Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 657249생성일: 2026년 10월 24일
Diisopropylethylamine → 4-(6,7-Dimethoxy-quinazolin-4-yl)-piperidine-1-carboxylic acid (4-azepan-1-yl-phenyl)-amide
https://huagongshe.com/ko/reaction/657249
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | Benzenamine, 4-(hexahydro-1H-azepin-1-yl)- | HCID 93643 | — |
| 반응물 | 4-(6,7-Dimethoxy-quinazolin-4-yl)-piperidine-1-carbonyl chloride | HCID 58770714 | — |
| 용매 | 1,4-Dioxane | HCID 31275 | — |
| 생성물 | 4-(6,7-Dimethoxy-quinazolin-4-yl)-piperidine-1-carboxylic acid (4-azepan-1-yl-phenyl)-amide | HCID 58770813 | 6.1% |
반응 단계
4-(6,7-Dimethoxy-quinazolin-4-yl)-piperidine-1-carbonyl chloride (37 mg, 0.11 mmol), prepared as described in Example 3a, was dissolved in anhydrous dioxane (2 mL) and to it was added 4-azepan-1-yl-phenylamine (19 mg, 0.1 mmol) followed by DIEA (20 uL, 0.11 mmol) and the mixture was stirred at 100° C. for 3 h. It was then concentrated in vacuo and the residue was purified by Preparative TLC (silica gel, 5% MeOH/DCM) to obtain 3 mg (6%) of pure 4-(6,7-dimethoxy-quinazolin-4-yl)-piperidine-1-carboxylic acid (4-azepan-1-yl-phenyl)-amide. 1H-NMR (300 MHz, CDCl3) 9.08 (s, 1H), 7.55-7.23 (m, 4H), 7.18 (d, 1H), 6.77 (d, 1H), 6.37 (s, 1H), 4.27 (m, 2H), 4.07 (s, 6H), 3.68-3.32 (m, 3H), 3.30-2.90 (m, 2H), 2.24-1.88 (m, 4H), 1.86-1.38 (m, 10H). LC/MS (ESI): 490.3 (MH)+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08071768B2 |
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| 출처 데이터셋 | uspto-grants-2011_12 |
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| ORD ID | ord-134e4c98d536485888c17fe23de3c6ad |
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| 출처 메모 | uspto-grants-2011_12 |
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