HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850142Generated: November 1, 2026
HCID 86730178, compound → HCID 86730179, compound
https://huagongshe.com/reaction/1850142
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 86730178 | HCID 86730178 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86730179 | HCID 86730179 | 69.5% |
Reaction Steps
2-(1-azidoethyl)-4-(4-fluorophenoxy)pyrimidine (120 mg, 0.463 mmol) was dissolved in 2 mL neat EtOH. 24.6 mg (0.023 mmol) of 10% Palladium on carbon catalyst was added. With vigorous stirring, the reaction vial was evacuated and purged 3 times with H2. The reaction vessel was fitted with an H2 balloon and stirred for 2 h. The mixture was filtered through Celite and concentrated in vacuo to give 75 mg (69%) 1-(4-(4-fluorophenoxy)pyrimidin-2-yl)ethanamine as a brown oil. 1H NMR (400 MHz, CDCl3) δ 8.45 (d, J=5.7 Hz, 1H), 7.13-6.92 (m, 4H), 6.59 (d, J=5.7 Hz, 1H), 4.00 (q, J=6.8 Hz, 1H), 1.34-1.30 (m, 3H). Anal. RP-HPLC tR=1.18 min. (Column=Inertsil C8 Column, 3.0 μm, 3.0×30 mm. Column Temperature=50° C. Eluents=A: Water (5 mM Ammonium formate, 2% ACN); B: ACN. Flow Rate=2 mL/min. Gradient=0 min 5% B; 5% to 95% B in 1.70 min; 0.3 min 95% B; 2.1 min 1% B.) MS m/z 234.2 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08957068B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-59719184d73747f28573378d2bec5326 |
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| Source note | uspto-grants-2015_02 |
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