ChemicalBook--->CAS DataBase List--->78686-77-8

78686-77-8

78686-77-8 Structure

78686-77-8 Structure
IdentificationBack Directory
[Name]

Methyl 5-bromo-6-chloropyridine-3-carboxylate
[CAS]

78686-77-8
[Synonyms]

Methyl 5-bromo-6-chl
METHYL 5-BROMO-6-CHLORONICOTINATE
Methyl-5-bromo-6-chloronicotinic acid
5-BROMO-6-CHLORONICOTINIC ACID METHYL ESTER
methyl 5-bromo-6-chloropyridine-3-carboxylate
Methyl 3-bromo-2-chloropyridine-5-carboxylate
3-Pyridinecarboxylic acid, 5-bromo-6-chloro-, methyl ester
Methyl 5-bromo-6-chloropyridine-3-carboxylate ISO 9001:2015 REACH
Methyl 5-bromo-6-chloropyridine-3-carboxylate, Methyl 3-bromo-2-chloropyridine-5-carboxylate
[EINECS(EC#)]

-0
[Molecular Formula]

C7H5BrClNO2
[MDL Number]

MFCD03844855
[MOL File]

78686-77-8.mol
[Molecular Weight]

250.48
Chemical PropertiesBack Directory
[Melting point ]

75-77°C
[Boiling point ]

279.2±35.0 °C(Predicted)
[density ]

1.684
[refractive index ]

1.568
[storage temp. ]

Inert atmosphere,2-8°C
[solubility ]

Chloroform (Slightly), Methanol (Slightly), Water (Slightly)
[form ]

Solid
[pka]

-2.84±0.10(Predicted)
[color ]

White to Off-White
[InChI]

InChI=1S/C7H5BrClNO2/c1-12-7(11)4-2-5(8)6(9)10-3-4/h2-3H,1H3
[InChIKey]

WINGWVOUOFMOJQ-UHFFFAOYSA-N
[SMILES]

C1=NC(Cl)=C(Br)C=C1C(OC)=O
[CAS DataBase Reference]

78686-77-8
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335-H302
[Precautionary statements ]

P301+P312+P330-P261-P280a-P304+P340-P305+P351+P338-P405-P501a
[Hazard Codes ]

Xi,Xn
[Risk Statements ]

22
[HazardClass ]

IRRITANT
[HS Code ]

2933399990
Hazard InformationBack Directory
[Uses]

Methyl 5-Bromo-6-chloronicotinate can be used to treat diseases related to S1PR1.
[Synthesis]

5-Bromo-6-chloronicotinic acid

29241-62-1

Iodomethane

74-88-4

Methyl 5-bromo-6-chloropyridine-3-carboxylate

78686-77-8

Step 1: Synthesis of methyl 5-bromo-6-chloronicotinate (61). A mixture of 5-bromo-6-chloronicotinic acid (60) (0.2 g, 0.84 mmol), potassium carbonate (K2CO3) (0.3 g, 2.1 mmol) and iodomethane (0.178 g, 1.2 mmol) in N,N-dimethylformamide (DMF) (10 mL) was stirred for 16 h at 0 °C and subsequently raised to room temperature. Upon completion of the reaction, the reaction mixture was diluted with water (20 mL) and extracted with ethyl acetate (EtOAc) (2 x 20 mL). The organic phases were combined and washed sequentially with saturated aqueous sodium bicarbonate (NaHCO3) (20 mL) and brine (2 x 20 mL), dried over anhydrous sodium sulfate (Na2SO4) and concentrated to afford the target product methyl 5-bromo-6-chloronicotinate (61) (0.2 g, 94.7% yield).

[References]

[1] Patent: WO2017/4608, 2017, A1. Location in patent: Paragraph 0183
Spectrum DetailBack Directory
[Spectrum Detail]

Methyl 5-bromo-6-chloropyridine-3-carboxylate(78686-77-8)1HNMR
Methyl 5-bromo-6-chloropyridine-3-carboxylate(78686-77-8)FT-IR
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