## Abstract [^3^H]SCH 211803, at a specific activity of 1.56 Ci/mmol, was prepared by direct exchange with tritiated water and platinum metal. [^2^H~4~]SCH 211803 was prepared from [^2^H]formaldehyde in a seven step synthesis in 10% yield. [^14^C]SCH 211803 was prepared from __N__βbenzylβ4βhydroxy[
Synthesis of 2H, 3H and 14C labelled Sch 40120
β Scribed by D. Hesk; T. Duelfer; S. Hickey; D. Hochman; D. Koharski; P. McNamara; S. Saluja
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- French
- Weight
- 376 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0022-2135
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β¦ Synopsis
Abstract
^2^H and ^3^H labelled Sch 40120 were prepared by Pt catalysed exchange with isotopic water. D7βSch 40120 was obtained in two exchanges in 53% yield and ^3^HβSch 40120 was prepared by a single exchange at a specific activity of 19.8 Ci/mmole. ^14^CβSch 40120 was prepared in 4 steps from ^14^Cβmβchloro aniline in overall 16% radiochemical yield.
π SIMILAR VOLUMES
3H-Sch 47949, racemic 3H-Sch 48461, was prepared at a specific activity of 40 mCi/mmole by Pt catalysed exchange with tritiated water. 3H-Sch 48461 was prepared at a specific activity of 64.6 Ci/mmole by a Pd/C catalysed reduction of an olefinic intermediate. 14C-Sch 48461 was prepared in 8 steps fr
## Abstract ^3^HβSch 58235 was prepared at a specific activity of 29.1 Ci/mmol by Ir(COD)(Cy~3~P)PyPF~6~ catalysed exchange with tritium gas. ^14^CβSch 58235 was prepared in three steps from __p__βhydroxy[ringβUβ^14^C]benzaldehyde with an overall radiochemical yield of 21%. ^13^C~6~βSch 58235 was s
## Abstract The preparation of [^3^H]Sch 727965 from unlabeled compound and tritiated water was base catalyzed. Diethyl [^13^C~3~]malonate was used to prepare [^13^C~3~]Sch 727965 in five steps in 21.8% overall yield. In a similar manner, [^14^C]Sch 727965 was prepared in five steps from diethyl [2
A synthesis of dibucaine labeled with l"C in the heterocyclic ring is described. starting with isatin and acetic anh~dride-2-~"C as shown in Scheme I. Two deutero analogs, dibucaine-d2 and dibucaine-dg, were also synthesized by the reactions shown in Scheme 11. Dibucaine-dg was synthesized by conden