## Abstract Tritium and ^14^Cโlabeled isomers of ethyl acetate are excellent substrates for competitive dualโlabeled radioactive isotopic measurements of ฮฒโdeuterium and ฮฒโtritium isotope effects. Methods are given for preparation of the ethyl esters of acetic acidโ2โ^3^H, acetic acidโ2โ^14^C, and
Syntheses of 14C and 3H labelled forms of donetidine - A histamine H2-antagonist
โ Scribed by M A Armitage; M M Cashyap; D Saunders
- Publisher
- John Wiley and Sons
- Year
- 1987
- Tongue
- French
- Weight
- 440 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
โฆ Synopsis
Three syntheses o f r a d i o l a b e l l e d 2-[2-(2-N.N-Dlmethylarnlnomethyl-5 -f uranyl-methyl thlo)ethylamlno]-5-( 6-hydroxy-l-plcolyl ) -4pyrlmldone t r i h y d r o c h l o r l d e (donetldlne t r i h y d r o c h l o r i d e ) are described. One descrlbes the preparatlon o f the f r e e base, and two o f I t s t r l h y d r o c h l o r l d e . 1. A f i v e stage synthesis (Scheme 1) whlch gave ''C-donetldlne * To whom correspondence should be addressed. 0362-4803/87/040431-15sO7.50 @ 1987 by John Wiley & Sons, Ltd.
๐ SIMILAR VOLUMES
## Abstract In support of a program to develop a treatment for depression, three isotopically labeled forms of the 5โHT~1B~ antagonist AZ12320927 were synthesized. A tritium labeled version was synthesized for autoradiography using Irโcatalyzed hydrogenโtritium exchange. A Cโ14 labeled version was
A novel hlstamlne H1 antagonist SKbF 93944 , 2-[4-(5-bromo-3methylpyrid-2-yl ) butylamino]-5-( 6-methylpyrid-3-yl-methyl)-4( 3H)pyrlmldone. has been labelled with carbon-14 in two dlfferent positions for use in metabolism and pharmacokinetic studies. four stage synthesis o f [p~rimldone-2-~~C] SKLF
## Abstract ^2^H and ^3^H labelled Sch 40120 were prepared by Pt catalysed exchange with isotopic water. D7โSch 40120 was obtained in two exchanges in 53% yield and ^3^HโSch 40120 was prepared by a single exchange at a specific activity of 19.8 Ci/mmole. ^14^CโSch 40120 was prepared in 4 steps from
In support of a program to develop an antipsychotic treatment for schizophrenia, three labeled forms of the NK3 receptor antagonist AZD2624 have been prepared. [ 3 H 2 ]AZD2624 was synthesized by tritiodehalogenation for use in receptor occupancy and autoradiographic studies. [ 13 C 6 ]AZD2624 was p