Acetone → HCID 12901337, 화합물
반응식
CC(C)=O.[F:5][C:6]1([C:15]([O:17][CH2:18][CH3:19])=[O:16])[CH:11]([OH:12])[NH:10][C:9](=[O:13])[NH:8][C:7]1=O.C(OC(=O)C)(=O)C.[NH:27]1[CH2:32][CH2:31][CH2:30][CH2:29][CH2:28]1>N1C=CC=CC=1>[F:5][C:6]1([C:15]([O:17][CH2:18][CH3:19])=[O:16])[CH:7]([N:27]2[CH2:32][CH2:31][CH2:30][CH2:29][CH2:28]2)[NH:8][C:9](=[O:13])[NH:10][C:11]1=[O:12]참가 물질
실험 절차
In 20 ml. of acetone is dissolved 4.40 g. of ethyl 5-fluoro-6-hydroxy-1,2,3,4,5,6-hexahydro-2,4-dioxo-pyrimidine-5-carboxylate, followed by the addition of 2.5 ml. of acetic anhydride. To this is further added dropwise 2 ml. of pyridine and the mixture is allowed to stand at room temperature for 24 hours. To the colorless reaction mixture thus obtained is added dropwise 5.9 ml. of piperidine, whereby the reaction takes place with evolution of heat. After 5.5 hours' standing at room temperature, volatiles are distilled off under reduced pressure and the yellow oily residue is dissolved in chloroform. The solution is subjected to column chromatography on silica gel (80 g., solvent:chloroform). The fractions rich in the desired compound are concentrated under reduced pressure to recover 5.20 g. of a white solid. Upon recrystallization from chloroform-hexane, 3.0 g. of ethyl 5-fluoro-6-piperidino-1,2,3,4,5,6-hexahydro-2,4-dioxopyrimidine-5-carboxylate is obtained as colorless needles.
후처리
- additionTo this is further added dropwise 2 ml
- customTo the colorless reaction mixture thus obtained
- additionis added dropwise 5.9 ml
- temperatureof heat
- waitAfter 5.5 hours' standing at room temperature
- distillationvolatiles are distilled off under reduced pressure
- dissolutionthe yellow oily residue is dissolved in chloroform
- concentrationThe fractions rich in the desired compound are concentrated under reduced pressure
- customto recover 5.20 g
- customUpon recrystallization from chloroform-hexane, 3.0 g
출처 및 근거
- ORD 기록
- ord-ca6dfab6485745dba958dcf5aa4ba3ad
- 출처 데이터셋
- uspto-grants-1982_05
- 특허 번호
- US04329460
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