Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Pharmaceutical intermediates >  Heterocyclic compound >  Pyridine compound >  Nitropyridine >  Methyl2-aMino-5-nitronicotinate

Methyl2-aMino-5-nitronicotinate

Basic information Safety Supplier Related

Methyl2-aMino-5-nitronicotinate Basic information

Product Name:
Methyl2-aMino-5-nitronicotinate
Synonyms:
  • Methyl2-aMino-5-nitronicotinate
  • 2-aMino-3-(Methoxycarbonyl)-5-nitropyridine
  • Methyl 2-aMino-5-nitropyridine-3-carboxylate
  • 2-aMino-5-nitronicotinic acid Methyl ester
  • Methyl2-aMino-5-nitronicotinate ISO 9001:2015 REACH
  • 3-Pyridinecarboxylic acid, 2-amino-5-nitro-, methyl ester
CAS:
88312-64-5
MF:
C7H7N3O4
MW:
197.15
Mol File:
88312-64-5.mol
More
Less

Methyl2-aMino-5-nitronicotinate Chemical Properties

Melting point:
199-200 °C
Boiling point:
372.3±37.0 °C(Predicted)
Density 
1.463±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
pka
0.62±0.49(Predicted)
Appearance
Off-white to light yellow Solid
More
Less

Methyl2-aMino-5-nitronicotinate Usage And Synthesis

Uses

Methyl 2-amino-5-nitronicotinate is a useful chemical for the synthesis of polyfunctionalized benzo[d]thiazole and its aza analog thiazolo[5,4-b]pyridine.

Synthesis

14667-47-1

88312-64-5

Methyl 2-aminopyridine-3-carboxylate (10.0 g, 72.4 mmol) was added slowly dropwise from concentrated nitric acid (65%, 3.2 mmol, 76 mmol, 1.05 eq.) to a stirred suspension of concentrated sulfuric acid (96%, 90.5 mL, 1.69 mol, 23.3 eq.) at 0 °C. The reaction mixture was gradually brought to room temperature and stirred continuously for 2 hours. The resulting brown mixture was carefully poured into ice water and solid Na2CO3 was added by batchwise addition until complete neutralization (pH > 8). Subsequently, the aqueous layer was extracted three times with ethyl acetate (AcOEt). The combined organic layers were washed sequentially with saturated saline and deionized water and dried over anhydrous magnesium sulfate (MgSO4). Finally, the solvent was removed by vacuum evaporation to afford the target product 2-amino-3-carboxylic acid methyl ester-5-nitropyridine (11.7 g, 82% yield) as a colorless solid with a purity meeting the analytical requirements.

References

[1] Tetrahedron, 2014, vol. 70, # 35, p. 5541 - 5549
[2] Patent: WO2015/189595, 2015, A1. Location in patent: Page/Page column 48; 49
[3] Patent: EP1782811, 2007, A1. Location in patent: Page/Page column 42
[4] Patent: EP1669348, 2006, A1. Location in patent: Page/Page column 50

Methyl2-aMino-5-nitronicotinateSupplier

PharmaBlock Sciences (Nanjing),Inc.
Tel
025-86918202 4000255188
Email
sales@pharmablock.com
SuZhou ShiYa Biopharmaceuticals, Inc.
Tel
86(512)5235 8471 17715136450
Email
sales@shiyabiopharm.com
Cantotech Chemicals, Ltd.
Tel
86-0755-86635001
Email
cantotech@126.com
Bide Pharmatech Ltd.
Tel
400-400-164-7117 18317119277
Email
product02@bidepharm.com
XiaMeng Kang Auke Pharma Co., Ltd
Tel
0086-592-7270133 612
Email
1934992149@qq.com