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(S)-3-N-Boc-aminopiperidine

CAS No.
216854-23-8
Chemical Name:
(S)-3-N-Boc-aminopiperidine
Synonyms
tert-butyl (R)-piperidin-3-ylcarbamate;tert-butyl (S)-piperidin-3-ylcarbamate;(S)-3-BOC-AMINOPIPERIDINE;(S)-3-(TERT-BUTOXYCARBONYLAMINO)PIPERIDINE;ZZ-7;Alogliptin Impurity 53;S-3-(Boc-Ao)piperidine;Linagliptin Impurity 108;(R)-Boc-3-aminopiperidine;(S)-tert-Butyl-(piperidin-
CBNumber:
CB5438435
Molecular Formula:
C10H20N2O2
Molecular Weight:
200.28
MDL Number:
MFCD03093383
MOL File:
216854-23-8.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 04:36:30

(S)-3-N-Boc-aminopiperidine Properties

Melting point 122-127°C
Boiling point 304.8±31.0 °C(Predicted)
alpha -3 º (c=1, DMF)
Density 1.02±0.1 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility Freely soluble in ethanol.
pka 12.37±0.20(Predicted)
form Crystalline Powder
color White to off-white
optical activity [α]/D -3.0±0.5°, c = 1 in DMF
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-/m0/s1
InChIKey WUOQXNWMYLFAHT-QMMMGPOBSA-N
SMILES CC(C)(C)OC(=O)N[C@H]1CCCNC1
CAS DataBase Reference 216854-23-8(CAS DataBase Reference)
UNSPSC Code 12352005
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Corrosion (GHS05)Exclamation Mark (GHS07)
GHS05,GHS07
Signal word  Danger
Hazard statements  H319-H315-H318-H335
Precautionary statements  P264-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313-P261-P280-P305+P351+P338-P280a-P304+P340-P405-P501a
target organs Respiratory system
PPE dust mask type N95 (US), Eyeshields, Gloves
Hazard Codes  Xi
Risk Statements  37/38-41-36/37/38
Safety Statements  26-39-37/39
WGK Germany  3
HS Code  29339900
Storage Class 11 - Combustible Solids
Hazard Classifications Eye Dam. 1
Skin Irrit. 2
STOT SE 3
NFPA 704
1
2 0

(S)-3-N-Boc-aminopiperidine price More Price(89)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 08601 (S)-3-(Boc-amino)piperidine ≥98.0% 216854-23-8 1g $108 2022-05-15 Buy
TCI Chemical B3660 (S)-3-(tert-Butoxycarbonylamino)piperidine >98.0%(GC) 216854-23-8 1g $34 2026-04-30 Buy
TCI Chemical B3660 (S)-3-(tert-Butoxycarbonylamino)piperidine >98.0%(GC) 216854-23-8 5g $106 2026-04-30 Buy
Usbiological 261896 S-3-N-Boc-Aminopiperidine 216854-23-8 10g $340 2026-06-03 Buy
Usbiological 261896 S-3-N-Boc-Aminopiperidine 216854-23-8 25g $489 2026-06-03 Buy
Product number Packaging Price Buy
08601 1g $108 Buy
B3660 1g $34 Buy
B3660 5g $106 Buy
261896 10g $340 Buy
261896 25g $489 Buy

(S)-3-N-Boc-aminopiperidine Chemical Properties, Uses, Production

Chemical Properties

White powder

Uses

(S)-3-N-Boc-aminopiperidine can be useful intermediate for the synthesis of a variety of chiral aminopiperidinyl quinolones as potent antibacterial agents against resistant pathogens; and alkynylpyrimidine amide derivatives as orally a vailable inhibitors of Tie-2 kinase.

Uses

(S)-3-(Boc-amino)piperidine, is used as an intermediate for pigments. It is also used as important raw material and intermediate used in organic Synthesis, pharmaceuticals, agrochemicals and dyestuff. It is also an useful intermediate for the synthesis of a variety of chiral aminopiperidinyl quinolones as potent antibacterial agents against resistant pathogens; and alkynylpyrimidine amide derivatives as orally available inhibitors of Tie-2 kinase.

Synthesis

(S)-3-BOC-AMINO-2-PIPERIDONE

92235-39-7

(S)-3-N-Boc-aminopiperidine

216854-23-8

General procedure for the synthesis of (S)-3-Boc-aminopiperidine from tert-butyl (S)-2-piperidone-3-carbamate: to a solution of THF (250 mL) of the product of Example 41A (20.1 g, 94 mmol) was added slowly and dropwise over a period of 45 min at 0 °C a borane-THF complex (162 mL, 1 M solution of THF 162 mmol; purchased from Aldrich). After the dropwise addition was completed, the reaction was kept at 0 °C with continued stirring for 1 hour. Subsequently, the ice bath was removed and the reaction mixture was allowed to stir at 20-25 °C for 6 hours. Upon completion of the reaction, methanol (100 mL) and 5% NaHCO3 solution (300 mL) were carefully added to quench the reaction. The mixture was stirred vigorously for 16 hours and subsequently concentrated under reduced pressure to reduce the volume. The residue was treated with methanol (200 mL), heated to reflux for 30 minutes, and then concentrated again under reduced pressure. This process was repeated twice. The final residue was suspended in 20% K2CO3 solution (200 mL) and extracted with ether (3 x 200 mL). The organic phases were combined, dried over MgSO4 and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent ratio of dichloromethane: methanol: NH4OH = 90:10:1) to afford (S)-3-Boc-aminopiperidine (5.64 g, 30% yield) in white solid form. The mass spectrum (CI/NH3) showed m/z 201 (M + H)+.

References

[1] Patent: EP1428824, 2004, A1. Location in patent: Page 44

Global Suppliers ( 358)
Supplier Tel Email Country ProdList Advantage
J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76
Meryer (Shanghai) Chemical Technology Co., Ltd. 4006356688 18621169109 market03@meryer.com China 40202 62
INTATRADE GmbH +49 3493/605464 sales@intatrade.de Germany 3563 66
3B Pharmachem (Wuhan) International Co.,Ltd. 18930552037 3bsc@sina.com China 15813 69
ChemFuture PharmaTech (Jiangsu) Ltd 5108538618 suger.wang@chemfuture.com China 832 65
Chembest Research Laboratories Limited 021-20908456 sales@BioChemBest.com China 5996 61
Alfa Aesar 400-6106006 saleschina@alfa-asia.com China 30103 84
TCI (Shanghai) Development Co., Ltd. 021-67121386 Sales-CN@TCIchemicals.com China 24512 81
Energy Chemical 400-0056266 sales8178@energy-chemical.com China 44850 61
Wuhan Chemwish Technology Co., Ltd 86-027-67849912 sales@chemwish.com China 35884 56

View Latest Price from (S)-3-N-Boc-aminopiperidine manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
(S)-3-N-Boc-aminopiperidine  pictures 2020-02-26 (S)-3-N-Boc-aminopiperidine
216854-23-8
100G 99.0%+ 100 tons Shaanxi Dideu Medichem Co. Ltd
(S)-3-N-Boc-aminopiperidine pictures 2019-07-06 (S)-3-N-Boc-aminopiperidine
216854-23-8
$1.00 1KG 98% 100KG Career Henan Chemical Co

(S)-3-N-Boc-aminopiperidine Spectrum

(3S)-3-Aminopiperidine, 3-BOC protected 95+% Alogliptin Impurity 53 (S)-3-amino-N-boc-piperidine Carbamic acid, N-(3S)-3-piperidinyl-, 1,1-dimethylethyl ester (3S)-3-Aminopiperidine, 3-BOC protected (S)-tert-butyl piperidin-3-ylcarbamate hydrochloride (S)-3-(Boc-aMino)piperidi... tert-butyl N-[(3S)-piperidin-3-yl]carbaMate (S)-tert-Butyl-(piperidin- N-(3S)-3-PiperidinylcarbaMic Acid 1,1-DiMethylethyl Ester tert-Butyl [(3S)-piperidin-3-yl]carbamate, (3S)-3-[(tert-Butoxycarbonyl)amino]piperidine (S)-3-(Boc-aMino)piperidine, 97+% (S)-3-(Boc-amino)piperidine >=98.0% S-3-(Boc-Ao)piperidine (S)-3-(N-Boc-amino)piperidine,99%e.e. CARBAMIC ACID, (3S)-3-PIPERIDINYL-, 1,1-DIMETHYLETHYL ESTER Carbamic acid, (3S)-3-piperidinyl-, 1,1-dimethylethyl ester (9CI) (R)-Boc-3-aminopiperidine (S)-3-Aminopiperidine, 3-BOC protected (S)-TERT-BUTYL-PIPERIDIN-3-YLCARBAMATE (S)-PIPERIDIN-3-YL-CARBAMIC ACID TERT-BUTYL ESTER (S)-(-)-3-TERT-BUTOXYCARBONYLAMINOPIPERIDINE (S)-3-(TERT-BUTOXYCARBONYLAMINO)PIPERIDINE (S)-3-N-BOC-AMINOPIPERIDINE (S)-3-(tert-Butoxycarbonylamino)piperidine > ert-butylN-[(3S)-piperidin-3-yl]carbamate (S)-3-N-Boc-aminopiperidine USP/EP/BP Linagliptin Impurity 108 tert-butyl N-[(3S)-3-piperidyl]carbamate ZZ-7 (S)-3-(Boc-amino)piperidine (S)-3-BOC-AMINOPIPERIDINE tert-butyl (S)-piperidin-3-ylcarbamate tert-butyl (R)-piperidin-3-ylcarbamate 216854-23-8 16854-23-8 Piperidines Heterocyclic Building Blocks Asymmetric Synthesis Chiral Building Blocks Heterocycle-other series Amines Heterocycles Chiral Building Blocks Heterocyclic Building Blocks Piperidines Piperidine Series pharmacetical Piperidine N-BOC