反応式
C1(C)C=CC=CC=1.[CH2:8]([O:24][C:25](Cl)=[O:26])[CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23].[CH:28]1([N:37]2[CH:44]=[CH:43][C:41]([NH2:42])=[N:40][C:38]2=[O:39])[O:34][C@H:33]([CH2:35][OH:36])[C@@H:31]([OH:32])[C@@H:29]1[OH:30].C(=O)([O-])O.[Na+]>CC(N(C)C)=O>[CH2:8]([O:24][C:25]([NH:42][C:41]1[CH:43]=[CH:44][N:37]([CH:28]2[O:34][C@H:33]([CH2:35][OH:36])[C@@H:31]([OH:32])[C@@H:29]2[OH:30])[C:38](=[O:39])[N:40]=1)=[O:26])[CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23]参加物
実験手順
A toluene solution containing 1.8 g of palmityloxycarbonyl chloride is added to 20 ml of a dimethylacetamide solution containing 1.5 g of arabinofuranosylcytosine and 1.7 g of sodium hydrogen carbonate. The reaction is carried out at room temperature with stirring of the mixture for 3 hours. After the reaction is completed, the reaction mixture is poured into an ice-water and the precipitated solids are collected by filtration, followed by washing successively with acetone and with hot chloroform. The resultant solids are dissolved in a mixture of chloroform-methanol and then subjected once to filtration, followed by removal of the solvent. The residue is subjected to crystallization from n-hexane to give 0.92 g of N4 -palmityloxycarbonylarabinofuranosylcytosine (Yield:30%).
後処理
- customis carried out at room temperature
- filtrationthe precipitated solids are collected by filtration
- washby washing successively with acetone and with hot chloroform
- dissolutionThe resultant solids are dissolved in a mixture of chloroform-methanol
- filtrationsubjected once to filtration
- customfollowed by removal of the solvent
- customThe residue is subjected to crystallization from n-hexane
出典と根拠
- ORDレコード
- ord-c831318232c74dc18a76d840e18e0fb7
- 出典データセット
- uspto-grants-1983_01
- 特許番号
- US04367332
関連ノート
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