Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 451412생성일: 2026년 10월 26일
Diisopropylethylamine → tert-butyl N-[1-(6-methylpyrimidin-4-yl)piperidin-4-yl]carbamate
https://huagongshe.com/reaction/451412
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | 4-Chloro-6-methylpyrimidine | HCID 581796 | — |
| 반응물 | 4-Amino-1-Boc-piperidine | HCID 1268291 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | 1,4-Dioxane | HCID 31275 | — |
| 생성물 | tert-butyl N-[1-(6-methylpyrimidin-4-yl)piperidin-4-yl]carbamate | HCID 67343276 | — |
반응 단계
A suspension of Boc-4-aminopiperidine (613 mg, 3 mmol), 4-chloro-6-methylpyrimidine (433 mg, 3.3 mmol) and N,N-diisopropylethyl amine (771 L, 4.5 mmol) in dioxane (12 mL) was heated to 150° C. in the microwave for 30 minutes. The reaction was diluted with water and extracted twice with ethyl acetate. The combined organic layers were washed with water, dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude product was purified by column chromatography on silica gel using a gradient from AcOEt to AcOEt/EtOH 9:1 as eluent. The title compound was obtained as a light yellow solid (693 mg, 79%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08486967B2 |
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| 출처 데이터셋 | uspto-grants-2013_07 |
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| ORD ID | ord-6de883d95cf14582bc0237df04c0840d |
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| 출처 메모 | uspto-grants-2013_07 |
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