Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1068006생성일: 2026년 10월 26일
N-Methylphenylethanolamine → N-(4-Chlorobenzyl)-6-{[(2-hydroxy-2-phenylethyl)(methyl)-amino]methyl}-1-methyl-4-oxo-1,4-dihydro-3quinolinecarboxamide
https://huagongshe.com/reaction/1068006
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | N-Methylphenylethanolamine | HCID 913 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | N-(4-Chlorobenzyl)-6-(chloromethyl)-1-methyl-4-oxo-1,4-dihydro-3-quinolinecarboxamide | HCID 21192571 | — |
| 용매 | N-methyl-2-pyrrolidone | HCID 13387 | — |
| 생성물 | N-(4-Chlorobenzyl)-6-{[(2-hydroxy-2-phenylethyl)(methyl)-amino]methyl}-1-methyl-4-oxo-1,4-dihydro-3quinolinecarboxamide | HCID 21192531 | 63.8% |
반응 단계
A solution of N-(4-chlorobenzyl)-6-(chloromethyl)-1-methyl-4-oxo-1,4-dihydro-3-quinolinecarboxamide (0.06 gm) from Preparation No. 35 in dry NMP (2 mL) containing diisopropylethylarnine (0.04 mL) is treated with α-(methylaminomethyl)-benzyl alcohol (0.04 gm). The reaction mixture is shaken at room temperature for 3 days then concentrated under reduced pressure. The residue is partioned between dichloromethane and water. The separated organic layer is washed with two additional portions of water, brine, dried (Na2SO4) and concentrated under reduced pressure. The residue is adsorbed onto silica and purified by flash column chromatography eluting with 2% to 6% methanol in dichloromethane and then by recrystallization from ethyl acetate-hexanes to afford 0.05 gm of the title compound as a white solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06248739B1 |
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| 출처 데이터셋 | uspto-grants-2001_06 |
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| ORD ID | ord-69358d5342f5415e8d81080eb6212e47 |
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| 출처 메모 | uspto-grants-2001_06 |
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