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106896-48-4

106896-48-4 Structure

106896-48-4 Structure
IdentificationBack Directory
[Name]

3-AMINO-2-BROMO-BENZOIC ACID METHYL ESTER
[CAS]

106896-48-4
[Synonyms]

Methyl 3-aMino-2-broMobenzoate
Methyl 3-aMino-2-broMobenzoate 95%
3-AMINO-2-BROMO-BENZOIC ACID METHYL ESTER
Benzoic acid, 3-amino-2-bromo-, methyl ester
[Molecular Formula]

C8H8BrNO2
[MDL Number]

MFCD03844437
[MOL File]

106896-48-4.mol
[Molecular Weight]

230.06
Chemical PropertiesBack Directory
[Boiling point ]

314.1±22.0 °C(Predicted)
[density ]

1.583 g/mL at 25 °C
[refractive index ]

n20/D1.601
[Fp ]

>110℃
[storage temp. ]

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

liquid
[pka]

1.39±0.10(Predicted)
[color ]

Clear, bright orange/amber
[InChI]

1S/C8H8BrNO2/c1-12-8(11)5-3-2-4-6(10)7(5)9/h2-4H,10H2,1H3
[InChIKey]

NIXWZYZFLFEHMB-UHFFFAOYSA-N
[SMILES]

COC(=O)c1cccc(N)c1Br
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

22-36/37/38
[Safety Statements ]

26
[RIDADR ]

2810
[WGK Germany ]

3
[HazardClass ]

6.1
[PackingGroup ]

Ⅲ
[HS Code ]

2922498590
[Storage Class]

6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
[Hazard Classifications]

Acute Tox. 3 Oral
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Hazard InformationBack Directory
[Uses]

Methyl 3-Amino-2-bromobenzoate is used in preparation of Carbazole-based compounds and its application as IDO inhibitor.
[Synthesis]

METHYL 2-BROMO-3-NITROBENZOATE

5337-09-7

3-AMINO-2-BROMO-BENZOIC ACID METHYL ESTER

106896-48-4

Methyl 2-bromo-3-nitrobenzoate (12.9 g, 49.5 mmol) was used as feedstock and prepared according to the method described by Webber ES et al. (Patent Application No. WO 01/16136 A2). The feedstock was refluxed with SnCl2 (42 g, 223 mmol) in a mixed solution of methanol (225 mL, 0.2 M) and H2O (5.3 g, 243 mmol) for 2 hours. After completion of the reaction, it was cooled to room temperature and diatomaceous earth (20 g) and dichloromethane (1 L) were added, followed by the slow addition of 3 N aqueous sodium hydroxide solution (150 mL) under vigorous stirring. The reaction mixture was filtered and the organic phase was washed with saturated aqueous sodium chloride solution. The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to remove all volatiles to afford the intermediate methyl 3-amino-2-bromobenzoate (11.4 g) in 98% yield.1H-NMR (d6-DMSO) δ: 7.12 (dd, 1H, J = 8.1, 7.5 Hz), 6.93 (dd, 1H, J = 8.1, 1.6 Hz), 6.80 ( dd, 1H, J = 7.4, 1.6 Hz), 5.57 (s, 2H), 3.81 (s, 3H).

[References]

[1] Patent: WO2004/63198, 2004, A1. Location in patent: Page 77
[2] Tetrahedron, 2010, vol. 66, # 29, p. 5402 - 5406
[3] Tetrahedron, 2000, vol. 56, # 2, p. 165 - 173
[4] Journal of Organic Chemistry, 1988, vol. 53, # 6, p. 1170 - 1176
[5] Patent: EP950657, 1999, A2
Spectrum DetailBack Directory
[Spectrum Detail]

3-AMINO-2-BROMO-BENZOIC ACID METHYL ESTER(106896-48-4)1HNMR
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