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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 886806생성일: 2026년 10월 26일

Sodium 2-methylbutan-2-olate → Tert-butyl 4-(4-(8-ethyl-4-methyl-7-oxo-6-(thiazol-2-yl)-7,8-dihydropyrido[2,3-d]pyrimidin-2-ylamino)phenyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/886806

반응식

참여 물질

역할이름HCID투입량
반응물Sodium 2-methylbutan-2-olateHCID 2733478—
반응물Tert-butyl 4-(4-iodophenyl)piperazine-1-carboxylateHCID 2795511—
반응물2-amino-8-ethyl-4-methyl-6-(1,3-thiazol-2-yl)pyrido[2,3-d]pyrimidin-7(8H)-oneHCID 16123381—
촉매2-(2'-Di-tert-butylphosphine)biphenylpalladium(II) acetateHCID 11982262—
용매TolueneHCID 1140—
생성물Tert-butyl 4-(4-(8-ethyl-4-methyl-7-oxo-6-(thiazol-2-yl)-7,8-dihydropyrido[2,3-d]pyrimidin-2-ylamino)phenyl)piperazine-1-carboxylateHCID 5760698236.9%

반응 조건

온도70 °C

반응 단계

Acetato(2′-di-t-butylphosphino-1,1′-biphenyl-2-yl)palladium(II) (45 mg, 0.098 mmol) was added to pressure tube charged with 2-amino-8-ethyl-4-methyl-6-(1,3-thiazol-2-yl)pyrido[2,3-d]pyrimidin-7(8H)-one (141 mg, 0.490 mmol), tert-butyl-4-(4-iodophenyl)tetrahydro-1(2H)pyrazinecarboxylate (209 mg, 0.539 mmol), and sodium tert-pentoxide (135 mg, 1.23 mmol) in dry toluene (1.5 mL). The pressure was capped under nitrogen and heated to 70° C.). After 60 hours, the reaction was cooled to room temperature and filtered through a pad of Celite. The filtrate was purified on silica gel (1:1 hexanes:ethyl acetate) to provide the product, tert-butyl 4-(4-(8-ethyl-4-methyl-7-oxo-6-(thiazol-2-yl)-7,8-dihydropyrido[2,3-d]pyrimidin-2-ylamino)phenyl)piperazine-1-carboxylate (99 mg, 34% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08247408B2
출처 데이터셋uspto-grants-2012_08
ORD IDord-609acabf051a43289017ec5bcc276045
출처 메모uspto-grants-2012_08