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Chemical Structure| 1017273-35-6 Chemical Structure| 1017273-35-6

Structure of 1017273-35-6

Chemical Structure| 1017273-35-6

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Product Details of [ 1017273-35-6 ]

CAS No. :1017273-35-6
Formula : C8H8N2O2S
M.W : 196.23
SMILES Code : O=C(C1=C(C)N2C(S1)=NC=C2)OC

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Application In Synthesis of [ 1017273-35-6 ]

* 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.

  • Downstream synthetic route of [ 1017273-35-6 ]

[ 1017273-35-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1017273-35-6 ]
  • [ 1017273-59-4 ]
YieldReaction ConditionsOperation in experiment
An aq. NaOH solution (1.0M, 23 mL) is added to a solution of the respective carboxylic ester derivative (11.3 mmol) in THF (12 mL) and MeOH (4.0 mL). The mixture is stirred for 16h, the organic volatiles are removed in vacuo and water (10 mL) is added. The mixture is cooled to 00C and made acidic (pH = 3-4) by addition of aq. HCl (1.0 M). The obtained precipitate is filtered off, washed with cold water and dried in vacuo to give the desired acid which is used without further purification.; 3-Methyl-imidazo[2,l-b]thiazole-2-carboxylic acid prepared by saponification of 3-methyl-imidazo[2,l-b]thiazole-2-carboxylic acid methyl ester. LC-MS: tR = 0.24 min; [M+H]+ = 183.0.
An aq. NaOH solution (1.0M, 23 mL) is added to a solution of the respective carboxylic ester derivative (11.3 mmol) in THF (12 mL) and MeOH (4.0 mL). The mixture is stirred for 16 h, the organic volatiles are removed in vacuo and water (10 mL) is added. The mixture is cooled to 0 C. and made acidic (pH=3-4) by addition of hydrochloric acid (1.0 M). The obtained precipitate is filtered off, washed with cold water and dried in vacuo to give the desired acid which is used without further purification.3-methyl-imidazo[2,1-b]thiazole-2-carboxylic acid prepared by saponification of 3-methyl-imidazo[2,1-b]thiazole-2-carboxylic acid methyl ester. LC-MS: tR=0.24 min; [M+H]+=183.0.
 

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