ChemicalBook--->CAS DataBase List--->1065181-58-9

1065181-58-9

1065181-58-9 Structure

1065181-58-9 Structure
IdentificationBack Directory
[Name]

Ethyl 5-broMo-1H-indole-7-carboxylate
[CAS]

1065181-58-9
[Synonyms]

Ethyl 5-broMo-1H-indole-7-carboxylate
1H-Indole-7-carboxylic acid, 5-bromo-, ethyl ester
[Molecular Formula]

C11H10BrNO2
[MDL Number]

MFCD21608002
[MOL File]

1065181-58-9.mol
[Molecular Weight]

268.11
Chemical PropertiesBack Directory
[storage temp. ]

2-8°C
[Appearance]

White to off-white Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
Spectrum DetailBack Directory
[Spectrum Detail]

Ethyl 5-broMo-1H-indole-7-carboxylate(1065181-58-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

ethyl 5-bromoindoline-7-carboxylate

1065181-56-7

Ethyl 5-broMo-1H-indole-7-carboxylate

1065181-58-9

Intermediate 4: Synthesis of ethyl 5-bromo-1H-indole-7-carboxylate. Ethyl 2,3-dihydro-5-bromo-1H-indole-7-carboxylate (129.1 g, 0.48 mmol) was dissolved in chloroform (1500 mL) and DDQ (119.3 g, 525.7 mmol) was added in batches. The reaction mixture was stirred at room temperature for 2 hours. After completion of the reaction, the mixture was filtered and the solids were washed with chloroform (3 x 500 mL). The combined filtrates were washed sequentially with 5% sodium hydroxide solution (3 x 500 mL), water (500 mL), and saturated brine (500 mL) and then dried with anhydrous sodium sulfate. The filtrate was concentrated under reduced pressure and the residue was recrystallized from ethanol to give ethyl 5-bromo-1H-indole-7-carboxylate (88 g, 69% yield). The product was analyzed by LC/MS: m/z 267.6 (M+H), retention time 1.14 min.

[References]

[1] Patent: WO2008/118724, 2008, A1. Location in patent: Page/Page column 66-67
[2] ACS Medicinal Chemistry Letters, 2018, vol. 9, # 12, p. 1164 - 1169
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