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Chemical Structure| 116861-31-5 Chemical Structure| 116861-31-5

Structure of 116861-31-5

Chemical Structure| 116861-31-5

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Product Details of [ 116861-31-5 ]

CAS No. :116861-31-5
Formula : C8H16ClNO2
M.W : 193.67
SMILES Code : CC(C)(C)OC(=O)NCCCCl
MDL No. :MFCD07781306
InChI Key :GLGLWGNZBMZWHG-UHFFFAOYSA-N
Pubchem ID :10932310

Safety of [ 116861-31-5 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of [ 116861-31-5 ]

* 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 [ 116861-31-5 ]

[ 116861-31-5 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 116861-31-5 ]
  • [ 939-69-5 ]
  • [ 882674-11-5 ]
  • 2
  • [ 105601-04-5 ]
  • [ 116861-31-5 ]
  • [ 1350432-40-4 ]
YieldReaction ConditionsOperation in experiment
65% With potassium carbonate; In N,N-dimethyl-formamide; for 24h;Heating / reflux; {2-[3-(1-dimethylamino-ethyl)-phenoxy]-ethyl}-carbamic acid ter-butyl ester (19b). A solution of 19a was synthesized following the procedure described for the corresponding (R,S)-3-[[1-di-(2H3) methylamino]ethyl]phenol in: Ciszewska, Grazyna; Pfefferkorn, Heidi; Tang, Y. S.; Jones, Lawrence; Tarapata, Richard; Sunay, Ustun B. Synthesis of tritium, deuterium, and carbon-14 labeled (s)-n-ethyl-n-methyl-3-[1-(dimethylamino)ethyl]carbamic acid, phenyl ester, (1) -2,3-dihydroxybutanedioic acid salt (SDZ ENA 713 hta), an investigational drug for the treatment of Alzheimer's disease. Journal of Labeled Compounds & Radiopharmaceuticals 1997, 39, 651-668) (350 mg, 2.17 mmol) (3-chloro-propyl)-carbamic acid terbutyl ester (420 mg, 2.17 mmol) and K2CO3 (300 mg, 2.17 mmol) in DMF (10 mL) was stirred under reflux conditions for 24 h. Evaporation of the solvent afforded a residue which was purified by gravity column. Elution with CHCl3/MeOH/aqueous 30% ammonia solution (9:1:0.02) afforded lab as an oil: 65% yield,
65% With potassium carbonate; In N,N-dimethyl-formamide; for 24h;Reflux; A solution of 14 (0.350 g, 2.17 mmol), tert-butyl 3-chloropropylcarbamate (0.420 g, 2.17 mmol) and K2CO3 (0.300 g, 2.17 mmol) in DMF (10 mL) was stirred under reflux conditions for 24 h. Evaporation of the solvent afforded a residue which was purified by gravity column. Elution with CHCl3/MeOH/aqueous 30% ammonia (9:1:0.02) afforded 15 (0.454 g, 65%) as an oil. 1H NMR (CDCl3, 200 MHz) delta 7.20 (t, J = 8.0 Hz, 1H), 6.79-6.89 (m, 3H), 4.92 (br s, 1H, exchangeable with D2O), 4.02 (t, J = 6.4 Hz, 2H), 3.20-3.33 (m, 3H), 2.20 (s, 6H), 1.93-1.99 (m, 2H), 1.44 (s, 9H), 1.35 (d, J = 6.6 Hz, 3H).
 

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