反応式
[N:1]#[N:2].[CH3:3][O:4][C:5]1[CH:10]=[CH:9][C:8]([C:11]([NH:24][C:25]2[NH:26][C:27](=[O:41])[C:28]3[N:29]=[CH:30][N:31]([CH2:34][O:35][CH:36]([CH2:39][OH:40])[CH2:37][OH:38])[C:32]=3[N:33]=2)([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[CH:7][CH:6]=1.[C:42](Cl)(=[O:50])[CH2:43][CH2:44][CH2:45][CH2:46][CH2:47][CH2:48][CH3:49].[OH2:52]>CN(C)C1C=CN=CC=1.N1C=CC=CC=1.C(Cl)Cl>[N:1]#[N:2].[CH3:3][O:4][C:5]1[CH:6]=[CH:7][C:8]([C:11]([NH:24][C:25]2[NH:26][C:27](=[O:41])[C:28]3[N:29]=[CH:30][N:31]([CH2:34][O:35][CH:36]([CH2:37][O:38][C:9](=[O:52])[CH2:10][CH2:5][CH2:6][CH2:7][CH2:8][CH2:11][CH3:12])[CH2:39][O:40][C:42](=[O:50])[CH2:43][CH2:44][CH2:45][CH2:46][CH2:47][CH2:48][CH3:49])[C:32]=3[N:33]=2)([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[C:18]2[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=2)=[CH:9][CH:10]=1参加物
7
反応物 3
生成物 1
試薬・触媒・溶媒 3
実験手順
To a magnetically stirred solution of 1.05 g of N2 -(4-methoxyphenyldiphenylmethyl)-9-(1,3-dihydroxy-2-propoxymethyl)guanine and 25 mg of 4-dimethylaminopyridine in 30 ml of dry pyridine was added dropwise a solution of 1.2 g of n-octanoyl chloride in 10 ml of methylene chloride. After 15 hour, 1.5 ml of water was added and the solution concentrated at reduced pressure. The residue was chromatographed over silica gel eluting with 1:9 methanol:methylene chloride to give a white solid which was recrystallized from ethyl acetate:hexane to N2 -(4-methoxyphenyldiphenylmethyl)-9-(1,3-din-octanoyloxy-2-propoxymethyl)guanine.
後処理
- concentrationthe solution concentrated at reduced pressure
- customThe residue was chromatographed over silica gel eluting with 1:9 methanol
- custommethylene chloride to give a white solid which
- customwas recrystallized from ethyl acetate
出典と根拠
- ORDレコード
- ord-4d67692707ba42fab27b37ab3e5eae3f
- 出典データセット
- uspto-grants-1986_09
- 特許番号
- US04612314
関連ノート
読み込み中…