Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 935생성일: 2026년 10월 24일
Dimethylformamide → cis-N-[1-[3-(4-Fluorophenoxy)propyl]-3-methoxy-4-piperidinyl]-4-amino-5-chloro-2-((S)-1-methyl-2-butynyl)oxybenzamide
https://huagongshe.com/ko/reaction/935
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Dimethylformamide | HCID 6228 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 1-(3-Bromopropoxy)-4-fluorobenzene | HCID 260004 | — |
| 반응물 | cis-N-(3-Methoxy-4-piperidinyl)-4-amino-5-chloro-2-((S)-1-methyl-2-butynyl)oxybenzamide | HCID 69232145 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | cis-N-[1-[3-(4-Fluorophenoxy)propyl]-3-methoxy-4-piperidinyl]-4-amino-5-chloro-2-((S)-1-methyl-2-butynyl)oxybenzamide | HCID 69229498 | 91.8% |
반응 단계
A mixture comprising 0.10 g of the cis-N-(3-methoxy-4-piperidinyl)-4-amino-5-chloro-2-((S)-1-methyl-2-butynyl)oxybenzamide, 0.07 g of 3-(4-fluorophenoxy)propyl bromide, 0.20 g of triethylamine and 10 ml of DMF was stirred at 50° C. for 2 hours and cooled. Ethyl acetate was poured into the resulting mixture. The obtained mixture was washed with water thrice, dried over magnesium sulfate, and freed from the solvent. The residue was purified by silica gel column chromatography (5% methanol/dichloromethane) to give 0.13 g of the title compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05723472 |
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| 출처 데이터셋 | uspto-grants-1998_03 |
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| ORD ID | ord-e90e3b33efd8427982a8d67e8d113a2f |
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| 출처 메모 | uspto-grants-1998_03 |
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