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【结 构 式】

【分子编号】59044

【品名】methyl (1R,5S)-8-(2-propynyl)-8-azabicyclo[3.2.1]oct-2-ene-2-carboxylate

【CA登记号】

【 分 子 式 】C12H15NO2

【 分 子 量 】205.25664

【元素组成】C 70.22% H 7.37% N 6.82% O 15.59%

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)

N-Demethylation of cocaine (I) is accomplished by treatment with 1-chloroethyl chloroformate, followed by methanolysis of the intermediate chloroethyl carbamate. The resultant nor-cocaine (II) is alkylated with propargyl bromide (III) to afford (IV). Acidic ester hydrolysis of (IV) furnishes hydroxy acid (V). Chlorination of (V) with POCl3, followed by treatment with methanol gives rise to the unsaturated ester (VI). Radical cyclization of the enyne system (VI) in the presence of Bu3SnH and AIBN affords a Z/E mixture of tricyclic vinyl stannanes (VIIa-b) that are separated by column chromatography. The major Z isomer is then subjected to Stille coupling with the aryl iodide (VIII), yielding adduct (IX). Then, reduction of the ester function of (IX) to the primary alcohol (X) is performed by means of either LiAlH4 or DIBAL.

1 Zhang, A.; Kozilowski, A.P.; Zhang, M.; Johnson, K.M.; Mukhopadhyaya, J.; Hoepping, A.; Zhou, G.; Further studies on conformationally constrained tricyclic tropane analogues and their uptake inhibition at monoamine transporter sites: Synthesis of (Z)-9-(substituted arylmethylene)-7-azatricyclo[4.3.1.0(3,7)]decanes as a novel class of serotonin transpo. J Med Chem 2002, 45, 9, 1930.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(VIIa) 59045 methyl (1S,2S,3R,6S)-9-[(Z)-(tributylstannyl)methylidene]-7-azatricyclo[4.3.1.0~3,7~]decane-2-carboxylate C24H43NO2Sn 详情 详情
(VIIb) 59046 methyl (1S,2S,3R,6S)-9-[(E)-(tributylstannyl)methylidene]-7-azatricyclo[4.3.1.0~3,7~]decane-2-carboxylate C24H43NO2Sn 详情 详情
(I) 21116 methyl (1R,2R,3S,5S)-3-(benzoyloxy)-8-methyl-8-azabicyclo[3.2.1]octane-2-carboxylate C17H21NO4 详情 详情
(II) 59041 methyl (1R,2R,3S,5S)-3-(benzoyloxy)-8-azabicyclo[3.2.1]octane-2-carboxylate C16H19NO4 详情 详情
(III) 11176 3-Bromopropyne; 3-Bromo-1-propyne 106-96-7 C3H3Br 详情 详情
(IV) 59042 methyl (1R,2R,3S,5S)-3-(benzoyloxy)-8-(2-propynyl)-8-azabicyclo[3.2.1]octane-2-carboxylate C19H21NO4 详情 详情
(V) 59043 (1R,2R,3S,5S)-3-hydroxy-8-(2-propynyl)-8-azabicyclo[3.2.1]octane-2-carboxylic acid C11H15NO3 详情 详情
(VI) 59044 methyl (1R,5S)-8-(2-propynyl)-8-azabicyclo[3.2.1]oct-2-ene-2-carboxylate C12H15NO2 详情 详情
(VIII) 59047 1-bromo-2-chloro-4-iodobenzene C6H3BrClI 详情 详情
(IX) 59048 methyl (1S,2S,3R,6S)-9-[(Z)-(4-bromo-3-chlorophenyl)methylidene]-7-azatricyclo[4.3.1.0~3,7~]decane-2-carboxylate C18H19BrClNO2 详情 详情
(X) 59049 {(1S,2S,3R,6S)-9-[(Z)-(4-bromo-3-chlorophenyl)methylidene]-7-azatricyclo[4.3.1.0~3,7~]dec-2-yl}methanol C17H19BrClNO 详情 详情
Extended Information