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Chemical Structure| 1082065-98-2 Chemical Structure| 1082065-98-2

Structure of 1082065-98-2

Chemical Structure| 1082065-98-2

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Product Details of [ 1082065-98-2 ]

CAS No. :1082065-98-2
Formula : C6H8N2O2
M.W : 140.14
SMILES Code : O=CC1=CN(CCO)N=C1
MDL No. :MFCD09941789

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Application In Synthesis of [ 1082065-98-2 ]

* 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 [ 1082065-98-2 ]

[ 1082065-98-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 35344-95-7 ]
  • [ 540-51-2 ]
  • [ 1082065-98-2 ]
YieldReaction ConditionsOperation in experiment
97% With potassium carbonate; In acetonitrile; at 150℃; for 0.333333h;Microwave irradiation; Preparation 12: 1 -(2-Hydroxy-ethyl)- lH-<strong>[35344-95-7]pyrazole-4-carbaldehyde</strong>Combine lH-<strong>[35344-95-7]pyrazole-4-carbaldehyde</strong> (0.110 g, 1.14 mmol), 2-bromoethanol(0.172 g, 1.37 mmol), and potassium carbonate (0.236 g, 1.71 mmol) in acetonitrile (2 mL). Heat in microwave at 150 0C for 20 min. Cool to room temperature and filter, wash with acetonitrile. Concentrate filtrate to give l-(2-hydroxy-ethyl)-lH-pyrazole-4- carbaldehyde (0.155 g, 97percent). GC-MS (m/z): 140 (M+).
97% With potassium carbonate; In acetonitrile; at 150℃; for 0.333333h;Microwave irradiation; Preparation 52: l-(2-Hydroxy-ethyl)-lH-<strong>[35344-95-7]pyrazole-4-carbaldehyde</strong> Combine lH-<strong>[35344-95-7]pyrazole-4-carbaldehyde</strong> (0.110 g, 1.14 mmol), 2-bromoethanol(0.172 g, 1.37 mmol), and potassium carbonate (0.236 g, 1.71 mmol) in acetonitrile (2 mL). Heat in microwave at 150 0C for 20 min.. Cool to room temperature and filter, washing with acetonitrile. Concentrate filtrate to give the title preparation (0.155 g, 97percent). GC-MS: m/z = 140 [M+].
89% With potassium carbonate; In acetonitrile; at 150℃; for 0.666667h;Sealed tube; Microwave irradiation; 1-(2-Hydroxyethyl)-<strong>[35344-95-7]1H-<strong>[35344-95-7]pyrazole-4-carbaldehyde</strong></strong> In a 30-mL sealed tube, <strong>[35344-95-7]1H-<strong>[35344-95-7]pyrazole-4-carbaldehyde</strong></strong> (500 mg, 5.20 mmol, 1.00 equiv), potassium carbonate (1.08 mg, 7.80 mmol, 1.50 equiv) and 2-bromoethan-1-ol (775.3 mg, 6.20 mmol, 1.19 equiv) were mixed in CH3CN (10 mL) at room temperature. The reaction mixture was then irradiated with microwave for 40 min at 150° C. After the reaction was done, the reaction mixture was cooled to room temperature, filtered through a celite pad and the filtrate was concentrated under reduced pressure. The residue was purified in a silica gel column eluting with dichloromethane/methanol (1percent to 5percent gradient) to afford 1-(2-hydroxyethyl)-<strong>[35344-95-7]1H-<strong>[35344-95-7]pyrazole-4-carbaldehyde</strong></strong> (650 mg, 89percent) as yellow solid. MS: m/z=140.8 [M+H]+
69% With potassium carbonate; In acetonitrile; at 150℃; for 0.5h;Microwave irradiation; 1H-Pyrazole-4-carboxaldehyde (0.50 g, 5.21 mmol), 2-bromoethanol (1.30 g, 10.41 mmol) and potassium carbonate (0.79 g, 5.73 mmol) combined with acetonitrile (5 mL) in a microwave vial. The microwave vial was heated at 150 °C in a microwave for 30 minutes. The reaction mixture was filtered and the solvent evaporated under reduced pressure. The residue was purified by flash column chromatography eluting with 0- 100percent ethyl acetate in iso-hexane to afford the title compound (0.50 g, 69percent). 1HNMR (400 MHz, CDCl3): delta 9.86 (s, 1 H); 8.02 (s, 1 H); 7.99 (s, 1 H); 4.33-4.25 (m, 2 H); 4.05 (t, J = 4.8 Hz, 2 H).

 

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• Appel Reaction • Barbier Coupling Reaction • Baylis-Hillman Reaction • Bucherer-Bergs Reaction • Buchwald-Hartwig C-N Bond and C-O Bond Formation Reactions • Chugaev Reaction • Clemmensen Reduction • Complex Metal Hydride Reductions • Corey-Chaykovsky Reaction • Corey-Fuchs Reaction • Corey-Kim Oxidation • Dess-Martin Oxidation • Fischer Indole Synthesis • Grignard Reaction • Hantzsch Dihydropyridine Synthesis • Henry Nitroaldol Reaction • Horner-Wadsworth-Emmons Reaction • Hydride Reductions • Jones Oxidation • Julia-Kocienski Olefination • Knoevenagel Condensation • Leuckart-Wallach Reaction • Martin's Sulfurane Dehydrating Reagent • McMurry Coupling • Meerwein-Ponndorf-Verley Reduction • Mitsunobu Reaction • Moffatt Oxidation • Mukaiyama Aldol Reaction • Nozaki-Hiyama-Kishi Reaction • Oxidation of Alcohols by DMSO • Passerini Reaction • Paternò-Büchi Reaction • Petasis Reaction • Pictet-Spengler Tetrahydroisoquinoline Synthesis • Preparation of Alcohols • Preparation of Aldehydes and Ketones • Preparation of Amines • Prins Reaction • Reactions of Alcohols • Reactions of Aldehydes and Ketones • Reactions of Amines • Reactions with Organometallic Reagents • Reformatsky Reaction • Ritter Reaction • Schlosser Modification of the Wittig Reaction • Schmidt Reaction • Sharpless Olefin Synthesis • Stetter Reaction • Stobbe Condensation • Swern Oxidation • Tebbe Olefination • Ugi Reaction • Wittig Reaction • Wolff-Kishner Reduction

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