Synthesis p. 482 - 483 (1988)
Update date:2022-07-29
Topics: Synthesis Column chromatography Melting point Yield Catalyst Solvent reflux Nucleophilic substitution Stirring TLC (thin-layer chromatography) NMR (nuclear magnetic resonance) Workup Purity IR (Infrared Spectroscopy) Acyl chloride
Tanabe, Yoo
Sanemitsu, Yuzuru
3-Chloromethyl-2(3H)-benzothiazolones 4 were synthesized from 1,3,5-triphenyl-1,3,5-triazines 2 and chlorocarbonylsulfenyl chloride in a one-pot procedure.The chlorine atom in 4 was substituted by three types of nucleophiles, namely, potassium acetate, p-
View MoreContact:17316303296
Address:240 Amboy Ave
Hebei Think-Do Environment Co., Ltd
website:http://www.thinkdo-environment.com
Contact:0311-86510809-
Address:No 6, Shilian Middle Street, Circular Chemical Industry Park
Changde Yungang Biotechnology Co., Ltd
website:http://www.cdyg.com
Contact:+86-736-7391178
Address:Qiaonan Industrial Park, Changde City, Hunan Province
Taizhou Elitechemie MediPharma Technology Co.,Ltd.
Contact:+86-523-86810021
Address:Building G14,NO.1 Avenue,China Medical City, Taizhou, Jiangsu,China
Chengdu King-tiger Pharm-chem. Tech. Co., Ltd
Contact:028-85317716
Address:Tianfu Life Science Park, No. 88 South Keyuan Road, Gaoxin District, Chengdu City, Sichuan Province, PRC.
Doi:10.1055/s-0029-1216636
(2009)Doi:10.1021/jo00260a014
(1988)Doi:10.1055/s-0028-1088110
(2009)Doi:10.1039/b822170g
(2009)Doi:10.1021/acs.orglett.7b03296
(2017)Doi:10.1002/chem.200802677
(2009)
