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Chemical Structure| 13781-65-2 Chemical Structure| 13781-65-2

Structure of 13781-65-2

Chemical Structure| 13781-65-2

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Product Details of [ 13781-65-2 ]

CAS No. :13781-65-2
Formula : C6H5ClOS
M.W : 160.62
SMILES Code : O=C(Cl)CC1=CSC=C1
MDL No. :MFCD03424732

Safety of [ 13781-65-2 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H314
Precautionary Statements:P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P310-P321-P363-P405-P501
Class:8
UN#:1760
Packing Group:

Application In Synthesis of [ 13781-65-2 ]

* 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 [ 13781-65-2 ]

[ 13781-65-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 6964-21-2 ]
  • [ 13781-65-2 ]
YieldReaction ConditionsOperation in experiment
With oxalyl dichloride;N,N-dimethyl-formamide; In tetrahydrofuran; The procedure described above for the synthesis of 1-chloro-3-[2-(3-methylbenzo[b]thiophen-2-yl)propan-2-one was followed, reacting thiophene-3-acetic acid (5.32 g, 37.4 mmol) with oxalyl chloride (3.6 mL, 5.2 g, 41 mmol, then ethereal diazomethane, then dry HCl gas. Work-up gave pure product, a brown oil which solidified upon refrigeration to a golden-brown, waxy solid (6.52 g, 100% yield): 1H NMR (400 MHz, CDCl3) δ 3.94 (s, 2H) 4.13 (s, 2H) 6.99 (d, J=5.1 Hz, 1H) 7.16 (dd, J=1.5, 0.8 Hz, 1H) 7.33 (dd, J=4.9, 2.9 Hz, 1H).
With oxalyl dichloride;N,N-dimethyl-formamide; In dichloromethane; at 20℃; for 3h; General method 2: preparation of ethyl-5-substituted-1 ,2,4-oxadiazole-3carboxylateStep I A mixture of a 2-aryl acetic acid (3.78 mmol; 1 equivalent) and oxalyl chloride (4.16 mmol,1.1 equivalents) in dichloromethane (12 ml_) with few drops of DMF was stirred at room temperature for 3 h.Step IlThe resulting solution from step I was added to a mixture of ethyl 2-amino-2- (hydroxyimino)acetate (3.78 mmol 1 equivalent) and N1N diisopropylethylamine (6.06 mmol, 1.60 equivalents) in dichloromethane (6 ml.) at -15C. The reaction mixture was then stirred at room temperature for 12 to 36 h and poured into a mixture of ice and water. The formed precipitate was filtered off. When a precipitate was not formed, the organic layer was separated, dried over magnesium sulphate, filtered and evaporated to dryness. Step III The precipitate or the residue from step Il was refluxed in a sealed tube with pyridine (18 ml.) for 20 h and concentrated under reduced pressure. The crude material was purified by flash chromatography on silica to yield the desired compound.; INTERMEDIATE 105 - PREPARATION OF ethyl 5-(thiophen-3-ylmethyl)-1 ,2,4- oxadiazole-3-carboxylate; This compound was prepared according to general method 2 with (step I) 2-(thiophen-3- yl)acetic acid (0.568 g; 3.78 mmol), oxalyl chloride (0.352 ml 4.16 mmol) in dichloromethane (12 ml.) with few drops of DMF; (step II) ethyl 2-amino-2- (hydroxyimino)acetate (0.5 g; 3.78 mmol); N, N diisopropylethylamine (1.05 ml 6.06 mmol) in dichloromethane (6 mL) and (step III) pyridine (18 ml_).The crude material was purified by flash chromatography on silica (eluent 20 to 100% ethyl acetate in heptane) to yield 0.343 g (38%) of ethyl 5-(thiophen-3-ylmethyl)-1 ,2,4-oxadiazole-3-carboxylate as a yellow solid. ESI/APCI(+): 239(M+H).
With oxalyl dichloride; N,N-dimethyl-formamide; In dichloromethane; at 20℃; for 18h;Inert atmosphere; General procedure: Carboxylic acid (0.735 mmol, 1.0 eq.) was added to a flame dried microwave vial under Argon. DCM (3 mL) was added, followed by oxalyl chloride (0.075mL, 0.885 mmol, 1.2 eq) and DMF (1 drop). The reaction mixture was stirred at room temperature under Argon for 18 hours. The solvent was removed under reduced pressure to afford the crude product. The resulting crude material was used directly for the next step without further purification.
 

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