The invention provides a synthetic metho...

METHOD FOR PRODUCING OPTICALLY ACTIVE 3-AMINOPIPERIDINE OR SALT THEREOF

-

Page/Page column 21, (2010/05/13)

The present invention relates to a metho...

AMIDE DERIVATIVE

-

Page/Page column 120, (2009/12/05)

The present invention relates to a compo...

188111-79-7 Process route

3-oxo-piperidine-1-carboxylic acid tert-butyl ester
98977-36-7

3-oxo-piperidine-1-carboxylic acid tert-butyl ester

tert-butyl (3R)3-aminopiperidine-1-carboxylate
188111-79-7

tert-butyl (3R)3-aminopiperidine-1-carboxylate

Conditions
Conditions Yield
With pyridoxal 5'-phosphate; immobilized Codex? amine ω-transaminase; isopropylamine; In dimethyl sulfoxide; at 50 ℃; pH=7.5; Temperature; enantioselective reaction; Enzymatic reaction;
70%
Multi-step reaction with 2 steps
1: ammonium acetate / ethanol / 7 h / Reflux; Large scale
2: bis(1,5-cyclooctadiene)rhodium(I) tetrafluoroborate; sodium hydride; C13H18FeP2; hydrogen / dichloromethane / Large scale
With bis(1,5-cyclooctadiene)rhodium(I) tetrafluoroborate; C13H18FeP2; ammonium acetate; hydrogen; sodium hydride; In ethanol; dichloromethane;
(R)-tert-butyl 3-carbamoylpiperidine-1-carboxylate
915226-43-6

(R)-tert-butyl 3-carbamoylpiperidine-1-carboxylate

tert-butyl (3R)3-aminopiperidine-1-carboxylate
188111-79-7

tert-butyl (3R)3-aminopiperidine-1-carboxylate

Conditions
Conditions Yield
With sodium hypochlorite; sodium hydroxide; In water; at 15 - 25 ℃; for 16h;
80%

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