ChemicalBook--->CAS DataBase List--->1253799-29-9

1253799-29-9

1253799-29-9 Structure

1253799-29-9 Structure
IdentificationBack Directory
[Name]

2-Benzyloxy-3-dibenzylaMino-5-fluoro-6-Methyl-benzoic acid phenyl ester
[CAS]

1253799-29-9
[Synonyms]

EOS-61973
2-Benzyloxy-3-dibenzylaMino-5-fluoro-6-Methyl-benzoic acid phenyl ester
phenyl 2-(benzyloxy)-3-(dibenzylamino)-5-fluoro-6-methylbenzoate TP-353
3-[Bis(phenylmethyl)amino]-5-fluoro-6-methyl-2-(phenylmethoxy)benzoic acid phenyl ester
Benzoic acid, 3-[bis(phenylmethyl)amino]-5-fluoro-6-methyl-2-(phenylmethoxy)-, phenyl ester
[Molecular Formula]

C35H30FNO3
[MDL Number]

MFCD28142365
[MOL File]

1253799-29-9.mol
[Molecular Weight]

531.62
Chemical PropertiesBack Directory
[Boiling point ]

695.5±55.0 °C(Predicted)
[density ]

1?+-.0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

2.69±0.50(Predicted)
[InChIKey]

VRXGVVAMXZXKNA-UHFFFAOYSA-N
[SMILES]

C(OC1=CC=CC=C1)(=O)C1=C(C)C(F)=CC(N(CC2=CC=CC=C2)CC2=CC=CC=C2)=C1OCC1=CC=CC=C1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H332-H312
[Precautionary statements ]

P280-P302+P352-P312-P322-P363-P501-P261-P271-P304+P340-P312-P264-P270-P301+P312-P330-P501
Hazard InformationBack Directory
[Uses]

Phenyl 2-(benzyloxy)-3-(dibenzylamino)-5-fluoro-6-methylbenzoate (CAS# 1253799-29-9) is most frequently used as a building block in the synthesis of tetracycline antibiotics.
[Synthesis]

3-AMino-2-benzyloxy-5-fluoro-6-Methyl-benzoic acid phenyl ester

1207284-89-6

Benzyl bromide

100-39-0

2-Benzyloxy-3-dibenzylaMino-5-fluoro-6-Methyl-benzoic acid phenyl ester

1253799-29-9

To a solution of 500 g of the compound (CAS:1207284-89-6) in 4.25 L of N-methylpyrrolidone was added N,N-diisopropylethylamine (620 mL), followed by benzyl bromide (425 mL, 2.5 equiv). The reaction mixture was heated at 100 °C for 18 h, after which it was cooled to 80 °C and treated with 25% w/w aqueous triethylamine solution for 10 min. The mixture was stirred at room temperature for 25 minutes and subsequently cooled to 15 °C and water (10 L) was added to precipitate the product. After 3 h of precipitation, the resulting light-colored suspension was filtered and washed with 2 L of water and subsequently dried. The crude product (750 g) was dissolved in 4.1 L of toluene and filtered through silica gel to give 762 g of yellow solid. This solid was recrystallized by acetone/heptane to give a final 606 g of the target compound 2-(benzyloxy)-3-(benzylamino)-5-fluoro-6-methylbenzoic acid (80% yield) as a white solid. Its 1H NMR (400 MHz, CDCl3) data were as follows: δ 7.48-7.03 (m, 20H), 6.60 (d, J=11.5 Hz, 1H), 5.31 (s, 2H), 4.33 (s, 4H), 2.30 (s, 3H).

[References]

[1] Patent: WO2010/126607, 2010, A2. Location in patent: Page/Page column 172/251
Spectrum DetailBack Directory
[Spectrum Detail]

2-Benzyloxy-3-dibenzylaMino-5-fluoro-6-Methyl-benzoic acid phenyl ester(1253799-29-9)1HNMR
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