反応式
[NH2:1][C:2]1[S:3][C:4]([S:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14])=[N:5][N:6]=1.C([O:17][CH:18]=[CH:19][C:20](OCC)=O)C>>[CH2:8]([S:7][C:4]1[S:3][C:2]2=[N:1][CH:20]=[CH:19][C:18](=[O:17])[N:6]2[N:5]=1)[CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14]参加物
3
実験手順
A mixture of 20.1 g of 2-amino-5-heptylthio-1,3,4-thiadiazole, 20.0 g of ethyl 3-ethoxypropenoate and 23 g of polyphosphoric acid was heated to 130°~140° C. and stirred for 30 minutes. The residue obtained by the same procedure as in Preparation Example 13 was purified by silica gel column chromatography using an ethyl acetate/toluene mixture as an eluent. Thus 12.6 g of 2-heptylthio-5H-1,3,4-thiadiazolo[3,2-a]pyrimidin-5-one was obtained. Yield 51%.
後処理
- temperaturewas heated to 130°~140° C.
- customThe residue obtained by the same procedure as in Preparation Example 13
- customwas purified by silica gel column chromatography
出典と根拠
- ORDレコード
- ord-8e87d93c0e0b4e6b870f0780bd7a170c
- 出典データセット
- uspto-grants-1990_11
- 特許番号
- US04971971
関連ノート
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