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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2275340생성일: 2026년 10월 25일

1,1'-Carbonyldiimidazole → (R)-N-(5-(4,4-difluoro-2-(3-fluorophenyl)pyrrolidin-1-yl)pyrazolo[1,5-a]pyrimidin-3-yl)-3-hydroxyazetidine-1-carboxamide

https://huagongshe.com/reaction/2275340

반응식

참여 물질

역할이름HCID투입량
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물DiisopropylethylamineHCID 81531—
반응물3-Hydroxyazetidine hydrochlorideHCID 2759290—
반응물(R)-5-(4,4-difluoro-2-(3-fluorophenyl)pyrrolidin-1-yl)pyrazolo[1,5-a]pyrimidin-3-amineHCID 67329839—
용매DichloromethaneHCID 6344—
생성물(R)-N-(5-(4,4-difluoro-2-(3-fluorophenyl)pyrrolidin-1-yl)pyrazolo[1,5-a]pyrimidin-3-yl)-3-hydroxyazetidine-1-carboxamideHCID 5838633748%

반응 단계

To a DCM (0.7 mL) solution of (R)-5-(4,4-difluoro-2-(3-fluorophenyl)pyrrolidin-1-yl)pyrazolo[1,5-a]pyrimidin-3-amine (25 mg, 0.074 mmol), was added CDI (18 mg, 0.11 mmol) at ambient temperature in one portion. After stirring two hours, azetidin-3-ol hydrochloride (16 mg, 0.15 mmol) was added in one portion, followed by addition of DIEA (0.039 mL, 0.22 mmol). The reaction was stirred overnight, then concentrated, and the residue was directly purified by reverse-phase column chromatography, eluting with 0 to 45% acetonitrile/water to yield the final product as a yellowish oil (15 mg, 48% yield). MS (apci) m/z=433.1 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09127013B2
출처 데이터셋uspto-grants-2015_09
ORD IDord-bf9630e6253d4e7486cb0ce0df9077e2
출처 메모uspto-grants-2015_09