돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 550825생성일: 2026년 10월 26일

Trifluoroacetic acid → 4-(4-Fluoro-3-trifluoromethyl-benzoylamino)-piperidine-1-carboxylic acid (7-methoxy-thiazolo[5,4-d]pyrimidin-2-yl)-amide

https://huagongshe.com/reaction/550825

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물TriethylamineHCID 8471—
반응물4-Fluoro-3-(trifluoromethyl)benzoyl ChlorideHCID 144253—
반응물4-Amino-piperidine-1-carboxylic acid (7-methoxy-thiazolo[5,4-d]pyrimidin-2-yl)-amideHCID 59011952—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물4-(4-Fluoro-3-trifluoromethyl-benzoylamino)-piperidine-1-carboxylic acid (7-methoxy-thiazolo[5,4-d]pyrimidin-2-yl)-amideHCID 5901197730.6%

반응 조건

온도25 °C

반응 단계

A suspension of the trifluoroacetic acid salt of 4-amino-piperidine-1-carboxylic acid (7-methoxy-thiazolo[5,4-d]pyrimidin-2-yl)-amide (prepared as in Example 83, 580 mg, 1.37 mmol), 4-fluoro-3-trifluoromethyl-benzoyl chloride (261 mL, 1.64 mmol) and triethylamine (573 μL, 4.11 mmol) in methylene chloride (15 mL) was stirred at 25° C. overnight. At this time, the reaction was diluted with water and was extracted with ethyl acetate. The organics were washed with a saturated aqueous sodium chloride solution and a saturated aqueous sodium bicarbonate solution, dried over sodium sulfate, filtered and concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 230-400 mesh, gradient elution 3:7 ethyl acetate/hexanes to 100% ethyl acetate) afforded 4-(4-fluoro-3-trifluoromethyl-benzoylamino)-piperidine-1-carboxylic acid (7-methoxy-thiazolo[5,4-d]pyrimidin-2-yl)-amide (21 mg, 30.6%) as an off-white solid; ES-HRMS m/e calcd for C20H18F4N6O3S (M+H)+ 499.1170, found 499.1170.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07947692B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-77228ead8fe5416ba38fd0e8a700ed4d
출처 메모uspto-grants-2011_05