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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 23734생성일: 2026년 10월 24일

Benzyl isocyanate → (4-{[Benzyl({[3,5-bis(trifluoromethyl)benzoyl]amino} sulfonyl)amino]methyl}cyclohexyl)methyl 3-methoxyphenylcarbamate

https://huagongshe.com/ko/reaction/23734

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl isocyanateHCID 76639—
반응물DiisopropylethylamineHCID 81531—
반응물3-Methoxyphenyl isocyanateHCID 87843—
반응물(4-{[Benzyl({[3,5-bis(trifluoromethyl)benzoyl]amino}sulfonyl)amino]methyl}cyclohexyl)methyl benzylcarbamateHCID 22574464—
용매TriethylamineHCID 8471—
생성물(4-{[Benzyl({[3,5-bis(trifluoromethyl)benzoyl]amino} sulfonyl)amino]methyl}cyclohexyl)methyl 3-methoxyphenylcarbamateHCID 22574485—

반응 단계

Following procedure to make (9), 3-methoxyphenyl isocyanate was substituted for benzyl isocyanate and diisopropylethylamine substituted for triethylamine to give the title compound after purification. 1H NMR (500 MHz, DMSO-d6): δ 9.50 (s, 1H), 8.45 (s, 2H), 8.10 (s, 1H), 7.38 (d, 2H), 7.24 (t, 2H), 7.14 (m, 3H), 6.96 (d, 1H), 6.52 (d, 1H), 4.35 (s, 2H), 3.75 (d, 2H), 3.68 (s, 3H), 3.30 (water), 2.89 (d, 2H), 2.48 (DMSO), 1.63 (m, 4H), 1.42 (m, 1H), 1.29 (m, 1H), 0.66 (m, 4H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06852738B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-3754d13e72ce47f49728e435d6baaf46
출처 메모uspto-grants-2005_02