HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 603172Generated: October 31, 2026
1,2-Dichloro-4-isothiocyanatobenzene → HCID 178462557, compound
https://huagongshe.com/reaction/603172
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,2-Dichloro-4-isothiocyanatobenzene | HCID 23065 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | Cyanamidnatrium | HCID 57375518 | — |
| Reactant | 1-{[(3R)-1-ethylpiperidin-3-yl]methyl}piperazine | HCID 57656847 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178462557 | HCID 178462557 | 37.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07906645B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-90ddf7e1382a455c943958080b3133a0 |
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| Source note | uspto-grants-2011_03 |
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