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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 532487생성일: 2026년 10월 25일

Sodium Carbonate → Tert-butyl 4-(7-(4-methanesulfonylphenyl)thieno[3,2-d]pyrimidin-4-yloxy)piperidin-1-carboxylate

https://huagongshe.com/reaction/532487

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물4-(Methanesulfonyl)phenylboronic acidHCID 2734364—
반응물Tert-butyl 4-(7-bromothieno[3,2-d]pyrimidin-4-yloxy)piperidine-1-carboxylateHCID 68299345—
촉매HCID 178418397HCID 178418397—
용매1,4-DioxaneHCID 31275—
생성물Tert-butyl 4-(7-(4-methanesulfonylphenyl)thieno[3,2-d]pyrimidin-4-yloxy)piperidin-1-carboxylateHCID 5741523721.2%

반응 조건

온도100 °C

반응 단계

Tert-butyl 4-(7-bromothieno[3,2-d]pyrimidin-4-yloxy)piperidine-1-carboxylate (100 mg), 4-methanesulfonyl-phenylboronic acid (72 mg), Pd(PPh3)4 (17 mg) and 2N Na2CO3 (0.72 mL) were added to 1,4-dioxane (2 mL), and stirred at 100° C. for 12 hours in a hermetically sealed reactor. The reaction mixture was cooled to room temperature, extracted with ethyl acetate and distilled water, and the organic layer thus obtained was washed with water and a saline solution. Subsequently, the washed organic layer was dried over anhydrous sodium sulfate, and concentrated under reduced pressure to obtain the title compound (25 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08853213B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-010bdb0c15e44f37a97dd9365cea8618
출처 메모uspto-grants-2014_10