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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 397436생성일: 2026년 10월 24일

4-(3-Chloro 4-fluoro-phenylamino)-5,7-dihydro-pyrrolo[2,3-d]pyrimidin-6-one → 4-(3-Chloro-4-fluoro-phenylamino)-5-{1-[5-(morpholine-4-carbonyl)-thiophen-2-yl]-methylidene}-5,7-dihydro-pyrrolo[2,3-d]pyrimidin-6-one

https://huagongshe.com/ko/reaction/397436

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참여 물질

역할이름HCID투입량
반응물4-(3-Chloro 4-fluoro-phenylamino)-5,7-dihydro-pyrrolo[2,3-d]pyrimidin-6-oneHCID 9878769—
반응물5-(Morpholine-4-carbonyl)-thiophene-2-carbaldehydeHCID 22390963—
촉매TriethylamineHCID 8471—
용매EthanolHCID 702—
생성물4-(3-Chloro-4-fluoro-phenylamino)-5-{1-[5-(morpholine-4-carbonyl)-thiophen-2-yl]-methylidene}-5,7-dihydro-pyrrolo[2,3-d]pyrimidin-6-oneHCID 6970906428%

반응 조건

온도90 °C

반응 단계

The mixture of 4-(3-chloro-4-fluoro-phenylamino)-5,7-dihydro-pyrrolo[2,3-d]pyrimidin-6-one (90 mg, 0.32 mmol), 5-(morpholine-4-carbonyl)-thiophene-2-carbaldehyde (82 mg, 0.36 mmol), and triethylamine (2 drops) in ethanol (3 mL) was heated at 90° C. oil bath for 2 hours, and cooled to room temperature. The solvent was evaporated and the residue was purified on a silica gel column eluting with methylene chloride-methanol (98:2 and 95:5) to provide pure 4-(3-chloro-4-fluoro-phenylamino)-5-{ 1-[5-(morpholine-4-carbonyl)-thiophen-2-yl]-methylidene-}-5,7-dihydro-pyrrolo[2,3-d]pyrimidin-6-one (41 mg, 28%). MS 486 [M++1].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06610688B2
출처 데이터셋uspto-grants-2003_08
ORD IDord-451d4e66646f48819c2976e5a7686409
출처 메모uspto-grants-2003_08