돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1015337생성일: 2026년 10월 25일

Benzylamine → 5-[1-(2,3-Difluorobenzyl)piperidin-4-ylmethoxy]quinazoline-2,4-diamine

https://huagongshe.com/reaction/1015337

반응식

참여 물질

역할이름HCID투입량
반응물BenzylamineHCID 7504—
반응물1-(Bromomethyl)-2,3-difluoro-benzeneHCID 517984—
반응물5-(Piperidin-4-ylmethoxy)quinazoline-2,4-diamineHCID 57576565—
생성물5-[1-(2,3-Difluorobenzyl)piperidin-4-ylmethoxy]quinazoline-2,4-diamineHCID 2500778653%

반응 단계

The benzylamine was obtained by reacting 5-(piperidin-4-ylmethoxy)quinazoline-2,4-diamine (50 mg; 0.18 mmol) and 2,3-difluorobenzyl bromide (77 mg; 0.37 mmol) via Method BB to yield 38 mg. (53% yield). 1HNMR (400 MHz, DMSO-d6) δ 8.26 (br s, 1H), 7.8 (br s, 1H), 7.55 (t, J=8.4 Hz, 1H), 7.33 (m, 1H), 7.2 (m, 2H), 6.99 (br s, 2H), 6.9 (d, J=8 Hz, 1H), 6.81 (d, J=8.0 Hz, 2H), 4.07 (d, J=6.4 Hz, 2H), 3.59 (s, 2H), 2.85 (m, 2H), 2.04 (t, J=11.2 Hz, 2H), 1.9 (m, 1H), 1.73 (d, J=10.4 Hz, 2H), 1.33 (m, 2H). 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-6cadd087a84c45209c4d7351ee0b5d24
출처 메모uspto-grants-2011_07