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Chemical Structure| 1159512-67-0 Chemical Structure| 1159512-67-0

Structure of 1159512-67-0

Chemical Structure| 1159512-67-0

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Product Details of [ 1159512-67-0 ]

CAS No. :1159512-67-0
Formula : C9H10F3NO2
M.W : 221.18
SMILES Code : NCC1=CC=C(OC)C=C1OC(F)(F)F
MDL No. :MFCD12026482

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Application In Synthesis of [ 1159512-67-0 ]

* 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 [ 1159512-67-0 ]

[ 1159512-67-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 4565-31-5 ]
  • [ 1159512-67-0 ]
  • 5-formyl-thiophene-2-carboxylic acid 4-methoxy-2-trifluoromethoxy-benzylamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
26% With 4-methyl-morpholine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In N,N-dimethyl-formamide; at 20℃; To a solution of of 5-Formyl- 2- thiophenecarboxylic acid (100 mg, 0.64 mmol) and (4-methoxy-2-(trifluoromethoxy)phenyl)methanamine (141 mg, 0.64 mmol) in 4 ml DMF, HOBt (117 mg, 196 mmol) and 4-methylmorpholine (196 mg, 1.9 mmol) were added. Then 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (168 mg, 0.83 mmol) was added and the mixture stirred at RT over night. The resulting solution was filtered, 0.1 mL TFA was added and purified by HPLC to give 5-Formyl-thiophene-2-carboxylic acid 4-methoxy-2-trifluoromethoxy-benzylamide (Intermediate 8)- (78 mg, 26percent). 1 H NMR (DMSO-d6, 500 MHz) delta ppm 9.9 (s, 1 H), 9.28 (t, 1 H), 8.05 (d, 1 H), 7.91 (d, 1 H), 7.40 (dd, 1 H), 6.99 (dd, 1 H), 6.90 (s, 1 H), 4.48 (d, 2H) 3.80 (s, 3H). LC/MS (Method 3); Rt = 1.88 min; detected mass: m/z = 314.10 ([M+H]+).
26% With 4-methyl-morpholine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In N,N-dimethyl-formamide; at 20 - 25℃; Intermediate 8: <strong>[4565-31-5]5-formyl-thiophene-2-carboxylic acid</strong> 4-methoxy-2-trifluoromethoxy-benzylamide To a solution of of 5-Formyl- 2- thiophenecarboxylic acid (100 mg, 0.64 mmol) and (4- methoxy-2-(trifluoromethoxy)phenyl)methanamine (141 mg, 0.64 mmol) in 4 ml DMF, HOBt (1 17 mg, 196 mmol) and 4-methylmorpholine (196 mg, 1 .9 mmol) were added. Then 1 -(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (168 mg, 0.83 mmol) was added and the mixture stirred at RT over night. The resulting solution was filtered, 0.1 ml_ TFA was added and purified by HPLC to give 5-Formyl-thiophene-2- carboxylic acid 4-methoxy-2-trifluoromethoxy-benzylamide (Intermediate 8)- (78 mg, 26percent). 1 H NMR (DMSO-d6, 500 MHz) delta ppm 9.9 (s, 1 H), 9.28 (t, 1 H), 8.05 (d, 1 H), 7.91 (d, 1 H), 7.40 (dd, 1 H), 6.99 (dd, 1 H), 6.90 (s, 1 H), 4.48 (d, 2H) 3.80 (s, 3H).LC/MS ( Method 3); Rt = 1 .88 min; detected mass: m/z = 314.10 ([M+H]+).
 

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