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HRID 48455作成日:2026年10月24日

Guanidine Hydrochloride → 5-(4-Ethoxy-1H-indol-6-ylmethyl)-pyrimidine-2,4-diamine

https://huagongshe.com/ja/reaction/48455

反応式

関与物質

役割名称HCID仕込み量
反応物Guanidine HydrochlorideHCID 5742—
反応物3-AnilinopropionitrileHCID 14100—
反応物4-ethoxy-1-(2-trimethylsilanyl-ethoxymethyl)-1H-indole-6-carbaldehydeHCID 22742926—
反応物Potassium tert-butoxideHCID 23665647—
反応物5-[4-Ethoxy-1-(2-trimethylsilanyl-ethoxymethyl)-1H-indol-6-ylmethyl]-pyrimidine-2,4-diamineHCID 69920554—
溶媒Dimethyl SulfoxideHCID 679—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
溶媒tert-ButanolHCID 6386—
生成物5-(4-Ethoxy-1H-indol-6-ylmethyl)-pyrimidine-2,4-diamineHCID 2274291962%

反応手順

5-[4-Ethoxy-1-(2-trimethylsilanyl-ethoxymethyl)-1H-indol-6-ylmethyl]-pyrimidine-2,4-diamine. A warm solution of potassium tert-butylate (900 mg, 8.02 mmol) in tert-butanol (7.5 mL) was added at room temperature to a solution of 4-ethoxy-1-(2-trimethylsilanyl-ethoxymethyl)-1H-indole-6-carbaldehyde (2.14 g, 6.69 mmol) and 3-anilinopropionitrile (1.08 g, 7.36 mmol) in methyl sulfoxide (25 mL). After 90 min the solution was treated with water and the suspension formed was stirred for 2 h. The precipitate was collected by filtration and dried. This material was added to a suspension of guanidine hydrochloride (1.90 g, 19.9 mmol) and potassium tert-butylate (2.23 g, 19.9 mmol) in ethanol (100 mL), and the reaction mixture was refluxed for 16 h, then most of the solvent was distilled off, and ether (50 mL) was added. Insoluble material was removed by filtration, the filtrate was washed with water, dried (MgSO4), and evaporated. The residue was washed with diethyl ether/n-hexane 4:3 (70 mL) to afford the title compound (1.71 g, 62%). Light brown solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06703397B2
出典データセットuspto-grants-2004_03
ORD IDord-9540ad39a2414b7abb810eca8ddaf9f3
出典メモuspto-grants-2004_03