HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1602856Generated: November 1, 2026
Methylamine hydrochloride → HCID 15886822, compound
https://huagongshe.com/reaction/1602856
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methylamine hydrochloride | HCID 6364545 | — |
| Reactant | HCID 9869513 | HCID 9869513 | — |
| Solvent | MeOH tetrahydrofuran | HCID 21899815 | — |
| Product | HCID 15886822 | HCID 15886822 | — |
Reaction Steps
Methylamine hydrochloride (37 mg, 0.546 mmol) was added to a solution of 4-(oxo)-N-[3-[4-methyl-1-(4-phenyl-1-piperazinyl)cyclohexyl]phenyl]-1-piperidinecarboxamide (cis isomer) (43 mg, 0.091 mmol) in THF/MeOH (1:1) and stirred at room temperature. When all the methylamine hydrochloride had dissolved, NaCNBH4 (6 mg, 0.091 mmol) was added and the reaction allowed to stir overnight at room temperature. The reaction mixture was concentrated, dissolved in an excess of 3N HCl, and the aqueous solution washed with ether (3×). The aqueous solution was made basic with 10N NaOH, extracted with EtOAc (4×), dried (Na2SO4), and concentrated to give 4-(methylamino)-N-[3-[4-methyl-1-(4-phenyl-1-piperazinyl)-cyclohexyl]phenyl]-1-piperidinecarboxamide (cis isomer) as a clear oil. The HCl salt was prepared by adding excess saturated EtOAc/HCl solution to the free base in dry MeOH. Concentration of the homogeneous solution yielded a white solid which was washed with EtOAc. mp=154-155° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05985873 |
|---|
| Source dataset | uspto-grants-1999_11 |
|---|
| ORD ID | ord-ece05cc3d4f84a529b13e0ecb7513957 |
|---|
| Source note | uspto-grants-1999_11 |
|---|