HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1027227Generated: November 1, 2026
HCID 86710633, compound → HCID 136377158, compound
https://huagongshe.com/reaction/1027227
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 86710633 | HCID 86710633 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 136377158 | HCID 136377158 | 52.3% |
Reaction Steps
A H2 purged mixture of 6-(3-(benzyloxy)-6-(piperidin-1-ylmethyl)naphthalen-2-yl)-N-methyl-N-(2,2,6,6-tetramethylpiperidin-4-yl)pyridazin-3-amine (34 mg, 0.059 mmol) and 10% wt Pd/C (0.3 mg, 3 μmol) in MeOH (3 mL) and EtOAc (3 mL) was stirred under a H2 atmosphere at RT overnight. The reaction mixture was filtered through celite, rinsed with MeOH and concentrated. The crude material was purified via HPLC to give the desired product as a yellow solid (15 mg, 52.3% yield). LCMS Rt=0.45 min [Method Q], MS (M−1)=486.4. 1H NMR (METHANOL-d4) δ 8.16 (s, 1H), 8.12 (d, J=10.1 Hz, 1H), 7.69 (d, J=8.6 Hz, 1H), 7.46 (s, 1H), 7.15-7.22 (m, 2H), 7.14 (s, 1H), 4.98 (t, J=12.1 Hz, 1H), 3.49 (s, 2H), 2.89 (s, 3H), 2.37 (br. s., 4H), 1.34-1.60 (m, 10H), 1.29 (s, 6H), 1.13 (s, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08729263B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-5171440cf56648b39d23a0845abbdff8 |
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| Source note | uspto-grants-2014_05 |
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