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1220910-89-3

1220910-89-3 Structure

1220910-89-3 Structure
IdentificationBack Directory
[Name]

CarbaMic acid, N-[3-fluoro-4-[6-(2-Methyl-2H-tetrazol-5-yl)-3-pyridinyl]phenyl]-, phenylMethyl ester
[CAS]

1220910-89-3
[Synonyms]

Torezolid-20
Tedizolid Impurity 46
Tedizolid Impurity 68
Torezolid Intermediate1
Intermediate of Tedazolamide
Tedizolid Phosphate Intermediate
N-[3-fluoro-4-[6-(2-Methyl-2H-tetrazol-5-yl)-3-pyridinyl]phenyl]-
benzyl N-[3-fluoro-4-[6-(2-methyltetrazol-5-yl)pyridin-3-yl]phenyl]carbamate
benzyl (3-fluoro-4-(6-(2-Methyl-2H-tetrazol-5-yl)pyridin-3-yl)phenyl)carbaMate
Benzyl {3-fluoro-4-[6-(2-methyl-2H-tetrazol-5-yl)-3-pyridinyl]phe nyl}carbamate
N- [3- fluoro-4- [6- (2-methyl--2H- tetrazol-5-yl) -3-pyridinyl] phenyl] carbamate
N-[3-fluoro-4-[6-(2-Methyl-2H-tetrazol-5-yl)-3-pyridinyl]phenyl]-, phenylMethyl ester
N- [3- fluoro-4- [6- (2-methyl--2H- tetrazol-5-yl) -3-pyridinyl] phenyl] carbamate carbamic acid
N-[3-Fluoro-4-[6-(2-Methyl-2H-tetrazol-5-yl)-3-pyridinyl]phenyl]carbaMic acid phenylMethyl ester
CarbaMic acid, N-[3-fluoro-4-[6-(2-Methyl-2H-tetrazol-5-yl)-3-pyridinyl]phenyl]-, phenylMethyl ester
Tedizolid impurity 29/Benzyl (3-fluoro-4-(6-(2-methyl-2H-tetrazol-5-yl)pyridin-3-yl)phenyl)carbamate
CarbaMic acid, N-[3-fluoro-4-[6-(2-Methyl-2H-tetrazol-5-yl)-3-pyridinyl]phenyl]-, phenylMethyl ester ISO 9001:2015 REACH
[Molecular Formula]

C21H17FN6O2
[MDL Number]

MFCD22418002
[MOL File]

1220910-89-3.mol
[Molecular Weight]

404.397
Chemical PropertiesBack Directory
[Melting point ]

168-170°C
[density ]

1.36±0.1 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,2-8°C
[solubility ]

Dichloromethane (Slightly), DMSO (Slightly), Methanol (Slightly)
[form ]

Solid
[pka]

12.52±0.70(Predicted)
[color ]

White to Off-White
[InChI]

InChI=1S/C21H17FN6O2/c1-28-26-20(25-27-28)19-10-7-15(12-23-19)17-9-8-16(11-18(17)22)24-21(29)30-13-14-5-3-2-4-6-14/h2-12H,13H2,1H3,(H,24,29)
[InChIKey]

GIBJIBYBOVNDET-UHFFFAOYSA-N
[SMILES]

C(OCC1=CC=CC=C1)(=O)NC1=CC=C(C2=CC=C(C3=NN(C)N=N3)N=C2)C(F)=C1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P501-P270-P264-P301+P312+P330
Hazard InformationBack Directory
[Uses]

N-[3-Fluoro-4-[6-(2-methyl-2H-tetrazol-5-yl)-3-pyridinyl]phenyl]carbamic Acid Phenylmethyl Ester is an intermediate in the synthesis of Tedizolid (T013750), an known oral and intravenous antibiotic.
[Synthesis]

CarbaMic acid, (4-borono-3-fluorophenyl)-, C-(phenylMethyl) ester (9CI)

874290-59-2

5-BROMO-2-(2-METHYL-2H-TETRAZOL-5-YL)-PYRIDINE

380380-64-3

CarbaMic acid, N-[3-fluoro-4-[6-(2-Methyl-2H-tetrazol-5-yl)-3-pyridinyl]phenyl]-, phenylMethyl ester

1220910-89-3

To a 5L three-necked round-bottomed flask was added (4-(((benzyloxy)carbonyl)amino)-2-fluorophenyl)boronic acid (200.0 g, 0.833 mol) followed by 1,4-dioxane (3L, 15 vol). The crude compound 2-(2-methyl-tetrazolyl)-5-bromopyridine (361.2 g, 1.249 mol, 1.5 eq.), tris(dibenzylideneacetone)dipalladium (11.44 g, 0.0125 mol, 0.015 eq.) and tricyclohexylphosphine (7.0 g, 0.025 mol, 0.03 eq.) were added and protected with nitrogen for 30 min. A solution of potassium carbonate (195.7 g, 1.7 eq.) in water (800 mL, 4 v/v) was added and the reaction was heated to 70 °C. After 1 h the reaction was complete with 0.5 area % of (4-(((benzyloxy)carbonyl)amino)-2-fluorophenyl)boronic acid remaining. The reaction was cooled to 50 °C, activated carbon Darco G-60 (40 g, 0.2 wt) was added and stirred for 30 min. Diatomaceous earth 545 (40 g, 0.2 wt) was added and the reaction was filtered through diatomaceous earth 545 (100 g, 0.5 wt) wetted with water (300 mL). Hot filtration from the diatomaceous earth into water resulted in precipitation of the product. Tetrahydrofuran (1.2 L, 6 vol) and brine (600 mL, 3 vol) were added and the product redissolved at room temperature. Phase separation was completely clean (Vmax = 28 vol). The dioxane was concentrated, ethanol (1L, 5 vol) was added and concentrated. The product was then re-slurried in ethanol: water (4:1,2L, 10 vol) at 70°C, cooled to room temperature over 3 h, filtered and washed with ethanol (2 x 400 mL). Benzyl (3-fluoro-4-(6-(2-methyl-2H-tetrazol-5-yl)pyridin-3-yl)phenyl)carbamate was isolated in 87% yield (292.6 g) by HPLC analysis with a purity of 97.7% (AUC).1H NMR and 19F NMR indicated the presence of a compound.Pd analysis showed that the product contained 135 ppm Pd.

[References]

[1] Patent: WO2010/42887, 2010, A2. Location in patent: Page/Page column 18-19
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