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

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

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

Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Warning

Hazard statements

H302Harmful if swallowed

H312Harmful in contact with skin

H332Harmful if inhaled

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P270Do not eat, drink or smoke when using this product.

P271Use only outdoors or in a well-ventilated area.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.

P312Call a POISON CENTER or doctor/physician if you feel unwell.

P322Specific measures (see …on this label).

P330Rinse mouth.

P363Wash contaminated clothing before reuse.

P501Dispose of contents/container to..…

2-Benzyloxy-3-dibenzylaMino-5-fluoro-6-Methyl-benzoic acid phenyl ester Chemical Properties,Usage,Production

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

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