HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615862Generated: October 31, 2026
Dimethylcarbamoyl Chloride → HCID 178491973, compound
https://huagongshe.com/reaction/1615862
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylcarbamoyl Chloride | HCID 6598 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 178491971 | HCID 178491971 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178491973 | HCID 178491973 | 72.1% |
Reaction Steps
0.92 g (2 mmol) trans-4-{2-[4-(2,3-dichloro-4-methoxy-phenyl)-piperazin-1-yl]-ethyl}-cyclohexyl-amine dihydrochloride was suspended in dichloromethane (60 ml), triethylamine (1.26 ml, 9 mmol) was added followed by 0.21 ml (2.3 mmol) N,N-dimethylcarbamoylchloride. The reaction mixture was stirred for 48 hours at room temperature. The solution was washed with water (2×10 ml), dried and evaporated in vacuo. Purification with flash chromatography gave 0.66 g trans-1-{4-[2-[4-(2,3-dichloro-4-methoxy-phenyl)-piperazin-1-yl]-ethyl]-cyclohexyl}-3,3-dimethyl-urea, melting at 196-8° C. This product was dissolved in dichloromethane (60 ml), then 6.4 ml (6.4 mmol) borontribromid solution (1M in CH2Cl2) was dropped in at 5° C. and the mixture stirred at room temperature for 24 hours. The reaction was monitored by TLC. 4 ml methanol was added, followed by 25 ml saturated NaHCO3 solution. After separation the organic layer was dried and evaporated in vacuo. Purification with flash chromatography gave 0.4 g of the title compound, melting at 278-80° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08765765B2 |
|---|
| Source dataset | uspto-grants-2014_07 |
|---|
| ORD ID | ord-8935ddbcccc24ea68e1b817df898687a |
|---|
| Source note | uspto-grants-2014_07 |
|---|