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CAS No. : | 1038509-28-2 | MDL No. : | MFCD13190218 |
Formula : | C9H7NO2S | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | SVEZOHPWBLWBNO-UHFFFAOYSA-N |
M.W : | 193.22 | Pubchem ID : | 59316815 |
Synonyms : |
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Signal Word: | Warning | Class: | |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | |
Hazard Statements: | H315-H319-H335 | Packing Group: | |
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 |
---|---|---|
With isopentyl nitrite; In tetrahydrofuran; for 4h;Heating / reflux; | Isoamyl nitrite (22.0 mmol) is added to a solution of 2-amino-benzothiazole-7-carboxylic acid methyl ester (10.1 mmol) in THF (29 mL). The mixture is heated to reflux for 4h, the solvents are removed in vacuo and the residue is purified by flash chromatography <n="80"/>(gradient: heptane to EtOAc/heptane 4/6) to give the desired product. LC-MS: tR = 0.85 min; [M+H]+ = 194.0. | |
With isopentyl nitrite; In tetrahydrofuran; for 4h;Heating / reflux; | Isoamyl nitrite (22.0 mmol) is added to a solution of 2-amino-benzothiazole- 7-carboxylic acid methyl ester (10.1 mmol) in THF (29 mL). The mixture is heated to reflux for 4h, the solvents are removed in vacuo and the residue is purified by FC (gradient: heptane to EtO Ac/heptane 4/6) to give the desired product. LC-MS: tR = 0.85 min; [M+H]+ = 194.0. | |
With isopentyl nitrite; In tetrahydrofuran; for 4h;Reflux; | A.4.3 Synthesis of benzothiazole-7-carboxylic acid methyl ester; Isoamyl nitrite (22.0 mmol) is added to a solution of 2-amino-benzothiazole-7-carboxylic acid methyl ester (10.1 mmol) in THF (29 mL). The mixture is heated to reflux for 4h, the solvents are removed in vacuo and the residue is purified by flash chromatography (gradient: heptane to EtOAc/heptane 4/6) to give the desired product. LC-MS: tR = 0.85 min; [M+H]+ = 194.0. |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
At 00C an aqueous NaOH solution (50%, 6.0 rnL) is added to a solution of benzothiazole- 7-carboxylic acid methyl ester in a mixture of MeOH (39 mL), THF (11.7 mL) and water (3.0 mL). The mixture is stirred for 4h and concentrated in vacuo. At 00C water (60 mL) is added and the mixture is made acidic (pH 5) by addition of cone, hydrochloric acid. After 30 min the precipitate is filtered off, washed with water and dried in vacuo to give the desired product. LC-MS : tR = 0.77 min; [M+CH3CN+H]+ = 221.1. | ||
A.4.4 Synthesis of benzothiazole-7-carboxylic acid; At 00C an aq. NaOH solution (50%, 6.0 mL) is added to a solution of benzothiazole-7- carboxylic acid methyl ester in a mixture of MeOH (39 mL), THF (11.7 mL) and water (3.0 mL). The mixture is stirred for 4h and concentrated in vacuo. At 00C water (60 mL) is added and the mixture is made acidic (pH 5) by addition of cone, hydrochloric acid. After <n="61"/>30 min the precipitate is filtered off, washed with water and dried in vacuo to give the desired product. LC-MS: tR = 0.77 min; [M+CH3CN+H]+ = 221.1. |
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