朱友成, C.Prenant, C.Crouzel, 池志强. 新的高强度高选择性阿片μ受体激动剂11C-羟甲芬太尼的合成J. 药学学报, 1994, 29(11): 823-828.
引用本文: 朱友成, C.Prenant, C.Crouzel, 池志强. 新的高强度高选择性阿片μ受体激动剂11C-羟甲芬太尼的合成J. 药学学报, 1994, 29(11): 823-828.
YC Zhu, C Prenant, C Crouzel, D.Comar , ZQ Chi, . SYNTHESIS OF 11C -OHMEFENTANYL,A NEW,HIGHLY POTENT AND SELECTIVE AGONIST FOR OPIATE μ-RECEPTORJ. Acta Pharmaceutica Sinica, 1994, 29(11): 823-828.
Citation: YC Zhu, C Prenant, C Crouzel, D.Comar , ZQ Chi, . SYNTHESIS OF 11C -OHMEFENTANYL,A NEW,HIGHLY POTENT AND SELECTIVE AGONIST FOR OPIATE μ-RECEPTORJ. Acta Pharmaceutica Sinica, 1994, 29(11): 823-828.

新的高强度高选择性阿片μ受体激动剂11C-羟甲芬太尼的合成

SYNTHESIS OF 11C -OHMEFENTANYL,A NEW,HIGHLY POTENT AND SELECTIVE AGONIST FOR OPIATE μ-RECEPTOR

  • 摘要: 羟甲芬太尼(I)是一个新的高强度高选择性阿片μ受体激动剂。本文用cis-A-N-1-(2-羟基-2-苯乙基)-3-甲基-4-哌啶基-苯胺(II)或cis-N-1-(苯甲酰甲基)-3-甲基-4-哌啶基-苯胺(III)作为前体合成了11C-羟甲芬太尼,以便用正电子发射断层扫描(PET)来观察μ受体。通过水解cis-A-羟甲芬太尼(I)和cis-N-1-(苯甲酰甲基)-3-甲基-4-哌啶-N-苯基丙酰胺(cis-IV)的4-N-丙酰基分别获得II和III。溴乙烷的格氏试剂与回旋加速器产生的11C-二氧化碳反应后继而直接加入邻苯二甲酸二酰氯和2,6-二叔丁基吡啶生成同位素标记中间体11C-丙酰氯。11C-丙酰氯与OH-前体(II)反应后再经HPLC分离纯化直接得11C-羟甲芬太尼;11C-丙酰氯与酮-前体(III)反应后,再用硼氢化钠甲醇溶液处理,然后进行HPLC分离纯化得11C-羟甲芬太尼。两种方法均可获得ll.1~14.8GBq/μmol的特异性放射化学纯11C-羟甲芬太尼。总共耗时为40~50min(EOB)。

     

    Abstract: Ohmefentanyl I is a new,highly potent and selective agonist for opiate μ-recptor. In order to visualize the μ-receptor by Positron Emission Tomography(PET),I labelcd with carbon-11 was synthesized using OH-precursor II or keto-precursor III.The OH-precursor Il was obtained by hydrolysis of cis-A-ohmefentanyl in 6 mol/L hydrochloric acid and the keto-precursor III was prepared by hydrolysis of cis-IV in 8 mol/L hydrochloric acid.The active intermediate11C-propionyl chloride was prepared by the reaction between Grignard reagent ethylmagnesium bromide and cyclotron-produced11C-carbon dioxide,followed by direct treatment of the radio-complex with phthaloyldichloride and 2,6-di-t-butylpyridine. Reaction of the OH-precursor Il with11C-propionyl chlorideorreaction of the keto-precursor IIl with11C-propionyl chloride and treatment with sodiumborohydride followed by HPLC separation all afforded11C-ohmefentanyl with high specific activityof ll.1~14.8 GBq/μmol(300~400 mCi/μmo1)at 45~50 minutes after the end of bombardment(EOB).

     

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