ChemicalBook--->CAS DataBase List--->115012-09-4

115012-09-4

115012-09-4 Structure

115012-09-4 Structure
IdentificationBack Directory
[Name]

5H-Pyrrolo[3,4-b]pyridin-5-one,6,7-dihydro-7-hydroxy-(9CI)
[CAS]

115012-09-4
[Synonyms]

7-Hydroxy-6,7-dihydro-5H-pyrrolo[3,4-b]pyridin-5-one
6,7-dihydro-7-hydroxy-5H-Pyrrolo[3,4-b]pyridin-5-one
5H-Pyrrolo[3,4-b]pyridin-5-one, 6,7-dihydro-7-hydroxy-
5H-Pyrrolo[3,4-b]pyridin-5-one,6,7-dihydro-7-hydroxy-(9CI)
[Molecular Formula]

C7H6N2O2
[MDL Number]

MFCD12924078
[MOL File]

115012-09-4.mol
[Molecular Weight]

150.13
Chemical PropertiesBack Directory
[storage temp. ]

2-8°C
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Hazard InformationBack Directory
[Synthesis]

5H-Pyrrolo[3,4-b]pyridine-5,7(6H)-dione

4664-00-0

5H-Pyrrolo[3,4-b]pyridin-5-one,6,7-dihydro-7-hydroxy-(9CI)

115012-09-4

7H-Pyrrolo[3,4-b]pyridin-7-one,5,6-dihydro-5-hydroxy-(9CI)

115012-10-7

The general procedure for the synthesis of 7-hydroxy-6,7-dihydro-5H-pyrrolo[3,4-b]pyridin-5-one and compounds (CAS:115012-10-7) from 2,3-pyridinedicarboximide was as follows: 0.74 g (5 mmol) of 2,3-pyridinedicarboximide was dissolved in 50 ml of a solvent mixture of methanol and chloroform at -20 °C ( methanol:chloroform=1:1, V/V). Subsequently, 0.283 g of sodium borohydride was added and the reaction was monitored by TLC until the disappearance of the feedstock spot. Upon completion of the reaction, the pH of the reaction solution was first adjusted to 3 with 3 mol/L hydrochloric acid, and then adjusted to pH 9 with 2 mol/L sodium hydroxide solution. the solvent was removed by concentration under reduced pressure, and the resulting mixture was separated by silica gel column chromatography (eluent: dichloromethane:methanol=15:1, V/V) to give a white solid (a mixture of compound a-1 and compound b-1 in the ratio of about 3:1 ). Finally, the two isomers were isolated by ethanol recrystallization in 45.1% yield of compound a-1.

[References]

[1] Bulletin of the Chemical Society of Japan, 1987, vol. 60, # 11, p. 4178 - 4180
[2] Patent: CN105541833, 2016, A. Location in patent: Paragraph 0152; 0153; 0154
[3] Bulletin of the Chemical Society of Japan, 1989, vol. 62, # 4, p. 1205 - 1210
[4] Bulletin of the Chemical Society of Japan, 1989, vol. 62, # 4, p. 1205 - 1210
[5] European Journal of Medicinal Chemistry, 2012, vol. 55, p. 58 - 66,9
115012-09-4 suppliers list
Company Name: BePharm Ltd  
Telephone: 400-685-9117
Website: www.bepharm.com
Company Name: Amadis Chemical Company Limited  
Telephone: 571-89925085
Website: http://www.amadischem.com
Company Name: Aikon International Limited  
Telephone: 025-58859352 19370895928
Website: www.aikonchem.com
Company Name: Shanghai Haohong Scientific Co., Ltd.  
Telephone: 400-8210725 4008210725
Website: https://www.leyan.com/
Company Name: Tangshan Jinyuan Biotechnology Co., Ltd  
Telephone: 15222523250
Website:
Tags:115012-09-4 Related Product Information
4664-00-0 40107-93-5 1256806-34-4 1211589-13-7 1256811-82-1