8-Oxa-bicyclo[3.2.1]oct-6-ene-3-carboxylic acid (6-amino-2,4-dioxo-1,3-dipropyl-1,2,3,4-tetrahydro-pyrimidin-5-yl)-amide → 8-(8-Oxa-bicyclo[3.2.1]oct-6-en-3-yl)-1,3-dipropyl-3,7-dihydro-purine-2,6-dione
反応式
[NH2:1][C:2]1[N:7]([CH2:8][CH2:9][CH3:10])[C:6](=[O:11])[N:5]([CH2:12][CH2:13][CH3:14])[C:4](=[O:15])[C:3]=1[NH:16][C:17]([CH:19]1[CH2:25][CH:24]2[O:26][CH:21]([CH:22]=[CH:23]2)[CH2:20]1)=O>[OH-].[Na+].CO>[CH:21]12[O:26][CH:24]([CH:23]=[CH:22]1)[CH2:25][CH:19]([C:17]1[NH:16][C:3]3[C:4](=[O:15])[N:5]([CH2:12][CH2:13][CH3:14])[C:6](=[O:11])[N:7]([CH2:8][CH2:9][CH3:10])[C:2]=3[N:1]=1)[CH2:20]2参加物
実験手順
A solution of 8-oxa-bicyclo[3.2.1]oct-6-ene-3-carboxylic acid (6-amino-2,4-dioxo-1,3-dipropyl-1,2,3,4-tetrahydro-pyrimidin-5-yl)-amide (0.185 mmol, 0.067 g) in 20% NaOH (1.23 ml) and MeOH (6.2 ml) was stirred and refluxed overnight. The reaction was cooled to room temperature and then concentrated to remove MeOH. The aqueous residue was extracted with Et2O and these extracts discarded. The aqueous was acidified (pH 2-3) with conc. HCl and then extracted with EtOAc. The combined EtOAc extracts were washed with H2O and brine and dried (MgSO4). Filtration and evaporation followed by flash column chromatography, eluting with 1:1 EtOAc/CH2Cl2, provided the title compound (0.037 g, 58%) as a beige solid. 1H NMR (300 MHz, CDCl3): 0.93-0.99 (m, 6H), 1.62-1.83 (m, 6H), 2.14-2.25 (m, 2H), 3.40-3.51 (m, 1H), 4.05-1.10 (m, 4H), 4.86 (br s, 2H), 6.25 (s, 2H).
後処理
- temperaturerefluxed overnight
- concentrationconcentrated
- customto remove MeOH
- extractionThe aqueous residue was extracted with Et2O
- extractionextracted with EtOAc
- washThe combined EtOAc extracts were washed with H2O and brine
- dry with materialdried (MgSO4)
- filtrationFiltration and evaporation
- washeluting with 1:1 EtOAc/CH2Cl2
出典と根拠
- ORDレコード
- ord-b2d8ec3403824642b5ffb25fea4b2fab
- 出典データセット
- uspto-grants-2003_08
- 特許番号
- US06605600B1
反応ノート
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