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3,4-Pyridinedicarboximide

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3,4-Pyridinedicarboximide manufacturers

3,4-Pyridinedicarboximide Basic information
Product Name:3,4-Pyridinedicarboximide
Synonyms:2,3-DIHYDRO-1H-PYRROLO[3,4-C]PYRIDINE-1,3-DIONE;CINCHOMERONIMIDE;BUTTPARK 48\06-51;3,4-Pyridinedicarboximide ,97%;2H-Pyrrolo[3,4-c]pyridine-1,3-dione;3,4-Pyridinedicarbimide;Pyridine-3,4-dicarbimide;pyrrolo[3,4-c]pyridine-1,3-quinone
CAS:4664-01-1
MF:C7H4N2O2
MW:148.12
EINECS:628-277-9
Product Categories:
Mol File:4664-01-1.mol
3,4-Pyridinedicarboximide Structure
3,4-Pyridinedicarboximide Chemical Properties
Melting point 232-235 °C(lit.)
Boiling point 268.69°C (rough estimate)
density 1.4015 (rough estimate)
refractive index 1.5300 (estimate)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
pka7.80±0.20(Predicted)
form Crystalline Powder
color White to tan
InChIInChI=1S/C7H4N2O2/c10-6-4-1-2-8-3-5(4)7(11)9-6/h1-3H,(H,9,10,11)
InChIKeySJSABZBUTDSWMJ-UHFFFAOYSA-N
SMILESC1=NC=CC2C(=O)NC(=O)C1=2
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-37/39
WGK Germany 3
RTECS US7966000
HazardClass IRRITANT
HS Code 29333990
MSDS Information
ProviderLanguage
SigmaAldrich English
3,4-Pyridinedicarboximide Usage And Synthesis
Chemical PropertiesWhite to light brown powder
Synthesis
3,4-Pyridinedicarboxylic acid

490-11-9

3,4-PYRIDINEDICARBOXIMIDE

4664-01-1

The general procedure for the synthesis of 3,4-pyridinedicarboxylic acid as a raw material for the synthesis of 3,4-pyridinedicarboximides was as follows: firstly, sublimated 3,4-pyridinedicarboxylic acid (50 g, 300 mmol) was suspended in acetic anhydride (123.5 g, 1,200 mmol), and heated to reflux (140-150 °C) until the solid was completely dissolved and the mixture presented homogeneous state. Subsequently, the reaction mixture was cooled and concentrated under vacuum. Next, acetamide (50 g, 846 mmol) was added to the concentrate and the mixture was heated and reacted at 140 °C for 3 hours. After completion of the reaction, the mixture was cooled to room temperature. The solid residue formed during cooling was pulverized, ground with 100 ml of water, filtered and washed with additional water. Finally, the resulting solid was dried in a desiccator to afford 3,4-pyridinedicarboximide (42.26 g, 95.1% yield), which met the purity requirements for use without further purification. The product was analyzed by LC-MS showing a m/z (ESP) of 149 [M + H]+ and a retention time (R/T) of 0.44 min.

References[1] Patent: US2006/199804, 2006, A1. Location in patent: Page/Page column 29
[2] Acta Chimica Hungarica, 1983, vol. 112, # 4, p. 487 - 500
3,4-Pyridinedicarboximide Preparation Products And Raw materials
Raw materialsAcetic anhydride-->Acetamide-->3,4-Pyridinedicarboxylic acid
Tag:3,4-Pyridinedicarboximide(4664-01-1) Related Product Information
2,3-Dihydro-1H-pyrrolo[3,4-c]pyridine 3,4-Pyridinedicarboximide N-Benzyl- 2,3-pyridinedicarboximide 5H-Pyrrolo[3,4-b]pyridine-5,7(6H)-dione 4-Chloro-6-methyl-2,3-dihydro-1H-pyrrolo[3,4-c]pyridine-1,3-dione 4-chloro-2-(2-chloro-6-fluoroBenzyl)-6-methyl-2,3-dihydro-1H-pyrrolo[3,4-c]pyridine-1,3-dione 4-Chloro-6-methyl-2-(4-methylbenzyl)-2,3-dihydro-1H-pyrrolo[3,4-c]pyridine-1,3-dione 4-Methyl-2,3-dihydro-1H-pyrrolo[3,4-c]quinoline-1,3-dione 4-Chloro-6-methyl-2-[3-(trifluoromethyl)Benzyl]-2,3-dihydro-1H-pyrrolo[3,4-c]pyridine-1,3-dione N-(2,6-dimethylphenyl)-2,3-pyridinedicarboximide N-(2,6-dimethylphenyl)-3,4-pyridinedicarboximide 2,3-Pyridinedicarboximide, N-(5,5-dimethyl-2-oxotetrahydro-3-furyl)- 4-chloro-2-(2,4-dichlorobenzyl)-6-methyl-2,3-dihydro-1H-pyrrolo[3,4-c]pyridine-1,3-dione 2-benzyl-4-chloro-6-methyl-2,3-dihydro-1H-pyrrolo[3,4-c]pyridine-1,3-dione 6-(tert-Butyl)-4-chloro-2,3-dihydro-1H-pyrrolo[3,4-c]pyridine-1,3-dione 4-[(Chloromethyl)thio]-6-methyl-2,3-dihydro-1H-pyrrolo[3,4-c]pyridine-1,3-dione Methyl 2-benzyl-7-hydroxy-1,3-dioxo-2,3-dihydro-1H-pyrrolo[3,4-c]pyridine-4-carboxylate 2-[[3-Chloro-5-(trifluoromethyl)-2-pyridinyl](methyl)amino]-1H-pyrrolo[3,4-c]pyridine-1,3(2H)-dione