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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 532590Generated: October 30, 2026

3-Bromophenyl Isothiocyanate → (3-Bromo-phenyl)-(4,7-dihydro-1-thia-4,5-diaza-cyclopenta[a]pentalen-6-yl)-amine

https://huagongshe.com/reaction/532590

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromophenyl IsothiocyanateHCID 16481—
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant4H,5H,6H-cyclopenta[b]thiophen-4-oneHCID 1958632—
ReactantLithium hexamethyldisilaneHCID 57425481—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(3-Bromo-phenyl)-(4,7-dihydro-1-thia-4,5-diaza-cyclopenta[a]pentalen-6-yl)-amineHCID 7181551134%

Reaction Steps

A mixture of 5,6-Dihydro-cyclopenta[b]thiophen-4-one (1.0 g, 7.4 mmol) and 1-Bromo-3-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 (3-Bromo-phenyl)-(4,7-dihydro-1-thia-4,5-diaza-cyclopenta[a]pentalen-6-yl)-amine as brown solid in 34% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853207B2
Source datasetuspto-grants-2014_10
ORD IDord-058c3630b1bd40d1b1a8d801e1610228
Source noteuspto-grants-2014_10