ChemicalBook--->CAS DataBase List--->1014613-64-9

1014613-64-9

1014613-64-9 Structure

1014613-64-9 Structure
IdentificationBack Directory
[Name]

4-Bromo-2-methyl-1H-pyrrolo[2,3-b]pyridine
[CAS]

1014613-64-9
[Synonyms]

4-Bromo-2-methyl-1H-pyrrolo[2,3-b]pyridine
1H-Pyrrolo[2,3-b]pyridine, 4-broMo-2-Methyl-
4-Bromo-2-methyl-1H-pyrrolo[2,3-b]pyridine 95%
(2R,3R,4R,5R)-2-(Acetoxymethyl)-5-(6-amino-9H-purin-9-yl)tetrahydrofuran-3,4-diyl diacetate
[EINECS(EC#)]

200-258-5
[Molecular Formula]

C8H7BrN2
[MDL Number]

MFCD15529172
[MOL File]

1014613-64-9.mol
[Molecular Weight]

211.059
Chemical PropertiesBack Directory
[density ]

1.654±0.06 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[form ]

solid
[pka]

13.52±0.40(Predicted)
[color ]

Light brown to brown
Safety DataBack Directory
[Symbol(GHS) ]

Corrosion (GHS05)Environment (GHS09)
GHS05,GHS09
[Signal word ]

Danger
[Hazard statements ]

H315-H318-H410
[Precautionary statements ]

P501-P273-P264-P280-P302+P352-P391-P362+P364-P332+P313-P305+P351+P338+P310
[HS Code ]

2933399990
Spectrum DetailBack Directory
[Spectrum Detail]

4-Bromo-2-methyl-1H-pyrrolo[2,3-b]pyridine(1014613-64-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

4-Bromo-2-methyl-1-phenylsulfonyl-7-azaindole

1014613-05-8

4-Bromo-2-methyl-1H-pyrrolo[2,3-b]pyridine

1014613-64-9

General procedure for the synthesis of 4-bromo-2-methyl-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine from 4-bromo-2-methyl-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine: To 4-bromo-2-methyl-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine (16 g, 0.045 mol) of 1,4-dioxane ( 320 mL) solution was added to 2M aqueous sodium hydroxide solution (114 mL, 0.228 mol). The reaction mixture was heated to 60°C and kept for 16 hours. After the reaction was completed, the mixture was cooled to room temperature. The organic layer was separated and the aqueous layer was extracted with ethyl acetate. The organic phases were combined, washed with saturated brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to give 4-bromo-2-methyl-1H-pyrrolo[2,3-b]pyridine as a milky white solid (10.07 g, 104% yield). lC/MS (Method B): m/z 211/213 [M+H]+, retention time 1.04 min.

[References]

[1] Patent: WO2009/112475, 2009, A1. Location in patent: Page/Page column 62
[2] Bioorganic and Medicinal Chemistry Letters, 2009, vol. 19, # 9, p. 2504 - 2508
[3] Patent: US2010/160647, 2010, A1. Location in patent: Page/Page column 21
[4] Patent: WO2012/170752, 2012, A1. Location in patent: Page/Page column 42
[5] Bioorganic and Medicinal Chemistry, 2015, vol. 23, # 15, p. 4344 - 4353
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