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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1889757생성일: 2026년 10월 23일

4-(3-Bromophenyl)morpholine → [8-(4-Methanesulfonyl-phenyl)-[1,2,4]triazolo[1,5-a]pyridin-2-yl]-(3-morpholin-4-yl-phenyl)-amine

https://huagongshe.com/ko/reaction/1889757

반응식

참여 물질

역할이름HCID투입량
반응물4-(3-Bromophenyl)morpholineHCID 4961268—
반응물8-(4-Methanesulfonyl-phenyl)-[1,2,4]triazolo[1,5-a]pyridin-2-ylamineHCID 57502376—
생성물[8-(4-Methanesulfonyl-phenyl)-[1,2,4]triazolo[1,5-a]pyridin-2-yl]-(3-morpholin-4-yl-phenyl)-amineHCID 57502382—

반응 단계

[8-(4-Methanesulfonyl-phenyl)-[1,2,4]triazolo[1,5-a]pyridin-2-yl]-(3-morpholin-4-yl-phenyl)-amine was prepared from 8-(4-methanesulfonyl-phenyl)-[1,2,4]triazolo[1,5-a]pyridin-2-ylamine (100.0 mg, 0.3468 mmol) and 4-(3-bromo-phenyl)-morpholine (126.0 mg, 0.5202 mmol) in a manner analogous to Step 2d and was isolated as a yellow solid (0.022 g, 14%). MP=234-236° C. 1H NMR (400 MHz, CDCl3, δ, ppm): 8.50 (dd, J=6.6, 1.1 Hz, 1H), 8.26-8.22 (m, 2H), 8.10-8.05 (m, 2H), 7.66 (dd, J=7.3, 1.1 Hz, 1H), 7.36 (t, J=2.2 Hz, 1H), 7.25 (t, J=8.0 Hz, 1H), 7.05-6.98 (m, 2H), 6.85 (s, 1H), 6.59 (dd, J=8.3, 1.9 Hz, 1H), 3.91-3.87 (m, 4H), 3.24-3.20 (m, 4H), 3.10 (s, 3H). MS=450 (MH)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08501936B2
출처 데이터셋uspto-grants-2013_08
ORD IDord-5a2f24114bb04e7ca6b4adb201c3416c
출처 메모uspto-grants-2013_08