The preparation of 5-indolyl-Mannich bases: an expedient source of 5-(chloromethyl)indoles
-
Add time:08/29/2019 Source:sciencedirect.com
Regioisomeric analogues of gramine, 5-(dialkylaminomethyl)indole-2-carboxylates were prepared by the Fischer indolization of 4-(dialkylaminomethyl)phenylhydrazones easily obtained from diazotized 4-(dialkylaminomethyl)anilines by the Japp–Klingemann reaction. These formal Mannich bases are valuable synthetic intermediates affording 5-(chloromethyl)indoles on reaction with acetyl chloride at rt within a few minutes in quantitative yields.
We also recommend Trading Suppliers and Manufacturers of 5-(CHLOROMETHYL)-N-PHENYL-1,3,4-THIADIAZOLE-2-CARBOXAMIDE (cas 113940-13-9). Pls Click Website Link as below: cas 113940-13-9 suppliers
Prev:Experimental studies towards optimization of the production of 5-(chloromethyl)furfural (CMF) from glucose in a two-phase reactor
Next:Original articleSynthesis and antiproliferative activity of 3-(2-chloroethyl)-5-methyl-6-phenyl-8-(trifluoromethyl)-5,6-dihydropyrazolo[3,4-f][1,2,3,5]tetrazepin-4-(3H)-one) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Experimental studies towards optimization of the production of 5-(chloromethyl)furfural (CMF) from glucose in a two-phase reactor08/28/2019
- Thermal degradation kinetics of functional polysiloxanes containing chloromethyl groups08/27/2019
- CommunicationChloromethyl pivalate based electrolyte for non-aqueous lithium oxygen batteries08/26/2019
- Evaluation of analgesic and antiplatelet activity of 2-((3-(chloromethyl)benzoyl)oxy)benzoic acid08/25/2019


