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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1173005생성일: 2026년 10월 24일

4-Methyl-2-[4-(trifluoromethyl)phenyl]-1,3-thiazole-5-carbaldehyde → (+)-(trans)-2-{4-[({4-Methyl-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl}methyl)amino]phenyl}cyclopropanecarboxylic acid

https://huagongshe.com/ko/reaction/1173005

반응식

참여 물질

역할이름HCID투입량
반응물4-Methyl-2-[4-(trifluoromethyl)phenyl]-1,3-thiazole-5-carbaldehydeHCID 2782899—
반응물(1R,2R)-2-(4-aminophenyl)cyclopropane-1-carboxylic acidHCID 68668314—
생성물(+)-(trans)-2-{4-[({4-Methyl-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl}methyl)amino]phenyl}cyclopropanecarboxylic acidHCID 11487291—

반응 단계

Experimental procedure analogous to that describing the synthesis of I-2a-I except that 4-methyl-2-(4-trifluoromethylphenyl)-1,3-thiazole-5-carbaldehyde and racemic-(trans)-2-(4-aminophenyl)cyclopropanecarboxylic acid (I-1) were used to give 1.05 g of the title compound as a light yellow solid. 1H NMR (400 MHz, CDCl3) δ 7.98 (d, J=8.78 Hz, 2H), 7.65 (d, J=8.78 Hz, 2H), 6.97 (d, J=8.60 Hz, 2H), 6.60 (d, J=8.60 Hz, 2H), 4.46 (s, 2H), 2.53 (m, 1H), 2.50 (s, 3H), 1.80 (m, 1H), 1.60 (m, 1H), 1.36 (m, 1H). ES-MS m/z 360 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07834013B2
출처 데이터셋uspto-grants-2010_11
ORD IDord-e4092ae1bb4a47d2955166f10cdeaefe
출처 메모uspto-grants-2010_11