ChemicalBook--->CAS DataBase List--->118768-13-1

118768-13-1

118768-13-1 Structure

118768-13-1 Structure
IdentificationBack Directory
[Name]

H-pyrrolo[1,2-b]pyridazine-6-carboxylic acid
[CAS]

118768-13-1
[Synonyms]

pyrrolo[1,2-b]pyridazine-6-carboxylic acid
H-pyrrolo[1,2-b]pyridazine-6-carboxylic acid
[EINECS(EC#)]

814-378-7
[Molecular Formula]

C8H6N2O2
[MDL Number]

MFCD20646267
[MOL File]

118768-13-1.mol
[Molecular Weight]

162.15
Chemical PropertiesBack Directory
[density ]

1.41±0.1 g/cm3(Predicted)
[storage temp. ]

2-8°C
[pka]

-0.15±0.41(Predicted)
[Appearance]

Brown to black Solid
Spectrum DetailBack Directory
[Spectrum Detail]

H-pyrrolo[1,2-b]pyridazine-6-carboxylic acid(118768-13-1)1HNMR
Hazard InformationBack Directory
[Synthesis]

Pyrrolo[1,2-b]pyridazine-5,6,7-tricarboxylic acid, 7-(1,1-dimethylethyl) 5,6-dimethyl ester

249513-32-4

H-pyrrolo[1,2-b]pyridazine-6-carboxylic acid

118768-13-1

The general procedure for the synthesis of pyrrolo[1,2-b]pyridazine-6-carboxylic acid from the compound (CAS: 249513-32-4) is as follows: intermediate B8: pyrrolo[1,2-b]pyridazine-6-carboxylic acid 7-tert-butyl 5,6-dimethyl pyrrolo[1,2-b]pyridazine-5,6,7-tricarboxylate was prepared with reference to the method reported by J. Mat. (1999 , 9, 2183-2188, which is incorporated herein by reference in its entirety). This was done as follows: the feedstock compound (3.25 g, 9.72 mmol) was suspended in a solution of water (12 mL) containing KOH (2.727 g, 48.6 mmol), and the reaction mixture was subsequently heated and reacted at 60 °C overnight. Upon completion of the reaction, the mixture was acidified to pH = 1 by addition of concentrated aqueous hydrochloric acid (9.41 mL) and stirring was continued at 80 °C overnight. After the reaction mixture was cooled to room temperature, the precipitate was collected by filtration to afford the target product pyrrolo[1,2-b]pyridazine-6-carboxylic acid (1.52 g, 9.37 mmol, 96% yield). The product was analyzed by mass spectrometry: MS/ESI+ m/z 163.1 [MH]+, retention time Rt = 0.61 min (analytical method A).

[References]

[1] Patent: US2015/361100, 2015, A1. Location in patent: Paragraph 0303; 0304
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