HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → HCID 69144794, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1,3-DI-Boc-2-methylisothiourea | HCID 546603 | — |
| Reactant | HCID 59714922 | HCID 59714922 | — |
| Catalyst | Mercuric Chloride | HCID 24085 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 69144794 | HCID 69144794 | 65% |
Reaction Steps
To a solution of N-[1-[2-[1-(2-aminoethyl)cyclohexyl]ethyl]piperidin-4-yl]-N-(5-methylpyridin-2-yl)-2-furancarboxamide (synthesized in Example 3F-5) (104 mg) and 1,3-bis(tert-butoxycarbonyl)-2-methyl-2-thiopseudourea (85 mg) in N,N-dimethylformamide (5 mL) were added N,N-diisopropylethylamine (0.12 g) and then mercury (II) chloride (113 mg) at room temperature. The solution was stirred at room temperature for 3 days. Dichloromethane was added to the solution and insolubles were filtered off with Celite. The solvent was distilled off under reduced pressure. The resulting residue was purified by chromatography [silica gel, dichloromethane-methanol-aqueous ammonia (97:3:0.2)] to give the title compound (0.1049 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07375115B2 |
| Source dataset | uspto-grants-2008_05 |
| ORD ID | ord-96ae96923ad34ada8ba48c9e421bf553 |
| Source note | uspto-grants-2008_05 |