ChemicalBook--->CAS DataBase List--->50735-34-7

50735-34-7

50735-34-7 Structure

50735-34-7 Structure
IdentificationBack Directory
[Name]

Methyl 2-amino-5-bromonicotinate
[CAS]

50735-34-7
[Synonyms]

2-AMINO-5-BROMONICOTINATE
METHYL 2-AMINO-5-BROMONICOTINAT
METHYL 2-AMINO-5-BROMONICOTINATE
2-AMino-5-broMo-nicotinic acid ethyl ester
2-AMINO-5-BROMO-NICOTINIC ACID METHYL ESTER
METHYL 2-AMINO-5-BROMOPYRIDINE-3-CARBOXYLATE
Methyl 2-amino-5-bromonicotinate ISO 9001:2015 REACH
3-Pyridinecarboxylic acid, 2-aMino-5-broMo-, Methyl e
TIANFU-CHEM Methyl 2-amino-5-bromonicotinate 50735-34-7
3-Pyridinecarboxylic acid, 2-aMino-5-broMo-, Methyl ester
Methyl 2-amino-5-bromopyridine-3-carboxylate, 2-Amino-5-bromo-3-(methoxycarbonyl)pyridine
[EINECS(EC#)]

229-486-4
[Molecular Formula]

C7H7BrN2O2
[MDL Number]

MFCD04117787
[MOL File]

50735-34-7.mol
[Molecular Weight]

231.05
Chemical PropertiesBack Directory
[Melting point ]

143-146°C
[Boiling point ]

275.2±35.0 °C(Predicted)
[density ]

1.662±0.06 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[pka]

2.45±0.49(Predicted)
[Appearance]

White to yellow Solid
[InChI]

InChI=1S/C7H7BrN2O2/c1-12-7(11)5-2-4(8)3-10-6(5)9/h2-3H,1H3,(H2,9,10)
[InChIKey]

POWKBBOOIZBIRZ-UHFFFAOYSA-N
[SMILES]

C1(N)=NC=C(Br)C=C1C(OC)=O
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H319
[Precautionary statements ]

P305+P351+P338
[HazardClass ]

IRRITANT
[HS Code ]

2933399990
Hazard InformationBack Directory
[Uses]

Methyl 2-Amino-5-bromonicotinate is a chemical reagent used in the synthesis of pharmaceutical agents.
[Synthesis]

Methyl 2-aminonicotinate

14667-47-1

Methyl 2-amino-5-bromonicotinate

50735-34-7

To a stirred solution of methyl 2-aminopyridine-3-carboxylate (2 g, 13.15 mmol) and sodium bicarbonate (2.2 g, 26.31 mmol) in dichloromethane (30 mL) was slowly added a dichloromethane solution of bromine dropwise (1.01 mL bromine dissolved in 20 mL dichloromethane). The reaction mixture was stirred at room temperature for 1 hour. Upon completion of the reaction, the reaction was quenched with sodium bisulfite solution (50 mL). The reaction mixture was extracted with dichloromethane (2 x 40 mL) and the combined organic phases were washed with brine (40 mL) and dried over anhydrous sodium sulfate. After filtration, the solvent was evaporated under reduced pressure to give methyl 2-amino-5-bromopyridine-3-carboxylate as a yellow solid (3 g, 99% yield).LCMS m/z (79Br/81Br) 231/233 (M+H)+.

[References]

[1] Patent: US2017/29420, 2017, A1. Location in patent: Paragraph 0034
Spectrum DetailBack Directory
[Spectrum Detail]

Methyl 2-amino-5-bromonicotinate(50735-34-7)1HNMR
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