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ChemicalBook--->CAS DataBase List--->221675-35-0

221675-35-0

221675-35-0 Structure

221675-35-0 Structure
IdentificationBack Directory
[Name]

1H-Pyrrolo[2,3-b]pyridine-2-carboxylic acid, ethyl ester
[CAS]

221675-35-0
[Synonyms]

ethyl 1H-pyrrolo[2
Ethyl 7-azaindole-2-carboxylate
ethyl1H-pyrrolo[2,3-b]pyridine-2-carbo
2-(Ethoxycarbonyl)-1H-pyrrolo[2,3-b]pyridine
ethyl 1H-pyrrolo[2,3-b]pyridine-2-carbo×ylate
1H-Prrolo[2,3-b]pyridine-2-carboxylic acid ethyl ester
1H-Pyrrolo[2,3-b]pyridine-2-carboxylic acid, ethyl ester
2-(Ethoxycarbonyl)-1H-pyrrolo[2,3-b]pyridine, Ethyl 1H-pyrrolo[2,3-b]pyridine-2-carboxylate
[Molecular Formula]

C10H10N2O2
[MDL Number]

MFCD09998715
[MOL File]

221675-35-0.mol
[Molecular Weight]

190.2
Chemical PropertiesBack Directory
[Boiling point ]

436.4±37.0 °C(Predicted)
[density ]

1.27±0.1 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

5.73±0.40(Predicted)
[Appearance]

Off-white to yellow Solid
[InChI]

InChI=1S/C10H10N2O2/c1-2-14-10(13)8-6-7-4-3-5-11-9(7)12-8/h3-6H,2H2,1H3,(H,11,12)
[InChIKey]

CBIVEMGUNRNUEB-UHFFFAOYSA-N
[SMILES]

C12NC(C(OCC)=O)=CC1=CC=CN=2
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P271-P280
[HS Code ]

2933998090
Spectrum DetailBack Directory
[Spectrum Detail]

1H-Pyrrolo[2,3-b]pyridine-2-carboxylic acid, ethyl ester(221675-35-0)1HNMR
Hazard InformationBack Directory
[Synthesis]

1H-Pyrrolo[2,3-b]pyridine-1,2-dicarboxylic acid, 2,3-dihydro-2-hydroxy-, 1-(1,1-dimethylethyl) 2-ethyl ester

287384-79-6

1H-Pyrrolo[2,3-b]pyridine-2-carboxylic acid, ethyl ester

221675-35-0

General procedure for the synthesis of ethyl 1H-pyrrolo[2,3-B]pyridine-2-carboxylate from compound (CAS: 287384-79-6): compound 29 (9.7 g, 31.4 mmol, 1 equiv.) was dissolved in 6 N hydrochloric acid solution (50 mL) and stirred for 2 hr at 50 °C, followed by continued stirring at room temperature overnight. Upon completion of the reaction, the pH of the reaction mixture was adjusted to 13 with solid potassium carbonate (K2CO3), followed by extraction with ethyl acetate (EtOAc). The organic phases were combined, dried with anhydrous sodium sulfate, filtered and concentrated under reduced pressure to afford the target product 30 (6.0 g, 100% yield). The structure of the product was confirmed by 1H NMR (400 MHz, DMSO-d6): δ 11.12 (br s, 1H), 8.59 (d, J = 4.8 Hz, 1H), 8.05 (dd, J = 8.0, 1.6 Hz, 1H), 7.19 (s, 1H), 7.18-7.15 (m, 1H), 4.46 (q, J = 6.8 Hz. 2H), 1.44 (t, J = 6.8 Hz, 3H).

[References]

[1] European Journal of Medicinal Chemistry, 2014, vol. 88, p. 3 - 9
[2] Patent: WO2015/187428, 2015, A1. Location in patent: Paragraph 00502; 00505; 00506
[3] Patent: US2009/318455, 2009, A1. Location in patent: Page/Page column 69; 93
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