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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 432281생성일: 2026년 10월 26일

4-(Trifluoromethoxy)benzoyl Chloride → HCID 178488217, 화합물

https://huagongshe.com/reaction/432281

반응식

참여 물질

역할이름HCID투입량
반응물4-(Trifluoromethoxy)benzoyl ChlorideHCID 142110—
반응물HCID 178488198HCID 178488198—
용매PyridineHCID 1049—
용매DichloromethaneHCID 6344—
생성물HCID 178488217HCID 17848821774%

반응 단계

4-(Trifluoromethoxy)-1-benzenecarbonyl chloride (283 mg, 1.256 mmol) in dichloromethane (1 mL) was added to a solution of trans-3-(4-amino-3-methoxyphenyl)-1-[4-(4-methylpiperazino)cyclohexyl]-1H-pyrazolo[3,4-d]pyrimidin-4-amine (500 mg, 1.145 mmol) in pyridine (8 mL) at 0° C. After 30 minutes, the ice bath was removed the reaction mixture was stirred at room temperature for 1.5 hour. Solvent was evaporated and the residue was purified by flash column chromatography using dichloromethane/methanol (80:20) as mobile phase to give trans-N1-(4-{4-amino-1-[4-(4-methylpiperazino)cyclohexyl]-1H-pyrazolo[3,4-d]pyrimidin-3-yl}-2-methoxyphenyl)-4-(trifluoromethoxy)benzamide (526 mg, 74%). 1H NMR (CDCl3) δ 1.57 (m, 2H), 1.74 (m, 2H), 2.10-2.27 (m, 6H), 2.30 (s, 3H), 2.51 (m, 4H), 2.66 (m, 3H), 4.03 (s, 3H), 4.77 (m, 3H), 5.56 (bs, 2H), 7.26-7.37 (m, 4H), 7.99 (m, 2H), 8.38 (s, 1H), 8.59 (s, 1H), 8.67 (d, J=8.21 Hz, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06660744B1
출처 데이터셋uspto-grants-2003_12
ORD IDord-85a49438e1dc44ef814cc401c69262dd
출처 메모uspto-grants-2003_12