Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2067908생성일: 2026년 10월 26일
Methyl isonipecotate → Methyl 1-(2-(5-(5-bromopyrimidin-2-ylamino)-2-fluorophenoxy)ethyl)piperidine-4-carboxylate
https://huagongshe.com/reaction/2067908
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Methyl isonipecotate | HCID 424914 | — |
| 반응물 | 2-(5-(5-Bromopyrimidin-2-ylamino)-2-fluorophenoxy)ethyl methanesulfonate | HCID 86660123 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | N-methyl-2-pyrrolidone | HCID 13387 | — |
| 생성물 | Methyl 1-(2-(5-(5-bromopyrimidin-2-ylamino)-2-fluorophenoxy)ethyl)piperidine-4-carboxylate | HCID 58542307 | — |
반응 단계
2-(5-(5-bromopyrimidin-2-ylamino)-2-fluorophenoxy)ethyl methanesulfonate 46b (0.24 mmol) and methyl piperidine-4-carboxylate (0.48 mmol) are dissolved in NMP (2 mL) and heated to 90° C. for 3 h. The reaction mixture is cooled to rt and diluted with water and extracted with EtOAc (2×30 mL). The organic layer is washed with water, brine, dried over sodium sulfate, and concentrated to dryness. The crude product is purified by short SiO2 chromatography using DCM:hexane=9:1 as eluant to yield methyl 1-(2-(5-(5-bromopyrimidin-2-ylamino)-2-fluorophenoxy)ethyl)piperidine-4-carboxylate 47 as light brown solid. MS (m/z) (M+1)+: 454.1.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08293757B2 |
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| 출처 데이터셋 | uspto-grants-2012_10 |
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| ORD ID | ord-5eacd9c8f44141448122ab8b1c12f878 |
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| 출처 메모 | uspto-grants-2012_10 |
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