반응식
[O:1]1[C:6]2[CH:7]=[CH:8][CH:9]=[CH:10][C:5]=2[O:4][CH2:3][CH:2]1[CH2:11][NH2:12].[C:13]([O:22][CH3:23])(=[O:21])[C:14]([CH2:16][C:17](OC)=[O:18])=[CH2:15]>>[CH3:23][O:22][C:13]([CH:14]1[CH2:16][C:17](=[O:18])[N:12]([CH2:11][CH:2]2[O:1][C:6]3[CH:7]=[CH:8][CH:9]=[CH:10][C:5]=3[O:4][CH2:3]2)[CH2:15]1)=[O:21]참가 물질
3
실험 절차
The title compound was prepared using 200 mg (1.21 mmol) of 2,3-dihydro-benzo[1,4]dioxin-2-ylmethylamine and 0.17 mL (1.21 mmol) of dimethyl itaconate according to the procedure for substituted pyrrolidines described in J. Org. Chem. 26 (1961) 1519-1524. Purification by column chromatography (silica gel, heptane/ethyl acetate, 1:2) afforded the pure product.
후처리
- customPurification by column chromatography (silica gel, heptane/ethyl acetate, 1:2)
- customafforded the pure product
출처 및 근거
- ORD 기록
- ord-3d3778256ba24e1bb4da7bb28f344f7d
- 출처 데이터셋
- uspto-grants-2014_04
- 특허 번호
- US08697723B2
연결된 노트
불러오는 중…