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【结 构 式】

【分子编号】12447

【品名】(5-Chloro-3-methyl-2-thienyl)(3-methyl-2-thienyl)methanol

【CA登记号】

【 分 子 式 】C11H11ClOS2

【 分 子 量 】258.79244

【元素组成】C 51.05% H 4.28% Cl 13.7% O 6.18% S 24.78%

与该中间体有关的原料药合成路线共 1 条

合成路线1

该中间体在本合成路线中的序号:(VI)

The synthesis of 5-hydroxytiagabine, a metabolite of tiagabine in humans, has been undertaken to confirm that it is present entirely as (E)- and (Z)-isomers of the tautomeric 5-oxo form: The bromination of 3-methylthiophene (I) with N-bromosuccinimide gives 2-bromo-3-methylthiophene (II), which is chlorinated with N-chlorosuccinimide to yield 2-bromo-5-chloro-3-methylthiophene (III). The reaction of (III) with Mg affords 5-chloro-3-methylthien-2-ylmagnesium bromide (IV), which is condensed with 3-methylthiophene-2-carboxaldehyde (V) (obtained from (II) by reaction with magnesium and dimethylformamide) to give the bisthienylmethanol (VI). The oxidation of (VI) with pyridinium chlorochromate (PCC) yields the bisthienyl ketone (VII), which is treated with sodium methoxide to afford the bis(2-thienyl)ketone (VIII). The Grignard reaction of (VIII) with cyclopropylmagnesium bromide (IX) gives the trisubstituted methanol (X), which is submitted to ring opening with trimethylsilyl bromide to afford the thiophenone (XI) as a mixture of the (E)- and (Z)-isomers. The condensation of (XI) with piperidine-3(R)-carboxylic acid ethyl ester (XII) by means of K2CO3 gives 1-[4-(3-methyl-5-oxo-2,5-dihydrothien-2-ylidene)-4-(3-methyl-2-thienyl) butyl]piperidine-3(R)-carboxylic acid ethyl ester (XIII) (also as a mixture of (E)- and (Z)-isomers). Finally, this compound is hydrolyzed to the free acid in HCl medium.

1 Thogersen, H.; Chorghade, M.S.; Lee, E.C.; Andersen, K.E.; Sorensen, P.O.; Lundt, B.F.; Begtrup, M.; Lau, J.; Petersen, H.; The synthesis of novel GABA uptake inhibitors. 2. Synthesis of 5-hdroxytiagabine, a human metabolite of the GABA reuptake inhibitor tiagabine. Tetrahedron 1994, 50, 29, 8699.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 12442 3-Methylthiophene 616-44-4 C5H6S 详情 详情
(II) 12443 2-Bromo-3-methylthiophene 14282-76-9 C5H5BrS 详情 详情
(III) 12444 2-Bromo-5-chloro-3-methylthiophene C5H4BrClS 详情 详情
(IV) 12445 Bromo(5-chloro-3-methyl-2-thienyl)magnesium C5H4BrClMgS 详情 详情
(V) 12446 3-Methyl-2-thiophenecarboxaldehyde; 3-Methyl-2-thiophenecarbaldehyde 5834-16-2 C6H6OS 详情 详情
(VI) 12447 (5-Chloro-3-methyl-2-thienyl)(3-methyl-2-thienyl)methanol C11H11ClOS2 详情 详情
(VII) 12448 (5-Chloro-3-methyl-2-thienyl)(3-methyl-2-thienyl)methanone C11H9ClOS2 详情 详情
(VIII) 12449 (5-Methoxy-3-methyl-2-thienyl)(3-methyl-2-thienyl)methanone C12H12O2S2 详情 详情
(IX) 12450 Bromo(cyclopropyl)magnesium;cyclopropylmagnesium bromide;cyclopropylmagnesiumbromide 23719-80-4 C3H5BrMg 详情 详情
(X) 12451 Cyclopropyl(5-methoxy-3-methyl-2-thienyl)(3-methyl-2-thienyl)methanol C15H18O2S2 详情 详情
(XI) 12452 5-[(E)-4-Bromo-1-(3-methyl-2-thienyl)butylidene]-4-methyl-2(5H)-thiophenone C14H15BrOS2 详情 详情
(XII) 12453 ethyl (3R)hexahydro-3-pyridinecarboxylate C8H15NO2 详情 详情
(XIII) 12454 ethyl (3R)-1-[4-[3-methyl-5-oxo-2(5H)-thiophenylidene]-4-(3-methyl-2-thienyl)butyl]hexahydro-3-pyridinecarboxylate C22H29NO3S2 详情 详情
Extended Information