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HRID 532575作成日:2026年10月24日

4-Bromophenyl isothiocyanate → (4-Bromo-phenyl)-(4,7-dihydro-1-thia-4,5-diaza-cyclopenta[a]pentalen-6-yl)-amine

https://huagongshe.com/ja/reaction/532575

反応式

関与物質

役割名称HCID仕込み量
反応物4-Bromophenyl isothiocyanateHCID 16133—
反応物Hydrazine hydrate (1:1)HCID 24654—
反応物4H,5H,6H-cyclopenta[b]thiophen-4-oneHCID 1958632—
反応物Lithium hexamethyldisilaneHCID 57425481—
溶媒Acetic AcidHCID 176—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物(4-Bromo-phenyl)-(4,7-dihydro-1-thia-4,5-diaza-cyclopenta[a]pentalen-6-yl)-amineHCID 7181538632%

反応手順

A mixture of 5,6-Dihydro-cyclopenta[b]thiophen-4-one (1.0 g, 7.4 mmol) and 1-Bromo-4-isothiocyanato-benzene (1.5 g, 7.2 mmol) in THF (2.0 mL) was added to lithium hexamethyl disilane (7.0 mL, 7.2 mmol) dropwise at room temperature. The reaction mixture was stirred for 8 hr. Hydrazine monohydrate (0.4 mL, 7.9 mmol) and glacial acetic acid (0.5 mL) were added to the reaction mixture, which was then heated at the reflux temperature for 24 hr. The resulting mixture was added to water (30 mL) and then extracted with ethyl acetate. The target product was purified by gravity column chromatography (50% EtOAc in hexane) to give (4-Bromo-phenyl)-(4,7-dihydro-1-thia-4,5-diaza-cyclopenta[a]pentalen-6-yl)-amine as brown solid in 32% yield.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08853207B2
出典データセットuspto-grants-2014_10
ORD IDord-b62f8fd057274d95b00d2f6fd690ce12
出典メモuspto-grants-2014_10