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[ CAS No. 91076-93-6 ] {[proInfo.proName]}

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Chemical Structure| 91076-93-6
Chemical Structure| 91076-93-6
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Product Details of [ 91076-93-6 ]

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 :

Safety of [ 91076-93-6 ]

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:

Application In Synthesis of [ 91076-93-6 ]

* 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.

  • Upstream synthesis route of [ 91076-93-6 ]

[ 91076-93-6 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 91076-93-6 ]
  • [ 187949-86-6 ]
YieldReaction ConditionsOperation 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).
Reference: [1] Patent: WO2007/11284, 2007, A1, . Location in patent: Page/Page column 22-23
[2] Patent: WO2007/11285, 2007, A1, . Location in patent: Page/Page column 19
[3] Patent: WO2007/11286, 2007, A1, . Location in patent: Page/Page column 20
[4] Patent: WO2005/66163, 2005, A2, . Location in patent: Page/Page column 109
[5] European Journal of Medicinal Chemistry, 2013, vol. 65, p. 223 - 231
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