HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 66953749, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 66954058 | HCID 66954058 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 66953749 | HCID 66953749 | 40% |
Reaction Steps
To a solution of N-(2-adamantyl)-1-oxo-1,3-dihydrospiro[indene-2,3′-piperidine]-1′-carboxamide (3.0 mg, 0.079 mmol) in MeOH (3 mL) was added NaBH4 (12 mg, 0.317 mmol) at 0° C. under nitrogen. The reaction mixture was stirred for 4 h under N2 at rt. The reaction mixture was evaporated to give a residue, which was purified by preparative HPLC to afford N-(2-adamantyl)-1-hydroxy-1,3-dihydrospiro[indene-2,3′-piperidine]-1′-carboxamide (12 mg, 40%). 1HNMR (CD3OD, 400 MHZ): δ=1.51-1.75 (m, 5H), 1.78˜1.81 (m, 4H), 1.82˜2.00 (m, 11H), 2.50 (m, 1H), 3.00 (d, 1H), 3.20 (m, 1H), 3.55 (m, 1H), 3.65 (m, 1H), 3.81 (s, 1H), 4.75 (s, 1H), 7.22 (m, 3H), 7.388 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08927715B2 |
| Source dataset | uspto-grants-2015_01 |
| ORD ID | ord-03168a6c06e54aca82c021a94a3d9392 |
| Source note | uspto-grants-2015_01 |