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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 532575생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물4-Bromophenyl isothiocyanateHCID 16133—
반응물Hydrazine hydrate (1:1)HCID 24654—
반응물4H,5H,6H-cyclopenta[b]thiophen-4-oneHCID 1958632—
반응물Lithium hexamethyldisilaneHCID 57425481—
용매Acetic AcidHCID 176—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물(4-Bromo-phenyl)-(4,7-dihydro-1-thia-4,5-diaza-cyclopenta[a]pentalen-6-yl)-amineHCID 7181538632%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08853207B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-b62f8fd057274d95b00d2f6fd690ce12
출처 메모uspto-grants-2014_10