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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

반응식

참여 물질

역할이름HCID투입량
반응물Tris(hydroxymethyl)aminomethaneHCID 6503—
반응물4-MethylmorpholineHCID 7972—
반응물4-(Bromomethyl)-1,2-difluorobenzeneHCID 581436—
반응물5-(Piperidin-4-ylmethoxy)quinazoline-2,4-diamineHCID 57576565—
용매DimethylformamideHCID 6228—
생성물5-[1-(3,4-Difluorobenzyl)piperidin-4-ylmethoxy]quinazoline-2,4-diamineHCID 2500778542%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07985755B2
출처 데이터셋uspto-grants-2011_07
ORD IDord-663fc5c7605d4ef899db475baada6a83
출처 메모uspto-grants-2011_07