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Type | HazMat fee for 500 gram (Estimated) |
Excepted Quantity | USD 0.00 |
Limited Quantity | USD 15-60 |
Inaccessible (Haz class 6.1), Domestic | USD 80+ |
Inaccessible (Haz class 6.1), International | USD 150+ |
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CAS No. : | 211943-13-4 | MDL No. : | MFCD02093928 |
Formula : | C6H4BrN5 | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | XJGDASCALCDOQH-UHFFFAOYSA-N |
M.W : | 226.03 g/mol | Pubchem ID : | 4173761 |
Synonyms : |
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Num. heavy atoms : | 12 |
Num. arom. heavy atoms : | 11 |
Fraction Csp3 : | 0.0 |
Num. rotatable bonds : | 1 |
Num. H-bond acceptors : | 4.0 |
Num. H-bond donors : | 1.0 |
Molar Refractivity : | 45.11 |
TPSA : | 67.35 Ų |
GI absorption : | High |
BBB permeant : | No |
P-gp substrate : | No |
CYP1A2 inhibitor : | No |
CYP2C19 inhibitor : | No |
CYP2C9 inhibitor : | No |
CYP2D6 inhibitor : | No |
CYP3A4 inhibitor : | No |
Log Kp (skin permeation) : | -7.09 cm/s |
Log Po/w (iLOGP) : | 0.84 |
Log Po/w (XLOGP3) : | 0.83 |
Log Po/w (WLOGP) : | 1.02 |
Log Po/w (MLOGP) : | 0.99 |
Log Po/w (SILICOS-IT) : | 1.82 |
Consensus Log Po/w : | 1.1 |
Lipinski : | 0.0 |
Ghose : | None |
Veber : | 0.0 |
Egan : | 0.0 |
Muegge : | 0.0 |
Bioavailability Score : | 0.85 |
Log S (ESOL) : | -2.38 |
Solubility : | 0.95 mg/ml ; 0.0042 mol/l |
Class : | Soluble |
Log S (Ali) : | -1.83 |
Solubility : | 3.37 mg/ml ; 0.0149 mol/l |
Class : | Very soluble |
Log S (SILICOS-IT) : | -3.5 |
Solubility : | 0.0723 mg/ml ; 0.00032 mol/l |
Class : | Soluble |
PAINS : | 0.0 alert |
Brenk : | 0.0 alert |
Leadlikeness : | 1.0 |
Synthetic accessibility : | 2.0 |
Signal Word: | Danger | Class: | 4.1 |
Precautionary Statements: | P240-P210-P241-P264-P280-P302+P352-P370+P378-P337+P313-P305+P351+P338-P362+P364-P332+P313 | UN#: | 1325 |
Hazard Statements: | H315-H319-H228 | Packing Group: | Ⅱ |
GHS Pictogram: |
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* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 2 steps 1: caesium carbonate; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2 / tetrahydrofuran; water / 3 h / 85 °C / Inert atmosphere; Sealed tube 2: trifluoroacetic acid / dichloromethane / 2 h / 23 °C |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
127 mg | With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; caesium carbonate In tetrahydrofuran; water at 85℃; for 3h; Inert atmosphere; Sealed tube; | 48.1 Example 48 (4S,6S)-4-(5-(5-(lH-tetrazol-5-yl)pyridin-3-yl)-2-fluorophenyl)-4-(fluoromethyl)-6- (trifluoromethyl)-5,6-dihydro-4H-l,3-oxazin-2-amine Step 1 : To a solution of (4S,6S)-N-(bis(4-methoxyphenyl)(phenyl)methyl)-4-(5-(5,5- dimethyl-l,3,2-dioxaborinan-2-yl)-2-fluorophenyl)-4-(fluoromethyl)-6-(trifluoromethyl)-5,6- dihydro-4H-l,3-oxazin-2-amine (Intermediate XXXIX-1, 223 mg) in THF (8.00 ml) and water (4.00 ml) was added at room temperature 3-bromo-5-(lH-tetrazol-5-yl)pyridine (CAS 211943- 13-4,107 mg) and cesium carbonate (410 mg). Under argon 1,1'- bis(diphenylphosphino)ferrocene-palladium(II)dichloride dichloromethane complex (25.7 mg) was added and the 2-phase-reaction mixture was stirred in a sealed tube at 85 °C for 3 hours. The aqueous layer was separated and extracted with ethyl acetate. The combined organic layers were dried over Na2S04, filtered and evaporated. The residue was chromatographed (Si02, 0-80% MeOH in dichloromethane) to give (4S,6S)-4-(5-(5-(lH-tetrazol-5-yl)pyridin-3-yl)-2- fluorophenyl)-N-(bis(4-methoxyphenyl)(phenyl)methyl)-4-(fluoromethyl)-6-(trifluoromethyl)- 5,6-dihydro-4H-l,3-oxazin-2-amine (127 mg) as brown oil. |
A1971549[ 1213234-85-5 ]
3-Bromo-5-(2H-tetrazol-5-yl)pyridine hydrochloride
Reason: Free-Salt