Structure of 96989-50-3
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The BI-3802 was designed by Boehringer Ingelheim and could be obtained free of charge through the Boehringer Ingelheim open innovation portal opnMe.com, associated with its negative control.
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CAS No. : | 96989-50-3 |
Formula : | C11H8N2O2S |
M.W : | 232.26 |
SMILES Code : | S=C(OC1=NC=CC=C1)OC2=NC=CC=C2 |
MDL No. : | MFCD00074870 |
InChI Key : | IKYOVSVBLHGFMA-UHFFFAOYSA-N |
Pubchem ID : | 719784 |
GHS Pictogram: |
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Signal Word: | Warning |
Hazard Statements: | H315-H319-H335 |
Precautionary Statements: | P261-P305+P351+P338 |
* 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 |
---|---|---|
In dichloromethane; | PREPARATION 32.1 2-Methoxy-5-(5-methylsulfonyl-1H-tetrazol-1-yl)benzoic Acid According to the method of Tet. Let., 26, 1661 (1985), combine <strong>[22802-67-1]methyl 2-methoxy-5-aminobenzoate</strong> (0.5 g, 2.76 mmol) and di-2-pyridyl thionocarbonate (0.64 g, 2.76 mmol) in dichloromethane (10 mL). After 30 minutes, dilute the reaction mixture with dichloromethane and extract five times with water. Dry the organic layer over Na2SO4, filter, and concentrate in vacuo to give methyl 2-methoxy-5-isothiocyanatobenzoate: Rf=0.51 (silica gel, dichloromethane). | |
In dichloromethane; | Treat a solution of 5-amino-2-methoxy-benzoic acid methyl ester (7.70 g, 42.5 mmol) and dichloromethane (50 mL) portionwise with a solution of di-2-pyridyl thionocarbonate (10.0 g, 43.1 mmol; Aldrich Chemical Company) and dichloromethane (70 mL) at room temperature under an argon atmosphere. After 3.5 hours, concentrate in vacuo and purify the residue by flash chromatography (silica gel, 5.5*17.8 cm) eluding with dichloromethane. Combine the appropriate fractions and concentrate to afford 5-isothiocyanato-2-methoxy-benzoic acid methyl ester (6,,9 g). | |
In dichloromethane; | PREPARATION 32.1 2-Methoxy-5-(5-methylsulfonyl-1H-tetrazol-1-yl)benzoic acid According to the method of Tet. Let., 26, 1661 (1985), combine <strong>[22802-67-1]methyl 2-methoxy-5-aminobenzoate</strong> (0.5 g, 2.76 mmol) and di-2-pyridyl thionocarbonate (0.64 g, 2.76 mmol) in dichloromethane (10 mL). After 30 minutes, dilute the reaction mixture with dichloromethane and extract five times with water. Dry the organic layer over Na2SO4, filter, and concentrate in vacuo to give methyl 2-methoxy-5-isothiocyanatobenzoate: Rf=0.51 (silica gel, dichloromethane). |
In dichloromethane; | Treat a solution of 5-amino-2-methoxy-benzoic acid methyl ester (7.70 g, 42.5 mmol) and dichloromethane (50 mL) portionwise with a solution of di-2-pyridyl thionocarbonate (10.0 g, 43.1 mmol; Aldrich Chemical Company) and dichloromethane (70 mL) at room temperature under an argon atmosphere. After 3.5 hours, concentrate in vacuo and purify the residue by flash chromatography (silica gel, 5.5*17.8 cm) eluding with dichloromethane. Combine the appropriate fractions and concentrate to afford 5-isothiocyanato-2-methoxy-benzoic acid methyl ester (6.9 g). | |
In dichloromethane; | Preparation 32.1 2-Methoxy-5-(5-methylsulfonyl-1H-tetrazol-1-yl)benzoic Acid According to the method of Tet. Let., 26, 1661 (1985), combine <strong>[22802-67-1]methyl 2-methoxy-5-aminobenzoate</strong> (0.5 g, 2.76 mmol) and di-2-pyridyl thionocarbonate (0.64 g, 2.76 mmol) in dichloromethane (10 mL). After 30 minutes, dilute the reaction mixture with dichloromethane and extract five times with water. Dry the organic layer over Na2SO4, filter, and concentrate in vacuo to give methyl 2-methoxy-5-isothiocyanatobenzoate: Rf=0.51 (silica gel, dichloromethane). | |
In dichloromethane; | PREPARATION 32 2-Methoxy-5-(5-methylsulfonyltetrazol-1-yl)benzoic acid According to the method of Tet. Let., 26, 1661 (1985), combine <strong>[22802-67-1]methyl 2-methoxy-5-aminobenzoate</strong> (0.5 g, 2.76 mmol) and di-2-pyridyl thionocarbonate (0.64 g, 2.76 mmol) in dichloromethane (10 mL). After 30 minutes, dilute the reaction mixture with dichloromethane and extract five times with water. Dry the organic layer over Na2SO4, filter, and concentrate in vacuo to give methyl 2-methoxy-5-thioisocyanatobenzoate: Rf=0.51 (silica gel, dichloromethane). |