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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1876591생성일: 2026년 10월 26일

Dichloromethane → 5-{8-[(3R)-4-Acetyl-3-methylpiperazin-1-yl]-9-(cyclopropylmethyl)-6-morpholin-4-yl-9H-purin-2-yl}pyrimidin-2-amine

https://huagongshe.com/reaction/1876591

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물Acetic AnhydrideHCID 7918—
반응물TriethylamineHCID 8471—
반응물5-{9-(cyclopropylmethyl)-8-[(3R)-3-methylpiperazin-1-yl]-6-morpholin-4-yl-9H-purin-2-yl}pyrimidin-2-amineHCID 59333522—
용매Dichloromethane methanolHCID 21226129—
생성물5-{8-[(3R)-4-Acetyl-3-methylpiperazin-1-yl]-9-(cyclopropylmethyl)-6-morpholin-4-yl-9H-purin-2-yl}pyrimidin-2-amineHCID 59333659100.9%

반응 단계

Triethylamine (77.3 μl, 0.55 mmol) was added to a methylene chloride solution (3.0 ml) of 5-{9-(cyclopropylmethyl)-8-[(3R)-3-methylpiperazin-1-yl]-6-morpholin-4-yl-9H-purin-2-yl}pyrimidin-2-amine (104.1 mg, 0.23 mmol) at room temperature followed by the addition of acetic anhydride (26.2 μl, 0.28 mmol) with ice cooling. The resulting mixture was stirred at room temperature for 95 minutes and the reaction mixture was poured into methylene chloride-methanol (10:1), washed with water, and dried over anhydrous sodium sulfate. After filtration, the filtrate was concentrated under reduced pressure and the resulting residue was purified by medium pressure silica gel column chromatography (methylene chloride:methanol=32:1 to 16:1) to give the title compound (114.3 mg, 100%) as a pale yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08309546B2
출처 데이터셋uspto-grants-2012_11
ORD IDord-3b02dc2e58754925b901fef4e75849ef
출처 메모uspto-grants-2012_11