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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2371130Generated: October 31, 2026

1,2-Dichloro-4-isothiocyanatobenzene → HCID 178462557, compound

https://huagongshe.com/reaction/2371130

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-Dichloro-4-isothiocyanatobenzeneHCID 23065—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantCyanamidnatriumHCID 57375518—
Reactant1-{[(3R)-1-ethylpiperidin-3-yl]methyl}piperazineHCID 57656847—
SolventEthanolHCID 702—
SolventDimethylformamideHCID 6228—
ProductHCID 178462557HCID 17846255737.6%

Reaction Steps

3,4-Dichlorophenylisothiocyanate (204 mg) and sodium hydrogen cyanamide (70 mg) were refluxed in ethanol (20 ml) for three hours. The mixture was allowed to cool to room temperature then 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (211 mg), 1-{[(3R)-1-ethylpiperidin-3-yl]methyl}piperazine (220 mg) and N,N-dimethylformamide (2 ml) were added and the reaction left to stir for 18 hours then concentrated in vacuo. The crude product was subjected to reverse phase HPLC using a gradient of 95% water/acetonitrile/0.1% TFA through to 50% water/acetonitrile/0.1% TFA. The combined product fractions were concentrated in vacuo then separated between dichloromethane (50 ml) and saturated sodium bicarbonate solution (100 ml). The dichloromethane layer was separated, dried over magnesium sulphate, filtered and concentrated in vacuo to give the title compound (159 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710224B2
Source datasetuspto-grants-2014_04
ORD IDord-a4bb133355e14354811bdf93fc91db2a
Source noteuspto-grants-2014_04