반응식
[N:1]1[N:2]([C:10]2[CH:11]=[C:12]([CH:19]=[C:20]([C:23]([CH3:26])([CH3:25])[CH3:24])[C:21]=2[OH:22])[CH2:13][CH2:14][C:15](OC)=[O:16])[N:3]=[C:4]2[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=12.[NH2:27][CH:28]1[CH2:33][C:32]([CH3:35])([CH3:34])[N:31]([O:36][CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH2:43][CH3:44])[C:30]([CH3:46])([CH3:45])[CH2:29]1>C(OCC)(=O)C>[CH2:37]([O:36][N:31]1[C:32]([CH3:35])([CH3:34])[CH2:33][CH:28]([NH:27][C:15](=[O:16])[CH2:14][CH2:13][C:12]2[CH:19]=[C:20]([C:23]([CH3:24])([CH3:25])[CH3:26])[C:21]([OH:22])=[C:10]([N:2]3[N:3]=[C:4]4[CH:9]=[CH:8][CH:7]=[CH:6][C:5]4=[N:1]3)[CH:11]=2)[CH2:29][C:30]1([CH3:45])[CH3:46])[CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH2:43][CH3:44]참가 물질
4
반응물 2
생성물 1
시약·촉매·용매 1
실험 절차
A mixture of 4.0 g (11.3 mmol) of methyl 3-(2H-benzotriazol-2-yl)-5-tert-butyl-4-hydroxyhydrocinnamate and 8.0 g (28.1 mmol) of 4-amino-1-octyloxy-2,2,6,6-tetramethylpiperidine is heated at 190°-200° C. for 2 hours. The reaction mixture is dissolved in ethyl acetate (300 ml). The organic solution is washed with 1N hydrochloric acid (2 ×100 ml) and saturated sodium bicarbonate solution (200 ml), then dried over magnesium sulfate and evaporated to obtain a solid. Purification by flash chromatography on silica gel (3:1 heptane: ethyl acetate) following by recrystallization from methanol affords 1.0 g (15% yield) of the title compound, a white solid, mp 153°-9° C.
후처리
- temperatureis heated at 190°-200° C. for 2 hours
- washThe organic solution is washed with 1N hydrochloric acid (2 ×100 ml) and saturated sodium bicarbonate solution (200 ml)
- dry with materialdried over magnesium sulfate
- customevaporated
- customto obtain a solid
- customPurification by flash chromatography on silica gel (3:1 heptane: ethyl acetate)
- customfollowing by recrystallization from methanol
출처 및 근거
- ORD 기록
- ord-62193cd13d364ebcb097d26237458510
- 출처 데이터셋
- uspto-grants-1991_06
- 특허 번호
- US05021478
연결된 노트
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