HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 59049327, compound → HCID 59049307, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 59049327 | HCID 59049327 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 59049307 | HCID 59049307 | — |
Reaction Steps
(2S)-1-(Benzyloxycarbonyl)-2-(1-[3-(3-pyridyl)-1-propyl]-1H-tetrazol-5-yl)azetidine from Reference Example 17 (125.3 mg, 0.331 mmol, 1.0 eq) was dissolved in ethanol (20 mL) and 10% Pd/C (49.9 mg, 0.047 mmol, 0.14 eq) was carefully added. The mixture was flushed with vacuum and nitrogen three times and stirred under a hydrogen atmosphere at about room temperature for about 26 hours. After removing the solid matter by filtration, the solvent was removed under vacuum to give 80.8 mg (quantitative yield) of the product as a colorless oil. 1H NMR (CDCl3) δ 2.18-3.24 (series of m, 7H); 3.46-4.68 (series of m, 5H); 7.19-7.33 (m, 1H); 7.51-7.63 (m, 1H); 8.38-8.57 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06544976B1 |
| Source dataset | uspto-grants-2003_04 |
| ORD ID | ord-019a7228a3f648b8b893780e04b9c643 |
| Source note | uspto-grants-2003_04 |