HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzenesulfonyl chloride → HCID 18630687, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 18630707 | HCID 18630707 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18630687 | HCID 18630687 | — |
Reaction Steps
In this case the title compound was prepared by sulfonylation of 1-(piperidin-4-yl)-3-(3-amidinophenyl)-5-ethenyl-2-imidazolidinone with phenylsulfonyl chloride in tetrahydrofuran with triethylamine followed by amidine formation as described above; HRMS (M+H)+ calc. 454.191287, found 454.191418.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05925635 |
| Source dataset | uspto-grants-1999_07 |
| ORD ID | ord-519c15d2445c46fa92c0c3e933e318d7 |
| Source note | uspto-grants-1999_07 |