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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7653생성일: 2026년 10월 24일

1-Phenethylamine, (-)- → 6-dimethylamino-2-(4-fluorophenyl)-3-[2-(1-(S)-phenylethylamino)-pyrimidin-4yl]-6,7-dihydro-5H-pyrazolo[1,2-a]pyrazol-1-one

https://huagongshe.com/ko/reaction/7653

반응식

참여 물질

역할이름HCID투입량
반응물1-Phenethylamine, (-)-HCID 75818—
반응물6-dimethylamino-2-(4-fluorophenyl)-3-(2-methanesulfonyl-pyrimidin-4-yl)-6,7-dihydro-5H-pyrazolo[1,2-a]pyrazol-1-oneHCID 21992208—
용매TolueneHCID 1140—
생성물6-dimethylamino-2-(4-fluorophenyl)-3-[2-(1-(S)-phenylethylamino)-pyrimidin-4yl]-6,7-dihydro-5H-pyrazolo[1,2-a]pyrazol-1-oneHCID 12133108—

반응 조건

온도140 °C

반응 단계

A solution of the crude 6-dimethylamino-2-(4-fluorophenyl)-3-(2-methanesulfonyl-pyrimidin-4-yl)-6,7-dihydro-5H-pyrazolo[1,2-a]pyrazol-1-one, 25, prepared as described herein above (4.2 g, 10 mmol) and (S)-(−)-α-methyl-benzyl amine (45.2 mL, 351 mmol) are dissolved in toluene (100 mL). The resulting mixture is heated to 140° C. for 12 hours, cooled to room temperature and the solvent removed in vacuo. The resulting residue is purified over silica (1:1 EtOAc/hexanes) to afford the desired product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087615B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-d25374737a9e4104a2fb69a179eedfcd
출처 메모uspto-grants-2006_08