HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1670201Generated: October 30, 2026
Diglyme → 6-(2-Fluoro-4-nitrophenoxy)-N-(4-methoxybenzyl)pyrimidin-4-amine
https://huagongshe.com/reaction/1670201
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diglyme | HCID 8150 | — |
| Reactant | 2-Fluoro-4-nitrophenol | HCID 9825 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 6-Chloro-N-(4-methoxybenzyl)pyrimidin-4-amine | HCID 22309497 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 6-(2-Fluoro-4-nitrophenoxy)-N-(4-methoxybenzyl)pyrimidin-4-amine | HCID 59301605 | 76% |
Reaction Steps
A mixture of N-(4-methoxybenzyl)-6-chloropyrimidin-4-amine (2.3 g, 9.2 mmol), 2-fluoro-4-nitrophenol (1.45 g, 9.2 mmol), DIPEA (15 mL), and 2-methoxyethyl ether (75 mL) was heated at 160° C. in a sealed pressure bottle for 50 h. The mixture was cooled, poured onto crushed ice (200 g), treated with EtOAc (200 mL). After vigorously stirring for 10 min, the insoluble material was filtered off. The EtOAc phase was washed with saturated aq. Na2CO3 solution (100 mL), brine (3×100 mL), dried (MgSO4) and concentrated in vacuo. The gummy solid obtained was triturated with isopropyl ether to give the title compound (1.75 g, 76%) as a brown solid. 1H NMR (DMSO-d6) δ 8.32 (dd, 1H, J=10.2, 2.0 Hz), 8.15 (d, 2H, J=9.2 Hz), 8.05 (br s, 1H), 7.61 (dd, 1H, J=8.4, 8.4 Hz), 7.26 (d, 2H, J=8.5 Hz), 6.91 (d, 2H, J=8.5 Hz), 6.14 (br s, 1H), 4.48 (br s, 2H), 3.74 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07989477B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-76156b78f019425687d74faf0b5a72eb |
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| Source note | uspto-grants-2011_08 |
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