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用于苯二氮䓬受体PET研究的Ro 15 - 1788在两个不同位置的¹¹C标记,以及其主要代谢物Ro 15 - 3890的¹¹C标记。

11C-labelling of Ro 15-1788 in two different positions, and also 11C-labelling of its main metabolite Ro 15-3890, for PET studies of benzodiazepine receptors.

作者信息

Halldin C, Stone-Elander S, Thorell J O, Persson A, Sedvall G

机构信息

Karolinska Pharmacy, Stockholm, Sweden.

出版信息

Int J Rad Appl Instrum A. 1988;39(9):993-7. doi: 10.1016/0883-2889(88)90044-5.

Abstract

The benzodiazepine receptor antagonist Ro 15-1788 has been labelled with 11C in two different positions [( methyl-11C]Ro 15-1788 (I) and [ethyl-11C]Ro 15-1788 (II]. Product I was prepared by N-alkylation of the desmethyl compound (Ro 15-5528) with [11C]methyl iodide and product II was prepared by esterification of the desethyl compound (Ro 15-3890) with [11C]ethyl iodide. Ro 15-3890, the main metabolic product of Ro 15-1788, was labelled by two synthetic routes. In route A, [methyl-11C]Ro 15-3890 (III) was prepared by N-alkylation of the corresponding desmethyl compound (Ro 15-6877) with [11C]methyl iodide. In route B, III was prepared by a subsequent hydrolysis of I. The radiochemical yields were on the order of 15-60% (EOB) with an overall synthesis time of 40-50 min. Compounds I, II and III were isolated by semi-preparative HPLC and the radiochemical purity was in all cases greater than 99%.

摘要

苯二氮䓬受体拮抗剂Ro 15 - 1788已在两个不同位置用11C标记,即[(甲基- 11C]Ro 15 - 1788(I)和[乙基- 11C]Ro 15 - 1788(II)。产物I是通过用[11C]碘甲烷对去甲基化合物(Ro 15 - 5528)进行N - 烷基化制备的,产物II是通过用[11C]碘乙烷对去乙基化合物(Ro 15 - 3890)进行酯化制备的。Ro 15 - 3890是Ro 15 - 1788的主要代谢产物,通过两条合成路线进行标记。在路线A中,[甲基- 11C]Ro 15 - 3890(III)是通过用[11C]碘甲烷对相应的去甲基化合物(Ro 15 - 6877)进行N - 烷基化制备的。在路线B中,III是通过对I进行后续水解制备的。放射化学产率约为15 - 60%(放化纯),总合成时间为40 - 50分钟。化合物I、II和III通过半制备高效液相色谱法分离,在所有情况下放射化学纯度均大于99%。

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