Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 593064생성일: 2026년 10월 25일
Dimethylformamide → tert-Butyl 2-(3-(2,5-Dimethyl-1H-pyrrol-1-yl)-5-(methoxy(methyl)carbamoyl)-1H-pyrazol-1-yl)ethylcarbamate
https://huagongshe.com/reaction/593064
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Dimethylformamide | HCID 6228 | — |
| 반응물 | Sodium Carbonate | HCID 10340 | — |
| 반응물 | N-Boc-2-chloroethylamine | HCID 3795708 | — |
| 반응물 | 3-(2,5-Dimethyl-1H-pyrrol-1-yl)-N-methoxy-N-methyl-1H-pyrazole-5-carboxamide | HCID 86684046 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | tert-Butyl 2-(3-(2,5-Dimethyl-1H-pyrrol-1-yl)-5-(methoxy(methyl)carbamoyl)-1H-pyrazol-1-yl)ethylcarbamate | HCID 86684523 | 66% |
반응 단계
A 250-mL round-bottomed flask equipped with a magnetic stirrer was charged with 287c (10.4 g, 1.0 eq., 41.9 mmol), tert-butyl 2-chloroethylcarbamate (37.7 g, 5.0 eq., 210.0 mmol), Na2CO3 (22.3 g, 5.0 eq., 210.0 mmol), and DMF (100 mL). The reaction mixture was stirred at 110° C. overnight. After cooling to room temperature, the resulting mixture was poured into water (200 mL) and extracted with ethyl acetate (3×100 mL). The combined organic layer was concentrated under reduced pressure. The resulting residue was purified by silica-gel column chromatography eluting with ethyl acetate to afford 287d (10.8 g, 66%) as yellow oil. MS-ESI: [M+H]+ 392.0
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09238655B2 |
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| 출처 데이터셋 | uspto-grants-2016_01 |
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| ORD ID | ord-24c7b5fe4cc94abaa163052284f9ccb8 |
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| 출처 메모 | uspto-grants-2016_01 |
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