반응 #6911
ord-5b2ee72421e84c96a53e63a90b2cd355
반응 방정식
product
N-(1-{6-[(Hydroxyamino)(imino)methyl]quinolin-2-yl}pyrrolidin-3-yl)-2,2-dimethylpropanamide
4-trifluoromethylphenylpropionic acid
EDC
→
2,2-Dimethyl-N-{1-[6-(5-{2-[4-(trifluoromethyl)phenyl]ethyl}-1,2,4-oxadiazol-3-yl)quinolin-2-yl]pyrrolidin-3-yl}propanamide
반응물
시약
없음
용매
반응 조건
온도
50°CELSIUS
상세 조건
See reaction.notes.procedure_details.
후처리
- 1온도the mixture was heated at 110° C. for 2 hr
- 2온도The mixture was cooled to r.t.
- 3기타quenched with water
- 4추출extracted with excess EtOAc
- 5기타The combined extracts were dried over a drying agent
- 6여과filtered
- 7기타the solvent removed under vacuum
- 8기타The residue was purified by preparative TLC
- 9세척eluting with EtOAc
- 10기타to afford the product, MS
실험 절차
To a mixture of the product of Step E, (66 mg) in anhydrous diglyme (2 mL) was added 4-trifluoromethylphenylpropionic acid (1.1 eq.) and EDC (2 eq.). The reaction mixture was heated to 50° C. overnight. After approximately 18 h, the mixture was heated at 110° C. for 2 hr. The mixture was cooled to r.t., quenched with water and extracted with excess EtOAc. The combined extracts were dried over a drying agent filtered and the solvent removed under vacuum. The residue was purified by preparative TLC eluting with EtOAc to afford the product, MS: m/z 538.