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METHYL 2-FLUORO-4-NITROBENZENECARBOXYLATE

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METHYL 2-FLUORO-4-NITROBENZENECARBOXYLATE Basic information

Product Name:
METHYL 2-FLUORO-4-NITROBENZENECARBOXYLATE
Synonyms:
  • METHYL 2-FLUORO-4-NITROBENZENECARBOXYLATE
  • METHYL 2-FLUORO-4-NITROBENZOATE
  • 3-Fluoro-4-(methoxycarbonyl)nitrobenzene
  • Benzoic acid, 2-fluoro-4-nitro-, Methyl ester
  • Benzoic acid, 2-fluoro-4-nitro-, methyl ester (8CI, 9CI, ACI)
  • 2-fluoro-4-nitro-Benzoic acid methyl ester (8CI 9CI ACI)
  • Enzalutamide Impurity 79
CAS:
392-09-6
MF:
C8H6FNO4
MW:
199.14
EINECS:
206-873-6
Mol File:
392-09-6.mol
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METHYL 2-FLUORO-4-NITROBENZENECARBOXYLATE Chemical Properties

Melting point:
73-75°C
Boiling point:
314.6±32.0 °C(Predicted)
Density 
1.388
storage temp. 
Sealed in dry,Room Temperature
form 
crystalline solid
color 
Pale lemon
InChI
InChI=1S/C8H6FNO4/c1-14-8(11)6-3-2-5(10(12)13)4-7(6)9/h2-4H,1H3
InChIKey
KJCVCRCYCOWPFY-UHFFFAOYSA-N
SMILES
C(OC)(=O)C1=CC=C([N+]([O-])=O)C=C1F
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Safety Information

Hazard Codes 
Xi
HazardClass 
IRRITANT
HS Code 
2916399090
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METHYL 2-FLUORO-4-NITROBENZENECARBOXYLATE Usage And Synthesis

Uses

Methyl 2-fluoro-4-nitrobenzoate is a pharmaceutical intermediate compound used in the preparation of the anticancer drug Venetoclax.  Venetoclax is a B-cell lymphoma-2 (BCL-2) inhibitor used in the treatment of adults with chronic lymphocytic leukaemia (CLL) or small lymphocytic lymphoma (SLL), or newly diagnosed chronic lymphocytic lymphoma (SLL).

Synthesis

67-56-1

403-24-7

392-09-6

Step 1: Concentrated sulfuric acid (2.9 ml) was slowly added to a methanolic solution of 2-fluoro-4-nitrobenzoic acid (1 g, 5.402 mmol). The reaction mixture was heated to reflux overnight and subsequently cooled to room temperature and concentrated under reduced pressure. The residue was diluted with ethyl acetate and washed with saturated sodium bicarbonate solution. The organic layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography to afford pure methyl 2-fluoro-4-nitrobenzoate (1.05 g, 98% yield).

References

[1] Patent: WO2013/68467, 2013, A1. Location in patent: Page/Page column 57; 59; 60; 61
[2] Bioorganic and Medicinal Chemistry, 2009, vol. 17, # 19, p. 7042 - 7051
[3] Bioorganic and Medicinal Chemistry Letters, 2005, vol. 15, # 2, p. 337 - 343
[4] Patent: WO2004/37814, 2004, A1. Location in patent: Page 166-167
[5] Patent: EP1810969, 2007, A1. Location in patent: Page/Page column 41

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