HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 66953749, compound → HCID 46231489, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 66953749 | HCID 66953749 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 46231489 | HCID 46231489 | 29% |
Reaction Steps
To a solution of N-(2-adamantyl)-1-hydroxy-1,3-dihydrospiro[indene-2,3′-piperidine]-1′-carboxamide (20 mg, 0.052 mmol) in ethanol (3 mL) was added Pd(OH)2 (10 mg), then the reaction mixture was stirred for 4 h at rt under a hydrogen atmosphere. The reaction mixture was filtered and the filtrate was evaporated to give a residue, which was purified by preparative HPLC to afford N-(2-adamantyl)-1,3-dihydrospiro[indene-2,3′-piperidine]-1′-carboxamide (5 mg, 29%): LC-MS Method 5 tR=3.057 min, m/z=365.2; 1H NMR (CD3OD, 400 MHz): δ=1.55 (m, 2H), 1.66 (m, 2H), 1.78 (m, 7H), 1.84 (m, 7H), 2.69-2.83 (m, 4H), 3.21 (s, 2H), 3.45 (m, 2H), 3.77 (s, 1H), 7.09 (m, 2H), 7.14 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08927715B2 |
| Source dataset | uspto-grants-2015_01 |
| ORD ID | ord-31d2108a5f2945c4b1389e9b46924a73 |
| Source note | uspto-grants-2015_01 |