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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1513938생성일: 2026년 10월 25일

Hydrochloric Acid → 7,9-Difluoro-5-[4-(2-piperidin-1-yl-ethoxy)-phenyl]-5H-6-thia-chrysen-2-ol hydrochloride salt

https://huagongshe.com/reaction/1513938

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Diethyl EtherHCID 3283—
반응물Potassium HydroxideHCID 14797—
반응물Ammonium ChlorideHCID 25517—
반응물Methanesulfonic acid 7,9-difluoro-5-[4-(2-piperidin-1-yl-ethoxy)-phenyl]-5H-6-thia-chrysen-2-yl esterHCID 11273238—
용매MethanolHCID 887—
용매DichloromethaneHCID 6344—
생성물7,9-Difluoro-5-[4-(2-piperidin-1-yl-ethoxy)-phenyl]-5H-6-thia-chrysen-2-ol hydrochloride saltHCID 6700473299%

반응 단계

Dissolve methanesulfonic acid 7,9-difluoro-5-[4-(2-piperidin-1-yl-ethoxy)-phenyl]-5H-6-thia-chrysen-2-yl ester (5.2 g, 9.0 mmol) in methanol (150 mL). Add potassium hydroxide (5.0 g, 90 mmol) and stir at room temperature. After 4 hours pour into saturated aqueous ammonium chloride and extract with methylene chloride. Dry over sodium sulfate, filter and concentrate. Dissolve residue in methylene chloride (90 mL) and add 2M HCl in ether (9 mL, 18 mmol). Concentrate in vacuo to yield 4.8 g (99%) of the title compound. LCMS Rt (0.01% heptafluorobutyric acid:1.0% isopropylalcohol:water is mobile phase A and 0.01% heptafluorobutyric acid:1.0% isopropylalcohol:acetonitrile is mobile phase B; gradient method 15 to 95% B, Purity@254 nm)=3.21 min (100%); mass spectrum (ion spray): m/z=504.3 (M+H). Chiral HPLC: 87%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08217032B2
출처 데이터셋uspto-grants-2012_07
ORD IDord-340c9335acb44245b8fc500147bec5d1
출처 메모uspto-grants-2012_07