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CAS No. : | 91076-93-6 | MDL No. : | MFCD00052591 |
Formula : | C12H10ClNO2S | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | MELGGDOYSMRBGA-UHFFFAOYSA-N |
M.W : | 267.73 | Pubchem ID : | 2777492 |
Synonyms : |
|
Signal Word: | Warning | Class: | N/A |
Precautionary Statements: | P261-P301+P312-P302+P352-P304+P340-P305+P351+P338 | UN#: | N/A |
Hazard Statements: | H302-H315-H319-H335 | Packing Group: | N/A |
GHS Pictogram: |
* 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 |
---|---|---|
98% | Stage #1: for 2 h; Heating / reflux Stage #2: With sodium hydrogen sulfate In water |
Example 1; EPO <DP n="24"/>6-(4-Chlorophenyl)-3-{4-[(3i?)-3-hydroxypyrrolidin-l-yl]-3- methoxyphenyl}thieno[3,2-^J[l;,2,3]triazin-4(3J9)-one; a) 3-Amino-5-(4-chIorophenyl)thiophene-2-carboxylic add; Methyl 3-amino-5-(4-chlorophenyl)thiophene-2-carboxylate (2.00 g, 7.47 mmol) was refluxed in a solution of KOH (2.0 g, 36 mmol) in 50 mL of water and 50 mL of MeOH for 2 h. The MeOH was evaporated and the residue was diluted to the double volume with water and washed with ethyl acetate. The aqueous layer was acidified with NaHSO4 (aq) and the precipitate was filtered, washed with water and dried to give 1.85 g (98percent) of the desired compound.1H NMR (DMSO-de) 5 7.62 (m, 2H), 7.48 (m, 2H)3 6.96 (s, IH). |
98% | Stage #1: for 2 h; Heating / reflux Stage #2: With sodium hydrogen sulfate In water |
Example 1; 6-(4-Chlorophenyl)-3-[2-(dimethyIamino)-l-methyl-lET-benzimidazol-6-yl]thieno[3,2- d\\ [l,2,3]triazin-4(3H)-one; a) 3-Amino-5-(4-chIorophenyI)thiophene-2-carboxylic acid; Methyl 3-armno-5-(4-chlorophenyl)thiophene-2-carboxylate (2.00 g, 7.47 mmol) was refluxed in a solution of potassium hydroxide (2.0 g, 36 mmol) in 50 mL of water and 50 mL of methanol for 2 h. Methanol was evaporated and the residue was diluted to the double volume with water and washed with ethyl acetate. The aqueous layer was acidified with NaHSO4 (aq) and the precipitate was filtered, washed with water and dried to give 1.85 g (98percent) of the desired compound. 1H NMR (DMSOd6) δ 7.62 (m, 2H), 7.48 (m, 2H), 6.96 (s, IH). |
98% | Stage #1: for 2 h; Heating / reflux |
Example 1; 6"(4-Chlorophenyl)-3-{4-[2-(3-hydroxypyrrolidin-l-yI)ethoxy]-3- methoxyphenyl}thieno[3,2-rf][l,2,3]triazin-4(3i)-one; a) 3-Amino-5-(4-chIorophenyl)thiophene-2-carboxylic acid; Methyl 3-amino-5-(4-chlorophenyl)thiophene-2-carboxylate (2.00 g, 7.47 rnmol) was refluxed in a solution of potassium hydroxide (2.0 g, 36 mmol) in 50 mL of water and 50 mL of methanol for 2 h. Methanol was evaporated and the residue was diluted to the double volume with water and washed with ethyl acetate. The aqueous layer was acidified with NaHSO4 (aq) and the precipitate was filtered, washed with water and dried to give 1.85 g (98percent) of the desired compound. 1H NMR (DMSO-d6) δ 7.62 (m, 2H), 7.48 (m, 2H), 6.96 (s, IH). |
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