Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1015336생성일: 2026년 10월 25일
Tris(hydroxymethyl)aminomethane → 5-[1-(3,4-Difluorobenzyl)piperidin-4-ylmethoxy]quinazoline-2,4-diamine
https://huagongshe.com/reaction/1015336
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Tris(hydroxymethyl)aminomethane | HCID 6503 | — |
| 반응물 | 4-Methylmorpholine | HCID 7972 | — |
| 반응물 | 4-(Bromomethyl)-1,2-difluorobenzene | HCID 581436 | — |
| 반응물 | 5-(Piperidin-4-ylmethoxy)quinazoline-2,4-diamine | HCID 57576565 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 5-[1-(3,4-Difluorobenzyl)piperidin-4-ylmethoxy]quinazoline-2,4-diamine | HCID 25007785 | 42% |
반응 단계
5-(Piperidin-4-ylmethoxy)quinazoline-2,4-diamine (50 mg; 0.18 mmol) was shaken for 60 hours at 60° C. in the presence of 3-(morpholino)propyl polystyrene sulfonamide (PS-NMM) (160 mg; 0.4 mmol) and 3,4-difluorobenzyl bromide (77 mg; 0.37 mmol) in 4 mL N,N-dimethylformamide. Tris-(2-aminoethyl)aminomethyl polystyrene (PS-Trisamine) (112 mg; 0.4 mmol) was then added to the mixture and continued to shake for an additional 2 hours. Resins were filtered off and rinsed with methanol. Filtrate was concentrated at reduced pressure, and residue was triturated with 2 mL 1 N NaOH and ethanol (1:1). Solids were collected by filtration to yield 5-[1-(3,4-difluorobenzyl)piperidin-4-ylmethoxy]quinazoline-2,4-diamine (30 mg; 42% yield). 1HNMR (400 MHz, DMSO-d6) δ 7.61 (m, 2H), 7.34 (m, 2H), 7.14 (m, 2H), 6.76 (m, 1H), 6.52 (m, 1H), 5.94 (br s, 2H), 3.99 (d, J=6.0 Hz, 2H), 3.46 (s, 3H), 3.12 (m, 1H), 2.82 (br d, J=10.8 Hz, 1H), 2.11 (m, 2H), 1.95 (m, 2H), 1.73 (br d, J=11.2 Hz, 1H), 1.34 (m, 1H). MS m/z (ESI) 400 (M+H)+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07985755B2 |
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| 출처 데이터셋 | uspto-grants-2011_07 |
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| ORD ID | ord-663fc5c7605d4ef899db475baada6a83 |
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| 출처 메모 | uspto-grants-2011_07 |
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