反応式
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([CH3:11])=[C:6]([N:8]=[C:9]=[S:10])[CH:7]=1.[CH3:12][C:13]1[N:14]=[C:15]([NH2:18])[O:16][CH:17]=1>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([CH3:11])=[C:6]([NH:8][C:9]([NH:18][C:15]2[O:16][CH:17]=[C:13]([CH3:12])[N:14]=2)=[S:10])[CH:7]=1参加物
3
実験手順
Prepared using Method A from 10.0 g (54.5 mmol) of 5-chloro-2-methyl-phenyl isothiocyanate and 5.39 g (55 mmol) of 4-methyl-2-amino-oxazole to give 8.3 g of title compound as a yellow solid, m.p. 207-208° C. An additional crop (4.8 g, m.p. 207-208° C.) was obtained from the mother liquor (86% combined yield).
後処理
- customPrepared
出典と根拠
- ORDレコード
- ord-44e731206ffe4858bf931064cf3976e5
- 出典データセット
- uspto-grants-2005_08
- 特許番号
- US06936630B2
関連ノート
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