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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 421403생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/421403

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물Acetic AnhydrideHCID 7918—
반응물TriethylamineHCID 8471—
반응물5-{9-(Cyclopropylmethyl)-8-[(3S)-3-methylpiperazin-1-yl]-6-morpholin-4-yl-9H-purin-2-yl}pyrimidin-2-amineHCID 59333528—
용매Dichloromethane methanolHCID 21226129—
생성물5-{8-[(3S)-4-Acetyl-3-methylpiperazin-1-yl]-9-(cyclopropylmethyl)-6-morpholin-4-yl-9H-purin-2-yl}pyrimidin-2-amineHCID 5933360398%

반응 단계

Triethylamine (80.3 μl, 0.58 mmol) was added to a methylene chloride solution (3.0 ml) of 5-{9-(cyclopropylmethyl)-8-[(3S)-3-methylpiperazin-1-yl]-6-morpholin-4-yl-9H-purin-2-yl}pyrimidin-2-amine (108.1 mg, 0.24 mmol) at room temperature followed by the addition of acetic anhydride (27.2 μl, 0.29 mmol) with ice cooling. The resulting mixture was stirred at room temperature for 2 hours and then 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=49:1 to 19:1) to give the title compound (115.8 mg, 98%) as a pale yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08097622B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-27a2d5a328bf4858ad8b791b614decd9
출처 메모uspto-grants-2012_01