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HRID 28678생성일: 2026년 10월 23일

2-Chloro-4-isocyanatoanisole → N-(6-Bromo-2,3,4,9-tetrahydro-1H-carbazol-1-yl)-N'-(3-chloro-4-methoxyphenyl)urea

https://huagongshe.com/ko/reaction/28678

반응식

참여 물질

역할이름HCID투입량
반응물2-Chloro-4-isocyanatoanisoleHCID 119947—
반응물6-bromo-2,3,4,9-tetrahydro-1H-carbazol-1-amineHCID 597879—
생성물N-(6-Bromo-2,3,4,9-tetrahydro-1H-carbazol-1-yl)-N'-(3-chloro-4-methoxyphenyl)ureaHCID 11419514—

반응 단계

N-(6-Bromo-2,3,4,9-tetrahydro-1H-carbazol-1-yl)-N′-(3-chloro-4-methoxyphenyl)urea was prepared from 6-bromo-2,3,4,9-tetrahydro-1H-carbazol-1-amine and 3-chloro-4-methoxyphenyl isocyanate in a similar manner as described above to give a tan solid (42% yield). 1H-NMR (DMSO-d6): δ 10.98 (s, 1H), 8.33 (s, 1H), 7.73 (d, 1H), 7.60 (d, 1H), 7.30 (d, 1H), 7.25-7.14 (m, 2H), 7.08 (d, 1H), 6.63 (d, 1H), 5.01 (m, 1H), 3.82 (s, 3H), 2.65 (m, 2H), 2.04 (m, 1H), 1.94-1.76 (m, 3H); MS m/z 448 (M−1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07419997B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-a9ba3fc031054932bfbd7a8f6da9c0f1
출처 메모uspto-grants-2008_09