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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 527923생성일: 2026년 10월 26일

Ammonium Chloride → (R)-N-methyl-N-(1-(7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)pyrrolidin-3-yl)-1H-pyrazolo[3,4-c]pyridin-5-amine

https://huagongshe.com/reaction/527923

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물Azane;hydrateHCID 12896473—
반응물Sodium NitriteHCID 23668193—
반응물(R)-N,4-dimethyl-5-nitro-N-(1-(7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)pyrrolidin-3-yl)pyridin-2-amineHCID 86692145—
촉매IronHCID 23925—
용매EthanolHCID 702—
용매WaterHCID 962—
생성물(R)-N-methyl-N-(1-(7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)pyrrolidin-3-yl)-1H-pyrazolo[3,4-c]pyridin-5-amineHCID 8669214633%

반응 단계

To a solution of (R)—N,4-dimethyl-5-nitro-N-(1-(7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)pyrrolidin-3-yl)pyridin-2-amine (0.248 mmol) in ethanol (20 mL) and water (5 mL), was added iron powder (0.752 mmol) and NH4Cl (1.495 mmol). The mixture was stirred at refluxing temperature for 2 hours, cooled, and filtered. The filtrate was concentrated, and dissolved in CH3COOH (1.5 mL) and water (2.5 mL). NaNO2 (0.304 mmol) was then slowly added, and the mixture was stirred at room temperature overnight, which was subsequently treated with NH3.H2O and extracted with EtOAc (3×20 mL). The combined extracts were concentrated and the residue was purified by column chromatography to give the title compound in 33.0% yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09346810B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-fd5238fc5b804296bb3e0cf629c60fe6
출처 메모uspto-grants-2016_05