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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1601906생성일: 2026년 10월 25일

Hydrochloric Acid → 5-[2-(4-Anilinopiperid-1-yl)ethyl]-3-[3,5-bis(trifluoromethyl)benzyl]-5-(3,4-dichlorophenyl)-tetrahydro-2H-1,3-oxazin-2-one dihydrochloride monohydrate

https://huagongshe.com/reaction/1601906

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Potassium CarbonateHCID 11430—
반응물4-AnilinopiperidineHCID 89982—
반응물3-[3,5-Bis(trifluoromethyl)benzyl]-5-(3,4-dichlorophenyl)-5-[2-(methanesulfonyloxy)ethyl]tetrahydro-2H-1,3-oxazin-2-oneHCID 15886677—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
용매AcetonitrileHCID 6342—
생성물5-[2-(4-Anilinopiperid-1-yl)ethyl]-3-[3,5-bis(trifluoromethyl)benzyl]-5-(3,4-dichlorophenyl)-tetrahydro-2H-1,3-oxazin-2-one dihydrochloride monohydrateHCID 21200476—

반응 조건

온도55 °C

반응 단계

A mixture of 0.3 g of 4-anilinopiperidine, 0.8 g of the compound obtained in step C of EXAMPLE 4 and 0.69 g of potassium carbonate in 5 ml of acetonitrile is heated at 50-60° C. for 5 hours. The reaction mixture is poured into water and extracted with AcOEt, the organic phase is washed twice with water and with saturated NaCl solution and dried over MgSO4 and the solvent is evaporated off under vacuum. The residue is chromatographed on silica H using DCM and then a DCM/MeOH mixture (96/4; v/v) as the eluent. The product obtained is taken up with a saturated solution of gaseous HCl in ether and the precipitate formed is wrung to give 0.12 g of the expected product. M.p.=158° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05977359
출처 데이터셋uspto-grants-1999_11
ORD IDord-410ba793fcef44a796f0d5dcbbb82886
출처 메모uspto-grants-1999_11