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1-BOC-4-(5-NITRO-2-PYRIDYL)PIPERAZINE

CAS No.
193902-78-2
Chemical Name:
1-BOC-4-(5-NITRO-2-PYRIDYL)PIPERAZINE
Synonyms
tert-Butyl 4-(5-nitropyridin-2-yl)piperazine-1-carboxylate;Palbociclib Impurity 102;Palbociclib Impurity SMA-7;1-Boc-4-(5-nitro-2-pyridinyl)-piperazine;1-Boc-4-(5-nitro-2-pyridyl)piperazine 97%;1-(tert-Butyloxycarbonyl)-4-(5-nitropyridin-2-yl)piperazine;4-(5-nitro-pyridin-2-yl)-piperazine-1-carboxylic acid tert-butyl ester;1-Boc-4-(5-nitro-2-pyridyl)piperazine;1-Piperazinecarboxylic acid, 4-(5-nitro-2-pyridinyl)-, 1,1-dimethylethyl ester;1-tert-Butoxycarbonyl-4-(5-nitropyrid-2-yl)piperazine, 2-(4-Boc-1-piperazinyl)-5-nitropyridine
CBNumber:
CB5973088
Molecular Formula:
C14H20N4O4
Molecular Weight:
308.33
MDL Number:
MFCD07369779
MOL File:
193902-78-2.mol
MSDS File:
SDS
Last updated:2026-05-28 03:48:50
Product description Number Pack Size Price
1-Boc-4-(5-nitro-2-pyridyl)piperazine 97% 654191 10g $263
tert-Butyl 4-(5-nitropyridin-2-yl)piperazine-1-carboxylate 105202 1.00g $1143
tert-butyl 4-(5-nitropyridin-2-yl)piperazine-1-carboxylate 97.0% B22095 1g $51
tert-butyl 4-(5-nitropyridin-2-yl)piperazine-1-carboxylate 97.0% B22095 5g $57
tert-butyl 4-(5-nitropyridin-2-yl)piperazine-1-carboxylate 97.0% B22095 10g $59

1-BOC-4-(5-NITRO-2-PYRIDYL)PIPERAZINE Properties

Melting point 168-172 °C (lit.)
Boiling point 468.7±45.0 °C(Predicted)
Density 1.258±0.06 g/cm3(Predicted)
pka 4.38±0.29(Predicted)
form solid
InChI 1S/C14H20N4O4/c1-14(2,3)22-13(19)17-8-6-16(7-9-17)12-5-4-11(10-15-12)18(20)21/h4-5,10H,6-9H2,1-3H3
InChIKey WWFJYZONBJARJT-UHFFFAOYSA-N
SMILES CC(C)(C)OC(=O)N1CCN(CC1)c2ccc(cn2)[N+]([O-])=O
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Skull and Crossbones (GHS06)
GHS06
Signal word  Danger
Hazard statements  H301
Precautionary statements  P264-P270-P301+P310-P405-P501
PPE Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
Hazard Codes  T
Risk Statements  25
Safety Statements  45
RIDADR  UN 2811 6.1/PG 3
WGK Germany  3
Storage Class 6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
Hazard Classifications Acute Tox. 3 Oral

1-BOC-4-(5-NITRO-2-PYRIDYL)PIPERAZINE price More Price(36)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 654191 1-Boc-4-(5-nitro-2-pyridyl)piperazine 97% 193902-78-2 10g $263 2023-06-20 Buy
Matrix Scientific 105202 tert-Butyl 4-(5-nitropyridin-2-yl)piperazine-1-carboxylate 193902-78-2 1.00g $1143 2026-05-18 Buy
Synthonix B22095 tert-butyl 4-(5-nitropyridin-2-yl)piperazine-1-carboxylate 97.0% 193902-78-2 1g $51 2026-05-06 Buy
Synthonix B22095 tert-butyl 4-(5-nitropyridin-2-yl)piperazine-1-carboxylate 97.0% 193902-78-2 5g $57 2026-05-06 Buy
Synthonix B22095 tert-butyl 4-(5-nitropyridin-2-yl)piperazine-1-carboxylate 97.0% 193902-78-2 10g $59 2026-05-06 Buy
Product number Packaging Price Buy
654191 10g $263 Buy
105202 1.00g $1143 Buy
B22095 1g $51 Buy
B22095 5g $57 Buy
B22095 10g $59 Buy

1-BOC-4-(5-NITRO-2-PYRIDYL)PIPERAZINE Chemical Properties,Uses,Production

Synthesis

2-Bromo-5-nitropyridine

4487-59-6

1-BOC-Piperazine

57260-71-6

1-BOC-4-(5-NITRO-2-PYRIDYL)PIPERAZINE

193902-78-2

General procedure: 2-bromo-5-nitropyridine (11.39 g, 56.1 mmol), tetrabutylammonium iodide (TBAI) (1.04 g, 0.05 mmol), potassium carbonate (8.53 g, 61.7 mmol), and N-BOC-piperazine (11.5 g, 61.7 mmol) were dissolved in DMSO (100 mL) and gently heated to 50 °C. The reaction was carried out for 3 h, followed by cooling to room temperature overnight. The reaction mixture was diluted with EtOAc (200 mL), filtered to remove the salt, and the DMSO solution was obtained by evaporating the EtOAc. The solution was diluted with water to form a precipitate. The precipitate was collected by filtration, washed with water and dried under vacuum to give 1-tert-butylcarbonyl-4-(5-nitro-2-pyridyl)piperazine (16.1 g, 93%) as a light orange solid.1H NMR (400 MHz, CDCl3) δ ppm 1.47 (s, 9H), 3.55 (m, 4H), 3.75 (m, 4H), 6.55 (d, J = 9.3 Hz, 1H), 8.21 (dd, J = 9.5, 2.7 Hz, 1H), 9.03 (d, J = 2.7 Hz, 1H). 1-tert-butylcarbonyl-4-(5-nitro-2-pyridinyl)piperazine (16.0 g, 51.9 mmol) was dissolved in THF (400 mL), Raney nickel (4 g) was added, and the reaction was carried out for 5 hr under 50 psi hydrogen atmosphere. The catalyst was removed by diatomaceous earth filtration and the solvent was evaporated in vacuum to give 1-tert-butylcarbonyl-4-(5-amino-2-pyridyl)piperazine (14.5 g, 100%).1H NMR (400 MHz, CDCl3) δ ppm 1.46 (s, 9H), 3.31 (m, 6H), 3.53 (m, 4H), 6.56 (d, J = 8.8 Hz. 1H), 6.98 (dd, J = 8.8, 2.9 Hz, 1H), 7.78 (dd, J = 2.9, 0.7 Hz, 1H). m/z 279.1 (M + 1).

References

[1] Patent: US2005/182078, 2005, A1. Location in patent: Page/Page column 9; 12
[2] Tetrahedron Letters, 2011, vol. 52, # 45, p. 5905 - 5909
[3] Patent: WO2004/9587, 2004, A1. Location in patent: Page 36
[4] Patent: EP2773638, 2015, B1. Location in patent: Paragraph 0753; 0754
[5] Patent: US2004/9988, 2004, A1. Location in patent: Page/Page column 10

1-BOC-4-(5-NITRO-2-PYRIDYL)PIPERAZINE Preparation Products And Raw materials

1-BOC-4-(5-NITRO-2-PYRIDYL)PIPERAZINE Suppliers

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1-Boc-4-(5-nitro-2-pyridinyl)-piperazine 4-(5-nitro-pyridin-2-yl)-piperazine-1-carboxylic acid tert-butyl ester 1-tert-Butoxycarbonyl-4-(5-nitropyrid-2-yl)piperazine, 2-(4-Boc-1-piperazinyl)-5-nitropyridine 1-Piperazinecarboxylic acid, 4-(5-nitro-2-pyridinyl)-, 1,1-dimethylethyl ester 1-Boc-4-(5-nitro-2-pyridyl)piperazine 97% Palbociclib Impurity SMA-7 Palbociclib Impurity 102 1-(tert-Butyloxycarbonyl)-4-(5-nitropyridin-2-yl)piperazine 1-Boc-4-(5-nitro-2-pyridyl)piperazine tert-Butyl 4-(5-nitropyridin-2-yl)piperazine-1-carboxylate 193902-78-2