Next Article in Journal
Fast Solvent-free Alkylation of Amides and Lactams under Microwave Irradiation
Previous Article in Journal
17O NMR Spectra of α,β-Unsaturated Carbonyl Compounds RCH=CHCOX: the Influence of Group X on the δ(17O) Value of the Carbonyl Oxygen and on the Shielding Effect of Group R
Molecules 1999, 4(11), 329-332; doi:10.3390/41100329
Article

8-Chloro-11-[4-(8-chloro-5H-dibenzo[b,e][1,4]diazepin-11-yl)piperazino]-5H-dibenzo[b,e][1,4]diazepine

Received: 13 August 1999; Accepted: 20 October 1999 / Published: 25 October 1999
Download PDF [22 KB, uploaded 18 June 2014]
Abstract: A method to synthesize desmethylclozapine, 3, is reported. The procedure afforded the target compound in 69% yield. A by-product, isolated from the reaction mixture in 11% yield, proved to be the title compound, 4.
Keywords: desmethylclozapine; amidine formation; titanium tetrachloride desmethylclozapine; amidine formation; titanium tetrachloride
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Export to BibTeX |
EndNote


MDPI and ACS Style

Capuano, B. 8-Chloro-11-[4-(8-chloro-5H-dibenzo[b,e][1,4]diazepin-11-yl)piperazino]-5H-dibenzo[b,e][1,4]diazepine. Molecules 1999, 4, 329-332.

AMA Style

Capuano B. 8-Chloro-11-[4-(8-chloro-5H-dibenzo[b,e][1,4]diazepin-11-yl)piperazino]-5H-dibenzo[b,e][1,4]diazepine. Molecules. 1999; 4(11):329-332.

Chicago/Turabian Style

Capuano, Ben. 1999. "8-Chloro-11-[4-(8-chloro-5H-dibenzo[b,e][1,4]diazepin-11-yl)piperazino]-5H-dibenzo[b,e][1,4]diazepine." Molecules 4, no. 11: 329-332.


Molecules EISSN 1420-3049 Published by MDPI AG, Basel, Switzerland RSS E-Mail Table of Contents Alert