• 제목/요약/키워드: 2-dimethyl-3

검색결과 1,193건 처리시간 0.028초

항응고성의 3-(N-Arylamino)-1,4-Naphthoquinone 유도체 합성(II) (Synthesis of Anticoagulant 3-(N-Arylamino)-1,4-Naphthoquinones(II))

  • 유충규;오재돈;서명은
    • 약학회지
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    • 제33권5호
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    • pp.273-279
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    • 1989
  • 2,3-Dichloro-1,4-naphthoquinone was reacted with o-fluoroaniline, p-sulfadiazine, p-acetoanline, N,N-dimethyl-1,4-phenylenediamine as a nucleophilic substitution to form 2-chloro-3-(N-arylamino)-1,4-naphthoquinones (1.-6.) in good yield. 2,3-Dibromo-1,4-naphthoquinone was also reacted with o-fluoroaniline, m-aminobenzoic acid, m-chloroaniline, morpholine, p-acetoaniline, N,N-dimethyl-1,4-phenylenediamine as a nucleophilic substitution to give 2-bromo-3-(N-arylamino)-1,4-naphthoquinones (7.-12.). These new compounds are expected to have a biological activities such as anticoagulant, cytotoxic.

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Determination of Stability Constants of the Inclusion Complexes of ${\beta}$-Blockers in Heptakis (2,3-Dimethyl-6-Sulfato)- ${\beta}$-Cyclodextrin

  • Phuong, Nuyen Thi;Lee, Kyung-Ah;Kim, Kyung-Ho;Choi, Jung-Kap;Kim, Jong-Moon;Kang , Jong-Seong
    • Archives of Pharmacal Research
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    • 제27권12호
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    • pp.1290-1294
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    • 2004
  • The ${\beta}$-blockers possess at least one chiral center and the S(-)-enantiomer shows higher affinity for binding to the ${\beta}$-adrenergic receptors than antipode. The stability constants of acebutolol, celiprolol, propranolol and terbutaline in the inclusion complexes with single-isomer heptakis (2,3-dimethyl-6-sulfato)- ${\beta}$-cyclodextrin (HDMS-${\beta}$-CD) were determined by capillary electrophoresis. The approximation and linear double reciprocal methods were adapted with comparable results. Among the ${\beta}$-blockers studied, propranolol had the lowest stability constant but the highest enantioselectivity, indicating that the magnitudes of the stability constants carried little information about enantioseparation. The magnitudes of enantioselectivities between the enantiomer pair were in the order of propranolol > celiprolol > terbutaline > acebutolol.

Effect of Biofilter Operation Parameters on Dimethyl Disulfide Removal : Loading, Time, and Concentration

  • Arpacioglu, Bora C.;Kim, Jo-Chun;Allen, Eric R.;Kim, Seoung-Hyun
    • 한국환경과학회지
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    • 제11권8호
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    • pp.783-791
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    • 2002
  • A laboratory-scale dual-column biofilter system was used to study the biofiltration of dimethyl disulfide(DMDS). The biofiltration of DMDS was found to depend on the pollutant loadings rather than the inlet concentrations. It was estimated that the pollutant was only inhibitory to the operation of the biofilters at DMDS concentrations greater than 5500 ppmv A residence time of 30 seconds(120 m$^3$/m$^2$/h volumetric loading) was determined as appropriate for efficient operation(>90%). The maximum elimination capacity for both compost mixtures under the current experimental conditions was found to range from 7.5 to 10 g-DMDS/m$^3$/h. A lower DMDS maximum elimination capacity was exhibited under acidified conditions.

Kinetics and Optimization of Dimethyl Carbonate Synthesis by Transesterification using Design of Experiment

  • Lee, Kilwoo;Yoo, Kye Sang
    • Korean Chemical Engineering Research
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    • 제56권3호
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    • pp.416-420
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    • 2018
  • A comprehensive kinetic study has been conducted on dimethyl carbonate synthesis by transesterification reaction of ethylene carbonate with methanol. An alkali base metal (KOH) was used as catalyst in the synthesis of DMC, and its catalytic ability was investigated in terms of kinetics. The experiment was performed in a batch reactor at atmospheric pressure. The reaction orders, the activation energy and the rate constants were determined for both forward and backward reactions. The reaction order for forward and backward reactions was 0.87 and 2.15, and the activation energy was 12.73 and 29.28 kJ/mol, respectively. Using the general factor analysis in the design of experiments, we analyzed the main effects and interactions according to the MeOH/EC, reaction temperature and KOH concentration. DMC yield with various reaction conditions was presented for all ranges using surface and contour plot. Furthermore, the optimal conditions for DMC yield were determined using response surface method.

비페닐디메칠디카르복실레이트의 결정다형 (Polymorphism of Biphenyl Dimethyl Dicarboxylate)

  • 손영택;박명숙;권순경
    • Journal of Pharmaceutical Investigation
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    • 제26권3호
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    • pp.193-199
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    • 1996
  • The polymorphism of biphenyl dimethyl dicarboxylate was investigated by DSC. From product five crystal forms. Form 1, Form 2, Form 3, Form 4, and Form 5, were characterized and three crystal forms. Form 6, Form 7, and Form 8, were prepared with the recrystallization method. The dissolution patterns of these eight crystal farms were also studied, but there was practically no difference in dissolution rate.

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DMT(Dimethylterephthalate), NDC(Dimethy1-2,6-Naphthalene Dicarboxylate)를 이용한 액상 폴리에스터 폴리올의 합성에 관한 연구 (Studies on Synthesis of Liquid Polyester Polyol by using DMT(Dimethylterephthalate) and NDC(Dimethyl-2,6-Naphthalene Dicarboxylate))

  • 김상헌
    • 한국응용과학기술학회지
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    • 제26권3호
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    • pp.317-327
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    • 2009
  • In this study DMT(Dimethylterephthalate), NDC(Dimethyl-2, 6-Naphthalene Dicarboxylate) were used to synthesize polyester polyol which shows enhanced storage stability, improved flame retardancy, and good compressive strength. If DMT and NDC react respectively with DEG(Diethylene Glycol) which is kind of linear diol, the obtained polyester polyols tend to crystallize easily after the reaction. In case of DMT, PA(Phthalic Anhydride) which has asymmetric structure was introduced to retard the crystallization. In case of NDC, DPG(Dipropylene Glycol) which has an methyl side chain was introduced to prevent the crystallization. It was found that to introduce DPG was much more effective method to prevent the crystallization than PA. NDC and DMT were reacted together with DPG for various compositions of NDC:DMT(8:2, 6:4, 4:6 mol ratio). The obtained NDC-DMT-DPG based polyester polyol showed improved flame retardancy, and good compressive strength with increasing the content of NDC.

Photochemical C$_4$-Cycloadduct Formation between 5(E)-Styryl-1,3-dimethyluracil and Some Olefins-Via Photochemical Diels-Alder Type [4 + 2] Adduct

  • Shim, Sang-Chul;Shin, Eun-Ju
    • Bulletin of the Korean Chemical Society
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    • 제8권5호
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    • pp.376-380
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    • 1987
  • The cyclobutane forming photocycloaddition reaction of 5(E)-styryl-1,3-dimethyluracil with some olefins occurs on the 5,6-double bond of uracil ring rather than the expected central double bond via an intermediate, probably the photochemical Diels-Alder type adduct. This intermediate formed on short term irradiation of 5(E)-styryl-1,3-dimethyluracil and 2,3-dimethyl-2-butene solution is converted into the $C_4$-cycloadduct on the prolonged irradiation. Quantum yield of the intermediate formation is not linear with the concentration of 2,3-dimethyl-2-butene probably due to the secondary reaction accompanied with the complex reaction kinetics. The intermediate is formed from the lowest excited singlet state.

Dimethyl Oxalate에 의한 균일 침전법으로 생성된 Barium Titanyl Oxalate의 형태학적 연구 (Morphology of Barium Titanyl Oxalate Produced by Homogeneous Precipitation from Acidic Solution of Dimethyl Oxalate)

  • 민천규;이철
    • 분석과학
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    • 제10권3호
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    • pp.203-208
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    • 1997
  • 출발물질로 $BaCl_2$$TiCl_4$를 사용하고 침전제로 dimethyl oxalate(DMO)를 사용하여 균일침전법에 의해 barium titanyl oxalate(BTO)를 제조하였다. 반응조건을 변화시켜 가면서 실험을 수행한 결과 반응 온도가 높을수록, [DMO]/[$Ba^{2+}+Ti^{4+}$]의 비율이 증가할수록 핵 형성시간이 단축되었으며 BTO 입자가 unimodal에서 bimodal을 거쳐 넓은 범위의 unimodal로 전환하는 속도가 빨랐다. 균일침전법으로 얻은 BTO를 $900^{\circ}C$에서 하소하여 얻은 barium titanate(BT)의 입자 크기는 통상의 공침법으로 합성한 BT 입자보다 큰 형태를 나타냈으며, 결정상은 tetragonal이었다. 또한 교반이 BTO 및 BT 분말의 특성에 큰 영향을 줌을 발견하였다.

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랫드에서 이황화메틸의 2주 반복투여 흡입독성연구 (Two-Week Repeated Inhalation Toxicity Study of Dimethyl Disulfide in Rats)

  • 김종춘;신진영;신동호;김성호;이성배;한정희;정용현;김현영;박승춘
    • Toxicological Research
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    • 제20권3호
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    • pp.273-280
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    • 2004
  • The present study was carried out to investigate the potential toxicity of dimethyl disulfide by a 2-week inhalation in F344 rats. The test article, dimethyl disulfide, was exposed by inhalation to male and female rats at dose levels of 0, 33, 100, or 300 ppm/6 hrs/day for 2 weeks. At the end of treatment period, all males and females were sacrificed. During the test period, clinical signs, mortality, body weights, food consumption, hematology, serum biochemistry, and gross findings were examined. The mean body weights of the male 300 ppm group and the female 33 ppm or higher dose groups were significantly lower than those of the control group, respectively. The mean food consumption at male 300 ppm and female 100 and 300 ppm were significantly decreased compared with the controls. Some treatment-related serum biochemical changes, including decreased alkaline phosphatase at male 300 ppm and female 100 and 300 ppm, reduced total bilirubin at male 300 ppm, and decreased alanine aminotransferase at female 300 ppm, were observed in a dose-dependent manner, but these findings were considered to be of no toxicological significance. There were no adverse effects on mortality, clinical signs, hematology, and necropsy findings in any treatment group. Based on these results, it was concluded that the 2-week repeated dose of dimethyl disulfide by inhalation resulted in suppressed body weight gain and decreased food consumption at the dose of male 300 ppm and suppressed or reduced body weight gain and decreased food consumption at the dose of female 33 ppm or higher. In the present experimental conditions, the no-observed-adverse-effect level (NOAEL) was considered to be 100 ppm/6 hrs/day for male rats and below 33 ppm/6 hrs/day for female rats.