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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 51538생성일: 2026년 10월 24일

Ammonium Hydroxide → HCID 178480948, 화합물

https://huagongshe.com/ko/reaction/51538

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium HydroxideHCID 14923—
반응물HCID 178480946HCID 178480946—
용매1,4-DioxaneHCID 31275—
생성물HCID 178480948HCID 178480948—

반응 단계

Trans-4-chloro-5-iodo-7-[4-(4-methylpiperazino)cyclohexyl]-7H-pyrrolo[2,3-d]pyrimidine (0.89 g, 1.9 nmol) in concentrated ammonium hydroxide (40 mL) and dioxane (40 mL) was heated at 120° C. in a pressure vessel for 18 hours. The mixture was allowed to cool to ambient temperature and the solvent was removed under reduced pressure. The residue was partitioned between saturated aqueous sodium bicarbonate solution and ethyl acetate. The water phase was further extracted with ethyl acetate and the combined organic extracts were washed with brine and dried over sodium sulfate. The solvent was removed under reduced pressure to yield trans-5-iodo-7-[4-(4-methylpiperazino)cyclohexyl]-7H-pyrrolo[2,3-d]pyrimidin-4-amine (0.35 g, 0.8 mmol). RP-HPLC (Hypersil C18, 5 μm, 250×4.6 mm; 25%-100% over 15 min with 0.1 M ammnonium acetate, 1 mL/min) Rt 4.01 min. MS: MH+441.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06713474B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-aeec641f13a74b2baf49f4c6da0d0a94
출처 메모uspto-grants-2004_03