Ethyl 4-chloroacetoacetate → S-[(3,4-Dihydro-2-(1-methylethyl)-4-oxo-6-pyrimidinyl)methyl] O,O-dimethyl phosphorodithioate
反応式
Cl[CH2:2][C:3]1[NH:8][C:7]([CH:9]([CH3:11])[CH3:10])=[N:6][C:5](=[O:12])[CH:4]=1.ClCC(=O)CC(OCC)=O.C(N)(=N)C(C)C.[P:29]([S-:35])(=[S:34])([O:32][CH3:33])[O:30][CH3:31].[NH4+]>CO.ClCCl>[P:29]([S:35][CH2:2][C:3]1[N:8]=[C:7]([CH:9]([CH3:11])[CH3:10])[NH:6][C:5](=[O:12])[CH:4]=1)(=[S:34])([O:32][CH3:33])[O:30][CH3:31]参加物
7
反応物 4
生成物 1
試薬・触媒・溶媒 2
実験手順
The intermediate, 6-(chloromethyl)-2-(1-methylethyl)-4(1H)pyrimidinone, was prepared according to Swiss patent 524617 from ethyl 4-chloroacetoacetate and isobutyramidine. m.p. 123°-125°. The intermediate chloromethyl compound (25 g) was stirred with 50 ml methanol at room temperature. To this mixture was added, dropwise, a solution of 25 g ammonium dimethyl phosphorodithioate dissolved in 500 ml methanol. The mixture was then heated to reflux for 6 hours, then the solvent was evaporated under reduced pressure yielding a solid. The solid was dissolved in dichloromethane and washed with water, separated, dried, and the solvent was evaporated. The remaining solid was recrystallized from toluene; yield: 15.9 g, m.p. 89°-93°.
後処理
- additionTo this mixture was added
- temperatureThe mixture was then heated
- temperatureto reflux for 6 hours
- customthe solvent was evaporated under reduced pressure
- customyielding a solid
- washwashed with water
- customseparated
- customdried
- customthe solvent was evaporated
- customThe remaining solid was recrystallized from toluene
出典と根拠
- ORDレコード
- ord-921e6e77ba944dc38469bfcabd59faa0
- 出典データセット
- uspto-grants-1983_07
- 特許番号
- US04395551
反応ノート
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