Sodium hydride → HCID 20034621、化合物
反応式
[CH3:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:8][S:9][C:10]2[NH:14][C:13]3=[CH:15][S:16][CH:17]=[C:12]3[N:11]=2)=[N:6][CH:7]=1.[H-].[Na+].[C:20](=O)([O:31]C1C=CC=CC=1)[O:21][CH2:22][C:23]1[CH:28]=[CH:27][C:26]([O:29][CH3:30])=[CH:25][CH:24]=1>CN(C=O)C>[CH3:30][O:29][C:26]1[CH:27]=[CH:28][C:23]([CH2:22][O:21][C:20]([N:11]2[C:12]3=[CH:17][S:16][CH:15]=[C:13]3[N:14]=[C:10]2[S:9][CH2:8][C:5]2[CH:4]=[CH:3][C:2]([CH3:1])=[CH:7][N:6]=2)=[O:31])=[CH:24][CH:25]=1参加物
実験手順
To 1.3 g (5 mmol) of 2-(5-methyl-2-picolylmercapto)-1H-thieno[3,4-d]imidazole dissolved in 15 ml of anhydrous DMF were added, under nitrogen, 275 mg (6 mmol) of sodium hydride. After the mixture had been heated at 40°-50° C. for 10 min, at room temperature 1.92 g (7.5 mmol) of 4-methoxybenzyl phenyl carbonate (prepared from 4-methoxybenzyl alcohol and phenyl chloroformate) were added, and the mixture was heated at 30°-40° C. for 10 minutes and stirred at room temperature for 1 hour. The solvent was removed by distillation in vacuo, and water was added to the residue. The oily/resinous precipitate was taken up in CH2Cl2, and the solution was dried over MgSO4 and the solvent was evaporated off. The residue crystallized from diethyl ether and was recrystallized from isopropanol. Melting point 120°-121° C.
後処理
- additionwere added, under nitrogen
- additionwere added
- temperaturethe mixture was heated at 30°-40° C. for 10 minutes
- customThe solvent was removed by distillation in vacuo, and water
- additionwas added to the residue
- dry with materialthe solution was dried over MgSO4
- customthe solvent was evaporated off
- customThe residue crystallized from diethyl ether
- customwas recrystallized from isopropanol
出典と根拠
- ORDレコード
- ord-449e5f0954f844debd26d10124aef7b7
- 出典データセット
- uspto-grants-1989_07
- 特許番号
- US04845118
反応ノート
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