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HRID 9583作成日:2026年10月24日

Dicyclohexylcarbodiimide → HCID 178418733、化合物

https://huagongshe.com/ja/reaction/9583

反応式

関与物質

役割名称HCID仕込み量
反応物DicyclohexylcarbodiimideHCID 10868—
反応物4-Trifluoromethyl-1,2-phenylenediamineHCID 520822—
反応物4-Bromo-2-fluorophenylisothiocyanateHCID 2757003—
溶媒DichloromethaneHCID 6344—
生成物HCID 178418733HCID 178418733—

反応条件

温度45 °C

反応手順

1,2-Diamino-5-trifluoromethylbenzene (0.50 g, 2.84 mmol) was diluted in dichloromethane (5 mL) and treated with 4-bromo-2-fluoro-phenylisothiocyanate (0.66 g, 2.84 mmol). The dark solution was stirred at 45° C. for 15 minutes, then 1,3-dicyclohexylcarbodiimide (0.44 g, 2.13 mmol) was added all at once. The reaction was heated in a 45° C. oil bath overnight, then cooled and concentrated at reduced pressure. The dark residue was diluted with ethyl acetate, and the organic layer was washed with water. The organic layer was dried (MgSO4) and concentrated in vacuo. The resulting dark brown oil was purified by flash chromatography on silica gel eluted on a gradient from 9:1 hexanes/ethyl acetate to 100% ethyl acetate. The title compound was collected as a light pink solid (0.60 g, 57%). 1H NMR (300 MHz, DMSO-d6) δ 11.3 (broad d, 1H), 9.87 (d, 1H), 7.50 (d, 2H), 7.61 (d, 1H), 7.55–7.41 (m, 3H), 7.35–7.30 (m, 1H); LC/MS m/z 356.2 (MH+), retention time 2.33 minutes.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091228B2
出典データセットuspto-grants-2006_08
ORD IDord-66414de28ead4eef90b6009cd06980d8
出典メモuspto-grants-2006_08