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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 587140생성일: 2026년 10월 25일

Potassium Carbonate → 3-[(4-(4,4-Difluoropiperidin-1-yl)-1,3,5-triazin-2-yl)amino]-benzenemethanesulfonamide

https://huagongshe.com/reaction/587140

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물4,4-Difluoropiperidine hydrochlorideHCID 2758351—
반응물3-[(4-Chloro-1,3,5-triazin-2-yl)amino]benzenemethanesulfonamideHCID 86679822—
용매Dimethyl SulfoxideHCID 679—
용매Ethyl AcetateHCID 8857—
생성물3-[(4-(4,4-Difluoropiperidin-1-yl)-1,3,5-triazin-2-yl)amino]-benzenemethanesulfonamideHCID 60197102—

반응 조건

온도80 °C

반응 단계

To a solution of triazine A1 (270 mg, 0.9 mmol) in DMSO (0.9 mL) were added K2CO3 (370 mg, 2.7 mmol) and 4,4-difluoropiperidine hydrochloride (140 mg, 0.9 mmol). The mixture was stirred for 2 hours at 80° C. After cooling to room temperature it was diluted with EtOAc and extracted with water. The organic layer was washed with brine, dried over MgSO4 and concentrated under reduced pressure. The residue was stirred with DCM to give the solid title compound B2 which was isolated by filtration and dried in vacuo (white powder, 110 mg, 32%). 1H NMR (300 MHz, d6-DMSO, 300K) δ 1.90-2.15 (m, 4H), 3.81-3.98 (m, 4H), 4.21 (s, 2H), 6.88 (s, 2H), 6.98-7.04 (m, 1H), 7.21-7.34 (m, 1H), 7.44-7.60 (m, 1H), 7.78-7.90 (m, 1H), 8.25 (s, 1H), 9.77 (s, 1H). MS (ES) C15H18F2N6O2S requires: 384. found: 385 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09226929B2
출처 데이터셋uspto-grants-2016_01
ORD IDord-99e9f0a35c3240d5a54ba40f06690f37
출처 메모uspto-grants-2016_01