HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,6-Lutidine → HCID 178483624, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,6-Lutidine | HCID 7937 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Trifluoromethyl-benzene sulfochloride | HCID 22294170 | — |
| Reactant | HCID 178483629 | HCID 178483629 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178483624 | HCID 178483624 | — |
Reaction Steps
In analogy to the sequence described in examples 17.3 and 17.4, trans-3-[4-(2-methylamino-ethyl)-cyclohexyl]-(E)-prop-2-en-1-ol HCl was reacted with 4-trifluoromethyl-benzene sulfochloride in dichloromethane in the presence of diisopropyl ethyl amine followed by treatment with methane sulfonylchloride and 2,6-lutidine in dichloromethane to yield trans-N-{2-[4-(3-chloro-(E)-propenyl)-cyclohexyl]-ethyl}-N-methyl-4-trifluoromethyl-benzenesulfonamide as colorless viscous oil, MS: 424 (MH+, 1Cl).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06953806B2 |
| Source dataset | uspto-grants-2005_10 |
| ORD ID | ord-a9f139d8336e4eb587d08d396e0cfbb6 |
| Source note | uspto-grants-2005_10 |