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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 48455생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Guanidine HydrochlorideHCID 5742—
반응물3-AnilinopropionitrileHCID 14100—
반응물4-ethoxy-1-(2-trimethylsilanyl-ethoxymethyl)-1H-indole-6-carbaldehydeHCID 22742926—
반응물Potassium tert-butoxideHCID 23665647—
반응물5-[4-Ethoxy-1-(2-trimethylsilanyl-ethoxymethyl)-1H-indol-6-ylmethyl]-pyrimidine-2,4-diamineHCID 69920554—
용매Dimethyl SulfoxideHCID 679—
용매EthanolHCID 702—
용매WaterHCID 962—
용매tert-ButanolHCID 6386—
생성물5-(4-Ethoxy-1H-indol-6-ylmethyl)-pyrimidine-2,4-diamineHCID 2274291962%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06703397B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-9540ad39a2414b7abb810eca8ddaf9f3
출처 메모uspto-grants-2004_03