ChemicalBook--->CAS DataBase List--->148760-75-2

148760-75-2

148760-75-2 Structure

148760-75-2 Structure
IdentificationBack Directory
[Name]

1-Boc-1H-pyrrolo[3,2-c]pyridine
[CAS]

148760-75-2
[Synonyms]

1-Boc-1H-pyrrolo[3,2-c]pyridine
1-Boc-pyrrolo[3,2-c]pyridine, 95%
1H-Pyrrolo[3,2-c]pyridine-1-carboxylic acid tert-butyl ester
1H-Pyrrolo[3,2-c]pyridine-1-carboxylic acid, 1,1-diMethylethyl ester
[Molecular Formula]

C12H14N2O2
[MDL Number]

MFCD11976180
[MOL File]

148760-75-2.mol
[Molecular Weight]

218.25
Chemical PropertiesBack Directory
[Boiling point ]

339.3±34.0 °C(Predicted)
[density ]

1.14±0.1 g/cm3(Predicted)
[storage temp. ]

2-8°C
[pka]

7.02±0.30(Predicted)
Hazard InformationBack Directory
[Synthesis]

5-Azaindole

271-34-1

Di-tert-butyl dicarbonate

24424-99-5

1-Boc-1H-pyrrolo[3,2-c]pyridine

148760-75-2

Step A: Preparation of tert-butyl 1H-pyrrolo[3,2-c]pyridine-1-carboxylate: To a stirred mixture of 5-azaindole (2.3 g, 20 mmol) and 4-dimethylaminopyridine (2.4 g, 20 mmol) in acetonitrile (20 mL) was added di-tert-butyl dicarbonate (3.9 g, 18 mmol). The reaction mixture was stirred at room temperature for 18 hours. Upon completion of the reaction, the mixture was concentrated under reduced pressure and subsequently purified by Biotage Flash 40S column chromatography using 1:1 ethyl acetate/hexane as eluent. The target product 1H-pyrrolo[3,2-c]pyridine-1-carboxylic acid tert-butyl ester was obtained as a colorless oil (4.0 g, 101% yield).

[References]

[1] Patent: US2007/238726, 2007, A1. Location in patent: Page/Page column 114
[2] Patent: WO2017/23987, 2017, A1. Location in patent: Paragraph 0703; 0704
[3] Patent: WO2017/24003, 2017, A1. Location in patent: Paragraph 0703; 0704
[4] Patent: WO2017/24010, 2017, A1. Location in patent: Paragraph 0650; 0651
[5] Patent: WO2017/23984, 2017, A1. Location in patent: Paragraph 0703
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