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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 12753생성일: 2026년 10월 25일

Sodium Iodide → 5-phenyl-1-(3-{(1S,5R)-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo-[3.1.0]hex-3-yl}propyl)-2,4(1H,3H)-pyrimidinedione hydrochloride

https://huagongshe.com/reaction/12753

반응식

참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물Ammonium ChlorideHCID 25517—
반응물1-(3-chloropropyl)-5-phenyl-2,4(1H,3H)-pyrimidinedioneHCID 58994186—
반응물(1S,5R)-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexaneHCID 59337591—
용매DimethylformamideHCID 6228—
생성물5-phenyl-1-(3-{(1S,5R)-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo-[3.1.0]hex-3-yl}propyl)-2,4(1H,3H)-pyrimidinedione hydrochlorideHCID 6869349388.9%

반응 단계

A mixture of (1S,5R)-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexane (Prep4, 40 mg) 1-(3-chloropropyl)-5-phenyl-2,4(1H,3H)-pyrimidinedione (Prep 4, 55 mg), TEA (0.050 mL) and NaI cat. Amount, in DMF (0.5 mL) was heated at 100° C. for 24 hours. Aqueous saturated NH4Cl solution was then added to the mixture and then it was extracted with DCM. The organic phase was dried and concentrated in vacuo. The crude product was purified by a SCX cartridge to give 77 mg of the title compound as free base. HCl (1M in diethyl ether) was added to a solution of the free base in dichloromethane. The mixture was evaporated and the residue triturated with diethyl ether to give the title compound (78 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07727988B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-6ec9f3d9adb8408a88df599667c67d5b
출처 메모uspto-grants-2010_06