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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1512136생성일: 2026년 10월 26일

Sodium Carbonate → 2-Amino-5-[2-morpholin-4-yl-6-(quinolin-3-ylamino)-pyrimidin-4-yl]-isonicotinonitrile

https://huagongshe.com/reaction/1512136

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물2-Amino-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine-4-carbonitrileHCID 59507509—
반응물N-(6-bromo-2-morpholinopyrimidin-4-yl)quinolin-3-amineHCID 59507540—
촉매CID 53485975HCID 53485975—
용매1,4-DioxaneHCID 31275—
생성물2-Amino-5-[2-morpholin-4-yl-6-(quinolin-3-ylamino)-pyrimidin-4-yl]-isonicotinonitrileHCID 5950773421.2%

반응 조건

온도120 °C

반응 단계

To the crude 2-amino-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine-4-carbonitrile (prepared as in Method 11) (25 mg, 0.13 mmol) solution in dioxane (1.8 mL) in a pressure vessel, was added (6-bromo-2-morpholin-4-yl-pyrimidin-4-yl)-quinolin-3-yl-amine (19.4 mg, 0.05 mmol) and aq. Na2CO3 (2 M, 0.6 mL, 1.2 mmol). After purging the reaction mixture with argon, dichloro[1,1′-bis(diphenylphosphino)ferrocene]palladium(II) dichloromethane adduct (10.3 mg, 0.01 mmol) was added in one portion. The pressure vessel was sealed and the mixture was heated in a microwave at 120° C. for 900 seconds. The crude mixture was filtered and concentrated under reduced pressure. The crude product was purified by reverse phase preparative HPLC to give 2-amino-5-[2-morpholin-4-yl-6-(quinolin-3-ylamino)-pyrimidin-4-yl]-isonicotinonitrile (4.5 mg, 20%). LC/MS (m/z): 425.0 (MH+), Rt 2.03 minutes.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08217035B2
출처 데이터셋uspto-grants-2012_07
ORD IDord-60d381057df44437bfbfcd3d9da6da70
출처 메모uspto-grants-2012_07