HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1832190Generated: October 25, 2026
Ammonia → N-[3-(1-{(3R)-3-[2-Fluoro-5-(Trifluoromethyl)Phenoxy]-3-Phenylpropyl}-4-Piperidinyl)Phenyl]-2-Methylpropanamide
https://huagongshe.com/reaction/1832190
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonia | HCID 222 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | 2-Fluoro-5-(trifluoromethyl)phenol | HCID 518888 | — |
| Reactant | N-(3-{1-[(3S)-3-Hydroxy-3-Phenylpropyl]-4-Piperidinyl}Phenyl)-2-Methylpropanamide | HCID 60078700 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-[3-(1-{(3R)-3-[2-Fluoro-5-(Trifluoromethyl)Phenoxy]-3-Phenylpropyl}-4-Piperidinyl)Phenyl]-2-Methylpropanamide | HCID 60078695 | 33.7% |
Reaction Steps
A mixture of N-(3-{1-[(3S)-3-hydroxy-3-phenylpropyl]-4-piperidinyl}phenyl)-2-methylpropanamide (5.20 mg, 0.0137 mmol), 2-fluoro-5-trifluoromethylphenol (100 mg), triphenylphosphine (30.0 mg, 0.115 mmol) and diethyl azodicarboxylate (7.42 mg, 0.0426 mmol) in THF (0.50 mL) was stirred at room temperature for 3 days. Chromatography using silica preparative TLC plates [2.5% of NH3 (2.0 M in methanol) in CHCl3] gave the desired product (2.50 mg, 33.7% yield) as a thick oil: 1H NMR (400 MHz, CDCl3) δ 8.07 (s, 1H), 7.67 (m, 1H), 7.54 (m, 1H), 7.45 (m, 2H), 7.30–7.10 (m, 6H), 7.14 (d, 1H, J=7.4 Hz), 6.97 (apparent d, 1H, J=7.7 Hz), 5.37 (apparent dd, 1H, J=5.0, 8.5 Hz), 3.4 (m, 2H), 2.8 (m, 2H), 2.6 (s, 1H), 2.53 (apparent sept, partially hidden, 1H, J=7.4 Hz), 2.30–2.10 (m, 6H), 1.80 (m, 2H), 1.25 (d, 6H, J=7.1 Hz, overlapped); ESMS m/e: 542.6 (M+), 543.54 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07067534B1 |
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| Source dataset | uspto-grants-2006_06 |
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| ORD ID | ord-d00b58242aab4ef4af99923aaeaf39a1 |
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| Source note | uspto-grants-2006_06 |
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