반응식
[CH3:1][C:2]1[NH:3][C:4]([CH3:24])=[C:5]([C:20]([O:22][CH3:23])=[O:21])[CH:6]([C:11]2[CH:16]=[CH:15][CH:14]=[C:13]([N+:17]([O-:19])=[O:18])[CH:12]=2)[C:7]=1[C:8]([OH:10])=[O:9].O[CH2:26][C:27]1[O:28][C:29]2[CH:35]=[C:34]([CH2:36][C:37]3[NH:38][CH:39]=[CH:40][N:41]=3)[CH:33]=[CH:32][C:30]=2[N:31]=1.C1(N=C=NC2CCCCC2)CCCCC1>C1(C)C=CC=CC=1>[CH3:1][C:2]1[NH:3][C:4]([CH3:24])=[C:5]([C:20]([O:22][CH3:23])=[O:21])[CH:6]([C:11]2[CH:16]=[CH:15][CH:14]=[C:13]([N+:17]([O-:19])=[O:18])[CH:12]=2)[C:7]=1[C:8]([O:10][CH2:26][C:27]1[O:28][C:29]2[CH:35]=[C:34]([CH2:36][C:37]3[NH:41][CH:40]=[CH:39][N:38]=3)[CH:33]=[CH:32][C:30]=2[N:31]=1)=[O:9]참가 물질
5
반응물 3
생성물 1
시약·촉매·용매 1
실험 절차
332 mg (1 mM) of 1,4-dihydro-2,6-dimethyl-5-methoxycarbonyl-4-(3-nitrophenyl)pyridine-3-carboxylic acid together with 229 mg (1 mM) of 2-hydroxymethyl-6-(1-imidazolylmethyl)benzoxazole 248 mg (1.2 mM) of dicyclohexylcarbodiimide and 134 mg (1.1 mM) of 4-N,N-dimethylaminopyridine were dissolved in 5 ml of toluene, while heating, and refluxed for six hours. The solution was cooled to room temperature, and the crystals produced were filtered off. The filtrate was washed with water and dried over anhydrous sodium sulfate. After the solvent was distilled off, the residue was purified by chromatography on a silica gel column, whereby the captioned compound was obtained. The yield was 542 mg (99.9%).
후처리
- temperaturewhile heating
- temperaturerefluxed for six hours
- customthe crystals produced
- filtrationwere filtered off
- washThe filtrate was washed with water
- dry with materialdried over anhydrous sodium sulfate
- distillationAfter the solvent was distilled off
- customthe residue was purified by chromatography on a silica gel column, whereby the captioned compound
- customwas obtained
출처 및 근거
- ORD 기록
- ord-226a9f9367aa4ac39fbe3ddc55086a66
- 출처 데이터셋
- uspto-grants-1994_02
- 특허 번호
- US05286869
연결된 노트
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