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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 60200생성일: 2026년 10월 24일

Tetrahydrofuran → [2-(2,6-Dichloro-benzyl)-5-methanesulfonyl-thiazolo[5,4-d]pyrimidin-7-yl]-(4-trifluoromethyl-phenyl)-amine

https://huagongshe.com/ko/reaction/60200

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참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물Potassium peroxymonosulphateHCID 10313463—
반응물HCID 42642138HCID 42642138—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물[2-(2,6-Dichloro-benzyl)-5-methanesulfonyl-thiazolo[5,4-d]pyrimidin-7-yl]-(4-trifluoromethyl-phenyl)-amineHCID 4264146485%

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온도40 °C

반응 단계

To a solution of [2-(2,6-dichloro-benzyl)-5-methylsulfanyl-thiazolo[5,4-d]pyrimidin-7-yl]-(4-trifluoromethyl-phenyl)-amine (110 mg, 0.22 mmol) in THF (6 mL) and MeOH (6 mL) was added a solution of potassium peroxymonosulfate (406 mg, 0.66 mmol) in H2O (6 mL). The resulting mixture was stirred vigorously at 40° C. After 24 h, the mixture was concentrated and the crude residue was diluted with satd. aq. NaHCO3 (10 mL) and extracted with EtOAc (10 mL×3). The combined organic layers were dried, concentrated, and purified by FCC to afford a colorless solid (100 mg, 85%). MS (ESI): mass calcd. for C20H13Cl2F3N4O2S2, 531.9; m/z found, 532.9 [M+H]+. 1H NMR ((CD3)2SO): 11.02 (s, 1H), 8.13 (d, J=8.6 Hz, 2H), 7.77 (d, J=8.7 Hz, 2H), 7.64 (d, J=8.1 Hz, 2H), 7.50 (dd, J=8.5, 7.8 Hz, 1H), 4.89 (s, 2H), 3.37 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09440978B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-3af7cce02cdd495bbb65d50b45a8dbd9
출처 메모uspto-grants-2016_09