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HRID 2298593作成日:2026年10月25日

Sodium Chloride → 5-Methylthio-4-(4-phenyl(1,3-thiazol-2-yl))thiophene-2-carbonitrile

https://huagongshe.com/reaction/2298593

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium ChlorideHCID 5234—
反応物Phosphorus oxide (P4O10)HCID 14812—
反応物HexamethyldisiloxaneHCID 24764—
反応物HCID 18536867HCID 18536867—
溶媒1,1-DichloroethaneHCID 6365—
生成物5-Methylthio-4-(4-phenyl(1,3-thiazol-2-yl))thiophene-2-carbonitrileHCID 1853726459%

反応条件

温度40 °C

反応手順

A slurry of P2O5 (2.7 g, 19 mmol) and hexamethyldisiloxane (6.7 mL) in dichloroethane (13 mL) was heated to 90° C., while stirring under a N2 atmosphere. After stirring for 2 h, the resulting clear solution was allowed to cool to 40° C. 5-methylthio-4-(4-phenyl(1,3-thiazol-2-yl))thiophene-2-carboxamide (0.9 g, 2.7 mmol) as prepared in previous step was added to this solution and the mixture was heated at 75° C. for 5 h. This solution was cooled to room temperature and stirred with aqueous NaCl (6 M, 100 mL) for 10 min. As the aqueous solution is added a yellow solid precipitated. After 10 min this solid was separated by filtration, and dried under vacuum to give (0.5 g, 59%) of 5-methylthio-4-(4-phenyl(1,3-thiazol-2-yl))thiophene-2-carbonitrile as a yellow solid. 1H-NMR (DMSO-d6; 300 MHz) δ2.76 (s, 3H), 7.35-7.40 (m, 1H), 7.45-7.50 (m, 2H), 8.05-8.08 (m, 2H), 8.22 (s, 1H), 8.51 (s, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06492403B1
出典データセットuspto-grants-2002_12
ORD IDord-d8807b7ea1ca4631b4300d47a6f2b090
出典メモuspto-grants-2002_12