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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 4-(3-Chloro 4-fluoro-phenylamino)-5,7-dihydro-pyrrolo[2,3-d]pyrimidin-6-one | HCID 9878769 | — |
| 반응물 | 5-(Morpholine-4-carbonyl)-thiophene-2-carbaldehyde | HCID 22390963 | — |
| 촉매 | Triethylamine | HCID 8471 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 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 | HCID 69709064 | 28% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06610688B2 |
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| 출처 데이터셋 | uspto-grants-2003_08 |
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| ORD ID | ord-451d4e66646f48819c2976e5a7686409 |
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| 출처 메모 | uspto-grants-2003_08 |
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