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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1912583생성일: 2026년 10월 25일

1-(4-(bromomethyl)phenyl)-1H-1,2,4-triazole → 2-Tert-butoxy-2-[4-chroman-6-yl-6-methyl-1-[[4-(1,2,4-triazol-1-yl)phenyl]methyl]pyrrolo[2,3-b]pyridin-5-yl]acetic acid

https://huagongshe.com/reaction/1912583

반응식

참여 물질

역할이름HCID투입량
반응물1-(4-(bromomethyl)phenyl)-1H-1,2,4-triazoleHCID 2776489—
반응물methyl 2-(tert-butoxy)-2-(4-(chroman-6-yl)-6-methyl-1H-pyrrolo[2,3-b]pyridin-5-yl)acetateHCID 71209024—
생성물2-Tert-butoxy-2-[4-chroman-6-yl-6-methyl-1-[[4-(1,2,4-triazol-1-yl)phenyl]methyl]pyrrolo[2,3-b]pyridin-5-yl]acetic acidHCID 71209215—

반응 단계

The title compound was prepared in a manner similar to that described in Example 27, Step H from methyl 2-(tert-butoxy)-2-(4-(chroman-6-yl)-6-methyl-1H-pyrrolo[2,3-b]pyridin-5-yl)acetate and 1-(4-(bromomethyl)phenyl)-1H-1,2,4-triazole. 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 8.61 (br. s., 1 H), 8.13 (br. s., 1 H), 7.67 (d, J=8.4 Hz, 2 H), 7.52-7.39 (m, 3 H), 7.24-7.17 (m, 1 H), 7.12 (t, J=3.1 Hz, 1 H), 6.95 (dd, J=4.7, 8.4 Hz, 1 H), 6.37 (dd, J=3.5, 11.3 Hz, 1 H), 5.80-5.70 (m, 1 H), 5.64-5.52 (m, 2 H), 4.30 (t, J=4.2 Hz, 2 H), 2.96-2.77 (m, 5 H), 2.16-2.05 (m, 2 H), 1.05-0.91 (s, 9 H); LC/MS (m/z) ES+=552.39 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08609653B2
출처 데이터셋uspto-grants-2013_12
ORD IDord-4c59a235e6ae406b8ba64128219316c3
출처 메모uspto-grants-2013_12