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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Carbonate | HCID 10340 | — |
| 반응물 | 4-(Methanesulfonyl)phenylboronic acid | HCID 2734364 | — |
| 반응물 | Tert-butyl 4-(7-bromothieno[3,2-d]pyrimidin-4-yloxy)piperidine-1-carboxylate | HCID 68299345 | — |
| 촉매 | HCID 178418397 | HCID 178418397 | — |
| 용매 | 1,4-Dioxane | HCID 31275 | — |
| 생성물 | Tert-butyl 4-(7-(4-methanesulfonylphenyl)thieno[3,2-d]pyrimidin-4-yloxy)piperidin-1-carboxylate | HCID 57415237 | 21.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US08853213B2 |
|---|
| 출처 데이터셋 | uspto-grants-2014_10 |
|---|
| ORD ID | ord-010bdb0c15e44f37a97dd9365cea8618 |
|---|
| 출처 메모 | uspto-grants-2014_10 |
|---|