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HRID 1723795作成日:2026年10月27日

Methyl iodide → 4,4-Dimethyl-2,3,4,9-tetrahydro-1H-beta-carboline-1-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1723795

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物beta,beta-Dimethyl-1H-indole-3-ethanamineHCID 27303—
反応物tert-Butyl 3-(cyanomethyl)-1H-indole-1-carboxylateHCID 15378323—
生成物4,4-Dimethyl-2,3,4,9-tetrahydro-1H-beta-carboline-1-carboxylic acid ethyl esterHCID 66640193—

反応手順

4,4-Dimethyl-2,3,4,9-tetrahydro-1H-beta-carboline-1-carboxylic acid ethyl ester was prepared in a manner similar to that described in Example 66A by replacing tryptamine-HCl with 2-(1H-indol-3-yl)-2-methylpropylamine, which was synthesized using 2 equivalents of iodomethane during alkylation of (1-tert-butoxycarbonylindol-3-yl)acetonitrile as described in Example 32B; MS(ESI): 273(MH+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07485634B2
出典データセットuspto-grants-2009_02
ORD IDord-a971a8d9f3624726a4b729c4df358154
出典メモuspto-grants-2009_02