HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2111579Generated: November 1, 2026
HCID 178418361, compound → HCID 178511722, compound
https://huagongshe.com/reaction/2111579
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Reactant | HCID 178420356 | HCID 178420356 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178511722 | HCID 178511722 | — |
Reaction Steps
Trans-N,N-dibenzyl-4-(2-(piperidin-1-yl)ethoxy)cyclohexanamine (4.7 g, 11.6 mmol), 20% Pd(OH)2/C (0.94 g) and methanol (40 mL) were charged into a septum-sealed flask. The reaction mixture was placed under balloon pressure of hydrogen for 18 h at ambient temperature, at which time LCMS indicated complete debenzylation to form the free amine. The catalyst was filtered off and the filtrate evaporated under reduced pressure to give 2.42 g of a crystalline material (93%). In some cases an additional portion of catalyst (ca. 50% of the initial charge) was needed in order to attain complete reaction. LRMS (ES) m/e 227.2 [MH]+; 1H NMR (300 MHz, CD3OD) δ 3.51(t, 2H), 3.12(m, 1H), 2.61(m, 1H), 2.42(t, 2H), 2.18(m, 4H), 1.93(m, 2H), 1.80(m, 2H), 1.50(m, 4H), 1.33(m, 2H), 1.12(m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07521446B2 |
|---|
| Source dataset | uspto-grants-2009_04 |
|---|
| ORD ID | ord-d6cc3112999c49ea85ceaaa80d6001a1 |
|---|
| Source note | uspto-grants-2009_04 |
|---|