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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 72191생성일: 2026년 10월 25일

Ethanamine, 2-(methylsulfonyl)-, hydrochloride (1:1) → (5)-1-(4-(1-methyl-7-(3-methylmorpholino)-1H-pyrazolo-[4,3-d]pyrimidin-5-yl)phenyl)-3-(2-(methylsulfonyl)ethyl)urea

https://huagongshe.com/reaction/72191

반응식

참여 물질

역할이름HCID투입량
반응물Ethanamine, 2-(methylsulfonyl)-, hydrochloride (1:1)HCID 17749886—
반응물(5)-1-(4-(1-methyl-7-(3-methylmorpholino)-1H-pyrazolo[4,3-d]pyrimidin-5-yl)phenyl)-3-(oxetan-3-yl)ureaHCID 51355347—
생성물(5)-1-(4-(1-methyl-7-(3-methylmorpholino)-1H-pyrazolo-[4,3-d]pyrimidin-5-yl)phenyl)-3-(2-(methylsulfonyl)ethyl)ureaHCID 51355346—

반응 단계

This compound was prepared in an analogous fashion to (S)-1-(4-(1-methyl-7-(3-methylmorpholino)-1H-pyrazolo[4,3-d]pyrimidin-5-yl)phenyl)-3-(oxetan-3-yl)urea, using 2-(methylsulfonyl)ethanamine hydrochloride as the starting material. 1H NMR (DMSO-d6, 400 MHz) δ ppm 8.96 (s, 1H), 8.25 (d, J=8.8 Hz, 2H), 8.21 (s, 1H), 7.51 (d, J=8.8 Hz, 2H), 6.42 (t, J=5.9 Hz, 1H), 4.25 to 4.13 (m, 4H), 3.96 to 3.83 (m, 2H), 3.78 to 3.79 (m, 1H), 3.79 to 3.60 (m, 2H), 3.60 to 3.47 (m, 3H), 3.37 to 3.30 (m, 5H), 1.27 (d, J=6.5 Hz, 3H); LC-MS m/z (method C1)=474.2 [M+H]+, RT=3.13 min

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08828990B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-c5cf6b4be41547f787cd5adab110e5ed
출처 메모uspto-grants-2014_09