Thionyl Chloride → [Rac]-5-(1-chloro-ethyl)-4-cyclopropyl-2-(4-trifluoromethyl-phenyl)-pyrimidine
반응식
[CH:1]1([C:4]2[C:9]([CH:10](O)[CH3:11])=[CH:8][N:7]=[C:6]([C:13]3[CH:18]=[CH:17][C:16]([C:19]([F:22])([F:21])[F:20])=[CH:15][CH:14]=3)[N:5]=2)[CH2:3][CH2:2]1.S(Cl)([Cl:25])=O>ClCCl>[Cl:25][CH:10]([C:9]1[C:4]([CH:1]2[CH2:2][CH2:3]2)=[N:5][C:6]([C:13]2[CH:14]=[CH:15][C:16]([C:19]([F:22])([F:21])[F:20])=[CH:17][CH:18]=2)=[N:7][CH:8]=1)[CH3:11]참가 물질
4
실험 절차
A solution of 357 mg (1.16 mmol) [rac]-1-[4-cyclopropyl-2-(4-trifluoromethyl-phenyl)-pyrimidin-5-yl]-ethanol and 0.09 ml (1.22 mmol) thionylchloride in 4 ml dichloromethane were stirred for 1 h at RT. The reaction mixture was concentrated under reduced pressure to provide 390 mg of pure [rac]-5-(1-chloro-ethyl)-4-cyclopropyl-2-(4-trifluoromethyl-phenyl)-pyrimidine.
후처리
- concentrationThe reaction mixture was concentrated under reduced pressure
출처 및 근거
- ORD 기록
- ord-fb340c30aeca4ce8b5fa56f90d7609ef
- 출처 데이터셋
- uspto-grants-2006_10
- 특허 번호
- US07115611B2
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