HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 392392Generated: October 29, 2026
HCID 10186648, compound → HCID 10160308, compound
https://huagongshe.com/reaction/392392
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 10186648 | HCID 10186648 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 10160308 | HCID 10160308 | 90% |
Reaction Steps
A solution of N-(3-(2-benzyloxyphenoxy)phenyl)-N-(2,2,2-trifluoroethylsulfonyl)pyrid-3-ylmethylamine (529 mg, 1.00 mmol) in methanol (50 mL) was carefully treated with Raney® nickel (one tsp.), placed on a Parr® apparatus, and hydrogenated at 45-50 psi pressure for 3 h. The mixture was carefully filtered through celite® under nitrogen without allowing the filter cake to dry, and the filtrate was concentrated in vacuo. The residual solid was triturated from petroleum ethers (30°-60°) to afford the title compound (394 mg, 90%) as a white solid; mp 57.5-60.0° C. The title compound was converted to the hydrochloride salt by treatment in methanol with ethereal HCl. 1H NMR: 8.50 (br s,1H), 8.25 (br s,1H), 7.68 (d,1H, J=8 Hz), 7.25-7.30 (m,2H); 6.95-7.10 (m,2H), 6.90-6.95 (m,2H), 6.70-6.85 (m,3H), 6.05 (br s,1H), 4.82 (s,2H), 3.75-3.85 (m,2H).MS calcd. 438.4; MS(M+1) 439.3
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06800651B2 |
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| Source dataset | uspto-grants-2004_10 |
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| ORD ID | ord-9d50956ba0ac44cca97e410de871a7cc |
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| Source note | uspto-grants-2004_10 |
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