## Abstract The novel [^14^C]‐labelled 3‐carbamoyl‐4‐hydroxycoumarins were prepared in two steps from 4‐chloro‐acetylsalicyloyl chloride (3). The isotope was incorporated by the reaction of diethyl malonate‐1,3‐^14^C with 4‐chloro‐acetylsalicyloyl chloride (3). Subsequent condensation of the result
Synthesis of carbon-14 and tritium labeled N,N′-(2-chloro-5-cyano-1,3-phenylene)dioxamic acid di-tham salt
✍ Scribed by Richard S. P. Hsi; Tommy D. Johnson
- Publisher
- John Wiley and Sons
- Year
- 1978
- Tongue
- French
- Weight
- 401 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Acetylation of tritium and carbon‐14 labeled 4‐chloro‐3,5‐diaminobenzonitrile (Ia and Ib) with ethyl oxalyl chloride afforded diethyl N,N′‐(2‐chloro‐5‐cyano‐1,3‐phenylene)dioxamate (IIa and IIb). The diester II was hydrolyzed to give N,N′‐(2‐chloro‐5‐cyano‐1,3‐phenylene)dioxamic acid, which was isolated as the tris‐hydroxymethylaminomethane (THAM) salt III.
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