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Chemical Structure| 90773-41-4 Chemical Structure| 90773-41-4

Structure of 90773-41-4

Chemical Structure| 90773-41-4

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Product Details of [ 90773-41-4 ]

CAS No. :90773-41-4
Formula : C5H8Cl2N2
M.W : 167.04
SMILES Code : CN1C(CCl)=CN=C1.[H]Cl
MDL No. :MFCD08668158

Safety of [ 90773-41-4 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H302-H314
Precautionary Statements:P264-P270-P271-P280-P303+P361+P353-P304+P340-P305+P351+P338-P310-P330-P331-P363-P403+P233-P501
Class:8
UN#:1759
Packing Group:

Application In Synthesis of [ 90773-41-4 ]

* 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 [ 90773-41-4 ]

[ 90773-41-4 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 38993-84-9 ]
  • [ 90773-41-4 ]
YieldReaction ConditionsOperation in experiment
98% With thionyl chloride; In 1,2-dichloro-ethane; at 20℃; for 18h; Add thionyl chloride (4.00 ml, 53.8 mmol) to a solution of (3-methyl-3H- imidazol-4-yl)-methanol (4.0 g, 35.7 mmol) in dichloroethane (30 mL) and stir at room temperature for 18 h. Concentrate the reaction mixture and add ether to the residue. Sonicate for 5 min, filter, and dry to give the title compound (5.8 g, 98percent). MS (ES+) 131 (M+l)+. 1H NMR (400 MHz, DMSO-d6): delta 14.99 (s, 1H), 9.18 (s, 1H), 7.75 (s, 1H), 5.00 (s, 2H), 3.85 (s, 3H).
86% With thionyl chloride; for 2h;Reflux; Methyl-1H-imidazol-5-yl)methanol (100 mg, 892 ).IDOl) was combined with thionylchloride (1 mL). The mixture was refluxed for 2 hand concentrated. The residue was dissolved in15 minimum amount of EtOH and ether was added. The mixture was sonicated to give 5-(chloromethyl)-1-methyl-1H-imidazole hydrochloride (128 mg, 86 percent, light yellow solid) whichwas used without purification. MS m/z 131 (MH+)
83% With thionyl chloride; for 3h;Heating / reflux; S-Methyl-SH-imidazole^-carboxylic acid ethyl ester (Chem. Pharm. Bull, 1994, 42,1463) (0.62 g, 4.02 mmol) in THF (5mL) was added dropwise over 1 min. to a slurry of lithium aluminum hydride (0.25 g, 6.60 mmol) in THF (20 mL). After stirring 16h at room temperature, the reaction was carefully quenched with excess sodium sulfate decahydrate, dried with anhydrous sodium sulfate and filtered through Celite. Concentration gave 0.33 g (73percent) of (3- methyl-3H-imidazol-4-yl)-methanol as a white solid which had: NMR (CDCI3) delta 7.38 (s, 1 H), 6.87 (s, 1 H), 4.60 (s, 2H)1 3.69 (s, 3H). A solution of this alcohol (0.150 g, 1.34 mmol) in thionyl chloride (5 mL) was refluxed for 3 h and concentrated. The residue was dissolved in a minimum of ethanol and ether was added to precipitate a white solid. This was collected to yield 0.185 g (83percent) of 5-chloromethyl-1-methyl-1H-imidazole hydrochloride which had: NMR (DMSOd6) delta 9.15 (s, 1 H), 7.75 (d, J = 1.2 Hz, 1 H), 4.99 (s, 2H), 3.84 (s, 3H).
28% With thionyl chloride; In DMF (N,N-dimethyl-formamide); at -5 - 20℃; for 1.66667h; A mixture of <strong>[38993-84-9](1-methyl-1H-imidazol-5-yl) methanol</strong> (500MG, 4.5 mmol) in DMF (5 ML) at-5 oC was slowly treated with thionyl chloride (0.49 ML, 6.7 mmol), stirred an additional 10 minutes AT-5 C, warmed to room temperature, stirred 1.5 hours, cooled TO-5 C, quenched with isopropyl alcohol and ethyl acetate, stirred 30 minutes AT-5 C, concentrated under vacuum, and filtered to collect the solid. The solid was rinsed with ethyl acetate and dried under vacuum to give (212mg, 28percent) of the desired product as the hydrochloride salt. MS (DCI) m/e 131 (M+H) + ; 1H NMR (300 MHz, DMSO-D6) 8 9.10 (S, 1H), 7.76 (s, 1H), 5.02 (s, 2H), 3.88 (s, 3H).

  • 2
  • [ 39998-25-9 ]
  • [ 90773-41-4 ]
  • [[2-[1-[(3-methylimidazol-4-yl)methyl]pyridin-1-ium-3-yl]acetyl]amino]ammonium bistrifluoroacetate [ No CAS ]
  • 3
  • [ 39998-25-9 ]
  • [ 90773-41-4 ]
  • [ 76-05-1 ]
  • methyl 2-[1-[(3-methylimidazol-4-yl)methyl]pyridin-1-ium-3-yl]acetate trifluoroacetate [ No CAS ]
YieldReaction ConditionsOperation in experiment
73% Methyl 3-pyridylacetate (52.0 mg, 0.344 mmol) was mixed with 5-(chloromethyl)- 1 -methyl- l77-imidazole hydrochloride (46.3 mg, 0.277 mmol) and dissolved in dry DMF (1 mL). The solution was stirred at 50 C for 1 d and was stopped by quenching with MeOH. The solvents were removed in vacuo and the crude mixture was subjected to preparative HPLC yielding 73.1 mg, 73%, of the desired product as a colorless oil. (0513) HPLC method C-18 column: (0514) 0 min: 100% H2O 0.1% TFA, 0% CHsCN 0.1% TFA; (0515) 0-60 min: 50% H2O 0.1% TFA, 50% CHsCN 0.1% TFA; 60-64 min: 2% H20 0.1% TFA; 98% CHsCN 0.1% TFA; (0516) 64-72 min: 2% H2O 0.1% TFA; 98% CHsCN 0.1% TFA; (0517) 72-74 min: 40% H2O 0.1% TFA; 60% CHsCN 0.1% TFA; (0518) 74-79 min: 40% H2O 0.1% TFA; 60% CHsCN 0.1% TFA; (0519) 79-80 min: 40% H2O 0.1% TFA; 60% CHsCN 0.1% TFA. (0520) NMR (400 MHz, METHANOL-^) d ppm 3.75 (s, 3 H) 3.91 (s, 3 H) 4.05 (s, 2 H) 6.14 (s, 2 H) 7.91 (s, 1 H) 8.15 (dd, =7.97, 6.21 Hz, 1 H) 8.63 (d, =8.03 Hz, 1 H) 8.95 - 9.07 (m, 2 H) 9.11 (s, 1 H). (0521) 13C NMR (101 MHz, METHANOL-) d ppm 32.99 (1 C) 36.14 (1 C) 51.71 (1 C) 52.28 (1 C) 122.98 (1 C) 126.59 (1 C) 127.99 (1 C) 136.95 (1 C) 138.29 (1 C) 143.08 (1 C) 145.22 (1 C) 148.02 (1 C) 170.03 (1 C). (0522) HPLC-MS (m/z) [M]+ calcd 246.12425 found 246.39.
 

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