ChemicalBook--->CAS DataBase List--->392-09-6

392-09-6

392-09-6 Structure

392-09-6 Structure
IdentificationBack Directory
[Name]

METHYL 2-FLUORO-4-NITROBENZENECARBOXYLATE
[CAS]

392-09-6
[Synonyms]

METHYL 2-FLUORO-4-NITROBENZOATE
3-Fluoro-4-(methoxycarbonyl)nitrobenzene
METHYL 2-FLUORO-4-NITROBENZENECARBOXYLATE
Benzoic acid, 2-fluoro-4-nitro-, Methyl ester
[EINECS(EC#)]

206-873-6
[Molecular Formula]

C8H6FNO4
[MDL Number]

MFCD08444028
[MOL File]

392-09-6.mol
[Molecular Weight]

199.14
Chemical PropertiesBack Directory
[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
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P271-P280
[Hazard Codes ]

Xi
[WGK Germany ]

WGK 3
[HazardClass ]

IRRITANT
[HS Code ]

2916399090
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Eye Irrit. 2
Hazard InformationBack Directory
[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]

Methanol

67-56-1

2-Fluoro-4-nitrobenzoic acid

403-24-7

METHYL 2-FLUORO-4-NITROBENZENECARBOXYLATE

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
Spectrum DetailBack Directory
[Spectrum Detail]

METHYL 2-FLUORO-4-NITROBENZENECARBOXYLATE(392-09-6)1HNMR
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