Sodium Iodide → HCID 18931124, 화합물
반응식
[O:1]=[C:2]1[NH:6][C:5](=[O:7])[C:4]2([CH2:12][CH2:11][N:10]([C:13]([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:14])[CH2:9][CH2:8]2)[NH:3]1.Br[CH2:21][CH:22]([OH:25])[CH2:23][OH:24].[I-].[Na+].C(=O)([O-])[O-].[K+].[K+]>CN(C=O)C>[O:1]=[C:2]1[N:6]([CH2:21][CH:22]([OH:25])[CH2:23][OH:24])[C:5](=[O:7])[C:4]2([CH2:8][CH2:9][N:10]([C:13]([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:14])[CH2:11][CH2:12]2)[NH:3]1참가 물질
반응 조건
- 온도
- 100 °C
실험 절차
A mixture of tert-butyl 2,4-dioxo-1,3,8-triaza-8-spiro[4.5]decanecarboxylate (6.9 g, 25.6 mmol), 3-bromo-1,2-propanediol (4.4 g, 28 mmol), sodium iodide (1.5 g, 10 mmol), potassium carbonate (14 g) and DMF (25 mL) was stirred approximately 48 hours at 100° C. Additional 3-bromo-1,2-propanediol (1.5 g, 10 mmol) was added, and the stirring and heating continued for an additional 72 hours. After cooling, the mixture was filtered, the solvent removed from the filtrate under vacuum, and the residue was purified by chromatography eluting with ethyl acetate containing 0.5-1% acetic acid. The fractions containing the product were combined and concentrated, and the residue was treated with ethyl acetate to give tert-butyl 2,4-dioxo-3-(2,3-dihydroxypropyl)-1,3,8-triaza-8-spiro[4.5]decanecarboxylate (1.5 g, 4.4 mmol) as a white solid, m.p. 167°-170° C.
후처리
- temperaturethe stirring and heating
- waitcontinued for an additional 72 hours
- temperatureAfter cooling
- filtrationthe mixture was filtered
- customthe solvent removed from the filtrate under vacuum
- customthe residue was purified by chromatography
- washeluting with ethyl acetate containing 0.5-1% acetic acid
- additionThe fractions containing the product
- concentrationconcentrated
- additionthe residue was treated with ethyl acetate
출처 및 근거
- ORD 기록
- ord-b16ae4bca1d4472196a882a508e07e35
- 출처 데이터셋
- uspto-grants-1998_04
- 특허 번호
- US05739336
반응 노트
불러오는 중…