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

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5H-Pyrrolo[3,4-b]pyridin-5-one,6,7-dihydro-7-hydroxy-(9CI) Basic information
Product Name:5H-Pyrrolo[3,4-b]pyridin-5-one,6,7-dihydro-7-hydroxy-(9CI)
Synonyms:5H-Pyrrolo[3,4-b]pyridin-5-one,6,7-dihydro-7-hydroxy-(9CI);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-
CAS:115012-09-4
MF:C7H6N2O2
MW:150.13
EINECS:
Product Categories:PYRROLIDINE;PYRIDINE
Mol File:115012-09-4.mol
5H-Pyrrolo[3,4-b]pyridin-5-one,6,7-dihydro-7-hydroxy-(9CI) Structure
5H-Pyrrolo[3,4-b]pyridin-5-one,6,7-dihydro-7-hydroxy-(9CI) Chemical Properties
storage temp. 2-8°C
Safety Information
MSDS Information
5H-Pyrrolo[3,4-b]pyridin-5-one,6,7-dihydro-7-hydroxy-(9CI) Usage And Synthesis
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] European Journal of Medicinal Chemistry, 2012, vol. 55, p. 58 - 66,9
5H-Pyrrolo[3,4-b]pyridin-5-one,6,7-dihydro-7-hydroxy-(9CI) Preparation Products And Raw materials
Raw materials5H-Pyrrolo[3,4-b]pyridine-5,7(6H)-dione-->Chloroform-->Methanol-->Sodium borohydride
Preparation Products3-Pyridinecarboxamide,2-(hydroxymethyl)-(9CI)
Tag:5H-Pyrrolo[3,4-b]pyridin-5-one,6,7-dihydro-7-hydroxy-(9CI)(115012-09-4) Related Product Information
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