## Abstract A one‐step synthesis for the preparation of a new series of substituted 7__H__‐pyrrolo[2,3‐__d__]pyrimidin‐4‐amines **2** is described. The method consists in heating the corresponding pyrrolo [2,3‐__d__]pyrimidin‐4(3__H__)‐ones **1** in a mixture of phosphorus pentoxide, __N__,__N__‐di
Phosphorus pentoxide in organic synthesis, VII. Synthesis of 3-aryl-3,7-dihydro-4H-pyrrolo[2,3-d]pyrimidin-4-imines
✍ Scribed by Girgis, Nabih S. ;Jørgensen, Anker ;Pedersen, Erik B.
- Publisher
- John Wiley and Sons
- Year
- 1983
- Tongue
- English
- Weight
- 399 KB
- Volume
- 1983
- Category
- Article
- ISSN
- 0947-3440
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The title compounds 2 were prepared by treating 2‐(acetylamino)‐3‐pyrrolecarbonitriles 1 with a mixture of phosphorus pentoxide, N,N‐dimethylcyclohexanamine, and an appropriate arylamine hydrochloride at 150–180°C. The importance of using absolutely anhydrous arylamine hydrochlorides is stressed because failing this, 4‐(arylamino)pyrrolo[2,3‐d]pyrimidines 4 can be formed as by‐products. – The results from pesticide and anticancer screenings are reported.
📜 SIMILAR VOLUMES
1,3-Dihydro-2H-indol-2-ones (oxindoles) and 1,3-dihydro-2H-pyrrolopyridin-2-ones (azaoxindoles) are useful scaffolds that have been explored for various pharmaceutical uses. Herein we report the synthesis of 2-chloro-5,7-dihydro-6H-pyrrolo [2,3d]pyrimidin-6-one (5) and its derivatives, and the appli
## Abstract 2‐Amino‐3,5‐dihydro‐7‐(3‐thienylmethyl)‐[6‐^14^C]‐4H‐pyrrolo [3,2‐d]pyrimidin‐4‐one monohydrochloride ([^14^C]Cl‐1000), a potent purine nucleoside phosphorylase inhibitor, was made in six steps from potassium [^14^C]cyanide. A key step was the reduction of a nitro and a nitrile group wi
Novel 2,3-substituted-2,4-dihydro-pyrazolo[4,3-d] pyrimidine-5,7-diones were successfully synthesized with moderate to good yields using a new synthetic approach. The structures of the regio-isomers in this series were determined by single crystal X-ray analysis and NMR spectra.