돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 472358생성일: 2026년 10월 27일

5-Bromo-[1,2,4]triazolo[1,5-a]pyridin-2-amine → 5-[4-[(1,1-Dioxo-1,4-thiazinan-4-yl)methyl]phenyl]-[1,2,4]triazolo[1,5-a]pyridin-2-amine

https://huagongshe.com/reaction/472358

반응식

참여 물질

역할이름HCID투입량
반응물5-Bromo-[1,2,4]triazolo[1,5-a]pyridin-2-amineHCID 25215939—
반응물(4-((1,1-Dioxidothiomorpholino)methyl)phenyl)boronic acidHCID 54970580—
생성물5-[4-[(1,1-Dioxo-1,4-thiazinan-4-yl)methyl]phenyl]-[1,2,4]triazolo[1,5-a]pyridin-2-amineHCID 6747944079.2%

반응 단계

5-{4-[(1,1-dioxidothiomorpholin-4-yl)methyl]phenyl}[1,2,4]triazolo[1,5-a]pyridin-2-amine was prepared from 5-bromo-[1,2,4]triazolo[1,5-a]pyridin-2-ylamine (368 mg, 1.73 mmol) and 4-[(4-boronophenyl)methyl]-thiomorpholine 1,1-dioxide (0.512 mg, 1.90 mmol), in a manner analogous to Step 73c. The residue was purified on a 12 g Isco silica gel column using a gradient of 0-15% methanol in dichloromethane as an eluent. 5-{4-[(1,1-dioxidothiomorpholin-4-yl)methyl]phenyl}[1,2,4]triazolo[1,5-a]pyridin-2-amine (490 mg, 79%) was isolated as a beige foam. 1H NMR (400 MHz, (D3C)2SO, δ, ppm): 7.93 (d, J=8.5 Hz, 2H), 7.50 (m, 3H), 7.37 (d, J=7.8 Hz, 1H), 7.07 (d, J=7.8 Hz, 1H), 6.02 (s, 2H), 3.78 (s, 2H), 3.15 (s, 4H), 2.91 (s, 4H). MS=358 (MH)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08633173B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-cfbe00f46f1d4efa99848f041ebdeae3
출처 메모uspto-grants-2014_01