<p>Reagents and conditions: a) 2-(4-chlorophenyl)acetonitrile, K<sub>2</sub>CO<sub>3</sub>, DMSO, reflux, 18<b> </b>h; b) 4-cyanobenzoyl chloride, Et<sub>3</sub>N, CH<sub>2</sub>Cl<sub>2</sub>, rt, 3<b> </b>h; c) 4-(chloromethyl)benzonitrile, THF, reflux, 2.5<b> </b>h; d) NaBH(OAc)<sub>3</sub>, CH<sub>2</sub>Cl<sub>2</sub>, rt, 12<b> </b>h; e) 4-fluorobenzoyl chloride, Et<sub>3</sub>N, CH<sub>2</sub>Cl<sub>2</sub>, rt, 3<b> </b>h; f) EDC.HCl, CH<sub>2</sub>Cl<sub>2</sub>, rt, 8<b> </b>h; g) 1-bromo-3-chloropropane, KI, CH<sub>3</sub>CN, MWI, 15<b> </b>min; h) 4-fluorobenzoyl chloride, Et<sub>3</sub>N, CH<sub>2</sub>Cl<sub>2</sub>, 0°C, 5<b> </b>h; i) KI, K<sub>2</sub>CO<sub>3</sub>, CH<sub>3</sub>CN, reflux, 24<b> </b>h.</p
Indian Institute of Experimental Medicine, Calcutta-32 Manuscript received 20 June 1973; revised 20...
The title compound was synthesized by N-alkylation of 4-(4-chlorophenyl)piperazine with ethyl 2-brom...
This article describes the development of a robust and scalable synthetic process for K-8986 (1). To...
<p>Reagents and conditions: a) SOCl<sub>2</sub>, EtOH, 0°C, 0.5<b> </b>h, rt, 3<b> </b>h, reflux, 1<...
W początkowej części pracy omówiono choroby: padaczkę i depresję oraz leki z grupy pochodnych pipera...
目的寻找并合成低毒、有较强抗肿瘤活性的哌嗪类化合物。方法和结果以1,4-二(3-溴丙酰基)哌嗪为先导物,合成了一系列1,4-二[3-(氨基硫代甲酰硫基)丙酰基]哌嗪类新化合物,并测试了这些化合物(4a...
Piperazine scaffolds are amongst the most extensively used backbones in medicinal chemistry and many...
<p>(a) (i) benzyl alcohol (BnOH), 4-dimethylaminopyridine, 1-ethyl-3-(3′-dimethylaminopropyl)carbodi...
The activity of pharmacologically active compounds can be increased by presenting a drug in a define...
Objective: Synthesis, anticancer and antituberculosis studies for 1-(4-Chlorophenyl) cyclopropyl] (p...
Department of Chemistry University of Lucknow, Lucknow-226 007 Manuscript received 11 January 199...
<p><i>Reagents and conditions</i>: (a) 4-bromoaniline, piperidine, 2-methoxyethanol, reflux, 72 h, 9...
923-928 Reaction of 2-(chloromethyl)-3-arylquinazolin-4(3H)-one 3 with N-BOC piperazine 4 in ...
<p><sup>a</sup>Piperazine is directly connected to the pteridine core without a secondary amine.</p>...
The title compds. (I; Q = bond, CH2, NR5, O; X = CH, N; Y = bond, CH2, NR6; Z = CH, N; R1, R2 = H, a...
Indian Institute of Experimental Medicine, Calcutta-32 Manuscript received 20 June 1973; revised 20...
The title compound was synthesized by N-alkylation of 4-(4-chlorophenyl)piperazine with ethyl 2-brom...
This article describes the development of a robust and scalable synthetic process for K-8986 (1). To...
<p>Reagents and conditions: a) SOCl<sub>2</sub>, EtOH, 0°C, 0.5<b> </b>h, rt, 3<b> </b>h, reflux, 1<...
W początkowej części pracy omówiono choroby: padaczkę i depresję oraz leki z grupy pochodnych pipera...
目的寻找并合成低毒、有较强抗肿瘤活性的哌嗪类化合物。方法和结果以1,4-二(3-溴丙酰基)哌嗪为先导物,合成了一系列1,4-二[3-(氨基硫代甲酰硫基)丙酰基]哌嗪类新化合物,并测试了这些化合物(4a...
Piperazine scaffolds are amongst the most extensively used backbones in medicinal chemistry and many...
<p>(a) (i) benzyl alcohol (BnOH), 4-dimethylaminopyridine, 1-ethyl-3-(3′-dimethylaminopropyl)carbodi...
The activity of pharmacologically active compounds can be increased by presenting a drug in a define...
Objective: Synthesis, anticancer and antituberculosis studies for 1-(4-Chlorophenyl) cyclopropyl] (p...
Department of Chemistry University of Lucknow, Lucknow-226 007 Manuscript received 11 January 199...
<p><i>Reagents and conditions</i>: (a) 4-bromoaniline, piperidine, 2-methoxyethanol, reflux, 72 h, 9...
923-928 Reaction of 2-(chloromethyl)-3-arylquinazolin-4(3H)-one 3 with N-BOC piperazine 4 in ...
<p><sup>a</sup>Piperazine is directly connected to the pteridine core without a secondary amine.</p>...
The title compds. (I; Q = bond, CH2, NR5, O; X = CH, N; Y = bond, CH2, NR6; Z = CH, N; R1, R2 = H, a...
Indian Institute of Experimental Medicine, Calcutta-32 Manuscript received 20 June 1973; revised 20...
The title compound was synthesized by N-alkylation of 4-(4-chlorophenyl)piperazine with ethyl 2-brom...
This article describes the development of a robust and scalable synthetic process for K-8986 (1). To...