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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1173006생성일: 2026년 10월 24일

Triethylamine → Racemic-(trans)-2-{4-[({4-isopropyl-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl}methyl)amino]phenyl}cyclopropanecarboxylic acid

https://huagongshe.com/ko/reaction/1173006

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Methanesulfonyl chlorideHCID 31297—
반응물4-Isopropyl-2-[4-(trifluoromethyl)phenyl]thiazole-5-methanolHCID 58765762—
반응물(1R,2R)-2-(4-aminophenyl)cyclopropane-1-carboxylic acidHCID 68668314—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물Racemic-(trans)-2-{4-[({4-isopropyl-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl}methyl)amino]phenyl}cyclopropanecarboxylic acidHCID 1120201119.7%

반응 조건

온도0 °C

반응 단계

To a solution of {(4-isopropyl-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl}methanol (0.10 g, 0.331 mmol) in dichloromethane (3 mL) was added Et3N (0.04 g, 0.39 mmol) and the mixture cooled to 0° C. The mixture stirred for 15 min after which methanesulfonyl chloride (0.04 g, 0.36 mmol) was added followed 30 min later by the addition of racemic-(trans)-2-(4-aminophenyl)cyclopropanecarboxylic acid (I-1) (0.09 g, 0.49 mmol). The solution stirred for 24 h after which it was poured into H2O, the organics extracted with dichloromethane, dried over MgSO4, and the solvents reduced in vacuo. The crude material was purified on silica gel eluting with an increasing gradient from hexanes to 30% ethyl acetate/hexanes to give the title compound as a yellow powder (0.03 g, 16%). 1H NMR (400 MHz, CDCl3) δ 8.01 (d, J=8.3 Hz, 2H), 7.65 (d, J=8.2 Hz, 2H), 6.98 (d, J=8.4 Hz, 2H), 6.62 (d, J=8.6 Hz, 2H), 4.47 (s, 2H), 3.50-3.47 (m, 1H), 3.18-3.15 (m, 1H), 2.53-2.51 (m, 1H), 1.80-1.77 (m, 1H), 1.61-1.58 (m, 1H), 1.37-1.26 (m, 7H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07834013B2
출처 데이터셋uspto-grants-2010_11
ORD IDord-ee78b6a53a9e4997a25bbcdb804911dd
출처 메모uspto-grants-2010_11