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Chemical Structure| 32519-70-3 Chemical Structure| 32519-70-3

Structure of 32519-70-3

Chemical Structure| 32519-70-3

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Product Details of [ 32519-70-3 ]

CAS No. :32519-70-3
Formula : C8H9ClN2O2S
M.W : 232.69
SMILES Code : O=C(NC1=NC(C)=C(C(C)=O)S1)CCl
MDL No. :MFCD05267743

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Application In Synthesis of [ 32519-70-3 ]

* 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 [ 32519-70-3 ]

[ 32519-70-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 30748-47-1 ]
  • [ 79-04-9 ]
  • [ 32519-70-3 ]
YieldReaction ConditionsOperation in experiment
With triethylamine; In tetrahydrofuran; at 0 - 20℃; General procedure: A solution of 2-amino-5-substituted-4-methylthiazole (1) (0.01 mol) (1a:1.2 g, 1b:1.3 g, 1c:1.6 g, 1d:1.9 g, 1e:1.9 g)[29, 30] and triethylamine (0.01 mol) (1.5 mL) was prepared by stirring in THF (50 mL) at room temperature. After cooling the mixture in an ice bath, chloroacetyl chloride (0.01mol) (0.8 mL) was added drop wise with constant stirring. Before evaporation of the solvent under reduced pressure,the reaction mixture was further stirred for 1 hour at room temperature. The precipitate formed was crystallised from ethanol [31, 12].
With potassium carbonate; In dichloromethane; General procedure: Aminothiazole (A1-A18, 50 mmol) and 100 mmol of potassiumcarbonate were dissolved in dichloromethane (100 mL), chloroacetylchloride (8.0 mL) was added dropwise under ice bath, andreacted at room temperature monitored by TLC. When the reactionis completed, the reaction solution is poured into water, andwashed with sodium bicarbonate solution, saturated saline andwater successively, dry the organic phase with anhydrous sodiumsulfate, remove the solvent under reduced pressure, and recrystallizewith ethanol to obtain raw product B1-B18. Then intermediate(30 mmol) and KSCN (45 mmol) were dissolved in 100 mLof ethanol, and reflux for 6 h. The reaction mixture were cooleddown, filtered, and washed with ethanol and water, the crudeproduct was recrystallized from ethanol/water to afford the pure 4-thiazolinone intermediate C1-C18.
 

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Technical Information

• Acyl Group Substitution • Alkyl Halide Occurrence • Baeyer-Villiger Oxidation • Barbier Coupling Reaction • Baylis-Hillman Reaction • Bucherer-Bergs Reaction • Buchwald-Hartwig C-N Bond and C-O Bond Formation Reactions • Chan-Lam Coupling Reaction • Clemmensen Reduction • Complex Metal Hydride Reductions • Corey-Bakshi-Shibata (CBS) Reduction • Corey-Chaykovsky Reaction • Fischer Indole Synthesis • General Reactivity • Grignard Reaction • Henry Nitroaldol Reaction • Hiyama Cross-Coupling Reaction • Horner-Wadsworth-Emmons Reaction • Hydride Reductions • Kinetics of Alkyl Halides • Kumada Cross-Coupling Reaction • Lawesson's Reagent • Leuckart-Wallach Reaction • Mannich Reaction • McMurry Coupling • Meerwein-Ponndorf-Verley Reduction • Passerini Reaction • Paternò-Büchi Reaction • Petasis Reaction • Peterson Olefination • Pictet-Spengler Tetrahydroisoquinoline Synthesis • Preparation of Aldehydes and Ketones • Preparation of Amines • Prins Reaction • Reactions of Aldehydes and Ketones • Reactions of Alkyl Halides with Reducing Metals • Reactions of Amines • Reformatsky Reaction • Robinson Annulation • Schlosser Modification of the Wittig Reaction • Schmidt Reaction • Specialized Acylation Reagents-Carbodiimides and Related Reagents • Specialized Acylation Reagents-Ketenes • Specialized Acylation Reagents-Vilsmeier Reagent • Stille Coupling • Stobbe Condensation • Substitution and Elimination Reactions of Alkyl Halides • Suzuki Coupling • Tebbe Olefination • Ugi Reaction • Wittig Reaction • Wolff-Kishner Reduction

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