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1245643-11-1

1245643-11-1 Structure

1245643-11-1 Structure
IdentificationBack Directory
[Name]

Methyl 3,4-diaMino-5-broMobenzoate
[CAS]

1245643-11-1
[Synonyms]

Methyl 3-bromo-4,5-diaminobenzoate
3,4-Diamino-5-bromo-benzoic acid methyl ester
Benzoic acid, 3,4-diamino-5-bromo-, methyl ester
3-Bromo-5-(methoxycarbonyl)benzene-1,2-diamine, 3-Bromo-5-(methoxycarbonyl)phenylene-1,2-diamine
[Molecular Formula]

C8H9BrN2O2
[MDL Number]

MFCD18072579
[MOL File]

1245643-11-1.mol
[Molecular Weight]

245.07
Chemical PropertiesBack Directory
[Boiling point ]

402.5±40.0 °C(Predicted)
[density ]

1.655±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,2-8°C
[form ]

light sensitive solid
[pka]

1.94±0.10(Predicted)
[color ]

Dark brown
[InChI]

InChI=1S/C8H9BrN2O2/c1-13-8(12)4-2-5(9)7(11)6(10)3-4/h2-3H,10-11H2,1H3
[InChIKey]

FJUXWCBISHILFS-UHFFFAOYSA-N
[SMILES]

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

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P271-P280
[Hazard Codes ]

Xn
[Risk Statements ]

22-43
[Safety Statements ]

36/37
[HS Code ]

2922498590
Hazard InformationBack Directory
[Uses]

Methyl 3,4-diamino-5-bromobenzoate
[Synthesis]

Methyl 4-amino-3-bromo-5-nitrobenzenecarboxylate

105655-17-2

Methyl 3,4-diaMino-5-broMobenzoate

1245643-11-1

Methyl 4-amino-3-bromo-5-nitrobenzoate (10 g, 36.3 mmol) was used as starting material to form a suspension with tin(II) chloride (33 g, 14.5 mmol) in methanol (100 mL). The suspension was heated to 60 °C and maintained at this temperature for the reaction. Upon completion of the reaction, the reaction mixture was cooled to room temperature and subsequently concentrated to give a residue. The residue was adjusted to pH 11 with saturated aqueous sodium bicarbonate and the aqueous phase was extracted with dichloromethane (3 x 200 mL). The organic phases were combined, washed with saturated aqueous sodium chloride solution (200 mL) and dried with anhydrous sodium sulfate. Concentration of the organic phase afforded the target compound methyl 3,4-diamino-5-bromobenzoate as an off-white solid (5 g, 58% yield).1H NMR (CDCl3) data were as follows: δ 7.74 (s, 1H), 7.35 (s, 1H), 4.18 (wide s, 2H), 3.85 (s, 3H), 3.38-3.56 (wide s, 2H).

[References]

[1] Patent: US2011/111046, 2011, A1. Location in patent: Page/Page column 19
[2] Patent: WO2011/58473, 2011, A1. Location in patent: Page/Page column 39; 40
[3] Patent: WO2016/77378, 2016, A1. Location in patent: Page/Page column 111; 112
Spectrum DetailBack Directory
[Spectrum Detail]

Methyl 3,4-diaMino-5-broMobenzoate(1245643-11-1)1HNMR
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